Abstract
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.
Highlights
Cervical cancer is the fourth most frequent cancer in women (Ferlay et al, 2019)
Between 2008 and 2012, 1,444 cervical samples from HIVpositive women were screened for Human papillomavirus (HPV) DNA
The Genomica CLART 2 Array failed to detect any HPV genotypes. These samples were submitted to Sanger sequencing, which allowed the identification of their HPV types: HPV13, HPV55, HPV69, HPV102 (n = 2), HPV118, and HPV120 (n = 2)
Summary
Cervical cancer is the fourth most frequent cancer in women (Ferlay et al, 2019). Statistical data suggest that almost 99% of cervical cancers are related to Human papillomavirus (HPV) infections (Walboomers et al, 1999; De Martel et al, 2012). The International Agency for Research on Cancer has indicated the 15 α-types as high-risk (HR) genotypes: HPV16, 18, 31, 33, 35, 39, 45, 51, 56, 58, 59, 66, 68, 73, and 82 (Muñoz et al, 2003). These genotypes are responsible of more than 90% of all cervical cancers (Luostarinen et al, 2018), and they are involved in anal and oropharynx cancers (Garbuglia et al, 2020). This disease is very difficult to treat, and it often has fatal outcomes (Garbuglia et al, 2020)
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