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海洋细菌中一种不寻常荚膜多糖生物合成基因座水平转移的证据。

Evidence for the horizontal transfer of an unusual capsular polysaccharide biosynthesis locus in marine bacteria.

机构信息

Department of Laboratory Medicine and Pathobiology, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.

出版信息

Infect Immun. 2010 Dec;78(12):5214-22. doi: 10.1128/IAI.00653-10. Epub 2010 Oct 4.

Abstract

The most intensely studied of the Vibrio vulnificus virulence factors is the capsular polysaccharide (CPS). All virulent strains produce copious amounts of CPS. Acapsular strains are avirulent. The structure of the CPS from the clinical isolate ATCC 27562 is unusual. It is serine modified and contains, surprisingly, N-acetylmuramic acid. We identified the complete 25-kb CPS biosynthesis locus from ATCC 27562. It contained 21 open reading frames and was allelic to O-antigen biosynthesis loci. Two of the genes, murA(CPS) and murB(CPS), were paralogs of the murA(PG) and murB(PG) genes of the peptidoglycan biosynthesis pathway; only a single copy of these genes is present in the strain CMCP6 and YJ016 genomes. Although MurA(CPS) and MurB(CPS) were functional when expressed in Escherichia coli, lesions in either gene had no effect on CPS production, virulence, or growth in V. vulnificus; disruption of 8 other genes within the locus resulted in an acapsular phenotype and attenuated virulence. Thus, murA(CPS) and murB(CPS) were functional but redundant. Comparative genomic analysis revealed that while completely different CPS biosynthesis loci were found in the same chromosomal region in other V. vulnificus strains, most of the CPS locus of ATCC 27562 was conserved in another marine bacterium, Shewanella putrefaciens strain 200. However, the average GC content of the CPS locus was significantly lower than the average GC content of either genome. Furthermore, several of the encoded proteins appeared to be of Gram-positive and archaebacterial origin. These data indicate that the horizontal transfer of intact and partial CPS loci drives CPS diversity in marine bacteria.

摘要

研究最为深入的创伤弧菌毒力因子是荚膜多糖(CPS)。所有毒力株都大量产生 CPS。无荚膜菌株无致病性。临床分离株 ATCC 27562 的 CPS 结构很不寻常。它是丝氨酸修饰的,并且出人意料地含有 N-乙酰胞壁酸。我们从 ATCC 27562 鉴定了完整的 25kb CPS 生物合成基因座。它包含 21 个开放阅读框,与 O-抗原生物合成基因座等位。两个基因,murA(CPS)和 murB(CPS),是肽聚糖生物合成途径中 murA(PG)和 murB(PG)基因的旁系同源物;在菌株 CMCP6 和 YJ016 基因组中仅存在这些基因的单个拷贝。尽管 MurA(CPS)和 MurB(CPS)在大肠杆菌中表达时具有功能,但这些基因中的任何一个基因的突变都不会影响 CPS 的产生、毒力或在创伤弧菌中的生长;该基因座内的另外 8 个基因的缺失导致无荚膜表型和减弱的毒力。因此,murA(CPS)和 murB(CPS)是有功能的但冗余的。比较基因组分析显示,虽然在其他创伤弧菌菌株的同一染色体区域发现了完全不同的 CPS 生物合成基因座,但 ATCC 27562 的大多数 CPS 基因座在另一种海洋细菌脱硫希瓦氏菌菌株 200 中是保守的。然而,CPS 基因座的平均 GC 含量明显低于两个基因组的平均 GC 含量。此外,编码的几种蛋白似乎来自革兰氏阳性菌和古细菌。这些数据表明,完整和部分 CPS 基因座的水平转移驱动了海洋细菌中 CPS 的多样性。

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