Characterization and Diagnostic Application of Trypanosoma cruzi Trypomastigote Excreted-Secreted Antigens Shed in Extracellular Vesicles Released from Infected Mammalian Cells

被引:40
作者
Bautista-Lopez, Norma L. [1 ,2 ]
Ndao, Momar [2 ,3 ]
Camargo, Fabio Vasquez [2 ,3 ]
Nara, Takeshi [4 ]
Annoura, Takeshi [5 ]
Hardie, Darryl B. [6 ]
Borchers, Christoph H. [6 ]
Jardim, Armando [1 ,2 ]
机构
[1] McGill Univ, Inst Parasitol, Montreal, PQ, Canada
[2] McGill Univ, Ctr Host Parasite Interact, Montreal, PQ, Canada
[3] McGill Univ, Natl Reference Ctr Parasitol, Ctr Hlth, Res Inst, Montreal, PQ, Canada
[4] Juntendo Univ, Dept Mol & Cellular Parasitol, Grad Sch Med, Tokyo, Japan
[5] Natl Inst Infect Dis, Dept Parasitol, Tokyo, Japan
[6] Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
parasite; proteomics; TESA; Trypanosoma cruzi; trypomastigote; CHAGAS-DISEASE; PROTEOMIC ANALYSIS; MONOCLONAL-ANTIBODIES; IMMUNE-RESPONSE; EXOSOMES; SERODIAGNOSIS; SURFACE; IDENTIFICATION; PROTEIN; ELISA;
D O I
10.1128/JCM.01649-16
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Chagas disease, caused by Trypanosoma cruzi, although endemic in many parts of Central and South America, is emerging as a global health threat through the potential contamination of blood supplies. Consequently, in the absence of a gold standard assay for the diagnosis of Chagas disease, additional antigens or strategies are needed. A proteomic analysis of the trypomastigote excreted-secreted antigens (TESA) associated with exosomal vesicles shed by T. cruzi identified similar to 80 parasite proteins, with the majority being trans-sialidases. Mass spectrometry analysis of immunoprecipitation products performed using Chagas immune sera showed a marked enrichment in a subset of TESA proteins. Of particular relevance for diagnostic applications were the retrotransposon hot spot (RHS) proteins, which are absent in Leishmania spp., parasites that often confound diagnosis of Chagas disease. Interestingly, serological screens using recombinant RHS showed a robust immunoreactivity with sera from patients with clinical stages of Chagas ranging from asymptomatic to advance cardiomyopathy and this immunoreactivity was comparable to that of crude TESA. More importantly, no cross-reactivity with RHS was detected with sera from patients with malaria, leishmaniasis, toxoplasmosis, or African sleeping sickness, making this protein an attractive reagent for diagnosis of Chagas disease.
引用
收藏
页码:744 / 758
页数:15
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