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20 pages, 3659 KiB  
Article
Exploring the Osteoinductive Potential of Bacterial Pyomelanin Derived from Pseudomonas aeruginosa in a Human Osteoblast Model
by Mateusz M. Urbaniak, Karolina Rudnicka, Przemysław Płociński and Magdalena Chmiela
Int. J. Mol. Sci. 2024, 25(24), 13406; https://doi.org/10.3390/ijms252413406 (registering DOI) - 14 Dec 2024
Viewed by 167
Abstract
Alkaptonuria (AKU) is a genetically determined disease associated with disorders of tyrosine metabolism. In AKU, the deposition of homogentisic acid polymers contributes to the pathological ossification of cartilage tissue. The controlled use of biomimetics similar to deposits observed in cartilage during AKU potentially [...] Read more.
Alkaptonuria (AKU) is a genetically determined disease associated with disorders of tyrosine metabolism. In AKU, the deposition of homogentisic acid polymers contributes to the pathological ossification of cartilage tissue. The controlled use of biomimetics similar to deposits observed in cartilage during AKU potentially may serve the development of new bone regeneration therapy based on the activation of osteoblasts. The proposed biomimetic is pyomelanin (PyoM), a polymeric biomacromolecule synthesized by Pseudomonas aeruginosa. This work presents comprehensive data on the osteoinductive, pro-regenerative, and antibacterial properties, as well as the cytocompatibility, of water-soluble (PyoMsol) or water-insoluble (PyoMinsol) PyoM. Both variants of PyoM support osteoinductive processes as well as the maturation of osteoblasts in cell cultures in vitro due to the upregulation of bone-formation markers, osteocalcin (OC), and alkaline phosphatase (ALP). Furthermore, the cytokines involved in these processes were elevated in cell cultures of osteoblasts exposed to PyoM: tumor necrosis factor (TNF)-α, interleukin (IL)-6, and IL-10. The PyoM variants are cytocompatible in a wide concentration range and limit the doxorubicin-induced apoptosis of osteoblasts. This cytoprotective PyoM activity is correlated with an increased migration of osteoblasts. Moreover, PyoMsol and PyoMinsol exhibit antibacterial activity against staphylococci isolated from infected bones. The osteoinductive, pro-regenerative, and antiapoptotic effects achieved through PyoM stimulation prompt the development of new biocomposites modified with this bacterial biopolymer for medical use. Full article
(This article belongs to the Section Macromolecules)
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<p>(<b>A</b>) The percentage of viable hFOB 1.19 osteoblasts after 24 h exposure to different concentrations of the water-soluble (PyoM<sub>sol</sub>) or water-insoluble pyomelanin (PyoM<sub>insol</sub>). Osteoblasts incubated only in medium (NC = 100% cell viability). (<b>B</b>) Diminishing cell apoptosis induced by doxorubicin (DOX) in the milieu of PyoM<sub>sol</sub> or PyoM<sub>insol</sub> at the concentration of 1 µg/mL. The Apoptotic Index was determined from the relative fluorescence units (RFUs) of cells exposed to PyoM vs. RFUs of non-stimulated osteoblasts (NS). The mean ± standard deviation results of four separate experiments are shown. Statistical significance for ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>(<b>A</b>) The migration effectiveness of hFOB 1.19 osteoblasts determined in a scratch assay. Osteoblasts were cultivated for 24 h, 48 h, or 72 h in the presence of water-soluble (PyoM<sub>sol</sub>) or water-insoluble pyomelanin (PyoM<sub>insol</sub>) at a concentration of 1 µg/mL Mean ± standard deviation of five separate experiments are shown. * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001, statistically significant differences. Cells not stimulated with PyoM (NS). The reference wound closure of non-stimulated cells is marked on the graph with dashed green line. (<b>B</b>) Representative images of hFOB 1.19 osteoblast migration after 24, 48, and 72 h of water-soluble (PyoM<sub>sol</sub>) or water-insoluble pyomelanin (PyoM<sub>insol</sub>) stimulation. In the microscopic images, the red dashed lines indicate the width of the overgrown crack.</p>
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<p>Transcriptomic changes in hFOB 1.19 osteoblasts upon treatment with soluble pyomelanin (PyoM<sub>sol</sub>). (<b>A</b>) Ontology analysis of differentially expressed genes overexpressed in hFOB1.19 osteoblasts during differentiation in osteoinductive media utilizing the ShinyGo 0.77 online platform [<a href="#B30-ijms-25-13406" class="html-bibr">30</a>]. (<b>B</b>) List of transcripts relevant to osteoblastic differentiation of hFOB cells in comparison between proliferative and differentiation conditions for PyoM<sub>sol</sub>-treated and non-treated cells. (<b>C</b>) A summary of transcriptomic changes observed between hFOB 1.19 cells differentiating under standard conditions versus cells differentiating in media supplemented with PyoM<sub>sol</sub>. RNA was isolated from cells incubated in proliferative or differentiation conditions for 14 days. The change in BMP-2 expression between non-treated and treated cells (marked in red) exceeded the Log 2 FC of 2, preset as the threshold for our analysis. ALPL, liver-/bone-/kidney-specific or tissue-nonspecific (TNSALP) ALP form, ALPP, placental ALP form; BMP, bone morphogenic protein; CGMP-PKG, cyclic guanosine monophosphate protein kinase G; COL, collagen; OCN, osteocalcin; OPG, osteoprotegrin, RUNX, runt-related transcription factors; TGF-Beta, transforming growth factor beta; PI3-Akt, PI3-Akt; phosphatidylinositol 3-kinase, serine/threonine kinase (protein kinase B); Rap1, Ras-proximate-1 or Ras-related protein-1.</p>
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<p>The influence of pyomelanin (PyoM) on cell growth, alkaline phosphatase production, and bone cell calcification. (<b>A</b>) Number of hFOB 1.19 osteoblasts after 1, 7, 14, 21, or 28 days of incubation with water-soluble pyomelanin (PyoM<sub>sol</sub>), water-insoluble pyomelanin (PyoM<sub>insol</sub>), or culture medium alone, i.e., unstimulated cells (NS). (<b>B</b>) The activity of alkaline phosphatase (ALP) produced by hFOB 1.19 osteoblasts in cell cultures exposed to PyoM<sub>sol</sub>, PyoM<sub>insol</sub>, or culture medium alone (NS) after 7, 14, 21, or 28 days are shown in international units (IU). Results are shown as mean ± standard deviation. The experiment was performed four times. Statistical significance is indicated by * at <span class="html-italic">p</span> &lt; 0.05. (<b>C</b>) Representative images of calcification process in cell culture of osteoblasts exposed for 24 days to PyoM<sub>sol</sub> or PyoM<sub>insol</sub> or not stimulated (NS). The cells were stained with 4% alizarin The stained mineralized extracellular matrix of osteoblasts was observed under an inverted-phase contrast microscope. Calcium deposits were assessed quantitatively on the basis of absorbance values at 405 nm using a standard curve developed with hydroxyapatite.</p>
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<p>Secretion of osteocalcin and cytokines by osteoblasts exposed to PyoM. (<b>A</b>) The levels of osteocalcin (OC), (<b>B</b>) the levels of interleukin (IL)-6, (<b>C</b>) the levels of IL-10, and (<b>D</b>) the levels of tumor necrosis factor (TNF)-α in cell cultures of hFOB 1.19 exposed to water-soluble pyomelanin (PyoM<sub>sol</sub>), water-insoluble pyomelanin (PyoM<sub>insol</sub>), or culture medium alone, i.e., non-stimulated cells (NS), after 1, 4, 7, 11, 14, 18, 21, 25, and 28 days. Results are shown as mean ± standard deviation. The experiment was performed four times. * <span class="html-italic">p</span> &lt; 0.05 indicates statistically significant differences.</p>
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<p>Antibacterial activity of studied PyoM variants. The figure shows dose–response curves supplemented with the minimum inhibitory concentration (MIC)<sub>50</sub> determined for (<b>1</b>) water-soluble piomelanin (PyoM<sub>sol</sub>) or (<b>2</b>) water-insoluble pyomelanin (PyoM<sub>insol</sub>). <span class="html-italic">Staphylococcus</span> strains: (<b>A</b>) reference <span class="html-italic">S. aureus</span> ATTC 29213, (<b>B</b>) clinical <span class="html-italic">S. aureus</span> strain resistant to methicillin (MRSA), and (<b>C</b>) <span class="html-italic">S. felis</span>. Results are shown as mean ± standard deviation. The experiment was performed five times. The green dashed line shows the 50% bacterial viability.</p>
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26 pages, 10324 KiB  
Article
Dual Differences, Dynamic Evolution and Convergence of Total Factor Carbon Emission Performance: Empirical Evidence from 116 Resource-Based Cities in China
by Jiaming Wang, Xiangyun Wang, Shuwen Wang, Xueyi Du and Li Yang
Sustainability 2024, 16(24), 10950; https://doi.org/10.3390/su162410950 - 13 Dec 2024
Viewed by 287
Abstract
Using panel data of Chinese cities from 2006 to 2020, this study constructs the carbon emission performance index from the perspective of the dual differences in the four stages of growth, maturity, decline and regeneration of eastern, central, western and resource-based cities (RBCs). [...] Read more.
