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18 pages, 3601 KiB  
Article
The Application of Near-Infrared Spectroscopy Combined with Chemometrics in the Determination of the Nutrient Composition in Chinese Cyperus esculentus L.
by Xiaobo Jiao, Dongliang Guo, Xinjun Zhang, Yunpeng Su, Rong Ma, Lewen Chen, Kun Tian, Jingyu Su, Tangnuer Sahati, Xiahenazi Aierkenjiang, Jingjing Xia and Liqiong Xie
Foods 2025, 14(3), 366; https://doi.org/10.3390/foods14030366 - 23 Jan 2025
Viewed by 388
Abstract
The nutritional content of tiger nut (Cyperus esculentus L.) is abundant, rich in oil, protein, and starch. Conventional methods for assessing the nutrient composition of tiger nuts (TNs) are time-consuming and labor-intensive. Near-infrared spectroscopy (NIR) combined with chemometrics has been widely applied [...] Read more.
The nutritional content of tiger nut (Cyperus esculentus L.) is abundant, rich in oil, protein, and starch. Conventional methods for assessing the nutrient composition of tiger nuts (TNs) are time-consuming and labor-intensive. Near-infrared spectroscopy (NIR) combined with chemometrics has been widely applied in rapidly predicting the nutritional content of various crops, but its application to TNs is rare. In order to enhance the practicality of the method, this study employed a portable NIR in conjunction with chemometrics to rapidly predict the contents of crude oil (CO), crude protein (CP), and total starch (TS) from TNs. In the period from 2022 to 2023, we collected a total of 75 TN tuber samples of 28 varieties from Xinjiang Uyghur Autonomous Region and Henan Province. The three main components were measured using common chemical analysis methods. Partial least squares regression (PLSR) was utilized to establish prediction models between NIR and chemical indicators. In addition, to further enhance the prediction performance of the models, various preprocessing and variable selection algorithms were utilized to optimize the prediction models. The optimal models for CO, CP, and TS exhibited coefficient of determination (R2) values of 0.8946, 0.8525, and 0.8778, with root mean square error of prediction (RMSEP) values of 1.1764, 0.7470, and 1.4601, respectively. The absolute errors between the predicted and actual values for the three-indicator spectral measurements were 0.80, 0.59, and 0.99. The results demonstrated that the portable NIR combined with chemometrics could be effectively utilized for the rapid analysis of quality-related components in TNs. With further refinements, this approach could revolutionize TN quality assessment and be used to determine optimal harvest times, as well as facilitate the graded marketing of TNs. Full article
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Graphical abstract

Graphical abstract
Full article ">Figure 1
<p>Near-infrared spectra of TNs. (<b>A</b>) Raw spectra. (<b>B</b>) Savitzky–Golay smoothing (S–G smoothing). (<b>C</b>) Standard Normal Variate (SNV). (<b>D</b>) Multiplicative Scatter Correction (MSC).</p>
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<p>The model results of full-spectrum analysis combined with three preprocessing methods, where (<b>A</b>–<b>D</b>) represent CO models for raw, S–G smoothing, SNV, and MSC, respectively. (<b>E</b>–<b>H</b>) are CP models for raw, S–G smoothing, SNV, and MSC, respectively. (<b>I</b>–<b>L</b>) are TS models for raw, S–G smoothing, SNV, and MSC, respectively. Red represents the training set, and blue represents the test set.</p>
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<p>The summary of the optimal model results for CO under different variable selection algorithms. (<b>A</b>–<b>D</b>) are the selected regions of MWPLS, iPLS, UVE-SPA, and ICO, respectively. (<b>E</b>–<b>H</b>) represent the model results by utilizing the corresponding selected regions. Red represents the training set, and blue represents the test set.</p>
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<p>The summary of optimal model results for CP under different variable selection algorithms. (<b>A</b>–<b>D</b>) are the selected regions of MWPLS, iPLS, UVE-SPA, and ICO, respectively. (<b>E</b>–<b>H</b>) represent the model results by utilizing the corresponding selected regions. Red represents the training set, and blue represents the test set.</p>
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<p>The summary of optimal model results for TS under different variable selection algorithms. (<b>A</b>–<b>D</b>) are the selected regions of MWPLS, iPLS, UVE-SPA, and ICO, respectively. (<b>E</b>–<b>H</b>) represent the model results by utilizing the corresponding selected regions. Red represents the trainging set, and blue represents the test set.</p>
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<p>Comparison of the R<sub>pre</sub><sup>2</sup> and RMSEP values by variable selection and full-spectrum PLS. (<b>A</b>) is R<sub>pre</sub><sup>2</sup>. (<b>B</b>) is RMSEP.</p>
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25 pages, 6999 KiB  
Article
From Young to Over-Mature: Long-Term Cultivation Effects on the Soil Nutrient Cycling Dynamics and Microbial Community Characteristics Across Age Chronosequence of Schima superba Plantations
by Yangyang Sun, Yajing Zhang, Liyan Wang, Xinyu Zhang, Yuhui Jiang, Mulualem Tigabu, Pengfei Wu, Ming Li and Xia Hu
Forests 2025, 16(1), 172; https://doi.org/10.3390/f16010172 - 17 Jan 2025
Viewed by 503
Abstract
Optimizing forest management requires a comprehensive understanding of how soil properties and microbial communities evolve across different plantation ages. This study examines variations in soil nutrient dynamics, enzyme activities, and bacterial communities in Schima superba Gardn. & Champ plantations of 10, 15, 27, [...] Read more.
Optimizing forest management requires a comprehensive understanding of how soil properties and microbial communities evolve across different plantation ages. This study examines variations in soil nutrient dynamics, enzyme activities, and bacterial communities in Schima superba Gardn. & Champ plantations of 10, 15, 27, 55, and 64 years. By analyzing soil from depths of 0–20 cm, 20–40 cm, and 40–60 cm, we identified significant age-related trends in soil characteristics. Notably, nutrient contents, including total organic carbon (TOC), total phosphorus (TP), total carbon (TC), total nitrogen (TN), and nitrate nitrogen (NO3-N), as well as soil water content (SWC), peaked in 55-year-old mature plantations and decreased in 64-year-old over-mature plantations. Enzyme activities, such as urease, sucrase, and acid phosphatase, decreased with soil depth and exhibited notable differences across stand ages. Microbial community analysis indicated the predominance of Acidobacteria, Chloroflexi, Proteobacteria, Actinobacteria, and Verrucomicrobiota in nutrient cycling, with their relative abundances varying significantly with age and depth. Mature and over-mature plantations exhibited higher absolute abundances of functional genes related to methane metabolism, nitrogen, phosphorus, and sulfur cycling. Reduced calcium ion levels were also linked to lower gene abundance in carbon degradation, carbon fixation, nitrogen, and phosphorus cycling, while increased TOC, NH4+-N, NO3-N, and AP correlated with higher gene abundance in methane metabolism and phosphorus cycling. Our findings suggest that long-term cultivation of Schima superba enhances soil nutrient cycling. Calcium ion was identified as a significant factor in assessing soil properties and microbial dynamics across different stand ages, suggesting that extended plantation rotations can improve soil health and nutrient cycling. Full article
(This article belongs to the Section Forest Ecology and Management)
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Figure 1

Figure 1
<p>Physical and chemical properties of soil in <span class="html-italic">Schima superba</span> plantations across different stand ages and soil layers. (<b>a</b>) the bulk density of soil (BD), (<b>b</b>) soil moisture content (SWC), (<b>c</b>) soil pH (pH), (<b>d</b>) the concentration of total organic carbon (TOC), (<b>e</b>) the concentration of total phosphorus (TP), (<b>f</b>) the concentration of total nitrogen (TN), (<b>g</b>) the concentration of total carbon (TC), (<b>h</b>) the concentration of ammonium nitrogen (<math display="inline"><semantics> <mrow> <msubsup> <mi>NH</mi> <mn>4</mn> <mo>+</mo> </msubsup> </mrow> </semantics></math>-N), (<b>i</b>) the concentration of available phosphorus (AP), (<b>j</b>) the concentration of total potassium (TN), (<b>k</b>) the concentration of nitrate nitrogen (<math display="inline"><semantics> <mrow> <msubsup> <mi>NO</mi> <mn>3</mn> <mo>−</mo> </msubsup> </mrow> </semantics></math>-N), and (<b>l</b>) the concentration of calcium ions (Ca<sup>2+</sup>). Different lowercase letters indicate significant differences among soil layers within the same stand age, while different uppercase letters indicate significant differences among stand ages within the same soil layer, both at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Soil enzyme activities in <span class="html-italic">Schima superba</span> plantations under different stand ages. (<b>a</b>) the activity of acid phosphatase (AP), (<b>b</b>) the activity of catalase (CAT), (<b>c</b>) the activity of urease (UE), and (<b>d</b>) the activity of sucrase (SC). Different lowercase letters indicate significant differences among soil layers within the same stand age, while different uppercase letters indicate significant differences among stand ages within the same soil layer, both at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Relative abundance of community composition at the level of bacterial phylum where panels (<b>a</b>), (<b>b</b>) and (<b>c</b>) represent soil layers of 0–20 cm, 20–40 cm, and 40–60 cm in sequence, respectively.</p>
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<p>Redundancy analysis of soil physicochemical properties, enzyme activities, and bacterial communities across different stand ages where panels (<b>a</b>), (<b>b</b>) and (<b>c</b>) represent soil layers of 0–20 cm, 20–40 cm, and 40–60 cm, respectively. Blue represents soil bacterial communities, orange represents soil physicochemical properties and enzyme activities.</p>
Full article ">Figure 4 Cont.
