Genomic analysis of antibiotic resistance genes and mobile genetic elements in eight strains of nontyphoid Salmonella.

IF 5 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2024-09-17 Epub Date: 2024-08-19 DOI:10.1128/msystems.00586-24
Haibing Liu, Lijie Zheng, Huimin Fan, Ji Pang
{"title":"Genomic analysis of antibiotic resistance genes and mobile genetic elements in eight strains of nontyphoid <i>Salmonella</i>.","authors":"Haibing Liu, Lijie Zheng, Huimin Fan, Ji Pang","doi":"10.1128/msystems.00586-24","DOIUrl":null,"url":null,"abstract":"<p><p>Nontyphoidal <i>Salmonella</i> (NTS) is the main etiological agent of human nontyphoidal salmonellosis. The aim of this study was to analyze the epidemiological characteristics and horizontal transfer mechanisms of antimicrobial resistance (AMR) genes from eight strains of NTS detected in Zhenjiang City, Jiangsu Province, China. Fecal samples from outpatients with food-borne diarrhea were collected in 2022. The NTS isolates were identified, and their susceptibility was tested with the Vitek 2 Compact system. The genomes of the NTS isolates were sequenced with the Illumina NovaSeq platform and Oxford Nanopore Technologies platform. The AMR genes and mobile genetic elements (MGEs) were predicted with the relevant open access resources. Eight strains of NTS were isolated from 153 specimens, and <i>Salmonella</i> Typhimurium ST19 was the most prevalent serotype. The AMR gene with the highest detection rate was AAC(6<i>'</i>)-Iaa (10.5%) followed by TEM-1 (7.9%), sul2 (6.6%), and tet(A) (5.3%). Eleven MGEs carrying 34 AMR genes were identified on the chromosomes of 3 of the 8 NTS, including 3 resistance islands, 6 composite transposons (Tns), and 2 integrons. Eighteen plasmids carrying 40 AMR genes were detected in the 8 NTS strains, including 6 mobilizable plasmids, 3 conjugative plasmids, and 9 nontransferable plasmids, 7 of which carried 10 composite Tns and 3 integrons. This study provided a theoretical basis, from a genetic perspective, for the prevention and control of NTS resistance in Zhenjiang City.</p><p><strong>Importance: </strong>Human nontyphoidal salmonellosis is one of the common causes of bacterial food-borne illnesses, with significant social and economic impacts, especially those caused by invasive multidrug-resistant nontyphoidal <i>Salmonella</i>, which entails high morbidity and mortality. Antimicrobial resistance is mainly mediated by drug resistance genes, and mobile genetic elements play key roles in the capture, accumulation, and dissemination of antimicrobial resistance genes. Therefore, it is necessary to study the epidemiological characteristics and horizontal transfer mechanisms of antimicrobial resistance genes of nontyphoidal <i>Salmonella</i> to prevent the spread of multidrug-resistant nontyphoidal <i>Salmonella</i>.</p>","PeriodicalId":18819,"journal":{"name":"mSystems","volume":" ","pages":"e0058624"},"PeriodicalIF":5.0000,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11406962/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"mSystems","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/msystems.00586-24","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Nontyphoidal Salmonella (NTS) is the main etiological agent of human nontyphoidal salmonellosis. The aim of this study was to analyze the epidemiological characteristics and horizontal transfer mechanisms of antimicrobial resistance (AMR) genes from eight strains of NTS detected in Zhenjiang City, Jiangsu Province, China. Fecal samples from outpatients with food-borne diarrhea were collected in 2022. The NTS isolates were identified, and their susceptibility was tested with the Vitek 2 Compact system. The genomes of the NTS isolates were sequenced with the Illumina NovaSeq platform and Oxford Nanopore Technologies platform. The AMR genes and mobile genetic elements (MGEs) were predicted with the relevant open access resources. Eight strains of NTS were isolated from 153 specimens, and Salmonella Typhimurium ST19 was the most prevalent serotype. The AMR gene with the highest detection rate was AAC(6')-Iaa (10.5%) followed by TEM-1 (7.9%), sul2 (6.6%), and tet(A) (5.3%). Eleven MGEs carrying 34 AMR genes were identified on the chromosomes of 3 of the 8 NTS, including 3 resistance islands, 6 composite transposons (Tns), and 2 integrons. Eighteen plasmids carrying 40 AMR genes were detected in the 8 NTS strains, including 6 mobilizable plasmids, 3 conjugative plasmids, and 9 nontransferable plasmids, 7 of which carried 10 composite Tns and 3 integrons. This study provided a theoretical basis, from a genetic perspective, for the prevention and control of NTS resistance in Zhenjiang City.

