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Detection of aac(6')-Ib-cr in avian pathogenic Escherichia coli isolates in Japan
Michiko Kawanishi1, Manao Ozawa, Mototaka Hiki
1National Veterinary Assay Laboratory, Ministry of Agriculture, Forestry and Fisheries, 1-15-1 Tokura, Kokubunji, Tokyo 185-8511, Japan.
Abstract:
We investigated the prevalence of plasmid-mediated quinolone resistance (PMQR) genes in avian pathogenic Escherichia coli (APEC) strains in Japan. A total of 117 APEC strains collected between 2004 and 2007 were examined for PMQR genes (qnrA, qnrB, qnrC, qnrD, qnrS, aac(6')-Ib-cr, qepA and oqxAB) by polymerase chain reaction. None of the APEC strains carried qnrA, qnrB, qnrC, qnrD, qnrS, qepA or oqxAB, but one of the isolates was identified as an AAC (6')-Ib-cr producer. Phylogenetic grouping, multi-locus sequence typing and serotyping showed that this isolate belonged to phylogenetic group A, sequence type 167 and untypable serogroup. To our knowledge, this is the first report of the aac (6')-Ib-cr gene in bacteria from food-producing animals in Japan.
Insights
The study found no common plasmid-mediated quinolone resistance genes in Japanese avian pathogenic E. coli (APEC). However, one APEC strain carried the AAC(6')-Ib-cr gene, a novel finding in Japan.
Area of Science:
- Veterinary Microbiology
- Antimicrobial Resistance
- Molecular Epidemiology
Background:
- Avian pathogenic Escherichia coli (APEC) poses a significant threat to poultry health and food safety.
- Plasmid-mediated quinolone resistance (PMQR) genes are a growing concern in bacterial pathogens.
- Understanding the prevalence of PMQR in APEC is crucial for monitoring and controlling antimicrobial resistance.
Purpose of the Study:
- To determine the prevalence of specific PMQR genes in APEC strains isolated in Japan.
- To identify the genetic characteristics of APEC isolates carrying PMQR genes.
Main Methods:
- Polymerase chain reaction (PCR) was used to detect nine PMQR genes (qnrA, qnrB, qnrC, qnrD, qnrS, aac(6 ime)-Ib-cr, qepA, and oqxAB).
- Phylogenetic grouping, multi-locus sequence typing (MLST), and serotyping were performed on positive isolates.
Main Results:
- None of the 117 APEC strains tested positive for qnrA, qnrB, qnrC, qnrD, qnrS, qepA, or oqxAB.
- One APEC isolate was identified as a producer of the aac(6 ime)-Ib-cr gene.
- The AAC(6 ime)-Ib-cr positive isolate belonged to phylogenetic group A, sequence type 167, and an untypable serogroup.
Conclusions:
- The study reports the first detection of the aac(6 ime)-Ib-cr gene in bacteria from food-producing animals in Japan.
- The limited prevalence of PMQR genes suggests specific resistance patterns in Japanese APEC strains.
- Further surveillance is needed to track the emergence and spread of antimicrobial resistance genes in APEC.
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