{"title":"尿路致病性克雷伯氏菌的全基因组序列、表型相关性和泛基因组分析","authors":"Abhirami Krishnamoorthy Sundaresan, Jaya Gangwar, Aravind Murugavel, Ganesh Babu Malli Mohan, Jayapradha Ramakrishnan","doi":"10.1186/s13568-024-01737-w","DOIUrl":null,"url":null,"abstract":"<p><p>Urinary tract infections (UTI) by antibiotic resistant and virulent K. pneumoniae are a growing concern. Understanding the genome and validating the genomic profile along with pangenome analysis will facilitate surveillance of high-risk clones of K. pneumoniae to underpin management strategies toward early detection. The present study aims to correlate resistome with phenotypic antimicrobial resistance and virulome with pathogenicity in Klebsiella spp. The present study aimed to perform complete genome sequences of Klebsiella spp. and to analyse the correlation of resistome with phenotypic antimicrobial resistance and virulome with pathogenicity. To understand the resistome, pangenome and virulome in the Klebsiella spp, the ResFinder, CARD, IS Finder, PlasmidFinder, PHASTER, Roary, VFDB were used. The phenotypic susceptibility profiling identified the uropathogenic kp3 to exhibit multi drug resistance. The resistome and in vitro antimicrobial profiling showed concordance with all the tested antibiotics against the study strains. Hypermucoviscosity was not observed for any of the test isolates; this phenotypic character matches perfectly with the absence of rmpA and magA genes. To the best of our knowledge, this is the first report on the presence of ste, stf, stc and sti major fimbrial operons of Salmonella enterica serotype Typhimurium in K. pneumoniae genome. The study identifies the discordance of virulome and virulence in Klebsiella spp. The complete genome analysis and phenotypic correlation identify uropathogenic K. pneumoniae kp3 as a carbapenem-resistant and virulent pathogen. The Pangenome of K. pneumoniae was open suggesting high genetic diversity. Diverse K serotypes were observed. Sequence typing reveals the prevalence of K. pneumoniae high-risk clones in UTI catheterised patients. The study also highlights the concordance of resistome and in vitro susceptibility tests. Importantly, the study identifies the necessity of virulome and phenotypic virulence markers for timely diagnosis and immediate treatment for the management of high-risk K. pneumoniae clones.</p>","PeriodicalId":7537,"journal":{"name":"AMB Express","volume":null,"pages":null},"PeriodicalIF":3.5000,"publicationDate":"2024-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11224175/pdf/","citationCount":"0","resultStr":"{\"title\":\"Complete genome sequence, phenotypic correlation and pangenome analysis of uropathogenic Klebsiella spp.\",\"authors\":\"Abhirami Krishnamoorthy Sundaresan, Jaya Gangwar, Aravind Murugavel, Ganesh Babu Malli Mohan, Jayapradha Ramakrishnan\",\"doi\":\"10.1186/s13568-024-01737-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Urinary tract infections (UTI) by antibiotic resistant and virulent K. pneumoniae are a growing concern. Understanding the genome and validating the genomic profile along with pangenome analysis will facilitate surveillance of high-risk clones of K. pneumoniae to underpin management strategies toward early detection. The present study aims to correlate resistome with phenotypic antimicrobial resistance and virulome with pathogenicity in Klebsiella spp. The present study aimed to perform complete genome sequences of Klebsiella spp. and to analyse the correlation of resistome with phenotypic antimicrobial resistance and virulome with pathogenicity. To understand the resistome, pangenome and virulome in the Klebsiella spp, the ResFinder, CARD, IS Finder, PlasmidFinder, PHASTER, Roary, VFDB were used. The phenotypic susceptibility profiling identified the uropathogenic kp3 to exhibit multi drug resistance. The resistome and in vitro antimicrobial profiling showed concordance with all the tested antibiotics against the study strains. Hypermucoviscosity was not observed for any of the test isolates; this phenotypic character matches perfectly with the absence of rmpA and magA genes. To the best of our knowledge, this is the first report