Proximity to humans is associated with antimicrobial-resistant enteric pathogens in wild bird microbiomes.

IF 8.1 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Current Biology Pub Date : 2024-09-09 Epub Date: 2024-08-13 DOI:10.1016/j.cub.2024.07.059
Evangelos Mourkas, José O Valdebenito, Hannah Marsh, Matthew D Hitchings, Kerry K Cooper, Craig T Parker, Tamás Székely, Håkan Johansson, Patrik Ellström, Ben Pascoe, Jonas Waldenström, Samuel K Sheppard
{"title":"Proximity to humans is associated with antimicrobial-resistant enteric pathogens in wild bird microbiomes.","authors":"Evangelos Mourkas, José O Valdebenito, Hannah Marsh, Matthew D Hitchings, Kerry K Cooper, Craig T Parker, Tamás Székely, Håkan Johansson, Patrik Ellström, Ben Pascoe, Jonas Waldenström, Samuel K Sheppard","doi":"10.1016/j.cub.2024.07.059","DOIUrl":null,"url":null,"abstract":"<p><p>Humans are radically altering global ecology, and one of the most apparent human-induced effects is urbanization, where high-density human habitats disrupt long-established ecotones. Changes to these transitional areas between organisms, especially enhanced contact among humans and wild animals, provide new opportunities for the spread of zoonotic pathogens. This poses a serious threat to global public health, but little is known about how habitat disruption impacts cross-species pathogen spread. Here, we investigated variation in the zoonotic enteric pathogen Campylobacter jejuni. The ubiquity of C. jejuni in wild bird gut microbiomes makes it an ideal organism for understanding how host behavior and ecology influence pathogen transition and spread. We analyzed 700 C. jejuni isolate genomes from 30 bird species in eight countries using a scalable generalized linear model approach. Comparing multiple behavioral and ecological traits showed that proximity to human habitation promotes lineage diversity and is associated with antimicrobial-resistant (AMR) strains in natural populations. Specifically, wild birds from urban areas harbored up to three times more C. jejuni genotypes and AMR genes. This study provides novel methodology and much-needed quantitative evidence linking urbanization to gene pool spread and zoonoses.</p>","PeriodicalId":11359,"journal":{"name":"Current Biology","volume":null,"pages":null},"PeriodicalIF":8.1000,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.cub.2024.07.059","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/13 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Humans are radically altering global ecology, and one of the most apparent human-induced effects is urbanization, where high-density human habitats disrupt long-established ecotones. Changes to these transitional areas between organisms, especially enhanced contact among humans and wild animals, provide new opportunities for the spread of zoonotic pathogens. This poses a serious threat to global public health, but little is known about how habitat disruption impacts cross-species pathogen spread. Here, we investigated variation in the zoonotic enteric pathogen Campylobacter jejuni. The ubiquity of C. jejuni in wild bird gut microbiomes makes it an ideal organism for understanding how host behavior and ecology influence pathogen transition and spread. We analyzed 700 C. jejuni isolate genomes from 30 bird species in eight countries using a scalable generalized linear model approach. Comparing multiple behavioral and ecological traits showed that proximity to human habitation promotes lineage diversity and is associated with antimicrobial-resistant (AMR) strains in natural populations. Specifically, wild birds from urban areas harbored up to three times more C. jejuni genotypes and AMR genes. This study provides novel methodology and much-needed quantitative evidence linking urbanization to gene pool spread and zoonoses.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
接近人类与野生鸟类微生物组中的抗菌肠道病原体有关。
人类正在从根本上改变全球生态,其中最明显的人为影响之一就是城市化,高密度的人类栖息地破坏了长期形成的生态区。这些生物之间过渡区域的变化,尤其是人类与野生动物之间接触的加强,为人畜共患病原体的传播提供了新的机会。这对全球公共卫生构成了严重威胁,但人们对生境破坏如何影响病原体的跨物种传播却知之甚少。在这里,我们研究了人畜共患肠道病原体空肠弯曲菌的变异。空肠弯曲菌在野生鸟类肠道微生物组中无处不在,这使其成为了解宿主行为和生态如何影响病原体过渡和传播的理想生物。我们采用可扩展的广义线性模型方法分析了来自 8 个国家 30 种鸟类的 700 个空肠大肠杆菌分离基因组。对多种行为和生态特征的比较表明,靠近人类居住区会促进血统多样性,并与自然种群中的抗菌素耐药(AMR)菌株有关。具体来说,来自城市地区的野生鸟类携带的空肠大肠杆菌基因型和 AMR 基因多达三倍。这项研究提供了将城市化与基因库传播和人畜共患病联系起来的新方法和急需的定量证据。
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 去求助
来源期刊
Current Biology
Current Biology 生物-生化与分子生物学
CiteScore
11.80
自引率
2.20%
发文量
869
审稿时长
46 days
期刊介绍: Current Biology is a comprehensive journal that showcases original research in various disciplines of biology. It provides a platform for scientists to disseminate their groundbreaking findings and promotes interdisciplinary communication. The journal publishes articles of general interest, encompassing diverse fields of biology. Moreover, it offers accessible editorial pieces that are specifically designed to enlighten non-specialist readers.
期刊最新文献
Parallel maturation of rodent hippocampal memory and CA1 task representations. Dynamic shape-shifting of the single-celled eukaryotic predator Lacrymaria via unconventional cytoskeletal components. Incorporating biotic interactions to better model current and future vegetation of the maritime Antarctic. Regulation of outer kinetochore assembly during meiosis I and II by CENP-A and KNL-2/M18BP1 in C. elegans oocytes. Positive serial dependence in ratings of food images for appeal and calories.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1