Structure-function analysis of apical membrane-associated molecules of the tegument of schistosome parasites of humans: Prospects for identification of novel targets for parasite control

18Citations
Citations of this article
46Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Neglected tropical diseases are a group of some 17 diseases that afflict poor and predominantly rural people in developing nations. One significant disease that contributes to substantial morbidity in endemic areas is schistosomiasis, caused by infection with one of five species of blood fluke belonging to the trematode genus Schistosoma. Although there is one drug available for treatment of affected individuals in clinics, or for mass administration in endemic regions, there is a need for new therapies. A prominent target organ of schistosomes, either for drug or vaccine development, is the peculiar epithelial syncytium that forms the body wall (tegument) of this parasite. This dynamic layer is maintained and organized by concerted activity of a range of proteins, among which are the abundant tegumentary annexins. In this review, we will outline advances in structure-function analyses of these annexins, as a means to understanding tegument cell biology in host-parasite interaction and their potential exploitation as targets for anti-schistosomiasis therapies. Linked Articles This article is part of a themed section on Annexins VII Programme. To view the other articles in this section visit http://dx.doi.org/10.1111/bph.2015.172.issue-7

Cite

CITATION STYLE

APA

Leow, C. Y., Willis, C., Hofmann, A., & Jones, M. K. (2015). Structure-function analysis of apical membrane-associated molecules of the tegument of schistosome parasites of humans: Prospects for identification of novel targets for parasite control. British Journal of Pharmacology. John Wiley and Sons Inc. https://doi.org/10.1111/bph.12898

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free