<p>Redundancy analysis of soil physicochemical properties, enzyme activities, and bacterial communities across different stand ages where panels (<b>a</b>), (<b>b</b>) and (<b>c</b>) represent soil layers of 0–20 cm, 20–40 cm, and 40–60 cm, respectively. Blue represents soil bacterial communities, orange represents soil physicochemical properties and enzyme activities.</p>
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<p>Heat map of correlations between soil physicochemical properties, enzyme activities, and bacterial communities across different stand ages where panels (<b>a</b>), (<b>b</b>) and (<b>c</b>) represent soil layers of 0–20 cm, 20–40 cm, and 40–60 cm, respectively.</p>
Full article ">Figure 5 Cont.
<p>Heat map of correlations between soil physicochemical properties, enzyme activities, and bacterial communities across different stand ages where panels (<b>a</b>), (<b>b</b>) and (<b>c</b>) represent soil layers of 0–20 cm, 20–40 cm, and 40–60 cm, respectively.</p>
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<p>Absolute abundance of soil bacterial functional genes across different stand ages. (<b>a</b>) the absolute abundances of 16SrDNA, (<b>b</b>) the absolute abundances of C degradation, (<b>c</b>) the absolute abundances of C fixation, (<b>d</b>) the absolute abundances of Methane metabolism, (<b>e</b>) the absolute abundances of N cycling, (<b>f</b>) the absolute abundances of P cycling, (<b>g</b>) the absolute abundances of S cycling, and (<b>h</b>) the absolute abundances of the sum of all functional genes. Different lowercase letters indicate significant differences among stand ages at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Heat map of the correlation between soil physicochemical properties and the bacterial functional gene abundance across different stand ages, where pink and orange indicate negative and positive correlations between variables, respectively. The darker the color, the closer the relationship. * and ** represent <span class="html-italic">p</span> &lt; 0.05 and <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Partial least squares pathway model (PLS-PM) illustrating the numerical values for the direct effects between modules were (<b>a</b>) the partial least squares pathway model of carbon degradation, (<b>b</b>) the partial least squares pathway model of carbon fixation, (<b>c</b>) the partial least squares pathway model of methane metabolism, (<b>d</b>) the partial least squares pathway model of N cycling, (<b>e</b>) the partial least squares pathway model of P cycling, and (<b>f</b>) the partial least squares pathway model of S cycling. Solid lines indicate positive effects, dashed lines indicate negative effects, and red lines denote significance levels with <span class="html-italic">p</span>-values of &lt;0.05 (*) and &lt;0.001 (***). The abbreviations are as follows: Soil PC (soil physicochemical), Ba. Com. (bacterial communities), and Ba. Div. (bacterial diversity).</p>
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21 pages, 6032 KiB  
Article
Developmental Proteomics Reveals the Dynamic Expression Profile of Global Proteins of Haemaphysalis longicornis (Parthenogenesis)
by Min-Xuan Liu, Xiao-Pei Xu, Fan-Ming Meng, Bing Zhang, Wei-Gang Li, Yuan-Yuan Zhang, Qiao-Ying Zen and Wen-Ge Liu
Life 2025, 15(1), 59; https://doi.org/10.3390/life15010059 - 6 Jan 2025
Viewed by 483
Abstract
H. longicornis is used as an experimental animal model for the study of three-host ticks due to its special life cycle and easy maintenance in the laboratory and in its reproduction. The life cycle of H. longicornis goes through a tightly regulated life [...] Read more.
H. longicornis is used as an experimental animal model for the study of three-host ticks due to its special life cycle and easy maintenance in the laboratory and in its reproduction. The life cycle of H. longicornis goes through a tightly regulated life cycle to adapt to the changing host and environment, and these stages of transition are also accompanied by proteome changes in the body. Here, we used the isobaric tags for a relative and absolute quantification (iTRAQ) technique to systematically describe and analyze the dynamic expression of the protein and the molecular basis of the proteome of H. longicornis in seven differential developmental stages (eggs, unfed larvae, engorged larvae, unfed nymphs, engorged nymphs unfed adults, and engorged adults). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis of the differentially expressed proteins (DEPs) were used. In our study, A total of 2044 proteins were identified, and their expression profiles were classified at different developmental stages. In addition, it was found that tissue and organ development-related proteins and metabolism-related proteins were involved in different physiological processes throughout the life cycle through the GO and KEGG analysis of DEPs. More importantly, we found that the up-regulated proteins of engorged adult ticks were mainly related to yolk absorption, degradation, and ovarian development-related proteins. The abundance of the cuticle proteins in the unfed stages was significantly higher compared with those of the engorged ticks in the previous stages. We believe that our study has made a significant contribution to the research on H. longicornis, which is an important vector of SFTSV. In this study, we identified changes in the proteome throughout the H. longicornis development, and functional analysis highlighted the important roles of many key proteins in developmental events (ovarian development, the molting process, the development of midgut, the development and degeneration of salivary glands, etc.). The revelation of this data will provide a reference proteome for future research on tick functional proteins and candidate targets for elucidating H. longicornis development and developing new tick control strategies. Full article
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Graphical abstract

Graphical abstract
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<p>(<b>A</b>) Wayne diagram of the total proteins identified by three repeated experiments on <span class="html-italic">H. longicornis</span>. R1, repeat 1; R2, repeat 2; and R3, repeat 3. (<b>B</b>) Distribution of the specific peptides and (<b>C</b>) protein coverage distribution.</p>
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<p>Comparative analysis of the differentially expressed proteins (DEPs) in the different developmental stages of <span class="html-italic">H. longicornis</span>. EE, egg; UL, unfed larva; FL, engorged larva; UN, unfed nymph.</p>
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<p>The heat map represents the proteome analysis results of six genes compared across different developmental stages, while the bar graph of (<b>A</b>–<b>F</b>) displays the RT-qPCR analysis results for CRK, flotillin, Mo-25, dystrophin, septin-1, and septin-2, respectively). EE, egg; UL, unfed larva; FL, engorged larva; UN, unfed nymph; FN, engorged nymph; UA, unfed adult; FA, engorged adult.</p>
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<p>Chitin-binding proteins. EE, egg; UL, unfed larva; FL, engorged larva; UN, unfed nymph; FN, engorged nymph; UA, unfed adult; FA, engorged adult.</p>
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<p>Digestion-related proteins. EE, egg; UL, unfed larva; FL, engorged larva; UN, unfed nymph; FN, engorged nymph; UA, unfed adult; FA, engorged adult.</p>
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<p>Vitellogenin (Vg)-related proteins. EE, egg; UL, unfed larva; FL, engorged larva; UN, unfed nymph; FN, engorged nymph; UA, unfed adult; FA, engorged adult.</p>
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<p>Cuticle-related proteins. EE, egg; UL, unfed larva; FL, engorged larva; UN, unfed nymph; FN, engorged nymph; UA, unfed adult; FA, engorged adult.</p>
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<p>Membrane proteins. EE, egg; UL, unfed larva; FL, engorged larva; UN, unfed nymph; FN, engorged nymph; UA, unfed adult; FA, engorged adult.</p>
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<p>Salivary proteins. EE, egg; UL, unfed larva; FL, engorged larva; UN, unfed nymph; FN, engorged nymph; UA, unfed adult; FA, engorged adult.</p>
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<p>Secreted proteins. EE, egg; UL, unfed larva; FL, engorged larva; UN, unfed nymph; FN, engorged nymph; UA, unfed adult; FA, engorged adult.</p>
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<p>Gene Ontology (GO) enrichment for the differentially expressed proteins (DEPs) (<span class="html-italic">p</span> &lt; 0.05) of the different life stages of <span class="html-italic">H. longicornis</span>. (<b>A</b>) Unfed larva vs. egg, (<b>B</b>) engorged larva vs. unfed larva, and (<b>C</b>) unfed nymph vs. engorged larva. GO functional annotations in the three main categories: molecular function, cellular component, and biological process.</p>
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<p>Gene Ontology (GO) enrichment for the differentially expressed proteins (DEPs) (<span class="html-italic">p</span> &lt; 0.05) of the different life stages of <span class="html-italic">H. longicornis</span>. (<b>A</b>) Engorged nymph vs. unfed nymph, (<b>B</b>) unfed adult vs. engorged nymph, and (<b>C</b>) engorged adult vs. unfed adult. The GO functional annotations are in three main categories: molecular function, cellular component, and biological process.</p>
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<p>Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis of the differentially expressed proteins (DEPs) (<span class="html-italic">p</span> &lt; 0.05) of the different life stages of <span class="html-italic">H. longicornis</span>. <span class="html-italic">p</span> &lt; 0.05 indicates significant enrichment in the development-related pathways. The top 20 pathways are shown. (<b>A</b>) Unfed larva vs. egg, (<b>B</b>) engorged larva vs. unfed larva, and (<b>C</b>) unfed nymph vs. engorged larva. The KEGG enrichment was measured by the Rich factor, <span class="html-italic">q</span>-value, and the number of genes enriched in this pathway. The colors and sizes of the spots represent the <span class="html-italic">q</span>-values and the number of target genes, respectively. EE, egg; UL, unfed larva; FL, engorged larva; UN, unfed nymph.</p>
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<p>Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis of the differentially expressed proteins (DEPs) (<span class="html-italic">p</span> &lt; 0.05) of the different life stages of <span class="html-italic">H. longicornis</span>. <span class="html-italic">p</span> &lt; 0.05 indicates significant enrichment in the development-related pathways. The top 20 pathways are shown. (<b>A</b>) engorged nymph vs. unfed nymph, (<b>B</b>) unfed adult vs. engorged nymph, and (<b>C</b>) engorged adult vs. unfed adult. The KEGG enrichment was measured by the Rich factor, <span class="html-italic">q</span>-value, and number of genes enriched in this pathway. The colors and sizes of the spots represent the <span class="html-italic">q</span>-values and the number of target genes, respectively. UN, unfed nymph; FN, engorged nymph; UA, unfed adult; FA, engorged adult.</p>
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12 pages, 3732 KiB  
Article
Analysis of the Distribution Pattern and Prophage Types in Candidatus Liberibacter Asiaticus ‘Cuimi’ Kumquat
by Wen-Ting Li, Xiao-Feng Teng, Li He, Bin Guan, Cui-Ling He, Jian-Jun Liu, Ke-Ling Chen, Zheng Zheng and Jian He
Plants 2025, 14(1), 94; https://doi.org/10.3390/plants14010094 - 31 Dec 2024
Viewed by 494
Abstract
The ‘Cuimi’ kumquat is a unique citrus cultivar known for its thin, crisp pulp and sweet, aromatic flavor. In addition to its use in fresh consumption and processing, this variety exhibits certain medicinal properties. This study aims to investigate the genetic diversity of [...] Read more.
