Volume 14, Number 6—June 2008
CME ACTIVITY - Research
Transmission of Human Papillomavirus in Heterosexual Couples
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|EID||Hernandez BY, Wilkens LR, Zhu X, Thompson P, McDuffie K, Shvetsov YB, et al. Transmission of Human Papillomavirus in Heterosexual Couples. Emerg Infect Dis. 2008;14(6):888-894. https://dx.doi.org/10.3201/eid1406.0706162|
|AMA||Hernandez BY, Wilkens LR, Zhu X, et al. Transmission of Human Papillomavirus in Heterosexual Couples. Emerging Infectious Diseases. 2008;14(6):888-894. doi:10.3201/eid1406.0706162.|
|APA||Hernandez, B. Y., Wilkens, L. R., Zhu, X., Thompson, P., McDuffie, K., Shvetsov, Y. B....Goodman, M. T. (2008). Transmission of Human Papillomavirus in Heterosexual Couples. Emerging Infectious Diseases, 14(6), 888-894. https://dx.doi.org/10.3201/eid1406.0706162.|
We examined the transmission of human papillomavirus (HPV) in 25 heterosexual, monogamous couples (25 men, 25 women), followed up over an average of 7.5 months. A total of 53 heterosexual transmission events were observed among 16 couples (14 male-to-female and 39 female-to-male). Sexual transmission involved 13 different oncogenic and nononcogenic HPV types; 8% were vaccine-covered types transmitted between partners. The overall rate of HPV transmission from the penis to the cervix was 4.9/100 person-months, which was substantially lower than that from the cervix to the penis (17.4/100 person-months). Transmission between the hands and genitals, as well as apparent self-inoculation events (primarily in men), were also observed. Couples who transmitted HPV were more sexually active and used condoms less frequently. These results have implications for HPV prevention and control strategies, including the targeting of prophylactic vaccines.
Cervical cancer remains a major source of illness and death among women globally, and infection with oncogenic human papillomaviruses (HPVs) is its principal cause (1,2). Men are assumed to be the main reservoirs of genital HPV infection for women, although comparatively little is known about the natural history of HPV in men.
A limited number of cross-sectional and case-control studies have evaluated genotype-specific HPV concordance in male-female couples (3–7). There are, however, no empirical data on the heterosexual transmission of HPV. Our investigation evaluates the transmission of HPV in a cohort of male-female sexual partners.
The study was conducted at the University Health Services of the University of Hawaii at Manoa from February 2005 through November 2006. Promotional efforts included flyers and email invitations, which were part of larger ongoing studies of HPV. The study was approved by the Committee on Human Studies of the University of Hawaii. All study participants provided written informed consent. Eligible participants were at least 18 years of age, English-speaking, not currently pregnant, and in a monogamous relationship with the index partner.
Couples attended concurrent study visits at 2-month intervals. Trained clinicians collected exfoliated cell samples for HPV DNA detection. For men, separate genital specimens from the penis glans/corona, penis shaft, scrotum, and inner foreskin (uncircumcised men) were collected by using textured paper and a saline-moistened swab (8,9). Anal canal specimens were collected by using a saline-moistened swab. A cytobrush was used to collect oral specimens (buccal cavity, tongue). Specimens from the dominant hand (palm, fingertips, under the fingernails) were collected by using a saline-moistened swab. Participants self-collected first-catch urine samples (30 mL) at the clinic. Using latex gloves, men collected semen specimens at home during masturbation within 24 hours of each visit.
For women, a cervical cytology (Papanicolaou [Pap]) smear was collected, and a swab and cytobrush were used to consecutively sample the ectocervix and endocervix, including the transformation zone. The same methods used for collection of anal, oral, hand, and urine specimens from men were used for collection of specimens from women.
HPV DNA Testing and Genotyping
DNA was extracted from specimens by using commercial reagents (QIAGEN, Valencia, CA, USA). The PCR used PGMY09/PGMY11 primers to amplify a 450-bp region of the L1 HPV genome (10). Amplification of the human β-globin gene was included as an internal control for sample sufficiency. HPV-positive specimens were subsequently genotyped by using commercial reagents (Roche Molecular Systems Inc., Branchburg, NJ, USA) originating from a prototype line blot assay (11). The assay detects 37 different HPV types, including oncogenic/probable oncogenic types (HPV 16, 18, 26, 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73, 82, and IS39, a subtype of HPV 82), nononcogenic types (HPV 6, 11, 40, 42, 54, 61, 70, 72, 81, and CP6108, also known as candidate HPV 89), and types with undetermined risk status (HPV 55, 62, 64, 67, 69, 71, 83, and 84) (12,13). This PCR-based assay has demonstrated a high degree of sensitivity and reproducibility (14–16). HPV testing and genotyping procedures have been given in detail previously (9).
