Application of Bruce-Ladder Multiplex PCR for Identification of Brucella abortus Isolated from Cattle in Kachia Grazing Reserve and Jos Plateau

W. Bertu, R. Ocholi, J. Kwaga, J. Kabir, A. Gusi, S. Ngulukun, E. Mwankon, Mohamed Hassan, M. Nanven, M. Ducrotoy, S. Andrés-Barranco, I. Moriyón
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Abstract

A study was carried out to isolate Brucella strains from cattle in Kachia Grazing Reserve (KGR) and some communities on Jos Plateau and to carry out phenotypic and molecular characterization of the isolates along with other isolates obtained from field submissions and those in the archive of National Veterinary Research Institute (NVRI), Vom. A total of 63 vaginal swabs, 36 milk samples, and 2 hygroma fluids were collected from KGR while 70 vaginal swabs, 50 milk samples and 2 hygroma fluids were collected on the Jos Plateau for Brucella isolation. They were cultured for Brucella isolation according to standard Brucella isolation protocol. Three Brucella abortus strains were isolated from KGR while 4 Brucella abortus strains were isolated from the Jos Plateau respectively. Eight isolates from field submissions and 5 from the archive were collected and resuscitated. Comprehensive characterization of the isolates in this study revealed that they were all Brucella abortus. Similarly, characterization of archived isolates and those from field submissions showed that they were Brucella abortus. The classical biotyping of all the isolates revealed that they were Brucella abortus biotype 3. Molecular characterization of all the isolates by Bruce-ladder multiplex Polymerase chain reaction (PCR) showed bands consistent with Brucella abortus. This is the first molecular characterization of Brucella isolates from Nigeria using the Bruce-ladder multiplex PCR and the first study that established that Brucella abortus biotype 3 is the predominant Brucella strain in Nigeria. The study established the endemicity of brucellosis due to Brucella abortus, in the two study areas. These findings have great veterinary and public health implications. There is therefore an urgent need for the institution and implementation of brucellosis control measures in these areas.
应用布鲁斯阶梯多重PCR技术鉴定Kachia放牧保护区和Jos高原牛的流产布鲁氏菌
本研究从Kachia放牧保护区(KGR)和Jos高原一些社区的牛中分离布鲁氏菌菌株,并对这些菌株以及从现场提交的材料和Vom国家兽医研究所(NVRI)档案中获得的其他菌株进行表型和分子鉴定。在KGR共采集63份阴道拭子、36份乳汁和2份湿液,在Jos高原共采集70份阴道拭子、50份乳汁和2份湿液进行布鲁氏菌分离。按照布鲁氏菌标准分离方案进行布鲁氏菌培养。从KGR分离到3株流产布鲁氏菌,在乔斯高原分离到4株流产布鲁氏菌。收集现场提交的8株分离株和档案中的5株分离株并进行复苏。本研究分离株的综合鉴定表明,它们均为流产布鲁氏菌。同样,对存档的分离株和现场提交的分离株的鉴定表明它们是流产布鲁氏菌。所有菌株的经典生物分型均为流产布鲁氏菌3型。通过布鲁斯阶梯多重聚合酶链反应(PCR)对分离菌株进行分子鉴定,发现与流产布鲁氏菌的条带一致。这是首次利用布鲁斯阶梯多重聚合酶链反应对尼日利亚布鲁氏菌分离物进行分子表征,也是首次确定流产布鲁氏菌生物型3是尼日利亚主要的布鲁氏菌菌株的研究。该研究确定了两个研究地区由流产布鲁氏菌引起的布鲁氏菌病的地方性。这些发现具有重大的兽医和公共卫生意义。因此,迫切需要在这些地区制定和实施布鲁氏菌病控制措施。
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