基于两种不同住房条件和寄生负荷的马肠道微生物群特征

IF 2.9 2区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Gopi Yalavarthi, Praveen Kosuri, Haswitha Sabbineni, Kendra Maas, Kristen E Govoni, Mary Anne Amalaradjou, Jenifer Nadeau
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引用次数: 0

摘要

圆形线虫是影响马大肠和盲肠的寄生线虫,导致胃肠道紊乱,包括肠绞痛和由于粘膜损伤和炎症导致的营养吸收受损。由于对驱虫药的广泛耐药性,有效的寄生虫管理越来越具有挑战性,因此需要替代策略。最近的研究表明,肠道微生物群与寄生虫感染之间存在复杂的相互作用,受饮食、免疫反应和住房条件等因素的影响。肠道微生物组调节已成为控制圆形线虫的潜在替代策略,因为特定的微生物群落可能增强寄生虫耐药性并减轻感染严重程度。该研究的目的是调查饲养条件(牧场与半集约化)对不同圆形粪卵计数(FEC)马肠道微生物群组成和多样性的影响,并探索微生物群落与寄生虫耐药性之间的潜在联系。25匹马分为两种饲养条件:放牧(n=13)和半集约化(SI; n=12)。在每一组中,根据圆形蛋数(<; 300个蛋/g =低,>;300个蛋/g =高)将马分为低或高产蛋量。采用因子设计。秋季收集粪便样本进行浮选分析和肠道微生物群评估。序列处理使用motherur 1.47.0,下游分析使用r3.2.7。放牧和si饲养的马在beta多样性指标(Bray-Curtis、Jaccard指数和Theta YC)上存在显著差异(P < 0.05),表明圈养条件对微生物群落结构的影响不同。热图和log2倍变化分析显示,低FEC的si饲养马在门水平上具有较高的厚壁菌门和elusiimicrobiota丰度(P < 0.05)。在分目水平上,低FEC和高FEC马在SI棚内的苔藓菌门、内生微生物门、土壤菌门和链霉菌门差异显著(P < 0.05)。通常在食草动物和昆虫肠道中发现的微生物群,以其在纤维素降解中的作用而闻名,可能有助于马的纤维消化。与反刍动物微生物群相关的肠道微生物可能促进纤维发酵和营养吸收。通常在土壤中发现的苔藓细菌和土壤细菌可能通过放牧进入肠道,并有助于养分循环和有机物降解。链霉菌以其生产抗生素的能力而闻名,可以帮助调节微生物平衡并抑制致病菌,这可能有助于寄生虫的耐药性。然而,在α多样性、丰富度或总体微生物多样性方面没有发现显著差异(P > 0.05)。这些发现强调了住房对马肠道微生物组的影响及其在寄生虫管理中的潜在作用。鉴于圆形线虫对传统驱虫药的抗性日益增强,靶向微生物组调节可以通过利用微生物组相关代谢物和激素反应之间的相互作用,为寄生虫控制提供另一种方法。未来的研究应进一步研究这些相互作用,以更好地了解它们在不同住房条件下对微生物组成和功能的集体影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PSV-22 Characterization of the gut microbiota of horses based on two different housing conditions and parasitic load.
Strongyles are parasitic nematodes affecting the large intestine and cecum of equines, leading to gastrointestinal disturbances, including colic and impaired nutrient absorption due to mucosal damage and inflammation. Effective parasite management is increasingly challenging due to widespread resistance to anthelmintic treatments, necessitating alternative strategies. Recent research suggests a complex interplay between gut microbiota and parasitic infections, influenced by factors such as diet, immune response, and housing conditions. Gut microbiome modulation has emerged as a potential alternative strategy for controlling strongyles, as specific microbial communities may enhance parasite resistance and mitigate infection severity. The objective of the study was to investigate the impact of housing conditions (pasture vs. semi-intensive) on gut microbiota composition and diversity in horses with varying strongyle fecal egg counts (FEC) and to explore potential links between microbial communities and parasite resistance. Twenty-five horses were divided into two housing conditions: pasture (n=13) and semi-intensive (SI; n=12). Within each group, horses were classified as low or high shedders based on strongyle egg counts (&lt; 300 eggs/g = low, &gt;300 eggs/g = high). A factorial design was used. Fecal samples were collected in the fall for flotation analysis and gut microbiota assessment. Sequence processing was performed using Mothur 1.47.0, with downstream analysis in R 3.2.7. Significant differences (P &lt; 0.05) in beta diversity metrics (Bray-Curtis, Jaccard Index, and Theta YC) were observed between pastured and SI-housed horses, indicating distinct microbial community structures influenced by housing conditions. Heatmaps and log2 fold-change analysis revealed a higher abundance (P &lt; 0.05) of Firmicutes and Elusimicrobiota at the phylum level in SI-housed horses with low FEC. At the order level, Bryobacterales, Endomicrobials, Pedosphaerales, and Streptomycetales showed significant differences (P &lt; 0.05) between low and high FEC horses in SI housing. Elusimicrobiota, commonly found in herbivore and insect guts, is known for its role in cellulose degradation, potentially aiding fiber digestion in horses. Endomicrobials, associated with ruminant microbiomes, may enhance fiber fermentation and nutrient absorption. Bryobacterales and Pedosphaerales, typically found in soil, may enter the gut through grazing and contribute to nutrient cycling and organic matter degradation. Streptomycetales, known for their antibiotic-producing capabilities, could help regulate microbial balance and inhibit pathogenic bacteria, potentially contributing to parasite resistance. However, no significant differences (P &gt; 0.05) were found in alpha diversity, richness, or overall microbial diversity. These findings highlight the impact of housing on the equine gut microbiome and its potential role in parasite management. Given the increasing resistance of strongyles to traditional anthelmintics, targeted microbiome modulation could offer an alternative approach for parasite control by leveraging the interplay between microbiome-associated metabolites and hormonal responses. Future research should further investigate these interactions to better understand their collective impact on microbial composition and function across different housing conditions.
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来源期刊
Journal of animal science
Journal of animal science 农林科学-奶制品与动物科学
CiteScore
4.80
自引率
12.10%
发文量
1589
审稿时长
3 months
期刊介绍: The Journal of Animal Science (JAS) is the premier journal for animal science and serves as the leading source of new knowledge and perspective in this area. JAS publishes more than 500 fully reviewed research articles, invited reviews, technical notes, and letters to the editor each year. Articles published in JAS encompass a broad range of research topics in animal production and fundamental aspects of genetics, nutrition, physiology, and preparation and utilization of animal products. Articles typically report research with beef cattle, companion animals, goats, horses, pigs, and sheep; however, studies involving other farm animals, aquatic and wildlife species, and laboratory animal species that address fundamental questions related to livestock and companion animal biology will be considered for publication.
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