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14 pages, 6506 KiB  
Article
Comparison of Fecal Microbiota and Metabolites Between Captive and Grazing Male Reindeer
by Fei Zhao, Quanmin Zhao, Songze Li, Yuhang Zhu, Huazhe Si, Jiang Feng and Zhipeng Li
Animals 2024, 14(24), 3606; https://doi.org/10.3390/ani14243606 - 14 Dec 2024
Viewed by 464
Abstract
The reindeer (Rangifer tarandus) is a circumpolar member of the Cervidae family, and has adapted to a harsh environment. Summer is a critical period for reindeer, with peak digestibility facilitating body fat accumulation. The gut microbiota plays a pivotal role in [...] Read more.
The reindeer (Rangifer tarandus) is a circumpolar member of the Cervidae family, and has adapted to a harsh environment. Summer is a critical period for reindeer, with peak digestibility facilitating body fat accumulation. The gut microbiota plays a pivotal role in nutrient metabolism, and is affected by captivity. However, differences in the composition of the gut microbiota and metabolites between captive and grazing reindeer during summer remain poorly understood. Here, we conducted a comparative study of the fecal microbiota and metabolites between captive (n = 6) and grazing (n = 6) male reindeer, using full-length 16S rRNA gene sequencing and gas chromatography–time-of-flight mass spectrometry, respectively. Our results indicated that Prevotella, Phocaeicola, Papillibacter, Muribaculum, and Bacteroides were the predominant genera in the feces of reindeer. However, microbial diversity was significantly higher in captive reindeer compared to their grazing counterparts. Principal coordinate analysis revealed significant differences in the fecal microbiota between captive and grazing reindeer. In captive reindeer, the relative abundances of the genera Clostridium, Paraprevotella, Alistipes, Paludibacter, Lentimicrobium, Paraclostridium, and Anaerovibrio were significantly higher, while those of the genera Prevotella, Phocaeicola, Pseudoflavonifractor, and Lactonifactor were significantly lower. A comparison of predicted functions indicated that pathways involved in fat digestion and absorption, histidine metabolism, lysine biosynthesis, and secondary bile acid biosynthesis were more abundant in captive reindeer, whereas the pathways of fructose and mannose metabolism and propanoate metabolism were less abundant. An untargeted metabolomic analysis revealed that 624 metabolites (e.g., amino acids, lipids, fatty acids, and bile acids) and 645 metabolites (e.g., carbohydrates and purines) were significantly increased in the feces of captive and grazing reindeer, respectively. In conclusion, we unveiled significant differences in fecal microbiota and metabolites between captive and grazing male reindeer, with the results suggesting a potentially enhanced ability to utilize plant fibers in grazing reindeer. Full article
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Figure 1
<p>Microbial community composition and diversity in the feces of captive and grazing reindeer. Microbial community composition in the feces of the Cap and Gra groups at the phylum (<b>A</b>) and genus (<b>B</b>) levels. (<b>C</b>) A comparison of alpha-diversity indices in feces between the Cap and Gra groups. (<b>D</b>) PCoA illustrating the differences in microbial community membership and structure in reindeer feces between the Cap and Gra groups at the OTU level, based on Bray–Curtis dissimilarity, Unweighted UniFrac distance, and Weighted UniFrac distance. * <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>The significantly different genera in the feces of captive and grazing reindeer. (<b>A</b>) A Venn diagram illustrating genera that were common and unique to the Cap and Gra groups. (<b>B</b>) A heatmap depicting the significantly different genera in feces between the Cap and Gra groups. Individuals are shaded from blue to red to represent relative abundances (low to high). * <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>A comparison of the potential functions of microbes in the feces of captive and grazing reindeer. (<b>A</b>) PCoA illustrating the variation in microbial functions at KEGG level 3, based on the Bray–Curtis dissimilarity matrix, in feces between the Cap and Gra groups. (<b>B</b>) A heatmap showing the significantly different metabolic pathways of fecal microbiota between the Cap and Gra groups. Individuals are shaded from blue to red to indicate relative abundances (low to high). * <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>Differences in fecal metabolites between captive and grazing reindeer. (<b>A</b>) A pie chart illustrating the classification of identified metabolites in feces. (<b>B</b>) PCA and PLS-DA plots highlighting the differences in fecal metabolites between the Cap (blue) and Gra (red) groups. (<b>C</b>) A comparison of the total concentrations of lipids, fatty acids, bile acids, carbohydrates, purines, pyrimidines, and amino acids between the Cap and Gra groups. (<b>D</b>) Volcano plots depicting the significantly different metabolites in feces between the Cap and Gra groups. (<b>E</b>) A heatmap showing the significantly different metabolites in reindeer feces when comparing the Gra group to the Cap group. Individuals are shaded from yellow to purple to indicate concentrations (low to high). (<b>F</b>) A lollipop chart displaying the enriched metabolic pathways of significantly different metabolites. * <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>The co-occurrence of significantly different microbiota and metabolites in the feces of captive (<b>A</b>) and grazing (<b>B</b>) reindeer. The Spearman correlation coefficient (|rho| &gt; 0.8 and <span class="html-italic">p</span> ≤ 0.05) was calculated from the abundances of microbiota and the concentrations of metabolites. Node colors indicate microbiota and metabolites, with yellow and blue edges representing positive and negative correlations, respectively.</p>
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14 pages, 5706 KiB  
Article
First Incidence of Peste des Petits Ruminants Virus in Cervidae Family from State Zoo of Assam, India
by Nagendra Nath Barman, Arpita Bharali, Durlav Prasad Bora, Biswajit Dutta, Mousumi Bora, Sophia M. Gogoi, Panchami Sharma, Sankar Sarma, Parikshit Kakati, Tejas Mariswamy, Ankita Choudhury and Lukumoni Buragohain
Viruses 2024, 16(12), 1829; https://doi.org/10.3390/v16121829 - 25 Nov 2024
Viewed by 555
Abstract
The present study aimed to investigate the episodes of per-acute mortality due to peste des petits ruminants (PPR) that resulted in the death of 30 animals of different species of cervids, namely, barking deer, four-horned antelope, hog deer, thamin, and mouse deer in [...] Read more.
