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Antimicrobial Resistance Profiles and Co-Existence of Multiple Antimicrobial Resistance Genes in mcr -Harbouring Colistin-Resistant Enterobacteriaceae Isolates Recovered from Poultry and Poultry Meats in Malaysia.

Md Rezaul KarimZakaria ZunitaLatiffah HassanNik Mohd FaizNur Indah Ahmad
Published in: Antibiotics (Basel, Switzerland) (2023)
The co-existence of the colistin resistance ( mcr ) gene with multiple drug-resistance genes has raised concerns about the possibility of the development of pan-drug-resistant bacteria that will complicate treatment. This study aimed to investigate the antibiotic resistance profiles and co-existence of antibiotic resistance genes among the colistin-resistant Enterobacteriaceae isolates recovered from poultry and poultry meats. The antibiotic susceptibility to various classes of antibiotics was performed using the Kirby-Bauer disk diffusion method and selected antimicrobial resistance genes were detected using PCR in a total of 54 colistin-resistant Enterobacteriaceae isolates including Escherichia coli ( E . coli ) (n = 32), Salmonella spp. (n = 16) and Klebsiella pneumoniae ( K . pneumoniae ) (n = 6) isolates. Most of the isolates had multi-drug resistance (MDR), with antibiotic resistance against up to seven classes of antibiotics. All mcr -harbouring, colistin-resistant Enterobacteriaceae isolates showed this MDR (100%) phenotype. The mcr-1 harbouring E . coli isolates were co-harbouring multiple antibiotic resistance genes. The seven most commonly identified resistance genes ( bla TEM , tetA , floR , aac-3-IV , aadA1 , fosA , aac ( 6_ ) -lb ) were detected in an mcr-1 -harbouring E . coli isolate recovered from a cloacal swab. The mcr-5 harbouring Salmonella spp. isolate recovered from poultry meats was positive for bla TEM , tetA , floR , aac-3-IV , fosA and aac ( 6_ ) -lb genes. In conclusion, the colistin-resistant Enterobacteriaceae with mcr genes co-existing multiple clinically important antimicrobial resistance genes in poultry and poultry meats may cause potential future threats to infection treatment choices in humans and animals.
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