Comparative analysis of the microbiome of sympatric wintering Bean Geese, Domestic Ducks, humans, and soil at Shengjin Lake of China reveals potential public risk to human health

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Gang Liu, Na Xu, Chongyang Yu
{"title":"Comparative analysis of the microbiome of sympatric wintering Bean Geese, Domestic Ducks, humans, and soil at Shengjin Lake of China reveals potential public risk to human health","authors":"Gang Liu,&nbsp;Na Xu,&nbsp;Chongyang Yu","doi":"10.1016/j.avrs.2024.100175","DOIUrl":null,"url":null,"abstract":"<div><p>The gut microbiota of migratory waterbirds is affected by various complex factors, including cross-species transmission, which increases the risk of pathogen spreading among sympatric animals and poses a potential public health risk to humans. In this study, we investigated the microbial communities of wintering Bean Geese (<em>Anser fabalis</em>), Domestic Ducks (<em>A</em>. <em>platyrhynchos domesticus</em>), humans, and soil using high-throughput sequencing of the 16S rRNA gene region in Shengjin Lake, China. In total, 6,046,677 clean reads were obtained, representing 41,119 operational taxonomic units (OTUs) across the four groups. The dominant microbial phyla were the Proteobacteria, Firmicutes, Bacteroidota, and Actinobacteriota. The Sorensen similarity index and alpha and beta diversity results showed that the gut microbial communities of Bean Geese and Domestic Ducks were more similar to those of the other pairs. Network analysis revealed that <em>Faecalibacterium prausnitzii</em>, <em>Pseudomonas fragi</em>, and <em>Bradyrhizobium elkanii</em> were hubs of the three major modules. Fourteen common microbiomes were identified in Bean Geese, Domestic Ducks, humans, and soil in Shengjin Lake. A total of 96 potential pathogens were identified among the four groups, with 20 specific potentially pathogenic microbiomes found in the gut of Bean Geese. Some of these pathogens are responsible for significant financial losses in the poultry industry and pose risks to human health. <em>Klebsiella pneumoniae</em>, <em>Morganella morganii</em>, <em>Escherichia coli</em>, and <em>Ralstonia insidiosa</em> are potential core pathogens found in the four groups at Shengjin Lake that can cause diseases in humans and animals and facilitate cross-species transmission through various media. Therefore, humans are at risk of contracting these pathogens from migratory birds because of their frequent contact with domestic poultry. However, further studies are required to explore the potential pathogenic species and transmission pathways among sympatric wintering Bean Geese, Domestic Ducks, humans, and soil.</p></div>","PeriodicalId":1,"journal":{"name":"Accounts of Chemical Research","volume":null,"pages":null},"PeriodicalIF":16.4000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2053716624000185/pdfft?md5=27cd002573c4004062dde466f331806d&pid=1-s2.0-S2053716624000185-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Accounts of Chemical Research","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2053716624000185","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

The gut microbiota of migratory waterbirds is affected by various complex factors, including cross-species transmission, which increases the risk of pathogen spreading among sympatric animals and poses a potential public health risk to humans. In this study, we investigated the microbial communities of wintering Bean Geese (Anser fabalis), Domestic Ducks (A. platyrhynchos domesticus), humans, and soil using high-throughput sequencing of the 16S rRNA gene region in Shengjin Lake, China. In total, 6,046,677 clean reads were obtained, representing 41,119 operational taxonomic units (OTUs) across the four groups. The dominant microbial phyla were the Proteobacteria, Firmicutes, Bacteroidota, and Actinobacteriota. The Sorensen similarity index and alpha and beta diversity results showed that the gut microbial communities of Bean Geese and Domestic Ducks were more similar to those of the other pairs. Network analysis revealed that Faecalibacterium prausnitzii, Pseudomonas fragi, and Bradyrhizobium elkanii were hubs of the three major modules. Fourteen common microbiomes were identified in Bean Geese, Domestic Ducks, humans, and soil in Shengjin Lake. A total of 96 potential pathogens were identified among the four groups, with 20 specific potentially pathogenic microbiomes found in the gut of Bean Geese. Some of these pathogens are responsible for significant financial losses in the poultry industry and pose risks to human health. Klebsiella pneumoniae, Morganella morganii, Escherichia coli, and Ralstonia insidiosa are potential core pathogens found in the four groups at Shengjin Lake that can cause diseases in humans and animals and facilitate cross-species transmission through various media. Therefore, humans are at risk of contracting these pathogens from migratory birds because of their frequent contact with domestic poultry. However, further studies are required to explore the potential pathogenic species and transmission pathways among sympatric wintering Bean Geese, Domestic Ducks, humans, and soil.

中国升金湖同域越冬豆雁、家鸭、人类和土壤微生物组的比较分析揭示了对人类健康的潜在公共风险
迁徙水鸟的肠道微生物群受到各种复杂因素的影响,包括跨物种传播,这增加了病原体在同域动物间传播的风险,并对人类构成潜在的公共卫生风险。在这项研究中,我们利用 16S rRNA 基因区高通量测序技术调查了中国升金湖越冬豆雁(Anser fabalis)、家鸭(A. platyrhynchos domesticus)、人类和土壤的微生物群落。总共获得了 6,046,677 个纯净读数,代表了四组中的 41,119 个操作分类单元(OTU)。主要的微生物门类是变形菌门、真菌门、类杆菌门和放线菌门。索伦森相似性指数以及阿尔法和贝塔多样性结果表明,豆雁和家鸭的肠道微生物群落与其他几对微生物群落更为相似。网络分析显示,普氏粪杆菌、弗拉基假单胞菌和麋鹿臂柄霉菌是三大模块的中心。在豆雁、家鸭、人类和升金湖土壤中发现了 14 个常见微生物组。在这四组微生物中,共鉴定出 96 种潜在病原体,其中在豆雁肠道中发现了 20 种特定的潜在致病微生物群。其中一些病原体对家禽业造成了重大经济损失,并对人类健康造成了威胁。肺炎克雷伯氏菌、摩根氏菌、大肠埃希氏菌和内生拉氏菌是在升金湖四个群体中发现的潜在核心病原体,可导致人类和动物疾病,并通过各种媒介促进跨物种传播。因此,由于候鸟与家禽的频繁接触,人类有可能从候鸟身上感染这些病原体。然而,还需要进一步的研究来探索同域越冬豆雁、家鸭、人类和土壤之间的潜在病原体种类和传播途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信