首页> 美国卫生研究院文献>Frontiers in Microbiology >The Complete Sequence and Comparative Analysis of a Multidrug-Resistance and Virulence Multireplicon IncFII Plasmid pEC302/04 from an Extraintestinal Pathogenic Escherichia coli EC302/04 Indicate Extensive Diversity of IncFII Plasmids
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The Complete Sequence and Comparative Analysis of a Multidrug-Resistance and Virulence Multireplicon IncFII Plasmid pEC302/04 from an Extraintestinal Pathogenic Escherichia coli EC302/04 Indicate Extensive Diversity of IncFII Plasmids

机译:来自肠道外致病性大肠杆菌EC302 / 04的多药耐药和毒力多复制子IncFII质粒pEC302 / 04的完整序列和比较分析表明IncFII质粒的广泛多样性

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摘要

Extraintestinal pathogenic Escherichia coli (ExPEC) that causes extraintestinal infections often harbor plasmids encoding fitness traits such as resistance and virulence determinants that are of clinical importance. We determined the complete nucleotide sequence of plasmid pEC302/04 from a multidrug-resistant E. coli EC302/04 which was isolated from the tracheal aspirate of a patient in Malaysia. In addition, we also performed comparative sequence analyses of 18 related IncFIIA plasmids to determine the phylogenetic relationship and diversity of these plasmids. The 140,232 bp pEC302/04 is a multireplicon plasmid that bears three replication systems (FII, FIA, and FIB) with subtype of F2:A1:B1. The plasmid is self-transmissible with a complete transfer region. pEC302/04 also carries antibiotic resistance genes such as blaTEM−1 and a class I integron containing sul1, cml and aadA resistance genes, conferring multidrug resistance (MDR) to its host, E. coli EC302/04. Besides, two iron acquisition systems (SitABCD and IutA-IucABCD) which are the conserved virulence determinants of ExPEC-colicin V or B and M (ColV/ColBM)-producing plasmids were identified in pEC302/04. Multiple toxin-antitoxin (TA)-based addiction systems (i.e., PemI/PemK, VagC/VagD, CcdA/CcdB, and Hok/Sok) and a plasmid partitioning system, ParAB, and PsiAB, which are important for plasmid maintenance were also found. Comparative plasmid analysis revealed only one conserved gene, the repA1 as the core genome, showing that there is an extensive diversity among the IncFIIA plasmids. The phylogenetic relationship of 18 IncF plasmids based on the core regions revealed that ColV/ColBM-plasmids and non-ColV/ColBM plasmids were separated into two distinct groups. These plasmids, which carry highly diverse genetic contents, are also mosaic in nature. The atypical combination of genetic materials, i.e., the MDR- and ColV/ColBM-plasmid-virulence encoding regions in a single ExPEC plasmid is rare but of clinical importance. Such phenomenon is bothersome when the plasmids are transmissible, facilitating the spread of virulence and resistance plasmids among pathogenic bacteria. Notably, certain TA systems are more commonly found in particular ExPEC plasmid types, indicating the possible relationships between certain TA systems and ExPEC pathogenesis.
机译:引起肠外感染的肠外致病性大肠杆菌(ExPEC)通常带有编码适合性状的质粒,例如具有临床重要性的抗性和毒力决定因素。我们从耐多药的大肠杆菌EC302 / 04中确定了质粒pEC302 / 04的完整核苷酸序列,该大肠杆菌是从马来西亚一名患者的气管抽吸物中分离得到的。此外,我们还对18个相关的IncFIIA质粒进行了比较序列分析,以确定这些质粒的系统发育关系和多样性。 140,232 bp pEC302 / 04是一个多复制子质粒,带有三个复制系统(FII,FIA和FIB),亚型为F2:A1:B1。质粒是自我传递的,具有完整的转移区。 pEC302 / 04还携带抗生素抗性基因,例如blaTEM-1和包含sul1,cml和aadA抗性基因的I类整倍体,从而向其宿主大肠杆菌EC302 / 04赋予多药抗性(MDR)。此外,在pEC302 / 04中鉴定了两个铁捕获系统(SitABCD和IutA-IucABCD),它们是ExPEC-colicin V或B和M(ColV / ColBM)产生质粒的保守毒力决定子。基于多种毒素-抗毒素(TA)的成瘾系统(即PemI / PemK,VagC / VagD,CcdA / CcdB和Hok / Sok)以及对质粒维护很重要的质粒分配系统ParAB和PsiAB也很重要。找到了。比较质粒分析显示只有一个保守基因repA1作为核心基因组,显示IncFIIA质粒之间存在广泛的多样性。基于核心区域的18种IncF质粒的系统发生关系显示,ColV / ColBM质粒和非ColV / ColBM质粒分为两个不同的组。这些具有高度遗传多样性的质粒,在自然界中也是镶嵌的。遗传物质的非典型组合,即单个ExPEC质粒中的MDR-和ColV / ColBM-质粒-毒力编码区很少见,但具有临床意义。当质粒是可传播的时,这种现象很麻烦,有利于致病性细菌中毒力和抗性质粒的传播。值得注意的是,在特定的ExPEC质粒类型中更常见地发现某些TA系统,这表明某些TA系统与ExPEC发病机理之间的可能关系。

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