The present study aimed to investigate the episodes of per-acute mortality due to peste des petits ruminants (PPR) that resulted in the death of 30 animals of different species of cervids, namely, barking deer, four-horned antelope, hog deer, thamin, and mouse deer in the State Zoo of Assam, a northeastern state of India. The affected animals showed no to limited clinical signs. However, the necropsy and histopathological findings were highly suggestive of PPR virus (PPRV) infection observed in domestic small ruminants. Representative tissue samples were screened for the presence of PPRV along with blue tongue virus (BTV) and epizootic hemorrhagic disease virus (EHDV) using RT-PCR or RT-qPCR and were found to be positive for PPRV. Considering the sudden outbreak of PPR in captive cervids, we sought to determine the role of domestic goats as the potential spillover host. To verify that, archived tissue samples of domestic goats collected during PPRV outbreaks in nearby localities and slaughtered goats used as meat for Carnivorous animals in the State Zoo were also screened and found to be positive for PPRV in RT-PCR. Phylogenetic analysis based on the Nucleocapsid (N) protein gene of PPRV from infected cervids, domestic goats, and goat meat revealed the virus to be of Lineage IV origin. Our findings provide evidence of probable spillover of PPRV from domestic goats to captive endangered cervids and circulation of Lineage IV PPRV strains among the small-ruminant population of this region. Full article
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<p>Map of Assam State Zoo cum Botanical Garden with location of dead animals in different species of cervids.</p>
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<p>Clinical manifestation of peste des petits ruminants virus infections in affected cervids. (<b>a</b>) Sudden death of four-horned antelopes (<b>b</b>) A death mouse deer due to PPR (<b>c</b>) An ailing four-horned antelope (<b>d</b>) Hemorrhages in the palpebral conjunctiva of an ailing four-horned antelope (<b>e</b>) Hemorrhages in ventral region and (<b>f</b>) Sloughing of the external nasal epithelium.</p>
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<p>Necropsy lesions observed in peste des petits ruminants virus-infected cervids: (<b>a</b>) Hemorrhages and congestion of the lung parenchyma; (<b>b</b>) Frothy trachea with congested lungs; (<b>c</b>) Ulcerative lesions on the tongue; (<b>d</b>) Hemorrhages on the peritoneum; (<b>e</b>) Hemorrhages and congestion on the omentum and mesentery; and (<b>f</b>) Fetal death following PPRV infection in four-horned antelopes.</p>
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<p>Histopathological changes in different tissues in peste des petits ruminants virus infected: (<b>a</b>) Presence of serous exudate in alveolar and bronchiolar spaces (arrowhead), hyperplasia of the bronchiolar epithelium (thick arrow) with thickening of interalveolar septa (thin arrow) due to infiltration of mononuclear cells in the lung (H&amp;E, 10×); (<b>b</b>) Depletion of lymphocytes from the lymphoid follicle (yellow circle) of the spleen (H&amp;E, 10×); (<b>c</b>) Presence of focal area of coagulative necrosis (arrows) in liver (H&amp;E, 40×); and (<b>d</b>) Dilatation and marked congestion (yellow circle) of renal capillaries (H&amp;E, 10×).</p>
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<p>Phylogenetic analysis of PPRV strains performed in MEGA 11 based on deduced nucleotide sequences of the partial Nucleocapsid (N) gene. Clades with four different colors represent four lineages (I–IV) of PPRV, and the eight PPRV strains detected in this study formed a clade with the lineage IV (blue-colored clade), which is highlighted with a solid red circular marker.</p>
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9 pages, 251 KiB  
Article
Comparison of Cortisol Levels in the Hair of Male European Roe Deer at the Beginning and End of the Stalking Hunting Season
by Katarzyna Dziki-Michalska, Katarzyna Tajchman, Patrycja Staniszewska and Aneta Strachecka
Animals 2024, 14(22), 3184; https://doi.org/10.3390/ani14223184 - 6 Nov 2024
Viewed by 594
Abstract
Roe deer (Capreolus capreolus), as a representative of the Cervidae family, are particularly sensitive to negative environmental stimuli due to their need to maintain increased vigilance during feeding. Intensive hunting seasons are undoubtedly also a stressful factor for this species. The [...] Read more.
Roe deer (Capreolus capreolus), as a representative of the Cervidae family, are particularly sensitive to negative environmental stimuli due to their need to maintain increased vigilance during feeding. Intensive hunting seasons are undoubtedly also a stressful factor for this species. The aim of this study was to analyze the cortisol levels in the hair of male roe deer collected at the beginning and the end of the hunting season in eastern Poland. In total, hair samples from 26 individuals collected in May and 31 individuals collected in September were analyzed. The concentration of cortisol in the hair was determined using the EIA kit. It was shown that the concentration of cortisol was significantly higher in samples collected in September compared to those collected in May (Pr. > |t| = 0.0017). Moreover, the age of animals and carcass mass did not significantly affect the concentration of the tested hormone. In summary, the concentration of cortisol in the fur of male roe deer depended on the season and was not influenced by the carcass mass or age of the animals studied. Full article
(This article belongs to the Section Wildlife)
27 pages, 402 KiB  
Review
Control of Helminth Infections in Captive Herbivores: An Overview of Experience
by Mariana S. Panayotova-Pencheva
J. Zool. Bot. Gard. 2024, 5(4), 641-667; https://doi.org/10.3390/jzbg5040043 - 30 Oct 2024
Viewed by 1120
Abstract
There are numerous challenges associated with helminth control in captive animals. The aim of the present paper is to provide an overview of the research on deworming of captive herbivorous mammals, the associated problems and the solutions sought, in order to derive recommendations [...] Read more.
There are numerous challenges associated with helminth control in captive animals. The aim of the present paper is to provide an overview of the research on deworming of captive herbivorous mammals, the associated problems and the solutions sought, in order to derive recommendations for practice in the relevant institutions. The research was conducted by searching electronic internet databases and following the bibliographies in the published articles. The articles found are presented in summarized form. Most of the results relate to herbivores of the family Bovidae, followed by the families Cervidae, Equidae, Elephantidae, Camelidae and Giraffidae. Systematic data are presented on the types of anthelmintics used, dosages and application regimens for different animal species. Anthelmintics were administered at doses similar to or even higher than those used in farm animals, with no evidence of side effects. Treatment results often depended on the animal and parasite species. Incomplete cure, reinfection, and resistance to anthelmintics were the most common problems in the field. Based on the literature reviewed, the optimal prevention measures include the following: quarantine of newly arrived animals; daily or as intensive as possible cleaning of droppings; regular change of substrate in the enclosures; and monitoring of possible infections and their qualitative and quantitative composition (monthly or at least every two months). For treatments and monitoring effectiveness, recommendations include the following: individual assessment of the need for treatment; selective choice of anthelmintics; post-treatment examination between the 10th and 14th day after deworming; carrying out a group treatment after a preliminary drug effect test; conducting mass deworming only in case of a significant increase in fecal egg counts, highly pathogenic helminth species and a deterioration in the condition of the animals. In the future, more attention should be paid to new approaches such as biological control by saprophytic fungi or natural compounds as an alternative to anthelmintics. This would help minimize the use of anthelmintics, protect refugia and allow animals to remain healthy by maintaining a balance with the low levels of parasites present. Full article
27 pages, 15755 KiB  
Article
A Craniometric Analysis of the Subfamily Cervinae (Cervidae, Mammalia)
by Roman Croitor
Foss. Stud. 2024, 2(3), 196-222; https://doi.org/10.3390/fossils2030010 - 9 Sep 2024
Viewed by 2121
Abstract
This study employs Principal Component Analysis to examine cranial measurements from both extant and fossil specimens spanning 38 species and comprising over 300 individuals within the subfamily Cervinae. Our findings elucidate craniometric distinctions among cervids characterized by varying body sizes and certain evolutionary [...] Read more.
