4.6 Article

Occurrence of Multiple, Extensive and Pan Drug-Resistant Pseudomonas aeruginosa and Carbapenemase Production from Presumptive Isolates Stored in a Biobank at Ethiopian Public Health Institute

Journal

INFECTION AND DRUG RESISTANCE
Volume 14, Issue -, Pages 3609-3618

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IDR.S327652

Keywords

P; aeruginosa; antimicrobial resistance; carbapenemase enzyme; Ethiopia

Funding

  1. Department of Medical Laboratory Sciences, College of Health Sciences, Addis Ababa University
  2. Ethiopian Public Health Institute

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Pseudomonas aeruginosa is a common cause of nosocomial infections with a high level of multidrug resistance, and this study in Ethiopia found an increasing rate of MDR and XDR isolates. Among the isolates tested, the highest resistance was observed against ceftazidime and the lowest against amikacin. Carbapenemase enzyme production was detected in only a small percentage of isolates, highlighting the need for infection prevention measures and guided treatment based on antibiotic susceptibility testing.
Purpose: Pseudomonas aeruginosa is a common cause of nosocomial infections with associated morbidity and mortality because the organism is unresponsive to commonly available antimicrobials. This study was undertaken to determine the multiple drug-resistant (MDR), extensive drug-resistant (XDR) and pan drug-resistant (PDR) phenotype of P. aeruginosa and its carbapenemase production rate from presumptive isolates stored in the biobank at the Ethiopian Public Health Institute (EPHI). Methods: A cross-sectional study was conducted at the EPHI laboratory, Addis Ababa, Ethiopia from March to June 2021. Stored isolates of Pseudomonas spp. which had been characterized by manual identification methods were further processed for species-level identification (ID) and antimicrobial susceptibility testing (AST) using a Becton Dickinson (BD) Phoenix automated system. The isolates were analyzed for carbapenemase enzyme production using the modified Carbapenem Inactivation Method (mCIM). The data analysis was done using SPSS version 20 software. Results: In this study, 110 presumptive Pseudomonas isolates from a biobank were re-analyzed, 100 of them were found to be Pseudomonas and among these P. aeruginosa accounted for 98% and P. putida accounted for 2%. The majority of isolates were recovered from wound (46%) specimens followed by ear swabs (18%). The highest level of resistance was observed against ceftazidime (35%) and the lowest level of resistance was observed against amikacin (2%). Twenty-seven isolates were identified as candidates for carbapenemase enzyme production testing, of which only 3/27 (11%) isolates were detected as carbapenemase enzyme producers. Conclusion: This study shows an increasing rate of MDR and XDR isolates and the appearance of PDR in P. aeruginosa strains; this is a serious problem in Ethiopia. The lack of newer anti-pseudomonal antibiotics adds to the problem. In order to alleviate this, infection prevention activities should be promoted, and treatment of bacterial infections should be guided by antibiotic susceptibility test results.

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