The main objective of the statistical analysis was to evaluate HPV transmission between partners. Each type-specific HPV infection was assigned a status of transmitted or not transmitted by time period and anatomic site. For some statistics, the penis anatomic site was further divided into foreskin, glans, shaft, and urine, which is a proxy for urethral infection. HPV in female urine, which has demonstrated type-specific concordance with cervical measurements (17), was considered to be a proxy for cervical and other lower genital tract infections. Therefore, cervix and urine were combined as 1 anatomic site. When there were >1 possible source sites, sites were grouped and evaluated as 1 transmission event. When there were >2 destination sites, each was counted as a separate transmission event.
Partner transmission was defined as the presence of a specific HPV genotype at an anatomic site in 1 partner and its absence in all sites of the other partner at a given visit, along with the presence of this HPV type in the unaffected partner at the subsequent visit. Auto-inoculation was defined as the presence of a particular HPV type at an anatomic site in 1 partner and its absence in all sites of the other partner at a given visit, and the presence of this HPV type in a different anatomic site in the affected partner at the subsequent visit. An event was defined as self-inoculation only after possible transmission from the partner was ruled out, i.e., when the partner was negative for the HPV genotype at prior and concurrent visits.
The rate of HPV transmission was calculated as the number of HPV type-specific transmission events divided by the number of person-months of exposure × 100 and expressed as the rate per 100 person-months. Exact confidence intervals (CIs) for transmission rates were calculated by assuming a Poisson distribution for the number of events (18). Person-months of exposure for each HPV infection by anatomic site were computed based on the period of time between successive visits. When HPV was detected at a given visit and HPV type was absent at the successive visit, the exposure period was estimated at half of the visit interval. Comparisons between couples by transmission status were made by using the t test, χ2 statistic, and linear rank statistic.
Thirty-eight couples (38 men, 38 women) were enrolled. Six couples left the study, including 2 whose relationships ended. The present analysis focuses on 25 couples with at least 2 visits. Couples were followed up at ≈2-month intervals over an average of 7.5 months.
The mean age was 28 years (range 18–59 years) for men and 26 years (range 18–57 years) for women. Participants comprised Caucasians (52%), Asians (8%), Pacific Islanders (6%), and persons of other single- or mixed-race backgrounds (34%). Couples were single/never married (48%), living together as married (32%), separated/divorced/widowed (12%), and married (8%). All participants indicated that the index partner was their only current sexual partner, and all reported vaginal intercourse with penile penetration during the follow-up period.
Five men were uncircumcised. At study entry, 1 woman had cervical low-grade squamous intraepithelial lesions, and 2 men had genital warts. Cervical atypia was diagnosed in 2 women during follow-up.
Overall, 957 (94%) of 1,015 specimens were adequate based on β-globin detection and were included in the present analyses. At study entry, 7 couples were HPV negative at all anatomic sites, 4 couples had 1 HPV-positive partner (3 were anal infections in the man), and 14 couples had both partners HPV positive. Of the 14 couples positive for HPV, 3 couples were positive for different HPV types, and 11 were positive for the same HPV type(s) at 1 or more anatomic sites (Table 1). All 11 HPV type-specific concordant infections involved the penis in the male partner and, with 2 exceptions, the cervix and/or urine in the female partner.
All transmission events occurred in couples with 1 or both partners positive for HPV at study entry. A total of 78 transmission events were observed in 16 couples, including 14 male-to-female, 39 female-to-male, 21 male auto-inoculation, and 4 female self-inoculation (Appendix Table [PDF - 33 KB - 2 pages]). Overall, 15 different genotypes were transmitted, including oncogenic types and nononcogenic/undetermined risk types. Partner transmission involved 13 genotypes. Forty-one (53%) of the 78 transmission events involved multiple potential sources of infection.
Male-to-female transmission was observed in 7 couples. All infections transmitted from male to female partners originated in the penis with or without additional involvement of the scrotum. In particular, the penis shaft was a predominant source of infection either alone or with other genital sites. The cervix and anus were the most frequent targets of transmission from the men. Transmission of oncogenic HPV 16 comprised 1 of the 5 genital-to-cervix events. Male genital to female hand transmission was observed in 3 couples (D, E, and G).
Female-to-male transmission was observed in 12 couples. Transmission from the cervix and/or urine to the male genitals comprised most female-to-male events. Within penis subsites, the glans was targeted more frequently than the shaft. The anus was frequently an additional source site along with the cervix/urine. In addition, the anus was the sole source of transmission to the male genitals on 4 occasions, of which 3 targeted the partner’s scrotum (couples A, B, and J). The penis and scrotum, respectively, were the most frequent targets of infection from women. There were 4 instances of transmission from the woman’s hands to the man’s genitals, including 1 case in which it was the sole source (couple I). Oncogenic HPV types 16 and 18 were transmitted in only 2 of the 39 female-to-male events.
