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首页> 外文期刊>Veterinary Microbiology >Analysis of the occurrence and distribution of the Omp25/Omp31 family of surface proteins in the six classical Brucella species
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Analysis of the occurrence and distribution of the Omp25/Omp31 family of surface proteins in the six classical Brucella species

机译:六个经典布鲁氏菌物种中表面蛋白Omp25 / Omp31家族的发生和分布分析

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摘要

Members of the Omp25/Omp31 family of surface proteins were previously shown to participate in the virulence of some Brucella species and a different distribution of the seven proteins of this family among species could be related to the difference in pathogenicity and host preference they exhibit. Accordingly, in this work we have analyzed the expression of the genes coding for the Omp25/Omp31 family in the six classical Brucella species and a set of B. ovis mutant strains with each omp gene inactivated. Immunoblot of whole-cell lysates with antibodies raised against the purified recombinant outer membrane proteins (OMPs) did not show the simultaneous presence of the seven OMPs in any of the Brucella strains studied, but different Omp25/Omp31 profiles were detected, in our experimental conditions, between the Brucella strains representative of the six classical species. Transcripts for omp31, omp25 and omp25c were, in general, the most abundant of the family and some hits were found in B. ovis for a posttranscriptional regulation mechanism and for a compensatory mechanism increasing the synthesis of a protein to compensate for the absence of another one. Finally, the potential interest of Omp25c and Omp31b as subcellular vaccines, considering their occurrence in the Brucella strains studied and their antigenic relatedness with other proteins of the family, is discussed.
机译:先前显示表面蛋白Omp25 / Omp31家族的成员参与某些布鲁氏菌物种的毒力,并且该家族的7种蛋白质在物种之间的不同分布可能与它们表现出的致病性和宿主偏好不同有关。因此,在这项工作中,我们分析了在六个经典布鲁氏菌属物种和一组灭活每个omp基因的B. ovis突变菌株中编码Omp25 / Omp31家族的基因的表达。用针对纯化的重组外膜蛋白(OMP)产生的抗体对全细胞裂解液进行的免疫印迹未显示在所研究的任何布鲁氏菌菌株中同时存在七个OMP,但是在我们的实验条件下检测到了不同的Omp25 / Omp31谱在代表六个经典种的布鲁氏菌之间。通常,omp31,omp25和omp25c的转录本是家族中最丰富的,在B. ovis中发现了一些命中点,这是因为转录后调节机制和补偿机制增加了蛋白质的合成,以弥补另一种蛋白质的缺失。一。最后,讨论了Omp25c和Omp31b作为亚细胞疫苗的潜在利益,考虑到它们在研究的布鲁氏菌菌株中的存在及其与该家族其他蛋白质的抗原相关性。

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