This study employs Principal Component Analysis to examine cranial measurements from both extant and fossil specimens spanning 38 species and comprising over 300 individuals within the subfamily Cervinae. Our findings elucidate craniometric distinctions among cervids characterized by varying body sizes and certain evolutionary adaptations. While our results generally corroborate previous assertions regarding the limited craniometric variability among plesiometacarpal deer, they also unveil specific cranial adaptations within certain genera and species. The Principal Component Analysis of craniometric data revealed that giant and large-sized deer display significantly broader ecomorphological diversity in cranial shape compared to small-sized deer. Secondly, small-sized deer exhibit greater uniformity in their cranial shape, appearing densely clustered on the factorial map. Thus, we conclude that body size imposes ecological constraints, limiting the available niches due to eco-physiological factors. This study demonstrates that endemic insular deer do not evolve consistent craniometric features attributable to insular isolation, while the cranial proportions of medium-to-small-sized deer delineate a ubiquitous morphological archetype characteristic of numerous cervid taxa spanning diverse phylogenetic lineages and sharing comparable body sizes. This group of “Dama-like” deer, characterized by similar body size, metabolic rates, ecological needs, and cranial morphometry, is referred to here as the fundamental eco-physiological type, typical of warm regions within the Palearctic and Oriental biogeographic realms. Full article
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<p>The scheme of cranial measurements used in the present study shown of a skull of <span class="html-italic">Cervus elaphus maral</span>: (<b>A</b>,<b>B</b>) side and dorsal views (skull drawings adapted from Flerov [<a href="#B6-fossstud-02-00010" class="html-bibr">6</a>]); (<b>C</b>) palatal view (adapted from Sokolov [<a href="#B18-fossstud-02-00010" class="html-bibr">18</a>]).</p>
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<p>Correlations of craniometrical data in the studied total sample of cranial material before missing data imputation.</p>
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<p>Correlations of craniometrical data in the studied total sample of cranial material after missing data imputation.</p>
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<p>Factorial plane 1: distribution of deer species following Principal Component Analysis of craniometric data.</p>
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<p>Variable factor map of cranial measurements used in Principal Component Analysis.</p>
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<p>Bregma position in various deer species: ratio of bregma-inion to bregma-prosthion measurements plotted against condylobasal length.</p>
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<p>Relative frontal breadth: ratio of frontal breadth at constriction to cranial length from upper second premolar to posterior side of occipital condyles plotted against condylobasal length.</p>
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<p>The relative breadth of rostrum, calculated as the ratio of rostrum breadth to condylobasal length, plotted against condylobasal length.</p>
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<p>Cranial shape of <span class="html-italic">Megaloceros giganteus</span> from Brühl (Koller), Rhine Valley, Germany (SMNS, collection number 166.16.17.11.80.37): (<b>A</b>) side view; (<b>B</b>) dorsal view; (<b>C</b>) palatal view.</p>
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<p>Relative length of braincase in <span class="html-italic">Megaloceros</span> and <span class="html-italic">Praemegaceros</span>, calculated as the ratio of braincase breadth behind pedicles to bregma-inion distance.</p>
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<p>Cranial shape of <span class="html-italic">Megaceroides algericus</span> from Guyotville (now Ain-Benian), Algeria (NMNH, “Collection Arambourg”’, no number): (<b>A</b>) side view; (<b>B</b>) dorsal view; (<b>C</b>) palatal view.</p>
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<p>Relative breadth of occiput calculated as the ratio of occipital breadth to cranial length measured from P<sup>2</sup> to the posterior side of occipital condyles, plotted against condylobasal length.</p>
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<p>Cranial shape of <span class="html-italic">Praemegaceros cazioti cazioti</span> from Coscia (Corsica): (<b>A</b>) side view (MNHN, no number); (<b>B</b>) dorsal view (Cos-6930; adapted from [<a href="#B36-fossstud-02-00010" class="html-bibr">36</a>]; (<b>C</b>) palatal view (MNHN, no number).</p>
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<p>Cranial shape of <span class="html-italic">Haploidoceros mediterraneus</span> from Cova del Rinoceront, Spain (CR-2413, FGUB): (<b>A</b>) side view; (<b>B</b>) dorsal view; (<b>C</b>) palatal view.</p>
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6 pages, 846 KiB  
Brief Report
A Case of Severe Abomasal Sand Impaction in a Farmed White-Tailed Deer (Odocoileus virginianus) in Florida
by Alireza Rahmani Shahraki, João H. J. Bittar, Samantha M. Wisely and Juan M. Campos-Krauer
Animals 2024, 14(11), 1602; https://doi.org/10.3390/ani14111602 - 29 May 2024
Viewed by 850
Abstract
The University of Florida’s Cervidae Health Research Initiative (CHeRI) conducted a post-mortem examination of a two-year-old white-tailed doe deceased at a northern Florida white-tailed deer farm. The carcass of the deer had notable emaciation and bloating. Upon opening of the carcass, there was [...] Read more.
