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dc.contributor.authorArroyo, Sara L.
dc.contributor.authorBasaras Ibarzabal, Miren ORCID
dc.contributor.authorArrese Arratibel, Miren Elixabete ORCID
dc.contributor.authorHernáez, Silvia
dc.contributor.authorAndia Ortiz, Daniel
dc.contributor.authorEsteban, Valetín
dc.contributor.authorGarcía Etxebarria, Koldo
dc.contributor.authorJugo Orrantia, Begoña Marina ORCID
dc.contributor.authorCisterna Cáncer, Ramón
dc.date.accessioned2013-05-28T09:59:20Z
dc.date.available2013-05-28T09:59:20Z
dc.date.issued2012
dc.identifier.citationVirology Journal 9 : (2012) // Article ID 258es
dc.identifier.issn1743-422X
dc.identifier.urihttp://hdl.handle.net/10810/10155
dc.description.abstractBackground:Human papillomavirus (HPV) variants differ in their biological and chemical properties, and therefore, may present differences in pathogenicity. Most authors classified variants based on the phylogenetic analysis of L1 region. Nevertheless, recombination in HPV samples is becoming a usual finding and thus, characterizing genetic variability in other regions should be essential. Objectives:We aimed to characterize the genetic variability of HPV 18 in 5 genomic regions: E6, E7, E4, L1 and the Upstream Regulatory Region (URR), working with both single infection and multiple HPV infection samples. Furthermore, we aimed to assess the prevalence of HPV 18 variants in our region and look for possible existence of recombination as well as analyze the relationship between these variants and the type of lesion. Methods: From 2007 to 2010, Clinical Microbiology and Infection Control Department analyzed 44 samples which were positive for HPV 18. Genetic variability was determined in PCR products and variants were assigned to European, Asian-amerindian or African lineage. Recombination and association of variants with different types of lesion was studied. Results: Genetic analysis of the regions revealed a total of 56 nucleotide variations. European, African and Asian-amerindian variants were found in 25/44 (56.8%), 10/44 (22.7%) and 5/44 (11.4%) samples, respectively. We detected the presence of recombinant variants in 2/44 (4.5%) cases. Samples taken from high-grade squamous intraepithelial lesions (H-SIL) only presented variants with specific-african substitutions. Conclusions: Multiple HPV infection, non-european HPV variants prevalence and existence of recombination are considered risk factors for HPV persistence and progression of intraepithelial abnormalities, and therefore, should be taken into consideration in order to help to design and optimize diagnostics protocols as well as improve epidemiologic studies. Our study is one of the few studies in Spain which analyses the genetic variability of HPV18 and we showed the importance of characterizing more than one genomic region in order to detect recombination and classify HPV variants properlyes
dc.language.isoenges
dc.publisherBioMed Centrales
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjecthuman papillomavirus infectiones
dc.subjectGenotype 18es
dc.subjectvariantses
dc.subjectrecombinationes
dc.subjectmultiple infectiones
dc.titleHuman Papillomavirus (HPV) genotype 18 variants in patients with clinical manifestations of HPV related infections in Bilbao, Spaines
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2012 Arroyo et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.es
dc.relation.publisherversionhttp://www.virologyj.com/content/9/1/258es
dc.identifier.doi10.1186/1743-422X-9-258
dc.departamentoesEspecialidades médico-quirúrgicases_ES
dc.departamentoeuMedikuntza eta kirurgia espezialitateakes_ES
dc.subject.categoriaINFECTIOUS DISEASES
dc.subject.categoriaVIROLOGY


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