Seroprevalence and bacteriological identification of brucellosis in buffaloes in Upper Egypt.

M. Ragaa, F. El-Seedy, Abou-Gazia K.A
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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 wasformat 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 identifiedat 731bp and B. abortus identified at 498bp. Finally, we made measures ofthe control program for eradication of brucellosis in buffaloes by areasonable system of compensation, Veterinarians for field work and statelaboratories capable of serological techniques.Also, information technologysolutions and further logistic means as animal identification techniques are inmany governorates in Egypt.
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上埃及水牛布鲁氏菌病的血清流行率和细菌学鉴定。
共采集样本1317份;在上埃及10个省的农场和村庄采集了1164个血清样本、122个牛奶样本、24个淋巴结和7个流产的水牛胎儿。用于诊断布鲁氏菌病的血清学试验有玫瑰孟加拉平板(RBT)、缓冲酸化平板抗原性(BABAT)、EDTA改良标准管凝集试验(MSAT)、Revanol试验(RT)。另一方面,对水牛乳进行乳环试验(MRT)。用革兰氏染色和改良ZeilNeelson染色对可疑菌落进行染色。将分离得到的布鲁氏菌在不含抗生素的布鲁氏菌琼脂培养基上进行co2需取量、H2S产量、脲酶活性、染料存在下的生长等生化鉴定试验,并根据血清和牛奶样品进行间接固相酶联免疫吸附试验。琼脂凝胶免疫扩散试验(AGID)和PCR技术在布鲁氏菌分离株中的应用。血清学检测结果为:孟加拉试验34.7%,BAPA (37%), Revanol试验(28.2%),改良SAT(23.7%),间接elisa (32.3%), AGPT(33.8%)。用培养法从屠宰水牛淋巴结中分离出布鲁氏菌3株(占13.64%);abortusbiovar1。从流产胎中分离到的菌株1株(14.29%)分型为melitensisbiovar 3。仅从Beni-Suef中分离。乳环试验(MRT)结果显示,10份乳样品为3型白耳白杆菌,占8.20%。多重检测格式可在2 - 3小时内一次快速鉴定布鲁氏菌、B. abortus和B.melitensis。B.melitensis在731bp处鉴定,B. abortus在498bp处鉴定。最后,通过合理的补偿制度、兽医的现场工作和具备血清学技术的国家实验室,制定了根除水牛布鲁氏菌病的控制方案。此外,信息技术解决方案和进一步的物流手段,如动物识别技术,在埃及的许多省份。
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