Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2017 Aug 8;17(1):531.
doi: 10.1186/s12885-017-3519-7.

High prevalence of co-infection between human papillomavirus (HPV) 51 and 52 in Mexican population

Affiliations

High prevalence of co-infection between human papillomavirus (HPV) 51 and 52 in Mexican population

Jazbet Gallegos-Bolaños et al. BMC Cancer. .

Abstract

Background: Human papillomavirus (HPV) is associated with the genesis of cervical carcinoma. The co-infection among HPV genotypes is frequent, but the clinical significance is controversial; in Mexico, the prevalence and pattern of co-infection differ depending on the geographic area of study. We analyzed the mono- and co-infection prevalence of multiple HPV genotypes, as well as preferential interactions among them in a Mexico City sample population.

Methods: This study was designed as a retrospective cohort study. Cervical cytology samples from 1163 women and 166 urethral scraping samples of men were analyzed between 2010 and 2012. The detection of HPV infection was performed using the hybrid capture and the genotyping was by PCR (HPV 6, 11, 16, 18, 30, 31, 33, 35, 45, 51, and 52).

Results: 36% of women were HPV-positive and the most prevalent genotypes were HPV 51, 52, 16, and 33 (42, 38, 37, and 34%, respectively). The prevalence of co-infection was higher (75.37%) than mono-infection in women HPV positives. All genotypes were co-infected with HPV 16, but the co-infection with 51-52 genotypes was the most frequent combination in all cases.

Conclusion: The co-infection was very common; each HPV genotype showed different preferences for co-infection with other genotypes, HPV 51-52 co-infection was the most frequent. The HPV 16, 33, 51 and 52 were the most prevalent and are a public health concern to the Mexican population.

Keywords: Co-infection; Genotypes; HPV; HPV 51; HPV 52; Human papillomavirus; Mexico; Prevalence.

PubMed Disclaimer

Conflict of interest statement

Ethics approval and consent to participate

The protocol was designed as a retrospective cohort study; we considered the results of 1329 individuals attended the laboratory clinical to practice the Papanicolaou test and scraping urethral between 2010 and 2012. We do not have informed consent because we conducted a retrospective study. We designed the protocol for the analysis of information according to the guidelines of the Declaration of Helsinki and to the Official Mexican Standard NOM-012-SSA3–2012 ensuring respect for all human beings and protect their health, their individual rights and confidentiality of personal information. This analysis protocol information was submitted for review and was approved by the ethics committee of the Laboratory Carpermor.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
The co-infection prevalence was higher than the mono-infection in HPV-positive patients. a The HPV-positive patients with mono- or co-infection in women and men. #p < 0.001 (mono- vs co-infection), *p = 0.009 (women vs men), z-test. b Frequency of patients with single or multiple HPV genotypes. Number of genotypes involved in co-infection was of two to eight different genotypes detected. *p = 0.005 (women vs men), z-test. c The infected patient prevalence with LR-HPV, HR-HPV or both. *p < 0.001 (LR-HPV vs HR-HPV/both); #p < 0.001 (HR-HPV vs both), z-test. d The prevalence of HPV 6, 11, 16, 18, 30, 31, 33, 35, 45, 51, 52, and other HPV genotypes was not sensitive to the method of genotyping (?). *p < 0.05, **p < 0.01 (women vs men); #p < 0.001 (prevalence within each gender), z-test
Fig. 2
Fig. 2
The frequency of low-risk HPV genotypes increased with the number of HPV genotypes in co-infection. Data represents the percentage of infected women with a) HPV 6 and b) HPV 11 in co-infection of 2, 3, 4, and 5 different genotypes *p < 0.05, **p < 0.01 (single- vs co-infection), z-test
Fig. 3
Fig. 3
The frequency of high-risk HPV genotypes increased with the number of HPV genotypes in co-infection. Data represents the percentage of infected women with a) HPV 16, b) 18, c) 30, d) 31, e) 33, f) 35, g) 51, and h) 52 in co-infection of 2, 3, 4, and 5 genotypes *p < 0.05, *p < 0.01, ***p < 0.001 (single- vs co-infection), z-test

Similar articles

Cited by

References

    1. Bosch FX, Manos MM, Munoz N, Sherman M, Jansen AM, Peto J, Schiffman MH, Moreno V, Kurman R, Shah KV. Prevalence of human papillomavirus in cervical cancer: a worldwide perspective. International biological study on cervical cancer (IBSCC) study group. J Natl Cancer Inst. 1995;87(11):796–802. doi: 10.1093/jnci/87.11.796. - DOI - PubMed
    1. zur Hausen H. Papillomaviruses and cancer: from basic studies to clinical application. Nat Rev Cancer. 2002;2(5):342–350. doi: 10.1038/nrc798. - DOI - PubMed
    1. Dahlstrom LA, Ylitalo N, Sundstrom K, Palmgren J, Ploner A, Eloranta S, Sanjeevi CB, Andersson S, Rohan T, Dillner J, et al. Prospective study of human papillomavirus and risk of cervical adenocarcinoma. Int J Cancer. 2010;127(8):1923–1930. doi: 10.1002/ijc.25408. - DOI - PMC - PubMed
    1. Cardoso JC, Calonje E. Cutaneous manifestations of human papillomaviruses: a review. Acta Dermatovenerol Alp Panonica Adriat. 2011;20(3):145–154. - PubMed
    1. You J. Papillomavirus interaction with cellular chromatin. Biochim Biophys Acta. 2010;1799(3-4):192–199. doi: 10.1016/j.bbagrm.2009.09.009. - DOI - PMC - PubMed

LinkOut - more resources