Infectious Agents and Cancer

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Open Access Highly Access Research article

Human papillomavirus type 16 variants in cervical intraepithelial neoplasia and invasive carcinoma in San Luis Potosí City, Mexico

Rubén López-Revilla1*, Marco A Pineda1,3, Julio Ortiz-Valdez2, Mireya Sánchez-Garza1 and Lina Riego1

Author Affiliations

1 División de Biología Molecular, Instituto Potosino de Investigación Científica y Tecnológica, Camino a la Presa San José 2055, 78216 San Luis Potosí, SLP, Mexico

2 Clínica de Colposcopía, Jurisdicción Sanitaria 1, Secretaría de Salud de San Luis Potosí, Calzada de Guadalupe 530, 78339 San Luis Potosí, SLP, Mexico

3 M.C. Marco Antonio Pineda, Área de Ciencias Químico-Biológicas, Universidad del Noreste, Prol. Av. Hidalgo 6315, 89337 Tampico, Tams., Mexico

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Infectious Agents and Cancer 2009, 4:3 doi:10.1186/1750-9378-4-3

Published: 16 February 2009

Abstract

Background

In San Luis Potosí City cervical infection by human papillomavirus type 16 (HPV16) associated to dysplastic lesions is more prevalent in younger women. In this work HPV16 subtypes and variants associated to low-grade intraepithelial lesions (LSIL), high-grade intraepithelial lesions (HSIL) and invasive cervical cancer (ICC) of 38 women residing in San Luis Potosí City were identified by comparing their E6 open reading frame sequences.

Results

Three European (E) variants (E-P, n = 27; E-T350G, n = 7; E-C188G, n = 2) and one AA-a variant (n = 2) were identified among the 38 HPV16 sequences analyzed. E-P variant sequences contained 23 single nucleotide changes, two of which (A334G, A404T) had not been described before and allowed the phylogenetic separation from the other variants. E-P A334G sequences were the most prevalent (22 cases, 57.9%), followed by the E-P Ref prototype (8 cases, 21.1%) and E-P A404T (1 case, 2.6%) sequences. The HSIL + ICC fraction was 0.21 for the E-P A334G variants and 0.00 for the E-P Ref variants.

Conclusion

We conclude that in the women included in this study the HPV16 E subtype is 19 times more frequent than the AA subtype; that the circulating E variants are E-P (71.1%) > E-T350G (18.4%) > E-C188G (5.3%); that 71.0% of the E-P sequences carry the A334G single nucleotide change and appear to correspond to a HPV16 variant characteristic of San Luis Potosi City more oncogenic than the E-P Ref prototype.