The ‘Cuimi’ kumquat is a unique citrus cultivar known for its thin, crisp pulp and sweet, aromatic flavor. In addition to its use in fresh consumption and processing, this variety exhibits certain medicinal properties. This study aims to investigate the genetic diversity of the Huanglongbing (HLB) bacterium across different tissues of the ‘Cuimi’ kumquat, offering a theoretical basis for understanding the HLB epidemic in Dechang County, Sichuan. The research focuses on the absolute quantification of the HLB bacterium in seven specific tissues of the ‘Cuimi’ kumquat, including new leaves, upper phloem of branches, fruit peduncle, pith, fruit axis, old leaves, and lower phloem of branches. Additionally, the types and contents of prophages were identified in these tissues. In the same diseased branch group, Candidatus Liberibacter asiaticus (CLas) exhibited an uneven distribution, with the highest concentration detected in the pith, significantly surpassing levels found in the stem and leaf tissues (new leaves, upper phloem of branches, old leaves, lower phloem of branches). Infected fruit peduncles and pith slices showed noticeable shrinkage and collapse in the phloem. Prophage analysis indicated that multiple types of prophages could be simultaneously detected within the same infected ‘Cuimi’ kumquat branch. New shoot tissues contained both Type 2 and Type 4 prophages, with a relatively higher abundance of Type 4 and a lower abundance of Type 2. The relative abundance of Type 1 prophage in the fruit tissues was generally higher than in other tissues. CLas primarily accumulates in the fruit tissues of the ‘Cuimi’ kumquat, and the situation in Dechang County suggests that individual trees may be infected with multiple prophage strains simultaneously. Full article
(This article belongs to the Special Issue Mycology and Plant Pathology)
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Figure 1

Figure 1
<p>Branches symptoms of ‘Cuimi’ kumquat infected with HLB. Note: 1: New Leaves, 2: Upper phloem of branches, 3: Pedicel, 4: Fruit axis, 5: Pith, 6: Old leaves, 7: Lower phloem of branches.</p>
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<p>Construction of the standard curves.</p>
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<p>Healthy and HLB-infected ‘Cuimi’ kumquat fruits.</p>
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<p>Anatomical structure of pith from healthy and infected fruits. Note: Pa: parenchyma; Ph: phloem; XY: xylem. Red arrows denote wrinkled phloem. Bars = 50 μm. (<b>A</b>) The upper section of healthy citrus pith with the horizontally cut; (<b>B</b>) The middle section of healthy citrus pith with the horizontally cut; (<b>C</b>) The lower section of healthy citrus pithwith the horizontally cut; (<b>D</b>) The upper section of HLB-infected citrus pith with the horizontally cut; (<b>E</b>) The middle section of HLB-infected citrus pith with the horizontally cut; (<b>F</b>) The lower section of HLB-infected citrus pith with the horizontally cut; (<b>G</b>) The upper section of healthy citrus pith with the vertically cut; (<b>H</b>) The middle section of healthy citrus pith with the vertically cut; (<b>I</b>) The lower section of healthy citrus pithwith the vertically cut; (<b>J</b>) The upper section of HLB-infected citrus pith with the vertically cut; (<b>K</b>) The middle section of HLB-infected citrus pith with the vertically cut; (<b>L</b>) The lower section of HLB-infected citrus pith with the vertically cut.</p>
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<p>The content of CLas in different tissues of ‘Cuimi’ kumquat. Note: different letters indicate significant differences in 95% confidence intervals (Duncan’s, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Content of CLas in different segments of ‘Cuimi’ kumquat peduncles. Note: Different patterns represent the copy number of CLas: 0–1 cm represents the upper pith, 1.0–2.0 cm represents the middle pith, 2.0–3.0 cm represents the lower pith. The numbers on the right represent the sample numbers.</p>
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16 pages, 3204 KiB  
Article
Dietary Quercetin Regulates Gut Microbiome Diversity and Abundance in Apis cerana (Hymenoptera Apidae)
by Haodong Wu, Conghui Ji, Ruisheng Wang, Lijiao Gao, Wenhua Luo and Jialin Liu
Insects 2025, 16(1), 20; https://doi.org/10.3390/insects16010020 - 28 Dec 2024
Viewed by 656
Abstract
Honeybee gut microbiota plays a crucial role in maintaining their health and digestive function. Studies have confirmed that quercetin improves honeybee health by enhancing their pesticide tolerance and survival rates. This study aimed to examine the effects of quercetin on the bee gut [...] Read more.
Honeybee gut microbiota plays a crucial role in maintaining their health and digestive function. Studies have confirmed that quercetin improves honeybee health by enhancing their pesticide tolerance and survival rates. This study aimed to examine the effects of quercetin on the bee gut microbiome by absolute quantification sequencing. We included 1800 bees from the experimental apiary and exposed them to 151.2, 75.6, and 37.8 mg/L of quercetin. Gut samples were collected on the 5th and 9th days, subjected to a polymerase chain reaction and 16S rRNA sequencing, and analyzed. After 5 days of quercetin treatment, the diversity of the honeybee gut microbiota was altered, and total bacterial copies and Lactobacillus abundance significantly decreased at high quercetin concentrations (151.2 and 75.6 mg/L). On day 9, the gut microbial community had recovered from the adverse effects, and Gilliamella abundance increased in response to 37.8 mg/L quercetin treatment. However, quercetin had no noticeable effects on survival rate, food consumption, and gut structure. Our study confirmed the effect of short-term quercetin intake on the gut microbiota of A. cerana, providing valuable insights into how phytochemicals alter the bee gut microbiome, and their repercussions on host physiology. Full article
(This article belongs to the Section Social Insects)
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Figure 1

Figure 1
<p>Worker survival rate and sucrose solution consumption. (<b>A</b>) Quercetin’s effect on honeybee survival is shown in Kaplan–Meier survival curves. (<b>B</b>) Sucrose solution consumption of honeybees under quercetin treatment over a 9-day period. Error bars showed the standard error of the mean. CK, control group. N = 5; 40 honeybees/replicate.</p>
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<p>Classification analysis of the gut microbiota community of the worker bees at phylum and genus levels. (<b>A</b>) Relative abundance of dominant bacterial communities at the phylum level; (<b>B</b>) absolute abundance of dominant bacterial communities at the phylum level; (<b>C</b>) relative abundance of dominant bacterial communities at the genus level; (<b>D</b>) absolute abundance of dominant bacterial communities at the genus level. CK, control group.</p>
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<p>Alpha diversity between the control and quercetin treatment groups, measured by the Shannon, Simpson, and Chao1 indices. (<b>A</b>) Shannon index at 5 days. (<b>B</b>) Simpson index at 5 days. (<b>C</b>) Chao1 index at 5 days. (<b>D</b>) Shannon index at 9 days. (<b>E</b>) Simpson index at 9 days. (<b>F</b>) Chao1 index at 9 days. Tested for differences between groups using Kruskal‒Wallis analysis, α = 0.05. CK, control group.</p>
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<p>The absolute abundance of total bacterial copies and the five most abundant bacterial genera of <span class="html-italic">A. cerana</span> workers were measured as copies of the 16S rRNA gene. (<b>A</b>) Total bacteria copies; (<b>B</b>) <span class="html-italic">Lactobacillus</span>; (<b>C</b>) <span class="html-italic">Gilliamella</span>; (<b>D</b>) <span class="html-italic">Snodgrassella</span>; (<b>E</b>) <span class="html-italic">Apibacter</span>; (<b>F</b>) <span class="html-italic">Bifidobacterium</span>. Tested for differences between groups using Kruskal‒Wallis analysis, α = 0.05. CK, control group.</p>
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<p>Absolute abundance of differentially non-dominant bacteria of <span class="html-italic">A. cerana</span> workers after quercetin treatment. (<b>A</b>) <span class="html-italic">Escherichia-shigella</span> copies differed after 5 days of quercetin treatment. (<b>B</b>) <span class="html-italic">Proteobactera</span>-unclassified copies differed after 9 days of quercetin treatment. Tested for differences between groups using Kruskal‒Wallis analysis, α = 0.05. CK, control group.</p>
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<p>Beta diversity analysis using principal coordinate analysis (PCoA) based on the Bray‒Curtis dissimilarity index for absolute abundance at 5 days (<b>A</b>) and 9 days (<b>B</b>). Tested for differences between groups using PERMANOVA analysis, α= 0.05. CK, control group.</p>
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<p>Cross sections of the gut of worker bees under quercetin treatment on days 5 and 9, with hematoxylin and eosin staining (200×).</p>
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16 pages, 2137 KiB  
Article
Influences of Growth-Related Myopathies on Peptide Patterns of In Vitro Digested Cooked Chicken Breast and Stress-Related Responses in an Intestinal Caco-2 Cell Model
by Yuwares Malila, Sunitta Saensa-ard, Chanikarn Kunyanee, Nalinrat Petpiroon, Nantanat Kosit, Sawanya Charoenlappanit, Narumon Phaonakrop, Yanee Srimarut, Sasitorn Aueviriyavit and Sittiruk Roytrakul
Foods 2024, 13(24), 4042; https://doi.org/10.3390/foods13244042 - 14 Dec 2024
Viewed by 680
Abstract
The objective of this study was to determine the effects of growth-related myopathies, i.e., normal, wooden breast (WB), white striping (WS), and the combined lesions of WS and WB (WS + WB), on the molecular response of Caco-2 cells. A total of 24 [...] Read more.
