4.6 Article

RNA Interference Targets Arbovirus Replication in Culicoides Cells

期刊

JOURNAL OF VIROLOGY
卷 87, 期 5, 页码 2441-2454

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AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.02848-12

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资金

  1. United Kingdom Medical Research Council
  2. Wellcome Trust
  3. Netherlands Organization for Scientific Research NWO (Rubicon Fellowship)
  4. BBSRC [BBS/E/D/20241864, BBS/E/D/20310000, BBS/E/D/20241866] Funding Source: UKRI
  5. MRC [MC_UP_A550_1031, G0801822, MR/K001744/1] Funding Source: UKRI
  6. Biotechnology and Biological Sciences Research Council [BBS/E/D/20241866, BBS/E/D/20310000, BBS/E/D/20241864] Funding Source: researchfish
  7. Medical Research Council [G0801822, MR/K001744/1, MC_UP_A550_1031] Funding Source: researchfish

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Arboviruses are transmitted to vertebrate hosts by biting arthropod vectors such as mosquitoes, ticks, and midges. These viruses replicate in both arthropods and vertebrates and are thus exposed to different antiviral responses in these organisms. RNA interference (RNAi) is a sequence-specific RNA degradation mechanism that has been shown to play a major role in the antiviral response against arboviruses in mosquitoes. Culicoides midges are important vectors of arboviruses, known to transmit pathogens of humans and livestock such as bluetongue virus (BTV) (Reoviridae), Oropouche virus (Bunyaviridae), and likely the recently discovered Schmallenberg virus (Bunyaviridae). In this study, we investigated whether Culicoides cells possess an antiviral RNAi response and whether this is effective against arboviruses, including those with double-stranded RNA (dsRNA) genomes, such as BTV. Using reporter gene-based assays, we established the presence of a functional RNAi response in Culicoides sonorensis-derived KC cells which is effective in inhibiting BTV infection. Sequencing of small RNAs from KC and Aedes aegypti-derived Aag2 cells infected with BTV or the unrelated Schmallenberg virus resulted in the production of virus-derived small interfering RNAs (viRNAs) of 21 nucleotides, similar to the viRNAs produced during arbovirus infections of mosquitoes. In addition, viRNA profiles strongly suggest that the BTV dsRNA genome is accessible to a Dicer-type nuclease. Thus, we show for the first time that midge cells target arbovirus replication by mounting an antiviral RNAi response mainly resembling that of other insect vectors of arboviruses.

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