Publications des scientifiques de l'IRD

Hongjaisee S., Braibant M., Barin F., Ngo-Giang-Huong Nicole, Sirirungsi W., Samleerat T. (2017). Effect of amino acid substitutions within the V3 region of HIV-1 CRF01_AE on interaction with CCR5-coreceptor. Aids Research and Human Retroviruses, 33 (9), p. 946-951. ISSN 0889-2229.

Titre du document
Effect of amino acid substitutions within the V3 region of HIV-1 CRF01_AE on interaction with CCR5-coreceptor
Année de publication
2017
Type de document
Article référencé dans le Web of Science WOS:000408495200010
Auteurs
Hongjaisee S., Braibant M., Barin F., Ngo-Giang-Huong Nicole, Sirirungsi W., Samleerat T.
Source
Aids Research and Human Retroviruses, 2017, 33 (9), p. 946-951 ISSN 0889-2229
Specific amino acids within the V3 loop of HIV-1 CRF01_AE envelope glycoprotein that are involved in the interaction with CCR5/CXCR4 coreceptors, are not well characterized. We generated V3 mutants using polymerase chain reaction (PCR)-based site-directed mutagenesis of HIV-1 CRF01_AE R5-env plasmids at specific positions. Mutant viruses were produced by env-pseudotyped virus assay, tested for coreceptor usage using U373.R5 and U373.X4 cells, and viral entry was assessed with luciferase activity measurement. All viruses, harboring either single or double mutations, used the CCR5 coreceptor. However, those containing a single substitution at positions 7, 11, 18, and 32 and those with mutations at positions 5/32 and 18/32 had reduced infectivity. Only virus with arginine substitution at position 11 seemed to be involved in CXCR4 coreceptor usage. Our results suggest that some V3 positions may be necessary for the binding to coreceptor, but not for the switch of coreceptor usage.
Plan de classement
Sciences fondamentales / Techniques d'analyse et de recherche [020] ; Entomologie médicale / Parasitologie / Virologie [052]
Localisation
Fonds IRD [F B010070953]
Identifiant IRD
fdi:010070953
Contact