A Mycobacterium marinum TesA mutant defective for major cell wall-associated lipids is highly attenuated in Dictyostelium discoideum and zebrafish embryos

被引:70
作者
Alibaud, Laeticia [1 ,2 ]
Rombouts, Yoann [4 ]
Trivelli, Xavier [4 ]
Burguiere, Adeline [1 ,2 ]
Cirillo, Suat L. G. [5 ]
Cirillo, Jeffrey D. [5 ]
Dubremetz, Jean-Francois [1 ,2 ]
Guerardel, Yann [4 ]
Lutfalla, Georges [1 ,2 ]
Kremer, Laurent [1 ,2 ,3 ]
机构
[1] Univ Montpellier 2, Lab Dynam Interact Membranaires Normales & Pathol, CNRS, UMR 5235, F-34095 Montpellier 05, France
[2] Univ Montpellier I, Lab Dynam Interact Membranaires Normales & Pathol, CNRS, UMR 5235, F-34095 Montpellier 05, France
[3] DIMNP, INSERM, F-34095 Montpellier 05, France
[4] Univ Sci & Technol Lille, Unite Glycobiol Struct & Fonct, CNRS, UMR 8576,IFR 147, F-59650 Villeneuve Dascq, France
[5] Texas A&M Hlth Sci Ctr, College Stn, TX 77843 USA
关键词
PHTHIOCEROL DIMYCOCEROSATE LOCUS; PHAGOSOME MATURATION; INTRACELLULAR SURVIVAL; DICENTRARCHUS-LABRAX; IMMUNE-RESPONSE; HOST MODEL; TUBERCULOSIS; INFECTION; VIRULENCE; BIOSYNTHESIS;
D O I
10.1111/j.1365-2958.2011.07618.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
P>Infection of the zebrafish with Mycobacterium marinum is regarded as a well-established experimental model to study the pathogenicity of Mycobacterium tuberculosis. Herein, a M. marinum transposon mutant library was screened for attenuated M. marinum phenotypes using a Dictyostelium discoideum assay. In one attenuated mutant, the transposon was located within tesA, encoding a putative type II thioesterase. Thin-layer chromatography analyses indicated that the tesA::Tn mutant failed to produce two major cell wall-associated lipids. Mass spectrometry and nuclear magnetic resonance clearly established the nature of missing lipids as phthioglycol diphthioceranates and phenolic glycolipids, respectively, indicating that TesA is required for the synthesis of both lipids. When injected into the zebrafish embryo bloodstream, the mutant was found to be highly attenuated, thus validating the performance and relevance of the Dictyostelium screen. Consistent with these in vivo findings, tesA::Tn exhibited increased permeability defects in vitro, which may explain its failure to survive in host macrophages. Unexpectedly, virulence was retained when bacteria were injected into the notochord. Histological and ultrastructural studies of the infected notochord revealed the presence of actively proliferating mycobacteria, leading to larval death. This work presents for the first time the notochord as a compartment highly susceptible to mycobacterial infection.
引用
收藏
页码:919 / 934
页数:16
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