The objective of this study was to determine the effects of growth-related myopathies, i.e., normal, wooden breast (WB), white striping (WS), and the combined lesions of WS and WB (WS + WB), on the molecular response of Caco-2 cells. A total of 24 cooked chicken breasts (n = 6 per myopathy) was subjected to an in vitro digestion using an enzymatic process mimicking human gastrointestinal digestion. Based on peptidomics, in vitro protein digestion of the abnormal samples, particularly WB meat, resulted in more peptides with lower molecular mass relative to those of normal samples. The cooked meat hydrolysates obtained at the end of the digestion were applied to a Caco-2 cell model for 4 h. The cell viability of treated normal and abnormal samples was not different (p ≥ 0.05). Absolute transcript abundances of genes associated with primary oxidative stress response, including nuclear factor erythroid 2 like 2, superoxide dismutase, and hypoxia-inducible factor 1 were determined using a droplet digital polymerase chain reaction. No significant differences in transcript abundance of those genes in Caco-2 cells were demonstrated between normal and the abnormal samples (p ≥ 0.05). Overall, the findings supported that, compared to normal meat, the cooked chicken meat with growth-related myopathies might be digested and absorbed to a greater extent. The cooked abnormal meat did not exert significant transcriptional impacts regarding oxidative stress on the human epithelial Caco-2 cells. Full article
(This article belongs to the Section Meat)
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<p>Different peptides (≤3000 Da) were released during in vitro digestion of cooked chicken breasts affected by various growth-related myopathies (normal, wooden breast (WB), white striping (WS), and WS + WB). (<b>a</b>) The scatter plot shows partial least squares discriminant analysis (PLS-DA). (<b>b</b>) Differential peptides (purple dots) are identified based on analysis of variance (FDR &lt; 0.05).</p>
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<p>Mass distribution of ≤3000 Da peptides in the hydrolyzed cooked chicken meat. The <span class="html-italic">x</span>-axis represents the mass (Da), and the <span class="html-italic">y</span>-axis represents the frequency of the occurrence. Each histogram depicts the mass distribution within the supernatants from (<b>a</b>) normal, (<b>b</b>) wooden breast (WB), (<b>c</b>) white striping (WS), (<b>d</b>) WS + WB, and (<b>e</b>) enzyme mixture samples.</p>
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<p>Caco-2 cell viability after treatment with 0.2 m of filtrate obtained from in vitro digested chicken breasts with different growth-related myopathies, including (<b>a</b>) normal, (<b>b</b>) wooden breast (WB), (<b>c</b>) white striping (WS), and (<b>d</b>) WS + WB samples. The filtrate obtained from enzyme mixture (<b>e</b>) was included in the experiment. Bars and error bars represent the mean and standard deviation, respectively. Different letters above bars indicate a significant difference (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Effects of different growth-related myopathies (i.e., normal, white striping (WS), wooden breast (WB), and WS + WB) among chicken breasts on Caco-2 cell viability. The cells were treated with (<b>a</b>) 2.5% (<span class="html-italic">v</span>/<span class="html-italic">v</span>), (<b>b</b>) 5.0% (<span class="html-italic">v</span>/<span class="html-italic">v</span>), and (<b>c</b>) 10% (<span class="html-italic">v</span>/<span class="html-italic">v</span>), with the supernatants obtained via in vitro protein digestion. Bars and error bars represent the mean and standard deviation, respectively. Different letters above bars indicate a significant difference (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Absolute transcript quantification in Caco-2 cells using a droplet digital polymerase chain reaction. Effects of different growth-related myopathies (i.e., normal, white striping (WS), wooden nreast (WB), and WS + WB) were analyzed on three oxidative-stress response genes, including (<b>a</b>,<b>b</b>) <span class="html-italic">HIF1A</span>, (<b>c</b>,<b>d</b>) <span class="html-italic">NFE2L2</span>, and (<b>e</b>,<b>f</b>) <span class="html-italic">SOD1</span>. (<b>a</b>,<b>c</b>,<b>e</b>) One-dimensional scatter plots illustrate the positive droplets (blue dots above pink lines), containing target amplicons, and the negative droplets (dark dots below pink lines) without any amplicons. (<b>b</b>,<b>d</b>,<b>e</b>) Bar graphs depict the average transcript abundance (copies in 20-μL PCR reaction per ng template). Bars and error bars represent the mean and standard error, respectively. Different letters above bars indicate a significant difference (<span class="html-italic">p</span> &lt; 0.05).</p>
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12 pages, 2727 KiB  
Article
Elevational Gradients of Soil Nematode Communities in Subtropical Forest Ecosystems
by Kexin Ding, Zhenyu Qiang, Zhengkun Hu, Saisai Cheng, Ruibo Sun, Heng Fang, Zhen Zhang and Chao Ma
Forests 2024, 15(12), 2149; https://doi.org/10.3390/f15122149 - 5 Dec 2024
Viewed by 709
Abstract
Soil biodiversity plays a critical role in supporting multiple ecosystem functions. As some of the most diverse and abundant metazoans on the Earth, soil nematode communities exhibit changes along environmental gradients, but the ways in which the abundance and diversity of nematode communities [...] Read more.
