TY - JOUR
T1 - Oral transmission of primate lentiviruses
AU - Ruprecht, Ruth M.
AU - Baba, Timothy W.
AU - Liska, Vladimir
AU - Ray, Nancy B.
AU - Martin, Louis N.
AU - Murphey-Corb, Michael
AU - Rizvi, Tahir A.
AU - Bernacky, Bruce J.
AU - Keeling, Michale E.
AU - McClure, Harold M.
AU - Andersen, Janet
N1 - Funding Information:
Grant support: NIH (AI-24845, AI-32330, AI-34266, and AI-35533 to R.M.R.; AI-15119 to L.N.M.; AI-15093 and AI-35550 to M.M.-C.; AI-38855 to J.A.; and AI-01327 to T.W.B.); Center for AIDS Research Core grant IP30 28691 (awarded to the Dana-Farber Cancer Institute as support for the Institute’s AIDS research efforts) and RR-00164 and RR-00165, providing base support for the Tulane Regional Primate Research Center and the Yerkes Regional Primate Research Center, respectively.
PY - 1999
Y1 - 1999
N2 - Oral transmission of human immunodeficiency virus type 1 (HIV-1) is well documented in children who become infected postnatally through breast milk. In contrast, epidemiologic surveys have yielded conflicting data regarding oral HIV-1 transmission among adults, even though case reports have described seroconversion and the development of AIDS in adults whose only risk was oral-genital contact. To study oral virus transmission in primate models, we exposed rhesus macaques of various ages to cell-free simian immunodeficiency virus (SIV), including uncloned and molecularly cloned viruses. In neonates, viremia and AIDS developed after nontraumatic oral exposure to several SIV strains. Furthermore, chimeric simian human immunodeficiency viruses containing the HIV-1 envelope can also cross intact upper gastrointestinal mucosal surfaces in neonates. In adult macaques, infection and AIDS have resulted from well-controlled, nontraumatic, experimental oral exposure to different strains of SIV. These findings have implications for the risks of HIV-1 transmission during oral-genital contact.
AB - Oral transmission of human immunodeficiency virus type 1 (HIV-1) is well documented in children who become infected postnatally through breast milk. In contrast, epidemiologic surveys have yielded conflicting data regarding oral HIV-1 transmission among adults, even though case reports have described seroconversion and the development of AIDS in adults whose only risk was oral-genital contact. To study oral virus transmission in primate models, we exposed rhesus macaques of various ages to cell-free simian immunodeficiency virus (SIV), including uncloned and molecularly cloned viruses. In neonates, viremia and AIDS developed after nontraumatic oral exposure to several SIV strains. Furthermore, chimeric simian human immunodeficiency viruses containing the HIV-1 envelope can also cross intact upper gastrointestinal mucosal surfaces in neonates. In adult macaques, infection and AIDS have resulted from well-controlled, nontraumatic, experimental oral exposure to different strains of SIV. These findings have implications for the risks of HIV-1 transmission during oral-genital contact.
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U2 - 10.1086/314794
DO - 10.1086/314794
M3 - Article
C2 - 10099108
AN - SCOPUS:0032953965
SN - 0022-1899
VL - 179
SP - S408-S412
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - SUPPL. 3
ER -