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土拉弗朗西斯菌wbt基因座在脂多糖O抗原生物合成及致病性中的作用

Role of the wbt locus of Francisella tularensis in lipopolysaccharide O-antigen biogenesis and pathogenicity.

作者信息

Raynaud Catherine, Meibom Karin L, Lety Marie-Annick, Dubail Iharilalao, Candela Thomas, Frapy Eric, Charbit Alain

机构信息

Université Paris Descartes, Faculté de Médecine René Descartes, Paris F-75015, France.

出版信息

Infect Immun. 2007 Jan;75(1):536-41. doi: 10.1128/IAI.01429-06. Epub 2006 Oct 9.

DOI:10.1128/IAI.01429-06
PMID:17030571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1828372/
Abstract

Francisella tularensis is a highly infectious bacterial pathogen, responsible for the zoonotic disease tularemia. We screened a bank of transposon insertion mutants of F. tularensis subsp. holarctica LVS for colony morphology alterations and selected a mutant with a transposon insertion in wbtA, the first gene of the predicted lipopolysaccharide O-antigen gene cluster. Inactivation of wbtA led to the complete loss of O antigen, conferred serum sensitivity, impaired intracellular replication, and severely attenuated virulence in the mouse model. Notably, this mutant afforded protection against a challenge against virulent LVS.

摘要

土拉弗朗西斯菌是一种具有高度传染性的细菌病原体,可引发人畜共患疾病兔热病。我们筛选了土拉弗朗西斯菌亚种全北区LVS的转座子插入突变体文库,以寻找菌落形态改变的突变体,并挑选出一个在wbtA基因(预测的脂多糖O抗原基因簇的第一个基因)中有转座子插入的突变体。wbtA基因的失活导致O抗原完全缺失,赋予血清敏感性,损害细胞内复制,并在小鼠模型中严重减弱毒力。值得注意的是,该突变体对强毒株LVS的攻击提供了保护。

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Role of the wbt locus of Francisella tularensis in lipopolysaccharide O-antigen biogenesis and pathogenicity.土拉弗朗西斯菌wbt基因座在脂多糖O抗原生物合成及致病性中的作用
Infect Immun. 2007 Jan;75(1):536-41. doi: 10.1128/IAI.01429-06. Epub 2006 Oct 9.
2
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本文引用的文献

1
Francisella tularensis travels a novel, twisted road within macrophages.土拉弗朗西斯菌在巨噬细胞内走出了一条独特而曲折的路径。
Trends Microbiol. 2006 Jan;14(1):37-44. doi: 10.1016/j.tim.2005.11.008. Epub 2005 Dec 13.
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Grey variants of the live vaccine strain of Francisella tularensis lack lipopolysaccharide O-antigen, show reduced ability to survive in macrophages and do not induce protective immunity in mice.土拉弗朗西斯菌活疫苗株的灰色变体缺乏脂多糖O抗原,在巨噬细胞中的存活能力降低,并且不能在小鼠中诱导保护性免疫。
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