利用芯片技术探索鲍曼不动杆菌的抗生素耐药基因表达

Nadia Parveen, Misbah Meharban, Zoha Tahir, Mavara Iqbal, Muhammad Bilal Gohar
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引用次数: 0

摘要

背景:抗生素耐药性是医疗保健领域的一项重大挑战,尤其是在鲍曼不动杆菌引起的医院内感染中。鲍曼不动杆菌的外排泵在介导抗生素耐药性方面起着至关重要的作用,但目前还缺乏对这些泵和获得性耐药性决定因素的全面评估。在此,我们介绍了一种基于寡核苷酸的 DNA 微阵列的开发和验证情况,该微阵列用于评估鲍曼不动杆菌中外排泵的基因表达和检测获得性抗生素耐药性决定因素:本研究的主要目的是开发一种稳健的微阵列平台,能够同时评估鲍曼不动杆菌外排泵基因的表达和检测获得性耐药性决定因素。此外,我们还旨在使用过表达或缺乏外排泵的突变体以及使用各种抗生素获得的单步突变体来验证芯片的性能:DNA 微阵列由针对 78 个基因的探针组成,包括 17 个外排系统、15 个抗性决定因子和 19 个看家基因。对突变体进行了比较分析,并进行了定量反转录酶 PCR 验证,以确认该芯片在检测外排泵过表达方面的准确性:验证实验发现,在使用庆大霉素、头孢噻肟或四环素的突变体中,RND外排泵AdeABC和AdeIJK过度表达,还发现了一种新型外排泵AdeFGH,它在暴露于氯霉素的突变体中过度表达。临床分离株显示出 AdeABC 和染色体编码的头孢菌素酶以及几个获得性耐药基因的过表达,这就是耐多药表型的原因:结论:所开发的芯片在检测鲍曼不动杆菌的外排泵表达和获得性耐药基因方面具有很高的灵敏度和特异性。它在鉴定抗生素耐药性和新型外排系统方面的潜在用途突出了其在临床环境中的重要性。
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Exploring Antibiotic Resistance Gene Expression in Acinetobacter baumannii Using Microarray Technology
Background: Antibiotic resistance is a significant challenge in healthcare, particularly in nosocomial infections caused by Acinetobacter baumannii. Efflux pumps play a crucial role in mediating antibiotic resistance in A. baumannii, yet comprehensive evaluation of these pumps and acquired resistance determinants is lacking. Here, we present the development and validation of an oligonucleotide-based DNA microarray for assessing gene expression of efflux pumps and detecting acquired antibiotic resistance determinants in A. baumannii. Objective: The primary objective of this study was to develop a robust microarray platform capable of simultaneously assessing the expression of efflux pump genes and detecting acquired resistance determinants in A. baumannii. Additionally, we aimed to validate the microarray's performance using mutants overexpressing or deficient in efflux pumps and single-step mutants obtained on various antibiotics. Methods: The DNA microarray consisted of probes targeting 78 genes, including 17 efflux systems, 15 resistance determinants, and 19 housekeeping genes. Comparative analysis of mutants, along with quantitative reverse transcriptase PCR validation, was conducted to confirm the microarray's accuracy in detecting efflux pump overexpression. Results: Validation experiments revealed overexpression of RND efflux pumps AdeABC and AdeIJK in mutants obtained on gentamicin, cefotaxime, or tetracycline, as well as identification of a novel efflux pump, AdeFGH, overexpressed in a mutant exposed to chloramphenicol. Clinical isolates showed overexpression of AdeABC and chromosomally encoded cephalosporinase, along with several acquired resistance genes, accounting for the multidrug-resistant phenotype. Conclusion: The developed microarray demonstrates high sensitivity and specificity in detecting efflux pump expression and acquired resistance determinants in A. baumannii. Its potential utility in identifying antibiotic resistance and novel efflux systems highlights its importance in clinical settings.
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