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编码碳青霉烯酶的质粒组特征及耐碳青霉烯类药物传播机制

Characterization of the Plasmidome Encoding Carbapenemase and Mechanisms for Dissemination of Carbapenem-Resistant .

作者信息

Abe Ryuichiro, Akeda Yukihiro, Sugawara Yo, Takeuchi Dan, Matsumoto Yuki, Motooka Daisuke, Yamamoto Norihisa, Kawahara Ryuji, Tomono Kazunori, Fujino Yuji, Hamada Shigeyuki

机构信息

Japan-Thailand Research Collaboration Centre on Emerging and Re-emerging Infections, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.

Department of Anaesthesiology and Intensive Care Medicine, Graduate School of Medicine, Osaka University, Osaka, Japan.

出版信息

mSystems. 2020 Nov 10;5(6):e00759-20. doi: 10.1128/mSystems.00759-20.

Abstract

Carbapenem-resistant (CRE) infections, high in morbidity and mortality, pose serious clinical challenges due to limited treatment options. A previous CRE surveillance study on 1,507 patients from 43 hospitals in Osaka, Japan, revealed that 12% of patients carried CRE and that 95% of the CRE isolates were IMP-type carbapenemase producers. Here, the mechanisms for this regional dissemination of a single carbapenemase gene were investigated. Since the dissemination of CRE is primarily due to the transmission of carbapenemase genes located on plasmids, we analyzed the plasmidome of 230 CRE isolates carrying by whole-genome sequencing and Southern blotting. was found to be predominantly disseminated among chromosomally distinct isolates through the pKPI-6 plasmid. Underlying the vast clonal dissemination of pKPI-6, various subpopulations deriving from pKPI-6 were identified, which had acquired advantages for the dissemination of CRE isolates. A cluster exhibiting heteroresistance against meropenem by the transcriptional regulation of caused an outbreak likely through covert transmission of For stable carriage of , they occasionally integrated on their chromosomes. In addition, we detected one isolate that broadened the range of antimicrobial resistance through a single point mutation in on pKPI-6. Multifaceted analysis of the plasmidome granted us more accurate perspectives on the horizontal spread of CRE isolates, which is difficult to trace only by comparing the whole genomes. This study revealed the predominant spread of a specific carbapenemase-encoding plasmid accompanying the emergence of phenotypically diverse derivatives, which may facilitate further dissemination of CRE in various environments. Global dissemination of carbapenem-resistant (CRE) threatens human health by limiting the efficacy of antibiotics even against common bacterial infections. Carbapenem resistance, mainly due to carbapenemase, is generally encoded on plasmids and is spread across bacterial species by conjugation. Most CRE epidemiological studies have analyzed whole genomes or only contigs of CRE isolates. Here, plasmidome analysis on 230 CRE isolates carrying was performed to shed light into the dissemination of a single carbapenemase gene in Osaka, Japan. The predominant dissemination of by the pKPI-6 plasmid among genetically distinct isolates was revealed, as well as the emergences of pKPI-6 derivatives that acquired advantages for further disseminations. Underlying vast clonal dissemination of a carbapenemase-encoding plasmid, heteroresistance was found in CRE offspring, which was generated by the transcriptional regulation of , stabilization of through chromosomal integration, or broadened antimicrobial resistance due to a single point mutation in .

摘要

耐碳青霉烯类肠杆菌科细菌(CRE)感染的发病率和死亡率很高,由于治疗选择有限,带来了严峻的临床挑战。此前一项针对日本大阪43家医院1507例患者的CRE监测研究显示,12%的患者携带CRE,且95%的CRE分离株是产IMP型碳青霉烯酶菌株。在此,对单一碳青霉烯酶基因在该地区传播的机制进行了研究。由于CRE的传播主要是由于位于质粒上的碳青霉烯酶基因的传递,我们通过全基因组测序和Southern印迹分析了230株携带该基因的CRE分离株的质粒组。发现该基因主要通过pKPI - 6质粒在染色体不同的分离株中传播。在pKPI - 6广泛的克隆传播背后,鉴定出了源自pKPI - 6的各种亚群,它们获得了促进CRE分离株传播的优势。一个通过该基因的转录调控对美罗培南表现出异质性耐药的簇可能通过该基因的隐匿传播导致了一次暴发。为了稳定携带该基因,它们偶尔会将其整合到染色体上。此外,我们检测到一株通过pKPI - 6上该基因的单点突变扩大了抗菌药物耐药范围的分离株。对质粒组的多方面分析使我们对CRE分离株的水平传播有了更准确的认识,仅通过比较全基因组很难追踪到这种传播。这项研究揭示了一种特定的编码碳青霉烯酶的质粒的主要传播方式,伴随着表型多样的衍生物的出现,这可能会促进CRE在各种环境中的进一步传播。耐碳青霉烯类肠杆菌科细菌(CRE)的全球传播通过限制抗生素对常见细菌感染的疗效威胁着人类健康。碳青霉烯耐药主要是由于碳青霉烯酶,通常由质粒编码,并通过接合在细菌物种间传播。大多数CRE流行病学研究分析了CRE分离株的全基因组或仅分析了重叠群。在此,对230株携带该基因的CRE分离株进行了质粒组分析,以阐明日本大阪单一碳青霉烯酶基因的传播情况。揭示了pKPI - 6质粒在基因不同的分离株中对该基因的主要传播情况,以及获得了进一步传播优势的pKPI - 6衍生物的出现。在编码碳青霉烯酶的质粒广泛的克隆传播背后,在CRE后代中发现了异质性耐药,这是由该基因的转录调控、通过染色体整合实现该基因的稳定化或由于该基因的单点突变导致抗菌药物耐药范围扩大所产生的。

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