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Molecular Characterization of Human Papillomavirus Type 159 (HPV159)
Human papillomavirus type 159 (HPV159) was identified in an anal swab sample and preliminarily genetically characterized by our group in 2012. Here we present a detailed molecular in silico analysis that showed that the HPV159 viral genome is 7443 bp in length and divided into five early and two lat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402796/ https://www.ncbi.nlm.nih.gov/pubmed/34452532 http://dx.doi.org/10.3390/v13081668 |
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author | Marković, Iva Hošnjak, Lea Seme, Katja Poljak, Mario |
author_facet | Marković, Iva Hošnjak, Lea Seme, Katja Poljak, Mario |
author_sort | Marković, Iva |
collection | PubMed |
description | Human papillomavirus type 159 (HPV159) was identified in an anal swab sample and preliminarily genetically characterized by our group in 2012. Here we present a detailed molecular in silico analysis that showed that the HPV159 viral genome is 7443 bp in length and divided into five early and two late genes, with conserved functional domains and motifs, and a non-coding long control region (LCR) with significant regulatory sequences that allow the virus to complete its life cycle and infect novel host cells. HPV159, clustering into the cutaneotropic Betapapillomavirus (Beta-PV) genus, is phylogenetically most similar to HPV9, forming an individual phylogenetic group in the viral species Beta-2. After testing a large representative collection of clinical samples with HPV159 type-specific RT-PCR, in addition to the anal canal from which the first HPV159 isolate was obtained, HPV159 was further detected in other muco-cutaneous (4/181, 2.2%), mucosal (22/764, 2.9%), and cutaneous (14/554, 2.5%) clinical samples, suggesting its extensive tissue tropism. However, because very low HPV159 viral loads were estimated in the majority of positive samples, it seemed that HPV159 mainly caused clinically insignificant infections of the skin and mucosa. Using newly developed, highly sensitive HPV159-specific nested PCRs, two additional HPV159 LCR viral variants were identified. Nevertheless, all HPV159 mutations were demonstrated outside important functional domains of the LCR, suggesting that the HPV159 viral variants were most probably not pathogenically different. This complete molecular characterization of HPV159 enhances our knowledge of the genome characteristics, tissue tropism, and phylogenetic diversity of Beta-PVs that infect humans. |
format | Online Article Text |
id | pubmed-8402796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84027962021-08-29 Molecular Characterization of Human Papillomavirus Type 159 (HPV159) Marković, Iva Hošnjak, Lea Seme, Katja Poljak, Mario Viruses Article Human papillomavirus type 159 (HPV159) was identified in an anal swab sample and preliminarily genetically characterized by our group in 2012. Here we present a detailed molecular in silico analysis that showed that the HPV159 viral genome is 7443 bp in length and divided into five early and two late genes, with conserved functional domains and motifs, and a non-coding long control region (LCR) with significant regulatory sequences that allow the virus to complete its life cycle and infect novel host cells. HPV159, clustering into the cutaneotropic Betapapillomavirus (Beta-PV) genus, is phylogenetically most similar to HPV9, forming an individual phylogenetic group in the viral species Beta-2. After testing a large representative collection of clinical samples with HPV159 type-specific RT-PCR, in addition to the anal canal from which the first HPV159 isolate was obtained, HPV159 was further detected in other muco-cutaneous (4/181, 2.2%), mucosal (22/764, 2.9%), and cutaneous (14/554, 2.5%) clinical samples, suggesting its extensive tissue tropism. However, because very low HPV159 viral loads were estimated in the majority of positive samples, it seemed that HPV159 mainly caused clinically insignificant infections of the skin and mucosa. Using newly developed, highly sensitive HPV159-specific nested PCRs, two additional HPV159 LCR viral variants were identified. Nevertheless, all HPV159 mutations were demonstrated outside important functional domains of the LCR, suggesting that the HPV159 viral variants were most probably not pathogenically different. This complete molecular characterization of HPV159 enhances our knowledge of the genome characteristics, tissue tropism, and phylogenetic diversity of Beta-PVs that infect humans. MDPI 2021-08-23 /pmc/articles/PMC8402796/ /pubmed/34452532 http://dx.doi.org/10.3390/v13081668 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Marković, Iva Hošnjak, Lea Seme, Katja Poljak, Mario Molecular Characterization of Human Papillomavirus Type 159 (HPV159) |
title | Molecular Characterization of Human Papillomavirus Type 159 (HPV159) |
title_full | Molecular Characterization of Human Papillomavirus Type 159 (HPV159) |
title_fullStr | Molecular Characterization of Human Papillomavirus Type 159 (HPV159) |
title_full_unstemmed | Molecular Characterization of Human Papillomavirus Type 159 (HPV159) |
title_short | Molecular Characterization of Human Papillomavirus Type 159 (HPV159) |
title_sort | molecular characterization of human papillomavirus type 159 (hpv159) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402796/ https://www.ncbi.nlm.nih.gov/pubmed/34452532 http://dx.doi.org/10.3390/v13081668 |
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