Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK.
Microb Pathog. 2011 Sep;51(3):169-77. doi: 10.1016/j.micpath.2011.04.004. Epub 2011 May 4.
A protein designated Bap-5 (GenBank accession no. AF081494) or BapC (GenBank accession no. AJ277634) has been identified as a member of the Bordetella pertussis autotransporter family and the present work suggests that this protein, like the previously characterised BrkA, is a Bvg-regulated serum resistance factor and virulence determinant. B. pertussis bapC and brkA, bapC mutants were created and, like a brkA mutant, showed greater sensitivity to killing by normal human serum than their parent strains but they were not as sensitive as a bvg mutant. Competition assays also showed an important role for BapC, like BrkA, in virulence of B. pertussis in mice after intranasal infection. Moreover, the bapC and brkA, bapC mutants, like the brkA mutant, were found to be more sensitive to the antimicrobial peptide cecropin P1 than the parent strains. In the genome sequence of B. pertussis strain Tohama, bapC is designated as a pseudogene due, in part, to a frameshift in a poly(C) tract near the 5' end of the gene which creates a truncated BapC protein. Sequence analyses of the bapC region spanning the poly(C) tract of a number of B. pertussis strains showed minor nucleotide and amino acid polymorphisms but it appeared that all had an ORF that would be able to produce BapC.
已鉴定出一种名为 Bap-5(GenBank 登录号 AF081494)或 BapC(GenBank 登录号 AJ277634)的蛋白,它是百日咳博德特氏菌自转运家族的成员,本研究表明,该蛋白与先前鉴定的 BrkA 一样,是一种 Bvg 调控的血清抗性因子和毒力决定因子。创建了 B. pertussis bapC 和 brkA、bapC 突变体,与 brkA 突变体一样,与亲本菌株相比,它们对正常人类血清的杀伤更为敏感,但不如 bvg 突变体敏感。竞争测定也表明,BapC 像 BrkA 一样,在鼻内感染后 B. pertussis 的小鼠毒力中发挥重要作用。此外,bapC 和 brkA、bapC 突变体与 brkA 突变体一样,对抗菌肽 cecropin P1 比亲本菌株更敏感。在 B. pertussis 菌株 Tohama 的基因组序列中,bapC 被指定为假基因,部分原因是基因 5'端附近的多(C)序列发生移码,导致截短的 BapC 蛋白。对跨越多个 B. pertussis 菌株多(C)序列的 bapC 区域进行的序列分析显示,核苷酸和氨基酸存在较小的多态性,但似乎所有菌株都有一个能够产生 BapC 的 ORF。