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Basic Characteristics of Mutations
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Mutation Site
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E138K |
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Mutation Site Sentence
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The mutations associated with resistance found in the NRTIs were: K103N with 6.36% (95% CI 3.5-10.4; N: 14/220), followed by K101E (1.8%; 95% CI 0.49-4.5; N 4/220), V106M (0.9%; 95% CI 0.11-3.24; N: 2/220) and G190E (0.9%; 95% CI 0.11-3.24; N: 2/220). The presence of E138A/K was also detected, 6.8% (95% CI 3.86-10.99). |
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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
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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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Y |
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Treatment
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NRTIs |
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Location
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Chile |
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Literature Information
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PMID
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33844760
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Title
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[Prevalence of transmitted drug resistance in HIV-infected treatment-naive patients in Chile]
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Author
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Palma P V,Leiva B I,Duran P M,Ramos V V,Sanchez C,Beltran B C,Afani S A,Ferrer C P
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Journal
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Revista medica de Chile
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Journal Info
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2020 Nov;148(11):1550-1557
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Abstract
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BACKGROUND: Transmitted drug resistance (TDR) occurs in patients with HIV infection who are not exposed to antiretroviral drugs but who are infected with a virus with mutations associated with resistance. AIM: To determine the prevalence of TDR and characterize HIV reverse transcriptase and protease mutation patterns. MATERIAL AND METHODS: HIV infected antiretroviral treatment-naive patients treated in three centers between 2014 and 2018 were studied. A genotyping study was carried out. The HIVdb Program (Stanford University) and the World Health Organization (WHO) TDR surveillance mutation list were used to register resistance-associated mutations. RESULTS: We enrolled 220 patients aged a median of 29 (interquartile range (IQR) 24-34) years, 99% men. Median CD4 count was 365 cells/muL (IQR 250-499 cells/muL) and median viral load was 39.150 copies/mL (IQR 9,270 -120,000). The overall prevalence of RTD was 10.45% (95% CI 6.7-15.2, N = 23/220). The higher frequency of TDR was against non-nucleoside reverse transcriptase inhibitors, reaching 9.0% (95% CI 5.6-13.6), followed by nucleoside reverse transcriptase inhibitors reaching 1.8% (95% CI 0.49-4.5) and protease inhibitors reaching 0.45% (95% CI 0.01-2.5). The mutations in reverse transcriptase were M41L, L210W, D67N, K70E, M184V, K103N (6.36%, 95% CI 3.5-10.4), G190A, E138A, K101E, and I84V in protease. CONCLUSIONS: These results should prompt a change in recommendations for starting antiretoviral therapy, especially in first-line regimens that include non-nucleoside reverse transcriptase inhibitors.
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Sequence Data
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-
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