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19血清群肺炎链球菌荚膜多糖生物合成的比较遗传学

Comparative genetics of capsular polysaccharide biosynthesis in Streptococcus pneumoniae types belonging to serogroup 19.

作者信息

Morona J K, Morona R, Paton J C

机构信息

Molecular Microbiology Unit, Women's and Children's Hospital, North Adelaide, South Australia 5006.

出版信息

J Bacteriol. 1999 Sep;181(17):5355-64. doi: 10.1128/JB.181.17.5355-5364.1999.

DOI:10.1128/JB.181.17.5355-5364.1999
PMID:10464207
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC94042/
Abstract

The genetic basis for the structural diversity of capsule polysaccharide (CPS) in Streptococcus pneumoniae serogroup 19 (consisting of types 19F, 19A, 19B, and 19C) has been determined for the first time. In this study, the genetic basis for the 19A and 19C serotypes is described, and the structures of all four serogroup 19 cps loci and their flanking sequences are compared. Transformation studies show that the structural difference between the 19A and 19F CPSs is likely to be a consequence of differences between their respective polysaccharide polymerase genes (cps19aI and cps19fI). The CPS of type 19C differs from that of type 19B by the addition of glucose. We have identified a single gene difference between the two cps loci (cps19cS), which is likely to encode a glucosyl transferase. The arrangement of the genes within the cps19 loci is highly conserved, with 13 genes (cps19A to -H and cps19K to -O) common to all four serogroup 19 members. These cps genes encode functions required for the synthesis of the shared trisaccharide component of the group 19 CPS repeat unit structures. Furthermore, the genetic differences between the group 19 cps loci identified are consistent with the CPS structures of the individual serotypes. Functions have been assigned to nearly all of the cps19 gene products, based on either gene complementation or similarity to other proteins with known functions, and putative biosynthetic pathways for production of all four group 19 CPSs have been proposed.

摘要

首次确定了肺炎链球菌19血清群(由19F、19A、19B和19C型组成)中荚膜多糖(CPS)结构多样性的遗传基础。在本研究中,描述了19A和19C血清型的遗传基础,并比较了所有四种19血清群cps基因座及其侧翼序列的结构。转化研究表明,19A和19F CPS之间的结构差异可能是其各自多糖聚合酶基因(cps19aI和cps19fI)差异的结果。19C型的CPS与19B型的CPS不同之处在于添加了葡萄糖。我们在两个cps基因座(cps19cS)之间发现了一个单一的基因差异,该差异可能编码一种葡萄糖基转移酶。cps19基因座内的基因排列高度保守,所有四种19血清群成员共有13个基因(cps19A至-H和cps19K至-O)。这些cps基因编码19血清群CPS重复单元结构共享三糖成分合成所需的功能。此外,所确定的19血清群cps基因座之间的遗传差异与各血清型的CPS结构一致。基于基因互补或与其他具有已知功能的蛋白质的相似性,几乎所有cps19基因产物的功能都已确定,并提出了所有四种19血清群CPS产生的推定生物合成途径。

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