The University of Florida’s Cervidae Health Research Initiative (CHeRI) conducted a post-mortem examination of a two-year-old white-tailed doe deceased at a northern Florida white-tailed deer farm. The carcass of the deer had notable emaciation and bloating. Upon opening of the carcass, there was pneumonia and the rumen was tympanic and enlarged. Additionally, the abomasum was distended and contained approximately 5 kg of sand. It is not uncommon for white-tailed deer to engage in geophagia (eating soil or sand), which typically does not result in diseases or fatalities. However, in this animal, we suspect a chronic process that created a physical barrier, hindering nutrient absorption and resulting in physical irritation of the abomasal mucosa with subsequent inflammation. This may have caused a disturbance in immune system function, allowing opportunistic bacteria to colonize and invade other organs, such as the lungs, contributing to the animal’s death. Full article
(This article belongs to the Special Issue Wildlife Diseases: Pathology and Diagnostic Investigation)
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<p>The yellow circle shows the lung lesion caused by <span class="html-italic">Trueperella pyogenes</span> in the white-tailed deer (<span class="html-italic">Odocoileus virginianus</span>) with severe abomasal sand impaction.</p>
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<p>The open abomasum of a female white-tailed deer (<span class="html-italic">Odocoileus virginianus</span>). The deer suffered from chronic abomasal sand impaction. The ear tag included in the image as a reference is 5.08 cm by 4.12 cm.</p>
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6 pages, 1200 KiB  
Brief Report
Mycobacterium kansasii Infection in a Farmed White-Tailed Deer (Odocoileus virginianus) in Florida, USA
by Sydney L. Cottingham, An-Chi Cheng, Pedro H. de Oliveira Viadanna, Kuttichantran Subramaniam, William F. Craft, Marley E. Iredale, Samantha M. Wisely and Juan M. Campos Krauer
Animals 2024, 14(10), 1511; https://doi.org/10.3390/ani14101511 - 20 May 2024
Viewed by 1445
Abstract
A 7-year-old farmed white-tailed deer doe was transported to a Levy County, Florida property and began to decline in health, exhibiting weight loss and pelvic limb weakness. The doe prematurely delivered live twin fawns, both of which later died. The doe was treated [...] Read more.
A 7-year-old farmed white-tailed deer doe was transported to a Levy County, Florida property and began to decline in health, exhibiting weight loss and pelvic limb weakness. The doe prematurely delivered live twin fawns, both of which later died. The doe was treated with corticosteroids, antibiotics, gastric cytoprotectants, and B vitamins but showed no improvement. The doe was euthanized, and a post mortem examination was performed under the University of Florida’s Cervidae Health Research Initiative. We collected lung tissue after the animal was euthanized and performed histological evaluation, using H&E and Ziehl–Neelsen (ZN) staining, and molecular evaluation, using conventional PCR, followed by Sanger sequencing. The microscopic observations of the H&E-stained lung showed multifocal granuloma, while the ZN-stained tissue revealed low numbers of beaded, magenta-staining rod bacteria inside the granuloma formation. Molecular analysis identified the presence of Mycobacterium kansasii. This isolation of a non-tuberculous Mycobacterium in a white-tailed deer emphasizes the importance of specific pathogen identification in cases of tuberculosis-like disease in farmed and free-ranging cervids. We report the first case of M. kansasii infection in a farmed white-tailed deer (Odocoileus virginianus) in Florida. Although M. kansasii cases are sporadic in white-tailed deer, it is important to maintain farm biosecurity and prevent farmed cervids from contacting wildlife to prevent disease transmission. Full article
(This article belongs to the Special Issue Wildlife Diseases: Pathology and Diagnostic Investigation)
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<p>Gross appearance of the lungs in the <span class="html-italic">M. kansasii</span>-infected deer. (<b>a</b>) Open thoracic cavity demonstrating lungs with multifocal, granulomatous pneumonia. Arrows indicate granulomas. (<b>b</b>) Focal area of atelectasis with numerous granulomas.</p>
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<p>Microscopic observations of lung tissue from the <span class="html-italic">M. kansasii</span>-infected deer. (<b>a</b>) H&amp;E-stained histologic section of lung with a focal granuloma (bar = 200 µm); asterisk indicates necrotic center. Arrow indicates fibrous capsule with macrophages. (<b>b</b>) Ziehl–Neelsen acid-fast stain with low numbers of beaded, magenta-staining rod bacteria (bar = 10 µm).</p>
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12 pages, 1274 KiB  
Article
Comparative Genomics Reveal Phylogenetic Relationship and Chromosomal Evolutionary Events of Eight Cervidae Species
by Lixin Tang, Shiwu Dong and Xiumei Xing
Animals 2024, 14(7), 1063; https://doi.org/10.3390/ani14071063 - 30 Mar 2024
Viewed by 2087
Abstract
Cervidae represents a family that is not only rich in species diversity but also exhibits a wide range of karyotypes. The controversies regarding the phylogeny and classification of Cervidae still persist. The flourishing development of the genomic era has made it possible to [...] Read more.
Cervidae represents a family that is not only rich in species diversity but also exhibits a wide range of karyotypes. The controversies regarding the phylogeny and classification of Cervidae still persist. The flourishing development of the genomic era has made it possible to address these issues at the genomic level. Here, the genomes of nine species were used to explore the phylogeny and chromosomal evolutionary events of Cervidae. By conducting whole-genome comparisons, we identified single-copy orthologous genes across the nine species and constructed a phylogenetic tree based on the single-copy orthologous genes sequences, providing new insights into the phylogeny of Cervidae, particularly the phylogenetic relationship among sika deer, red deer, wapiti and Tarim red deer. Gene family analysis revealed contractions in the olfactory receptor gene family and expansions in the histone gene family across eight Cervidae species. Furthermore, synteny analysis was used to explore the chromosomal evolutionary events of Cervidae species, revealing six chromosomal fissions during the evolutionary process from Bovidae to Cervidae. Notably, specific chromosomal fusion events were found in four species of Cervus, and a unique chromosomal fusion event was identified in Muntiacus reevesi. Our study further completed the phylogenetic relationship within the Cervidae and demonstrated the feasibility of inferring species phylogeny at the whole-genome level. Additionally, our findings on gene family evolution and the chromosomal evolutionary events in eight Cervidae species lay a foundation for comprehensive research of the evolution of Cervidae. Full article
(This article belongs to the Section Small Ruminants)
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<p>Phylogeny and gene family analysis of Cervidae. (<b>a</b>) Phylogeny with divergence time and gene family expansion and contraction in the eight Cervidae species, with <span class="html-italic">Bos taurus</span> used as an outgroup. The numbers of expanded (red) and contracted (green) gene families are shown on branches. (<b>b</b>) Horizontal bar plots indicate the number of orthogroups that are species-specific (red), present in all nine species (orange), or present in more than one but less than all species (green) in the analysis.</p>
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<p>The chromosome collinearity of seven species of Cervidae (<span class="html-italic">Cervus elaphus yarkandensis</span>, <span class="html-italic">Cervus nippon</span>, <span class="html-italic">Cervus elaphus</span>, <span class="html-italic">Cervus canadensis</span>, <span class="html-italic">Rangifer tarandus</span>, <span class="html-italic">Muntiacus reevesi</span> and <span class="html-italic">Muntiacus muntjac</span>), with <span class="html-italic">Bos taurus</span> as the reference. <span class="html-italic">Odocoileus virginianus</span> was excluded, as it is not a chromosome-level genome. The cirves are in the same colors, grey. The different colors are the chromosomes of different species.</p>
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19 pages, 360 KiB  
Review
A Review of Cervidae Visual Ecology
by Blaise A. Newman and Gino J. D’Angelo
Animals 2024, 14(3), 420; https://doi.org/10.3390/ani14030420 - 27 Jan 2024
Cited by 2 | Viewed by 2637
Abstract
This review examines the visual systems of cervids in relation to their ability to meet their ecological needs and how their visual systems are specialized for particular tasks. Cervidae encompasses a diverse group of mammals that serve as important ecological drivers within their [...] Read more.
