ArticleNature communications2025
Synchronized seasonal excretion of multiple coronaviruses coincides with high rates of coinfection in immature bats.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
6 citing papers in PubMed.
- Periodic shifts in viral load increase risk of Hendra virus spillover fromScience advances · 2026Article
- Serum proteome of the Egyptian rousette bat (Rousettus aegyptiacus) reveals signatures of immunity, proteostasis, and metabolism.Scientific reports · 2026Article
- Coronavirus Nsp3 Hijacks CLTC to Modulate Autophagosome Nucleation for Promoting DMV Formation and Viral Replication.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
- Cohorts of immature Pteropus bats show interannual variation in Hendra virus serology.The Journal of animal ecology · 2026Article
- Virus-host associations of bat coronaviruses along a land-use gradient in the Yucatán Peninsula, México.Virus evolution · 2026Article
- Biosurveillance of coronaviruses inVirus evolution · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
15 authors.
Funding
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.
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Registered trials
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