The s48/45 six-cysteine proteins: mediators of interaction throughout the Plasmodium life cycle

被引:46
作者
Arredondo, Silvia A. [1 ]
Kappe, Stefan H. I. [1 ,2 ]
机构
[1] Seattle Biomed Res Inst, Ctr Infect Dis Res, 4 Nickerson St, Seattle, WA 98109 USA
[2] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
基金
比尔及梅琳达.盖茨基金会;
关键词
Malaria; Plasmodium; s48/45; 6-cys proteins; Adhesion proteins; Host-pathogen interactions; Malaria vaccine; TRANSMISSION-BLOCKING IMMUNITY; GAMETE-SURFACE PROTEIN; VACCINE CANDIDATE PFS48/45; MALARIA PARASITE INVASION; SEXUAL-STAGE ANTIGEN; TOXOPLASMA-GONDII; RECOMBINANT PROTEINS; FALCIPARUM MALARIA; TARGET ANTIGEN; NATURAL INFECTIONS;
D O I
10.1016/j.ijpara.2016.10.002
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程]; 100103 [病原生物学];
摘要
During their life cycle Plasmodium parasites rely upon an arsenal of proteins that establish key interactions with the host and vector, and between the parasite sexual stages, with the purpose of ensuring infection, reproduction and proliferation. Among these is a group of secreted or membrane-anchored proteins known as the six-cysteine (6-cys) family. This is a small but important family with only 14 members thus far identified, each stage-specifically expressed during the parasite life cycle. 6-cys proteins often localise at the parasite surface or interface with the host and vector, and are conserved in different Plasmodium species. The unifying feature of the family is the s48/45 domain, presumably involved in adhesion and structurally related to Ephrins, the ligands of Eph receptors. The most prominent s48/45 members are currently under functional investigation and are being pursued as vaccine candidates. In this review, we examine what is known about the 6-cys family, their structure and function, and discuss future research directions. (C) 2016 Australian Society for Parasitology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:409 / 423
页数:15
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