This review examines the visual systems of cervids in relation to their ability to meet their ecological needs and how their visual systems are specialized for particular tasks. Cervidae encompasses a diverse group of mammals that serve as important ecological drivers within their ecosystems. Despite evidence of highly specialized visual systems, a large portion of cervid research ignores or fails to consider the realities of cervid vision as it relates to their ecology. Failure to account for an animal’s visual ecology during research can lead to unintentional biases and uninformed conclusions regarding the decision making and behaviors for a species or population. Our review addresses core behaviors and their interrelationship with cervid visual characteristics. Historically, the study of cervid visual characteristics has been restricted to specific areas of inquiry such as color vision and contains limited integration into broader ecological and behavioral research. The purpose of our review is to bridge these gaps by offering a comprehensive review of cervid visual ecology that emphasizes the interplay between the visual adaptations of cervids and their interactions with habitats and other species. Ultimately, a better understanding of cervid visual ecology allows researchers to gain deeper insights into their behavior and ecology, providing critical information for conservation and management efforts. Full article
(This article belongs to the Special Issue Evolution, Ecology and Management of Wild Boar and Deer)
16 pages, 1601 KiB  
Article
X Chromosome-Specific Repeats in Non-Domestic Bovidae
by Svatava Kubickova, Olga Kopecna, Halina Cernohorska, Jiri Rubes and Miluse Vozdova
Genes 2024, 15(2), 159; https://doi.org/10.3390/genes15020159 - 25 Jan 2024
Viewed by 1288
Abstract
Repetitive sequences form a substantial and still enigmatic part of the mammalian genome. We isolated repetitive DNA blocks of the X chromosomes of three species of the family Bovidae: Kobus defassa (KDEXr sequence), Bos taurus (BTAXr sequence) and Antilope cervicapra (ACEXr sequence). The [...] Read more.
Repetitive sequences form a substantial and still enigmatic part of the mammalian genome. We isolated repetitive DNA blocks of the X chromosomes of three species of the family Bovidae: Kobus defassa (KDEXr sequence), Bos taurus (BTAXr sequence) and Antilope cervicapra (ACEXr sequence). The copy numbers of the isolated sequences were assessed using qPCR, and their chromosomal localisations were analysed using FISH in ten bovid tribes and in outgroup species. Besides their localisation on the X chromosome, their presence was also revealed on the Y chromosome and autosomes in several species. The KDEXr sequence abundant in most Bovidae species also occurs in distant taxa (Perissodactyla and Carnivora) and seems to be evolutionarily older than BTAXr and ACEXr. The ACEXr sequence, visible only in several Antilopini species using FISH, is probably the youngest, and arised in an ancestor common to Bovidae and Cervidae. All three repetitive sequences analysed in this study are interspersed among gene-rich regions on the X chromosomes, apparently preventing the crossing-over in their close vicinity. This study demonstrates that repetitive sequences on the X chromosomes have undergone a fast evolution, and their variation among related species can be beneficial for evolutionary studies. Full article
(This article belongs to the Section Animal Genetics and Genomics)
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<p>FISH results with KDEXr, BTAXr and ACEXr probes (red). (<b>a</b>) FISH with the KDEXr probe on chromosomes of <span class="html-italic">K. defassa</span>. (<b>b</b>) FISH with the BTAXr probe on chromosomes of <span class="html-italic">B. taurus</span>. (<b>c</b>) FISH with the ACEXr probe on chromosomes of <span class="html-italic">A. cervicapra</span>. Chromosomes were counterstained with DAPI (blue). Scale bar represents 5 µm.</p>
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<p>FISH with the KDEXr probe (red) to chromosomes X and BTA13 of Tragelaphini species: <span class="html-italic">T. strepsiceros</span> (TST), <span class="html-italic">T. angasii</span> (TAN), <span class="html-italic">T. eurycerus</span> (TEU), <span class="html-italic">T. oryx</span> (TOR), <span class="html-italic">A. imberbis</span> (AIM) and <span class="html-italic">T. spekii</span> (TSP). The dashed white lines indicate the position of centromeres.</p>
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<p>FISH with KDEXr and ACEXr probes (red) to chromosomes of <span class="html-italic">E. thomsonii</span>. Scale bar represents 5 µm.</p>
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<p>FISH with KDEXr and BTAXr probes (red) to X chromosomes of (<b>a</b>) <span class="html-italic">C. hircus</span> representing the caprine type of the X chromosome, (<b>b</b>) <span class="html-italic">B. taurus</span> representing the bovine type of the X chromosome, (<b>c</b>) <span class="html-italic">B. bubalis</span> representing the eland type of the X chromosome. The dashed white lines indicate the position of centromeres.</p>
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8 pages, 1958 KiB  
Communication
Potential Tick Defense Associated with Skin and Hair Characteristics in Korean Water Deer (Hydropotes inermis argyropus)
by Sang-Joon Lee, Ki-Yoon Kim, Gyurae Kim, Subin Moon, Yung-Chul Park, Ho-Seong Cho and Yeonsu Oh
Animals 2024, 14(2), 185; https://doi.org/10.3390/ani14020185 - 5 Jan 2024
Cited by 3 | Viewed by 1766
Abstract
The Korean water deer (WD), a predominant wildlife species in South Korea, is listed as vulnerable by the IUCN Red List. Despite belonging to the same family, Cervidae, WD show significantly fewer adult ixodid tick infestations compared to roe deer (RD). Ticks, which [...] Read more.