Using panel data of Chinese cities from 2006 to 2020, this study constructs the carbon emission performance index from the perspective of the dual differences in the four stages of growth, maturity, decline and regeneration of eastern, central, western and resource-based cities (RBCs). This study employs the Dagum Gini coefficient and kernel density estimation to explore σ convergence and β convergence for understanding the dual differences, dynamic evolutionary trend and convergence. Results indicate that during the sample period, the carbon emission performance index of RBCs shows a fluctuating upward trend with regional and typological imbalance influenced by geographical location and division of labour. The carbon emission performance index of RBCs of different regions and types (Growing, Mature, Declining and Regenerative) shows a fluctuating downward trend. However, the carbon emission performance index gap between the 116 RBCs in China is gradually expanding, further corroborating the influence of “excellent but outliers”. The overall level of carbon emission performance index of RBCs exhibits σ convergence, absolute β convergence and conditional β convergence phenomena. Notably, growing and regenerative RBCs demonstrate a clear “catching-up” trend compared to mature and declining RBCs. Furthermore, the inclusion of control variables reveals varying degrees of increased convergence speed. Environmental regulation intensity (ERI), gross domestic product (GDP), energy consumption structure (ECS), technology development level (T), industrial structure (IS) and foreign direct investment demonstrate significant regional and type heterogeneity in the changes in the carbon emission performance index of RBCs. Finally, based on the analysis results, implications are proposed to enhance the carbon emission performance of RBCs of different types, as well as at the national and regional levels. Full article
(This article belongs to the Section Environmental Sustainability and Applications)
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<p>Changes in NMTCPI and decomposition mean for different regions and types.</p>
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<p>Changes in NMTCPI and decomposition mean for different regions and types.</p>
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<p>Regional overall difference and its contribution proportion decomposition diagram.</p>
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<p>Intra-regional differences and inter-regional differences line chart.</p>
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<p>The overall difference of type and its contribution percentage decomposition diagram.</p>
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<p>Intra-type difference and inter-type difference line chart.</p>
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<p>Kernel density map of the dynamic evolution of NMTCPI in China’s 116 RBCs across the country and in three major regions.</p>
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<p>The <span class="html-italic">σ</span> convergence line chart by region and type of NMTCPI.</p>
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25 pages, 1472 KiB  
Review
A Comprehensive Review of Multiple Physical and Data-Driven Model Fusion Methods for Accurate Lithium-Ion Battery Inner State Factor Estimation
by Junjie Tao, Shunli Wang, Wen Cao, Carlos Fernandez and Frede Blaabjerg
Batteries 2024, 10(12), 442; https://doi.org/10.3390/batteries10120442 - 13 Dec 2024
Viewed by 304
Abstract
With the rapid global growth in demand for renewable energy, the traditional energy structure is accelerating its transition to low-carbon, clean energy. Lithium-ion batteries, due to their high energy density, long cycle life, and high efficiency, have become a core technology driving this [...] Read more.
With the rapid global growth in demand for renewable energy, the traditional energy structure is accelerating its transition to low-carbon, clean energy. Lithium-ion batteries, due to their high energy density, long cycle life, and high efficiency, have become a core technology driving this transformation. In lithium-ion battery energy storage systems, precise state estimation, such as state of charge, state of health, and state of power, is crucial for ensuring system safety, extending battery lifespan, and improving energy efficiency. Although physics-based state estimation techniques have matured, challenges remain regarding accuracy and robustness in complex environments. With the advancement of hardware computational capabilities, data-driven algorithms are increasingly applied in battery management, and multi-model fusion approaches have emerged as a research hotspot. This paper reviews the fusion application between physics-based and data-driven models in lithium-ion battery management, critically analyzes the advantages, limitations, and applicability of fusion models, and evaluates their effectiveness in improving state estimation accuracy and robustness. Furthermore, the paper discusses future directions for improvement in computational efficiency, model adaptability, and performance under complex operating conditions, aiming to provide theoretical support and practical guidance for developing lithium-ion battery management technologies. Full article
(This article belongs to the Section Battery Modelling, Simulation, Management and Application)
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<p>Flowchart of model-based state estimation.</p>
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<p>Common types of equivalent circuit models. (<b>a</b>) Randles ECM; (<b>b</b>) Thevenin ECM; (<b>c</b>) PNGV ECM; (<b>d</b>) Second-order RC ECM; (<b>e</b>) Fractional-order ECM.</p>
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<p>Schematic diagrams of the SPM and P2D model. (<b>a</b>) Single particle model; (<b>b</b>) Pseudo-2D model.</p>
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<p>Flowchart of state estimation based on data-driven models.</p>
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14 pages, 11542 KiB  
Article
Open-Source High-Throughput Phenotyping for Blueberry Yield and Maturity Prediction Across Environments: Neural Network Model and Labeled Dataset for Breeders
by Jing Zhang, Jerome Maleski, Hudson Ashrafi, Jessica A. Spencer and Ye Chu
Horticulturae 2024, 10(12), 1332; https://doi.org/10.3390/horticulturae10121332 - 13 Dec 2024
Viewed by 326
Abstract
Time to maturity and yield are important traits for highbush blueberry (Vaccinium corymbosum) breeding. Proper determination of the time to maturity of blueberry varieties and breeding lines informs the harvest window, ensuring that the fruits are harvested at optimum maturity and [...] Read more.