Male self-inoculation was observed in 11 men, including 3 for whom no heterosexual transmission was observed during the entire period of follow-up. Sixteen events involved transmission between different genital sites, 2 involved anal-to-genital transmission, and 3 involved genital-to-hand transmission. Most genital-to-genital events involved transmission between penis subsites. In 3 instances, male self-inoculation immediately preceded transmission of HPV to female partners (couples A and B).
Female self-inoculation was observed in 4 females. All involved urine as a source site and 3 of these targeted the hands.
Heterosexual transmission of the same HPV genotype to >1 anatomic site (excluding penis subsites) was observed on 13 occasions. Eight of these cases involved transmission from the cervix/urine to the penis and scrotum.
Heterosexual transmission of multiple genotypes to the same anatomic site during the same period was observed in 5 instances (couples A, B, D, F, and G); the scrotum was the target site on 3 of these occasions. In 1 case, different genotypes in the cervix and urine were each transmitted to both the penis glans and shaft (couple K).
Transmission of some HPV types in preference to others was also observed. In couple L, after cervical infection with HPV 16 and 31 was detected at study entry, only HPV 31 was transmitted to the penis (glans, shaft) and scrotum. Alternatively, the female anus may have been the source of infection because HPV 31, not HPV 16, was present in the anus at baseline. In couple D, HPV 16, 59, and 62 were present in the penis shaft at baseline. Subsequently, only HPV 16 was transmitted to the woman’s cervix/urine and anus by the second visit.
A number of instances indicated apparent reinfection after viral clearance. In 1 couple (A), the woman’s anus was positive for HPV 39 infection at baseline and at visit 2. By visit 3, HPV 39 had been transmitted to the man’s scrotum, and the woman was negative for HPV 39. HPV 39 had been transmitted (presumably by auto-inoculation) to the penis by visit 4, and the infection remained through visit 5. By visit 6, or 9 months after initial clearance in the woman, HPV 39 had been transmitted to the woman’s anus.
Four cases of transmission to the female anus required >4 months of exposure to an infected partner. In 27 incident infections, no source of infection could be ascertained; 17 of these infections were in the male genitals.
The rates of HPV transmission by source site are shown in Table 2. Overall, the rate of transmission from the penis to the cervix/urine was 4.9 per 100 person-months of exposure (95% CI 1.6–10.0). By contrast, the overall rate of transmission from the cervix/urine to the penis was 17.4 per 100 person-months of exposure (95% CI 10.6–25.8). Transmission of oncogenic types to the male genitals was greater from the female urine alone than from the cervix alone. Transmission of HPV from the penis to the female anus was higher than that to the cervix; this was particularly true for transmission of oncogenic types to the anus (12.2 per 100 person-months of exposure, 95% CI 3.9–24.9). The highest rates of transmission were observed from the female anus to the male genitals (47.1 per 100 person-months of exposure, 95% CI 30.2–67.7), followed by cervix to the male genitals (27.8 per 100 person-months of exposure, 95% CI 19.0–38.3). In men, the rate of transmission by auto-inoculation was comparable to that of transmission from women. For example, the rate of transmission from the scrotum alone to the penis (6.0 per 100 person-months of exposure, 95% CI 1.2–14.5) was comparable to that of cervix only to penis (5.0 per 100 person-months of exposure, 95% CI 1.0–11.9).
All couples with genital-to-genital transmission reported vaginal intercourse during the period corresponding to the transmission event. Among the 5 couples with penis-to-anus transmission, 4 reported anal intercourse during the corresponding time period.
Table 3 compares baseline characteristics of couples with and without HPV transmission. Male partners in transmitting couples had had more sexual partners over their lifetime. Transmitting couples had more frequent sexual intercourse with one another, were more likely to have contact between the male’s mouth and the female’s anus, were more likely to use birth control injections and have withdrawal before ejaculation, and had fewer periods of abstinence. Over half of nontransmitting couples reported use of condoms 100% of the time during sexual intercourse within the previous 4 months, compared with only 3% of transmitting couples.
This study demonstrates that HPV is efficiently transmitted between sexual partners and that multiple transmission events can occur within a couple. The rates of genital transmission from women to men were substantially higher than from men to women. Greater rates of female-to-male transmission should imply higher HPV prevalence in men. Studies in men to date, including our own cohort, have reported male genital HPV prevalences at least as high as in women, with most reporting prevalences of at least 20% and up to 73% (9,19). The penis shaft was the primary source of transmission to the cervix; the cervix and urine were the primary sources of infection to male genitals.
Sexual transmission also involved the scrotum, the anus of women, and the hands of both sexes. The oral cavity and semen were not involved in transmission.
