产OXA-244-碳青霉烯酶大肠埃希菌的长期携带使流行病学调查复杂化

IF 4.5 3区 医学 Q1 MICROBIOLOGY
Felix Reichert , Simon Brinkwirth , Niels Pfennigwerth , Sebastian Haller , Lena Sophie Fritsch , Tim Eckmanns , Guido Werner , Sören Gatermann , Jörg B. Hans
{"title":"产OXA-244-碳青霉烯酶大肠埃希菌的长期携带使流行病学调查复杂化","authors":"Felix Reichert ,&nbsp;Simon Brinkwirth ,&nbsp;Niels Pfennigwerth ,&nbsp;Sebastian Haller ,&nbsp;Lena Sophie Fritsch ,&nbsp;Tim Eckmanns ,&nbsp;Guido Werner ,&nbsp;Sören Gatermann ,&nbsp;Jörg B. Hans","doi":"10.1016/j.ijmm.2023.151595","DOIUrl":null,"url":null,"abstract":"<div><p>The rapid increase of OXA-244-producing <em>Escherichia coli</em>, predominantly driven by genetically clustered isolates of sequence type (ST)38, has been observed in at least nine European countries, including Germany. However, the reasons for the spread of OXA-244-producing <em>E. coli</em> remain unclear. Here, we aim to evaluate the possibility of prolonged carriage. We identified a total of six different patients with repeated detection of OXA-244-producing <em>E. coli</em> isolates, which were subjected to both short and long-read whole-genome sequencing (WGS). Besides allelic differences using core genome multilocus sequence typing (cgMLST) analyses, we obtained numbers of single-nucleotide polymorphisms (SNPs) to calculate individual base-pair substitution (BPS) rates. To assess possible re-exposure and risk factors for prolonged carriage, case interviews were conducted. The time between detections ranged from eleven months to more than three years. Initial isolates originated in three+ out of six cases from clinical samples, whereas remaining samples were from screening, mostly in the inpatient setting. As expected, cgMLST analyses showed low numbers of allelic differences between isolates of each case ranging from 1 to 4, whereas numbers of SNPs were between 2 and 99 (mean = 36), thus clearly highlighting the discrepancy between these different bacterial typing approaches. For five out of six cases, observed BPS rates suggest that patients can be colonized with OXA-244-producing <em>E. coli</em>, including ST38 cluster isolates, for extensively long times. Thus, we may have previously missed the epidemiological link between cases because exposure to OXA-244-producing <em>E. coli</em> could have occurred in a time frame, which has not been evaluated in previous investigations. Our results may help to guide future epidemiological investigations as well as to support the interpretation of genetic diversity of OXA-244-producing <em>E. coli</em>, particularly among ST38 cluster isolates.</p></div>","PeriodicalId":50312,"journal":{"name":"International Journal of Medical Microbiology","volume":"314 ","pages":"Article 151595"},"PeriodicalIF":4.5000,"publicationDate":"2023-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1438422123000231/pdfft?md5=a87c9eb916322b02a19c3f1f71b45702&pid=1-s2.0-S1438422123000231-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Prolonged carriage of OXA-244-carbapenemase-producing Escherichia coli complicates epidemiological investigations\",\"authors\":\"Felix Reichert ,&nbsp;Simon Brinkwirth ,&nbsp;Niels Pfennigwerth ,&nbsp;Sebastian Haller ,&nbsp;Lena Sophie Fritsch ,&nbsp;Tim Eckmanns ,&nbsp;Guido Werner ,&nbsp;Sören Gatermann ,&nbsp;Jörg B. Hans\",\"doi\":\"10.1016/j.ijmm.2023.151595\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The rapid increase of OXA-244-producing <em>Escherichia coli</em>, predominantly driven by genetically clustered isolates of sequence type (ST)38, has been observed in at least nine European countries, including Germany. However, the reasons for the spread of OXA-244-producing <em>E. coli</em> remain unclear. Here, we aim to evaluate the possibility of prolonged carriage. We identified a total of six different patients with repeated detection of OXA-244-producing <em>E. coli</em> isolates, which were subjected to both short and long-read whole-genome sequencing (WGS). Besides allelic differences using core genome multilocus sequence typing (cgMLST) analyses, we obtained numbers of single-nucleotide polymorphisms (SNPs) to calculate individual base-pair substitution (BPS) rates. To assess possible re-exposure and risk factors for prolonged carriage, case interviews were conducted. The time between detections ranged from eleven months to more than three years. Initial isolates originated in three+ out of six cases from clinical samples, whereas remaining samples were from screening, mostly in the inpatient setting. As expected, cgMLST analyses showed low numbers of allelic differences between isolates of each case ranging from 1 to 4, whereas numbers of SNPs were between 2 and 99 (mean = 36), thus clearly highlighting the discrepancy between these different bacterial typing approaches. For five out of six cases, observed BPS rates suggest that patients can be colonized with OXA-244-producing <em>E. coli</em>, including ST38 cluster isolates, for extensively long times. Thus, we may have previously missed the epidemiological link between cases because exposure to OXA-244-producing <em>E. coli</em> could have occurred in a time frame, which has not been evaluated in previous investigations. Our results may help to guide future epidemiological investigations as well as to support the interpretation of genetic diversity of OXA-244-producing <em>E. coli</em>, particularly among ST38 cluster isolates.</p></div>\",\"PeriodicalId\":50312,\"journal\":{\"name\":\"International Journal of Medical Microbiology\",\"volume\":\"314 \",\"pages\":\"Article 151595\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2023-12-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S1438422123000231/pdfft?md5=a87c9eb916322b02a19c3f1f71b45702&pid=1-s2.0-S1438422123000231-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Medical Microbiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1438422123000231\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Medical Microbiology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1438422123000231","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