Soil biodiversity plays a critical role in supporting multiple ecosystem functions. As some of the most diverse and abundant metazoans on the Earth, soil nematode communities exhibit changes along environmental gradients, but the ways in which the abundance and diversity of nematode communities vary along elevational gradients remain poorly understood. Taking advantage of an investigation on Huangshan Mountain, Southeast China, with elevation ranging from 500 to 1200 m, we assessed the abundance and diversity of soil nematodes, as well as the soil physicochemical properties, across subtropical forest ecosystems. Nematode communities were analyzed at the genus level, and the α-diversity was calculated as the genus richness, while the β-diversity was based on the Bray–Curtis dissimilarity. The results showed that, among the top 20 nematode genera ranked by absolute abundance, most genera, such as Eucephalobus, Prismatolaimus, Filenchus, and Rotylenchulus, reached their peak abundance at the highest elevation (1000 m). Additionally, the abundances of Oriverutus, Tylenchus, Criconema, and Tripyla exhibited a positive correlation with the elevation. Moreover, the abundance and α-diversity of the total nematodes and each trophic group of nematodes increased linearly with the elevation, likely due to increased soil moisture at higher elevation. In contrast, the β-diversity of the total nematodes, bacterivores, and herbivores decreased with increasing elevation, indicating the importance of stochastic processes in shaping community assembly at high altitudes. This pattern suggests that as the elevation increases, the nematode communities become more homogeneous in structure. Taken together, our study’s findings demonstrate the divergent responses of nematodes’ α- and β-diversity to an elevation gradient, highlighting the importance of the soil nematode diversity in maintaining ecosystem functions such as nutrient cycling and food web stability in mountainous regions. These results emphasize the need to incorporate the below-ground biodiversity into conservation strategies, particularly in the face of environmental changes driven by climate and human activities. Full article
(This article belongs to the Section Forest Soil)
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<p>Nematode abundance and diversity with increasing elevation. (<b>a</b>–<b>e</b>) abundance; (<b>f</b>–<b>j</b>) α-diversity; (<b>k</b>–<b>o</b>) β-diversity; (<b>p</b>–<b>t</b>) β-deviation. α-Diversity is measured by genera numbers of nematodes. β-Diversity is measured by Bray–Curtis dissimilarity. β-Deviation is the standardized effect size of the β-diversity, calculated by comparing the observed β-diversity to the null models. Significant regression lines are shown.</p>
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<p>Ordination plot of distance-based redundancy analysis (dbRDA) and decomposition of nematode β-diversity along elevational gradient. (<b>a</b>) dbRDA result illustrating the variation in nematode communities along elevational gradient. Percentage values in axis titles represent the explained community composition variation by each constrained axis. The contour lines in different colors indicate altitudes added passively using the <span class="html-italic">ordisurf</span> function from the <span class="html-italic">vegan</span> package with the default parameters. (<b>b</b>) Abundance-based Bray–Curtis dissimilarity was decomposed into balanced variation and abundance gradient components.</p>
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<p>Relative contributions of soil physicochemical properties to nematode abundance and diversity (α- and β-deviation). (<b>a</b>–<b>e</b>) abundance; (<b>f</b>–<b>j</b>) α-diversity; (<b>k</b>–<b>o</b>) β-deviation. The analysis was performed using linear mixed models and variance decomposition. The optimal model was selected based on the Akaike Information Criterion (AIC) and coefficients of determination. Significant differences at: *, <span class="html-italic">p</span> &lt; 0.05; **, <span class="html-italic">p</span> &lt; 0.01.</p>
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23 pages, 2768 KiB  
Article
Optimizing Green Extraction Methods for Maximizing the Biological Potential of Dandelion, Milk Thistle, and Chamomile Seed Extracts
by Stoja Milovanovic, Katarzyna Tyśkiewicz, Marcin Konkol, Agnieszka Grzegorczyk, Kinga Salwa and Łukasz Świątek
Foods 2024, 13(23), 3907; https://doi.org/10.3390/foods13233907 - 3 Dec 2024
Viewed by 1210
Abstract
This study investigates the underutilized potential of agri-crops from the Asteraceae family by employing sustainable and green technologies (supercritical fluid, ultrasound, and Soxhlet extractions) to enhance the recovery of bioactive compounds. A total of 21 extracts from native and waste seeds of dandelion, [...] Read more.
This study investigates the underutilized potential of agri-crops from the Asteraceae family by employing sustainable and green technologies (supercritical fluid, ultrasound, and Soxhlet extractions) to enhance the recovery of bioactive compounds. A total of 21 extracts from native and waste seeds of dandelion, milk thistle, and chamomile were systematically compared utilizing a combination of solvents (supercritical CO2 and absolute or aqueous ethanol). Supercritical CO2 extraction yielded up to 281 mg/g of oils from native seeds, while conventional techniques with ethanol recovered an additional 142 mg/g of extracts from waste seeds. Notably, waste seed extracts exhibited superior biological activity, including potent antioxidant properties (IC50 values as low as 0.3 mg/mL in the DPPH assay) and broad-spectrum antimicrobial activity against 32 microbial strains, including methicillin-resistant Staphylococcus aureus, Gram-negative bacteria, and yeast strains. Phenolic compounds were abundant, with up to 2126 mg GAE/g, alongside 25.9 mg QE/g flavonoids, and 805.5 mg/kg chlorophyll A. A selective anticancer activity of waste milk thistle extracts was observed, with a selectivity index of 1.9 to 2.7. The oils recovered from native seeds demonstrated lower bioactivity and are well-suited for applications in food. The potent bioactivity of the smaller quantities of waste seed extracts positions them as valuable candidates for pharmaceutical use. Full article
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<p>Extraction yield for native and waste seeds of (<b>a</b>) dandelion, (<b>b</b>) milk thistle, and (<b>c</b>) chamomile obtained by SFE, SXE, and USE using sc-CO<sub>2</sub>, absolute ethanol, or aqueous ethanol as solvents. Different letters (a–d) suggest that values are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Total phenolic content in oils and extracts from (<b>a</b>) dandelion, (<b>b</b>) milk thistle, and (<b>c</b>) chamomile native and waste seeds obtained via SFE, SXE, and USE using sc-CO<sub>2</sub>, absolute ethanol, or aqueous ethanol as solvents. Different letters (a–e) suggest that values are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Total phenolic content in oils and extracts from (<b>a</b>) dandelion, (<b>b</b>) milk thistle, and (<b>c</b>) chamomile native and waste seeds obtained via SFE, SXE, and USE using sc-CO<sub>2</sub>, absolute ethanol, or aqueous ethanol as solvents. Different letters (a–e) suggest that values are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Total flavonoid content in oils and extracts from (<b>a</b>) dandelion, (<b>b</b>) milk thistle, and (<b>c</b>) chamomile native and waste seeds obtained by SFE, SXE, and USE using sc-CO<sub>2</sub>, absolute ethanol, or aqueous ethanol as solvents. Different letters (a–f) suggest that values are significantly different (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Images of samples from native and waste seeds of dandelion (D), milk thistle (MT), and chamomile (C) obtained by SFE, SXE, and USE using sc-CO<sub>2</sub>, absolute ethanol, or aqueous ethanol as solvents.</p>
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<p>Antimicrobial data (MIC—minimum inhibitory concentration, MBC—minimum bactericidal concentration, and MFC—minimum fungicidal concentration) for extracts from dandelion (D), milk thistle (MT), and chamomile (C) seeds obtained by SXE using aqueous ethanol against reference microorganisms.</p>
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<p>Cytotoxicity of selected extracts from dandelion (D), milk thistle (MT), and chamomile (C) seeds obtained by SXE using aqueous ethanol. (CC<sub>50</sub>—concentration resulting in a 50% reduction in cell viability; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001; **** <span class="html-italic">p</span> &lt; 0.0001).</p>
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12 pages, 4591 KiB  
Article
Polypyrrole-Derived Nitrogen-Doped Tubular Carbon Materials as a Promising Cathode for Aqueous Aluminum-Ion Batteries
by Xiaoming Zhou, Xiaolei Li, Jiaming Duan, Lihao Zhang, Xinyu Mo, Qing Wu, Yang Liu, Guohui Yuan and Miaosen Yang
Polymers 2024, 16(23), 3276; https://doi.org/10.3390/polym16233276 - 25 Nov 2024
Viewed by 520
Abstract
The advantages of aluminum-ion batteries in the area of power source systems are: inexpensive manufacture, high capacity, and absolute security. However, due to the limitations of cathode materials, the capacity and durability of aluminum-ion batteries ought to be further advanced. Herein, we synthesized [...] Read more.
The advantages of aluminum-ion batteries in the area of power source systems are: inexpensive manufacture, high capacity, and absolute security. However, due to the limitations of cathode materials, the capacity and durability of aluminum-ion batteries ought to be further advanced. Herein, we synthesized a nitrogen-doped tubular carbon material as a potential cathode to achieve advanced aqueous aluminum-ion batteries. Nitrogen-doped tubular carbon materials own an abundant space (367.6 m2 g−1) for electrochemical behavior, with an aperture primarily concentrated around 2.34 nm. They also exhibit a remarkable service lifespan, retaining a specific capacity of 78.4 mAh g−1 at 50 mA g−1 after 300 cycles. Additionally, from 2 to 300 cycles, the material achieves an appreciable reversibility (coulombic efficiency CE: 99.7%) demonstrating its excellent reversibility. The tubular structural material possesses a distinctive hollow architecture that mitigates volumetric expansion during charging and discharging, thereby preventing structural failure. This material offers several advantages, including a straightforward synthesis method, high yield, and ease of mass production, making it highly significant for the research and development of future aluminum-ion batteries. Full article
(This article belongs to the Special Issue Polymeric Conductive Materials for Energy Storage)
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<p>Schematic diagram of the fabrication process of tubular carbon materials.</p>
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<p>(<b>a</b>–<b>c</b>) SEM image for tubular polypyrrole polymer precursor. (<b>d</b>–<b>f</b>) SEM image of tubular carbon material. (<b>g</b>–<b>j</b>) EDS mapping images of tubular carbon material.</p>
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<p>(<b>a</b>,<b>b</b>) The different TEM images of hollow tubular carbon material. (<b>c</b>) XRD pattern of tubular carbon material. (<b>d</b>) Nitrogen adsorption-desorption isotherms, and (<b>e</b>) aperture distribution of tubular carbon material.</p>
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<p>(<b>a</b>) XPS element full spectrum of tubular carbon material. Regional XPS spectra of (<b>b</b>) C 1s, (<b>c</b>) O 1s and (<b>d</b>) N 1s. (<b>e</b>) Structural illustration for nitrogen-doped carbon materials.</p>
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<p>(<b>a</b>) Rate properties and (<b>b</b>) GCD curves of tubular carbon material at various operating rates. (<b>c</b>) GCD curves during cycling at 50 mA g<sup>−1</sup>. (<b>d</b>) Cycling lifespan and (<b>e</b>) coulombic efficiency of tubular carbon material at an operating rate of 50 mA g<sup>−1</sup>. (<b>f</b>) CV curve of tubular carbon material recorded at a test rate of 0.1 mV s<sup>−1</sup>.</p>
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<p>(<b>a</b>,<b>b</b>) SEM images of fresh nitrogen-doped tubular carbon electrode. (<b>c</b>,<b>d</b>) SEM images of nitrogen-doped tubular carbon electrode after rate capability test.</p>
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22 pages, 2227 KiB  
Article
Zic-HILIC MS/MS Method for NADomics Provides Novel Insights into Redox Homeostasis in Escherichia coli BL21 Under Microaerobic and Anaerobic Conditions
by Divyata Vilas Rane, Laura García-Calvo, Kåre Andre Kristiansen and Per Bruheim
Metabolites 2024, 14(11), 607; https://doi.org/10.3390/metabo14110607 - 9 Nov 2024
Viewed by 887
Abstract
Background: Nicotinamide adenine dinucleotide (NAD+), its precursors, and its derivatives (collectively NADome) play a crucial role in cellular processes and maintain redox homeostasis. Understanding the dynamics of these metabolic pools and redox reactions can provide valuable insights into metabolic functions, especially [...] Read more.
