Back to Search Start Over

Identification and characterization of the Onchocerca volvulus Excretory Secretory Product Ov28CRP, a putative GM2 activator protein

Authors :
Njume, Ferdinand Ngale
Ghogomu, Stephen M
Shey, Robert Adamu
Tchouate Gainkam, Lea Olive
Poelvoorde, Philippe
Humblet, Claire Perrine
Kamgno, Joseph
Robert, Annie
Mutesa, Léon
Lelubre, Christophe
Edelweiss, Evelina
Poterszman, Arnaud
Anheuser, Susi
Vanhamme, Luc
Souopgui, Jacob
Njume, Ferdinand Ngale
Ghogomu, Stephen M
Shey, Robert Adamu
Tchouate Gainkam, Lea Olive
Poelvoorde, Philippe
Humblet, Claire Perrine
Kamgno, Joseph
Robert, Annie
Mutesa, Léon
Lelubre, Christophe
Edelweiss, Evelina
Poterszman, Arnaud
Anheuser, Susi
Vanhamme, Luc
Souopgui, Jacob
Source :
P L o S Neglected Tropical Diseases, 13 (7
Publication Year :
2019

Abstract

Onchocerca volvulus is the nematode pathogen responsible for human onchocerciasis also known as “River blindness”, a neglected tropical disease that affects up to 18 million people worldwide. Helminths Excretory Secretory Products (ESPs) constitute a rich repertoire of molecules that can be exploited for host-parasite relationship, diagnosis and vaccine studies. Here, we report, using a range of molecular techniques including PCR, western blot, recombinant DNA technology, ELISA, high performance thin-layer chromatography and mass spectrometry that the 28 KDa cysteine-rich protein (Ov28CRP) is a reliable component of the O. volvulus ESPs to address the biology of this parasite. We showed that (1) Ov28CRP is a putative ganglioside GM2 Activator Protein (GM2AP) conserved in nematode; (2) OvGM2AP gene is transcriptionally activated in all investigated stages of the parasitic life cycle, including larval and adult stages; (3) The full-length OvGM2AP was detected in in-vitro O. volvulus ESPs of adult and larval stages; (4) the mass expressed and purified recombinant OvGM2AP purified from insect cell culture medium was found to be glycosylated at asparagine 173 and lacked N-terminal signal peptide sequence; (5) the recombinant OvGM2AP discriminated serum samples of infected and uninfected individuals; (6) OvGM2AP competitively inhibits MUG degradation by recombinant β-hexosaminidase A but not MUGS, and could not hydrolyze the GM2 to GM3; (7) humoral immune responses to the recombinant OvGM2AP revealed a negative correlation with ivermectin treatment. Altogether, our findings suggest for the first time that OvGM2AP is an antigenic molecule whose biochemical and immunological features are important to gain more insight into our understanding of host-parasite relationship, as well as its function in parasite development at large.<br />SCOPUS: ar.j<br />info:eu-repo/semantics/published

Details

Database :
OAIster
Journal :
P L o S Neglected Tropical Diseases, 13 (7
Notes :
1 full-text file(s): application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1192449344
Document Type :
Electronic Resource