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publication name Characterization of some virulence properties of subclinical mastitis-associated Escherichia coli in Egyptian cows and buffalos
Authors Ibrahim N. Alkhouly1,2, Abdelmoneim M. Moustafa1 , Nahla A. Abou El Roos2, and Sahar A. Kandeel1 ,*
year 2023
keywords mastitis,coliform bacteria
journal Benha Veterinary Medical Journal
volume Not Available
issue Not Available
pages Not Available
publisher Not Available
Local/International Local
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Abstract

Bovine mastitis is a common worldwide infection caused by different types of pathogens including coliform bacteria. Understanding mastitis pathogens and their dominance, as well as risk factors, is required to facilitate disease prevention and control, and to enhance udder health within the herd. Our objectives were to investigate the prevalence of different mastitiscausing pathogens and describe some genetic traits which outline mastitis-associated E.coli (MAEC). Four-hundred twenty-eight quarter foremilk samples were collected from 107 apparently healthy lactating cows and buffaloes from El-Menofia Governorate between 2020- 2022. The California Mastitis Test (CMT) was used to estimate the quarter somatic cell count (SCC), with subclinical mastitis (SCM) defined as non-negative CMT score. The bacterial culture of milk was used as a reference method to identify SCM based on the isolation of the causative pathogens. VITEK-2 compact system was used for isolates identification. Serological identification of E.coli serotypes and molecular identification of some virulence genes using PCR were also performed. The prevalence of SCM was 60.7% with E.coli being the most commonly isolated organism. The enteropathogenic serotypes of E.coli isolated from the examined milk samples showed; O26:H11 (EHEC) 21.70%, O15:H2 (ETEC) 13.04%, O127:H6 (ETEC) 4.34%, O121:H7 (EHEC) 13.04%, O117:H4 (EHEC) 17.39%, O146:H21 (EPEC) 17.39% and O103:H2 (EHEC) 13.04%. The molecular identification of the most common virulence genes of E.coli revealed the presence of sfa, papC, and traT genes in 100% of the examined samples while cnf1 gene was present in only 30% of the samples

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