Time to maturity and yield are important traits for highbush blueberry (Vaccinium corymbosum) breeding. Proper determination of the time to maturity of blueberry varieties and breeding lines informs the harvest window, ensuring that the fruits are harvested at optimum maturity and quality. On the other hand, high-yielding crops bring in high profits per acre of planting. Harvesting and quantifying the yield for each blueberry breeding accession are labor-intensive and impractical. Instead, visual ratings as an estimation of yield are often used as a faster way to quantify the yield, which is categorical and subjective. In this study, we developed and shared a high-throughput phenotyping method using neural networks to predict blueberry time to maturity and to provide a proxy for yield, overcoming the labor constraints of obtaining high-frequency data. We aim to facilitate further research in computer vision and precision agriculture by publishing the labeled image dataset and the trained model. In this research, true-color images of blueberry bushes were collected, annotated, and used to train a deep neural network object detection model [You Only Look Once (YOLOv11)] to detect mature and immature berries. Different versions of YOLOv11 were used, including nano, small, and medium, which had similar performance, while the medium version had slightly higher metrics. The YOLOv11m model shows strong performance for the mature berry class, with a precision of 0.90 and an F1 score of 0.90. The precision and recall for detecting immature berries were 0.81 and 0.79. The model was tested on 10 blueberry bushes by hand harvesting and weighing blueberries. The results showed that the model detects approximately 25% of the berries on the bushes, and the correlation coefficients between model-detected and hand-harvested traits were 0.66, 0.86, and 0.72 for mature fruit count, immature fruit count, and mature ratio, respectively. The model applied to 91 blueberry advance selections and categorized them into groups with diverse levels of maturity and productivity using principal component analysis (PCA). These results inform the harvest window and yield of these breeding lines with precision and objectivity through berry classification and quantification. This model will be helpful for blueberry breeders, enabling more efficient selection, and for growers, helping them accurately estimate optimal harvest windows. This open-source tool can potentially enhance research capabilities and agricultural productivity. Full article
(This article belongs to the Special Issue AI-Powered Phenotyping of Horticultural Plants)
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<p>Map of the locations of the blueberry orchards where images were collected.</p>
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<p>The picture is cropped into smaller sections for labeling, model training, and prediction.</p>
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<p>Cropped images and their annotations of two classes: mature (purple box) and immature fruits (yellow box). The image contains 184 mature and 48 immature annotations.</p>
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<p>Histogram showing distributions of (<b>A</b>) immature fruit count, (<b>B</b>) mature fruit count, (<b>C</b>) mature ratio predicted from the model, and (<b>D</b>) visual ratings of mature ratio on a 1 to 6 scale in a blueberry population consisting of 91 breeding lines in Alapaha, GA, 2023.</p>
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<p>Pearson correlation among immature fruit count, mature fruit count, total fruit count, mature ratio detected by the model and visual ratings of mature ratio in a blueberry mapping population in Alapaha, GA, 2023. **, and *** indicate significance at 0.05, 0.01, and 0.001 <span class="html-italic">P</span> level.</p>
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<p>Principal component analysis (PCA) showing (<b>A</b>) variable contributions for berry count, mature ratio, and visual ratings of maturity and (<b>B</b>) cluster results based on the PCA analysis.</p>
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20 pages, 5085 KiB  
Article
Antioxidant Effects and Potential Mechanisms of Citrus reticulata ‘Chachi’ Components: An Integrated Approach of Network Pharmacology and Metabolomics
by Jiahao Xiao, Tian Sun, Shengyu Jiang, Zhiqiang Xiao, Yang Shan, Tao Li, Zhaoping Pan, Qili Li and Fuhua Fu
Foods 2024, 13(24), 4018; https://doi.org/10.3390/foods13244018 - 12 Dec 2024
Viewed by 437
Abstract
Citrus reticulata ‘Chachi’ (CRC), recognized for its considerable edible and medicinal significance, is a valuable source of metabolites beneficial to human health. This research investigates the metabolic distinctions and antioxidant properties across four different parts of CRC, using multivariate statistical analysis to interpret [...] Read more.
Citrus reticulata ‘Chachi’ (CRC), recognized for its considerable edible and medicinal significance, is a valuable source of metabolites beneficial to human health. This research investigates the metabolic distinctions and antioxidant properties across four different parts of CRC, using multivariate statistical analysis to interpret metabolomic data and network pharmacology to identify potential antioxidant targets and relevant signaling pathways. The results indicate considerable metabolic differences in different parts of the sample, with 1622 metabolites showing differential expression, including 816 secondary metabolites, primarily consisting of terpenoids (31.02%) and flavonoids (25.22%). The dried mature citrus peel (CP) section demonstrates the highest level of total phenolics (6.8 mg/g), followed by the pulp without seed (PU) (4.52 mg/g), pulp with seed (PWS) (4.26 mg/g), and the seed (SE) (2.16 mg/g). Interestingly, targeted high-performance liquid chromatography of flavonoids reveals the highest level of nobiletin and tangeretin in CP, whereas PU has the highest level of hesperidin, narirutin, and didymin. Furthermore, all four sections of CRC exhibit robust antioxidant properties in in vitro assessments (CP > PU > PWS > SE). Lastly, the network pharmacology uncovered potential antioxidant mechanisms in CRC. This research offers deeper insights into the development and utilization of byproducts in the CRC processing industry. Full article
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<p>(<b>A</b>) Classification of primary metabolites. (<b>B</b>) Classification of secondary metabolites. (<b>C</b>) Three-dimensional PCA score plot. (<b>D</b>) PLS-DA score plot. (<b>E</b>) Permutation test plot with 200 permutations. (<b>F</b>) Sample correlation heat map.</p>
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<p>(<b>A</b>–<b>C</b>) OPLS-DA score plots. (<b>A</b>) CP and PU; (<b>B</b>) PWS and PU; (<b>C</b>) SE and PU. (<b>D</b>–<b>F</b>) Volcano plots of differential metabolite expression levels. (<b>D</b>) CP and PU; (<b>E</b>) PWS and PU; (<b>F</b>) SE and PU.</p>
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<p>(<b>A</b>) Venn diagram of differential metabolites; (<b>B</b>) Classification of 816 secondary differential metabolites.</p>
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<p>Heat maps display the levels of secondary differentially expressed metabolites in four parts of CRC. (<b>A</b>) Flavonoids; (<b>B</b>) Terpenoids; (<b>C</b>) Phenolic acids and derivatives; (<b>D</b>) Steroids and steroid derivatives.</p>
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<p>Heat maps display the levels of secondary differentially expressed metabolites in four parts of CRC. (<b>A</b>) Coumarins and derivatives; (<b>B</b>) Organic acids and derivatives; (<b>C</b>) Alkaloids and derivatives; (<b>D</b>) Others.</p>
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<p>Bubble chart of KEGG enrichment pathways for secondary differential metabolites.</p>
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<p>HPLC chromatograms of 16 flavonoid standards (1, Verbascoside; 2, Taxifolin; 3, Narirutin; 4, Naringin; 5, Hesperidin; 6, Neohesperidin; 7, Rutin; 8, Rhoifolin; 9, Diosmin; 10, Didymin; 11, Hesperetin; 12, Luteolin; 13, Diosmetin; 14, Sinensetin; 15, Nobiletin; 16, Tangeretin) and samples. (<b>A</b>) Flavonoid standard mixture, 283 nm. (<b>B</b>) Flavonoid standard mixture, 330 nm. (<b>C</b>) PU, 283 nm. (<b>D</b>) CP, 330 nm. (<b>E</b>) PWS, 283 nm. (<b>F</b>) SE, 283 nm.</p>
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<p>(<b>A</b>) Venn diagram of overlapping targets between flavonoid active components and oxidative damage. (<b>B</b>,<b>C</b>) Protein–protein interaction (PPI) analysis network diagram. (<b>C</b>) Top 10 GO enrichment analysis bar chart. (<b>D</b>) Top 20 KEGG enrichment analysis bubble chart of signaling pathways.</p>
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15 pages, 1825 KiB  
Review
Evaluation of Breeding Progress and Agronomic Traits for Japonica Rice in Anhui Province, China (2005–2024)
by Yu Zou, Muhammad Ahmad Hassan, Ending Xu, Yi Ren, Jie Wang, Xinchun Zhan, Dahu Ni and Peijiang Zhang
Agronomy 2024, 14(12), 2957; https://doi.org/10.3390/agronomy14122957 - 12 Dec 2024
Viewed by 265
Abstract
Rice is the staple diet for most of the world’s population and is considered a major staple crop in China. Anhui province of China is among the leading provinces for rice production, consumption, and commodities; it is well-known as the “land of fish [...] Read more.
