Presence of Intact vpu and nef genes in nonpathogenic SHIV is essential for acquisition of pathogenicity of this virus by serial passage in macaques.
Virology
; 295(1): 133-46, 2002 Mar 30.
Article
en En
| MEDLINE
| ID: mdl-12033772
ABSTRACT
Use of the macaque model of human immunodeficiency virus (HIV) pathogenesis has shown that the accessory genes nef and vpu are important in the pathogenicity of simian immunodeficiency virus (SIV) and simian-human immunodeficiency virus (SHIV). We examined the ability of two nonpathogenic SHIVs, SHIV(PPC) and DeltavpuDeltanefSHIV(PPC), to gain pathogenicity by rapid serial passage in macaques. In this study, each virus was passaged by blood intravenously four times at 4-week intervals in macaques. Animals were monitored for 40 weeks for levels of CD4 T cells and quantitative measures of virus infection. DeltavpuDeltanefSHIV(PPC) maintained a limited phase of productive replication in the four animals, with no loss of CD4(+) T cells, whereas SHIV(PPC) became more pathogenic in later passages, judging by plasma viral load and viral mRNA in lymph nodes, infectious peripheral blood mononuclear cells and CD4(+) T cell loss. The nef, LTR, and env of the SHIV(PPC) viruses underwent numerous mutations, compared to DeltavpuDeltanefSHIV(PPC). This study confirms the seminal role that nef, LTR, and vpu could play in regulation of pathogenesis of HIV infection.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Genes nef
/
Genes vpu
/
Síndrome de Inmunodeficiencia Adquirida
/
VIH-1
/
Virus de la Inmunodeficiencia de los Simios
/
Virus Reordenados
Límite:
Animals
/
Humans
Idioma:
En
Revista:
Virology
Año:
2002
Tipo del documento:
Article
País de afiliación:
Estados Unidos