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水平基因转移 共同携带毒力和抗菌耐药基因的外膜囊泡是耐碳青霉烯类高毒力菌株传播的一种新途径。

Horizontal gene transfer OMVs co-carrying virulence and antimicrobial-resistant genes is a novel way for the dissemination of carbapenem-resistant hypervirulent .

作者信息

Li Ping, Luo Wanying, Xiang Tian-Xin, Jiang Yuhuan, Liu Peng, Wei Dan-Dan, Fan Linping, Huang Shanshan, Liao Wenjian, Liu Yang, Zhang Wei

机构信息

Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Nanchang University, Nanchang University, Nanchang, China.

Jiangxi Institute of Respiratory Disease, The First Affiliated Hospital of Nanchang University, Nanchang, China.

出版信息

Front Microbiol. 2022 Dec 1;13:945972. doi: 10.3389/fmicb.2022.945972. eCollection 2022.

Abstract

INTRODUCTION

The rapidly increased isolation rate of CR-HvKP worldwide has brought great difficulties in controlling clinical infection. Moreover, it has been demonstrated that the transmission of drug-resistant genes among bacteria can be mediated by outer membrane vesicles (OMVs), which is a new way of horizontal gene transfer (HGT). The transmission of virulence genes among bacteria has also been well studied; however, it remains unclear whether virulence and drug-resistant genes can be co-transmitted simultaneously. Co-transmission of virulence and drug-resistant genes is essential for the formation and prevalence of CR-HvKP.

METHODS

First, we isolated OMVs from CR-HvKP by cushioned-density gradient ultracentrifugation (C-DGUC). TEM and DLS were used to examine the morphology and size of bacterial OMVs. OMV-mediated gene transfer in liquid cultures and the acquisition of the carbapenem gene and virulence gene was confirmed using colony-PCR. Antimicrobial susceptibility testing, mCIM and eCIM were conducted for the resistance of transformant. Serum killing assay, assessment of the anti-biofilm effect and galleria mellonella infection model, mucoviscosity assay, extraction and quantification of capsules were verified the virulence of transformant. Pulsed-field gel electrophoresis (PFGE), S1 nuclease-pulsed-field gel electrophoresis (S1-PFGE), Southern blotting hybridization confirmed the plasmid of transformant.

RESULTS

Firstly, OMVs were isolated from CR-HvKP NUHL30457 (K2, ST86). TEM and DLS analyses revealed the spherical morphology of the vesicles. Secondly, our study demonstrated that CR-HvKP delivered genetic material, incorporated DNA within the OMVs, and protected it from degradation by extracellular exonucleases. Thirdly, the vesicular lumen DNA was delivered to the recipient cells after determining the presence of virulence and carbapenem-resistant genes in the CR-HvKP OMVs. Importantly, S1-PFGE and Southern hybridization analysis of the 700603 transformant strain showed that the transformant contained both drug-resistant and virulence plasmids.

DISCUSSION

In the present study, we aimed to clarify the role of CRHvKP-OMVs in transmitting CR-HvKP among . Collectively, our findings provided valuable insights into the evolution of CR-HvKP.

摘要

引言

全球范围内耐碳青霉烯类高毒力肺炎克雷伯菌(CR-HvKP)分离率的迅速上升给临床感染控制带来了巨大困难。此外,已有研究表明细菌间耐药基因的传递可由外膜囊泡(OMV)介导,这是水平基因转移(HGT)的一种新方式。细菌间毒力基因的传递也已得到充分研究;然而,毒力基因和耐药基因是否能同时共传递仍不清楚。毒力基因和耐药基因的共传递对于CR-HvKP的形成和流行至关重要。

方法

首先,我们通过缓冲密度梯度超速离心法(C-DGUC)从CR-HvKP中分离出OMV。利用透射电子显微镜(TEM)和动态光散射(DLS)检测细菌OMV的形态和大小。使用菌落聚合酶链反应(colony-PCR)确认液体培养物中OMV介导的基因转移以及碳青霉烯基因和毒力基因的获得。对转化体进行药敏试验、改良Carba NP试验(mCIM)和乙酰胺试验(eCIM)以检测其耐药性。通过血清杀菌试验、抗生物膜效果评估、大蜡螟感染模型、黏液粘度测定、荚膜提取和定量来验证转化体的毒力。脉冲场凝胶电泳(PFGE)、S1核酸酶脉冲场凝胶电泳(S1-PFGE)、Southern印迹杂交确认转化体的质粒。

结果

首先,从CR-HvKP NUHL30457(K2,ST86)中分离出OMV。TEM和DLS分析显示囊泡呈球形。其次,我们的研究表明CR-HvKP传递遗传物质,将DNA整合到OMV中,并保护其免受细胞外核酸酶的降解。第三,在确定CR-HvKP OMV中存在毒力基因和耐碳青霉烯基因后,囊泡腔内的DNA被传递到受体细胞。重要的是,对700603转化体菌株的S1-PFGE和Southern杂交分析表明,转化体同时含有耐药质粒和毒力质粒。

讨论

在本研究中,我们旨在阐明CR-HvKP-OMV在CR-HvKP传播中的作用。总体而言,我们的研究结果为CR-HvKP的进化提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c918/9751880/0e2c8873ec99/fmicb-13-945972-g001.jpg

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