Rice is the staple diet for most of the world’s population and is considered a major staple crop in China. Anhui province of China is among the leading provinces for rice production, consumption, and commodities; it is well-known as the “land of fish and rice”. Japonica rice cultivation in Anhui Province is mainly categorized into late-maturing medium, early-maturing medium, and early-maturing late japonica. This review explores the suitable ecological zone distribution and corresponding climate characteristics of the three types of japonica rice in Anhui Province. Data on japonica rice varieties approved in the province over the past twenty years were collected, illustrating the development process of japonica rice varieties in the province and their quality and resistance to rice blast disease. The review shows that the yield is positively and significantly correlated with agronomic traits, such as the number of effective panicles and the total number of grains per panicle, plant height, etc. In addition, it elucidates the major problems faced by Anhui’s japonica rice breeding and cultivation, such as frequent events of high temperatures, rice blast disease, and medium to low soil fertility levels. Considering the existing issues in breeding japonica rice varieties in Anhui Province, this review proposes a strategy for breeding high-yield and disease-resistant japonica rice varieties, particularly varieties adaptable to medium and low fertility soil conditions. In brief, this article provides a theoretical basis and practical recommendations for the sustainable development of japonica rice in the Anhui Province of China. Full article
(This article belongs to the Special Issue Innovative Research on Rice Breeding and Genetics)
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<p>Rice geographical distribution map of the five major rice areas in Anhui province of China: (<b>a</b>) the location of Anhui province in China; (<b>b</b>) the administrative division of Anhui province; (<b>c</b>) the distribution of the five major rice cultivation areas and three types of <span class="html-italic">japonica</span> rice in Anhui province.</p>
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<p>AMMI2 biplots of 30 <span class="html-italic">japonica</span> rice genotypes were tested in four environments for regional trial yield. Regional Trial Yield—RTY; First principal component—PC1; Second principal component—PC2; Environment—E; Genotype—G.</p>
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<p>(<b>a</b>) Rainfall during rice growth from May to November for Fengtai, Nanling, and Quanjiao between 2005 and 2023; (<b>b</b>) Effective accumulate temperature during rice growth from May to November for Fengtai, Nanling, and Quanjiao between 2005 and 2023; (<b>c</b>) Sunshine hours during rice growth from May to November for Fengta, Nanling, and Quanjiao between 2005 and 2023.</p>
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<p>Analysis of significant differences in average rainfall (<b>a</b>), effective accumulated temperature (<b>b</b>), and sunshine hours (<b>c</b>) in Nanling, Quanjiao, and Fengtai between 2005 and 2023. Differential letters indicate statistical differences (LSD test, <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Genetic progress from the generalized linear regression of grain yield by year. Estimations were performed using EML <span class="html-italic">japonica</span> rice (<b>a</b>) and LMM <span class="html-italic">japonica</span> rice (<b>b</b>) varieties released from 2005 to 2024.</p>
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17 pages, 3630 KiB  
Article
Porcine Epidemic Diarrhea Virus Infection of Porcine Intestinal Epithelial Cells Causes Mitochondrial DNA Release and the Activation of the NLRP3 Inflammasome to Mediate Interleukin-1β Secretion
by Di Bao, Shushuai Yi, Luobing Zhao, Han Zhao, Jiuyuan Liu, Yiming Wei, Guixue Hu and Xinxin Liu
Vet. Sci. 2024, 11(12), 643; https://doi.org/10.3390/vetsci11120643 - 12 Dec 2024
Viewed by 369
Abstract
Porcine epidemic diarrhea virus (PEDV) induces enteritis and diarrhea in piglets. Mitochondrial DNA (mtDNA) contributes to virus-induced inflammatory responses; however, the involvement of inflammasomes in PEDV infection responses remains unclear. We investigated the mechanism underlying inflammasome-mediated interleukin (IL)-1β secretion during the PEDV infection [...] Read more.
Porcine epidemic diarrhea virus (PEDV) induces enteritis and diarrhea in piglets. Mitochondrial DNA (mtDNA) contributes to virus-induced inflammatory responses; however, the involvement of inflammasomes in PEDV infection responses remains unclear. We investigated the mechanism underlying inflammasome-mediated interleukin (IL)-1β secretion during the PEDV infection of porcine intestinal epithelial (IPEC-J2) cells. IL-1β production and caspase-1 activity were assessed by quantitative PCR and enzyme-linked immunosorbent assay. NLRP3 inflammasome activation was assessed using immunoprecipitation experiments. Mitochondrial damage was evaluated by analyzing the mitochondrial membrane potential and ATP levels and by the flow cytometry examination of mitochondrial reactive oxygen species (mtROS). Mitochondria and mtDNA localization were observed using immunofluorescence. The inhibition of mtROS and mtDNA production allowed NLRP3 inflammasome and IL-1β expression detection and the evaluation of the pathway underlying NLRP3 inflammasome activation in PEDV-infected IPEC-J2 cells. IPEC-J2 cells upregulated IL-1β upon PEDV infection, where mature IL-1β secretion depended on caspase-1 activity, triggered NLRP3 inflammasome expression and assembly, and caused mitochondrial dysfunction, leading to mtDNA release and NLRP3 inflammasome activation, while mtROS contributed to NF-κB pathway activation, enhancing IL-1β secretion. This is the first demonstration of the mechanism underlying mtDNA release and NLRP3 inflammasome activation facilitating IL-1β secretion from PEDV-infected IPEC-J2 cells. These data enhance our understanding of the inflammatory mechanisms triggered by PEDV. Full article
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<p>Porcine epidemic diarrhea virus (PEDV) infects IPEC-J2 cells to promote the secretion of mature interleukin (IL)-1β. PEDV (multiplicity of infection (MOI) = 1) was used to infect IPEC-J2 cells for the specified periods of time. Detection of PEDV N protein expression via Western blot following PEDV infection in IPEC-J2 cells (<b>a</b>). mRNA expression (<b>b</b>) and Western blot (<b>f</b>) analyses of IL-1β levels, as well as the results of an enzyme-linked immunosorbent assay (ELISA) to assess IL-1β secretion in the cell supernatants (<b>c</b>). IPEC-J2 cells were infected with PEDV at the specified dose for 24 h, followed by fluorescence quantification (<b>d</b>), Western blotting (<b>g</b>), and the ELISA detection of IL-1β secretion in the cell supernatant (<b>e</b>). Data represent the mean ± SD (<span class="html-italic">n</span> = 3). * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>PEDV promotes caspase-1 enzymatic activity in IPEC-J2 cells. Caspase-1 enzyme activity (<b>a</b>) and Western blot results (<b>b</b>) at the specified time points after the PEDV infection of IPEC-J2 cells (MOI = 1). Caspase-1 enzyme activity (<b>c</b>) and Western blot results (<b>d</b>) of IPEC-J2 cells infected with PEDV at the specified doses for 24 h. IPEC-J2 cells were treated with the caspase-1 inhibitor, Ac-YVAD-cmk, at the specified concentration for 1 h and then inoculated with PEDV (MOI = 1). ELISA was used to detect IL-1β secretion in the cell supernatant 24 h after infection (<b>e</b>). Data represent the mean ± SD (<span class="html-italic">n</span> = 3). * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>PEDV infection of IPEC-J2 cells activates the NLRP3 inflammasome. PEDV was used to infect IPEC-J2 cells at the specified doses for 24 h and then the <span class="html-italic">NLRP3</span> inflammasome (<b>a</b>) and <span class="html-italic">ASC</span> (<b>c</b>) mRNA expression were analyzed. <span class="html-italic">NLRP3</span> (<b>b</b>) and <span class="html-italic">ASC</span> (<b>d</b>) mRNA expression in IPEC-J2 cells infected with PEDV (MOI = 1) for the specified times. NLRP3 (<b>e</b>) and ASC (<b>f</b>) rabbit-derived primary antibodies were used as bait antibodies and rabbit serum was used as the negative control antibody in a co-immunoprecipitation experiment. Data represent the mean ± SD (<span class="html-italic">n</span> = 3). * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>PEDV-infected IPEC-J2 cells secrete IL-1β through NLRP3 inflammasome activity. IPEC-J2 cells were treated with 10 µM MCC950 for 1 h, and negative control cells were treated with DMSO for the same time. After 24 h of cell infection with PEDV (MOI = 1), IL-1β