追踪黏菌素和碳青霉烯耐药肺炎克雷伯菌的克隆和质粒传播。

IF 5 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-01-10 DOI:10.1128/msystems.01128-24
Ifeoluwa Akintayo, Marko Siroglavic, Daria Frolova, Mabel Budia Silva, Hajo Grundmann, Zamin Iqbal, Ana Budimir, Sandra Reuter
{"title":"追踪黏菌素和碳青霉烯耐药肺炎克雷伯菌的克隆和质粒传播。","authors":"Ifeoluwa Akintayo, Marko Siroglavic, Daria Frolova, Mabel Budia Silva, Hajo Grundmann, Zamin Iqbal, Ana Budimir, Sandra Reuter","doi":"10.1128/msystems.01128-24","DOIUrl":null,"url":null,"abstract":"<p><p>The surveillance of mobile genetic elements facilitating the spread of antimicrobial resistance genes has been challenging. Here, we tracked both clonal and plasmid transmission in colistin- and carbapenem-resistant <i>Klebsiella pneumoniae</i> using short- and long-read sequencing technologies. We observed three clonal transmissions, all containing Incompatibility group (Inc) L plasmids and New Delhi metallo-beta-lactamase <i>bla</i><sub>NDM-1</sub>, although not co-located on the same plasmid. One IncL-<i>bla</i><sub>NDM-1</sub> plasmid had been transferred between sequence type (ST) 392 and ST15, and the promiscuous IncL-<i>bla</i><sub>OXA-48</sub> plasmid was likely shared between a singleton and a clonal transmission of ST392. Plasmids within clonal outbreaks and between clusters and STs had 0-2 single nucleotide polymorphism (SNP) differences, showing high stability upon transfer to same or different STs. The simplest explanation, without a comprehensive analysis with long-read sequencing, would be the spread of a single common IncL-<i>bla</i><sub>NDM-1</sub> plasmid. However, here, we report <i>bla</i><sub>NDM-1</sub> in five different plasmids, emphasizing the need to investigate plasmid-mediated transmission for effective containment of outbreaks.IMPORTANCEAntimicrobial resistance occupies a central stage in global public health emergencies. Recently, efforts to track the genetic elements that facilitate the spread of resistance genes in plasmids outbreaks, utilizing short-read sequencing technologies, have been described. However, incomplete plasmid reconstruction from short-read sequencing data hinders full knowledge about plasmid structure, which makes the exploration very challenging. In this study, we used both short- and long-read sequencing in clinical <i>Klebsiella pneumoniae</i> from University Hospital Centre Zagreb, Croatia, which was resistant to both last-resort antibiotics colistin and carbapenem. Our results show complex transmission networks and sharing of plasmids, emphasizing multiple transmissions of plasmids harboring carbapenem and/or colistin resistance genes between and within <i>K. pneumoniae</i> clones. Only full-length sequencing plus a novel way of determining plasmid clusters resulted in the complete picture, showing how future active monitoring of plasmids as a vital tool for infection prevention and control could be implemented.</p>","PeriodicalId":18819,"journal":{"name":"mSystems","volume":" ","pages":"e0112824"},"PeriodicalIF":5.0000,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tracking clonal and plasmid transmission in colistin- and carbapenem-resistant <i>Klebsiella pneumoniae</i>.\",\"authors\":\"Ifeoluwa Akintayo, Marko Siroglavic, Daria Frolova, Mabel Budia Silva, Hajo Grundmann, Zamin Iqbal, Ana Budimir, Sandra Reuter\",\"doi\":\"10.1128/msystems.01128-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The surveillance of mobile genetic elements facilitating the spread of antimicrobial resistance genes has been challenging. Here, we tracked both clonal and plasmid transmission in colistin- and carbapenem-resistant <i>Klebsiella pneumoniae</i> using short- and long-read sequencing technologies. We observed three clonal transmissions, all containing Incompatibility group (Inc) L plasmids and New Delhi metallo-beta-lactamase <i>bla</i><sub>NDM-1</sub>, although not co-located on the same plasmid. One IncL-<i>bla</i><sub>NDM-1</sub> plasmid had been transferred between sequence type (ST) 392 and ST15, and the promiscuous IncL-<i>bla</i><sub>OXA-48</sub> plasmid was likely shared between a singleton and a clonal transmission of ST392. Plasmids within clonal outbreaks and between clusters and STs had 0-2 single nucleotide polymorphism (SNP) differences, showing high stability upon transfer to same or different STs. The simplest explanation, without a comprehensive analysis with long-read sequencing, would be the spread of a single common IncL-<i>bla</i><sub>NDM-1</sub> plasmid. However, here, we report <i>bla</i><sub>NDM-1</sub> in five different plasmids, emphasizing the need to investigate plasmid-mediated transmission for effective containment of outbreaks.IMPORTANCEAntimicrobial resistance occupies a central stage in global public health emergencies. Recently, efforts to track the genetic elements that facilitate the spread of resistance genes in plasmids outbreaks, utilizing short-read sequencing technologies, have been described. However, incomplete plasmid reconstruction from short-read sequencing data hinders full knowledge about plasmid structure, which makes the exploration very challenging. In this study, we used both short- and long-read sequencing in clinical <i>Klebsiella pneumoniae</i> from University Hospital Centre Zagreb, Croatia, which was resistant to both last-resort antibiotics colistin and carbapenem. Our results show complex transmission networks and sharing of plasmids, emphasizing multiple transmissions of plasmids harboring carbapenem and/or colistin resistance genes between and within <i>K. pneumoniae</i> clones. Only full-length sequencing plus a novel way of determining plasmid clusters resulted in the complete picture, showing how future active monitoring of plasmids as a vital tool for infection prevention and control could be implemented.</p>\",\"PeriodicalId\":18819,\"journal\":{\"name\":\"mSystems\",\"volume\":\" \",\"pages\":\"e0112824\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2025-01-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"mSystems\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/msystems.01128-24\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"mSystems","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/msystems.01128-24","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

