Michael J Rothrock, Benjamin Zwirzitz, Walid G Al Hakeem, Adelumola Oladeinde, Jean Y Guard, Xiang Li
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While distinct microbiota were found for each sample type category and hatchery area, microbial community analyses revealed that Egg microbiota trended towards clustering with the facility-related samples when moving from the prehatch to post-hatch areas, highlighting the potential effect of the hatchery environment in shaping the pre-harvest broiler-related microbiota. Prevalence analyses revealed 20 ASVs (Core20) present in the core microbiota of all sample types and areas, with each ASV possessing a unique distribution throughout the hatchery. Interestingly, three Enterobacteriaceae ASVs were in the Core20, including Salmonella. Subsequent analyses showed that Salmonella, while a minor prehatch and hatch Core20ASV, dominated the Enterobacteriaceae niche and total microbiota in the chick pad feces in the post-hatch area of the hatchery, and the presence of this Salmonella ASV in the post-hatch feces was associated with swabs of breakroom tables. These findings highlight the complexity of commercial hatchery microbiota, including identifying chick pad feces and breakroom tables as potentially important sampling or disinfection targets for hatchery managers to focus their Salmonella mitigation efforts to reduce loads entering live production farms.</p>","PeriodicalId":72201,"journal":{"name":"Animal microbiome","volume":"6 1","pages":"46"},"PeriodicalIF":4.9000,"publicationDate":"2024-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11312677/pdf/","citationCount":"0","resultStr":"{\"title\":\"16S amplicon-based microbiome biomapping of a commercial broiler hatchery.\",\"authors\":\"Michael J Rothrock, Benjamin Zwirzitz, Walid G Al Hakeem, Adelumola Oladeinde, Jean Y Guard, Xiang Li\",\"doi\":\"10.1186/s42523-024-00334-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Hatcheries, where eggs from multiple breeder farms are incubated and hatched before being sent to different broiler farms, represent a nexus point in the commercial production of broilers in the United States. 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Prevalence analyses revealed 20 ASVs (Core20) present in the core microbiota of all sample types and areas, with each ASV possessing a unique distribution throughout the hatchery. Interestingly, three Enterobacteriaceae ASVs were in the Core20, including Salmonella. Subsequent analyses showed that Salmonella, while a minor prehatch and hatch Core20ASV, dominated the Enterobacteriaceae niche and total microbiota in the chick pad feces in the post-hatch area of the hatchery, and the presence of this Salmonella ASV in the post-hatch feces was associated with swabs of breakroom tables. 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引用次数: 0
摘要
孵化场是美国肉鸡商业化生产的关键点,来自多个种鸡场的种蛋在孵化场孵化后被送往不同的肉鸡养殖场。考虑到肉鸡生产的所有下游微生物质量和安全方面(活体生产、加工、消费者使用)都可能受到孵化场的影响,因此更好地了解商业孵化场内的微生物生态至关重要。因此,利用基于 16S rRNA 扩增子的微生物组分析,对孵化前、孵化中和孵化后五个不同地点的四类样本(空气、蛋、水、设施)进行了生物绘图。虽然在每个样品类型类别和孵化区都发现了不同的微生物群,但微生物群落分析表明,从孵化前到孵化后,蛋类微生物群趋向于与设施相关的样品聚集在一起,这突显了孵化环境在形成孵化前肉鸡相关微生物群方面的潜在影响。流行率分析表明,在所有样本类型和区域的核心微生物群中存在 20 种 ASV(Core20),每种 ASV 在整个孵化场都有独特的分布。有趣的是,Core20 中有三种肠杆菌科 ASV,其中包括沙门氏菌。随后的分析表明,沙门氏菌虽然是孵化前和孵化时的次要核心 20 ASV,但在孵化后区域的雏鸡垫粪便中却主宰了肠杆菌科生态位和总微生物群,孵化后粪便中沙门氏菌 ASV 的存在与休息室桌子上的拭子有关。这些发现突显了商业孵化场微生物群的复杂性,包括确定雏鸡垫粪便和休息室桌子可能是孵化场管理者的重要采样或消毒目标,以集中精力减轻沙门氏菌的危害,减少进入活体生产养殖场的沙门氏菌量。
16S amplicon-based microbiome biomapping of a commercial broiler hatchery.
Hatcheries, where eggs from multiple breeder farms are incubated and hatched before being sent to different broiler farms, represent a nexus point in the commercial production of broilers in the United States. Considering all downstream microbial quality and safety aspects of broiler production (live production, processing, consumer use) can be potentially affected by the hatchery, a better understanding of microbial ecology within commercial hatcheries is essential. Therefore, a commercial broiler hatchery was biomapped using 16S rRNA amplicon-based microbiome analyses of four sample type categories (Air, Egg, Water, Facility) across five different places in the pre-hatch, hatch, and post-hatch areas. While distinct microbiota were found for each sample type category and hatchery area, microbial community analyses revealed that Egg microbiota trended towards clustering with the facility-related samples when moving from the prehatch to post-hatch areas, highlighting the potential effect of the hatchery environment in shaping the pre-harvest broiler-related microbiota. Prevalence analyses revealed 20 ASVs (Core20) present in the core microbiota of all sample types and areas, with each ASV possessing a unique distribution throughout the hatchery. Interestingly, three Enterobacteriaceae ASVs were in the Core20, including Salmonella. Subsequent analyses showed that Salmonella, while a minor prehatch and hatch Core20ASV, dominated the Enterobacteriaceae niche and total microbiota in the chick pad feces in the post-hatch area of the hatchery, and the presence of this Salmonella ASV in the post-hatch feces was associated with swabs of breakroom tables. These findings highlight the complexity of commercial hatchery microbiota, including identifying chick pad feces and breakroom tables as potentially important sampling or disinfection targets for hatchery managers to focus their Salmonella mitigation efforts to reduce loads entering live production farms.