Six RNA viruses and forty-one hosts: viral small RNAs and modulation of small RNA repertoires in vertebrate and invertebrate systems
We have used multiplexed high-throughput sequencing to characterize changes in small RNA populations that occur during viral infection in animal cells. Small RNA-based mechanisms such as RNA interference (RNAi) have been shown in plant and invertebrate systems to play a key role in host responses to...
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Published in: | PLoS pathogens Vol. 6; no. 2; p. e1000764 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Public Library of Science
01-02-2010
Public Library of Science (PLoS) |
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Online Access: | Get full text |
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Summary: | We have used multiplexed high-throughput sequencing to characterize changes in small RNA populations that occur during viral infection in animal cells. Small RNA-based mechanisms such as RNA interference (RNAi) have been shown in plant and invertebrate systems to play a key role in host responses to viral infection. Although homologs of the key RNAi effector pathways are present in mammalian cells, and can launch an RNAi-mediated degradation of experimentally targeted mRNAs, any role for such responses in mammalian host-virus interactions remains to be characterized. Six different viruses were examined in 41 experimentally susceptible and resistant host systems. We identified virus-derived small RNAs (vsRNAs) from all six viruses, with total abundance varying from "vanishingly rare" (less than 0.1% of cellular small RNA) to highly abundant (comparable to abundant micro-RNAs "miRNAs"). In addition to the appearance of vsRNAs during infection, we saw a number of specific changes in host miRNA profiles. For several infection models investigated in more detail, the RNAi and Interferon pathways modulated the abundance of vsRNAs. We also found evidence for populations of vsRNAs that exist as duplexed siRNAs with zero to three nucleotide 3' overhangs. Using populations of cells carrying a Hepatitis C replicon, we observed strand-selective loading of siRNAs onto Argonaute complexes. These experiments define vsRNAs as one possible component of the interplay between animal viruses and their hosts. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 d: Current address: Harvard University, Cambridge, Massachusetts, United States of America f: Current address: Department of Microbiology and Molecular Genetics, Center for Biopreparedness and Infectious Diseases, Medical College of Wisconsin, Milwaukee, Wisconsin, United States of America i: Current address: Laboratório de Flavivirus, Pav. Helio e Peggy Pereira, sala B 102, Instituto Oswaldo Cruz/Fundação Oswaldo Cruz, Rio de Janeiro, Brazil j: Current address: Dept. of Virology, University of Heidelberg, Heidelberg, Germany Conceived and designed the experiments: PP AZF. Performed the experiments: PP. Analyzed the data: PP AZF. Contributed reagents/materials/analysis tools: PP ES CW TB MAS RL KMA VH SE WJ TD SP CP FBdS RJ FB BG DG MK SK PS MR SWD EH MC MSD KK JSG AZF. Wrote the paper: PP AZF. g: Current address: Science and Technology Policy Fellowship Program, American Association for the Advancement of Sciences, Washington, D.C., United States of America a: Current address: Department of Clinical Microbiology and Immunology, Tel-Aviv University, Ramat-Aviv, Tel-Aviv, Israel b: Current address: Department of Immunology, University of Washington School of Medicine, Seattle, Washington, United States of America e: Current address: Department of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana, United States of America h: Current address: National Veterinary Institute, Lindholm, Denmark c: Current address: Sg2, Evanston, Illinois, United States of America k: Current address: Illumina, San Diego, California, United States of America |
ISSN: | 1553-7374 1553-7366 1553-7374 |
DOI: | 10.1371/journal.ppat.1000764 |