The role of the microbiota in respiratory virus-bacterial pathobiont relationships in the upper respiratory tract.

Matthew S Kelly, Pixu Shi, Sefelani C Boiditswe, Emily Qin, Andrew P Steenhoff, Tiny Mazhani, Mohamed Z Patel, Coleen K Cunningham, John F Rawls, Kathy Luinstra, Jodi Gilchrist, Julia Maciejewski, Jillian H Hurst, Patrick C Seed, David Bulir, Marek Smieja
{"title":"The role of the microbiota in respiratory virus-bacterial pathobiont relationships in the upper respiratory tract.","authors":"Matthew S Kelly, Pixu Shi, Sefelani C Boiditswe, Emily Qin, Andrew P Steenhoff, Tiny Mazhani, Mohamed Z Patel, Coleen K Cunningham, John F Rawls, Kathy Luinstra, Jodi Gilchrist, Julia Maciejewski, Jillian H Hurst, Patrick C Seed, David Bulir, Marek Smieja","doi":"10.1101/2024.10.22.24315478","DOIUrl":null,"url":null,"abstract":"<p><p>The mechanisms by which respiratory viruses predispose to secondary bacterial infections remain poorly characterized. Using 2,409 nasopharyngeal swabs from 300 infants in Botswana, we performed a detailed analysis of factors that influence the dynamics of bacterial pathobiont colonization during infancy. We quantify the extent to which viruses increase the acquisition of <i>Haemophilus influenzae</i>, <i>Moraxella catarrhalis</i>, and <i>Streptococcus pneumoniae</i>. We provide evidence of cooperative interactions between these pathobionts while identifying host characteristics and environmental exposures that influence the odds of pathobiont colonization during early life. Using 16S rRNA gene sequencing, we demonstrate that respiratory viruses result in losses of putatively beneficial <i>Corynebacterium</i> and <i>Streptococcus</i> species that are associated with a lower odds of pathobiont acquisition. These findings provide novel insights into viral-bacterial relationships in the URT of direct relevance to respiratory infections and suggest that the URT bacterial microbiota is a potentially modifiable mechanism by which viruses promote bacterial respiratory infections.</p>","PeriodicalId":94281,"journal":{"name":"medRxiv : the preprint server for health sciences","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11537323/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv : the preprint server for health sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.10.22.24315478","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The mechanisms by which respiratory viruses predispose to secondary bacterial infections remain poorly characterized. Using 2,409 nasopharyngeal swabs from 300 infants in Botswana, we performed a detailed analysis of factors that influence the dynamics of bacterial pathobiont colonization during infancy. We quantify the extent to which viruses increase the acquisition of Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae. We provide evidence of cooperative interactions between these pathobionts while identifying host characteristics and environmental exposures that influence the odds of pathobiont colonization during early life. Using 16S rRNA gene sequencing, we demonstrate that respiratory viruses result in losses of putatively beneficial Corynebacterium and Streptococcus species that are associated with a lower odds of pathobiont acquisition. These findings provide novel insights into viral-bacterial relationships in the URT of direct relevance to respiratory infections and suggest that the URT bacterial microbiota is a potentially modifiable mechanism by which viruses promote bacterial respiratory infections.

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
上呼吸道微生物群在呼吸道病毒-细菌致病关系中的作用。
呼吸道病毒导致继发性细菌感染的机制仍不甚明了。我们使用来自博茨瓦纳 300 名婴儿的 2,409 份鼻咽拭子,对影响婴儿期细菌病原菌定植动态的因素进行了详细分析。我们对病毒增加流感嗜血杆菌、白喉摩拉菌和肺炎链球菌感染的程度进行了量化。我们提供了这些病原菌之间合作互动的证据,同时确定了影响生命早期病原菌定植几率的宿主特征和环境暴露。利用 16S rRNA 基因测序,我们证明呼吸道病毒会导致假定有益的棒状杆菌和链球菌物种的损失,而这些物种与较低的病原菌感染几率有关。这些发现为了解与呼吸道感染直接相关的URT中病毒与细菌的关系提供了新的视角,并表明URT细菌微生物群是病毒促进细菌呼吸道感染的潜在可改变机制。
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
自引率
0.00%
发文量
0
期刊最新文献
A Unified Rubric and Similarity Metric for Biomedical Publication Types and Study Designs. Social Determinants of Health Associated with Multiple Myeloma Incidence and Survival among a Low-Income Cohort in the Southeastern U.S. Evaluation of a serum protein signature as monitoring biomarker for Duchenne Muscular Dystrophy in a long-term clinical trial with corticosteroids. Ultrasound-guided skeletal muscle biopsy technique permits measurement of structural, functional, cellular and biochemical properties. Personas Shift Clinical Action Thresholds in Large Language Models.
×
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:604180095
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