TY - JOUR
T1 - Human Papillomavirus Infections in Cervical Samples From HIV-Positive Women
T2 - Evaluation of the Presence of the Nonavalent HPV Genotypes and Genetic Diversity
AU - Sias, Catia
AU - Guarrasi, Valerio
AU - Minosse, Claudia
AU - Lapa, Daniele
AU - Nonno, Franca Del
AU - Capobianchi, Maria Rosaria
AU - Garbuglia, Anna Rosa
AU - Del Porto, Paola
AU - Paci, Paola
N1 - Funding Information:
This work was supported by Ricerca Corrente Funding from the Italian Ministry of Health.
Publisher Copyright:
© Copyright © 2020 Sias, Guarrasi, Minosse, Lapa, Nonno, Capobianchi, Garbuglia, Del Porto and Paci.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/11/25
Y1 - 2020/11/25
N2 - Non-nonavalent vaccine (9v) Human papillomavirus (HPV) types have been shown to have high prevalence among HIV-positive women. Here, 1444 cervical samples were tested for HPV DNA positivity. Co-infections of the 9v HPV types with other HPV types were evaluated. The HPV81 L1 and L2 genes were used to investigate the genetic variability of antigenic epitopes. HPV-positive samples were genotyped using the HPVCLART2 assay. The L1 and L2 protein sequences were analyzed using a self-optimized prediction method to predict their secondary structure. Co-occurrence probabilities of the 9v HPV types were calculated. Non9v types represented 49% of the HPV infections; 31.2% of the non9v HPV types were among the low-grade squamous intraepithelial lesion samples, and 27.3% among the high-grade squamous intraepithelial lesion samples, and several genotypes were low risk. The co-occurrence of 9v HPV types with the other genotypes was not correlated with the filogenetic distance. HPV81 showed an amino-acid substitution within the BC loop (N75Q) and the FGb loop (T315N). In the L2 protein, all of the mutations were located outside antigenic sites. The weak cross-protection of the 9v types suggests the relevance of a sustainable and effective screening program, which should be implemented by HPV DNA testing that does not include only high-risk types.
AB - Non-nonavalent vaccine (9v) Human papillomavirus (HPV) types have been shown to have high prevalence among HIV-positive women. Here, 1444 cervical samples were tested for HPV DNA positivity. Co-infections of the 9v HPV types with other HPV types were evaluated. The HPV81 L1 and L2 genes were used to investigate the genetic variability of antigenic epitopes. HPV-positive samples were genotyped using the HPVCLART2 assay. The L1 and L2 protein sequences were analyzed using a self-optimized prediction method to predict their secondary structure. Co-occurrence probabilities of the 9v HPV types were calculated. Non9v types represented 49% of the HPV infections; 31.2% of the non9v HPV types were among the low-grade squamous intraepithelial lesion samples, and 27.3% among the high-grade squamous intraepithelial lesion samples, and several genotypes were low risk. The co-occurrence of 9v HPV types with the other genotypes was not correlated with the filogenetic distance. HPV81 showed an amino-acid substitution within the BC loop (N75Q) and the FGb loop (T315N). In the L2 protein, all of the mutations were located outside antigenic sites. The weak cross-protection of the 9v types suggests the relevance of a sustainable and effective screening program, which should be implemented by HPV DNA testing that does not include only high-risk types.
KW - genetic variability
KW - HPV mixed infection
KW - HPV vaccine
KW - Human papillomavirus
KW - intraepithelial lesions
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U2 - 10.3389/fmicb.2020.603657
DO - 10.3389/fmicb.2020.603657
M3 - Article
AN - SCOPUS:85097398562
VL - 11
SP - 1
EP - 14
JO - Frontiers in Microbiology
JF - Frontiers in Microbiology
SN - 1664-302X
M1 - 603657
ER -