The Korean water deer (WD), a predominant wildlife species in South Korea, is listed as vulnerable by the IUCN Red List. Despite belonging to the same family, Cervidae, WD show significantly fewer adult ixodid tick infestations compared to roe deer (RD). Ticks, which cannot fly, engage in questing behavior in natural environments to latch onto hosts. They detect signals like body temperature and host skin chemicals to navigate through the hair coat to the preferred epidermis. In light of this, we performed an extensive comparative study of the skin tissue and hair characteristics of both deer species, focusing on elements contributing to the reduced tick bite incidence in WD. Remarkably, WD exhibited more prominent blood vessels, sebaceous glands, and sweat glands, which are crucial for skin barrier functions (p < 0.005). Moreover, WD had irregular scale patterns on their hair cuticles and possessed hair that was significantly stiffer and 2.83 times thicker than that of RD (p < 0.001). These characteristics potentially impede ticks from reaching the epidermis hair in WD and RD in the context of tick bite prevention. Further investigations in this area could enhance our understanding of tick–host dynamics and contribute to developing preventive measures against tick-borne diseases in other deer species. Full article
(This article belongs to the Special Issue Advances in Wildlife and Exotic Animals Anatomy)
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<p>Hair cuticle and medulla characteristics. (<b>A</b>) Roe deer (<span class="html-italic">Capreolus pygargus</span>) hair cuticles exhibited transversal scale alignment, smooth scale edges, moderate distance between scales, and a consistent wave-like pattern. Scale bar = 20 μm. (<b>B</b>) Korean water deer (<span class="html-italic">Hydropotes inermis argyropus</span>) hair cuticles featured transversal scale alignment, slightly wavy scale edges, close proximity between scales, and an irregular wave pattern. Scale bar = 20 μm. (<b>C</b>) Roe deer (<span class="html-italic">Capreolus pygargus</span>) hair medullas were composed of multiple cells, a semi-filled lattice structure, a steady pattern, and scalloped edges. Scale bar = 50 μm. (<b>D</b>) Korean water deer (<span class="html-italic">Hydropotes inermis argyropus</span>) hair medullas were similar in structure with multiple cells, a semi-filled lattice, consistent pattern, and scalloped edges. Scale bar = 50 μm.</p>
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<p>Cross-section of skin. (<b>A</b>) Roe deer (<span class="html-italic">Capreolus pygargus</span>) and (<b>B</b>) Korean water deer (<span class="html-italic">Hydropotes inermis argyropus</span>). In WD, the skin appendages were larger in size. The hair follicles in RD showed a compound primary with secondary follicle structure, more intricate compared to the basic primary follicle pattern seen in WD. WD had broader blood vessel diameters. The epidermal thickness did not show any notable variation. Scale bar = 200 μm. H&amp;E staining.</p>
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17 pages, 3878 KiB  
Article
Description of Bisbalus, a New Genus for the Gray Brocket, Mazama cita Osgood, 1912 (Mammalia, Cervidae), as a Step to Solve the Neotropical Deer Puzzle
by Eluzai Dinai Pinto Sandoval, Wlodzimierz Jędrzejewski, Jesús Molinari, Miluse Vozdova, Halina Cernohorska, Svatava Kubickova, Agda Maria Bernegossi, Renato Caparroz and José Mauricio Barbanti Duarte
Taxonomy 2024, 4(1), 10-26; https://doi.org/10.3390/taxonomy4010002 - 2 Jan 2024
Cited by 3 | Viewed by 3533
Abstract
The Neotropical deer genus Mazama is characterized by homoplastic morphological characters, a high karyotypic diversity, and a polyphyletic condition. The species of the genus have been recovered into two multigeneric lineages, the subtribes Odocoileina and Blastocerina, of the tribe Odocoileini (New World deer) [...] Read more.
The Neotropical deer genus Mazama is characterized by homoplastic morphological characters, a high karyotypic diversity, and a polyphyletic condition. The species of the genus have been recovered into two multigeneric lineages, the subtribes Odocoileina and Blastocerina, of the tribe Odocoileini (New World deer) in the family Cervidae. Within the Blastocerina, gray brockets include two non-sister species, Subulo gouazoubira, occurring south of the Amazon region, and Passalites nemorivagus, occurring in the Guianas and in the Amazon region. We clarify the taxonomic status and phylogenetic position of Mazama americana citus Osgood, 1912 (referred to as either S. gouazoubira or P. nemorivagus by other authors). We collected a topotype of M. a. citus from the eastern shore of Lake Maracaibo, Venezuela, characterize it morphologically and cytogenetically (conventional banding and fluorescence in situ hybridization), and carry out a phylogenetic analysis of its whole mitogenome and Cytb alongside two additional specimens of M. a. citus from northwestern Venezuela. Our analyses reveal the topotype to be a large gray brocket with a cinnamon band above the eyes and 2n = 61 and FN = 70 karyotype. Using cattle whole chromosome painting and bacterial artificial chromosome X probes, we determined its karyotype to differ in at least 10 rearrangements from that of S. gouazoubira. Bayesian inference recovers M. a. citus within the Blastocerina subtribe, separated phylogenetically from other gray brockets (100% branch value), revealing the Osgood’s gray brocket to be a valid species that should be assigned to a new genus. We propose the generic name Bisbalus, with Bisbalus citus (Osgood, 1912) as the type species. Full article
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<p>Male topotype of <span class="html-italic">Mazama cita</span> (Osgood, 1912) collected in El Consejo de Ciruma, Zulia, Venezuela. (<b>A</b>) Lateral view of the body. (<b>B</b>) Close up of the head. (<b>C</b>) Ventral view of the body. (<b>D</b>) Dorsal view of the body.</p>
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<p>Skull of the male topotype of <span class="html-italic">Mazama cita</span> (Osgood, 1912) collected in El Consejo de Ciruma, Zulia, Venezuela (<b>A</b>) Dorsal view. (<b>B</b>) Ventral view. (<b>C</b>) Right lateral view. (<b>D</b>) Left lateral view.</p>
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<p>Conventional Giemsa-stained karyotype of the male topotype of <span class="html-italic">Mazama cita</span> (Osgood, 1912). Groups of chromosomal relative lengths: A—large biarmed autosome; C—small biarmed autosomes; E—small acrocentric autosome; B—Supernumerary chromosomes; XY—Simple sexual system. Number of each chromosomal pair from 1 to 29.</p>
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<p>Karyotype of a male topotype of <span class="html-italic">Mazama cita</span> (Osgood, 1912) (MCI) and homologies with the karyotype of <span class="html-italic">Subulo gouazoubira</span> (SGO). Left to right: C-band, schematic representation of C-band and G-band of MCI, and homology with <span class="html-italic">Subulo gouazoubira</span> SGO [<a href="#B24-taxonomy-04-00002" class="html-bibr">24</a>], adapted. Localization of Ag-NOR staining is indicated by arrows. Positions of bovine BAC probes on the MCI X chromosome are shown. PAR corresponds to pseudo-autosomal region probe, comprising clones BAC 453C5 and 326B13. Number of each chromosomal pair from 1 to 29.</p>
