Detection by PCR of human papillomavirus in Colombia: Comparison of GP5+/6+ and MY09/11 primer sets

The aims of this study were to determine the prevalence of HPV infection and evaluate the concordance and performance of two primer sets for detecting single and multiple viral infections. A total of 1810 Colombian women were enrolled in the study, and molecular, cytological and epidemiological anal...

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Autores:
Tipo de recurso:
Fecha de publicación:
2011
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/22493
Acceso en línea:
https://doi.org/10.1016/j.jviromet.2011.08.014
https://repository.urosario.edu.co/handle/10336/22493
Palabra clave:
Virus DNA
Adult
Aged
Article
Beta globin gene
Colombia
Controlled study
Cytology
Disease severity
Female
Gene
Gene dosage
Human
Human tissue
Major clinical study
Mixed infection
Nonhuman
Papillomavirus infection
Performance measurement system
Polymerase chain reaction
Prevalence
Priority journal
Screening test
Sensitivity and specificity
Virus detection
Virus load
Wart virus
Adolescent
Adult
Aged
Coinfection
Colombia
DNA Primers
Female
Humans
Middle Aged
Molecular Diagnostic Techniques
Papillomaviridae
Papillomavirus Infections
Polymerase Chain Reaction
Virology
Young Adult
Human papillomavirus
Colombia
GP5+/6+
Human papillomavirus (HPV)
Multiple infections
MY09/11
Rights
License
Abierto (Texto Completo)
Description
Summary:The aims of this study were to determine the prevalence of HPV infection and evaluate the concordance and performance of two primer sets for detecting single and multiple viral infections. A total of 1810 Colombian women were enrolled in the study, and molecular, cytological and epidemiological analyses were performed. Both concordance and performance of two different PCR amplification primer sets (GP5+/6+ and MY09/11) were assessed. The results showed that 60.2% of females with positive HPV DNA were infected by more than one viral type. The OR for multiple infections was 18.2 when using the MY09/11 primer set and 6.52 with the GP5+/6+ primer set. The results also showed an association between GP5+/6+ positivity and the severity of the disease regarding the cytological findings. It was also found that using a single primer set led to underestimating the prevalence for HPV infection. The simultaneous use of these primer sets is an important tool for the detection of HPV DNA, being equally relevant for identifying multiple infections and low viral DNA copies. This study highlights the importance of suitable assessment of HPV epidemiological profiles; screening programs must also be strengthened to broaden the coverage of the most vulnerable populations. © 2011 Elsevier B.V.