| Literature DB >> 25987709 |
Bo Wang1, Feng Lu2, Yang Cheng3, Jun-Hu Chen4, Hye-Yoon Jeon5, Kwon-Soo Ha5, Jun Cao6, Myat Htut Nyunt7, Jin-Hee Han4, Seong-Kyun Lee4, Myat Phone Kyaw8, Jetsumon Sattabongkot9, Eizo Takashima10, Takafumi Tsuboi11, Eun-Taek Han12.
Abstract
Tryptophan-rich antigens (TRAgs) are an antigen family that has been identified in human and rodent malaria parasites. TRAgs have been proposed as candidate antigens for potential vaccines. The Plasmodium vivax TRAg (PvTRAg) family includes 36 members. Each PvTRAg contains a tryptophan-rich (TR) domain in the C-terminal region. In this study, we recombinantly expressed all 36 PvTRAgs using a cell-free expression system, and, for the first time, profiled the IgG antibody responses against all PvTRAgs in the sera from 96 vivax malaria patients and 40 healthy individuals using protein microarray technology. The mean seropositive rate for all PvTRAgs was 60.3%. Among them, nine PvTRAgs were newly identified in this study and showed a seropositive rate of >50%. Five of them, PvTRAg_13, PvTRAg_15, PvTRAg_16, PvTRAg_26, and PvTRAg_29, produced higher levels of IgG antibody, even in low-endemicity countries. In addition, the results of an immunofluorescence analysis suggest that PvTRAgs are, at least in part, associated with caveola-vesicle complexes, a unique structure of P. vivax-infected erythrocytes. The mechanism of formation and the function of these abundant membrane structures are not known. Further investigation aimed at determining the functions of these proteins would lead to a better understanding of the blood-stage biology of P. vivax.Entities:
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Year: 2015 PMID: 25987709 PMCID: PMC4496608 DOI: 10.1128/IAI.03067-14
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441