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HPV infection, risk factors and viral load among Mexican male college students The study has been approved by the Institutional Review Board from the National Institute of Public Health from Mexico (code 88-6417), and we obtained written informed consent from all participants. The paper has been seen and approved by all the authors, the manuscript has not been simultaneously submitted or published elsewhere. This work was supported by the CONACyT, Grant: SALUD-2004-C01-34 and CVU was the recipient of a master degree scholarship by CONACyT.

Abstract

Objectives:

To determine the prevalence of HPV and the risky sexual behaviors associated to it in a sample of male college students, taking into account genotype and viral load.

Methods:

From 2002 to 2003, male students from the Autonomous University of Morelos State completed a questionnaire and provided self-collected genital samples to detect and quantify HPV. We performed a bivariate and a multivariate logistic regression analysis to identify correlates associated with the infection and to assess the viral load as a function of the viral infecting type. The fragments of β-globin gene and L1 of HPV, were amplified, purified and cloned, to evaluate viral load.

Results:

Among 253 subjects, HPV prevalence was 19.4%, and HPV16 was the most common subtype. History of STIs (OR = 4.8; 95% CI 1.2–18.9), contraceptive pill use by female partner (OR = 2.6; 95% CI 1.1–6.3) and exchanging sex for money (OR = 4.9; 95% CI 1.2–20) were associated to the HPV infection. HPV16 viral load was 7.8 copies (HPV/beta-globin) compared to 0.9 copies for other HPV types.

Discussion:

HPV16 displayed the highest viral load, and it was the most prevalent. It was found that using contraceptive pills by female partners was associated with HPV infection.

HPV; Viral load; Contraceptive pills; Risky sexual behaviors; Male; Students


Introduction

HPV is the most common sexually transmitted infection (STI) around the world and the majority of the infections have an asymptomatic course; however, HPV chronic infection may cause cervical, penis or anal cancer.11. Muñoz N, Castellsagué X, de González AB, Gissmann L. Chapter 1: HPV in the etiology of human cancer. Vaccine. 2006;24 suppl 3. S3/1–S3/10. It has been proven that men can transmit the infection to their sexual partners; one study in women within three months of sexual debut and with only one sexual partner showed 28.5% of HPV infection after one year of follow up.22. Winer RL, Feng Q, Hughes JP, O'Reilly S, Kiviat NB, Koutsky LA. Risk of female human papillomavirus acquisition associated with first male sex partner. J Infect Dis. 2008;197:279–82. The number of male sexual partners was a major risk for HPV infection.

