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1.
Mem. Inst. Oswaldo Cruz ; 112(10): 728-731, Oct. 2017. tab
Article in English | LILACS | ID: biblio-894837

ABSTRACT

The classification of human papillomavirus (HPV) intratypic lineages by complete genome sequencing is a determinant in understanding biological differences in association with this disease. In this work, we have characterised complete HPV genomes from southern Brazil. Fifteen cervicovaginal Pap smear negative samples previously categorised as HPV-positive were sequenced using ultradeep sequencing, and 18 complete genomes from 13 different HPV types were assembled. Phylogenetic and genetic distance analyses were performed to classify the HPV genomes into lineages and sublineages. This is the first report describing the distribution of HPV intratype lineages of high and low oncogenic risk in asymptomatic women from southern Brazil.


Subject(s)
Humans , Female , Adult , Papillomaviridae , Papillomaviridae/genetics , Vaginal Smears , DNA, Viral , Uterine Cervical Diseases/virology , Genome, Viral , Papillomavirus Infections/virology , Risk Factors
2.
Mem. Inst. Oswaldo Cruz ; 111(2): 120-127, Feb. 2016. tab
Article in English | LILACS | ID: lil-772616

ABSTRACT

This study investigated the rate of human papillomavirus (HPV) persistence, associated risk factors, and predictors of cytological alteration outcomes in a cohort of human immunodeficiency virus-infected pregnant women over an 18-month period. HPV was typed through L1 gene sequencing in cervical smears collected during gestation and at 12 months after delivery. Outcomes were defined as nonpersistence (clearance of the HPV in the 2nd sample), re-infection (detection of different types of HPV in the 2 samples), and type-specific HPV persistence (the same HPV type found in both samples). An unfavourable cytological outcome was considered when the second exam showed progression to squamous intraepithelial lesion or high squamous intraepithelial lesion. Ninety patients were studied. HPV DNA persistence occurred in 50% of the cases composed of type-specific persistence (30%) or re-infection (20%). A low CD4+T-cell count at entry was a risk factor for type-specific, re-infection, or HPV DNA persistence. The odds ratio (OR) was almost three times higher in the type-specific group when compared with the re-infection group (OR = 2.8; 95% confidence interval: 0.43-22.79). Our findings show that bonafide (type-specific) HPV persistence is a stronger predictor for the development of cytological abnormalities, highlighting the need for HPV typing as opposed to HPV DNA testing in the clinical setting.


Subject(s)
Adult , Female , Humans , Pregnancy , Young Adult , DNA, Viral/classification , HIV , HIV Seropositivity/virology , Papillomaviridae/isolation & purification , Papillomavirus Infections/diagnosis , Pregnancy Complications, Infectious/virology , Squamous Intraepithelial Lesions of the Cervix/diagnosis , Chronic Disease , Coinfection , Cytopathogenic Effect, Viral , DNA, Viral/isolation & purification , HIV , Longitudinal Studies , Molecular Typing/methods , Phylogeny , Predictive Value of Tests , Prospective Studies , Papillomaviridae/classification , Papillomavirus Infections/virology , Recurrence , Risk Factors , Reproductive Tract Infections/virology , Socioeconomic Factors
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