不动杆菌广泛耐药(XDR) IV型分泌系统编码质粒在宿主范围内多样性的表征

IF 3.3 3区 医学 Q2 MICROBIOLOGY
Kailey Martz, Dalya Alomar, Marisha Karim, Sara Knezevic, Vanessa M D'Costa
{"title":"不动杆菌广泛耐药(XDR) IV型分泌系统编码质粒在宿主范围内多样性的表征","authors":"Kailey Martz, Dalya Alomar, Marisha Karim, Sara Knezevic, Vanessa M D'Costa","doi":"10.3390/pathogens14060606","DOIUrl":null,"url":null,"abstract":"<p><p>The World Health Organization (WHO) cites antimicrobial resistance as among the greatest threats to human health. The multidrug-resistant pathogen <i>Acinetobacter baumannii</i>, recognized as a priority pathogen for healthcare and research, is responsible for a diverse array of infections including respiratory tract, soft tissue and wound, and bloodstream infections. Despite this importance, the mechanisms of its pathogenesis remain poorly understood. Conjugation represents a central mechanism for bacterial adaptation and evolution and is responsible for the spread of genes that promote pathogen survival, antibiotic resistance, virulence, and biofilm formation. Our laboratory recently characterized a large group of almost 120 Type IV Secretion System (T4SS)-encoding plasmids in <i>Acinetobacter</i>, distributed globally across 20 countries spanning four continents, and demonstrated that an XDR <i>A. baumannii</i> plasmid from this family was transmissible to another <i>A. baumannii</i> strain. This research investigated the potential diversity of host strains for this representative member plasmid. Using the GC1 lineage strain <i>A. baumannii</i> AB5075-UW harbouring the XDR plasmid p1AB5075 and a series of previously characterized clinical and environmental <i>Acinetobacter</i> strains, conjugative analyses demonstrated transfer of the XDR plasmid to both <i>A. baumannii</i> strains of more genetically divergent sequence types and to non-<i>baumannii Acinetobacter</i> species both inside and outside the <i>Acinetobacter calcoaceticus-baumannii</i> (ACB) complex. Successful recipients included diverse strains of both clinical and environmental origin within the <i>Acinetobacter</i> genus. Collectively, this research could provide insights into an important genetic element for future surveillance.</p>","PeriodicalId":19758,"journal":{"name":"Pathogens","volume":"14 6","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12196012/pdf/","citationCount":"0","resultStr":"{\"title\":\"Characterization of the Diversity in Host Range of an Extensively Drug-Resistant (XDR) Type IV Secretion System-Encoding Plasmid in <i>Acinetobacter</i>.\",\"authors\":\"Kailey Martz, Dalya Alomar, Marisha Karim, Sara Knezevic, Vanessa M D'Costa\",\"doi\":\"10.3390/pathogens14060606\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The World Health Organization (WHO) cites antimicrobial resistance as among the greatest threats to human health. The multidrug-resistant pathogen <i>Acinetobacter baumannii</i>, recognized as a priority pathogen for healthcare and research, is responsible for a diverse array of infections including respiratory tract, soft tissue and wound, and bloodstream infections. Despite this importance, the mechanisms of its pathogenesis remain poorly understood. Conjugation represents a central mechanism for bacterial adaptation and evolution and is responsible for the spread of genes that promote pathogen survival, antibiotic resistance, virulence, and biofilm formation. Our laboratory recently characterized a large group of almost 120 Type IV Secretion System (T4SS)-encoding plasmids in <i>Acinetobacter</i>, distributed globally across 20 countries spanning four continents, and demonstrated that an XDR <i>A. baumannii</i> plasmid from this family was transmissible to another <i>A. baumannii</i> strain. This research investigated the potential diversity of host strains for this representative member plasmid. Using the GC1 lineage strain <i>A. baumannii</i> AB5075-UW harbouring the XDR plasmid p1AB5075 and a series of previously characterized clinical and environmental <i>Acinetobacter</i> strains, conjugative analyses demonstrated transfer of the XDR plasmid to both <i>A. baumannii</i> strains of more genetically divergent sequence types and to non-<i>baumannii Acinetobacter</i> species both inside and outside the <i>Acinetobacter calcoaceticus-baumannii</i> (ACB) complex. Successful recipients included diverse strains of both clinical and environmental origin within the <i>Acinetobacter</i> genus. Collectively, this research could provide insights into an important genetic element for future surveillance.</p>\",\"PeriodicalId\":19758,\"journal\":{\"name\":\"Pathogens\",\"volume\":\"14 6\",\"pages\":\"\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-06-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12196012/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pathogens\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3390/pathogens14060606\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pathogens","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/pathogens14060606","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

