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质粒R64的细菌毛PilV粘附素识别受体细胞脂多糖分子的特定结构。

Thin pilus PilV adhesins of plasmid R64 recognize specific structures of the lipopolysaccharide molecules of recipient cells.

作者信息

Ishiwa Akiko, Komano Teruya

机构信息

Department of Biology, Tokyo Metropolitan University, Minamiohsawa, Hachioji, Tokyo 192-0397, Japan.

出版信息

J Bacteriol. 2003 Sep;185(17):5192-9. doi: 10.1128/JB.185.17.5192-5199.2003.

Abstract

IncI1 plasmid R64 encodes a type IV pilus called a thin pilus, which includes PilV adhesins. Seven different sequences for the C-terminal segments of PilV adhesins can be produced by shufflon DNA rearrangement. The expression of the seven PilV adhesins determines the recipient specificity in liquid matings of plasmid R64. Salmonella enterica serovar Typhimurium LT2 was recognized by the PilVA' and PilVB' adhesins, while Escherichia coli K-12 was recognized by the PilVA', PilVC, and PilVC' adhesins. Lipopolysaccharide (LPS) on the surfaces of recipient cells was previously shown to be the specific receptor for the seven PilV adhesins. To identify the specific receptor structures of LPS for various PilV adhesins, R64 liquid matings were carried out with recipient cells consisting of various S. enterica serovar Typhimurium LT2 and E. coli K-12 waa mutants and their derivatives carrying various waa genes of different origins. From the mating experiments, including inhibition experiments, we propose that the GlcNAc(alpha1-2)Glc and Glc(alpha1-2)Gal structures of the LPS core of S. enterica serovar Typhimurium LT2 function as receptors for the PilVB' and PilVC' adhesins, respectively, while the PilVC' receptor in the wild-type LT2 LPS core may be masked. We further propose that the GlcNAc(beta1-7)Hep and Glc(alpha1-2)Glc structures of the LPS core of E. coli K-12 function as receptors for the PilVC and PilVC' adhesins, respectively.

摘要

IncI1质粒R64编码一种名为细菌毛的IV型菌毛,其中包括PilV黏附素。通过洗牌子DNA重排可产生7种不同的PilV黏附素C末端片段序列。这7种PilV黏附素的表达决定了质粒R64液体交配中的受体特异性。鼠伤寒沙门氏菌LT2血清型可被PilVA'和PilVB'黏附素识别,而大肠杆菌K-12可被PilVA'、PilVC和PilVC'黏附素识别。先前已证明受体细胞表面的脂多糖(LPS)是这7种PilV黏附素的特异性受体。为了确定各种PilV黏附素的LPS特异性受体结构,用由各种鼠伤寒沙门氏菌LT2血清型和大肠杆菌K-12 waa突变体及其携带不同来源各种waa基因的衍生物组成的受体细胞进行了R64液体交配。从包括抑制实验在内的交配实验中,我们提出,鼠伤寒沙门氏菌LT2 LPS核心的GlcNAc(α1-2)Glc和Glc(α1-2)Gal结构分别作为PilVB'和PilVC'黏附素的受体,而野生型LT2 LPS核心中的PilVC'受体可能被掩盖。我们进一步提出,大肠杆菌K-12 LPS核心的GlcNAc(β1-7)Hep和Glc(α1-2)Glc结构分别作为PilVC和PilVC'黏附素的受体。

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