Complete Genome Sequence of a Novel Human Gammapapillomavirus Isolated from a Cervical Swab in Luxembourg

ABSTRACT A novel human papillomavirus genotype was detected in a cervical swab specimen by next-generation sequencing after rolling circular amplification. It was fully cloned and characterized. The L1 open reading frame showed 77% nucleotide similarity with the closest genotype, HPV101, belonging to the gamma-6 species.

H uman papillomaviruses (HPVs) are small, circular, double-stranded DNA viruses that are linked to the malignant transformation of epithelia of various human sites (1). Currently, more than 200 HPV genotypes have been fully characterized, including five genera of papillomaviruses-alpha, beta, gamma, mu, and nu (2,3). An HPV genome is considered a novel type if its L1 genomic region shares less than 90% similarity with the closest known HPV genotype (3,4). Here, we describe the discovery of a novel gammapapillomavirus isolated from a cervical swab specimen (stored in PreservCyt liquid) taken from a 24-year-old woman participating in a vaccine efficacy study and vaccinated with two doses of quadrivalent HPV vaccine. The cytological result was negative for intraepithelial lesion and malignancy.
The L1 open reading frame (ORF) of HPV isolate 16031680A showed 77% nucleotide identity with the closest genotype, HPV101, belonging to the gamma-6 species, and analysis using BLAST showed 77% pairwise identity for the full genome. The complete genome of this novel HPV genotype consists of 7,313 nucleotides with a GϩC content of 42.6%. It has four early (E1, E2, E4, and E7) and two late (L1 and L2) ORFs. The ORF coding the early protein E6 is absent, as it is for other known members of the gamma-6 species, namely, 101, 103, and 108 (7)(8)(9). The long control region of 735 nucleotides found between the L1 and E7 genes contains one TATA box (TATAAA) and three palindromic E2-binding sites (ACC-N 6 -GGT). One conserved zinc-binding domain was identified in the E7 protein [CxxC(x) 29 CxxC], and the ATP-binding site of the ATPdependent helicase (GPPDTGKS) was identified in the carboxy-terminal region of E1 (7).
To conclude, we discovered a novel genotype of the gamma-6 papillomavirus species. Members of this species are adapted to the mucosal niche (9) and may be associated with low-grade (8) and high-grade cervical lesions (7). The clinical relevance and prevalence of gamma-6 genotypes deserves further investigation.
Accession number(s). The complete genome sequence for human gammapapillomavirus isolate 16031680A is available in GenBank under accession number MG813996.

ACKNOWLEDGMENTS
This study received financial support from the Fonds National de la Recherche Luxembourg (FNR number 14/BM/7932582). M.A. was supported by the Papillux Project and the COHEAHR Network (number 603019), funded by the 7th Framework Program of DG Research and Innovation, European Commission (Brussels, Belgium). The study was approved by the Comité National d'Ethique de Recherche (CNER number 201501/ 02) and authorized by the Commission Nationale pour la Protection des Données (CNPD number 288/2016).
We thank Catherine Ragimbeau for help with sequencing, the Inspection Générale de la Sécurité Social for providing vaccination data, and Planning Familial for study recruitment and sample collection.