HPV prevalence among male college students from different countries ranged from 1.3% in Japan,33. Takahashi S, Shimizu T, Takeyama K, et al. Detection of human papillomavirus DNA on the external genitalia of healthy men and male patients with urethritis. Sex Transm Dis. 2003;30:629–33. 8.5% in Mexico,44. Sánchez-Alemán MA, Uribe-Salas F, Conde-González CJ. Human papillomavirus infection, a possible biological marker of sexual behavior among university students. Salud Publica Mex. 2002;44:442–7. 10.6% in South Korea,55. Shin HR, Franceschi S, Vaccarella S, et al. Prevalence and determinants of genital infection with papillomavirus, in female and male university students in Busan, South Korea. J Infect Dis. 2004;190:468–76. 25.8% and 33% in Washington State,66. Partridge JM, Hughes JP, Feng Q, et al. Genital human papillomavirus infection in men: incidence and risk factors in a cohort of university students. J Infect Dis. 2007;196:1128–36.,77. Weaver BA, Feng Q, Holmes KK, et al. Evaluation of genital sites and sampling techniques for detection of human papillomavirus DNA in men. J Infect Dis. 2004;189:677–85. 42.8% in Hawaii,88. Hernandez BY, McDuffie K, Goodman MT, et al. Comparison of physician and self-collected genital specimens for detection of human papillomavirus in men. J Clin Microbiol. 2006;44:513–7. to 84% in Chile.99. Guzmán P, Ili C, Rifo P, et al. Prevalence of human papillomavirus genital infection among male university students. Rev Med Chil. 2008;136:1381–9. Age at sexual debut, number of sexual partners and relationship with sexual workers have been associated with HPV infection among males.1010. Svare EI, Kjaer SK, Worm AM, Osterlind A, Meijer CJ, van den Brule AJ. Risk factors for genital HPV DNA in men resemble those found in women: a study of male attendees at a Danish STD clinic. Sex Transm Infect. 2002;78:215–8.1313. Vaccarella S, Lazcano-Ponce E, Castro-Garduño JA, et al. Prevalence and determinants of human papillomavirus infection in men attending vasectomy clinics in Mexico. Int J Cancer. 2006;119:1934–9. Circumcision and condom use have been reported as protective factors but with inconsistent results1010. Svare EI, Kjaer SK, Worm AM, Osterlind A, Meijer CJ, van den Brule AJ. Risk factors for genital HPV DNA in men resemble those found in women: a study of male attendees at a Danish STD clinic. Sex Transm Infect. 2002;78:215–8.,1111. Lajous M, Mueller N, Cruz-Valdéz A, et al. Determinants of prevalence, acquisition and persistence of human papillomavirus in healthy Mexican military men. Cancer Epidemiol Biomarkers Prev. 2005;14:1710–6.,1313. Vaccarella S, Lazcano-Ponce E, Castro-Garduño JA, et al. Prevalence and determinants of human papillomavirus infection in men attending vasectomy clinics in Mexico. Int J Cancer. 2006;119:1934–9.1616. Backes DM, Snijders PJ, Hudgens MG, et al. Sexual behaviour and less frequent bathing are associated with higher human papillomavirus incidence in a cohort study of uncircumcised Kenyan men. Sex Transm Infect. 2013;89:148–55.; this could be explained by the different anatomical sampling sites, the HPV detection method and the different population studied.1717. Partridge JM, Koutsky LA. Genital human papillomavirus infection in men. Lancet Infect Dis. 2006;6:21–31. Nevertheless, HPV risk factors have been insufficiently studied in young males. Korean male students with sexual debut at 18–19 years old had 4.4 times greater risk of HPV infection than students ≥20 years old at sexual debut.55. Shin HR, Franceschi S, Vaccarella S, et al. Prevalence and determinants of genital infection with papillomavirus, in female and male university students in Busan, South Korea. J Infect Dis. 2004;190:468–76. Students from the USA with past smoking displayed 1.6 times greater risk of HPV infection than students that had never smoked, and students with ≥ one sexual partner during the last four months had 2 times greater risk of HPV infection than students without sexual partners,66. Partridge JM, Hughes JP, Feng Q, et al. Genital human papillomavirus infection in men: incidence and risk factors in a cohort of university students. J Infect Dis. 2007;196:1128–36. and African young men with ≥ two female sexual partners during last year had 1.6 times greater risk of HPV infection.1616. Backes DM, Snijders PJ, Hudgens MG, et al. Sexual behaviour and less frequent bathing are associated with higher human papillomavirus incidence in a cohort study of uncircumcised Kenyan men. Sex Transm Infect. 2013;89:148–55.

These studies have evaluated demographic and sexual behavior characteristics; however, it is also necessary to study viral factors, i.e. the viral load, because it points to efficient viral transmission, as has been the case in relation to HIV and Herpes Simplex Virus (HSV).1818. Quinn TC, Wawer MJ, Sewankambo N, et al. Viral load and heterosexual transmission of human immunodeficiency virus type 1. Rakai Project Study Group. N Eng J Med. 2000;342:921–9.In fact, HPV viral load has been associated with high-grade cervical lesions.1919. Hart KW, Williams OM, Thelwell N, et al. Novel method for detection, typing, and quantification of human papillomaviruses in clinical samples. J Clin Microbiol. 2001;39:3204–12.2121. Peitsaro P, Johansson B, Syrjänen S. Integrated human papillomavirus type 16 is frequently found in cervical cancer precursors as demonstrated by a novel quantitative real-time PCR technique. J Clin Microbiol. 2002;40:886–91. Nevertheless, the relation between HPV infection and viral load in men is unknown. The present study evaluated the prevalence, risk factors for HPV infection, and viral load in Mexican male college students.