世界卫生组织(WHO)将抗菌素耐药性列为对人类健康的最大威胁之一。多药耐药病原体鲍曼不动杆菌被认为是卫生保健和研究的重点病原体,可导致多种感染,包括呼吸道、软组织和伤口以及血液感染。尽管如此,其发病机制仍然知之甚少。偶联是细菌适应和进化的核心机制,是促进病原体生存、抗生素耐药性、毒力和生物膜形成的基因传播的原因。我们的实验室最近对分布在全球四大洲20个国家的不动杆菌中近120个IV型分泌系统(T4SS)编码质粒进行了鉴定,并证明该家族的XDR鲍曼不动杆菌质粒可传播给另一株鲍曼不动杆菌。本研究探讨了该代表性成员质粒的寄主菌株的潜在多样性。利用含有XDR质粒p1AB5075的鲍曼不动杆菌GC1谱系菌株AB5075-UW和一系列先前鉴定的临床和环境不动杆菌菌株,结合分析表明,XDR质粒可以转移到基因序列更多样化的鲍曼不动杆菌菌株和ACB不动杆菌内外的非鲍曼不动杆菌物种。成功的接受者包括不动杆菌属中临床和环境来源的各种菌株。总的来说,这项研究可以为未来的监测提供一个重要的遗传因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of the Diversity in Host Range of an Extensively Drug-Resistant (XDR) Type IV Secretion System-Encoding Plasmid in Acinetobacter.

The World Health Organization (WHO) cites antimicrobial resistance as among the greatest threats to human health. The multidrug-resistant pathogen Acinetobacter baumannii, recognized as a priority pathogen for healthcare and research, is responsible for a diverse array of infections including respiratory tract, soft tissue and wound, and bloodstream infections. Despite this importance, the mechanisms of its pathogenesis remain poorly understood. Conjugation represents a central mechanism for bacterial adaptation and evolution and is responsible for the spread of genes that promote pathogen survival, antibiotic resistance, virulence, and biofilm formation. Our laboratory recently characterized a large group of almost 120 Type IV Secretion System (T4SS)-encoding plasmids in Acinetobacter, distributed globally across 20 countries spanning four continents, and demonstrated that an XDR A. baumannii plasmid from this family was transmissible to another A. baumannii strain. This research investigated the potential diversity of host strains for this representative member plasmid. Using the GC1 lineage strain A. baumannii AB5075-UW harbouring the XDR plasmid p1AB5075 and a series of previously characterized clinical and environmental Acinetobacter strains, conjugative analyses demonstrated transfer of the XDR plasmid to both A. baumannii strains of more genetically divergent sequence types and to non-baumannii Acinetobacter species both inside and outside the Acinetobacter calcoaceticus-baumannii (ACB) complex. Successful recipients included diverse strains of both clinical and environmental origin within the Acinetobacter genus. Collectively, this research could provide insights into an important genetic element for future surveillance.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Pathogens
Pathogens Medicine-Immunology and Allergy
CiteScore
6.40
自引率
8.10%
发文量
1285
审稿时长
17.75 days
期刊介绍: Pathogens (ISSN 2076-0817) publishes reviews, regular research papers and short notes on all aspects of pathogens and pathogen-host interactions. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodical details must be provided for research articles.
×
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