Whole Genomic Analysis and Comparison of Two Canine Papillomavirus Type 9 Strains in Malignant and Benign Skin Lesions
Autor: | Kazuyuki Uchida, Wei-Tao Chen, Hui-Wen Chang, James K. Chambers, Pei-Shiue Tsai, Sonoka Tomizawa, I-Li Liu, Nanako Yamashita-Kawanishi, Wei-Hsiang Huang, Takeshi Haga, Kinji Shirota, Yen-Chen Chang, Chia-Yu Chang |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Male Pathology medicine.medical_specialty Skin Neoplasms canine papillomavirus type 9 (CPV9) Sequence analysis 030106 microbiology Genome Viral medicine.disease_cause Article law.invention Malignant transformation 03 medical and health sciences Dogs E2 law Risk Factors Virology medicine Animals Dog Diseases Papillomaviridae Gene Polymerase chain reaction E7 E6 Skin biology Whole Genome Sequencing Papillomavirus Infections squamous cell carcinoma (SCC) Genomics medicine.disease biology.organism_classification Viral plaque 030104 developmental biology Infectious Diseases oncoprotein DNA Viral Carcinoma Squamous Cell Papilloma Neoplasm Recurrence Local Carcinogenesis |
Zdroj: | Viruses Volume 12 Issue 7 |
ISSN: | 1999-4915 |
Popis: | Papillomaviruses (PVs) usually cause benign proliferative lesions in the stratified epithelium of various animal species. However, some high-risk types of PVs have been proven to lead to malignant transformations. In dogs, several canine papillomaviruses (CPVs) have been identified in malignant lesions and are suggested as one of the risk factors for the development of squamous cell carcinomas (SCCs). In the present study, the full genomes of two CPV9 strains from recurrent SCCs of Dog 1 and skin viral papilloma (viral plaque) of Dog 2 were sequenced. Alignment of the two CPV9 sequences with the genome of the reference CPV9 strain (accession no. JF800656.1) derived from a solitary pigmented plaque was performed. Compared with the reference strain, a 27 bp in-frame insertion in the E1 gene was identified in both CPV9 strains in this study. In comparison with the CPV9 strains derived from benign lesions, the CPV9 from the SCCs of Dog 1 exhibited a 328 bp deletion at the 3′ end of the E2 and spacer sequence, which encoded a truncated deduced E2 protein and a chimeric E8^E2 protein. However, there was no difference in the mRNA expression levels of viral oncoproteins of E6 and E7 between the two CPV9 cases, suggesting that the oncogenesis of CPV9 for malignant transformation might be different from that of human papillomaviruses. The roles of E2 and E8^E2 deleted CPV9 in the oncogenesis of benign and malignant lesions should be further investigated. |
Databáze: | OpenAIRE |
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