J. Virol., 07 1996, 4474-4483, Vol 70, No. 7
Copyright © 1996, American Society for Microbiology

Characterization of human immunodeficiency virus type 1 p17 matrix protein motifs associated with mother-to-child transmission

R Narwa, P Roques, C Courpotin, F Parnet-Mathieu, F Boussin, A Roane, D Marce, G Lasfargues and D Dormont
Service de Neurovirologie, Departement de Recherche Medicale, Direction des Sciences du Vivant, Service de Sante des Armees, Commissariat a l'Energie Atomique, France.

In order to determine if viral selection occurs during mother-to-child transmission of human immunodeficiency virus type 1 (HIV-1), we used a direct solid-phase sequencing method to sequence the p17 matrix protein- encoding regions of viral isolates from 12 HIV-1-infected mother-and- child pairs, 4 infected infants, 4 transmitting mothers, and 22 nontransmitting mothers and compared the sequences. The blood samples were collected during the delivery period for the mothers and during the first month of life for most of the children. The p17 nucleic sequences were distributed among several clades corresponding to the HIV-1 A, B, and G subtypes. At the amino acid level, no significant differences within the known p17 functional regions were observed among the subtypes. Statistical analyses could be performed with the B subtype. Within the major p17 antibody binding site, a constant KIEEEQN motif (amino acids 103 to 109) was found in all mother-and-child isolates from the B subtype. On the other hand, 9 of 17 nontransmitting mother isolates were variable in this 103 to 109 region. Thus, this motif was significantly associated with the transmitting status (chi square, P = 0.0034). A valine residue at position 104 was significantly associated with the nontransmitting phenotype (chi square, P = 0.014), suggesting that it has a protective role during vertical transmission. The C-terminal end of p17 was globally conserved among nontransmitting mother isolates (chi square, P = 0.0037). These results might improve the understanding of the pathogenesis of HIV-1 vertical transmission and might allow the screening of seropositive mothers by a rapid molecular or peptide test.

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