secretion in the cell supernatants was detected by ELISA (<b>a</b>) and <span class="html-italic">IL-1β</span> mRNA quantified by fluorescence (<b>c</b>). siNLRP3 and siCtrl (control) were transfected into IPEC-J2 cells. PEDV was used to infect cells (MOI = 1) for 24 h, IL-1β secretion in the cell supernatants was detected by ELISA (<b>b</b>), and <span class="html-italic">IL-1β</span> mRNA expression was quantified by fluorescence (<b>d</b>). Western blot of IPEC-J2 cells treated with 10 µM MCC950 (<b>e</b>) and siNLRP3 transfection of IPEC-J2 cells to detect the expression of inflammasome proteins (<b>f</b>). Data represent the mean ± SD (<span class="html-italic">n</span> = 3),** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>PEDV infection causes mitochondrial dysfunction and results in mitochondrial reactive oxygen species (mtROS) production and mitochondrial DNA (mtDNA) release. Mitochondrial membrane potential was decreased (<b>a</b>). Reduced ATP production after PEDV infection (<b>b</b>). Flow cytometry fluorescence intensity analysis of mtROS production after PEDV infection (<b>c</b>). Immunofluorescence showing mtDNA release after PEDV infection (<b>d</b>). Data represent mean ± SD (<span class="html-italic">n</span> = 3), ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>mtROS are involved in NF-κB activation in PEDV-infected IPEC-J2 cells. IPEC-J2 cells were infected with PEDV at the specified doses for 24 h and the expression levels of pp65 and p65 detected by Western blot (<b>a</b>). IPEC-J2 cells were treated with the NF-κB inhibitor BAY11-7082 (10 μM). <span class="html-italic">IL-1β</span> mRNA expression was detected 24 h after PEDV infection (MOI = 1) (<b>b</b>) and IL-1β secretion in the cell supernatant detected by ELISA (<b>c</b>). Western blot to assess the expression of pp65, p65, and IL-1β proteins (<b>d</b>). After IPEC-J2 cells were treated with 10 µM Mito-TEMPO for 1 h, <span class="html-italic">IL-1β</span> mRNA expression was detected following PEDV infection (MOI = 1) for 24 h (<b>e</b>) and IL-1β secretion in the cell supernatant detected by ELISA (<b>f</b>). Data represent mean ± SD (<span class="html-italic">n</span> = 3), ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>mtDNA participates in NLRP3 inflammasome activation in PEDV-infected IPEC-J2 cells. After transfection with DNase I, IPEC-J2 cells were infected with PEDV (MOI = 1). IL-1β mRNA expression (<b>a</b>) and secretion in cell supernatants detected by ELISA (<b>b</b>). <span class="html-italic">NLRP3</span> inflammasome mRNA expression (<b>c</b>) and caspase-1 enzyme activity (<b>d</b>). Western blot detection of NLRP3 inflammasome and downstream protein expression after transfection with DNase I protein (<b>e</b>). Data represent mean ± SD (<span class="html-italic">n</span> = 3). ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Schematic showing that PEDV infection leads to cytoplasmic mitochondrial DNA release and the activation of the NLPR3 inflammasome.</p>
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24 pages, 6400 KiB  
Article
Holistic Dynamic Modeling and Simulation of Alkaline Water Electrolysis Systems Based on Heat Current Method
by Yi-Chong Jiang, Shi-Meng Dong, Zheng Liang, Xiao-Li Wang, Lei Shi, Bing Yan and Tian Zhao
Energies 2024, 17(23), 6202; https://doi.org/10.3390/en17236202 - 9 Dec 2024
Viewed by 412
Abstract
Hydrogen production technology is becoming increasingly important with the rapid development of hydrogen energy. Among existing hydrogen production technologies, alkaline water electrolysis (AWE) is drawing wide attention due to its advantages such as high maturity and low cost, and its performance analysis and [...] Read more.
Hydrogen production technology is becoming increasingly important with the rapid development of hydrogen energy. Among existing hydrogen production technologies, alkaline water electrolysis (AWE) is drawing wide attention due to its advantages such as high maturity and low cost, and its performance analysis and optimization are important for applications. However, the AWE system contains processes with different physical and mathematical properties such as electrochemical reaction and heat transport processes, bringing difficulties to the system modeling. Moreover, the electrical and thermal processes have different characteristic time scales, and the system shows a sophisticated dynamic behavior, which has not been well studied yet. Here, a homomorphic dynamic model of the AWE system in the form of electrical circuit is built to describe the thermal and electrochemical processes uniformly, where the two parts are integrated via the energy conservation seamlessly. The model is verified by comparing with the experimental data and shows a high accuracy. The dynamic simulation analysis is conducted to investigate the dynamic response characteristics of the system under current step changes and fluctuations. The temperature overshoot and oscillation phenomena caused by delays in heat transport processes are studied. Results show that the time delay yields a maximum temperature overshoot of 10 °C, which would reduce the lifespan of the stack. This also highlights the importance of dynamic system analysis. Full article
(This article belongs to the Section A5: Hydrogen Energy)
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<p>Sketch of the AWE system.</p>
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<p>Electrical circuit model of a cell in the stack.</p>
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<p>Heat balance diagram of the stack.</p>
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<p>Sketch of the heat transport process in the stack, the stack is simplified as a pipeline for clarity.</p>
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<p>Heat current model of the stack.</p>
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<p>Heat balance of the hydrogen gas-liquid separator.</p>
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<p>Heat current model of the hydrogen gas-liquid separator and the pipeline.</p>
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<p>Heat balance of the oxygen gas-liquid separator.</p>
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<p>Heat current model of the oxygen gas-liquid separator and the pipeline.</p>
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<p>Mixer model, (<b>a</b>) schematic diagram of the mixer, (<b>b</b>) heat current model of the mixer.</p>
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<p>Dynamic heat current model of heat exchanger, (<b>a</b>) schematic diagram of the heat exchanger, (<b>b</b>) heat current model of the heat exchanger.</p>
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<p>Dynamic heat current model of the segmented heat exchanger. (<b>a</b>) heat exchanger with multiple segments, (<b>b</b>) heat current model of the entire heat exchanger.</p>
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<p>Overall heat current model of the AWE system.</p>
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<p>Comparison of polarization curves of the HRI stack.</p>
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<p>Comparison of the results of the dynamic temperature model of the inlet and outlet of the stack and the steady-state model.</p>
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<p>Average stack temperature variation with the current variation.</p>
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<p>Voltage and voltage efficiency over time in the case of current steps.</p>
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<p>Input current in evaluation of hydrogen production rate and Faraday efficiency.</p>
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<p>Hydrogen production rate over time.</p>
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<p>Faraday efficiency over time.</p>
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<p>Cooling water flow, temperature, and power of the stack for 15–40 h.</p>
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16 pages, 2783 KiB  
Article
Functional Analysis of TAAR1 Expression in the Intestine Wall and the Effect of Its Gene Knockout on the Gut Microbiota in Mice
by Anastasia N. Vaganova, Ilya S. Zhukov, Taisiia S. Shemiakova, Konstantin A. Rozhkov, Lyubov S. Alferova, Alena B. Karaseva, Elena I. Ermolenko and Raul R. Gainetdinov
Int. J. Mol. Sci. 2024, 25(23), 13216; https://doi.org/10.3390/ijms252313216 - 9 Dec 2024
Viewed by 415
Abstract
Currently, the TAAR1 receptor has been identified in various cell groups in the intestinal wall. It recognizes biogenic amine compounds like phenylethylamine or tyramine, which are products of decarboxylation of phenylalanine and tyrosine by endogenous or bacterial decarboxylases. Since several gut bacteria produce [...] Read more.
