Taking the Scenic Route: Polyomaviruses Utilize Multiple Pathways to Reach the Same Destination

Members of the <i>Polyomaviridae</i> family differ in their host range, pathogenesis, and disease severity. To date, some of the most studied polyomaviruses include human JC, BK, and Merkel cell polyomavirus and non-human subspecies murine and simian virus 40 (SV40) polyomavirus. Althoug...

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Main Authors: Colleen L. Mayberry, Melissa S. Maginnis
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:Viruses
Subjects:
Online Access:https://www.mdpi.com/1999-4915/12/10/1168
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author Colleen L. Mayberry
Melissa S. Maginnis
author_facet Colleen L. Mayberry
Melissa S. Maginnis
author_sort Colleen L. Mayberry
collection DOAJ
description Members of the <i>Polyomaviridae</i> family differ in their host range, pathogenesis, and disease severity. To date, some of the most studied polyomaviruses include human JC, BK, and Merkel cell polyomavirus and non-human subspecies murine and simian virus 40 (SV40) polyomavirus. Although dichotomies in host range and pathogenesis exist, overlapping features of the infectious cycle illuminate the similarities within this virus family. Of particular interest to human health, JC, BK, and Merkel cell polyomavirus have all been linked to critical, often fatal, illnesses, emphasizing the importance of understanding the underlying viral infections that result in the onset of these diseases. As there are significant overlaps in the capacity of polyomaviruses to cause disease in their respective hosts, recent advancements in characterizing the infectious life cycle of non-human murine and SV40 polyomaviruses are key to understanding diseases caused by their human counterparts. This review focuses on the molecular mechanisms by which different polyomaviruses hijack cellular processes to attach to host cells, internalize, traffic within the cytoplasm, and disassemble within the endoplasmic reticulum (ER), prior to delivery to the nucleus for viral replication. Unraveling the fundamental processes that facilitate polyomavirus infection provides deeper insight into the conserved mechanisms of the infectious process shared within this virus family, while also highlighting critical unique viral features.
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spelling doaj.art-b2990a76e86b426e8ad41cadacffe2302023-11-20T17:11:57ZengMDPI AGViruses1999-49152020-10-011210116810.3390/v12101168Taking the Scenic Route: Polyomaviruses Utilize Multiple Pathways to Reach the Same DestinationColleen L. Mayberry0Melissa S. Maginnis1Department of Molecular and Biomedical Sciences, The University of Maine, Orono, ME 04469, USADepartment of Molecular and Biomedical Sciences, The University of Maine, Orono, ME 04469, USAMembers of the <i>Polyomaviridae</i> family differ in their host range, pathogenesis, and disease severity. To date, some of the most studied polyomaviruses include human JC, BK, and Merkel cell polyomavirus and non-human subspecies murine and simian virus 40 (SV40) polyomavirus. Although dichotomies in host range and pathogenesis exist, overlapping features of the infectious cycle illuminate the similarities within this virus family. Of particular interest to human health, JC, BK, and Merkel cell polyomavirus have all been linked to critical, often fatal, illnesses, emphasizing the importance of understanding the underlying viral infections that result in the onset of these diseases. As there are significant overlaps in the capacity of polyomaviruses to cause disease in their respective hosts, recent advancements in characterizing the infectious life cycle of non-human murine and SV40 polyomaviruses are key to understanding diseases caused by their human counterparts. This review focuses on the molecular mechanisms by which different polyomaviruses hijack cellular processes to attach to host cells, internalize, traffic within the cytoplasm, and disassemble within the endoplasmic reticulum (ER), prior to delivery to the nucleus for viral replication. Unraveling the fundamental processes that facilitate polyomavirus infection provides deeper insight into the conserved mechanisms of the infectious process shared within this virus family, while also highlighting critical unique viral features.https://www.mdpi.com/1999-4915/12/10/1168polyomavirusviral entryviral traffickingviral disassemblyJC polyomavirusBK polyomavirus
spellingShingle Colleen L. Mayberry
Melissa S. Maginnis
Taking the Scenic Route: Polyomaviruses Utilize Multiple Pathways to Reach the Same Destination
Viruses
polyomavirus
viral entry
viral trafficking
viral disassembly
JC polyomavirus
BK polyomavirus
title Taking the Scenic Route: Polyomaviruses Utilize Multiple Pathways to Reach the Same Destination
title_full Taking the Scenic Route: Polyomaviruses Utilize Multiple Pathways to Reach the Same Destination
title_fullStr Taking the Scenic Route: Polyomaviruses Utilize Multiple Pathways to Reach the Same Destination
title_full_unstemmed Taking the Scenic Route: Polyomaviruses Utilize Multiple Pathways to Reach the Same Destination
title_short Taking the Scenic Route: Polyomaviruses Utilize Multiple Pathways to Reach the Same Destination
title_sort taking the scenic route polyomaviruses utilize multiple pathways to reach the same destination
topic polyomavirus
viral entry
viral trafficking
viral disassembly
JC polyomavirus
BK polyomavirus
url https://www.mdpi.com/1999-4915/12/10/1168
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