{"title":"中国产碳青霉烯类耐药肺炎克雷伯菌序列 1 型 NDM-5 的基因组序列。","authors":"","doi":"10.1016/j.jgar.2024.05.001","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><p>The emergence of carbapenem-resistant <em>Klebsiella pneumoniae</em> presents significant health challenges. Here, we present the structural genome sequence of an NDM-5–producing <em>K. pneumoniae</em> (HZKP2) in China.</p></div><div><h3>Methods</h3><p>Antimicrobial susceptibility tests were conducted via broth microdilution. Whole-genome sequencing was performed for genomic analysis. Wzi and capsular polysaccharide (KL) were analysed using Kaptive. Resistance genes, virulence factors, and comparative genomics analyses were also conducted. Multilocus sequence typing (MLST), replicons type, and core genome MLST analysis were further conducted using BacWGSTdb server.</p></div><div><h3>Results</h3><p>HZKP2 was resistant to cefepime, ceftazidime, ciprofloxacin, ciprofloxacin, meropenem, and ertapenem. It harboured <em>fosA, bla</em><sub>SHV-187</sub>, <em>oqxA, oqxB, sul1, dfrA1, tet(A), floR, aph(6)-Id, aph(3′')-Ib, sul2, bla</em><sub>CTX-M-55</sub>, and <em>bla</em><sub>NDM-5</sub>. Based on the RAST results, 5563 genes that belonged to 398 subsystems were annotated. The complete genome sequence of HZKP2 was characterized as ST1, <em>wzi</em> 19, and KL19, 5 five contigs totalling 5 654 446 bp, including one chromosome and four plasmids. Further analysis found that <em>bla</em><sub>NDM-5</sub> was located in a 46 161 bp IncX3 plasmid (pHZKP2-3). The genetic structure of <em>bla</em><sub>NDM-5</sub> gene was IS<em>Kox3</em>-IS<em>26</em>-<em>ble</em><sub>MBL</sub>-<em>bla</em><sub>NDM-5</sub>-IS<em>5</em>-IS<em>Ab125</em>-IS<em>3000</em>. Further analysis revealed that insertion sequences mediated the dissemination of <em>bla</em><sub>NDM-5</sub> from other species of <em>Enterobacterales</em>. Phylogenetic analysis showed that the closest relative was from a human stool specimen in China, which differed by 53 core genome MLST alleles.</p></div><div><h3>Conclusions</h3><p>Our study provides the first structural perspective of the ST1 <em>K. pneumoniae</em> isolate producing NDM-5 in China. These results could provide valuable insights into the genetic characteristics, antimicrobial resistance mechanisms, and transmission dynamics of carbapenem-resistant <em>K. pneumoniae</em> in clinical settings.</p></div>","PeriodicalId":15936,"journal":{"name":"Journal of global antimicrobial resistance","volume":null,"pages":null},"PeriodicalIF":3.7000,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213716524000833/pdfft?md5=a6a41cda4d6df31b523c42f62d8363e9&pid=1-s2.0-S2213716524000833-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Genome sequence of a sequence type 1 NDM-5-producing carbapenem-resistant Klebsiella pneumoniae in China\",\"authors\":\"\",\"doi\":\"10.1016/j.jgar.2024.05.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objectives</h3><p>The emergence of carbapenem-resistant <em>Klebsiella pneumoniae</em> presents significant health challenges. Here, we present the structural genome sequence of an NDM-5–producing <em>K. pneumoniae</em> (HZKP2) in China.</p></div><div><h3>Methods</h3><p>Antimicrobial susceptibility tests were conducted via broth microdilution. Whole-genome sequencing was performed for genomic analysis. Wzi and capsular polysaccharide (KL) were analysed using Kaptive. Resistance genes, virulence factors, and comparative genomics analyses were also conducted. Multilocus sequence typing (MLST), replicons type, and core genome MLST analysis were further conducted using BacWGSTdb server.</p></div><div><h3>Results</h3><p>HZKP2 was resistant to cefepime, ceftazidime, ciprofloxacin, ciprofloxacin, meropenem, and ertapenem. It harboured <em>fosA, bla</em><sub>SHV-187</sub>, <em>oqxA, oqxB, sul1, dfrA1, tet(A), floR, aph(6)-Id, aph(3′')-Ib, sul2, bla</em><sub>CTX-M-55</sub>, and <em>bla</em><sub>NDM-5</sub>. Based on the RAST results, 5563 genes that belonged to 398 subsystems were annotated. The complete genome sequence of HZKP2 was characterized as ST1, <em>wzi</em> 19, and KL19, 5 five contigs totalling 5 654 446 bp, including one chromosome and four plasmids. Further analysis found that <em>bla</em><sub>NDM-5</sub> was located in a 46 161 bp IncX3 plasmid (pHZKP2-3). The genetic structure of <em>bla</em><sub>NDM-5</sub> gene was IS<em>Kox3</em>-IS<em>26</em>-<em>ble</em><sub>MBL</sub>-<em>bla</em><sub>NDM-5</sub>-IS<em>5</em>-IS<em>Ab125</em>-IS<em>3000</em>. Further analysis revealed that insertion sequences mediated the dissemination of <em>bla</em><sub>NDM-5</sub> from other species of <em>Enterobacterales</em>. Phylogenetic analysis showed that the closest relative was from a human stool specimen in China, which differed by 53 core genome MLST alleles.