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<p>Bayesian Inference (BI) of the mtDNA of several species of Neotropical deer. (<b>A</b>) Complete mitochondrion. (<b>B</b>) Partial Cyt<span class="html-italic">b</span> 1040 bp. The values above clade nodes represent posterior probabilities. Blastocerina subtribe (light yellow square). <span class="html-italic">Mazama cita</span> (Osgood, 1912) clade (blue), topotype (black star). Odocoileina subtribe (melon red square). <span class="html-italic">S. gouazoubira</span> (blue dashed lines). <span class="html-italic">P. nemorivagus</span> (green dashed line). Outgroup, <span class="html-italic">A. alces</span>.</p>
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11 pages, 1119 KiB  
Article
Molecular Detection and Genotyping of Theileria spp. in Deer (Cervidae) in Korea
by Chang Uk Chung, Haeseung Lee, Min-Goo Seo, Seung-Hun Lee, Kyoo-Tae Kim, Kaifa Nazim, Jung-Sun Song, Dong Hwa Bae, Man Hee Rhee, Oh-Deog Kwon and Dongmi Kwak
Microorganisms 2023, 11(11), 2740; https://doi.org/10.3390/microorganisms11112740 - 9 Nov 2023
Cited by 2 | Viewed by 1419
Abstract
Major clinical symptoms of Theileria infection include fever, anemia, anorexia, jaundice, and decreased milk production. Although several studies have been conducted on tick-borne pathogens, including Theileria in Korea, only a few have focused on Theileria infection in deer, including the Korean water deer. [...] Read more.
Major clinical symptoms of Theileria infection include fever, anemia, anorexia, jaundice, and decreased milk production. Although several studies have been conducted on tick-borne pathogens, including Theileria in Korea, only a few have focused on Theileria infection in deer, including the Korean water deer. Blood samples from 160 deer were collected and subjected to DNA extraction and polymerase chain reaction (PCR). Next, PCR-positive samples were sequenced and analyzed by constructing a phylogenetic tree. The results showed that the overall infection rate of Theileria was 8.1% (13/160). Infection rates of 100% were observed in the northern and southern regions. However, the study’s limitation was its small sample size, wherein five and one samples were analyzed from the northern and southern regions, respectively. The central region exhibited the lowest infection rate of 2.9% (4/140). Infection rates also differed based on seasons, with the highest (18.4%, 9/49) being observed in spring, followed by that in summer (8.9%, 4/45). However, no infection was observed during autumn and winter. A phylogenetic analysis indicated that the PCR-positive samples contained Theileria luwenshuni, which usually infects small ruminants, such as goats and sheep. Full article
(This article belongs to the Special Issue Ticks and Tick-Borne Diseases in Animals)
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<p>Map representing the regions from which samples were collected. Based on the provincial areas, the country was categorized into three regions: northern (Gangwon (GW) and Gyeonggi (GG) provinces), central (Chungbuk (CB), Chungnam (CN), and Gyeongbuk (GB) provinces), and southern (Jeonbuk (JB), Jeonnam (JN), Gyeongnam (GN), and Jeju (JJ) provinces) regions. Yellow spots indicate the sampling site.</p>
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<p>Genera corresponding to the piroplasm 18S rRNA (including <span class="html-italic">Theileria</span> and <span class="html-italic">Babesia</span>) were analyzed by constructing a phylogenetic tree, and the acquired sequences belonged to <span class="html-italic">Theileria</span>. The sequences obtained in this study are indicated using black arrows.</p>
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<p>Phylogenetic tree of the <span class="html-italic">Theileria</span> 18S rRNA. The sequence obtained in this study is indicated using a black arrow.</p>
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12 pages, 1429 KiB  
Review
Analysis of the Intestinal and Faecal Bacterial Microbiota of the Cervidae Family Using 16S Next-Generation Sequencing: A Review
by Irene Pacheco-Torres, David Hernández-Sánchez, Cristina García-De la Peña, Luis A. Tarango-Arámbula, María M. Crosby-Galván and Paulino Sánchez-Santillán
Microorganisms 2023, 11(7), 1860; https://doi.org/10.3390/microorganisms11071860 - 24 Jul 2023
Cited by 4 | Viewed by 2258
Abstract
The Cervidae family has a wide distribution due to its adaptation to numerous ecological environments, which allows it to develop a diverse microbial community in its digestive tract. Recently, research has focused on the taxonomic composition and functionality of the intestinal and faecal [...] Read more.
The Cervidae family has a wide distribution due to its adaptation to numerous ecological environments, which allows it to develop a diverse microbial community in its digestive tract. Recently, research has focused on the taxonomic composition and functionality of the intestinal and faecal microbiota of different cervid species worldwide, as well as their microbial diversity and variation under different associated factors such as age, sex, diet, distribution, and seasonal variation. In addition, there is special interest in knowing how cervids act as reservoirs of zoonotic pathogenic microorganisms, which represent a threat to public health. This review provides a synthesis of the growing field of microbiota determination in cervids worldwide, focusing on intestinal and faecal samples using 16S next-generation sequencing. It also documents factors influencing microbial diversity and composition, the microorganisms reported as pathogenic/zoonotic, and the perspectives regarding the conservation of these species. Knowing the interactions between bacteria and cervid health can drive management and conservation strategies for these species and help develop an understanding of their evolutionary history and the interaction with emerging disease-causing microorganisms. Full article
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<p>Heatmap representing the number of publications on the intestinal and faecal microbiota of cervids throughout the world based on the information and references in <a href="#microorganisms-11-01860-t001" class="html-table">Table 1</a>.</p>
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<p>Number of publications on microbiota by species of cervids throughout the world. The numbers inside the graph are related to the amount of publications available for each deer species (elaboration based on the information and references in <a href="#microorganisms-11-01860-t001" class="html-table">Table 1</a>).</p>
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14 pages, 4229 KiB  
Article
Macroscopic Anatomy of the Stifle Joint in the Pampa’s Deer (Ozotoceros bezoarticus-Linnaeus, 1758)
by Horst Erich König, Sokol Duro and William Pérez
Anatomia 2023, 2(2), 124-137; https://doi.org/10.3390/anatomia2020012 - 23 Apr 2023
Viewed by 3241
Abstract
The objective of this paper was to describe the anatomy of the stifle joint (Articulatio genus) of the pampas deer (Ozotoceros bezoarticus, Linnaeus, 1758) by dissection and imaging studies. Twenty-six pelvic limbs were used for gross dissection, and four [...] Read more.
