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Human Protoparvoviruses

Next-generation sequencing and metagenomics have revolutionized the discovery of novel viruses. In recent years, three novel protoparvoviruses have been discovered in fecal samples of humans: bufavirus (BuV) in 2012, tusavirus (TuV) in 2014, and cutavirus (CuV) in 2016. BuV has since been studied th...

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Autores principales: Väisänen, Elina, Fu, Yu, Hedman, Klaus, Söderlund-Venermo, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707561/
https://www.ncbi.nlm.nih.gov/pubmed/29165368
http://dx.doi.org/10.3390/v9110354
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author Väisänen, Elina
Fu, Yu
Hedman, Klaus
Söderlund-Venermo, Maria
author_facet Väisänen, Elina
Fu, Yu
Hedman, Klaus
Söderlund-Venermo, Maria
author_sort Väisänen, Elina
collection PubMed
description Next-generation sequencing and metagenomics have revolutionized the discovery of novel viruses. In recent years, three novel protoparvoviruses have been discovered in fecal samples of humans: bufavirus (BuV) in 2012, tusavirus (TuV) in 2014, and cutavirus (CuV) in 2016. BuV has since been studied the most, disclosing three genotypes that also represent serotypes. Besides one nasal sample, BuV DNA has been found exclusively in diarrheal feces, but not in non-diarrheal feces, suggesting a causal relationship. According to both geno- and seroprevalences, BuV appears to be the most common of the three novel protoparvoviruses, whereas TuV DNA has been found in only a single fecal sample, with antibody detection being equally rare. Moreover, the TuV sequence is closer to those of non-human protoparvoviruses, and so the evidence of TuV being a human virus is thus far insufficient. Interestingly, besides in feces, CuV has also been detected in skin biopsies of patients with cutaneous T-cell lymphoma and a patient with melanoma, while all other skin samples have tested PCR negative. Even if preliminary disease associations exist, the full etiological roles of these viruses in human disease are yet to be resolved.
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spelling pubmed-57075612017-12-05 Human Protoparvoviruses Väisänen, Elina Fu, Yu Hedman, Klaus Söderlund-Venermo, Maria Viruses Review Next-generation sequencing and metagenomics have revolutionized the discovery of novel viruses. In recent years, three novel protoparvoviruses have been discovered in fecal samples of humans: bufavirus (BuV) in 2012, tusavirus (TuV) in 2014, and cutavirus (CuV) in 2016. BuV has since been studied the most, disclosing three genotypes that also represent serotypes. Besides one nasal sample, BuV DNA has been found exclusively in diarrheal feces, but not in non-diarrheal feces, suggesting a causal relationship. According to both geno- and seroprevalences, BuV appears to be the most common of the three novel protoparvoviruses, whereas TuV DNA has been found in only a single fecal sample, with antibody detection being equally rare. Moreover, the TuV sequence is closer to those of non-human protoparvoviruses, and so the evidence of TuV being a human virus is thus far insufficient. Interestingly, besides in feces, CuV has also been detected in skin biopsies of patients with cutaneous T-cell lymphoma and a patient with melanoma, while all other skin samples have tested PCR negative. Even if preliminary disease associations exist, the full etiological roles of these viruses in human disease are yet to be resolved. MDPI 2017-11-22 /pmc/articles/PMC5707561/ /pubmed/29165368 http://dx.doi.org/10.3390/v9110354 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Väisänen, Elina
Fu, Yu
Hedman, Klaus
Söderlund-Venermo, Maria
Human Protoparvoviruses
title Human Protoparvoviruses
title_full Human Protoparvoviruses
title_fullStr Human Protoparvoviruses
title_full_unstemmed Human Protoparvoviruses
title_short Human Protoparvoviruses
title_sort human protoparvoviruses
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707561/
https://www.ncbi.nlm.nih.gov/pubmed/29165368
http://dx.doi.org/10.3390/v9110354
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