4.5 Article

Genetic mechanisms and correlated risk factors of antimicrobial-resistant ESKAPEE pathogens isolated in a tertiary hospital in Malaysia

Journal

Publisher

BMC
DOI: 10.1186/s13756-021-00936-5

Keywords

AMR-conferring genes; Minimum inhibitory concentration; Molecular epidemiology; Multidrug-resistant organisms; Nosocomial infections; Risk factors analysis

Funding

  1. United States of America Naval Medical Research Unit [TWO (NAMRU-2), IF004-2020]
  2. Armed Forces Health Surveillance Division, Global Emerging Infections Surveillance [P0107_19_NA, WUN D0016]

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High rates of multidrug resistance were observed in A. baumannii, K. pneumoniae, E. coli, and S. aureus in a tertiary hospital in Malaysia. These pathogens, except E. coli, were frequently associated with hospital-acquired infections (HAIs). Non-susceptibility to last-resort drugs like vancomycin, carbapenems, and colistin was commonly observed.
Background Knowledge on the epidemiology, genotypic and phenotypic features of antimicrobial-resistant (AMR) ESKAPEE pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Enterobacter spp., and Escherichia coli) and their association with hospital-acquired infections (HAIs) are limited in Malaysia. Therefore, we evaluated the AMR features and resistance mechanisms of the ESKAPEE pathogens collected in a tertiary hospital located in the capital of Malaysia. Methods A total of 378 AMR-ESKAPEE strains were obtained based on convenience sampling over a nine-month study period (2019-2020). All strains were subjected to disk diffusion and broth microdilution assays to determine the antimicrobial susceptibility profiles. Polymerase chain reaction (PCR) and DNA sequence analyses were performed to determine the AMR genes profiles of the non-susceptible strains. Chi-square test and logistic regression analyses were used to correlate the AMR profiles and clinical data to determine the risk factors associated with HAIs. Results High rates of multidrug resistance (MDR) were observed in A. baumannii, K. pneumoniae, E. coli, and S. aureus (69-89%). All organisms except E. coli were frequently associated with HAIs (61-94%). Non-susceptibility to the last-resort drugs vancomycin (in Enterococcus spp. and S. aureus), carbapenems (in A. baumannii, P. aeruginosa, and Enterobacteriaceae), and colistin (in Enterobacteriaceae) were observed. Both A. baumannii and K. pneumoniae harbored a wide array of extended-spectrum beta-lactamase genes (bla(TEM), bla(SHV), bla(CTX-M), bla(OXA)). Metallo-beta-lactamase genes (bla(VEB), bla(VIM), bla(NDM)) were detected in carbapenem-resistant strains, at a higher frequency compared to other local reports. We detected two novel mutations in the quinolone-resistant determining region of the gyrA in fluoroquinolone-resistant E. coli (Leu-102-Ala; Gly-105-Val). Microbial resistance to ampicillin, methicillin, and cephalosporins was identified as important risk factors associated with HAIs in the hospital. Conclusion Overall, our findings may provide valuable insight into the microbial resistance pattern and the risk factors of ESKAPEE-associated HAIs in a tertiary hospital located in central Peninsular Malaysia. The data obtained in this study may contribute to informing better hospital infection control in this region.

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