The objective of this paper was to describe the anatomy of the stifle joint (Articulatio genus) of the pampas deer (Ozotoceros bezoarticus, Linnaeus, 1758) by dissection and imaging studies. Twenty-six pelvic limbs were used for gross dissection, and four stifle regions from two animals were used for radiography and magnetic resonance imaging (MRI). The stifle joint of the pampas deer comprised the femoropatellar joint (joint between the distal part of the femur and the patella), and the femorotibial joint joined the femoral condyles to the proximal extremity of the tibia. The general anatomy of the stifle joint, including the overall morphology of the joint with its bones, complementary parts, means of attachment, and anatomical relationships, was like that of other ruminant species of similar size. Imaging techniques such as MRI allow adequate visualization of most components of the stifle joint. Full article
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<p>Distal extremity of the left femur of the pampas deer and sheep, cranial view. (<bold>1</bold>): Medial lip of femoral trochlea; (<bold>2</bold>): femoral trochlea, central depression; (<bold>3</bold>): lateral lip of femoral trochlea; (<bold>4</bold>): medial condyle; (<bold>5</bold>): lateral condyle.</p>
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<p>Distal extremity of the left femur of pampas deer and sheep, caudal view. (<bold>1</bold>): Lateral condyle; (<bold>2</bold>): intercondylar fossa; (<bold>3</bold>): medial condyle.</p>
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<p>Caudal view of the articular surface of the left patella of the pampas deer. (<bold>1</bold>): Patellar ligament; (<bold>2</bold>): medial relief; (<bold>3</bold>): medial articular surface; (<bold>4</bold>): lateral articular surface; (<bold>5</bold>): lateral parapatellar fibrocartilage; (<bold>6</bold>): medial parapatellar fibrocartilage.</p>
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<p>Proximal extremity of the tibia of the pampas deer, dorsal view. (<bold>1</bold>): Tibia tuberosity; (<bold>2</bold>): fibula; (<bold>3</bold>): lateral condyle; (<bold>4</bold>): central intercondylar fossa; (<bold>5</bold>): medial condyle.</p>
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<p><bold>Left</bold> panel: plain radiograph of the left pelvic limb to show the bones involved in the stifle joint of the pampas deer. (<bold>1</bold>): Patella; (<bold>2</bold>): femoral condyle; (<bold>3</bold>); proximal extremity of tibia. <bold>Right</bold> panel: left pelvic limb, lateral view. (<bold>4</bold>): Patella; (<bold>5</bold>): patellar ligament; (<bold>6</bold>): articular capsule; (<bold>7</bold>): tibial tuberosity; (<bold>8</bold>): popliteus muscle.</p>
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<p>Proximal view of the proximal extremity of the right tibia and its menisci in the pampas deer. (<bold>1</bold>): Extensor sulcus; (<bold>2</bold>): cranial part of the medial meniscus; (<bold>3</bold>): central part of the medial meniscus; (<bold>4</bold>): caudal insertion of the medial meniscus; (<bold>5</bold>): cranial cruciate ligament; (<bold>6</bold>): cranial insertion of the lateral meniscus; (<bold>7</bold>): central part of the lateral meniscus.</p>
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<p>Cranial view after wide opening of the left stifle joint of the pampas deer. (<bold>1</bold>): Intermediate relief of the patellar articular surface; (<bold>2</bold>): lateral articular surface of the patella; (<bold>3</bold>): medial articular surface; (<bold>4</bold>): patellar insertion of the patellar ligament; (<bold>5</bold>): lateral parapatellar fibrocartilage; (<bold>6</bold>): synovial stratum of the patellofemoral joint capsule; (<bold>7</bold>): femoral trochlea; 8: lateral lip of the femoral trochlea; (<bold>9</bold>): infrapatellar adipose body.</p>
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<p><bold>Left</bold> panel: MRI of the right stifle joint of the pampas deer, caudal view. (<bold>2</bold>): Meniscofemoral ligament; (<bold>4</bold>): lateral meniscus. <bold>Right</bold> panel: caudal view of the right stifle of the pampas deer after removal of the gastrocnemius muscles. (<bold>1</bold>): Medial condyle; (<bold>2</bold>): meniscofemoral ligament; (<bold>3</bold>): caudal cruciate ligament; (<bold>4</bold>): lateral meniscus.</p>
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<p>Lateral view of the right thigh and leg of the pampas deer after removal of fasciae and gastrocnemius muscles. (<bold>1</bold>): Lateral collateral ligament; (<bold>2</bold>): tendon of the popliteus muscle; (<bold>3</bold>): tendon of the extensor digitorum longus.</p>
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<p>Lateral view of the right femur and leg of the pampas deer after removal of fasciae and gastrocnemius muscles. (<bold>1</bold>): Femoral trochlea; (<bold>2</bold>): lateral collateral ligament incised and reclined proximally; (<bold>3</bold>): lateral border of the lateral meniscus; (<bold>4</bold>): popliteus muscle transversely sectioned at the level of its tendinous part.</p>
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<p>Medial view of the right femur and leg of the pampas deer after removal of fasciae and gastrocnemius muscles. (<bold>1</bold>): Patellar insertion of the patellar ligament; (<bold>2</bold>): patellar ligament; (<bold>3</bold>): articular capsule; (<bold>4</bold>): popliteus muscle.</p>
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<p><bold>Left</bold> panel: MRI of the right stifle joint of the pampas deer. (<bold>1</bold>): Patella; (<bold>2</bold>): distal part of <xref ref-type="fig" rid="anatomia-02-00012-f003">Figure 3</xref> infrapatellar adipose body; (<bold>4</bold>): proximal extremity of tibia. <bold>Right</bold> panel: medial view of the right stifle of the pampas deer, sagittal section. (<bold>1</bold>): Patella; (<bold>2</bold>): distal part of femur; (<bold>3</bold>): infrapatellar adipose body; (<bold>4</bold>): proximal extremity of tibia.</p>
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