Identification of Trans-Sialidases as a Common Mediator of Endothelial Cell Activation by African Trypanosomes

PLoS Pathogens

Nicolas Plazolles¹  Virginie Coustou¹  Théo Baltz¹  Zeinab Ammar¹ 

[1] French National Centre for Scientific Research (CNRS), Université Bordeaux Segalen, Microbiologie fondamentale et Pathogénicité, UMR 5234, Bordeaux, France

关键词: Trypanosoma;    Endothelial cells;    Transcription factors;    Lectins;    Inflammation;    Trypanosoma congolense;    Host-pathogen interactions;    Trypanosoma vivax;   

DOI  :  10.1371/journal.ppat.1003710

学科分类：生物科学（综合）

来源: Public Library of Science

【 摘 要 】

Understanding African Trypanosomiasis (AT) host-pathogen interaction is the key to an “anti-disease vaccine”, a novel strategy to control AT. Here we provide a better insight into this poorly described interaction by characterizing the activation of a panel of endothelial cells by bloodstream forms of four African trypanosome species, known to interact with host endothelium. T. congolense, T. vivax, and T. b. gambiense activated the endothelial NF-κB pathway, but interestingly, not T. b. brucei. The parasitic TS (trans-sialidases) mediated this NF-κB activation, remarkably via their lectin-like domain and induced production of pro-inflammatory molecules not only in vitro but also in vivo, suggesting a considerable impact on pathogenesis. For the first time, TS activity was identified in T. b. gambiense BSF which distinguishes it from the subspecies T. b. brucei. The corresponding TS were characterized and shown to activate endothelial cells, suggesting that TS represent a common mediator of endothelium activation among trypanosome species with divergent physiopathologies.

【 授权许可】

CC BY