Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/119393
Título: Nationwide study of drug resistance mutations in hiv-1 infected individuals under antiretroviral therapy in Brazil
Autor: Santos-Pereira, Ana
Triunfante, Vera
Araújo, Pedro M.M.
Martins, Joana
Soares, Helena
Poveda, Eva
Souto, Bernardino
Osório, Nuno S.
Palavras-chave: Antiretroviral treatment failure
Brazilian cohort study
Drug resistance mutations
HIV-1
K65R
Tenofovir
Catalysis
Molecular Biology
Spectroscopy
Computer Science Applications
Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry
SDG 3 - Good Health and Well-being
Data: 2-Mai-2021
Resumo: The success of antiretroviral treatment (ART) is threatened by the emergence of drug resistance mutations (DRM). Since Brazil presents the largest number of people living with HIV (PLWH) in South America we aimed at understanding the dynamics of DRM in this country. We analyzed a total of 20,226 HIV-1 sequences collected from PLWH undergoing ART between 2008– 2017. Results show a mild decline of DRM over the years but an increase of the K65R reverse tran-scriptase mutation from 2.23% to 12.11%. This increase gradually occurred following alterations in the ART regimens replacing zidovudine (AZT) with tenofovir (TDF). PLWH harboring the K65R had significantly higher viral loads than those without this mutation (p < 0.001). Among the two most prevalent HIV-1 subtypes (B and C) there was a significant (p < 0.001) association of K65R with subtype C (11.26%) when compared with subtype B (9.27%). Nonetheless, evidence for K65R transmission in Brazil was found both for C and B subtypes. Additionally, artificial neural network-based immunoinformatic predictions suggest that K65R could enhance viral recognition by HLA-B27 that has relatively low prevalence in the Brazilian population. Overall, the results suggest that tenofovir-based regimens need to be carefully monitored particularly in settings with subtype C and specific HLA profiles.
Descrição: Funding: This work has been funded by Portuguese National funds, through the Foundation for Science and Technology (FCT) (project UIDB/50026/2020 and UIDP/50026/2020; by the projects NORTE-01-0145-FEDER-000013 and NORTE-01-0145-FEDER-000023, supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF) and by Gilead Génese PGG/009/2017. ASP and PMMA were funded by FCT PhD scholarships PD/BD/127827/2016, and PDE/BDE/113599/2015, respectively.
Peer review: yes
URI: http://hdl.handle.net/10362/119393
DOI: https://doi.org/10.3390/ijms22105304
ISSN: 1661-6596
Aparece nas colecções:NMS: CEDOC - Artigos em revista internacional com arbitragem científica

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