Currently, the TAAR1 receptor has been identified in various cell groups in the intestinal wall. It recognizes biogenic amine compounds like phenylethylamine or tyramine, which are products of decarboxylation of phenylalanine and tyrosine by endogenous or bacterial decarboxylases. Since several gut bacteria produce these amines, TAAR1 is suggested to be involved in the interaction between the host and gut microbiota. The purpose of this present study was to clarify the TAAR1 function in the intestinal wall and estimate the TAAR1 gene knockout effect on gut microbiota composition. By analyzing public transcriptomic data of the GEO repository, we identified TAAR1 expression in enterocytes, enteroendocrine cells, tuft cells, and myenteric neurons in mice. The analysis of genes co-expressed with TAAR1 in enteroendocrine cells allows us to suggest the TAAR1 involvement in enteroendocrine cell maturation. Also, in myenteric neurons, we identified the co-expression of TAAR1 with calbindin, which is specific for sensory neurons. The 16S rRNA gene-based analysis of fecal microbiota revealed a slight but significant impact of TAAR1 gene knockout in mice on the gut microbial community, which manifests in the higher diversity, accompanied by low between-sample variability and reorganization of the microbial co-occurrence network. Full article
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<p>Sources of trace amines (TA) in the gut. The major process of TA biogenesis marked by the bold arrows is the decarboxylation of amino acids by bacterial aromatic amino acid decarboxylases (AADCs). Additionally, mammalian AADC (encoded by gene <span class="html-italic">DOPA decarboxylase</span>, <span class="html-italic">DDC</span>) is produced by intestine epithelial cells involved in the TA biogenesis in the gastrointestinal tract as marked by dotted arrows.</p>
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<p>TAAR1 mRNA expression in the fractionated murine intestine wall cell samples. The expression of TAAR1 mRNA in various cell fractions described in different datasets is represented. Threshold level (0.1 CPM) is marked with a dotted line (<b>a</b>). Functional analysis of top 50 genes co-expressed (cut-off values were ρ &gt; 0.7, <span class="html-italic">p</span> &lt; 0.05) with TAAR1 in normal adult wild-type mice enteroendocrine cells (GSE121489) with Gene Ontology (GO) Biologic process (BP) term enrichment analysis, (<b>b</b>) GO molecular function (MF) term enrichment analysis (<b>c</b>), or Kyoto Encyclopedia of Genes and Genomes (KEGG)-pathway enrichment analysis (<b>d</b>). Functional analysis of genes (<span class="html-italic">n</span> = 26) co-expressed with TAAR1 in enteric neurons (cut-off values were ρ &gt; 0.7, <span class="html-italic">p</span> &lt; 0.05, GSE140291) by (<b>e</b>) GO MF term enrichment analysis or (<b>f</b>) KEGG pathway enrichment analysis.</p>
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<p>TAAR1 mRNA expression in the fractionated murine intestine wall cell samples. The expression of TAAR1 mRNA in various cell fractions described in different datasets is represented. Threshold level (0.1 CPM) is marked with a dotted line (<b>a</b>). Functional analysis of top 50 genes co-expressed (cut-off values were ρ &gt; 0.7, <span class="html-italic">p</span> &lt; 0.05) with TAAR1 in normal adult wild-type mice enteroendocrine cells (GSE121489) with Gene Ontology (GO) Biologic process (BP) term enrichment analysis, (<b>b</b>) GO molecular function (MF) term enrichment analysis (<b>c</b>), or Kyoto Encyclopedia of Genes and Genomes (KEGG)-pathway enrichment analysis (<b>d</b>). Functional analysis of genes (<span class="html-italic">n</span> = 26) co-expressed with TAAR1 in enteric neurons (cut-off values were ρ &gt; 0.7, <span class="html-italic">p</span> &lt; 0.05, GSE140291) by (<b>e</b>) GO MF term enrichment analysis or (<b>f</b>) KEGG pathway enrichment analysis.</p>
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<p>The basic structure of the bacterial community composition. Relative abundance of fecal microbiota composition at the phylum level in each sample (<b>a</b>) and study group (<b>b</b>) for TAAR1-KO mice and wild-type littermates. The top ten phyla are presented. Each bar in (<b>a</b>) represents a single fecal sample, and each bar in (<b>b</b>) represents a group.</p>
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<p>The comparison of gut microbiota α-diversity among TAAR1-knockout (TAAR1-KO) and wild-type (WT) mice. α-diversity was measured by observed OTUs, Chao1, abundance-based coverage estimator (ACE), Shannon, Simpson, and Pielou. Box plots and violin plots depict microbiome diversity and abundance differences according to each test. The horizontal line inside the box represents the median. Individual sample values are represented by dots. Wilcoxon’s test was applied to compare groups.</p>
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<p>Heatmap (<b>a</b>) representing the Bray–Curtis dissimilarity (bray) in the bacterial community structure between samples. The genotype is marked by color. No clustering of samples based on the genotype (i.e., WT or TAAR1-KO) was identified. Box plots (<b>b</b>) of the Bray–Curtis dissimilarity index within groups and between groups represent significant differences between phenotypes. Wilcoxon’s test was applied to compare Bray–Curtis dissimilarity values in TAAR1-KO and WT groups. These results confirm the differences in β-diversity among TAAR1-KO and wild-type (WT) mice. *—<span class="html-italic">p</span> value &lt; 0.05, **—<span class="html-italic">p</span> value &lt; 0.01, ***—<span class="html-italic">p</span> value &lt; 0.001.</p>
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18 pages, 671 KiB  
Article
Impact of French Oak Chip Maturation on the Volatile Composition and Sensory Profile of Agiorgitiko Wine
by Ioannis Ligas and Yorgos Kotseridis
Beverages 2024, 10(4), 121; https://doi.org/10.3390/beverages10040121 - 9 Dec 2024
Viewed by 475
Abstract
The traditional practice of aging wines in oak barrels has long been associated with the evolution of wine aromas. However, due to rising costs, alternative approaches like aging with oak chips have gained popularity. The aging time, addition dose, and type of toasting [...] Read more.
The traditional practice of aging wines in oak barrels has long been associated with the evolution of wine aromas. However, due to rising costs, alternative approaches like aging with oak chips have gained popularity. The aging time, addition dose, and type of toasting of the oak chips are critical parameters affecting the quality of the wine’s aroma. In this study, we focus on wines from Agiorgitiko variety and explore the impact of oak chip maturation on both volatile composition and sensory profile. By analyzing volatile compounds of wine aroma using GC-MS/MS and conducting descriptive sensory analysis, we investigate the effects of three different oak chip toasting levels, three dosages, and three aging periods. Our findings reveal that almost all wines aged with oak chips exhibit higher ester concentrations compared to the control. Notably, heavily toasted oak chips contribute to the sensory attribute of smoky aroma, while medium oak chips are associated with the sensory attribute of barrel aroma. This study provides valuable data for winemakers to determine the most suitable application for their product. Full article
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<p>PCA for the sensory attributes fruity aroma, barrel aroma, smoky aroma, aroma complexity, flavor intensity, the compounds acetovanillone, 4-ethylguaiacol, guaiacol, vanillin, <span class="html-italic">trans</span>-whiskey lactone, <span class="html-italic">cis</span>-whiskey lactone, the OAV Fruity and OAV Oak Compounds in score plot form.</p>
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<p>PCA for the sensory attributes fruity aroma, barrel aroma, smoky aroma, aroma complexity, flavor intensity, the compounds acetovanillone, 4-ethylguaiacol, guaiacol, vanillin, <span class="html-italic">trans</span>-whiskey lactone, <span class="html-italic">cis</span>-whiskey lactone, the OAV Fruity and OAV Oak Compounds in loading plot form.</p>
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15 pages, 524 KiB  
Study Protocol
Describing Biological Vulnerability in Small, Vulnerable Newborns in Urban Burkina Faso (DenBalo): Gut Microbiota, Immune System, and Breastmilk Assembly
by Lionel Olivier Ouédraogo, Lishi Deng, Cheick Ahmed Ouattara, Anderson Compaoré, Moctar Ouédraogo, Alemayehu Argaw, Carl Lachat, Eric R. Houpt, Queen Saidi, Filomeen Haerynck, Justin Sonnenburg, Meghan B. Azad, Simon J. Tavernier, Yuri Bastos-Moreira, Laeticia Celine Toe and Trenton Dailey-Chwalibóg
Nutrients 2024, 16(23), 4242; https://doi.org/10.3390/nu16234242 - 9 Dec 2024
Viewed by 441
Abstract
Background: Small vulnerable newborns (SVNs), including those born preterm, small for gestational age, or with low birth weight, are at higher risk of neonatal mortality and long-term health complications. Early exposure to maternal vaginal microbiota and breastfeeding plays a critical role in [...] Read more.
