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1.
J Infect Dis ; 184(8): 998-1006, 2001 Oct 15.
Article in English | MEDLINE | ID: mdl-11574914

ABSTRACT

Phylogenetic analysis of the reverse transcriptase (RT) and protease of 117 published complete human immunodeficiency virus (HIV) type 1 genome sequences demonstrated that these genes cluster into distinct subtypes. There was a slightly higher proportion of informative sites in the RT (40.4%) than in the protease (34.8%; P= .03). Although most variation between subtypes was due to synonymous nucleotide substitutions, several subtype-specific amino acid patterns were observed. In the protease, the subtype-specific variants included 7 positions associated with drug resistance. Variants at positions 10, 20, 36, and 82 were more common in non-B isolates, whereas variants at positions 63, 77, and 93 were more common in subtype B isolates. In the RT, the subtype-specific mutations did not include positions associated with anti-retroviral drug resistance. RT and protease sequences from 2246 HIV-infected persons in northern California were also examined: 99.4% of the sequences clustered with subtype B, whereas 0.6% clustered with subtype A, C, or D.


Subject(s)
HIV Protease/genetics , HIV Reverse Transcriptase/genetics , HIV-1/genetics , Mutation , Amino Acid Sequence , Genome, Viral , Humans , North Carolina , Phylogeny , Sequence Alignment , Sequence Homology, Amino Acid
2.
Nucleic Acids Res ; 29(1): 296-9, 2001 Jan 01.
Article in English | MEDLINE | ID: mdl-11125118

ABSTRACT

The HIV Reverse Transcriptase and Protease Sequence Database is an on-line relational database that catalogs evolutionary and drug-related sequence variation in the human immunodeficiency virus (HIV) reverse transcriptase (RT) and protease enzymes, the molecular targets of anti-HIV therapy (http://hivdb.stanford.edu). The database contains a compilation of nearly all published HIV RT and protease sequences, including submissions from International Collaboration databases and sequences published in journal articles. Sequences are linked to data about the source of the sequence sample and the antiretroviral drug treatment history of the individual from whom the isolate was obtained. During the past year 3500 sequences have been added and the data model has been expanded to include drug susceptibility data on sequenced isolates. Database content has also been integrated with didactic text and the output of two sequence analysis programs.


Subject(s)
Databases, Factual , HIV Protease/genetics , HIV Reverse Transcriptase/genetics , Amino Acid Sequence , Anti-HIV Agents/therapeutic use , HIV Infections/drug therapy , HIV Infections/virology , Humans , Information Storage and Retrieval , Internet , Molecular Sequence Data , Sequence Alignment
3.
J Virol Methods ; 86(2): 143-53, 2000 May.
Article in English | MEDLINE | ID: mdl-10785289

ABSTRACT

The reproducibility of population-based human immunodeficiency virus type 1 (HIV-1) protease and reverse transcriptase (RT) sequencing was assessed using replicate aliquots of cryopreserved plasma samples obtained from seven heavily treated HIV-1-infected individuals. The sequence of each sample replicate was compared with the consensus sequence for that sample and 99.4% of 35128 amino acids were found to be concordant with the sample consensus. Partial discordances were present at 0.5% of positions and complete discordances were present at <0.1% of positions. To assess the reproducibility at detecting mutations (defined here as differences from the subtype B consensus sequence), the proportion of sequences having a mutation when at least two sequences from that sample had the same mutation were examined. There was a median of 13 protease and 18 RT mutations per sample for a total of 3126 mutations; 95% of these mutations were detected. However, sequencing of multiple clones from two samples demonstrated that those mutations present in a minority of clones were often not detected by population-based sequencing. These results suggest that HIV-1 protease and RT sequencing of circulating plasma virus is highly reproducible but that the sensitivity at detecting mutations may be low if those mutations are present as minor variants.


Subject(s)
Anti-HIV Agents/therapeutic use , HIV Infections/drug therapy , HIV Infections/virology , HIV Protease/genetics , HIV Reverse Transcriptase/genetics , HIV-1/genetics , Anti-HIV Agents/pharmacology , Base Sequence , Cloning, Molecular , Drug Resistance, Microbial/genetics , Drug Resistance, Multiple/genetics , Drug Therapy, Combination , HIV Infections/blood , HIV-1/drug effects , HIV-1/enzymology , Humans , Mutation , RNA, Viral/blood , Reproducibility of Results , Reverse Transcriptase Inhibitors/pharmacology , Reverse Transcriptase Inhibitors/therapeutic use , Sensitivity and Specificity , Sequence Analysis, DNA
4.
Nucleic Acids Res ; 28(1): 346-8, 2000 Jan 01.
Article in English | MEDLINE | ID: mdl-10592270

ABSTRACT

The HIV RT and Protease Sequence Database is an online relational database that catalogs evolutionary and drug-related human immunodeficiency virus (HIV) reverse transcriptase (RT) and protease sequence variation (http://hivdb.stanford.edu). The database contains a compilation of nearly all published HIV RT and protease sequences including International Collaboration database submissions (e.g., GenBank) and sequences published in journal articles. Sequences are linked to data about the source of the sequence sample and the antiretroviral drug treatment history of the individual from whom the isolate was obtained. The database is curated and sequences are annotated with data from >230 literature references. Users can retrieve additional data and view alignments of sequence sets meeting specific criteria (e.g., treatment history, subtype, presence of a particular mutation). A gene-specific sequence analysis program, new user-defined queries and nearly 2000 additional sequences were added in 1999.


Subject(s)
Databases, Factual , HIV Protease/chemistry , HIV Reverse Transcriptase/chemistry , Drug Resistance, Microbial/genetics , HIV Protease/genetics , HIV Reverse Transcriptase/genetics , Internet , Mutation , User-Computer Interface
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