Title of article :
Phenotypic and Genotypic Characterization of Salmonella enterica Serovars Isolated from Imported Poultry
Author/Authors :
Badr, Heba Reference Laboratory for Veterinary Quality Control on Poultry production - Animal Health Research Institute - Agricultural Research Center (ARC), Egypt , Roshdy, Heba Reference Laboratory for Veterinary Quality Control on Poultry production - Animal Health Research Institute - Agricultural Research Center (ARC), Egypt , Sorour, Hend K. Reference Laboratory for Veterinary Quality Control on Poultry production - Animal Health Research Institute - Agricultural Research Center (ARC), Egypt , AbdelRahman, Mona A.A. Reference Laboratory for Veterinary Quality Control on Poultry production - Animal Health Research Institute - Agricultural Research Center (ARC), Egypt , Erfan, Ahmed M. Reference Laboratory for Veterinary Quality Control on Poultry production - Animal Health Research Institute - Agricultural Research Center (ARC), Egypt , Salem, Noha Reference Laboratory for Veterinary Quality Control on Poultry production - Animal Health Research Institute - Agricultural Research Center (ARC), Egypt , Nasef, Soad A. Reference Laboratory for Veterinary Quality Control on Poultry production - Animal Health Research Institute - Agricultural Research Center (ARC), Egypt , Hassan, Wafaa M. Reference Laboratory for Veterinary Quality Control on Poultry production - Animal Health Research Institute - Agricultural Research Center (ARC), Egypt , Abdelaty, May F. Reference Laboratory for Veterinary Quality Control on Poultry production - Animal Health Research Institute - Agricultural Research Center (ARC), Egypt
Abstract :
Monitoring of imported 1-day-old poultry is mandated in Egypt to prevent the possible introduction of
new Salmonella serovars into the country’s poultry industry. Such serovars are considered to be a major public health
threat. We examined 391 imported poultry flocks for the presence of salmonellae (231 duckling, 84 chick, and 76
turkey poult), serotyped all isolated salmonellae, and performed antimicrobial susceptibility testing. Molecular profiles
were also constructed based on results of conventional polymerase chain reaction assays to detect virulence genes (stn,
avrA, and sopB) and antibiotic resistance genes (blaTEM, tetA(A), and qnrS) in the Salmonella isolates. Thirty Salmonella strains were isolated from the 391 samples (7.7%). By poultry type, salmonellae were isolated from 21 of 231
(9.1%) duckling samples, 6 of 84 (7.1%) of chick samples, and 3 of 76 (3.9%) turkey poult samples. Serotyping of the
isolates identified 16 different serovars: S. Enteritidis, S. Typhimurium, S. Sinstorf, S. Muenster, S. Vejle, S. Cuckmere,
S. Indiana, S. Infantis, S. Koenigstuhl, S. Macallen, S. Nchanga, S. Neftenbach, S. Newlands, S. Nigeria, S. Nyborg,
and S. Regent. The isolates showed variable degrees of antibiotic resistance across species. All tested Salmonella strains
harbored the virulence and antibiotic resistance genes, with the exception of qnrS, which was found in only 50% of the
isolates. In conclusion, examination of imported poultry is a critical point of control to prevent poultry from becoming
a reservoir for human health hazards, including salmonellae with antimicrobial resistance phenotypes.
Keywords :
Imported poultry , Salmonella serovars , sensitivity , virulence genes , antibiotic genes
Journal title :
Advances in Animal and Veterinary Sciences