Background: Small vulnerable newborns (SVNs), including those born preterm, small for gestational age, or with low birth weight, are at higher risk of neonatal mortality and long-term health complications. Early exposure to maternal vaginal microbiota and breastfeeding plays a critical role in the development of the neonatal microbiota and immune system, especially in low-resource settings like Burkina Faso, where neonatal mortality rates remain high. Objectives: The DenBalo study aims to investigate the role of maternal and neonatal factors, such as vaginal and gut microbiota, immune development, and early nutrition, in shaping health outcomes in SVNs and healthy infants. Methods: This prospective cohort observational study will recruit 141 mother-infant pairs (70 SVNs and 71 healthy controls) from four health centers in Bobo-Dioulasso, Burkina Faso. The mother-infant pairs will be followed for six months with anthropometric measurements and biospecimen collections, including blood, breast milk, saliva, stool, vaginal swabs, and placental biopsies. Multi-omics approaches, encompassing metagenomics, metabolomics, proteomics, and immune profiling, will be used to assess vaginal and gut microbiota composition and functionality, immune cell maturation, and cytokine levels at critical developmental stages. Conclusions: This study will generate comprehensive data on how microbiota, metabolomic, and proteomic profiles, along with immune system development, differ between SVNs and healthy infants. These findings will guide targeted interventions to improve neonatal health outcomes and reduce mortality, particularly in vulnerable populations. Full article
(This article belongs to the Section Pediatric Nutrition)
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<p>Flow chart of the DenBalo study schedule.</p>
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14 pages, 4118 KiB  
Article
Differentiation of Soybean Genotypes Concerning Seed Physiological Quality Using Hyperspectral Bands
by Izabela Cristina de Oliveira, Dthenifer Cordeiro Santana, Victoria Toledo Romancini, Ana Carina da Silva Cândido Seron, Charline Zaratin Alves, Paulo Carteri Coradi, Carlos Antônio da Silva Júnior, Regimar Garcia dos Santos, Fábio Henrique Rojo Baio, Paulo Eduardo Teodoro and Larissa Ribeiro Teodoro
AgriEngineering 2024, 6(4), 4752-4765; https://doi.org/10.3390/agriengineering6040272 - 9 Dec 2024
Viewed by 347
Abstract
The use of summarized spectral data in bands obtained by hyperspectral sensors can make it possible to obtain biochemical information about seeds and, thus, relate the results to seed viability and vigor. Thus, the hypothesis of this work is based on the possibility [...] Read more.
The use of summarized spectral data in bands obtained by hyperspectral sensors can make it possible to obtain biochemical information about seeds and, thus, relate the results to seed viability and vigor. Thus, the hypothesis of this work is based on the possibility of obtaining information about the physiological quality of seeds through hyperspectral bands and distinguishing seed lots regarding their quality through wavelengths. The objective was then to evaluate the possibility of differentiating soybean genotypes regarding the physiological quality of seeds using spectral data. The experiment was conducted during the 2021/2022 harvest at the Federal University of Mato Grosso do Sul in a randomized block design with four replicates and 10 F3 soybean populations (G1, G8, G12, G15, G19, G21, G24, G27, G31, and G36). After the maturation of each genotype, seeds were harvested from the central rows of each plot, which consisted of five one-meter rows. Seed samples from each experimental unit were placed in a Petri dish to collect spectral data. Readings were performed in the laboratory at a temperature of 26 °C and using two 60 W halogen lamps as the light source, positioned 15 cm between the sensor and the sample. The sensor used was the Ocean Optics (Florida, USA) model STS-VIS-L-50-400-SMA, which captured the reflectance of the seed sample at wavelengths between 450 and 824 nm. After readings from the hyperspectral sensor, the seeds were subjected to tests for water content, germination, first germination count, electrical conductivity, and tetrazolium. The data obtained were subjected to an analysis of variance and the means were compared by the Scott–Knott test at 5% probability, analyzed using R software version 4.2.3 (Auckland, New Zealand). The data on the physiological quality of the seeds of the soybean genotypes were subjected to principal component analysis (PCA) and associated with the K-means algorithm to form groups according to the similarity and distinction between the genetic materials. After the formation of these groups, spectral curve graphs were constructed for each soybean genotype and for the groups that were formed. The physiological quality of the soybean genotypes can be differentiated using hyperspectral bands. The spectral bands, therefore, provide important information about the physiological quality of soybean seeds. Through the use of hyperspectral sensors and the observation of specific bands, it is possible to differentiate genotypes in terms of seed quality, complementing and/or replacing traditional tests in a fast, accurate, and non-destructive way, reducing the time and investment spent on obtaining information on seed viability and vigor. The results found in this study are promising, and further research is needed in future studies with other species and genotypes. The interval between 450 and 649 nm was the main spectrum band that contributed to the differentiation between soybean genotypes of superior and inferior physiological quality. Full article
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<p>Principal component analysis for the variables PCG (first germination count), GERM (germination), EC (electrical conductivity), vigor, and viability to form two groups (C1—group with superior seed physiological quality and C2—group with inferior seed physiological quality) based on the K-means algorithm.</p>
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<p>Reflectance of seeds from 10 soybean genotypes (<b>A</b>) and the clusters (<b>B</b>) formed based on principal component analysis and the K-means algorithm (C1—group with superior seed physiological quality and C2—group with inferior seed physiological quality).</p>
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<p>Principal component analysis for the variables PCG (first germination count), GERM (germination), EC (electrical conductivity), vigor, and viability, for bands B1 (450–475 nm), B2 (480 nm), B3 (481–500 nm), B4 (501–530 nm), B5 (531–539 nm), B6 (540 nm), B7 (541–649 nm), B8 (650 nm), B9 (661–670 nm), B10 (675 nm), B11 (676–684 nm), B12 (685–689 nm), B13 (690–700 nm), B14 (701–709 nm), B15 (710 nm), and B16 (711–730 nm) of 10 soybean genotypes to form two groups (C1—group with superior seed physiological quality and C2—group with inferior seed physiological quality) based on the K-means algorithm.</p>
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<p>Reflectance of the spectral bands of the seeds of 10 soybean genotypes (<b>A</b>) and the clusters (<b>B</b>) formed based on principal component analysis and the K-means algorithm (C1—group with superior seed physiological quality and C2—group with inferior seed physiological quality).</p>
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<p>Scatterplot for the variables PCG (first germination count), GERM (germination), EC (electrical conductivity), vigor, and viability, and bands B1 (450–475 nm), B2 (480 nm), B3 (481–500 nm), B4 (501–530 nm), B5 (531–539 nm), B6 (540 nm), B7 (541–649 nm), B8 (650 nm), B9 (661–670 nm), B10 (675 nm), B11 (676–684 nm), B12 (685–689 nm), B13 (690–700 nm), B14 (701–709 nm), B15 (710 nm), and B16 (711–730 nm) of 10 soybean genotypes. *, ** and ***: significant at 5, 1 and 0.01% respectively.</p>
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14 pages, 3762 KiB  
Article
Detection of Pear Quality Using Hyperspectral Imaging Technology and Machine Learning Analysis
by Zishen Zhang, Hong Cheng, Meiyu Chen, Lixin Zhang, Yudou Cheng, Wenjuan Geng and Junfeng Guan
Foods 2024, 13(23), 3956; https://doi.org/10.3390/foods13233956 - 8 Dec 2024
Viewed by 514
Abstract
The non-destructive detection of fruit quality is indispensable in the agricultural and food industries. This study aimed to explore the application of hyperspectral imaging (HSI) technology, combined with machine learning, for a quality assessment of pears, so as to provide an efficient technical [...] Read more.
