Sequence Variability in p6 gag Protein and gag/pol Coevolution in Human Immunodeficiency Type 1 Subtype F Genomes
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作者:
Rossi, Andres H.
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Hosp Pediat Juan P Garran, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, ArgentinaHosp Pediat Juan P Garran, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, Argentina
Rossi, Andres H.
[1
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Rocco, Carlos A.
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Hosp Pediat Juan P Garran, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, ArgentinaHosp Pediat Juan P Garran, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, Argentina
Rocco, Carlos A.
[1
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Mangano, Andrea
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Hosp Pediat Juan P Garran, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, ArgentinaHosp Pediat Juan P Garran, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, Argentina
Mangano, Andrea
[1
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Sen, Luisa
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Hosp Pediat Juan P Garran, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, ArgentinaHosp Pediat Juan P Garran, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, Argentina
Sen, Luisa
[1
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Aulicino, Paula C.
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Hosp Pediat Juan P Garran, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, ArgentinaHosp Pediat Juan P Garran, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, Argentina
Aulicino, Paula C.
[1
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机构:
[1] Hosp Pediat Juan P Garran, Lab Biol Celular & Retrovirus, CONICET, Buenos Aires, DF, Argentina
Polymorphisms occurring at the p6(gag) protein of HIV-1 have been previously found to have an impact on viral fitness and antiretroviral (ARV) resistance, mainly on subtype B genomes. We compared p6(gag) variability in a large group of 165 subtype F gag-pol sequences, with 36 subtype B sequences from the same study source, and identified sites of gag-pol coevolution under ARV selection pressure. Subtype-specific differences in the frequency of point mutations, insertions, and deletions previously associated with ARV resistance were found. Also, in our dataset of subtype F genomes a strong association between mutation P5L in the p1/p6 cleavage region of gag and the nelfinavir (NFV) resistance mutation N88D(PR) was found with no impact on the preference for any of the NFV resistance pathways.
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NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702
GORELICK, RJ
OTT, DE
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NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702
OTT, DE
SOWDER, RC
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NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702
SOWDER, RC
NIGIDA, SM
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NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702
NIGIDA, SM
HENDERSON, LE
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NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702
HENDERSON, LE
ARTHUR, LO
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NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702NCI,FREDERICK CANC RES & DEV CTR,PRI DYNCORP,AIDS VACCINE PROGRAM,FREDERICK,MD 21702