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Viral MicroRNA Effects on Pathogenesis of Polyomavirus SV40 Infections in Syrian Golden Hamsters

Effects of polyomavirus SV40 microRNA on pathogenesis of viral infections in vivo are not known. Syrian golden hamsters are the small animal model for studies of SV40. We report here effects of SV40 microRNA and influence of the structure of the regulatory region on dynamics of SV40 DNA levels in vi...

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Autores principales: Zhang, Shaojie, Sroller, Vojtech, Zanwar, Preeti, Chen, Chun Jung, Halvorson, Steven J., Ajami, Nadim J., Hecksel, Corey W., Swain, Jody L., Wong, Connie, Sullivan, Christopher S., Butel, Janet S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916418/
https://www.ncbi.nlm.nih.gov/pubmed/24516384
http://dx.doi.org/10.1371/journal.ppat.1003912
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author Zhang, Shaojie
Sroller, Vojtech
Zanwar, Preeti
Chen, Chun Jung
Halvorson, Steven J.
Ajami, Nadim J.
Hecksel, Corey W.
Swain, Jody L.
Wong, Connie
Sullivan, Christopher S.
Butel, Janet S.
author_facet Zhang, Shaojie
Sroller, Vojtech
Zanwar, Preeti
Chen, Chun Jung
Halvorson, Steven J.
Ajami, Nadim J.
Hecksel, Corey W.
Swain, Jody L.
Wong, Connie
Sullivan, Christopher S.
Butel, Janet S.
author_sort Zhang, Shaojie
collection PubMed
description Effects of polyomavirus SV40 microRNA on pathogenesis of viral infections in vivo are not known. Syrian golden hamsters are the small animal model for studies of SV40. We report here effects of SV40 microRNA and influence of the structure of the regulatory region on dynamics of SV40 DNA levels in vivo. Outbred young adult hamsters were inoculated by the intracardiac route with 1×10(7) plaque-forming units of four different variants of SV40. Infected animals were sacrificed from 3 to 270 days postinfection and viral DNA loads in different tissues determined by quantitative real-time polymerase chain reaction assays. All SV40 strains displayed frequent establishment of persistent infections and slow viral clearance. SV40 had a broad tissue tropism, with infected tissues including liver, kidney, spleen, lung, and brain. Liver and kidney contained higher viral DNA loads than other tissues; kidneys were the preferred site for long-term persistent infection although detectable virus was also retained in livers. Expression of SV40 microRNA was demonstrated in wild-type SV40-infected tissues. MicroRNA-negative mutant viruses consistently produced higher viral DNA loads than wild-type SV40 in both liver and kidney. Viruses with complex regulatory regions displayed modestly higher viral DNA loads in the kidney than those with simple regulatory regions. Early viral transcripts were detected at higher levels than late transcripts in liver and kidney. Infectious virus was detected infrequently. There was limited evidence of increased clearance of microRNA-deficient viruses. Wild-type and microRNA-negative mutants of SV40 showed similar rates of transformation of mouse cells in vitro and tumor induction in weanling hamsters in vivo. This report identified broad tissue tropism for SV40 in vivo in hamsters and provides the first evidence of expression and function of SV40 microRNA in vivo. Viral microRNA dampened viral DNA levels in tissues infected by SV40 strains with simple or complex regulatory regions.
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spelling pubmed-39164182014-02-10 Viral MicroRNA Effects on Pathogenesis of Polyomavirus SV40 Infections in Syrian Golden Hamsters Zhang, Shaojie Sroller, Vojtech Zanwar, Preeti Chen, Chun Jung Halvorson, Steven J. Ajami, Nadim J. Hecksel, Corey W. Swain, Jody L. Wong, Connie Sullivan, Christopher S. Butel, Janet S. PLoS Pathog Research Article Effects of polyomavirus SV40 microRNA on pathogenesis of viral infections in vivo are not known. Syrian golden hamsters are the small animal model for studies of SV40. We report here effects of SV40 microRNA and influence of the structure of the regulatory region on dynamics of SV40 DNA levels in vivo. Outbred young adult hamsters were inoculated by the intracardiac route with 1×10(7) plaque-forming units of four different variants of SV40. Infected animals were sacrificed from 3 to 270 days postinfection and viral DNA loads in different tissues determined by quantitative real-time polymerase chain reaction assays. All SV40 strains displayed frequent establishment of persistent infections and slow viral clearance. SV40 had a broad tissue tropism, with infected tissues including liver, kidney, spleen, lung, and brain. Liver and kidney contained higher viral DNA loads than other tissues; kidneys were the preferred site for long-term persistent infection although detectable virus was also retained in livers. Expression of SV40 microRNA was demonstrated in wild-type SV40-infected tissues. MicroRNA-negative mutant viruses consistently produced higher viral DNA loads than wild-type SV40 in both liver and kidney. Viruses with complex regulatory regions displayed modestly higher viral DNA loads in the kidney than those with simple regulatory regions. Early viral transcripts were detected at higher levels than late transcripts in liver and kidney. Infectious virus was detected infrequently. There was limited evidence of increased clearance of microRNA-deficient viruses. Wild-type and microRNA-negative mutants of SV40 showed similar rates of transformation of mouse cells in vitro and tumor induction in weanling hamsters in vivo. This report identified broad tissue tropism for SV40 in vivo in hamsters and provides the first evidence of expression and function of SV40 microRNA in vivo. Viral microRNA dampened viral DNA levels in tissues infected by SV40 strains with simple or complex regulatory regions. Public Library of Science 2014-02-06 /pmc/articles/PMC3916418/ /pubmed/24516384 http://dx.doi.org/10.1371/journal.ppat.1003912 Text en © 2014 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Shaojie
Sroller, Vojtech
Zanwar, Preeti
Chen, Chun Jung
Halvorson, Steven J.
Ajami, Nadim J.
Hecksel, Corey W.
Swain, Jody L.
Wong, Connie
Sullivan, Christopher S.
Butel, Janet S.
Viral MicroRNA Effects on Pathogenesis of Polyomavirus SV40 Infections in Syrian Golden Hamsters
title Viral MicroRNA Effects on Pathogenesis of Polyomavirus SV40 Infections in Syrian Golden Hamsters
title_full Viral MicroRNA Effects on Pathogenesis of Polyomavirus SV40 Infections in Syrian Golden Hamsters
title_fullStr Viral MicroRNA Effects on Pathogenesis of Polyomavirus SV40 Infections in Syrian Golden Hamsters
title_full_unstemmed Viral MicroRNA Effects on Pathogenesis of Polyomavirus SV40 Infections in Syrian Golden Hamsters
title_short Viral MicroRNA Effects on Pathogenesis of Polyomavirus SV40 Infections in Syrian Golden Hamsters
title_sort viral microrna effects on pathogenesis of polyomavirus sv40 infections in syrian golden hamsters
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916418/
https://www.ncbi.nlm.nih.gov/pubmed/24516384
http://dx.doi.org/10.1371/journal.ppat.1003912
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