The non-destructive detection of fruit quality is indispensable in the agricultural and food industries. This study aimed to explore the application of hyperspectral imaging (HSI) technology, combined with machine learning, for a quality assessment of pears, so as to provide an efficient technical method. Six varieties of pears were used for inspection, including ‘Sucui No.1’, ‘Zaojinxiang’, ‘Huangguan’, ‘Akizuki’, ‘Yali’, and ‘Hongli No.1’. Spectral data within the 398~1004 nm wavelength range were analyzed to compare the predictive performance of the Least Squares Support Vector Machine (LS-SVM) models on various quality parameters, using different preprocessing methods and the selected feature wavelengths. The results indicated that the combination of Fast Detrend-Standard Normal Variate (FD-SNV) preprocessing and Competitive Adaptive Reweighted Sampling (CARS)-selected feature wavelengths yielded the best improvement in model predictive ability for forecasting key quality parameters such as firmness, soluble solids content (SSC), pH, color, and maturity degree. They could enhance the predictive capability and reduce computational complexity. Furthermore, in order to construct a quality prediction model, integrating hyperspectral data from six pear varieties resulted in an RPD (Ratio of Performance to Deviation) exceeding 2.0 for all the quality parameters, indicating that increasing the fruit sample size and variety number further strengthened the robustness of the model. The Backpropagation Neural Network (BPNN) model could accurately distinguish six distinct pear varieties, achieving prediction accuracies of above 99% for both the calibration and test sets. In summary, the combination of HSI and machine learning models enabled an efficient, rapid, and non-destructive detection of pear quality and provided a practical value for quality control and the commercial processing of pears. Full article
(This article belongs to the Special Issue Spectroscopic Methods Applied in Food Quality Determination)
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<p>The reflectance spectra of the six different pear varieties.</p>
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<p>BP neural network classification model: (<b>a</b>) Calibration set; (<b>b</b>) Prediction set. These abbreviations are detailed as follows: Sucui No.1: SC; Huangguan: HG; Zaojinxiang: ZJX; Akizuki: AK; Hongli No.1: HL; Yali: YL. The same form is used in <a href="#foods-13-03956-f003" class="html-fig">Figure 3</a>, <a href="#foods-13-03956-f004" class="html-fig">Figure 4</a> and <a href="#foods-13-03956-f005" class="html-fig">Figure 5</a>.</p>
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<p>SVM classification model: (<b>a</b>) Calibration set; (<b>b</b>) Prediction set.</p>
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<p>RF classification model: (<b>a</b>) Calibration set; (<b>b</b>) Prediction set.</p>
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<p>ELM classification model: (<b>a</b>) Calibration set; (<b>b</b>) Prediction set.</p>
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14 pages, 3160 KiB  
Article
Determining Hydroxyapatite Filling Volume for the Treatment of Post-Extraction Alveoli Based on Measurements of Alveolar Volume in Relation to the Body Weight of Dogs
by Anna Misztal-Kunecka, Przemysław Prządka, Maja Jeż and Stanisław Dzimira
Vet. Sci. 2024, 11(12), 633; https://doi.org/10.3390/vetsci11120633 - 7 Dec 2024
Viewed by 360
Abstract
Filling post-extraction alveoli with hydroxyapatite-based materials is becoming an increasingly common procedure in veterinary dentistry. In dogs, tooth roots vary in structure depending on the weight of the dog, but data on tooth length and volume have not yet been described. This study [...] Read more.
Filling post-extraction alveoli with hydroxyapatite-based materials is becoming an increasingly common procedure in veterinary dentistry. In dogs, tooth roots vary in structure depending on the weight of the dog, but data on tooth length and volume have not yet been described. This study aimed to establish reference data on tooth root length and post-extraction alveolar volume for mature maxillary and mandibular incisors and canines in dogs. We determined the mean length and volume of these teeth in dogs in the weight ranges of 1–5 kg, 5–10 kg, 10–20 kg, and over 20 kg. The obtained values given showed a correlation between tooth length and alveolar volume in a specific weight range. A review of the commercially available hydroxyapatite-based bone substitute materials was then conducted. A table is presented which shows how to calculate the volume of bone substitute material required to fill a post-extraction alveolus with a given material. Statistics were used to assess significant differences between the mass of the bone substitute product used (μL) for specific weight ranges and to demonstrate the correlation between tooth length and alveolar volume for a specific weight range. The data obtained in this study can serve as reference values for tooth crown length and alveolar volume, allowing operators to plan a specific volume of bone substitute material for filling post-extraction alveoli. This research is interesting because it shows that the weight of an animal is an important aspect in planning the amount of bone substitute material for tooth extraction. In clinical work, it is much easier to weigh an animal than it is to make calculations based on the length of the tooth root. Full article
(This article belongs to the Section Veterinary Biomedical Sciences)
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<p>The length measurement of the maxillary second incisor.</p>
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<p>The measurement of the length of the canine. The green lines represent a triangle with the base of the length of the tooth neck and the apex at the longest end of the root apex. The red arrow shows the bisector of the angle, which determines the length of the tooth root.</p>
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<p>A tooth immersed in dental silicone while waiting for the material to polymerise.</p>
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<p>Tooth impression with accurate representation of anatomical structure prepared for filling with water to calculate tooth volume.</p>
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<p>The box-and-whisker plot for incisors I and II for the variable volume of the alveolus (µL) vs. the cluster variable weight.</p>
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<p>The box-and-plot for incisor III for the variable volume of alveolus (µL) vs. the cluster variable weight.</p>
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<p>The box-and-whisker plot for the canine tooth for the variable volume of alveolus (µL) vs. the cluster variable weight.</p>
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<p>The box-and-whisker plot for incisors I and II for the variable length (mm) vs. the cluster variable weight.</p>
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<p>The box-and-whisker plot for incisor III for the variable length (mm) vs. the cluster variable weight.</p>
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<p>The box-and-whisker plot for the canine for the variable length (mm) vs. the cluster variable weight.</p>
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<p>A schematic diagram showing the filling of alveoli with a bone substitute material (<b>a</b>) in the form of a cylindrical pellet after plasticity has been achieved (FlexiOssVet<sup>®</sup>), (<b>b</b>) in the form of granules (Adbone<sup>®</sup>, SinossGraft<sup>®</sup>), (<b>c</b>) in the form of cylindrical pellets (PerOssal<sup>®</sup>), and (<b>d</b>) in the form of a block/cylinder (Adbone<sup>®</sup>).</p>
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15 pages, 1172 KiB  
Article
Identification and Preliminary Analysis of Granulosa Cell Biomarkers to Predict Oocyte In Vitro Maturation Outcome in the Southern White Rhinoceros (Ceratotherium simum simum)
by Elena Ruggeri, Kristin Klohonatz, Barbara Durrant and Marc-André Sirard
Animals 2024, 14(23), 3538; https://doi.org/10.3390/ani14233538 - 7 Dec 2024
Viewed by 442
Abstract
In recent years, biomarkers in granulosa cells (GC) have been determined and associated in several species with oocyte maturation, in vitro fertilization success, and embryo development outcomes. The identification of biomarkers of oocyte competence can aid in improving assisted reproductive technologies (ARTs) in [...] Read more.
In recent years, biomarkers in granulosa cells (GC) have been determined and associated in several species with oocyte maturation, in vitro fertilization success, and embryo development outcomes. The identification of biomarkers of oocyte competence can aid in improving assisted reproductive technologies (ARTs) in the southern white rhino (SWR). This study aimed to identify biomarkers present in SWR GC associated with oocytes that either did or did not mature in vitro. We evaluated follicle development (FD), meiotic competence (MC), cell death and atresia (CDA), and embryonic genome activation (EGA). Our objective was to design biomarkers to predict oocyte in vitro maturation results in the SWR. RNA was isolated from GC obtained during ovum pick up (OPU) for qPCR analysis. Overall, 22 genes were assessed, and nine were differentially expressed between GC from oocytes that did or did not mature in vitro (FD-GDF9 and mTOR; MC-GGPS1, JMY, and NPR2; CDA-COL4A1, MACIR, and TMPO; EGA-NFYA). From these data, we determined that GC can be used as a predictor for oocyte in vitro maturation outcome in the SWR. Our results provide crucial information needed to improve in vitro maturation and ARTs in this species. Full article
(This article belongs to the Special Issue The Application of Reproductive Technologies for Wildlife Management)
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<p>Fold changes in genes associated with follicle development in granulosa cells associated with oocytes that did or did not mature in vitro. A positive fold change indicates gene expression was higher in cells from oocytes that matured (PB) while a negative fold change indicates gene expression was higher in cells associated with oocytes that did not mature (no PB) after in vitro culture. * <span class="html-italic">p</span> ≤ 0.05.</p>
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<p>Fold changes in genes associated with meiotic competence in granulosa cells associated with oocytes that did or did mature in vitro. A positive fold change indicates gene expression was higher in cells from oocytes that matured (PB) while a negative fold change indicates gene expression was higher in cells associated with oocytes that did not mature (no PB) after in vitro culture. * <span class="html-italic">p</span> ≤ 0.05.</p>
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<p>Fold changes in genes associated with cell death and atresia in granulosa cells associated with oocytes that did or did mature in vitro. A negative fold change indicates gene expression was higher in cells associated with oocytes that did not mature (no PB) after in vitro maturation culture. * <span class="html-italic">p</span> ≤ 0.05.</p>
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<p>Fold changes in genes associated with embryonic genome activation in granulosa cells associated with oocytes that did or did mature in vitro. A negative fold change indicates gene expression was higher in cells associated with oocytes that did not mature (no PB) after in vitro maturation. * <span class="html-italic">p</span> ≤ 0.05.</p>
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