Methods

Study design

The first and second year male students of Medicine, Psychology and Pharmacy of the Autonomous University of Morelos State, at central Mexico, were invited to participate in August 2002, and male students of first year in August 2003. The project was approved by the bioethics committee from Instituto Nacional de Salud Publica, Mexico. The research team visited each classroom, explained the purpose of the study and invited all male students to participate. It was not the aim to obtain a representative sample of the student population. Afterwards, they signed a consent form, answered a self-applied questionnaire (demographic and sexual behaviors sections) and provided a self-collected genital sample obtained from their penis, glans and sulcus.

Each participant received verbal instructions from trained personnel, so that the sample was directly taken through vigorous rubbing with a sterile swab; if the subject was not circumcised, he had to proceed after retraction of the foreskin. The swab material collected was deposited in a tube with maintenance medium (Digene Specimen Collection Kit, USA), that was then transported immediately to the laboratory and frozen at −20°C until processing. DNA was extracted from the genital samples by Qiagen columns (QIAamp DNA Mini Kit). A fragment of the β-globin gene was first amplified by PCR to check the sample quality with GH20 and PC04 primers.2222. Bauer HM, Greer CE, Manos MM. Determination of genital human papillomavirus using consensus PCR. In: Herrington CS, McGee JOD, editors. Diagnostics molecular pathology: a practical approach. Oxford, UK: Oxford University Press; 1992. p. 132–52. The detection of HPV DNA by PCR was carried out with primers MY09/MY112222. Bauer HM, Greer CE, Manos MM. Determination of genital human papillomavirus using consensus PCR. In: Herrington CS, McGee JOD, editors. Diagnostics molecular pathology: a practical approach. Oxford, UK: Oxford University Press; 1992. p. 132–52. only for the β-globin-positive samples. After this stage, all HPV-negative samples were further analyzed with GP5/GP6 primers2323. de Roda Husman AM, Walboomers JM, van den Brule AJ, Meijer CJ, Snijders PJ. The use of general primers GP5 and GP6 elongated at their 3′ ends with adjacent highly conserved sequences improves human papillomavirus detection by PCR. J Genl Virol. 1995;76:1057–62. to optimize HPV detection.2424. Karlsen F, Kalantari M, Jenkins A, et al. Use of multiple PCR primer sets for optimal detection of human papillomavirus. J Clin Microbiol. 1996;34:2095–100. HPV-positive samples with either set of primers were typified by means of a linear array HPV genotyping test (Roche, Branchburg, NJ, USA) and classified as single or multiple infections.

Viral load quantification

The 268-bp fragments of the β-globin gene and the 450-bp fragments of the HPV L1 gene were amplified by PCR (GH20/PC04 and MY09/MY11 primers sets respectively) and purified by QIAquick Spin (QIAGEN, Germany). Subsequently, fragments were cloned separately using the pCR2.1-TOPO system (TOPO TA Cloning, Invitrogen, USA); finally, the plasmid DNA purification was performed by QIAprep Miniprep (QIAGEN, Germany). HPV plasmid fragment was 4381 bp with concentration of 260 ng/μL, the β-globin plasmid was 4199 bp and 210 ng/μL of concentration, considering the molecular weight average 650 g/bp, the stock concentration was 5.5 × 1010 copies/μL of HPV and 4.6 × 1010 copies/μL of β-globin. Six dilutions of each plasmid were made in triplicate for each run, ranging from 1:1000 to 1:100,000,000 to generate a standard curve of HPV from 55,120,000 to 551.2 copies/μL and a β-globin curve from 46,620,000 to 466.2 copies/μL. Determination of the viral load was performed by SYBR Green I real-time PCR (FastStart Master SYBR Green Rox, Roche, Germany). The reaction mixture contained 1× master mix, 1 μL of DNA and 0.3 pmol of primers GH20/PC04 (β-globin) and 0.5 pmol GP5/GP6 (HPV) to a final volume of 15 μL. Each sample was run in triplicate, if the coefficient of variation (CV) was higher than 5%, the sample was repeated.

