Human Papillomavirus Infections in Cervical Samples From HIV-Positive Women: Evaluation of the Presence of the Nonavalent HPV Genotypes and Genetic Diversity

被引:3
作者
Sias, Catia [1 ]
Guarrasi, Valerio [2 ]
Minosse, Claudia [1 ]
Lapa, Daniele [1 ]
Nonno, Franca Del [3 ]
Capobianchi, Maria Rosaria [1 ]
Garbuglia, Anna Rosa [1 ]
Del Porto, Paola [4 ]
Paci, Paola [2 ]
机构
[1] IRCCS, Lazzaro Spallanzani Natl Inst Infect Dis, Lab Virol, Rome, Italy
[2] Sapienza Univ Roma, Dipartimento Ingn Informat Automat & Gest A Ruber, Rome, Italy
[3] IRCCS, Lazzaro Spallanzani Natl Inst Infect Dis, Lab Pathol, Rome, Italy
[4] Sapienza Univ, Dept Biol & Biotechnol C Darwin, Rome, Italy
关键词
Human papillomavirus; HPV mixed infection; genetic variability; intraepithelial lesions; HPV vaccine; MINOR CAPSID PROTEIN; VIRUS-LIKE PARTICLES; INTRAEPITHELIAL NEOPLASIA; NEUTRALIZING ANTIBODIES; VACCINE; RISK; CANCER; CLASSIFICATION; VARIABILITY; CARCINOMA;
D O I
10.3389/fmicb.2020.603657
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页数:14
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