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Basic Characteristics of Mutations
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Mutation Site
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L210W |
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Mutation Site Sentence
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The main resistance mutations that we identified were D30N, M46I, I54LV, V82A, N88D, and L90M for PIs;M41L, K65R, D67N, K70R, M184V, L210W, and T215FY for NRTIs;and L100I, K103N, and G190A for NNRTIs. |
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Mutation Level
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Amino acid level |
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Mutation Type
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Nonsynonymous substitution |
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Gene/Protein/Region
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RT |
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Standardized Encoding Gene
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gag-pol:155348
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Genotype/Subtype
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HIV-1 |
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Viral Reference
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-
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Functional Impact and Mechanisms
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Disease
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HIV Infections
Acquired Immunodeficiency Syndrome
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Immune
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- |
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Target Gene
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-
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Clinical and Epidemiological Correlations
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Clinical Information
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- |
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Treatment
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NRTIs |
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Location
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Brazil |
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Literature Information
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PMID
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32218587
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Title
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Characterization of HIV-1 genetic diversity and antiretroviral resistance in the state of Maranhao, Northeast Brazil
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Author
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Leal E,Arrais CR,Barreiros M,Farias Rodrigues JK,Silva Sousa NP,Duarte Costa D,Rodrigo Pereira Santos FD,Dantas Silva A,Silva Viana AIE,Barros AK,Lima K
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Journal
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PloS one
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Journal Info
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2020 Mar 27;15(3):e0230878
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Abstract
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The HIV-1 epidemic in Brazil has been growing in northeast and north regions, particularly an increase in AIDS cases among the younger male population has been observed. This study aims to characterize the HIV-1 genetic diversity and to evaluate its antiretroviral resistance profile among individuals presenting virological failure in the state of Maranhao-Brazil. HIV-1 pol gene sequences from 633 patients on antiretroviral therapy were obtained from the Department of Surveillance, Prevention and Control of Sexually Transmitted Infections, HIV/AIDS and Viral Hepatitis of the Brazilian Ministry of Health. Phylogenetic and recombination analyses were performed to characterize viral genetic diversity. The presence of antiretroviral resistance mutations was assessed using the HIV Drug Resistance Database online platform of Stanford University. A predominance of subtype B (84.5%) was observed, followed by recombinant BF (9.5%), where more than half of the sequences were dispersed in 3 clusters. Antiretroviral resistance was detected in 74.1% of the sequences, and it was significantly higher for nucleoside analogue reverse-transcriptase inhibitors (NRTIs) than for non-nucleoside analogue reverse-transcriptase inhibitors (NNRTIs) and protease inhibitors (PIs). Inference of putative transmissions clusters identified 11 clusters with 22 query sequences (22/633, 3.5%). Thus, we conclude that continuous monitoring of the molecular epidemiology of HIV-1 is essential for prevention strategies, epidemic control, and treatment adequacy.
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Sequence Data
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-
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