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巴基斯坦肺炎克雷伯菌分离株中脂质 A-Ara4N 作为(黏菌素)耐药的替代途径。

Lipid A-Ara4N as an alternate pathway for (colistin) resistance in Klebsiella pneumonia isolates in Pakistan.

机构信息

Department of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.

Health Security Partners, Washington, DC, 20009, USA.

出版信息

BMC Res Notes. 2021 Dec 14;14(1):449. doi: 10.1186/s13104-021-05867-3.

Abstract

OBJECTIVES

This study aimed to explore mechanism of colistin resistance amongst Klebsiella pneumoniae isolates through plasmid mediated mcr-1 gene in Pakistan. Carbapenem and Colistin resistant K. pneumoniae isolates (n  = 34) stored at - 80 °C as part of the Aga Khan University Clinical Laboratory strain bank were randomly selected and subjected to mcr-1 gene PCR. To investigate mechanisms of resistance, other than plasmid mediated mcr-1 gene, whole genome sequencing was performed on 8 clinical isolates, including 6 with colistin resistance (MIC  >  4 μg/ml) and 2 with intermediate resistance to colistin (MIC  >  2 μg/ml).

RESULTS

RT-PCR conducted revealed absence of mcr-1 gene in all isolates tested. Whole genome sequencing results revealed modifications in Lipid A-Ara4N pathway. Modifications in Lipid A-Ara4N pathway were detected in ArnA_ DH/FT, UgdH, ArnC and ArnT genes. Mutation in ArnA_ DH/FT gene were detected in S3, S5, S6 and S7 isolates. UgdH gene modifications were found in all isolates except S3, mutations in ArnC were present in all except S1, S2 and S8 and ArnT were detected in all except S4 and S7. In the absence of known mutations linked with colistin resistance, lipid pathway modifications may possibly explain the phenotype resistance to colistin, but this needs further exploration.

摘要

目的

本研究旨在探索巴基斯坦肺炎克雷伯菌分离株中通过质粒介导的 mcr-1 基因产生粘菌素耐药的机制。从阿克巴汗大学临床实验室菌株库中随机选择储存在 -80°C 的耐碳青霉烯类和粘菌素的肺炎克雷伯菌分离株(n=34),并进行 mcr-1 基因 PCR。为了研究除质粒介导的 mcr-1 基因以外的耐药机制,对 8 株临床分离株(包括 6 株对粘菌素耐药(MIC>4μg/ml)和 2 株对粘菌素中度耐药(MIC>2μg/ml))进行了全基因组测序。

结果

RT-PCR 结果显示所有检测的分离株均未检测到 mcr-1 基因。全基因组测序结果显示脂 A-Ara4N 途径发生了修饰。在 ArnA_DH/FT、UgdH、ArnC 和 ArnT 基因中检测到脂 A-Ara4N 途径的修饰。在 S3、S5、S6 和 S7 分离株中检测到 ArnA_DH/FT 基因突变。除 S3 外,所有分离株均发现 UgdH 基因修饰,除 S1、S2 和 S8 外,所有分离株均存在 ArnC 基因突变,除 S4 和 S7 外,所有分离株均检测到 ArnT。在缺乏与粘菌素耐药相关的已知突变的情况下,脂类途径的修饰可能可以解释对粘菌素的表型耐药,但这需要进一步探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b7d/8670247/d51bdf276e31/13104_2021_5867_Fig1_HTML.jpg

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