Cargando…

Quantification of human polyomaviruses MCPyV and HPyV6 in malignant and non-malignant skin lesions()

BACKGROUND: Human Polyomaviruses such as MCPyV and HPyV6 are frequently found as part of healthy skin microbiota and have been associated with Merkel cell carcinoma (MCC), pruritic and dyskeratotic dermatoses, respectively. Their presence in other types of skin conditions varies greatly depending on...

Descripción completa

Detalles Bibliográficos
Autores principales: Venceslau, Marianna T., Costa, Gabriella R.M. da, Guimarães, Maria Angelica A.M., Varella, Rafael B., Luz, Flavio B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984872/
https://www.ncbi.nlm.nih.gov/pubmed/36635157
http://dx.doi.org/10.1016/j.abd.2022.02.006
_version_ 1784900828434268160
author Venceslau, Marianna T.
Costa, Gabriella R.M. da
Guimarães, Maria Angelica A.M.
Varella, Rafael B.
Luz, Flavio B.
author_facet Venceslau, Marianna T.
Costa, Gabriella R.M. da
Guimarães, Maria Angelica A.M.
Varella, Rafael B.
Luz, Flavio B.
author_sort Venceslau, Marianna T.
collection PubMed
description BACKGROUND: Human Polyomaviruses such as MCPyV and HPyV6 are frequently found as part of healthy skin microbiota and have been associated with Merkel cell carcinoma (MCC), pruritic and dyskeratotic dermatoses, respectively. Their presence in other types of skin conditions varies greatly depending on lesion type and population. OBJECTIVE: To analyse comparatively the presence of MCPyV and HPyV6 in nonmelanoma skin cancers and healthy skin. METHODS: The authors utilized qPCR techniques to quantify these pathogens in NMSC, premalignant diseases, and healthy skin of 87 patients. RESULTS: MCPyV was detected in over 40% of samples, while HPyV6 was in 9.6%. MCPyV load was higher in squamous cell carcinomas (SCC) compared to basal cell carcinomas (BCC) (p = 0.016) and HPyV6 showed a higher percentage of infected cells in areas of low solar exposure as well as normal skin (p = 0.012). A fair agreement (kappa = 0.301) was found between MCPyV detection in lesions and their respective perilesional skin, indicating a random process of local dissemination of the virus. STUDY LIMITATIONS: The lack of a larger sampling of different lesion types and protein expression analyses limits the correlation findings. CONCLUSION: This is the first report of HPyV6 detection in the healthy skin of a Brazilian population, but the role of both polyomaviruses in NMSC has yet to be demonstrated.
format Online
Article
Text
id pubmed-9984872
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Sociedade Brasileira de Dermatologia
record_format MEDLINE/PubMed
spelling pubmed-99848722023-03-05 Quantification of human polyomaviruses MCPyV and HPyV6 in malignant and non-malignant skin lesions() Venceslau, Marianna T. Costa, Gabriella R.M. da Guimarães, Maria Angelica A.M. Varella, Rafael B. Luz, Flavio B. An Bras Dermatol Original Article BACKGROUND: Human Polyomaviruses such as MCPyV and HPyV6 are frequently found as part of healthy skin microbiota and have been associated with Merkel cell carcinoma (MCC), pruritic and dyskeratotic dermatoses, respectively. Their presence in other types of skin conditions varies greatly depending on lesion type and population. OBJECTIVE: To analyse comparatively the presence of MCPyV and HPyV6 in nonmelanoma skin cancers and healthy skin. METHODS: The authors utilized qPCR techniques to quantify these pathogens in NMSC, premalignant diseases, and healthy skin of 87 patients. RESULTS: MCPyV was detected in over 40% of samples, while HPyV6 was in 9.6%. MCPyV load was higher in squamous cell carcinomas (SCC) compared to basal cell carcinomas (BCC) (p = 0.016) and HPyV6 showed a higher percentage of infected cells in areas of low solar exposure as well as normal skin (p = 0.012). A fair agreement (kappa = 0.301) was found between MCPyV detection in lesions and their respective perilesional skin, indicating a random process of local dissemination of the virus. STUDY LIMITATIONS: The lack of a larger sampling of different lesion types and protein expression analyses limits the correlation findings. CONCLUSION: This is the first report of HPyV6 detection in the healthy skin of a Brazilian population, but the role of both polyomaviruses in NMSC has yet to be demonstrated. Sociedade Brasileira de Dermatologia 2023 2023-01-10 /pmc/articles/PMC9984872/ /pubmed/36635157 http://dx.doi.org/10.1016/j.abd.2022.02.006 Text en © 2022 Sociedade Brasileira de Dermatologia. Published by Elsevier España, S.L.U. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Venceslau, Marianna T.
Costa, Gabriella R.M. da
Guimarães, Maria Angelica A.M.
Varella, Rafael B.
Luz, Flavio B.
Quantification of human polyomaviruses MCPyV and HPyV6 in malignant and non-malignant skin lesions()
title Quantification of human polyomaviruses MCPyV and HPyV6 in malignant and non-malignant skin lesions()
title_full Quantification of human polyomaviruses MCPyV and HPyV6 in malignant and non-malignant skin lesions()
title_fullStr Quantification of human polyomaviruses MCPyV and HPyV6 in malignant and non-malignant skin lesions()
title_full_unstemmed Quantification of human polyomaviruses MCPyV and HPyV6 in malignant and non-malignant skin lesions()
title_short Quantification of human polyomaviruses MCPyV and HPyV6 in malignant and non-malignant skin lesions()
title_sort quantification of human polyomaviruses mcpyv and hpyv6 in malignant and non-malignant skin lesions()
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984872/
https://www.ncbi.nlm.nih.gov/pubmed/36635157
http://dx.doi.org/10.1016/j.abd.2022.02.006
work_keys_str_mv AT venceslaumariannat quantificationofhumanpolyomavirusesmcpyvandhpyv6inmalignantandnonmalignantskinlesions
AT costagabriellarmda quantificationofhumanpolyomavirusesmcpyvandhpyv6inmalignantandnonmalignantskinlesions
AT guimaraesmariaangelicaam quantificationofhumanpolyomavirusesmcpyvandhpyv6inmalignantandnonmalignantskinlesions
AT varellarafaelb quantificationofhumanpolyomavirusesmcpyvandhpyv6inmalignantandnonmalignantskinlesions
AT luzflaviob quantificationofhumanpolyomavirusesmcpyvandhpyv6inmalignantandnonmalignantskinlesions