Characterization of mother-infant HIV type 1 gag p17 sequences associated with perinatal transmission

Citation
T. Hahn et al., Characterization of mother-infant HIV type 1 gag p17 sequences associated with perinatal transmission, AIDS RES H, 15(10), 1999, pp. 875-888
Citations number
73
Categorie Soggetti
Immunology
Journal title
AIDS RESEARCH AND HUMAN RETROVIRUSES
ISSN journal
08892229 → ACNP
Volume
15
Issue
10
Year of publication
1999
Pages
875 - 888
Database
ISI
SICI code
0889-2229(19990701)15:10<875:COMHT1>2.0.ZU;2-M
Abstract
The gag p17 matrix sequences of human immunodeficiency virus type (HIV-1) f rom seven infected mother-infant pairs were analyzed after perinatal transm ission. The p17 matrix open reading frame was maintained in 143 of the 166 clones analyzed (86.2% frequency of intact p17 open reading frames), The fu nctional domains essential for p17 matrix function in HIV-1 replication, in cluding targeting of Gag to the plasma membrane, virus assembly and release , envelope glycoprotein incorporation into virus particle, virus entry, and localization of the virus preintegration complex to the nucleus of nondivi ding cells, were highly conserved in most of the sequences. In addition, ex amination of the three-dimensional structure of the p17 matrix protein in m other-infant isolates showed a high degree of conservation of amino acids r equired for correct folding and biological activity, Several amino acid mot ifs common to most of the mother-infant pairs sequences, including pair-spe cific signature sequences, were observed, There was a low degree of heterog eneity of gag p17 sequences within mothers, within infants, and between mot her-infant pairs, but the distances were greater between epidemiologically unlinked individuals. Phylogenetic analyses of 166 mother-infant pairs and 181 other p17 sequences available from HIV-1 databases revealed distinct cl usters for each mother-infant pair and for other p17 sequences. In conclusi on, these findings indicate that an intact and functional gag p17 matrix is maintained during maternal-fetal transmission and that several motifs in p 17 may be associated with perinatal transmission.