par Xong, H V;Vanhamme, Luc 
;Chamekh, Mostafa ;Chimfwembe, C E;Van Den Abbeele, J;Pays Deschutter, Annette ;Van Meirvenne, N;Hamers, Raymond ;De Baetselier, Patrick;Pays, Etienne
Référence Cell, 95, 6, page (839-846)
Publication Publié, 1998-12
;Chamekh, Mostafa ;Chimfwembe, C E;Van Den Abbeele, J;Pays Deschutter, Annette ;Van Meirvenne, N;Hamers, Raymond ;De Baetselier, Patrick;Pays, Etienne Référence Cell, 95, 6, page (839-846)
Publication Publié, 1998-12
Article révisé par les pairs
| Résumé : | Infectivity of Trypanosoma brucei rhodesiense to humans is due to its resistance to a lytic factor present in human serum. In the ETat 1 strain this character was associated with antigenic variation, since expression of the ETat 1.10 variant surface glycoprotein was required to generate resistant (R) clones. In addition, in this strain transcription of a gene termed SRA was detected in R clones only. We show that the ETat 1.10 expression site is the one selectively transcribed in R variants. This expression site contains SRA as an expression site-associated gene (ESAG) and is characterized by the deletion of several ESAGs. Transfection of SRA into T.b. brucei was sufficient to confer resistance to human serum, identifying this gene as one of those responsible for T.b. rhodesiense adaptation to humans. |