on the presence of ste, stf, stc and sti major fimbrial operons of Salmonella enterica serotype Typhimurium in K. pneumoniae genome. The study identifies the discordance of virulome and virulence in Klebsiella spp. The complete genome analysis and phenotypic correlation identify uropathogenic K. pneumoniae kp3 as a carbapenem-resistant and virulent pathogen. The Pangenome of K. pneumoniae was open suggesting high genetic diversity. Diverse K serotypes were observed. Sequence typing reveals the prevalence of K. pneumoniae high-risk clones in UTI catheterised patients. The study also highlights the concordance of resistome and in vitro susceptibility tests. 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引用次数: 0
摘要
由耐药性和毒性肺炎双球菌引起的尿路感染(UTI)日益受到关注。了解基因组和验证基因组图谱以及庞基因组分析将有助于监测肺炎克雷伯菌的高风险克隆,为早期发现的管理策略提供依据。本研究旨在分析克雷伯氏菌的抗药性基因组与表型抗菌药耐药性以及致病性病毒组之间的相关性。 本研究旨在对克雷伯氏菌进行完整的基因组测序,并分析抗药性基因组与表型抗菌药耐药性以及致病性病毒组之间的相关性。为了解克雷伯氏菌的耐药性组、泛基因组和病毒组,使用了 ResFinder、CARD、IS Finder、PlasmidFinder、PHASTER、Roary 和 VFDB。表型药敏谱分析发现尿路致病菌 kp3 具有多重耐药性。耐药性组和体外抗菌谱分析显示,研究菌株对所有测试过的抗生素都有一致的耐药性。在所有测试分离物中都没有观察到高粘液性;这一表型特征与 rmpA 和 magA 基因的缺失完全吻合。据我们所知,这是首次报道肺炎克氏菌基因组中存在肠炎沙门氏菌血清型鼠伤寒沙门氏菌的 ste、stf、stc 和 sti 主要fimbrial操作子。通过完整的基因组分析和表型相关性研究发现,尿路致病性肺炎克雷伯菌 kp3 是一种耐碳青霉烯类抗生素的强毒力病原体。肺炎克雷伯菌的庞基因组是开放的,表明其具有高度遗传多样性。观察到了多种 K 血清型。序列分型揭示了肺炎克氏菌高风险克隆在UTI导管插入患者中的流行情况。该研究还强调了耐药性组和体外药敏试验的一致性。重要的是,该研究确定了病毒组和表型毒力标记的必要性,以便及时诊断和立即治疗高危肺炎克隆。
Complete genome sequence, phenotypic correlation and pangenome analysis of uropathogenic Klebsiella spp.
Urinary tract infections (UTI) by antibiotic resistant and virulent K. pneumoniae are a growing concern. Understanding the genome and validating the genomic profile along with pangenome analysis will facilitate surveillance of high-risk clones of K. pneumoniae to underpin management strategies toward early detection. The present study aims to correlate resistome with phenotypic antimicrobial resistance and virulome with pathogenicity in Klebsiella spp. The present study aimed to perform complete genome sequences of Klebsiella spp. and to analyse the correlation of resistome with phenotypic antimicrobial resistance and virulome with pathogenicity. To understand the resistome, pangenome and virulome in the Klebsiella spp, the ResFinder, CARD, IS Finder, PlasmidFinder, PHASTER, Roary, VFDB were used. The phenotypic susceptibility profiling identified the uropathogenic kp3 to exhibit multi drug resistance. The resistome and in vitro antimicrobial profiling showed concordance with all the tested antibiotics against the study strains. Hypermucoviscosity was not observed for any of the test isolates; this phenotypic character matches perfectly with the absence of rmpA and magA genes. To the best of our knowledge, this is the first report on the presence of ste, stf, stc and sti major fimbrial operons of Salmonella enterica serotype Typhimurium in K. pneumoniae genome. The study identifies the discordance of virulome and virulence in Klebsiella spp. The complete genome analysis and phenotypic correlation identify uropathogenic K. pneumoniae kp3 as a carbapenem-resistant and virulent pathogen. The Pangenome of K. pneumoniae was open suggesting high genetic diversity. Diverse K serotypes were observed. Sequence typing reveals the prevalence of K. pneumoniae high-risk clones in UTI catheterised patients. The study also highlights the concordance of resistome and in vitro susceptibility tests. Importantly, the study identifies the necessity of virulome and phenotypic virulence markers for timely diagnosis and immediate treatment for the management of high-risk K. pneumoniae clones.
期刊介绍:
AMB Express is a high quality journal that brings together research in the area of Applied and Industrial Microbiology with a particular interest in ''White Biotechnology'' and ''Red Biotechnology''. The emphasis is on processes employing microorganisms, eukaryotic cell cultures or enzymes for the biosynthesis, transformation and degradation of compounds. This includes fine and bulk chemicals, polymeric compounds and enzymes or other proteins. Downstream processes are also considered. Integrated processes combining biochemical and chemical processes are also published.