| dc.contributor.author | Murray, MC | |
| dc.contributor.author | Embree, JE | |
| dc.contributor.author | Ramdahin, SG | |
| dc.contributor.author | Anzala Aggrey O. | |
| dc.contributor.author | Njenga, S | |
| dc.contributor.author | Plummer, FA | |
| dc.date.accessioned | 2013-04-26T13:09:43Z | |
| dc.date.available | 2013-04-26T13:09:43Z | |
| dc.date.issued | 2000 | |
| dc.identifier.citation | J Infect Dis. 2000 Feb;181(2):746-9 | en |
| dc.identifier.uri | http://www.ncbi.nlm.nih.gov/pubmed/10669368 | |
| dc.identifier.uri | http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/17181 | |
| dc.description.abstract | The objective of this study was to determine whether the maternal infecting human immunodeficiency virus (HIV) type 1 clade affects mother-to-child transmission frequency. Mothers in the mother-to-child HIV-1 transmission study in Nairobi, Kenya, were grouped by HIV-1 status of their first enrolled child: uninfected, perinatally infected, or postnatally infected. Restriction fragment length polymorphism (RFLP) analysis was used to determine HIV-1 viral clades of nested polymerase chain reaction products from HIV-1 protease or p24 genes. When inconclusive, sequencing determined the clade. Clade distributions within the groups were compared. The 3 groups displayed a uniform clade distribution. The predominant clades were A (59%) and D (20%). Clades B, C, F, mixed, and recombinant infections comprised the remainder (21%). No significant association was seen between clades A and D and either frequency or mode of vertical transmission. RFLP analysis revealed 2 clade B infections, 9 mixed, and 5 p24/protease recombinant infections in the study population. | en |
| dc.language.iso | en | en |
| dc.title | Effect of human immunodeficiency virus (HIV) type 1 viral genotype on mother-to-child transmission of HIV-1. | en |
| dc.type | Article | en |
| local.publisher | Department of Medical Microbiology, University of Manitoba, Winnipeg, Canada | en |
| local.publisher | Department of Medical Microbiology, University of Nairobi, Nairobi, Kenya | en |
| local.publisher | Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom | en |