The Mycobacterium tuberculosis capsule: a cell structure with key implications in pathogenesis

被引:87
作者
Kalscheuer, Rainer [1 ]
Palacios, Ainhoa [2 ]
Anso, Itxaso [2 ]
Cifuente, Javier [2 ]
Anguita, Juan [2 ,3 ]
Jacobs, William R., Jr. [4 ,5 ]
Guerin, Marcelo E. [2 ,3 ]
Prados-Rosales, Rafael [2 ,4 ,6 ]
机构
[1] Heinrich Heine Univ Dusseldorf, Inst Pharmaceut Biol & Biotechnol, Dusseldorf, Germany
[2] CIC bioGUNE, Bizkaia Technol Pk,Ed 801A, Derio 48160, Spain
[3] Ikerbasque, Basque Fdn Sci, Bilbao 48013, Spain
[4] Albert Einstein Coll Med, Dept Microbiol & Immunol, New York, NY 10461 USA
[5] Albert Einstein Coll Med, Howard Hughes Med Inst, New York, NY 10461 USA
[6] Univ Autonoma Madrid, Dept Prevent Med & Publ Hlth & Microbiol, Madrid 28029, Spain
关键词
ELECTRON-TRANSPARENT ZONE; BACILLUS-CALMETTE-GUERIN; RECEPTOR-TYPE; 3; MANNOSE-RECEPTOR; ALPHA-GLUCAN; IN-VITRO; DC-SIGN; MACROPHAGE PHAGOCYTOSIS; INOSITOL MANNOSIDES; FREEZE-SUBSTITUTION;
D O I
10.1042/BCJ20190324
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
Bacterial capsules have evolved to be at the forefront of the cell envelope, making them an essential element of bacterial biology. Efforts to understand the Mycobacterium tuberculosis (Mtb) capsule began more than 60 years ago, but the relatively recent development of mycobacterial genetics combined with improved chemical and immunological tools have revealed a more refined view of capsule molecular composition. A glycogen-like a-glucan is the major constituent of the capsule, with lower amounts of arabinomannan and mannan, proteins and lipids. The major Mtb capsular components mediate interactions with phagocytes that favor bacterial survival. Vaccination approaches targeting the mycobacterial capsule have proven successful in controlling bacterial replication. Although the Mtb capsule is composed of polysaccharides of relatively low complexity, the concept of antigenic variability associated with this structure has been suggested by some studies. Understanding how Mtb shapes its envelope during its life cycle is key to developing anti-infective strategies targeting this structure at the host-pathogen interface.
引用
收藏
页码:1995 / 2016
页数:22
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