Background: Nicotinamide adenine dinucleotide (NAD+), its precursors, and its derivatives (collectively NADome) play a crucial role in cellular processes and maintain redox homeostasis. Understanding the dynamics of these metabolic pools and redox reactions can provide valuable insights into metabolic functions, especially cellular regulation and stress response mechanisms. The accurate quantification of these metabolites is challenging due to the interconversion between the redox forms. Methods: Our laboratory previously developed a zwitterionic hydrophilic interaction liquid chromatography (zic-HILIC)–tandem mass spectrometry method for the quantification of five essential pyridine nucleotides, including NAD+ derivatives and it’s reduced forms, with 13C isotope dilution and matrix-matched calibration. In this study, we have improved the performance of the chromatographic method and expanded its scope to twelve analytes for a comprehensive view of NAD+ biosynthesis and utilization. The analytical method was validated and applied to investigate Escherichia coli BL21 under varying oxygen supplies including aerobic, microaerobic, and anaerobic conditions. Conclusions: The intracellular absolute metabolite concentrations ranged over four orders of magnitude with NAD+ as the highest abundant, while its precursors were much less abundant. The composition of the NADome at oxygen-limited conditions aligned more with that in the anaerobic conditions rather than in the aerobic phase. Overall, the NADome was quite homeostatic and E. coli rapidly, but in a minor way, adapted the metabolic activity to the challenging shift in the growth conditions and achieved redox balance. Our findings demonstrate that the zic-HILIC-MS/MS method is sensitive, accurate, robust, and high-throughput, providing valuable insights into NAD+ metabolism and the potential significance of these metabolites in various biological contexts. Full article
(This article belongs to the Section Metabolomic Profiling Technology)
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<p>NAD<sup>+</sup> biosynthesis in <span class="html-italic">E. coli</span>, adapted from Gholson et al., Begley et al., and Sugiyama et al. [<a href="#B5-metabolites-14-00607" class="html-bibr">5</a>,<a href="#B6-metabolites-14-00607" class="html-bibr">6</a>,<a href="#B10-metabolites-14-00607" class="html-bibr">10</a>]. Figure created using BioRender.com. Abbreviations: Fructose-6-P: Fructose 6-phosphate; PYR: Pyruvate; Asp: Aspartate; QA: Quinolinic acid; NAM: Nicotinamide; NCA: Nicotinic acid; NAMN: Nicotinic acid mononucleotide; NAAD: Nicotinic acid adenine dinucleotide; NAD: Nicotinamide adenine dinucleotide; NR: Nicotinamide riboside; NADP: Nicotinamide adenine dinucleotide phosphate; NMN: Nicotinamide mononucleotide; NADH: Reduced form of NAD<sup>+</sup>; NADPH: Reduced form of NADP<sup>+</sup>; PncA: Nicotinamidase; PncB: Nicotinate phosphoribosyltransferase (NAPRT); PncC: NMN amidohydrolase; NadC: Quinolinic acid phosphoribosyltransferase; NadD: NAMN adenyltransferase; NadE: NAD synthase; NadR: Trifunctional NAD biosynthesis/regulator protein; NadK: NAD<sup>+</sup> kinase; NadV: Nicotinamide phosphoribosyltransferase; ADPR: Adenosine diphosphate ribose.</p>
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<p>Cultivation of <span class="html-italic">E. coli</span> BL21 with oxygen limitation at OD<sub>600</sub>~2.0 (red dotted line) and anaerobiosis at OD<sub>600</sub>~4.0 (purple dotted line). The plot represents one of the biological replicates, while the other replicate displays similar growth parameters. Gray lines indicate sampling times for pyridine nucleotide metabolite analysis experiments (T1–T5). Error bars in glucose estimation indicate SD between technical replicates.</p>
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<p>Combined 2D scores for plot and biplot of principal component analysis (PCA) displaying principal components of metabolite concentrations in <span class="html-italic">E. coli</span> BL21 over sampling time points (T1, T2, T3, T4, and T5). Each metabolite’s contribution is represented as loadings (red arrows). The data used for plotting represent two biological replicates. For each biological replicate, an average of absolute concentrations of five technical replicates corresponding to one time point was plotted. Data were normalized by autoscale (mean-centered and divided by SD of each variable) and plotted using RStudio v. 4.3.1 (packages used: ‘ggplot2’, ’ggfortify’, ’factorextra’) [<a href="#B53-metabolites-14-00607" class="html-bibr">53</a>,<a href="#B54-metabolites-14-00607" class="html-bibr">54</a>,<a href="#B55-metabolites-14-00607" class="html-bibr">55</a>]. The plot shows 46.63% variation along PC1 and 25.02% along PC2.</p>
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<p>(<b>a</b>) Heatmap showing absolute concentrations of metabolites (nmol g <sup>−1</sup> CDW) at aerobic (T1), microaerobic (T2), and anaerobic (T3, T4, and T5) sampling intervals. Data were obtained from one of the biological replicates and an average of five technical replicates (for one sampling point) is plotted on the heatmap. (<b>b</b>) Heatmap displaying log2 fold changes in metabolite concentrations at microaerobic (T2) and anaerobic (T3, T4, and T5) sampling intervals compared to aerobic sampling point (T1) (*: <span class="html-italic">p</span> ≤ 0.05; **: <span class="html-italic">p</span> ≤ 0.01; and *** <span class="html-italic">p</span> ≤ 0.001).</p>
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<p>Intracellular (<b>a</b>) NADPH/NADH, (<b>b</b>) NADP/NAD<sup>+</sup>, (<b>c</b>) NADH/NAD<sup>+</sup>, and (<b>d</b>) NADPH/NADP<sup>+</sup> ratios at aerobic (T1), microaerobic (T2), and anaerobic (T3, T4, and T5) sampling intervals (ns: not significant; *: <span class="html-italic">p</span> ≤ 0.05; **: <span class="html-italic">p</span> ≤ 0.01; and *** <span class="html-italic">p</span> ≤ 0.001). Graphs created using GraphPad Prism 10.</p>
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12 pages, 4211 KiB  
Article
Generalized Ketogenic Diet Induced Liver Impairment and Reduced Probiotics Abundance of Gut Microbiota in Rat
by Ge Song, Dan Song, Yongwei Wang, Li Wang and Weiwei Wang
Biology 2024, 13(11), 899; https://doi.org/10.3390/biology13110899 - 4 Nov 2024
Viewed by 1248
Abstract
The ketogenic diet is becoming an assisted treatment to control weight, obesity, and even type 2 diabetes. However, there has been no scientific proof supporting that the ketogenic diet is absolutely safe and sustainable. In this study, Sprague–Dawley (SD) rats were fed different [...] Read more.
