Seroprevalence and bacteriological identification of brucellosis in buffaloes in Upper Egypt. | ||
| Journal of Veterinary Medical Research | ||
| Article 15, Volume 25, Issue 1, June 2018, Pages 148-156 PDF (536.98 K) | ||
| Document Type: Original Article | ||
| DOI: 10.21608/jvmr.2018.43312 | ||
| Authors | ||
| Ragaa M.1; El-Seedy F.2; Abou-Gazia K.A1 | ||
| 1Dept. of Reproductive Diseases, ARRI, ARC, Giza, Egypt. | ||
| 2Dept. of Bacteriology, Mycology and Immunology, Faculty of Veterinary Medicine. Beni-Suef, Egypt. | ||
| Abstract | ||
| A total of 1317 samples were collected; 1164 serum samples, 122 milk samples, 24 lymph nodes and 7 aborted foeti from buffaloes in 10 Governorates from farms and villages in Upper Egypt. The serological tests used for the diagnosis of brucellosis on blood sera were the Rose Bengal plate (RBT) , Buffered acidified plate antigentest (BABAT), EDTA modifiedstandard tube agglutination test (MSAT), Revanol test (RT). On the other hand, the milk ring test (MRT) was performed on buffalo-cow's milk. Suspected colonies were stained with Gram, s stain and Modified ZeilNeelson stain. The isolated Brucella organisms on antibiotic free Brucella agar medium were subjected to the following tests for biochemical identification tests as CO2requirement, H2S production, Urease activity, growth in the presence of dyes,The indirect solid phase ELISA technique was carried out according to serum and milk samples.Agar gel immune diffusion test (AGID) and PCR applied on isolated Brucella strains. The results of the serological tests wereRose Bengal test 34.7%, BAPA (37%), Revanol test (28.2%),modified SAT (23.7%), indirect ELISAwere (32.3%) and AGPT (33.8%)in this study.Brucellaorganisms from lymph nodes of slaughtered buffaloes by culturing method showed that 3 (13.64%) isolates(2) of B. melitensisbiovar 3 and (1)B. abortusbiovar1. The isolated strain from aborted foeti was one isolate (14.29%) typed as B.melitensisbiovar 3. isolated only from Beni-Suef.By milk ring test (MRT) milk samples were 10 (8.20%) of B. melitensis biotype 3. A multiplex was format that will allow the rapid identification of Brucella spp., B. abortus, and B.melitensis in a single test within 2 to 3 h. B. melitensis was identified at 731bp and B. abortus identified at 498bp. Finally, we made measures of the control program for eradication of brucellosis in buffaloes by a reasonable system of compensation, Veterinarians for field work and state laboratories capable of serological techniques.Also, information technology solutions and further logistic means as animal identification techniques are in many governorates in Egypt. | ||
| Keywords | ||
| Brucellosis; buffaloes; Egypt | ||
|
Statistics Article View: 230 PDF Download: 252 |
||
