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  4. Data from: Synchronized seasonal excretion of multiple coronaviruses coincides with high rates of coinfection in immature bats

Data from: Synchronized seasonal excretion of multiple coronaviruses coincides with high rates of coinfection in immature bats

File(s)
combined_out_variant.csv (459.63 KB)
individual_variant_covariates.csv (518.91 KB)
PeelEtAl_Data_README.txt (5.05 KB)
Permanent Link(s)
https://doi.org/10.7298/w7sw-6161
https://hdl.handle.net/1813/116957
Collections
CVM Research
Author
Peel, Alison J.
Ruiz-Aravena, Manuel
Kim, Karan
Scherting, Braden
Falvo, Caylee A.
Crowley, Dan
Munster, Vincent J.
Annand, Ed
Plain, Karren
Jones, Devin N.
Lunn, Tamika J.
Dale, Adrienne S.
Hoegh, Andrew
Eden, John-Sebastian
Plowright, Raina K.
Abstract

Bats host a high diversity of coronaviruses, including betacoronaviruses that have caused outbreaks and pandemics in humans and other species. Here, we study the spatiotemporal dynamics of co-circulating coronaviruses in Pteropus spp bats (flying foxes) in eastern Australia over a three-year period across five roost sites (n = 2537 fecal samples). In total, we identify six betacoronavirus clades, all within the nobecovirus subgenus. Genome sequencing supports overall clade assignments, however, also demonstrates the important role recombination has played in both the long-term and contemporary evolution of these viruses. Using a statistical framework that integrates individual and population level data, we assess the variability in prevalence of viral clades over space and time. Coronavirus infections and co-infections are highest among juveniles and subadults, particularly around the time of weaning. The overlapping shedding dynamics across multiple clades suggest opportunities for recombination, especially in younger bats. Understanding the ecological and host-viral drivers of these seasonally dynamic infections, co-infections, and recombination events will inform future predictive frameworks for coronavirus emergence in humans and other animals.

Description
Please cite as:
Alison Peel, Manuel Ruiz-Aravena, Karan Kim, Braden Scherting, Caylee A. Falvo, Dan Crowley, Vincent J. Munster, Edward J. Annand, Karren Plain, Devin N. Jones, Tamika J. Lunn, Adrienne S. Dale, Andrew Hoegh, John-Sebastian Eden, Raina K. Plowright. (2025) Data from: Synchronized seasonal excretion of multiple coronaviruses coincides with high rates of coinfection in immature bats. [dataset] Cornell University Library eCommons Repository. https://doi.org/10.7298/w7sw-6161
Sponsorship
Information about funding sources that supported the collection of the data:
The project was supported by the National Science Foundation (DEB1716698, EF2133763, EF-2231624), and the DARPA PREEMPT program Cooperative Agreement # D18AC00031. The content of the information does not necessarily reflect the position or the policy of the U.S. government, and no official endorsement should be inferred.
AJP was supported by an ARC DECRA fellowship (DE190100710) and a University of Sydney Horizons Fellowship.
Date Issued
2025-05-21
Keywords
coronaviruses
•
betacoronavirus
•
nobecovirus
•
flying foxes
•
Australia
Related Publication(s)
Peel, A., Ruiz-Aravena, M., Kim, K., Scherting, B., Falvo, C., Crowley, D. E., Munster, V., Annand, E. J., Plain, K., Jones, D., Lunn, T. J., Dale, A., Hoegh, A., Eden, J.-S., & Plowright, R. (2025). andyhoegh/CovOz_submission: Manuscript Code (v1.0.0). Zenodo. https://doi.org/10.5281/zenodo.15399029
Peel, A.J., Ruiz-Aravena, M., Kim, K. et al. Synchronized seasonal excretion of multiple coronaviruses coincides with high rates of coinfection in immature bats. Nat Commun 16, 6579 (2025). https://doi.org/10.1038/s41467-025-61521-7
Link(s) to Related Publication(s)
https://doi.org/10.5281/zenodo.15399029
https://doi.org/10.1038/s41467-025-61521-7
Rights
CC0 1.0 Universal
Rights URI
http://creativecommons.org/publicdomain/zero/1.0/
Type
dataset
Accessibility Hazard
none

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