BACKGROUND: Recently three previously unknown polyomaviruses (KI, WU and Merkel cell polyomaviruses) have been identified from human specimens. The spectrum of clinical manifestations and their tissue tropism are currently unknown. Since a member of this virus family, JC virus, is well-known for its capacity to establish latency in human brain tissue where reactivation in immunocompromised individuals can result in fatal progressive multifocal leukoencephalopathy, we sought to examine for the presence of all the five known human polyomaviruses in a series of human brain tissues. OBJECTIVES: To investigate the possibility of neuropersistence of the newly identified human polyomaviruses. STUDY DESIGN: Autopsy brain tissues were collected from 10 different brain regions of 30 individuals who died from diseases unrelated to viral infections. Nested PCR was used to assess the presence or absence of viral DNA. RESULTS: Ten samples collected from five individuals were found to harbour JCV DNA. In contrast, none of the 300 brain tissues examined showed positive results for BK, KI, WU or Merkel cell polyomavirus. CONCLUSION: The newly identified KI, WU and Merkel cell polyomaviruses either do not, or have a much lower neuropersistent potential compared to JCV. Copyright 2010 Elsevier B.V. All rights reserved.
BACKGROUND: Recently three previously unknown polyomaviruses (KI, WU and Merkel cell polyomaviruses) have been identified from human specimens. The spectrum of clinical manifestations and their tissue tropism are currently unknown. Since a member of this virus family, JC virus, is well-known for its capacity to establish latency in human brain tissue where reactivation in immunocompromised individuals can result in fatal progressive multifocal leukoencephalopathy, we sought to examine for the presence of all the five known humanpolyomaviruses in a series of human brain tissues. OBJECTIVES: To investigate the possibility of neuropersistence of the newly identified humanpolyomaviruses. STUDY DESIGN: Autopsy brain tissues were collected from 10 different brain regions of 30 individuals who died from diseases unrelated to viral infections. Nested PCR was used to assess the presence or absence of viral DNA. RESULTS: Ten samples collected from five individuals were found to harbour JCV DNA. In contrast, none of the 300 brain tissues examined showed positive results for BK, KI, WU or Merkel cell polyomavirus. CONCLUSION: The newly identified KI, WU and Merkel cell polyomaviruses either do not, or have a much lower neuropersistent potential compared to JCV. Copyright 2010 Elsevier B.V. All rights reserved.
Authors: Xin Dang; Seweryn Bialasiewicz; Michael D Nissen; Theo P Sloots; Igor J Koralnik; Chen S Tan Journal: PLoS One Date: 2011-03-16 Impact factor: 3.240
Authors: Spyros Chalkias; Joshua M Gorham; Erica Mazaika; Michael Parfenov; Xin Dang; Steve DePalma; David McKean; Christine E Seidman; Jonathan G Seidman; Igor J Koralnik Journal: PLoS One Date: 2018-01-23 Impact factor: 3.240
Authors: Manuel Schibler; Francisco Brito; Marie-Céline Zanella; Evgeny M Zdobnov; Florian Laubscher; Arnaud G L'Huillier; Juan Ambrosioni; Noémie Wagner; Klara M Posfay-Barbe; Mylène Docquier; Eduardo Schiffer; Georges L Savoldelli; Roxane Fournier; Lauriane Lenggenhager; Samuel Cordey; Laurent Kaiser Journal: Genes (Basel) Date: 2019-08-19 Impact factor: 4.096