The anus of women was both a major source and target of heterosexual transmission. We observed consistency between penis-to-female anus transmission and reported anal intercourse during the corresponding period. We previously demonstrated high genotypic concordance between concurrent cervical-anal infections in women, which indicates possible common sources of infection (20).
Transmission through nonpenetrative sexual contact was demonstrated between the female anus and the scrotum, as well as the female hand and male genitals. The male anus was not a major source or a target of HPV transmission. However, 3 of the 4 couples with baseline infection in only 1 partner involved anal infection in men.
Male self-transmission frequently involved the scrotum, likely facilitated by passive contact between proximate genital sites. The scrotum may be an important reservoir of infection for penile infections that can subsequently be transmitted to partners. Hands may also serve as reservoirs of infection in both men and women. Auto-inoculation involving the hands may result from casual contact or masturbation.
To some extent, our study results suggest that HPV is relatively indiscriminate in its patterns of transmission. We observed the transmission of a given viral genotype to multiple anatomic sites in a partner and concurrent transmission of multiple genotypes to the same site.
Other observations suggest that HPV transmission is not entirely arbitrary and may reflect tissue or genotype differences or both. Rates of transmission of oncogenic types to the male genitals from the urine were higher than from the cervix. This may reflect differences in genotypes found in the vagina and vulva compared with those found in the cervix. All transmission events requiring extended periods of exposure involved the female anus target site.
A total of 15 genotypes were transmitted, including 13 which were transmitted through heterosexual means. HPV 16 and 18 and nononcogenic HPV 6 and 11, the 4 types included in the current quadrivalent vaccine, comprised <10% of transmitted types. Notably, we observed greater transmission of HPV 16 to the cervix than such transmission by other types, which underscores the possibility of selective transmission of some HPV types.
Compared with couples not experiencing HPV transmission, transmitting couples were more sexually active and were more likely to use certain nonbarrier forms of contraception. Few HPV-transmitting couples reported always using condoms during recent sexual activity, compared with over half of nontransmitting couples.
A major limitation of our study was the potential for misclassification of HPV transmission events. Variable detection of HPV could be due to natural fluctuation in viral levels or variable sampling of sites could confound the observation of viral transmission. For example, instances of apparent reinfection of sites may alternatively represent possible reactivation of latent infections.
Another potential source of misclassification was the lack of a priori knowledge of the time required for HPV to be acquired from an infected partner. Viral transmission could have occurred more frequently than the 2-month visit intervals used in the study, and transmission events could have been missed.
Another limitation of the study was the inclusion of couples who had already had sexual contact with one another; initial viral transmission was likely to have occurred before study entry. Indeed, nearly half of the couples had type-specific concordant infections at study entry, indicating previous transmission of HPV, which limited our ability to evaluate incident infections.
Because our study relied on self-reported sexual activity, it was subject to recall bias. Furthermore, although all persons reported monogamous relationships, some of the incident infections without a source, most of which involved the male genitals, could have been acquired through sexual activity with another partner. Despite these limitations, the present study included intensive follow-up of a well-characterized cohort, sampling of multiple genital and nongenital sites, and state-of-the-art HPV testing and genotyping methods.
The development of comprehensive HPV prevention and control strategies, which incorporate HPV vaccine usage and contraceptive practices, is impeded by lack of information on the risk and routes of sexual transmission between heterosexual partners and potential genotype-specific differences in transmission efficiency. The small size of the cohort and the diversity of genotypes precluded type-specific analysis of transmission.
This study contributes to a growing body of knowledge of HPV in men because we directly examined HPV transmission. However, study results are preliminary and need to be verified in larger cohorts. Future HPV transmission studies are critical to address major gaps in our knowledge of the natural history of this virus.
Dr Hernandez is an epidemiologist at the Cancer Research Center of Hawaii, University of Hawaii. Her research focuses on the molecular epidemiology of cancer including the role of infectious agents in the development and progression of cancer. She has investigated the epidemiology of HPV in both women and men.
We extend our gratitude to the staff of the University of Hawaii, Cancer Research Center of Hawaii, and the University of Hawaii University Health Services whose clinical staff conducted specimen collection for the study.
This project was supported in part by the Centers of Biomedical Research Excellence Program award P20 RR018727 from the National Center for Research Resources, and National Cancer Institute grant R01 CA077813.
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- Table 1. HPV status of couples at study entry
- Table 2. Rate of HPV transmission by source and target site in male-female couples
- Table 3. Characteristics of male-female couples by HPV transmission status
- Appendix Table. HPV transmission events in male-female couples by anatomic site* 33 KB
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Brenda Y. Hernandez, Cancer Research Center of Hawaii, University of Hawaii, 1236 Lauhala St, Honolulu, HI 96813, USA;
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