</p></div><div><h3>Conclusions</h3><p>Our study provides the first structural perspective of the ST1 <em>K. pneumoniae</em> isolate producing NDM-5 in China. These results could provide valuable insights into the genetic characteristics, antimicrobial resistance mechanisms, and transmission dynamics of carbapenem-resistant <em>K. pneumoniae</em> in clinical settings.</p></div>\",\"PeriodicalId\":15936,\"journal\":{\"name\":\"Journal of global antimicrobial resistance\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2024-05-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2213716524000833/pdfft?md5=a6a41cda4d6df31b523c42f62d8363e9&pid=1-s2.0-S2213716524000833-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of global antimicrobial resistance\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2213716524000833\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of global antimicrobial resistance","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213716524000833","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
Genome sequence of a sequence type 1 NDM-5-producing carbapenem-resistant Klebsiella pneumoniae in China
Objectives
The emergence of carbapenem-resistant Klebsiella pneumoniae presents significant health challenges. Here, we present the structural genome sequence of an NDM-5–producing K. pneumoniae (HZKP2) in China.
Methods
Antimicrobial susceptibility tests were conducted via broth microdilution. Whole-genome sequencing was performed for genomic analysis. Wzi and capsular polysaccharide (KL) were analysed using Kaptive. Resistance genes, virulence factors, and comparative genomics analyses were also conducted. Multilocus sequence typing (MLST), replicons type, and core genome MLST analysis were further conducted using BacWGSTdb server.
Results
HZKP2 was resistant to cefepime, ceftazidime, ciprofloxacin, ciprofloxacin, meropenem, and ertapenem. It harboured fosA, blaSHV-187, oqxA, oqxB, sul1, dfrA1, tet(A), floR, aph(6)-Id, aph(3′')-Ib, sul2, blaCTX-M-55, and blaNDM-5. Based on the RAST results, 5563 genes that belonged to 398 subsystems were annotated. The complete genome sequence of HZKP2 was characterized as ST1, wzi 19, and KL19, 5 five contigs totalling 5 654 446 bp, including one chromosome and four plasmids. Further analysis found that blaNDM-5 was located in a 46 161 bp IncX3 plasmid (pHZKP2-3). The genetic structure of blaNDM-5 gene was ISKox3-IS26-bleMBL-blaNDM-5-IS5-ISAb125-IS3000. Further analysis revealed that insertion sequences mediated the dissemination of blaNDM-5 from other species of Enterobacterales. Phylogenetic analysis showed that the closest relative was from a human stool specimen in China, which differed by 53 core genome MLST alleles.
Conclusions
Our study provides the first structural perspective of the ST1 K. pneumoniae isolate producing NDM-5 in China. These results could provide valuable insights into the genetic characteristics, antimicrobial resistance mechanisms, and transmission dynamics of carbapenem-resistant K. pneumoniae in clinical settings.
期刊介绍:
The Journal of Global Antimicrobial Resistance (JGAR) is a quarterly online journal run by an international Editorial Board that focuses on the global spread of antibiotic-resistant microbes.
JGAR is a dedicated journal for all professionals working in research, health care, the environment and animal infection control, aiming to track the resistance threat worldwide and provides a single voice devoted to antimicrobial resistance (AMR).
Featuring peer-reviewed and up to date research articles, reviews, short notes and hot topics JGAR covers the key topics related to antibacterial, antiviral, antifungal and antiparasitic resistance.