z-logo
open-access-imgOpen Access
Prevalence and Genetic Characterization of Carbapenem- and Polymyxin-ResistantAcinetobacter baumanniiIsolated from a Tertiary Hospital in Terengganu, Malaysia
Author(s) -
Soo Sum Lean,
Zarizal Suhaili,
Salwani Ismail,
Nor Iza A. Rahman,
Norlela Othman,
Fatimah Haslina Abdullah,
Zakaria Jusoh,
Chew Chieng Yeo,
Kwai Lin Thong
Publication year - 2014
Publication title -
isrn microbiology
Language(s) - English
Resource type - Journals
eISSN - 2090-7486
pISSN - 2090-7478
DOI - 10.1155/2014/953417
Subject(s) - polymyxin , acinetobacter baumannii , microbiology and biotechnology , polymyxin b , carbapenem , biology , drug resistance , multiple drug resistance , antibiotics , acinetobacter , bacteria , genetics , pseudomonas aeruginosa
Nosocomial infection caused by Acinetobacter baumannii is of great concern due to its increasing resistance to most antimicrobials. In this study, 54 nonrepeat isolates of A. baumannii from the main tertiary hospital in Terengganu, Malaysia, were analyzed for their antibiograms and genotypes. Out of the 54 isolates, 39 (72.2%) were multidrug resistant (MDR) and resistant to carbapenems whereas 14 (25.9%) were categorized as extensive drug resistant (XDR) with additional resistance to polymyxin B, the drug of “last resort.” Pulsed-field gel electrophoresis analyses showed that the polymyxin-resistant isolates were genetically diverse while the carbapenem-resistant isolates were clonally related. The 14 XDR isolates were further investigated for mutations in genes known to mediate polymyxin resistance, namely, pmrCAB , and the lipopolysaccharide biosynthesis genes, lpxA , lpxC , lpxD, and lpsB . All 14 isolates had a P102H mutation in pmrA with no mutation detected in pmrC and pmrB . No mutation was detected in lpxA but each polymyxin-resistant isolate had 2–4 amino acid substitutions in lpxD and 1-2 substitutions in lpxC . Eight resistant isolates also displayed a unique H181Y mutation in lpsB . The extent of polymyxin resistance is of concern and the novel mutations discovered here warrant further investigations.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom