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首页> 外文期刊>Clinical and diagnostic laboratory immunology >Identification of an IS711 Element Interrupting the wboA Gene of Brucella abortusVaccine Strain RB51 and a PCR Assay To Distinguish Strain RB51 from Other Brucella Species and Strains
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Identification of an IS711 Element Interrupting the wboA Gene of Brucella abortusVaccine Strain RB51 and a PCR Assay To Distinguish Strain RB51 from Other Brucella Species and Strains

机译:中断流产布鲁氏菌疫苗RB51的wboA基因的IS711元件的鉴定和区别其他布鲁氏菌属和菌株的RB51的PCR分析

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Brucella abortus vaccine strain RB51 is a natural stable attenuated rough mutant derived from the virulent strain 2308. The genetic mutations that are responsible for the roughness and the attenuation of strain RB51 have not been identified until now. Also, except for an assay based on pulsed-field gel electrophoresis, no other simple method to differentiate strain RB51 from its parent strain 2308 is available. In the present study, we demonstrate that thewboA gene encoding a glycosyltransferase, an enzyme essential for the synthesis of O antigen, is disrupted by an IS711 element in B. abortus vaccine strain RB51. Exploiting this feature, we developed a PCR assay that distinguishes strain RB51 from all other Brucella species and strains tested.
机译:流产布鲁氏菌疫苗菌株RB51是一种自然稳定的减毒粗糙突变体,衍生自有毒力菌株2308。到目前为止,尚未确定导致RB51菌株粗糙和减毒的遗传突变。而且,除了基于脉冲场凝胶电泳的测定法之外,没有其他简单的方法可以将菌株RB51与其亲本菌株2308区分。在本研究中,我们证明了 wboA 基因编码糖基转移酶(一种合成O抗原所必需的酶)被中的IS 711 元件破坏B.流产疫苗菌株RB51。利用此功能,我们开发了一种PCR检测方法,可将RB51菌株与所有其他 Brucella 物种和测试菌株区分开。

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