MOLECULAR DETECTION AND SEROTYPING OF FOOT AND MOUTH DISEASE VIRUS IN TONGUE EPITHELIUM SAMPLES | ||||
Mansoura Veterinary Medical Journal | ||||
Article 42, Volume 18, Issue 1, June 2017, Page 397-404 PDF (488.92 K) | ||||
DOI: 10.21608/mvmj.2017.127703 | ||||
View on SCiNiTO | ||||
Authors | ||||
A. A. El-Kenawy* 1; E. E. Younis2; Hiam M. Fakhry3; R. Karam4 | ||||
1Department of Virology, Faculty of Veterinary Medicine , Mansoura University. Phone: +20-50-2372593, Fax: +20-50-237995 | ||||
2Department of Internal Medicine, Infectious and Fish diseases, Faculty of Veterinary Medicine, Mansoura University. | ||||
3Veterinary Serum and Vaccine Research Institute, FMD Department, Abbassia, Cairo, Egypt | ||||
4Department of Virology, Faculty of Veterinary Medicine , Mansoura University. Phone: +20-50-2372593, Fax: +20-50-2379952 | ||||
Abstract | ||||
The aim of the present study is molecular identification and typing of FMDV circulating in Dakahlia governorate in Egypt, 2014. The study was accomplished on pooled nine tongue epithelium samples collected from diseased cattle and buffaloes expected to be infected with FMDV. The diseased animals showed fever , excessive salivation and ulceration on tongue and gum. Conventional reverse transcription polymerase chain reaction (RT-PCR) was used for identification of FMDV using universal primers. Then serotyping of the identified virus was done using RT-PCR for serotype O and A and Real time RT-PCR for serotype SAT2 . FMDV was identified in all the examined nine samples. Five of them were of serotype O, two of serotype A, one of serotype SAT2 and one sample was neither O, A nor SAT2. In conclusion, molecular techniques are sensitive and rapid methods for FMDV detection. In addition, serotypes O, A and SAT2 are circulating in Dakahlia Governorate, Egypt, 2014. | ||||
Keywords | ||||
FMD; Egypt; Serotype | ||||
Statistics Article View: 148 PDF Download: 163 |
||||