Primary resistance to integrase strand transfer inhibitors in Spain using ultrasensitive HIV-1 genotyping


Por: Casadella, M, Santos, JR, Noguera-Julian, M, Mican-Rivera, R, Domingo, P, Antela, A, Portilla, J, Sanz, J, Montero-Alonso, M, Navarro, J, Masia, M, Valcarce-Pardeiro, N, Ocampo, A, Perez-Martinez, L, Pasquau, J, Vivancos, MJ, Imaz, A, Carmona-Oyaga, P, Munoz-Medina, L, Villar-Garcia, J, Barrufet, P and Paredes, R

Publicada: 1 dic 2020
Resumen:
Background: Transmission of resistance mutations to integrase strand transfer inhibitors (INSTIs) in HIV-infected patients may compromise the efficacy of first-Line antiretroviral regimens currently recommended worldwide. Continued surveillance of transmitted drug resistance (TDR) is thus warranted. Objectives: We evaluated the rates and effects on virological outcomes of TDR in a 96 week prospective multicentre cohort study of ART-naive HIV-1-infected subjects initiating INSTI-based ART in Spain between April 2015 and December 2016. Methods: Pre-ART plasma samples were genotyped for integrase, protease and reverse transcriptase resistance using Sanger population sequencing or MiSeq (TM) using a >= 20% mutant sensitivity cut-off. Those present at 1%-19% of the virus population were considered to be Low-frequency variants. Results: From a total of 214 available samples, 173 (80.8%), 210 (98.1%) and 214 (100.0%) were successfully amplified for integrase, reverse transcriptase and protease genes, respectively. Using a Sanger-Like cut-off, the overall prevalence of any TDR, INSTI-, NRTI-, NNRTI- and protease inhibitor (PI)-associated mutations was 13.1%, 1.7%, 3.8%, 7.1% and 0.9%, respectively. Only three (1.7%) subjects had INSTI TDR (R263K, E138K and G163R), while minority variants with integrase TDR were detected in 9.6% of subjects. There were no virological failures during 96 weeks of follow-up in subjects harbouring TDR as majority variants. Conclusions: Transmitted INSTI resistance remains rare in Spain and, to date, is not associated with virological failure to first-Line INSTI-based regimens.

Filiaciones:
:
 IrsiCaixa AIDS Res Inst, Badalona, Catalonia, Spain

:
 Lluita SIDA Fdn, Hosp Univ Germans Trias & Pujol, Badalona, Spain

:
 IrsiCaixa AIDS Res Inst, Badalona, Catalonia, Spain

Mican-Rivera, R:
 Univ Hosp La Paz, Madrid, Spain

Domingo, P:
 Hosp Santa Creu & Sant Pau, Infect Dis Unit, Barcelona, Spain

Antela, A:
 Santiago de Compostela Clin Univ Hosp, Infect Dis Unit, Santiago De Compostela, Spain

Portilla, J:
 Hosp Gen Univ Alicante, Alicante, Spain

Sanz, J:
 Univ Hosp La Princesa, Madrid, Spain

Montero-Alonso, M:
 La Fe Univ & Polytech Hosp, Infect Dis Unit, Valencia, Spain

Navarro, J:
 Hosp Univ Vall dHebron, Infect Dis Dept, Barcelona, Spain

Masia, M:
 Elche Univ, Gen Hosp, Infect Dis Unit, Elche, Spain

Valcarce-Pardeiro, N:
 Hosp Arquitecto Marcide, Infect Dis Unit, Ferrol, Spain

Ocampo, A:
 Hosp Alvaro Cunqueiro, HIV Unit, Vigo, Spain

Perez-Martinez, L:
 Hosp San Pedro CIBIR, Infect Dis Area, Logrono, Spain

Pasquau, J:
 Univ Hosp Virgen de las Nieves, Granada, Spain

Vivancos, MJ:
 Ramon & Cajal Hosp, Infect Dis Unit, Madrid, Spain

Imaz, A:
 Bellvitge Univ Hosp, HIV & STI Unit, Bellvitge Biomed Res Inst IDIBELL, Infect Dis Dept, Lhospitalet De Llobregat, Spain

Carmona-Oyaga, P:
 Donostia Univ Hosp, Infect Dis Unit, San Sebastian, Spain

Munoz-Medina, L:
 Univ Hosp San Cecilio, Granada, Spain

Villar-Garcia, J:
 Hosp del Mar IMIM, Infect Dis Dept, Barcelona, Spain

Barrufet, P:
 Mataro Hosp, Infect Dis Unit, Mataro, Spain

:
 IrsiCaixa AIDS Res Inst, Badalona, Catalonia, Spain

 Lluita SIDA Fdn, Hosp Univ Germans Trias & Pujol, Badalona, Spain
ISSN: 03057453





Journal of Antimicrobial Chemotherapy
Editorial
Oxford University Press, GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 75 Número: 12
Páginas: 3517-3524
WOS Id: 000593526100013
ID de PubMed: 32929472

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