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HPyV6 and HPyV7 in urine from immunocompromised patients

BACKGROUND: Human polyomavirus 6 (HPyV6) and HPyV7 are two of the novel polyomaviruses that were originally detected in non-diseased skin. Serological studies have shown that these viruses are ubiquitous in the healthy adult population with seroprevalence up to 88% for HPyV6 and 72% for HPyV7. Both...

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Autores principales: Prezioso, Carla, Van Ghelue, Marijke, Moens, Ugo, Pietropaolo, Valeria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821732/
https://www.ncbi.nlm.nih.gov/pubmed/33482864
http://dx.doi.org/10.1186/s12985-021-01496-1
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author Prezioso, Carla
Van Ghelue, Marijke
Moens, Ugo
Pietropaolo, Valeria
author_facet Prezioso, Carla
Van Ghelue, Marijke
Moens, Ugo
Pietropaolo, Valeria
author_sort Prezioso, Carla
collection PubMed
description BACKGROUND: Human polyomavirus 6 (HPyV6) and HPyV7 are two of the novel polyomaviruses that were originally detected in non-diseased skin. Serological studies have shown that these viruses are ubiquitous in the healthy adult population with seroprevalence up to 88% for HPyV6 and 72% for HPyV7. Both viruses are associated with pruritic skin eruption in immunocompromised patients, but a role with other diseases in immunoincompetent patients or malignancies has not been established. METHODS: PCR was used to determine the presence of HPyV6 and HPyV7 DNA in urine samples from systemic lupus erythematosus (n = 73), multiple sclerosis (n = 50), psoriasis vulgaris (n = 15), arthritic psoriasis (n = 15) and HIV-positive patients (n = 66). In addition, urine from pregnant women (n = 47) and healthy blood donors (n = 20) was investigated. RESULTS: HPyV6 DNA was detected in 21 (28.8%) of the urine specimens from SLE patients, in 6 (9.1%) of the urine samples from the HIV-positive cohort, and in 19 (40.4%) samples from pregnant women. HPyV7 DNA was only found in 6 (8.2%) of the urine specimens from SLE patients and in 4 (8.5%) samples from pregnant women. No HPyV6 and HPyV7 viruria was detected in the urine samples from the other patients. CONCLUSIONS: HPyV6, and to a lesser extend HPyV7, viruria seems to be common in SLE and HIV-positive patients, and pregnant women. Whether these viruses are of clinical relevance in these patients is not known.
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spelling pubmed-78217322021-01-25 HPyV6 and HPyV7 in urine from immunocompromised patients Prezioso, Carla Van Ghelue, Marijke Moens, Ugo Pietropaolo, Valeria Virol J Research BACKGROUND: Human polyomavirus 6 (HPyV6) and HPyV7 are two of the novel polyomaviruses that were originally detected in non-diseased skin. Serological studies have shown that these viruses are ubiquitous in the healthy adult population with seroprevalence up to 88% for HPyV6 and 72% for HPyV7. Both viruses are associated with pruritic skin eruption in immunocompromised patients, but a role with other diseases in immunoincompetent patients or malignancies has not been established. METHODS: PCR was used to determine the presence of HPyV6 and HPyV7 DNA in urine samples from systemic lupus erythematosus (n = 73), multiple sclerosis (n = 50), psoriasis vulgaris (n = 15), arthritic psoriasis (n = 15) and HIV-positive patients (n = 66). In addition, urine from pregnant women (n = 47) and healthy blood donors (n = 20) was investigated. RESULTS: HPyV6 DNA was detected in 21 (28.8%) of the urine specimens from SLE patients, in 6 (9.1%) of the urine samples from the HIV-positive cohort, and in 19 (40.4%) samples from pregnant women. HPyV7 DNA was only found in 6 (8.2%) of the urine specimens from SLE patients and in 4 (8.5%) samples from pregnant women. No HPyV6 and HPyV7 viruria was detected in the urine samples from the other patients. CONCLUSIONS: HPyV6, and to a lesser extend HPyV7, viruria seems to be common in SLE and HIV-positive patients, and pregnant women. Whether these viruses are of clinical relevance in these patients is not known. BioMed Central 2021-01-22 /pmc/articles/PMC7821732/ /pubmed/33482864 http://dx.doi.org/10.1186/s12985-021-01496-1 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Prezioso, Carla
Van Ghelue, Marijke
Moens, Ugo
Pietropaolo, Valeria
HPyV6 and HPyV7 in urine from immunocompromised patients
title HPyV6 and HPyV7 in urine from immunocompromised patients
title_full HPyV6 and HPyV7 in urine from immunocompromised patients
title_fullStr HPyV6 and HPyV7 in urine from immunocompromised patients
title_full_unstemmed HPyV6 and HPyV7 in urine from immunocompromised patients
title_short HPyV6 and HPyV7 in urine from immunocompromised patients
title_sort hpyv6 and hpyv7 in urine from immunocompromised patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821732/
https://www.ncbi.nlm.nih.gov/pubmed/33482864
http://dx.doi.org/10.1186/s12985-021-01496-1
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