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重新探讨毒力决定因子 magA 及其周围基因在导致化脓性肝脓肿的肺炎克雷伯菌中的重要性:在血清型 K1 荚膜形成中的确切作用。

Revisiting the importance of virulence determinant magA and its surrounding genes in Klebsiella pneumoniae causing pyogenic liver abscesses: exact role in serotype K1 capsule formation.

机构信息

Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan, Republic of China.

出版信息

J Infect Dis. 2010 Apr 15;201(8):1259-67. doi: 10.1086/606010.

Abstract

BACKGROUND

Mucoviscosity-associated gene A (magA) is proposed to play a decisive role in the pathogenesis of liver abscesses due to Klebsiella pneumoniae. Although some investigators consider MagA to be a putative O-antigen ligase, it is also reportedly associated with the K1 antigen.

METHODS

Using magA-positive serotype K1 K. pneumoniae STL43 isolated from a patient with liver abscess, we constructed 3 bacterial mutants by targeting genes within the same transcription unit, including magA, wcaG, and rfbP. The virulence of these mutants was determined by neutrophil phagocytosis and inoculation of mice. Transmission electron microscopy and Western blot analysis were used to define their surface polysaccharides.

RESULTS

STL43 was resistant, and all 3 mutants were highly susceptible, to phagocytosis. None of the mutant strains caused death in mice at the lethal dose of STL43. In contrast to previous reports, transmission electron microscopy revealed that all 3 mutants were nonencapsulated. Analysis of surface polysaccharides revealed that all 3 mutants retained their O antigen but lost their K antigen/capsule. Furthermore, amino acid analysis showed that MagA shared a conserved domain of Wzy, the serotype-specific capsular polysaccharide polymerase.

CONCLUSIONS

In accordance with the bacterial polysaccharide gene nomenclature (BPGN) scheme, MagA should be renamed Wzy(KpK1), the capsular polymerase specific to K. pneumoniae serotype K1.

摘要

背景

黏附相关基因 A(magA)被认为在肺炎克雷伯菌导致的肝脓肿发病机制中起决定性作用。尽管一些研究人员认为 MagA 是一种假定的 O-抗原连接酶,但它也与 K1 抗原有关。

方法

我们使用从肝脓肿患者中分离出的 magA 阳性血清型 K1 肺炎克雷伯菌 STL43 构建了 3 种细菌突变体,这些突变体针对同一转录单元内的基因,包括 magA、wcaG 和 rfbP。通过中性粒细胞吞噬和小鼠接种来确定这些突变体的毒力。通过透射电子显微镜和 Western blot 分析来定义它们的表面多糖。

结果

STL43 对吞噬作用具有抗性,而所有 3 种突变体均高度敏感。与之前的报道相反,透射电子显微镜显示所有 3 种突变体均无包膜。表面多糖分析表明,所有 3 种突变体均保留了 O 抗原,但失去了 K 抗原/荚膜。此外,氨基酸分析表明 MagA 与 Wzy 共享一个保守结构域,Wzy 是血清型特异性荚膜多糖聚合酶。

结论

根据细菌多糖基因命名法(BPGN)方案,MagA 应更名为 Wzy(KpK1),这是肺炎克雷伯菌血清型 K1 特有的荚膜聚合酶。

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