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比较同一患者中两种不同的肺炎克雷伯菌 ST16 亚群。

Comparison of Two Distinct Subpopulations of Klebsiella pneumoniae ST16 Co-Occurring in a Single Patient.

机构信息

Department of Pathogenic Biology, School of Basic Medicine, Southwest Medical University, Luzhou, Sichuan, China.

Department of Laboratory Medicine, The Affiliated Wuxi No.2 People's Hospital of Nanjing Medical University, Wuxi, Jiangsu, China.

出版信息

Microbiol Spectr. 2022 Jun 29;10(3):e0262421. doi: 10.1128/spectrum.02624-21. Epub 2022 Apr 25.

DOI:10.1128/spectrum.02624-21
PMID:35467408
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9241866/
Abstract

The higher resistance rate to ceftazidime-avibactam (CZA) is mainly related to carbapenem resistance, especially New Delhi metallo-β-lactamase (NDM). The CZA-susceptible Klebsiella pneumoniae (K191663) and the later CZA-resistant isolates (K191724, K191725, K191773) co-producing NDM-4 and OXA-181 were obtained from the same hospitalized patient returning from Vietnam. Our study aims to elucidate the diversity of K. pneumoniae ST16 through comparative analysis of whole-genome sequencing (WGS) data and identify the potential evolution of plasmids by sequencing longitudinal clinical isolates during antibiotic treatment. Firstly, multilocus sequence typing analysis and phylogenic analysis suggested that these strains belong to the two lineages of K. pneumoniae ST16. Surprisingly, the CZA-resistant strains were closely related to K. pneumoniae ST16 described in South Korea, instead of the - or -carrying ST16 reported in Vietnam. Secondly, , , and co-existed on a self-conjugative IncFII(Yp)-like plasmid, which played a significant role in CZA resistance. It could transfer into the recipient Escherichia coli J53 at high frequency, indicating the risk of mobile carbapenemases. In addition, the loss of 12-kbp fragment occurred in -positive isolate (K191773), which was likely caused by insertion sequence-mediated homologous recombination. Last but not least, as a repressor of operon system, was truncated by a frameshift mutation in K191663. Thus, our study provided baseline information for monitoring the occurrence and development of bacterial resistance. As a leading health care-acquired infection pathogen, Klebsiella pneumoniae is threatening a large number of inpatients due to its diverse antibiotic resistance and virulence factors. Heretofore, with a growing number of reports about the coexistence of several carbapenemases in carbapenem-resistant K. pneumoniae (CRKP), epidemiologic surveillance has been strengthened. Nevertheless, the nosocomial outbreaks by CRKP ST16 are gradually increasing worldwide. Our study provides a deeper insight into the diversification of clinical isolates of CRKP ST16 in China. In addition, the comparison analysis of resistant plasmids may reveal the transmission of carbapenemase-encoding genes. Furthermore, our study also highlights the importance of longitudinal specimen collection and continuous monitoring during the treatment, which play a crucial role in understanding the development of antibiotic resistance and the evolution of resistance plasmids.

摘要

对头孢他啶-阿维巴坦(CZA)的更高耐药率主要与碳青霉烯类耐药有关,尤其是新德里金属β-内酰胺酶(NDM)。从从越南返回的同一位住院患者中获得了对 CZA 敏感的肺炎克雷伯菌(K191663)和后来的 CZA 耐药分离株(K191724、K191725、K191773),这些分离株均共同产生 NDM-4 和 OXA-181。我们的研究旨在通过比较全基因组测序(WGS)数据阐明肺炎克雷伯菌 ST16 的多样性,并通过在抗生素治疗期间对纵向临床分离株进行测序来鉴定质粒的潜在进化。首先,多位点序列分型分析和系统发育分析表明,这些菌株属于肺炎克雷伯菌 ST16 的两个谱系。令人惊讶的是,CZA 耐药株与韩国描述的肺炎克雷伯菌 ST16 密切相关,而不是越南报道的携带-或-的 ST16。其次,IncFII(Yp)-样可自我转移的质粒上同时存在 、 和 ,这对 CZA 耐药性起着重要作用。它可以高频转移到受体大肠杆菌 J53 中,表明存在移动碳青霉烯酶的风险。此外,在 -阳性分离株(K191773)中发生了 12-kbp 片段的缺失,这可能是由插入序列介导的同源重组引起的。最后但并非最不重要的是,作为 操纵子系统的阻遏物,在 K191663 中发生了移码突变导致其截断。因此,我们的研究为监测细菌耐药性的发生和发展提供了基线信息。作为主要的医疗保健获得性感染病原体,由于其具有多种抗生素耐药性和毒力因子,肺炎克雷伯菌正在威胁大量住院患者。迄今为止,由于越来越多的关于碳青霉烯类耐药肺炎克雷伯菌(CRKP)中几种碳青霉烯酶共存的报告,已经加强了流行病学监测。然而,CRKP ST16 的医院感染暴发在全球范围内逐渐增加。我们的研究提供了对中国 CRKP ST16 临床分离株多样化的更深入了解。此外,对耐药质粒的比较分析可能揭示了碳青霉烯酶编码基因的传播。此外,我们的研究还强调了在治疗过程中纵向标本采集和持续监测的重要性,这对于了解抗生素耐药性的发展和耐药质粒的进化至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/9241866/6b9f9eb94f54/spectrum.02624-21-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/9241866/eea3c4dded40/spectrum.02624-21-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/9241866/44ee84c3b007/spectrum.02624-21-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/9241866/99d84fb13dd4/spectrum.02624-21-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/9241866/ff4e2b217e0b/spectrum.02624-21-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/9241866/6b9f9eb94f54/spectrum.02624-21-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/9241866/eea3c4dded40/spectrum.02624-21-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/9241866/44ee84c3b007/spectrum.02624-21-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/9241866/99d84fb13dd4/spectrum.02624-21-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/9241866/ff4e2b217e0b/spectrum.02624-21-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e4/9241866/6b9f9eb94f54/spectrum.02624-21-f005.jpg

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