Author
Listed:
- Ivan Haralampiev
(IRI Life Sciences, Humboldt-Universität zu Berlin
Crystallography, Max Delbrück Center for Molecular Medicine)
- Simon Prisner
(IRI Life Sciences, Humboldt-Universität zu Berlin)
- Mor Nitzan
(The Hebrew University of Jerusalem)
- Matthias Schade
(IRI Life Sciences, Humboldt-Universität zu Berlin)
- Fabian Jolmes
(IRI Life Sciences, Humboldt-Universität zu Berlin
PicoQuant)
- Max Schreiber
(Institute for Applied Informatics e.V. at Leipzig University)
- Maria Loidolt-Krüger
(Max-Planck-Institute for Biophysical Chemistry
PicoQuant)
- Kalle Jongen
(IRI Life Sciences, Humboldt-Universität zu Berlin)
- Jasmine Chamiolo
(Humboldt-Universität zu Berlin)
- Niklaas Nilson
(IRI Life Sciences, Humboldt-Universität zu Berlin)
- Franziska Winter
(Max-Planck-Institute for Biophysical Chemistry
Abberior Instruments GmbH)
- Nir Friedman
(The Hebrew University of Jerusalem
The Hebrew University of Jerusalem)
- Oliver Seitz
(Humboldt-Universität zu Berlin)
- Thorsten Wolff
(Robert Koch Institut, Unit 17, Influenza and Other Respiratory Viruses)
- Andreas Herrmann
(IRI Life Sciences, Humboldt-Universität zu Berlin)
Abstract
The genome of influenza A viruses (IAV) is encoded in eight distinct viral ribonucleoproteins (vRNPs) that consist of negative sense viral RNA (vRNA) covered by the IAV nucleoprotein. Previous studies strongly support a selective packaging model by which vRNP segments are bundling to an octameric complex, which is integrated into budding virions. However, the pathway(s) generating a complete genome bundle is not known. We here use a multiplexed FISH assay to monitor all eight vRNAs in parallel in human lung epithelial cells. Analysis of 3.9 × 105 spots of colocalizing vRNAs provides quantitative insights into segment composition of vRNP complexes and, thus, implications for bundling routes. The complexes rarely contain multiple copies of a specific segment. The data suggest a selective packaging mechanism with limited flexibility by which vRNPs assemble into a complete IAV genome. We surmise that this flexibility forms an essential basis for the development of reassortant viruses with pandemic potential.
Suggested Citation
Ivan Haralampiev & Simon Prisner & Mor Nitzan & Matthias Schade & Fabian Jolmes & Max Schreiber & Maria Loidolt-Krüger & Kalle Jongen & Jasmine Chamiolo & Niklaas Nilson & Franziska Winter & Nir Fried, 2020.
"Selective flexible packaging pathways of the segmented genome of influenza A virus,"
Nature Communications, Nature, vol. 11(1), pages 1-13, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-18108-1
DOI: 10.1038/s41467-020-18108-1
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