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Basic Characteristics of Mutations
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|
Mutation Site
|
I54V |
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Mutation Site Sentence
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For protease inhibitors (PIs), the most common mutations observed were as follows: any 37 (10.1%); V82A 25 (6.8%); M46I/L 24 (6.6%); L76V 12 (3.3%); I54V 10 (2.7%); L90M 7 (1.9%); and I84V 6 (1.6%). |
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Mutation Level
|
Amino acid level |
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Mutation Type
|
Nonsynonymous substitution |
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Gene/Protein/Region
|
PR |
|
Standardized Encoding Gene
|
gag-pol
|
|
Genotype/Subtype
|
HIV-1 |
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Viral Reference
|
-
|
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Functional Impact and Mechanisms
|
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Disease
|
HIV Infections
|
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Immune
|
- |
|
Target Gene
|
-
|
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Clinical and Epidemiological Correlations
|
|
Clinical Information
|
- |
|
Treatment
|
PIs |
|
Location
|
Namibia |
|
Literature Information
|
|
PMID
|
30568984
|
|
Title
|
Human Immunodeficiency Virus-1 Drug Resistance Patterns Among Adult Patients Failing Second-Line Protease Inhibitor-Containing Regimens in Namibia, 2010-2015
|
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Author
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Sawadogo S,Shiningavamwe A,Roscoe C,Baughman AL,Negussie T,Mutandi G,Yang C,Hamunime N,Agolory S
|
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Journal
|
Open forum infectious diseases
|
|
Journal Info
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2018 Jan 12;5(2):ofy014
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Abstract
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Three hundred sixty-six adult patients in Namibia with second-line virologic failures were evaluated for human immunodeficiency virus drug-resistant (HIVDR) mutations. Less than half (41.5%) harbored >/=1 HIVDR mutations to standardized second-line antiretroviral therapy (ART) regimen. Optimizing adherence, viral load monitoring, and genotyping are critical to prevent emergence of resistance, as well as unnecessary switching to costly third-line ART regimens.
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|
Sequence Data
|
-
|