A genomic and phenotypic investigation of pigeon-adaptive Salmonella.

IF 4.9 1区 医学 Q1 MICROBIOLOGY PLoS Pathogens Pub Date : 2025-03-17 eCollection Date: 2025-03-01 DOI:10.1371/journal.ppat.1012992
Zining Wang, Zenghai Jiang, Qianzhe Cao, Chenghao Jia, Haiyang Zhou, Chenghu Huang, Linlin Huang, Yingying Huang, Yan Li, Min Yue
{"title":"A genomic and phenotypic investigation of pigeon-adaptive Salmonella.","authors":"Zining Wang, Zenghai Jiang, Qianzhe Cao, Chenghao Jia, Haiyang Zhou, Chenghu Huang, Linlin Huang, Yingying Huang, Yan Li, Min Yue","doi":"10.1371/journal.ppat.1012992","DOIUrl":null,"url":null,"abstract":"<p><p>Salmonella, a significant threat to public safety, inflicts substantial economic losses on the poultry industry. The unique \"parental feeding\" breeding model of pigeon farms, against the \"all-in & all-out\" biosecurity strategy, makes them susceptible to Salmonella infections and subsequent outbreaks of pigeon paratyphoid. This study initially studied three pigeon paratyphoid outbreak incidents in Henan, China, in which 53 strains of pigeon-origin Salmonella Typhimurium (STM) were identified. Whole-genome sequencing (WGS) and antimicrobial-resistant profile analysis revealed that the three outbreaks were caused by distinct STM clones (ST128-DT2, ST19-DT99). Global phylogenetic analysis suggested that the United States is a possible origin, indicating a risk of intercontinental transmission via pigeon eggs. Further bacterial virulence and invasion assays, including in vitro and in vivo assays, revealed that pigeon-host-adaptive STM, compared to broad-host-range STM, carried fewer resistance genes, exhibited higher invasion indices and pseudogene levels, displayed a non-rdar (red dry and rough) phenotype, and had strong biofilm formation capability. Additionally, they showed reduced virulence and invasiveness in mice but a pigeon-adaptive feature in cogent models. The collective results support the host adaptation for pigeons among DT2 and DT99 phage-type isolates.</p>","PeriodicalId":48999,"journal":{"name":"PLoS Pathogens","volume":"21 3","pages":"e1012992"},"PeriodicalIF":4.9000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11957392/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"PLoS Pathogens","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1371/journal.ppat.1012992","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Salmonella, a significant threat to public safety, inflicts substantial economic losses on the poultry industry. The unique "parental feeding" breeding model of pigeon farms, against the "all-in & all-out" biosecurity strategy, makes them susceptible to Salmonella infections and subsequent outbreaks of pigeon paratyphoid. This study initially studied three pigeon paratyphoid outbreak incidents in Henan, China, in which 53 strains of pigeon-origin Salmonella Typhimurium (STM) were identified. Whole-genome sequencing (WGS) and antimicrobial-resistant profile analysis revealed that the three outbreaks were caused by distinct STM clones (ST128-DT2, ST19-DT99). Global phylogenetic analysis suggested that the United States is a possible origin, indicating a risk of intercontinental transmission via pigeon eggs. Further bacterial virulence and invasion assays, including in vitro and in vivo assays, revealed that pigeon-host-adaptive STM, compared to broad-host-range STM, carried fewer resistance genes, exhibited higher invasion indices and pseudogene levels, displayed a non-rdar (red dry and rough) phenotype, and had strong biofilm formation capability. Additionally, they showed reduced virulence and invasiveness in mice but a pigeon-adaptive feature in cogent models. The collective results support the host adaptation for pigeons among DT2 and DT99 phage-type isolates.

Abstract Image

Abstract Image

Abstract Image

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
鸽子适应性沙门氏菌的基因组和表型研究。
沙门氏菌是对公共安全的重大威胁,给家禽业造成了巨大的经济损失。鸽子养殖场独特的“亲代饲养”饲养模式,与“全力以赴”的生物安全战略背道而驰,使它们容易受到沙门氏菌感染和随后爆发的鸽子副伤寒的影响。本研究对中国河南省3起鸽子副伤寒暴发事件进行了初步研究,共鉴定出53株鸽源性鼠伤寒沙门菌(STM)。全基因组测序(WGS)和耐药谱分析显示,这三次暴发是由不同的STM克隆(ST128-DT2, ST19-DT99)引起的。全球系统发育分析表明,美国是一个可能的起源,表明有通过鸽子蛋进行洲际传播的风险。进一步的细菌毒力和侵袭实验(包括体内和体外实验)表明,与广泛宿主范围的STM相比,鸽子-宿主适应性STM携带的抗性基因较少,具有更高的侵袭指数和假基因水平,表现出非rdar(红色干燥和粗糙)表型,具有较强的生物膜形成能力。此外,它们在小鼠中表现出毒性和侵袭性降低,但在cogent模型中表现出鸽子适应特征。这些结果支持了DT2和DT99噬菌体型分离株对鸽子宿主的适应性。
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
PLoS Pathogens
PLoS Pathogens MICROBIOLOGY-PARASITOLOGY
自引率
3.00%
发文量
598
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
期刊最新文献
Identification of essential genes for conjugative transfer in antimicrobial resistance-associated pELF-type linear plasmids of opportunistic pathogen Enterococcus faecium. Glutamine supports human cytomegalovirus induced lipidome remodeling through reductive carboxylation. Multisensory pathogen detection drives rapid escape and shapes host-microbe interactions in Drosophila larvae. Viral inhibition of the anaphase promoting complex enhances replication by elevating nucleotide pools. Spatial dynamics of viral replication drive biphasic lymphoid activation and systemic alphavirus immune responses.
×
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