Abstract

Background: Acinetobacter baumannii is an opportunistic pathogen associated with healthcare infections and high mortality rates in intensive care units all over the globe. Porins and efflux pumps over-expression have been reported as contributing factors in escalating drug resistance and rendering treatment ineffective. In this study, we investigated the mechanisms of multidrug resistance (MDR) in A. baumannii clinical isolates. Methods: A total of 30 A. baumannii isolates were included in the present study from Nehru Hospital (PGIMER-Chandigarh) located in North India. Kirby Bauer disk diffusion assay and MIC were performed to determine the antimicrobial susceptibility pattern. Screening of beta-lactamases was performed using PCR. Relative gene expression of four RND, one MATE efflux pump, and two outer membrane proteins were determined using RT-PCR. Molecular typing of 22 isolates was carried out using MLST Oxford scheme. Results: CarO porin genes showed over-expression in 63% isolates followed by adeGandabeM efflux pump downregulation/underexpression (<0.5 fold), suggesting the carbapenem-susceptible phenotypic nature of the isolates. High prevalence of VIM-2, NDM-1, and OXA-23 genes was observed in A. baumannii isolates. Interestingly, NDM-1 and OXA-58 were traced in 10 and3 A. baumannii isolates respectively; 13 of 22 (59%) isolates showed novel Sequence Types (STs) in the Multi-Locus Sequence Typing (MLST) analysis. ST 1087 was most commonly found ST among all others (16 STs). Conclusions: This study indicated a possible role of carO porin genes and adeG (RND) andabeM (MATE) efflux pumps in carbapenem susceptibility of A. baumannii. New STs were also reported in the majority of the isolates.

Highlights

  • Carbapenem-resistant Acinetobacter baumannii has recently surfaced as a significant nosocomial bug

  • 30 carbapenem-susceptible Acinetobacter baumannii (CSAB) isolates were included in the present study, which were collected from 12 different wards/intensive care units (ICUs)/centers of a tertiary care hospital and from three sources: blood, cerebrospinal fluids (CSF), and sterile body fluid

  • regulation of adeG (RND)-type efflux pumps are encoded by chromosomal genes and their over-expression contributes to multidrug resistance in A. baumannii [24]

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Summary

Introduction

Carbapenem-resistant Acinetobacter baumannii has recently surfaced as a significant nosocomial bug. According to the recent reports, carbapenem resistance in A. baumannii poses a significant threat to public health [1]. A. baumannii commonly causes healthcareassociated infections (HAIs), in intensive care units (ICUs) where the incidence has rampantly escalated over time. Multidrug-resistant (MDR) isolates of A. baumannii have been associated with a medical history of long hospitalization, patients on mechanical ventilation, presence of catheters, and with immunocompromised or severely ill patients [2]. Carbapenem-susceptible Acinetobacter baumannii (CSAB) has gained lesser attention in pathogenesis [4]. Acinetobacter baumannii is an opportunistic pathogen associated with healthcare infections and high mortality rates in intensive care units all over the globe. We investigated the mechanisms of multidrug resistance (MDR) in A. baumannii clinical isolates.

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