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临床分离株 的毒力因子、抗生素耐药模式和分子分型。

Virulence factors, antibiotic resistance patterns, and molecular types of clinical isolates of .

机构信息

Department of Microbiology, Shahr-e-Qods Branch, Islamic Azad University, Tehran, Iran.

Molecular Biology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.

出版信息

Expert Rev Anti Infect Ther. 2022 Mar;20(3):463-472. doi: 10.1080/14787210.2022.1990040. Epub 2021 Oct 28.

Abstract

BACKGROUND

is armed with a wide range of antibiotic resistance mechanisms that mostly challenge effective treatment. The aims of the current study were to identify the clinical strains of also to determine their phenotypes and molecular characterization related to antimicrobial resistance and virulence genes.

RESEARCH DESIGN AND METHODS

In this investigation, clinical specimens from different hospitals located in Tehran, Iran, were collected during a nine-month period (December 2018 to August 2019). The strains were isolated and identified through standard microbial and biochemical assays. Additionally, disk diffusion, combined disk, Modified Hodge Test (MHT) and PCR were performed for antibiotic resistance and virulence gene analysis, respectively.

RESULTS

Eighty-four isolates of were subjected to the study. According to the combined disk and modified Hodge test results, 27 (52%) and 15 pathotypes (62.5%) out of resistant strains of isolated were detected as ESBL and KPC producers. The virulence genes of mrkD (94%) and magA (11%) were the highest and lowest among isolates, respectively.

CONCLUSIONS

The high prevalence of antibiotic resistance and virulence genes in conjunction with a significant relationship between the strains revealed a high pathogenic capacity of the isolated pathotypes of .

摘要

背景

拥有广泛的抗生素耐药机制,这在很大程度上挑战了有效的治疗。本研究的目的是鉴定临床分离株,同时确定与抗菌药物耐药性和毒力基因相关的表型和分子特征。

研究设计与方法

在这项研究中,收集了 2018 年 12 月至 2019 年 8 月期间来自伊朗德黑兰不同医院的临床标本。通过标准微生物和生化检测鉴定 菌株。此外,通过纸片扩散法、联合纸片法、改良 Hodge 试验(MHT)和 PCR 分别进行抗生素耐药性和毒力基因分析。

结果

对 84 株 进行了研究。根据联合纸片法和改良 Hodge 试验结果,检测出 27 株(52%)和 15 种(62.5%)耐药株为 ESBL 和 KPC 产酶株。mrkD(94%)和 magA(11%)的毒力基因在分离株中最高和最低。

结论

耐药基因和毒力基因的高流行率以及菌株之间的显著关系表明,分离株的致病性很高。

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