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Original Article
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Volume 343:1369-1377 November 9, 2000 Number 19
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Mucosal Shedding of Human Herpesvirus 8 in Men
John Pauk, M.D., M.P.H., Meei-Li Huang, Ph.D., Scott J. Brodie, D.V.M., Ph.D., Anna Wald, M.D., M.P.H., David M. Koelle, M.D., Timothy Schacker, M.D., Connie Celum, M.D., M.P.H., Stacy Selke, M.S., and Lawrence Corey, M.D.

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ABSTRACT

Background Epidemiologic studies suggest that human herpesvirus 8 (HHV-8) is sexually transmitted among men who have sex with men; however, the mode of transmission is unclear.

Methods To evaluate the patterns of shedding of HHV-8, we obtained mucosal-secretion samples from a cohort of HHV-8–seropositive men who had sex with men and had no clinical evidence of Kaposi's sarcoma. Quantitative polymerase-chain-reaction (PCR) assays, in situ PCR assays, and in situ RNA hybridization were used to identify potential sources of infectious HHV-8.

Results We detected HHV-8 in at least one mucosal sample from 30 of 50 men who were seropositive for HHV-8 (60 percent). Overall, HHV-8 was detected in 30 percent of oropharyngeal samples, as compared with 1 percent of anal and genital samples (P<0.001). In 39 percent of the HHV-8–seropositive men, HHV-8 was detected in saliva on more than 35 percent of the consecutive days on which samples were obtained. The median log titer of HHV-8 from the oral cavity was approximately 2.5 times as high as the titer at all other sites. In situ hybridization studies indicated that HHV-8 DNA and messenger RNA were present in oral epithelial cells. Among 92 men who had sex with men and who were seronegative for the human immunodeficiency virus (HIV), a history of sex with a partner who had Kaposi's sarcoma, deep kissing with an HIV-positive partner, and the use of amyl nitrite capsules ("poppers") or inhaled nitrites were independent risk factors for infection with HHV-8.

Conclusions Oral exposure to infectious saliva is a potential risk factor for the acquisition of HHV-8 among men who have sex with men. Hence, currently recommended safer sex practices may not protect against HHV-8 infection.


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From the Departments of Medicine (J.P., A.W., D.M.K., C.C., S.S., L.C.), Laboratory Medicine (M.-L.H., S.J.B., D.M.K., L.C.), and Epidemiology (A.W., S.S.), University of Washington, Seattle; the Department of Medicine, University of Minnesota, Minneapolis (T.S.); and the Program in Infectious Diseases, Fred Hutchinson Cancer Research Center, Seattle (L.C.).

Address reprint requests to Dr. Corey at the Program in Infectious Diseases, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave. N. (D3-100), Seattle, WA 98109.

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