Variable definitions

Sexually active students were persons with anal or vaginal intercourses. The variables “warts on the penis” and “previous STIs” were self-reported when filling out the questionnaire. In regard to “frequency of condom use”, the “not always” category was built with the following answers: “most of the time”, “half of the time” or “rarely”. In the case of the “always” category, it was confirmed that the participants answered yes to having used a condom at first sexual intercourse, at some other time in their life, and at last sexual intercourse. Age at sexual debut was stratified as ≤15 years old or ≥16 years old, in function to first quartile; the number of sexual partners was stratified as 1–2 sexual partners or ≥3 sexual partners during last year, in function to third quartile, both variables were not normally distributed. Contraceptive pills used by female partners during last sexual relationships were considered according to the response given by the participants.

Statistical analysis

The factors associated to HPV infection were evaluated using a logistic regression model; backward stepwise elimination method was employed in multivariate analysis, the final model being selected when all variables had p < 0.10. Viral load and continuous variables are presented as median and interquartile range (IQR) and the Mann–Whitney test was used to compare subgroups. The statistical analyses were performed using SPSS 15.0 (IBM Company), p-values ≤0.05 were considered as statistically significant.

Results

We contacted 450 students, 67.5% (304 students) sexually active, out of these 84.2% (256 students) provided genital samples. Three students were excluded because β-globin was not detected; thus, 253 students were included in the analyses. The median age of the participants was 21 years (IQR 20–23); on average, students had their sexual debut at 17 years old (IQR 15–18) with 18 year old (IQR 16–19) sexual partners. The students mentioned three (IQR 2–6.5) lifetime sexual partners and one (IQR 1–2) during last year. Forty percent of the students reported illegal drug consumption, 4.0% reported a history of STIs, 20% mentioned always using a condom, and more than 10% reported sexual relationship with sexual workers. Table 1 shows the demographic and sexual behavior characteristics.

Table 1
Demographic, clinical and sexual behavior characteristics in Mexican male college students.

Forty nine samples were detected as HPV-positive (34 with MY primers and 15 with GP primers), yielding an HPV prevalence of 19.4% (95% CI 14.5–24.2). High-risk genotypes prevalence was 17.4% (95% CI 12.7–22.1), low-risk genotypes 1.6%, (95% CI 0.0–3.1) and one sample remained undetermined. Table 2 shows the different HPV genotypes detected, multiple infection was detected in 3.2% of the students (seven students with two types and one student with three types). HPV16 was the most prevalent in the male college students analyzed (17.4%, 95% CI 12.7–22.1).

Table 2
Type of HPV infection in Mexican male college students.

The β-globin copies/μL among the samples ranged from 35,721 to 10,791,496 and the HPV copies/μL ranged from 14,348 to 81,376,686. The viral load was normalized (HPV copies/μL/β-globin copies/μL), the minimum value was 0.40 and the maximum value 37.6, with a median of 7.1 (IQR 2.1–11.3 HPV/β-globin). Single infection (median = 6.6; IQR, 2.6–11.5) in comparison with multiple infection (median = 10; IQR, 3.1–11.3) was not different (p = 0.894, Mann–Whitney test). However, the HPV16-positive samples had 7.8 HPV/β-globin (IQR, 4.5–11.4) higher than other HPV types which displayed 0.9 HPV/β-globin (IQR 0.5–10.6), (p= 0.034, Mann–Whitney test).

HPV prevalence was higher in students that consumed illegal drugs and in males with a history of genital warts, but without statistical significance. Nonetheless, half of the students with history of STIs presented HPV infection (p< 0.05). Students with sexual debut at 16 years or older had 2.3-fold higher risk to HPV infection than students with sexual debut at 15 years or younger (ORa = 2.3; 95% CI 0.96–5.6). Male students with later sexual debut and three or more sexual partners during last year, had 45.0% HPV infection and students with later sexual debut and two or less sexual partners during last year, had 18.0% HPV prevalence (p = 0.005). The subjects who had had three or more sexual partners during last year had twice the risk of acquiring an HPV infection (ORa = 2.1; 95% CI 0.9–5.0) than those with two sexual partners. Students who exchanged sex for money showed almost five times greater risk of having HPV, with statistical significance in multivariate analysis.