The ketogenic diet is becoming an assisted treatment to control weight, obesity, and even type 2 diabetes. However, there has been no scientific proof supporting that the ketogenic diet is absolutely safe and sustainable. In this study, Sprague–Dawley (SD) rats were fed different ratios of fat to carbohydrates under the same apparent metabolizable energy level to evaluate the effects of a ketogenic diet on healthy subjects. The results showed that the ketogenic diet could relatively sustain body weight and enhance the levels of serum alanine aminotransferase (ALT) and serum alkaline phosphatase (SAP), leading to more moderate lipoidosis and milder local non-specific inflammation in the liver compared with the high-carbohydrate diet. In addition, the abundance of probiotic strains such as Lactobacillus, Lactococcus, and Faecalitalea were reduced with the ketogenic diet in rats, while an abundance of pathogenic strains such as Anaerotruncus, Enterococcus, Rothia, and Enterorhabdus were increased with both the ketogenic diet and the high-carbohydrate diet. This study suggests that the ketogenic diet can lead to impairments of liver function and changed composition of the gut microbiota in rats, which to some extent indicates the danger of consuming a generalized ketogenic diet. Full article
(This article belongs to the Special Issue Metabolic Interactions between the Gut Microbiome and Host)
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<p>Body weight of SD rats (<span class="html-italic">n =</span> 10) fed diets with different ratios of fat/carbohydrates (10/70, 20/60, 30/50, 40/40, and 50/50).</p>
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<p>Serum total triglyceride (<b>a</b>), total protein (<b>b</b>), serum alanine aminotransferase (<b>c</b>), and serum alkaline phosphatase (<b>d</b>) levels of SD rats fed diets with different ratios of fat/carbohydrates (10/70, 20/60, 30/50, 40/40, and 50/50). Values are shown as means ± SEM, <span class="html-italic">n =</span> 10. Means in a list without a common letter differ, <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Light photomicrographs of live tissue of SD rats fed diets with different ratios of fat/carbohydrates (10/70, 20/60, 30/50, 40/40, and 50/50) for 8 weeks. (Hematoxylin–eosin-stained, captured in original magnification of 200×), <span class="html-italic">n =</span> 10. (<b>a</b>) 10/70 (F10). (<b>b</b>) 20/60 (F20). (<b>c</b>) 30/50 (F30). (<b>d</b>) 40/40 (F40). (<b>e</b>) 20/60 (F50). Arrows present pathological changes of rats.</p>
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<p>Alpha diversity of F10 (control) SD rats and SD rats fed diets with different ratios of fat/carbohydrates (10/70, 20/60, 30/50, 40/40, and 50/50), <span class="html-italic">n =</span> 4. (<b>a</b>) Rarefaction curve. (<b>b</b>) Chao1 index levels.</p>
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<p>Gut bacteria composition at the genus level in SD rats fed diets with different ratios of fat/carbohydrates (10/70, 20/60, 30/50, 40/40, and 50/50) <span class="html-italic">n =</span> 4. (<b>a</b>) Principal coordinate analysis (PCoA) used un-weighted UniFrac distance metrics. (<b>b</b>) Hierarchical clustered heat map with Z-score normalized relative abundance of Top 35.</p>
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<p>LEfSe analysis of taxonomic biomarkers of F10 (control) SD rats and SD rats fed with different ratios of fat (30% (F30) and 50% (F50)), <span class="html-italic">n =</span> 4.</p>
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18 pages, 3227 KiB  
Article
Time Prediction in Ship Block Manufacturing Based on Transfer Learning
by Jinghua Li, Pengfei Lin, Dening Song, Zhe Yan, Boxin Yang and Lei Zhou
J. Mar. Sci. Eng. 2024, 12(11), 1977; https://doi.org/10.3390/jmse12111977 - 2 Nov 2024
Viewed by 654
Abstract
Accurate time prediction is critical to the success of ship block manufacturing. However, the emergence of new ship types with limited historical data poses challenges to existing prediction methods. In response, this paper proposes a novel framework for ship block manufacturing time prediction, [...] Read more.
Accurate time prediction is critical to the success of ship block manufacturing. However, the emergence of new ship types with limited historical data poses challenges to existing prediction methods. In response, this paper proposes a novel framework for ship block manufacturing time prediction, integrating clustering and the transfer learning algorithm. Firstly, the concept of distributed centroids was innovatively adopted to achieve the clustering of categorical attribute features. Secondly, abundant historical data from other types of blocks (source domain) were incorporated into the neural network model to explore the effects of block features on manufacturing time, and the model was further transferred to blocks with limited data (target domain). Leveraging the similarities and differences between source and target domain blocks, actions involving freezing and fine-tuning parameters were adopted for the predictive model development. Despite a small sample size of only 80, our proposed block time prediction method achieves an impressive mean absolute percentage error (MAPE) of 8.62%. In contrast, the MAPE for the predictive model without a transfer learning algorithm is notably higher at 14.97%. Experimental validation demonstrates the superior performance of our approach compared to alternative methods in scenarios with small sample datasets. This research addresses a critical gap in ship block manufacturing time prediction. Full article
(This article belongs to the Section Ocean Engineering)
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<p>(<b>a</b>) The framework of block time prediction; (<b>b</b>) cluster process; (<b>c</b>) PSO-BPNN framework.</p>
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<p>Prediction flow chart of TL-PSO-BPNN model.</p>
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<p>Source block time prediction results of (<b>a</b>) MAPE values and (<b>b</b>) <math display="inline"><semantics> <mrow> <msubsup> <mrow> <mi>R</mi> </mrow> <mrow> <mi>a</mi> <mi>d</mi> <mi>j</mi> </mrow> <mrow> <mn>2</mn> </mrow> </msubsup> </mrow> </semantics></math> values.</p>
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<p>Parameter freezing and fine-tuning information of TR-PSO-BPNN.</p>
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<p>Comparisons of target block time predict results: (<b>a</b>) with-TR models; (<b>b</b>) without-TR models.</p>
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<p>Comparison of different methods and true values.</p>
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<p>Comparison of different methods: absolute errors.</p>
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<p>Comparison of different methods: MAPE.</p>
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<p>The effect of sample size on the MAPE of TR and without-TR models.</p>
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17 pages, 982 KiB  
Article
Proteomic Analysis of Follicular Fluid in Polycystic Ovary Syndrome: Insights into Protein Composition and Metabolic Pathway Alterations
by Janusz Przewocki, Adam Łukaszuk, Grzegorz Jakiel, Izabela Wocławek-Potocka, Karolina Kłosińska, Jolanta Olszewska and Krzysztof Łukaszuk
Int. J. Mol. Sci. 2024, 25(21), 11749; https://doi.org/10.3390/ijms252111749 - 1 Nov 2024
Viewed by 1129
Abstract
This study explores the proteomic composition of follicular fluid (FF) from women undergoing oocyte retrieval for in vitro fertilisation (IVF), with a focus on the effects of polycystic ovary syndrome (PCOS). FF samples were collected from 74 patients, including 34 with PCOS and [...] Read more.
This study explores the proteomic composition of follicular fluid (FF) from women undergoing oocyte retrieval for in vitro fertilisation (IVF), with a focus on the effects of polycystic ovary syndrome (PCOS). FF samples were collected from 74 patients, including 34 with PCOS and 40 oocyte donors. Proteomic profiling using machine learning identified significant differences in protein abundance between the PCOS and control groups. Of the 484 quantified proteins, 20 showed significantly altered levels in the PCOS group. Functional annotation and pathway enrichment analysis pointed to the involvement of protease inhibitors and immune-related proteins in the pathophysiology of PCOS, suggesting that inflammation and immune dysregulation may play a key role. Additionally, HDL assembly was identified as a significant pathway, with apolipoprotein-AI (APOA1) and alpha-2-macroglobulin (A2M) as the major proteins involved. Notably, myosin light polypeptide 6 was the most downregulated protein, showing the highest absolute fold change, and may serve as a novel independent biomarker for PCOS. Full article
(This article belongs to the Special Issue New Breakthroughs in Molecular Diagnostic Tools for Human Diseases)
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<p>Correlation matrix calculated with the robust algorithm based on winsorisation [<a href="#B14-ijms-25-11749" class="html-bibr">14</a>].</p>
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<p>A protein–protein interaction network functional enrichment analysis created using STRING v.12.0. Predicted interactions are summarised using coloured lines: gene co-expression by a black line, gene neighbourhood by a green line, experimental evidence by a purple line, database evidence by a light blue line, and text-mining evidence by a yellow line. The proteins are labelled by the names of their corresponding genes (see <a href="#ijms-25-11749-t002" class="html-table">Table 2</a>).</p>
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18 pages, 1463 KiB  
Review
Depletion Estimation, Stock–Recruitment Relationships, and Interpretation of Biomass Reference Points
by Mark N. Maunder and Kevin R. Piner
Fishes 2024, 9(11), 447; https://doi.org/10.3390/fishes9110447 - 1 Nov 2024
Viewed by 976
Abstract
Stock depletion level is an important concept in the assessment and management of exploited fish stocks because it is often used in conjunction with reference points to infer stock status. Both the depletion level and reference points can be highly dependent on the [...] Read more.
