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Code from: Periodic shifts in viral load increase risk of spillover from bats

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Abstract

This code, and the associated dataset, support the findings of the results reported in Lunn, et al, 2023 (https://doi.org/10.1101/2023.09.06.556454), where we found: Prediction and management of zoonotic pathogen spillover requires an understanding of infection dynamics within reservoir host populations. Transmission risk is often assessed using prevalence of infected hosts, with infection status based on the presence of genomic material. However, detection of viral genomic material alone does not necessarily indicate the presence of infectious virus, which could decouple prevalence from transmission risk. We undertook a multi-faceted investigation of Hendra virus shedding in Pteropus bats, combining insights from virus isolation, viral load proxies, viral prevalence, and longitudinal patterns of shedding, from 6,151 samples. In addition to seasonal and interannual fluctuation in prevalence, we found evidence for periodic shifts in the distribution of viral loads. The proportion of bats shedding high viral loads was higher during peak prevalence periods during which spillover events were observed, and lower during non-peak periods when there were no spillovers. We suggest that prolonged periods of low viral load and low prevalence reflect prolonged shedding of non-infectious RNA, or viral loads that are insufficient or unlikely to overcome dose barriers to spillover infection. These findings show that incorporating viral load (or proxies of viral load), into longitudinal studies of virus excretion will better inform predictions of spillover risk than prevalence alone.

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This code is shared under a MIT license: Copyright 2025 Permission is hereby granted, free of charge, to any person obtaining a copy of this software and associated documentation files (the “Software”), to deal in the Software without restriction, including without limitation the rights to use, copy, modify, merge, publish, distribute, sublicense, and/or sell copies of the Software, and to permit persons to whom the Software is furnished to do so, subject to the following conditions: The above copyright notice and this permission notice shall be included in all copies or substantial portions of the Software. THE SOFTWARE IS PROVIDED “AS IS”, WITHOUT WARRANTY OF ANY KIND, EXPRESS OR IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM, OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN THE SOFTWARE.

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The project was supported by the National Science Foundation (DEB1716698, EF-4172133763), and the DARPA PREEMPT program Cooperative Agreement #418D18AC00031. 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. TJL was supported by an Endeavour Postgraduate Leadership Award and a Research Training Program scholarship sponsored by the Australian Government. AJP was supported by an ARC DECRA fellowship (DE190100710), and a Queensland Government Accelerate Postdoctoral Research Fellowship. VJM and KCY are supported by the Division of Intramural Research of NIAID. MKK was supported by the Fulbright U.S. Student Program, which is sponsored by the U.S. Department of State and the Australian-American Fulbright Commission.

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2025

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flying fox; Henipavirus; Pteropodidae; viral load distribution; detection limit; fruit bat; RT-PCR; viral replication

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Lunn, Tamika J., Benny Borremans, Devin Slobodian, Maureen Kessler, Adrienne Dale, Claude Yinda Kwe, Manuel Ruiz-Aravena, Caylee Falvo, Daniel Crowley, James Lloyd-Smith, Vincent Munster, Peggy Eby, Hamish McCallum, Peter Hudson, Olivier Restif, McGuire, Liam P., Smith, Ina L., Raina Plowright, and Alison Peel. 2025 Data from: Periodic shifts in viral load increase risk of spillover from bats. [Dataset] Cornell University Library eCommons Repository. https://doi.org/10.7298/dh0d-yc86

Lunn, Tamika J., Benny Borremans, Devin N. Jones, Maureen K. Kessler, Adrienne S. Dale, Kwe C. Yinda, Manuel Ruiz-Aravena, Caylee A Falvo, Dan Crowley, James O. Lloyd-Smith, Vincent J. Munster, Peggy Eby, Hamish McCallum, Peter Hudson, Olivier Restif, Liam P. McGuire, Ina L. Smith, Raina K. Plowright, Alison J. Peel. 2023. Periodic shifts in viral load increase risk of spillover from bats. bioRxiv 2023.09.06.556454; https://doi.org/10.1101/2023.09.06.556454

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