Molecular characterization of virulence and resistance genes in Salmonella strains isolated from chickens sold at the informal chicken market in Gauteng Province, South Africa

Author:

Mokgophi Thelma M.1,Gcebe Nomakorinte2,Fasina Folorunso34ORCID,Adesiyun Abiodun A.15ORCID

Affiliation:

1. Department of Production Animal Studies, Faculty of Veterinary Science University of Pretoria Pretoria South Africa

2. Bacteriology Department, Serology Section, Onderstepoort Veterinary Research Agricultural Research Council Pretoria South Africa

3. Food and Agriculture Organization of the UN Rome Italy

4. Department of Veterinary Tropical Diseases, Faculty of Veterinary Science University of Pretoria Pretoria South Africa

5. School of Veterinary Medicine, The University of West Indies St. Augustine Trinidad and Tobago

Abstract

AbstractThis cross‐sectional study determined the occurrence of virulence and antimicrobial resistance genes in Salmonella strains recovered from chicken obtained from informal markets in Gauteng province, South Africa. The study also assessed the relationship between these characteristics, the source, the type of samples, and the serotypes of Salmonella isolates. A total of 151 samples (cloacal swabs, chicken carcasses, and carcass drips) were randomly collected from 47 informal market outlets in six townships in Gauteng province. Salmonella spp. was isolated and identified based on ISO 6579:2002 methods and confirmed by polymerase chain reaction (PCR) targeting invA gene fragment. Conventional PCR was used to detect 12 virulence and 18 antimicrobial resistance (AMR) genes in Salmonella spp. The most frequently detected virulence genes were invA (100%), shdA (91%), mgtB (87.7%), and sopE (81%), but considerably low for spvC (2.2%), sefC (1.5%), and pefC (0.4%). The differences in detection frequency were statistically significant (p < 0.05). Tetracycline‐resistant genes tetA (34.7%) and tetB (16%) were the most frequently detected, while Beta‐lactam‐resistant genes blaTEM (0.4%), blaCMY‐2 (0.4%) and quinolones resistant gene qnrS (0.4%) were detected in low frequency (p < 0.05). The locations of the outlets and the types of samples were significantly associated with detecting some virulence and AMR genes. Significant but moderately to substantial positive correlations were observed for qnrS, sul2; shdA, and mgtB genes. The pipA and spiC were, however, substantially negatively correlated. Our findings show that detecting these virulence and AMR genes in Salmonella isolates serves as a potential health hazard to the public, environment, and poultry farming in Gauteng, South Africa.

Funder

Gauteng Department of Agriculture and Rural Development

Publisher

Wiley

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