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在医院感染爆发期间,碳青霉烯酶 OXA-48 的体内水平基因转移。

In vivo horizontal gene transfer of the carbapenemase OXA-48 during a nosocomial outbreak.

机构信息

Institute for Medical Microbiology and Infection Control, Hospital of Johann Wolfgang Goethe University, Frankfurt.

Max-von-Pettenkofer Institute, Ludwig-Maximilians-University German Center for Infection Research (DZIF), Munich.

出版信息

Clin Infect Dis. 2015 Jun 15;60(12):1808-15. doi: 10.1093/cid/civ191. Epub 2015 Mar 10.

Abstract

BACKGROUND

OXA-48 is a highly prevalent carbapenemase and has been isolated worldwide. Here, we investigate the in vivo horizontal gene transfer (HGT) of blaOXA-48 from Klebsiella pneumoniae to Escherichia coli in an infected patient.

METHODS

Bacterial isolates were characterized by susceptibility testing, multilocus sequence typing, DiversiLab, and plasmid analyses. Transferability of blaOXA-48 was evaluated by in vitro transconjugation using the outbreak strain and E. coli J53. In vivo transconjugation was investigated using the larvae of the greater wax moth (Galleria mellonella) and low-complexity-microbiota mice.

RESULTS

OXA-48-harboring K. pneumoniae isolates belonging to ST14 were isolated during a nosocomial outbreak from 6 patients. Molecular and epidemiological analyses revealed the HGT of an approximately 60-kb OXA-48-containing IncL/M-type plasmid from K. pneumoniae to E. coli belonging to the novel ST666 in a patient. In vitro conjugation experiments revealed a transconjugation frequency of 8.7 × 10(-7). HGT of OXA-48 in a newly developed in vivo model using G. mellonella larvae revealed a higher transconjugation frequency of 1.3 × 10(-4). The conjugation frequency of OXA-48 from K. pneumoniae and E. coli in the gut of low-complexity-microbiota mice was determined to be 2.9 × 10(-5).

CONCLUSIONS

The in vivo intergenus gene transfer of OXA-48 in the gut of an infected patient was verified in vitro and in 2 in vivo models, which both showed even higher transmission frequencies vs in vitro conditions. This implies that the current in vitro protocols might not correctly reflect the HGT of carbapenemase genes in vivo.

摘要

背景

OXA-48 是一种广泛流行的碳青霉烯酶,已在全球范围内分离出来。在这里,我们研究了感染患者中产 OXA-48 的肺炎克雷伯菌向大肠杆菌的体内水平基因转移(HGT)。

方法

通过药敏试验、多位点序列分型、DiversiLab 和质粒分析对细菌分离株进行特征描述。使用暴发株和大肠杆菌 J53 进行体外转导评估 blaOXA-48 的可转移性。使用大蜡螟(Galleria mellonella)幼虫和低复杂度微生物群小鼠研究体内转导。

结果

从 6 名患者的医院感染暴发中分离出携带 OXA-48 的肺炎克雷伯菌 ST14 株。分子和流行病学分析显示,来自肺炎克雷伯菌的大约 60kb OXA-48 携带 IncL/M 型质粒通过 HGT 转移到患者中新出现的 ST666 大肠杆菌中。体外接合实验显示转导频率为 8.7×10(-7)。在使用大蜡螟幼虫的新开发的体内模型中,OXA-48 的 HGT 显示出更高的转导频率为 1.3×10(-4)。在低复杂度微生物群小鼠肠道中,来自肺炎克雷伯菌和大肠杆菌的 OXA-48 的接合频率为 2.9×10(-5)。

结论

在感染患者的体内,通过体外和 2 种体内模型证实了 OXA-48 的属间基因转移,这两种模型的传播频率都高于体外条件。这意味着目前的体外方案可能无法正确反映体内碳青霉烯酶基因的 HGT。

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