在包括德国在内的至少九个欧洲国家,主要由序列类型(ST)38 的基因聚类分离物引起的产 OXA-244 大肠杆菌迅速增加。然而,产 OXA-244 大肠杆菌扩散的原因仍不清楚。在此,我们旨在评估长期携带的可能性。我们共发现了六名重复检测到产 OXA-244 大肠杆菌分离物的不同患者,并对其进行了短线程和长线程全基因组测序(WGS)。除了利用核心基因组多焦点序列分型(cgMLST)分析等位基因差异外,我们还获得了单核苷酸多态性(SNP)的数量,以计算单个碱基对置换(BPS)率。为了评估可能的再次接触和长期携带的风险因素,我们对病例进行了访谈。两次检测之间的间隔时间从 11 个月到三年多不等。在六个病例中,有三个以上病例的初始分离株来自临床样本,而其余样本则来自筛查,主要是在住院环境中筛查。不出所料,cgMLST 分析显示每个病例分离物之间的等位基因差异数量较少,从 1 个到 4 个不等,而 SNP 的数量则从 2 个到 99 个不等(平均值 = 36 个),这清楚地表明了这些不同细菌分型方法之间的差异。在 6 个病例中,有 5 个病例观察到的 BPS 率表明,患者可能长期定植于产 OXA-244 大肠杆菌(包括 ST38 群分离菌)。因此,我们以前可能忽略了病例之间的流行病学联系,因为暴露于产 OXA-244 大肠杆菌的时间框架可能是在以前的调查中没有评估过的。我们的研究结果可能有助于指导未来的流行病学调查,并支持对产 OXA-244 大肠杆菌遗传多样性的解释,尤其是在 ST38 群体分离物中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prolonged carriage of OXA-244-carbapenemase-producing Escherichia coli complicates epidemiological investigations

The rapid increase of OXA-244-producing Escherichia coli, predominantly driven by genetically clustered isolates of sequence type (ST)38, has been observed in at least nine European countries, including Germany. However, the reasons for the spread of OXA-244-producing E. coli remain unclear. Here, we aim to evaluate the possibility of prolonged carriage. We identified a total of six different patients with repeated detection of OXA-244-producing E. coli isolates, which were subjected to both short and long-read whole-genome sequencing (WGS). Besides allelic differences using core genome multilocus sequence typing (cgMLST) analyses, we obtained numbers of single-nucleotide polymorphisms (SNPs) to calculate individual base-pair substitution (BPS) rates. To assess possible re-exposure and risk factors for prolonged carriage, case interviews were conducted. The time between detections ranged from eleven months to more than three years. Initial isolates originated in three+ out of six cases from clinical samples, whereas remaining samples were from screening, mostly in the inpatient setting. As expected, cgMLST analyses showed low numbers of allelic differences between isolates of each case ranging from 1 to 4, whereas numbers of SNPs were between 2 and 99 (mean = 36), thus clearly highlighting the discrepancy between these different bacterial typing approaches. For five out of six cases, observed BPS rates suggest that patients can be colonized with OXA-244-producing E. coli, including ST38 cluster isolates, for extensively long times. Thus, we may have previously missed the epidemiological link between cases because exposure to OXA-244-producing E. coli could have occurred in a time frame, which has not been evaluated in previous investigations. Our results may help to guide future epidemiological investigations as well as to support the interpretation of genetic diversity of OXA-244-producing E. coli, particularly among ST38 cluster isolates.

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
CiteScore
9.70
自引率
0.00%
发文量
18
审稿时长
45 days
期刊介绍: Pathogen genome sequencing projects have provided a wealth of data that need to be set in context to pathogenicity and the outcome of infections. In addition, the interplay between a pathogen and its host cell has become increasingly important to understand and interfere with diseases caused by microbial pathogens. IJMM meets these needs by focussing on genome and proteome analyses, studies dealing with the molecular mechanisms of pathogenicity and the evolution of pathogenic agents, the interactions between pathogens and host cells ("cellular microbiology"), and molecular epidemiology. To help the reader keeping up with the rapidly evolving new findings in the field of medical microbiology, IJMM publishes original articles, case studies and topical, state-of-the-art mini-reviews in a well balanced fashion. All articles are strictly peer-reviewed. Important topics are reinforced by 2 special issues per year dedicated to a particular theme. Finally, at irregular intervals, current opinions on recent or future developments in medical microbiology are presented in an editorial section.
×
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