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参与核心脂多糖生物合成的肺炎克雷伯菌 waa 基因簇的遗传特征分析。

Genetic characterization of the Klebsiella pneumoniae waa gene cluster, involved in core lipopolysaccharide biosynthesis.

作者信息

Regué M, Climent N, Abitiu N, Coderch N, Merino S, Izquierdo L, Altarriba M, Tomás J M

机构信息

Departamento de Microbiología y Parasitología Sanitarias, División de Ciéncias de la Salud, Facultad de Farmacia, Universidad de Barcelona, Barcelona, Spain.

出版信息

J Bacteriol. 2001 Jun;183(12):3564-73. doi: 10.1128/JB.183.12.3564-3573.2001.

Abstract

A recombinant cosmid containing genes involved in Klebsiella pneumoniae C3 core lipopolysaccharide biosynthesis was identified by its ability to confer bacteriocin 28b resistance to Escherichia coli K-12. The recombinant cosmid contains 12 genes, the whole waa gene cluster, flanked by kbl and coaD genes, as was found in E. coli K-12. PCR amplification analysis showed that this cluster is conserved in representative K. pneumoniae strains. Partial nucleotide sequence determination showed that the same genes and gene order are found in K. pneumoniae subsp. ozaenae, for which the core chemical structure is known. Complementation analysis of known waa mutants from E. coli K-12 and/or Salmonella enterica led to the identification of genes involved in biosynthesis of the inner core backbone that are shared by these three members of the Enterobacteriaceae. K. pneumoniae orf10 mutants showed a two-log-fold reduction in a mice virulence assay and a strong decrease in capsule amount. Analysis of a constructed K. pneumoniae waaE deletion mutant suggests that the WaaE protein is involved in the transfer of the branch beta-D-Glc to the O-4 position of L-glycero-D-manno-heptose I, a feature shared by K. pneumoniae, Proteus mirabilis, and Yersinia enterocolitica.

摘要

通过赋予大肠杆菌K-12对细菌素28b抗性的能力,鉴定出一个含有参与肺炎克雷伯菌C3核心脂多糖生物合成相关基因的重组黏粒。该重组黏粒包含12个基因,即完整的waa基因簇,两侧分别是kbl和coaD基因,正如在大肠杆菌K-12中所发现的那样。PCR扩增分析表明,该基因簇在代表性的肺炎克雷伯菌菌株中是保守的。部分核苷酸序列测定显示,在肺炎克雷伯菌亚种臭鼻亚种中发现了相同的基因和基因顺序,其核心化学结构是已知的。对来自大肠杆菌K-12和/或肠炎沙门氏菌的已知waa突变体进行互补分析,从而鉴定出参与这三种肠杆菌科成员共有的内核骨架生物合成的基因。肺炎克雷伯菌orf10突变体在小鼠毒力试验中显示出两个对数级的降低,并且荚膜量大幅减少。对构建的肺炎克雷伯菌waaE缺失突变体的分析表明,WaaE蛋白参与将分支β-D-葡萄糖转移至L-甘油-D-甘露庚糖I的O-4位,这是肺炎克雷伯菌、奇异变形杆菌和小肠结肠炎耶尔森菌共有的特征。

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