Male students, who had sex within one month after meeting a partner in comparison to those who reported a longer time to do so, had nearly twice the risk of becoming infected with HPV (ORa = 1.8; 95% CI 0.9–3.6). This subgroup had higher rate of intercourse with sexual workers (14.1% vs. 6.8%, p = 0.057), more casual sexual partners (47% vs. 32.9%, p = 0.019) and a greater number of sexual partners (median 4 vs. 3, p = 0.023, Mann Whitney). Finally, students whose partners had been using contraceptive pills during their last intercourse showed an HPV prevalence of 34.5%, i.e. a 2.6-fold higher risk than those students whose partners did not use contraceptive pills (p < 0.05). Table 3 shows HPV prevalence according to risky sexual behaviors, and univariate and multivariate analyses.

Table 3
Demographic and sexual behavior characteristics associated with HPV infection in Mexican male college students.

Discussion

HPV prevalence among Mexican male college students analyzed stands at midpoint in comparison to other university populations: Japan33. Takahashi S, Shimizu T, Takeyama K, et al. Detection of human papillomavirus DNA on the external genitalia of healthy men and male patients with urethritis. Sex Transm Dis. 2003;30:629–33. and South Korea55. Shin HR, Franceschi S, Vaccarella S, et al. Prevalence and determinants of genital infection with papillomavirus, in female and male university students in Busan, South Korea. J Infect Dis. 2004;190:468–76. displayed an HPV prevalence of 1.3% and 10.6%, respectively, while students from Chile99. Guzmán P, Ili C, Rifo P, et al. Prevalence of human papillomavirus genital infection among male university students. Rev Med Chil. 2008;136:1381–9. showed 83.6%. Studies from the US66. Partridge JM, Hughes JP, Feng Q, et al. Genital human papillomavirus infection in men: incidence and risk factors in a cohort of university students. J Infect Dis. 2007;196:1128–36.88. Hernandez BY, McDuffie K, Goodman MT, et al. Comparison of physician and self-collected genital specimens for detection of human papillomavirus in men. J Clin Microbiol. 2006;44:513–7. reported HPV prevalence between 25.8 and 42.8% in college students. However, the sampling sites and the diagnostic techniques were different; therefore the comparison between populations is difficult. HPV prevalence in Mexican male students analyzed was 19.4% and HPV16 was the prevailing detected type in the current study, similar to studies among young men in Kenya,2525. Smith JS, Moses S, Hudgens MG, et al. Human papillomavirus detection by penile site in young men from Kenya. Sex Transm Dis. 2007;34:928–34.Chile99. Guzmán P, Ili C, Rifo P, et al. Prevalence of human papillomavirus genital infection among male university students. Rev Med Chil. 2008;136:1381–9. and the US.66. Partridge JM, Hughes JP, Feng Q, et al. Genital human papillomavirus infection in men: incidence and risk factors in a cohort of university students. J Infect Dis. 2007;196:1128–36. Further analysis taking into account genotypes revealed that HPV16 (single- or multiple-infection) displayed the highest viral load in comparison to other viral types. Higher viral load has been related to increased HPV transmission2626. Bleeker MC, Hogewoning CJ, Berkhof J, et al. Concordance of specific human papillomavirus types in sex partners is more prevalent than would be expected by chance and is associated with increased viral loads. Clin Infect Dis. 2005;41:612–20. and higher HPV16 viral load has been associated with persistence of infection in women.2727. Fontaine J, Hankins C, Money D, et al. Human papillomavirus type 16 (HPV-16) viral load and persistence of HPV-16 infection in women infected or at risk for HIV. J Clin Virol. 2008;43:307–12. Therefore, the male college students analyzed in our study are more likely to transmit HPV16 to their sexual partners.