Importance: Human nontyphoidal salmonellosis is one of the common causes of bacterial food-borne illnesses, with significant social and economic impacts, especially those caused by invasive multidrug-resistant nontyphoidal Salmonella, which entails high morbidity and mortality. Antimicrobial resistance is mainly mediated by drug resistance genes, and mobile genetic elements play key roles in the capture, accumulation, and dissemination of antimicrobial resistance genes. Therefore, it is necessary to study the epidemiological characteristics and horizontal transfer mechanisms of antimicrobial resistance genes of nontyphoidal Salmonella to prevent the spread of multidrug-resistant nontyphoidal Salmonella.

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
八株非伤寒沙门氏菌耐抗生素基因和移动遗传因子的基因组分析。
非伤寒沙门氏菌(NTS)是人类非伤寒沙门氏菌病的主要病原菌。本研究旨在分析中国江苏省镇江市检出的8株NTS的流行病学特征和抗菌药耐药性(AMR)基因的水平转移机制。该研究收集了 2022 年食源性腹泻门诊患者的粪便样本。对 NTS 分离物进行了鉴定,并使用 Vitek 2 Compact 系统检测了它们的药敏性。用 Illumina NovaSeq 平台和 Oxford Nanopore Technologies 平台对 NTS 分离物的基因组进行了测序。利用相关开放资源对 AMR 基因和移动遗传元件(MGEs)进行了预测。从 153 份标本中分离出 8 株 NTS 菌株,伤寒沙门氏菌 ST19 是最常见的血清型。检出率最高的 AMR 基因是 AAC(6')-Iaa (10.5%),其次是 TEM-1 (7.9%)、sul2 (6.6%) 和 tet(A) (5.3%)。在 8 个 NTS 中的 3 个的染色体上发现了 11 个携带 34 个 AMR 基因的 MGE,包括 3 个抗性岛、6 个复合转座子(Tns)和 2 个整合子。在 8 株 NTS 中检测到携带 40 个 AMR 基因的 18 个质粒,包括 6 个可迁移质粒、3 个共轭质粒和 9 个不可迁移质粒,其中 7 个质粒携带 10 个复合转座子和 3 个整合子。该研究从遗传学角度为镇江市防控NTS耐药性提供了理论依据:人类非伤寒沙门氏菌病是细菌性食源性疾病的常见病因之一,具有重大的社会和经济影响,尤其是由具有多重耐药性的侵袭性非伤寒沙门氏菌引起的非伤寒沙门氏菌病,具有很高的发病率和死亡率。抗菌药耐药性主要是由耐药基因介导的,而移动遗传因子在抗菌药耐药基因的捕获、积累和传播中起着关键作用。因此,有必要研究非伤寒沙门氏菌抗菌基因的流行病学特征和水平转移机制,以防止耐多药非伤寒沙门氏菌的传播。
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
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.
期刊最新文献
Association of body index with fecal microbiome in children cohorts with ethnic-geographic factor interaction: accurately using a Bayesian zero-inflated negative binomial regression model. Cigarette smoke-induced disordered microbiota aggravates the severity of influenza A virus infection. Deep learning enabled integration of tumor microenvironment microbial profiles and host gene expressions for interpretable survival subtyping in diverse types of cancers. Advancing microbiome research in Māori populations: insights from recent literature exploring the gut microbiomes of underrepresented and Indigenous peoples. Pan-genome-scale metabolic modeling of Bacillus subtilis reveals functionally distinct groups.
×
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学术文献互助
Book学术文献互助群
群 号:481959085
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