对促进抗菌素耐药基因传播的移动遗传元件的监测一直具有挑战性。在这里,我们使用短读和长读测序技术追踪了克隆和质粒在粘菌素和碳青霉烯耐药肺炎克雷伯菌中的传播。我们观察到三个克隆传递,它们都含有不相容组(Inc) L质粒和新德里金属- β -内酰胺酶blaNDM-1,尽管它们不在同一质粒上。一个c - blandm -1质粒在序列型(ST) 392和ST15之间转移,而混杂的c - blaoxa -48质粒可能在ST392的单例和克隆传播中共享。克隆爆发内的质粒以及簇与STs之间的质粒存在0-2的单核苷酸多态性(SNP)差异,在转移到相同或不同STs时表现出高度的稳定性。最简单的解释是,如果没有长读测序的全面分析,可能是一个常见的包括- blandm -1质粒的传播。然而,在这里,我们报告了五种不同质粒中的blaNDM-1,强调有必要调查质粒介导的传播,以有效遏制疫情。抗菌素耐药性在全球突发公共卫生事件中占据中心地位。最近,利用短读测序技术追踪在质粒暴发中促进抗性基因传播的遗传因素的努力已经得到了描述。然而,短读测序数据中质粒重构的不完整阻碍了对质粒结构的全面了解,这给质粒的探索带来了很大的挑战。在这项研究中,我们对来自克罗地亚萨格勒布大学医院中心的临床肺炎克雷伯菌使用了短读和长读测序,该菌株对最后的抗生素粘菌素和碳青霉烯都具有耐药性。我们的研究结果显示了复杂的传播网络和质粒的共享,强调了肺炎克雷伯菌克隆之间和内部含有碳青霉烯类和/或粘菌素抗性基因的质粒的多重传播。只有全长测序加上一种确定质粒簇的新方法才能得到完整的图像,显示如何在未来对质粒进行主动监测,作为预防和控制感染的重要工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tracking clonal and plasmid transmission in colistin- and carbapenem-resistant Klebsiella pneumoniae.

The surveillance of mobile genetic elements facilitating the spread of antimicrobial resistance genes has been challenging. Here, we tracked both clonal and plasmid transmission in colistin- and carbapenem-resistant Klebsiella pneumoniae using short- and long-read sequencing technologies. We observed three clonal transmissions, all containing Incompatibility group (Inc) L plasmids and New Delhi metallo-beta-lactamase blaNDM-1, although not co-located on the same plasmid. One IncL-blaNDM-1 plasmid had been transferred between sequence type (ST) 392 and ST15, and the promiscuous IncL-blaOXA-48 plasmid was likely shared between a singleton and a clonal transmission of ST392. Plasmids within clonal outbreaks and between clusters and STs had 0-2 single nucleotide polymorphism (SNP) differences, showing high stability upon transfer to same or different STs. The simplest explanation, without a comprehensive analysis with long-read sequencing, would be the spread of a single common IncL-blaNDM-1 plasmid. However, here, we report blaNDM-1 in five different plasmids, emphasizing the need to investigate plasmid-mediated transmission for effective containment of outbreaks.IMPORTANCEAntimicrobial resistance occupies a central stage in global public health emergencies. Recently, efforts to track the genetic elements that facilitate the spread of resistance genes in plasmids outbreaks, utilizing short-read sequencing technologies, have been described. However, incomplete plasmid reconstruction from short-read sequencing data hinders full knowledge about plasmid structure, which makes the exploration very challenging. In this study, we used both short- and long-read sequencing in clinical Klebsiella pneumoniae from University Hospital Centre Zagreb, Croatia, which was resistant to both last-resort antibiotics colistin and carbapenem. Our results show complex transmission networks and sharing of plasmids, emphasizing multiple transmissions of plasmids harboring carbapenem and/or colistin resistance genes between and within K. pneumoniae clones. Only full-length sequencing plus a novel way of determining plasmid clusters resulted in the complete picture, showing how future active monitoring of plasmids as a vital tool for infection prevention and control could be implemented.

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
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
×
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:481959085
Book学术官方微信