It was noteworthy that a later sexual debut as considered in this paper (≥16 years) was associated with an HPV infection, in contrast to another study in which early sexual debut (≤17 years) was associated with HPV.55. Shin HR, Franceschi S, Vaccarella S, et al. Prevalence and determinants of genital infection with papillomavirus, in female and male university students in Busan, South Korea. J Infect Dis. 2004;190:468–76. In a previous study with the same population, we documented that HSV-2 antibodies were associated with a later sexual debut (≥18 years),2828. Sánchez-Alemán MA, Uribe-Salas FJ, Lazcano-Ponce EC, García-Cisneros S, Eguiza-Fano S, Conde-Glez CJ. HSV-2 seroincidence among Mexican college students: the delay of sexual debut is not enough to avoid risky sexual behaviours and virus transmission. Sex Transm Infect. 2010;86:565–9. because we found a subgroup of students with delayed sexual debut and a high turnover of sexual partners. Similarly, in the current analysis, male students with later sexual debut and higher turnover of sexual partners during last year had higher HPV infection (45%). Men whose partners were using contraceptive pills during their last relationship had more than twice the risk of acquiring HPV infection. The use of this contraceptive method is considered as an approximation of the lack of use of condoms. In a Canadian contraception study, only 27% of female contraceptive users reported concurrent use of condoms.2929. Boroditsky R, Fisher WA, Sand M. The 1995 Canadian Contraception Study. J Obstet Gynaecol Can. 1996;18 suppl:S1–31. Mexican male students who reported contraceptive pill use and no condom use (simultaneously) had 54.5% of HPV, in comparison to students taking contraceptive pills and using condom who had 22.2% of HPV prevalence (p = 0.076). Moreover, Mexican female students from the same university who used the emergency contraceptive pill had twice the risk of acquiring HPV infection than non-users, because they had not used condoms.3030. Sánchez-Alemán MA, Uribe-Salas FJ, Lazcano-Ponce EC, Conde-Glez CJ. HPV incidence and risk factors among Mexican female college students. Sex Transm Dis. 2011;38:275–8. Male students with STIs history had almost five times the odds of getting HPV infection. Self-report of STIs could point to risky sexual practices,33. Takahashi S, Shimizu T, Takeyama K, et al. Detection of human papillomavirus DNA on the external genitalia of healthy men and male patients with urethritis. Sex Transm Dis. 2003;30:629–33. but in this sample of Mexican male students we have not detected any difference between students with and without self-report of STIs. This finding will need further assessment because the design of the study does not allow for a possible explanation. Exchanging sex for money and the number of sexual partners were the main risk factors for the acquisition of HPV infections, because both factors increase the likelihood of running into sexual partners with HPV infection. This association is consistent with other studies in young people.66. Partridge JM, Hughes JP, Feng Q, et al. Genital human papillomavirus infection in men: incidence and risk factors in a cohort of university students. J Infect Dis. 2007;196:1128–36.,1616. Backes DM, Snijders PJ, Hudgens MG, et al. Sexual behaviour and less frequent bathing are associated with higher human papillomavirus incidence in a cohort study of uncircumcised Kenyan men. Sex Transm Infect. 2013;89:148–55.,2525. Smith JS, Moses S, Hudgens MG, et al. Human papillomavirus detection by penile site in young men from Kenya. Sex Transm Dis. 2007;34:928–34.,3131. Johnson AM, Mercer CH, Beddows S, et al. Epidemiology of, and behavioural risk factors for, sexually transmitted human papillomavirus infection in men and women in Britain. Sex Transm Infect. 2012;88:212–7.

The current study does not represent all male students from the University, but could be indicative of the magnitude of HPV infection in that setting. Genital samples from young people are very difficult to obtain, but self-sampling allowed the HPV test to be performed. However, as not all college students participated, this could have generated a selection bias. We identified certain sexual behavior factors associated with HPV infection and we also showed that HPV16 was the most prevalent in the male college students analyzed and HPV16 was the genotype with the highest viral load. Longitudinal studies are needed to delve into the persistence and the elimination of the infection, to know more about HPV natural history in men, and to implement preventive measures in the student population, like condom promotion and vaccine use.

  • The study has been approved by the Institutional Review Board from the National Institute of Public Health from Mexico (code 88-6417), and we obtained written informed consent from all participants. The paper has been seen and approved by all the authors, the manuscript has not been simultaneously submitted or published elsewhere. This work was supported by the CONACyT, Grant: SALUD-2004-C01-34 and CVU was the recipient of a master degree scholarship by CONACyT.

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Publication Dates

  • Publication in this collection
    Jan-Feb 2014

History

  • Received
    11 Jan 2013
  • Accepted
    23 May 2013
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