Distinct adaptation and epidemiological success of different genotypes within Salmonella enterica serovar Dublin.

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2025-06-25 DOI:10.7554/eLife.102253
Cheryll M Sia, Rebecca L Ambrose, Mary Valcanis, Patiyan Andersson, Susan A Ballard, Benjamin P Howden, Deborah A Williamson, Jaclyn S Pearson, Danielle J Ingle
{"title":"Distinct adaptation and epidemiological success of different genotypes within <i>Salmonella enterica</i> serovar Dublin.","authors":"Cheryll M Sia, Rebecca L Ambrose, Mary Valcanis, Patiyan Andersson, Susan A Ballard, Benjamin P Howden, Deborah A Williamson, Jaclyn S Pearson, Danielle J Ingle","doi":"10.7554/eLife.102253","DOIUrl":null,"url":null,"abstract":"<p><p><i>Salmonella</i> Dublin is a host-adapted, invasive nontyphoidal <i>Salmonella</i> (iNTS) serovar that causes bloodstream infections in humans and demonstrates increasing prevalence of antimicrobial resistance (AMR). Using a global dataset of 1303 genomes, coupled with in vitro assays, we examined the evolutionary, resistance, and virulence characteristics of <i>S</i>. Dublin. Our analysis revealed strong geographical associations between AMR profiles and plasmid types, with highly resistant isolates confined predominantly to North America, linked to IncC plasmids co-encoding AMR and heavy metal resistance. By contrast, Australian isolates were largely antimicrobial-susceptible, reflecting differing AMR pressures. We identified two phylogenetically distinct Australian lineages, ST10 and ST74, with a small number of ST10 isolates harbouring a novel hybrid plasmid encoding both AMR and mercuric resistance. Whereas the ST10 lineage remains globally dominant, the ST74 lineage was less prevalent. ST74 exhibited unique genomic features including a larger pan genome compared to ST10 and the absence of key virulence loci, including <i>Salmonella</i> pathogenicity island (SPI)-19 which encodes a type VI secretion system (T6SS). Despite these genomic differences, the ST74 lineage displayed enhanced intracellular replication in human macrophages and induced less pro-inflammatory responses compared with ST10, suggesting alternative virulence strategies that may support systemic dissemination of ST74. The Vi antigen was absent in all ST10 and ST74 genomes, highlighting challenges for serotyping and vaccine development, and has implications for current diagnostic and control strategies for <i>S.</i> Dublin infections. Collectively, this study represents the most comprehensive investigation of <i>S</i>. Dublin to date and, importantly, has revealed distinct adaptations of two genotypes within the same serovar, leading to different epidemiological success. The regional emergence and evolution of distinct <i>S.</i> Dublin lineages highlight the need to understand the divergence of intra-serovar virulence mechanisms which may impact the development of effective control measures against this important global pathogen.</p>","PeriodicalId":11640,"journal":{"name":"eLife","volume":"13 ","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12194135/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"eLife","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.7554/eLife.102253","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Salmonella Dublin is a host-adapted, invasive nontyphoidal Salmonella (iNTS) serovar that causes bloodstream infections in humans and demonstrates increasing prevalence of antimicrobial resistance (AMR). Using a global dataset of 1303 genomes, coupled with in vitro assays, we examined the evolutionary, resistance, and virulence characteristics of S. Dublin. Our analysis revealed strong geographical associations between AMR profiles and plasmid types, with highly resistant isolates confined predominantly to North America, linked to IncC plasmids co-encoding AMR and heavy metal resistance. By contrast, Australian isolates were largely antimicrobial-susceptible, reflecting differing AMR pressures. We identified two phylogenetically distinct Australian lineages, ST10 and ST74, with a small number of ST10 isolates harbouring a novel hybrid plasmid encoding both AMR and mercuric resistance. Whereas the ST10 lineage remains globally dominant, the ST74 lineage was less prevalent. ST74 exhibited unique genomic features including a larger pan genome compared to ST10 and the absence of key virulence loci, including Salmonella pathogenicity island (SPI)-19 which encodes a type VI secretion system (T6SS). Despite these genomic differences, the ST74 lineage displayed enhanced intracellular replication in human macrophages and induced less pro-inflammatory responses compared with ST10, suggesting alternative virulence strategies that may support systemic dissemination of ST74. The Vi antigen was absent in all ST10 and ST74 genomes, highlighting challenges for serotyping and vaccine development, and has implications for current diagnostic and control strategies for S. Dublin infections. Collectively, this study represents the most comprehensive investigation of S. Dublin to date and, importantly, has revealed distinct adaptations of two genotypes within the same serovar, leading to different epidemiological success. The regional emergence and evolution of distinct S. Dublin lineages highlight the need to understand the divergence of intra-serovar virulence mechanisms which may impact the development of effective control measures against this important global pathogen.

都柏林肠沙门氏菌血清中不同基因型的不同适应和流行病学成功。
都柏林沙门氏菌是一种适应宿主的侵入性非伤寒沙门氏菌(iNTS)血清型,可引起人类血液感染,并显示出越来越普遍的抗微生物药物耐药性(AMR)。利用1303个基因组的全球数据集,结合体外试验,研究了S. Dublin的进化、抗性和毒力特征。我们的分析显示,AMR谱和质粒类型之间存在很强的地理关联,高抗性分离株主要局限于北美,与共同编码AMR和重金属抗性的IncC质粒有关。相比之下,澳大利亚的分离株大多对抗菌素敏感,反映了不同的抗菌素耐药性压力。我们鉴定了两个系统发育上不同的澳大利亚谱系,ST10和ST74,其中少量ST10分离株含有一种新型杂交质粒,编码AMR和抗汞性。尽管ST10谱系仍在全球占主导地位,但ST74谱系的流行程度较低。与ST10相比,ST74具有独特的基因组特征,包括更大的泛基因组和缺乏关键毒力位点,包括沙门氏菌致病岛(SPI)-19,该基因编码VI型分泌系统(T6SS)。尽管存在这些基因组差异,但与ST10相比,ST74谱系在人巨噬细胞中表现出增强的细胞内复制,诱导的促炎反应更少,这表明其他毒力策略可能支持ST74的全身传播。在所有ST10和ST74基因组中都没有Vi抗原,这突出了血清分型和疫苗开发的挑战,并对当前都柏林S.感染的诊断和控制策略具有重要意义。总的来说,这项研究代表了迄今为止对S. Dublin最全面的调查,重要的是,它揭示了同一血清型中两种基因型的不同适应,导致不同的流行病学成功。不同都柏林葡萄球菌谱系的区域出现和进化突出表明需要了解血清内毒力机制的差异,这可能会影响针对这一重要全球病原体的有效控制措施的发展。
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
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
×
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:604180095
Book学术官方微信