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一株高毒力肺炎克雷伯菌 25 型序列型单接合质粒中同时存在多重耐药性和毒力

Coexistence of Multidrug Resistance and Virulence in a Single Conjugative Plasmid from a Hypervirulent Klebsiella pneumoniae Isolate of Sequence Type 25.

机构信息

Department of Laboratory Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

出版信息

mSphere. 2022 Dec 21;7(6):e0047722. doi: 10.1128/msphere.00477-22. Epub 2022 Dec 6.

Abstract

Carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKP) has received considerable attention. Typically, the genetic elements that confer virulence are harbored by nonconjugative plasmids. In this study, we report a CR-hvKP strain, CY814036, of high-risk sequence type 25 (ST25) and the K2 serotype, which is uncommon among K. pneumoniae isolates but caused serious lung infection in a tertiary teaching hospital in China. Whole-genome sequencing (WGS) revealed a rare conjugative plasmid, pCY814036-iucA, carrying a virulence-associated operon () coding for aerobactin and determinants of multidrug resistance (MDR), coexisting with a conjugative -bearing plasmid, pCY814036-KPC2, in the same strain. A conjugation assay showed that pCY814036-iucA and pCY814036-KPC2 could be efficiently cotransmitted from CY814036 to Escherichia coli EC600. Further phenotypic investigation, including antimicrobial susceptibility tests, serum resistance assays, and mouse infection models, confirmed that pCY814036-iucA was capable of cotransferring multidrug resistance and hypervirulence features to the recipient. pCY814036-KPC2 also conferred resistance to antibiotics, including β-lactams and aminoglycosides. Overall, the rare coexistence of a conjugative MDR-virulence plasmid and a -bearing plasmid in a K. pneumoniae isolate offers a possible mechanism for the formation of CR-hvKP strains and the potential to significantly accelerate the propagation of high-risk phenotypes. The increased reporting of carbapenem-resistant hypervirulent K. pneumoniae is considered a worrisome concern to human health care and has restricted the choice of effective antibiotics for clinical treatment. Moreover, virulence plasmids with complete conjugation modules have been identified, which evolved via homologous recombination. Here, we characterize an ST25 CR-hvKP strain, CY814036, harboring both a conjugative MDR-virulence plasmid and a -bearing plasmid in China. This study highlights that the cotransmission of drug resistance and virulence plasmids increases therapeutic difficulties and worsens clinical prognoses. Also, active surveillance of the conjugative MDR-virulence plasmid is necessary.

摘要

碳青霉烯类耐药高毒力肺炎克雷伯菌(CR-hvKP)受到了广泛关注。通常,赋予毒力的遗传元件位于非接合性质粒上。在本研究中,我们报告了一株高风险序列型 25(ST25)和 K2 血清型的 CR-hvKP 菌株 CY814036,该菌株在中国的一家三级教学医院引起了严重的肺部感染,但在肺炎克雷伯菌分离株中并不常见。全基因组测序(WGS)揭示了一种罕见的接合性质粒 pCY814036-iucA,该质粒携带一个与毒力相关的 操纵子(),编码铁载体和多种药物耐药性(MDR)决定因素,与同一菌株中的另一个携带的质粒 pCY814036-KPC2 共存。接合试验表明,pCY814036-iucA 和 pCY814036-KPC2 可从 CY814036 高效地转移到大肠杆菌 EC600 中。进一步的表型研究,包括药敏试验、血清抗性试验和小鼠感染模型,证实了 pCY814036-iucA 能够将多药耐药性和高毒力特征共同转移给受体。pCY814036-KPC2 还赋予了对包括β-内酰胺类和氨基糖苷类在内的抗生素的抗性。总的来说,肺炎克雷伯菌分离株中罕见的接合性 MDR-毒力质粒和 质粒的共存为 CR-hvKP 菌株的形成提供了一种可能的机制,并有可能显著加速高危表型的传播。耐碳青霉烯类高毒力肺炎克雷伯菌的报道增加被认为是对人类医疗保健的一个令人担忧的关注,并限制了临床治疗有效的抗生素的选择。此外,已经鉴定出具有完整接合模块的毒力质粒,这些质粒是通过同源重组进化而来的。在这里,我们在中国描述了一株 ST25 CR-hvKP 菌株 CY814036,该菌株同时携带一种接合性 MDR-毒力质粒和一种 质粒。本研究强调了耐药性和毒力质粒的共同转移增加了治疗的难度并恶化了临床预后。此外,有必要对具有接合功能的 MDR-毒力质粒进行主动监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eaa/9769751/6bfa7b453151/msphere.00477-22-f001.jpg

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