Vol. 35 No. 1 (2018): February
Original Article

Genetic analysis of the mutations in HIV-1 infected population in Ecuador

Manuel González-González
Universidad de Guayaquil; Instituto Nacional de Investigación en Salud Pública “Leopoldo Izquieta Pérez”
Consuelo Correa-Sierra
Instituto Nacional de Investigación en Salud Pública “Leopoldo Izquieta Pérez”
Katherine Hermida-Álava
Instituto Nacional de Investigación en Salud Pública “Leopoldo Izquieta Pérez”
Ana Machado-Díaz
Instituto Nacional de Investigación en Salud Pública “Leopoldo Izquieta Pérez”
L. Fernando Gómez-Andrade
Centro Nacional de Referencia de Retrovirus, Hepatitis y otros Virus de Transmisión Sexual
Martha Castillo-Segovia
Instituto Nacional de Investigación en Salud Pública “Leopoldo Izquieta Pérez”
C. Lissette Pérez-Santos
Instituto de Medicina Tropical Pedro Kourí
Vivian Kourí-Cardelláciones
Instituto de Medicina Tropical Pedro Kourí

Published 2018-02-28

How to Cite

1.
González-González M, Correa-Sierra C, Hermida-Álava K, Machado-Díaz A, Gómez-Andrade LF, Castillo-Segovia M, Pérez-Santos CL, Kourí-Cardelláciones V. Genetic analysis of the mutations in HIV-1 infected population in Ecuador. Rev. Chilena. Infectol. [Internet]. 2018 Feb. 28 [cited 2025 Nov. 27];35(1). Available from: https://revinf.cl/index.php/revinf/article/view/22

Abstract

Background: The international recommendations of antiretroviral treatment include resistance tests to guide the treatment regimen in each patient, which is not available on a regular basis in Ecuador. Aim: To describe mutations that confer resistance to antiretrovirals in a population of Ecuadorian patients. Methods: Plasma samples from 101 HIV-1 patients with failure to antiretroviral therapy, divided into 15 children and 86 adults, were studied with the GS Junior (Roche) and the sequences were analyzed with the DeepChek program. Results: The most frequent mutations were M184V/I, K101E/P/H, K103N/S, D30N, M46L/I, I54L/M, V82T/F/A/S/L and L90M in adults and F77L, K103N/S, M46L/I, V82T/F/A/S/L and L90M in children. High resistance to non-nucleoside reverse transcriptase (RT) inhibitors in minority viral populations of adults and children (34.9% and 70%) was detected; in children both viral populations (majority and minority viral populations) (> 45%) were protease inhibitor resistant. Patients who had a greater number of therapeutic regimens had higher levels of resistance to antiretrovirals. Most of the samples were subtype B in the TR and protease region, and CRF25_cpx in integrase. Conclusions: Mutations and resistance to antiretrovirals are shown in a population of Ecuadorian patients with HIV-1. These results will make it possible to issue a warning to health authorities about the need for resistance studies.