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Peer-reviewedCC BY-NC-NDNature communications

Live imaging and interactome analysis of Zika and chikungunya viral RNAs via dual-action aptamer tag.

  1. 1Department of Biochemistry and Molecular Biology, The Pennsylvania State University Park, University Park, PA, USA.
  2. 2Department of Biochemistry and Molecular Biology, The Pennsylvania State University Park, University Park, PA, USA. [email protected].
  3. 3The Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, PA, USA. [email protected].

Abstract

Arthropod-borne, positive-sense RNA viruses encompass many human pathogens posing significant health threats worldwide. Understanding intracellular dynamics and host-factor interactions of the viral genome is essential for devising effective antiviral strategies. Here, we engineer dual-labeled Zika and chikungunya viruses incorporating a Mango-II aptamer for RNA pulldown and real-time imaging, achieving high-resolution imaging of flavivirus RNA in live cells. Tandem imaging with viral replication proteins revealed intracellular dynamics of replication complexes and RNA molecules of these viruses. We identify >200 high-confidence host interactors of viral RNA and corroborated 355 hits from existing data sets. Spliceosome factor SFPQ is as a common interactor decreasing RNA production in both viruses when depleted. Intracellular colocalization of SFPQ-ZIKV and SFPQ-CHIKV RNA is confirmed through confocal microscopy imaging of infected cells. Thus, we demonstrate Mango-II aptamer tagging as an innovative strategy for identifying spatiotemporal dynamics and virus-host interactions of viral genomes in positive-strand RNA viruses.

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BibTeX
@article{jablunovsky2026live,
  title = {{Live imaging and interactome analysis of Zika and chikungunya viral RNAs via dual-action aptamer tag.}},
  author = {Anastazia Jablunovsky and Benjamin M Kropff and Anoop Narayanan and Joyce Jose},
  journal = {Nature communications},
  year = {2026},
  month = sep,
  doi = {10.1038/s41467-026-77830-4},
  url = {https://europepmc.org/article/MED/42901910},
  note = {CC BY-NC-ND},
}
RIS
TY  - JOUR
TI  - Live imaging and interactome analysis of Zika and chikungunya viral RNAs via dual-action aptamer tag.
AU  - Anastazia Jablunovsky
AU  - Benjamin M Kropff
AU  - Anoop Narayanan
AU  - Joyce Jose
PY  - 2026
DA  - 2026/09/21
JO  - Nature communications
DO  - 10.1038/s41467-026-77830-4
UR  - https://europepmc.org/article/MED/42901910
AB  - Arthropod-borne, positive-sense RNA viruses encompass many human pathogens posing significant health threats worldwide. Understanding intracellular dynamics and host-factor interactions of the viral genome is essential for devising effective antiviral strategies. Here, we engineer dual-labeled Zika and chikungunya viruses incorporating a Mango-II aptamer for RNA pulldown and real-time imaging, achieving high-resolution imaging of flavivirus RNA in live cells. Tandem imaging with viral replication proteins revealed intracellular dynamics of replication complexes and RNA molecules of these viruses. We identify >200 high-confidence host interactors of viral RNA and corroborated 355 hits from existing data sets. Spliceosome factor SFPQ is as a common interactor decreasing RNA production in both viruses when depleted. Intracellular colocalization of SFPQ-ZIKV and SFPQ-CHIKV RNA is confirmed through confocal microscopy imaging of infected cells. Thus, we demonstrate Mango-II aptamer tagging as an innovative strategy for identifying spatiotemporal dynamics and virus-host interactions of viral genomes in positive-strand RNA viruses.
SN  - 2041-1723
ER  -