Stock depletion level is an important concept in the assessment and management of exploited fish stocks because it is often used in conjunction with reference points to infer stock status. Both the depletion level and reference points can be highly dependent on the stock–recruitment relationship. Here, we show how depletion level is estimated in stock assessment models, what data inform the depletion level, and how the stock–recruitment relationship influences the depletion level. There are a variety of data that provide information on abundance. In addition, to estimate the depletion level, unexploited absolute abundance needs to be determined. This often means extrapolating the abundance back in time to the start of the fishery, accounting for the removals and the productivity. Uncertainty in the depletion level arises because the model can account for the same removals by either estimating low productivity (e.g., low natural mortality) and high carrying capacity or high productivity and a low carrying capacity, and by estimating different relationships between productivity and depletion level, which are strongly controlled by the stock–recruitment relationship. Therefore, estimates of depletion are particularly sensitive to uncertainty in the biological processes related to natural mortality and the stock–recruitment relationship and to growth when length composition data are used. In addition, depletion-based reference points are highly dependent on the stock–recruitment relationship and need to account for recruitment variability, particularly autocorrelation, trends, and regime shifts. Future research needs to focus on estimating natural mortality, the stock–recruitment relationship, asymptotic length, shape of the selectivity curve, or management strategies that are robust to uncertainty in these parameters. Tagging studies, including close-kin mark-recapture, can address some of these issues. However, the stock–recruitment relationship will remain uncertain. Full article
(This article belongs to the Special Issue Assessment and Management of Fishery Resources)
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<p>Illustration of the calculation of the depletion level corresponding to MSY. The upper figure shows that the biomass of a cohort changes as it ages due to a tradeoff between increases from individual growth and reductions from natural mortality. The maximum yield-per-recruit (YPR) is obtained when all the individuals are caught at the age that maximizes the biomass of the cohort, which occurs when the growth rate equals natural mortality. For illustrative purposes, natural mortality is assumed to be constant across age, while individual growth rates reduce as they age, forming a peak in population biomass growth. The lower figure shows how MSY is calculated by combing the YPR curve with the stock–recruitment relationship, which also gives the shape of the production function. For a given selectivity that catches multiple ages of fish, fish are caught at a younger age as the fishing mortality increases and the population becomes more depleted. The YPR initial increases with fishing mortality because fewer fish are left in the population and lost due to natural mortality, then decreases as more fish are caught at an age younger than the age that maximizes the biomass of the cohort. Yield is a tradeoff between increases in yield-per-recruit as the stock becomes more depleted and individuals are caught before the loss due to natural mortality is greater than the gain due to growth and losses in recruitment due to reduced spawning stock size through the stock–recruitment relationship.</p>
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<p>Estimates of historic abundance reconstructed with different steepness values of the stock–recruitment relationship from a given absolute abundance level in year 10 (<b>top</b>) under a given catch trajectory (<b>bottom</b>). Units in number of individuals. The simple population dynamics model is described in <a href="#app1-fishes-09-00447" class="html-app">Appendix A</a> and is fit to an absolute biomass estimate in year 10.</p>
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<p>Uncertainty in depletion level represented by the posterior distribution for a total catch history model (<span class="html-italic">R</span><sub>0</sub> estimated) (<b>left</b>) with known h = 0.75 and no recruitment variation (<b>top</b>), uniform prior on h = U(0.5, 1.0) and no recruitment variation (<b>middle</b>), uniform prior on h = U(0.5, 1.0) and recruitment variation sd = 0.6 (<b>bottom</b>) versus short-term model (<span class="html-italic">R</span><sub>0</sub>, initial recruitment, and initial fishing mortality estimated) (<b>right</b>) using the simple model described in <a href="#app1-fishes-09-00447" class="html-app">Appendix A</a> fit to an absolute biomass estimate in year 10. The prior on <span class="html-italic">R</span><sub>0</sub> is U(0, 200).</p>
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<p>Recruitment as a fraction of virgin recruitment (<b>top</b>) and yield and a fraction of maximum sustainable yield (MSY, <b>bottom</b>) for different levels of depletion (spawning biomass divided by virgin spawning biomass, S/S<sub>0</sub>) and different steepness values of the stock–recruitment relationship. The latter represents the production function.</p>
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<p>The age-structure of an exploited population at the start of the modeling time period in a short-term model is represented by <span class="html-italic">R<sub>init</sub></span> that scales the recruitment and compensates for the stock–recruitment relationship and any other trends or regime shifts in recruitment that occurred before the start of the modeling time period, <span class="html-italic">F<sub>init</sub></span> that represents the historic fishing, and <span class="html-italic">R<sub>dev</sub></span> that represents individual variation in recruitment (and fishing mortality or other process variation) related to that cohort [<a href="#B27-fishes-09-00447" class="html-bibr">27</a>].</p>
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<p>Estimates of depletion of a hypothetical application under different assumed values of <span class="html-italic">h</span> and the associated MSY-based biomass reference points when fit to an absolute abundance estimate in year 10 (<b>top</b>) and to the change in the index from year 10 to year 11 (<b>bottom</b>).</p>
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<p>Estimates of depletion of a hypothetical application under different assumed values of <span class="html-italic">h</span> and the associated MSY-based biomass reference points when fit to an absolute abundance estimate in year 10 (<b>top</b>) and to the change in the index from year 10 to year 11 (<b>bottom</b>).</p>
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19 pages, 7630 KiB  
Article
Investigation into Critical Gut Microbes Influencing Intramuscular Fat Deposition in Min Pigs
by Long Jin, Ke Li, Zhimin Li, Xuankai Huang, Li Wang, Xibiao Wang, Shengwei Di, Shiquan Cui and Yuan Xu
Animals 2024, 14(21), 3123; https://doi.org/10.3390/ani14213123 - 30 Oct 2024
Viewed by 821
Abstract
To determine the pivotal microorganisms affecting intramuscular fat (IMF) accumulation in Min pigs and to discern the extent of the influence exerted by various intestinal segments on IMF-related traits, we sequenced 16S rRNA from the contents of six intestinal segments from a high [...] Read more.
To determine the pivotal microorganisms affecting intramuscular fat (IMF) accumulation in Min pigs and to discern the extent of the influence exerted by various intestinal segments on IMF-related traits, we sequenced 16S rRNA from the contents of six intestinal segments from a high IMF group (Group H) and a low IMF group (Group L) of Min pigs weighing 90 ± 1 kg. We then compared their diversity and disparities in bacterial genera. Group H exhibited considerably higher α diversity in the jejunum and colon than Group L (p < 0.05). When 95% confidence levels were considered, the main β diversity components for the ileum, caecum, and colon within Groups H and L exhibited absolute segregation. Accordingly, 31 differentially abundant genera across Group H were pinpointed via LEfSe and the Wilcoxon test (p < 0.05) and subsequently scrutinised based on their distribution and abundance across distinct intestinal segments and their correlation with IMF phenotypes. The abundances of Terrisporobacter, Acetitomaculum, Bacteroides, Fibrobacter, Treponema, Akkermansia, Blautia, Clostridium sensu stricto 1, Turicibacter, Subdoligranulum, the [Eubacterium] siraeum group, and dgA 11 gut groups were positively correlated with IMF content (p < 0.05), whereas those of Bacillus, the Lachnospiraceae NK4A136 group, Streptococcus, Roseburia, Solobacterium, Veillonella, Lactobacillus, the Rikenellaceae RC9 gut group, Anaerovibrio, and the Lachnospiraceae AC2044 group were negatively associated with IMF content (p < 0.05). Employing PICRUSt2 for predicting intergenic metabolic pathways that differ among intestinal microbial communities revealed that within the 95% confidence interval the colonic microbiome was enriched with the most metabolic pathways, including those related to lipid metabolism. The diversity results, bacterial genus distributions, and metabolic pathway disparities revealed the colonic segment as an influential region for IMF deposition. Full article
(This article belongs to the Section Pigs)
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<p>Sample clustering and comparison of IMF content. (<b>A</b>): Conceptual clustering diagram for the Min pig population on the basis of IMF content. Red lines (M1–M9): individuals in the low IMF group; Blue lines (M10–M20): individuals with intermediate IMF levels; Green lines (M21–M30): individuals in the high IMF group. (<b>B</b>): Difference in IMF contents between Groups L and H, *** <span class="html-italic">p</span>&lt; 0.0001.</p>
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<p>Paraspinal longissimus muscle oil-red-O-stained sections from Groups L and H. (<b>A</b>,<b>B</b>): Section from Group L. (<b>C</b>,<b>D</b>): Section from Group H.</p>
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<p>Sequencing depth chart of the entire sample. (<b>A</b>): Dilution curve. (<b>B</b>): Shannon curve.</p>
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<p>The exclusive and shared OTU taxa among the contents of different intestinal segments in Groups H and L. (<b>A</b>): Duodenum. (<b>B</b>): Jejunum. (<b>C</b>): Ileum. (<b>D</b>): Caecum. (<b>E</b>): Colon. (<b>F</b>): Rectum.</p>
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<p>The α diversity indices of specific intestinal segments from Groups H and L. (<b>A</b>): ACE index. (<b>B</b>): Chao1 index. (<b>C</b>): Shannon index. (<b>D</b>): Simpson index, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>β diversity indices of the respective intestinal segments in Groups H and L. (<b>A</b>): Duodenum. (<b>B</b>): Jejunum. (<b>C</b>): Ileum. (<b>D</b>): Caecum. (<b>E</b>): Colon. (<b>F</b>): Rectum.</p>
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<p>Distribution of prominent microbial populations at both the phylum and genus levels for each intestinal segment. (<b>A</b>–<b>F</b>): Phylum level. (<b>G</b>–<b>L</b>): Genus level.</p>
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<p>The microbiome profile analysis results for each intestinal segment (using an LDA &gt; 4.0 as a discernment criterion). (<b>A</b>): Duodenum. (<b>B</b>): Jejunum. (<b>C</b>): Ileum. (<b>D</b>): Caecum. (<b>E</b>): Colon. (<b>F</b>): Rectum.</p>
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<p>Significant differences were identified in the Group H and Group L genera across intestinal segments, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01. (<b>A</b>): Duodenum. (<b>B</b>): Jejunum. (<b>C</b>): Ileum. (<b>D</b>): Caecum. (<b>E</b>): Colon. (<b>F</b>): Rectum.</p>
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<p>Genomic variations in the microbiome communities of Groups H and L revealed significant KEGG pathway enrichment (95% confidence interval), <span class="html-italic">p</span> &lt; 0.05, Red dashed boxes indicate KEGG pathways related to metabolism. The circles show deviations from the 95% confidence interval, indicating inter-group differences. (<b>A</b>): duodenum, (<b>B</b>): ileum, (<b>C</b>): caecum, (<b>D</b>): colon, (<b>E</b>): rectum.</p>
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