s'authentifier
version française rss feed
Fiche concise
Inhibition of Chikungunya virus infection in cultured human muscle cells by furin inhibitors: impairment of the maturation of the E2 surface glycoprotein.
Ozden S., Lucas-Hourani M., Ceccaldi P.-E., Basak A., Valentine M., Benjannet S., Hamelin J., Jacob Y., Mamchaoui K., Mouly V. et al
The Journal of Biological Chemistry 283, 32 (2008) 21899-908 - http://hal-pasteur.archives-ouvertes.fr/pasteur-00330695
(18559340)
Inhibition of Chikungunya virus infection in cultured human muscle cells by furin inhibitors: impairment of the maturation of the E2 surface glycoprotein.
Simona Ozden1, Marianne Lucas-Hourani2, Pierre-Emmanuel Ceccaldi1, Ajoy Basak3, Menogh Valentine3, Suzanne Benjannet4, Josée Hamelin4, Yves Jacob5, Kamel Mamchaoui6, Vincent Mouly6, Philippe Desprès7, Antoine Gessain1, Gillian Butler-Browne6, 8, Michel Chrétien4, Frédéric Tangy2, Pierre-Olivier Vidalain2, Nabil G. Seidah () 4
1 :  Epidémiologie et Physiopathologie des Virus Oncogènes
Institut Pasteur de Paris – CNRS : URA3015
25-28 rue du Docteur Roux F-75724 Paris Cedex 15
France
2 :  Génomique Virale et Vaccination
Institut Pasteur de Paris – CNRS : URA3015
25-28 rue du Docteur Roux, F-75724 Paris Cedex 15
France
3 :  Regional Protein Chemistry Center
Health Research Institute
Chronic Disease Program Ottawa, Ontario
Canada
4 :  Biochemical Neuroendocrinology
Clinical Research Institute of Montreal
110 Pine Avenue West, Montreal, QC, Canada H2W 1R7
Canada
5 :  Génétique, Papillomavirus et Cancer Humain
Institut Pasteur de Paris
25-28 rue du Docteur Roux, F-75724 Paris Cedex 15
France
6 :  Groupe Myologie
INSERM : U787 – Université Pierre et Marie Curie [UPMC] - Paris VI – Institut de myologie
Faculte de Medecine Pitie-Salpetriere 105 Boulevard de L'Hopital 75634 PARIS
France
7 :  Interactions Moléculaires Flavivirus-Hôtes
Institut Pasteur de Paris
25-28 rue du Docteur Roux, F-75724 Paris Cedex 15
France
8 :  UMR S 787
Université Pierre et Marie Curie [UPMC] - Paris VI
France
Chikungunya virus (CHIKV) is a mosquito-transmitted Alphavirus that causes in humans an acute infection characterized by polyarthralgia, fever, myalgia, and headache. Since 2005 this virus has been responsible for an epidemic outbreak of unprecedented magnitude. By analogy with other alphaviruses, it is thought that cellular proteases are able to process the viral precursor protein E3E2 to produce the receptor-binding E2 protein that associates as a heterodimer with E1. Destabilization of the heterodimer by exposure to low pH allows viral fusion and infection. We show that among a large panel of proprotein convertases, membranous furin but also PC5B can process E3E2 from African CHIKV strains at the HRQRR(64) / ST site, whereas a CHIKV strain of Asian origin is cleaved at RRQRR(64) / SI by membranous and soluble furin, PC5A, PC5B, and PACE4 but not by PC7 or SKI-1. Using fluorogenic model peptides and recombinant convertases, we observed that the Asian strain E3E2 model peptide is cleaved most efficiently by furin and PC5A. This cleavage was also observed in CHIKV-infected cells and could be blocked by furin inhibitor decanoyl-RVKR-chloromethyl ketone. This inhibitor was compared with chloroquine for its ability to inhibit CHIKV spreading in myoblast cell cultures, a cell-type previously described as a natural target of this virus. Our results demonstrate the role of furin-like proteases in the processing of CHIKV particles and point out new approaches to inhibit this infection.
Sciences du Vivant/Biochimie, Biologie Moléculaire
Sciences du Vivant/Biologie cellulaire
Anglais
0021-9258

Articles dans des revues avec comité de lecture
10.1074/jbc.M802444200
The Journal of Biological Chemistry
internationale
08/08/2008
17/06/2008
283
32
21899-908

Alphavirus Infections – Amino Acid Chloromethyl Ketones – Antimalarials – Cell Line – Chikungunya virus – Chloroquine – Furin – Humans – Myoblasts – Proprotein Convertases – Protein Synthesis Inhibitors – Viral Envelope Proteins – Virus Internalization – Virus Replication