Evidence map›Paper›PMID 41394910›Full record

ArticleFrontiers in veterinary science2025

The final frontier: using carcasses for one health surveillance at the ecosystem interface.

Katie A Barton, Patrick B Finnerty, Ruwini Rupasinghe, Carlos González-Crespo, Jackie E Mahar, John-Sebastian Eden, Niraj Y Meisuria, Beatriz Martínez-López, Thomas M Newsome, Alison J Peel and 2 more

Abstract read
In one paragraph

Article in Frontiers in veterinary science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Katie A BartonSydney School of Veterinary Science, Faculty of Science, The University of Sydney, Camperdown, NSW, Australia.
Patrick B FinnertySchool of Life and Environmental Sciences, Faculty of Science, The University of Sydney, Camperdown, NSW, Australia.
Ruwini RupasingheCenter for Animal Disease Modeling and Surveillance, University of California, Davis, Davis, CA, United States.
Carlos González-CrespoCenter for Animal Disease Modeling and Surveillance, University of California, Davis, Davis, CA, United States.
Jackie E MaharAustralian Animal Health Laboratory and Health and Biosecurity, Commonwealth Scientific and Industrial Research Organisation, Geelong, VIC, Australia.
John-Sebastian EdenCentre for Virus Research, Westmead Institute for Medical Research, Westmead, NSW, Australia.
Niraj Y MeisuriaSydney School of Veterinary Science, Faculty of Science, The University of Sydney, Camperdown, NSW, Australia.
Beatriz Martínez-LópezCenter for Animal Disease Modeling and Surveillance, University of California, Davis, Davis, CA, United States.
Thomas M NewsomeSchool of Life and Environmental Sciences, Faculty of Science, The University of Sydney, Camperdown, NSW, Australia.
Alison J PeelSydney School of Veterinary Science, Faculty of Science, The University of Sydney, Camperdown, NSW, Australia.
Justine A SmithDepartment of Wildlife, Fish, and Conservation Biology, University of California, Davis, Davis, CA, United States.
Victoria J BrookesSydney School of Veterinary Science, Faculty of Science, The University of Sydney, Camperdown, NSW, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anthropogenic activities such as agricultural intensification, urbanisation, globalisation, and climate change are accelerating disease emergence globally, yet surveillance systems have largely overlooked the critical role of vertebrate carcasses in pathogen transmission. This omission is concerning because animal mass mortality events (MMEs) are increasing in frequency and magnitude, while populations of key vertebrate scavengers, especially obligate scavengers like vultures, are declining, resulting in longer carcass persistence and altered disease risks. Carcasses serve as essential resources in food webs but also act as complex microbe transmission hubs through direct consumption, environmental contamination, vector-mediated dispersal, and increased host aggregation, facilitating cross-species and trophic spillover events. Scavengers can amplify or mitigate microbe transmission: their consumption of carcasses can remove infectious material, but their mobility and sociality may also disperse potential pathogens across large areas. Technological advances, including remote sensing, camera traps, GPS telemetry, and machine learning, now enable detailed tracking of scavenger-carcass interactions and identification of transmission hotspots. Simultaneously, metagenomic sequencing allows untargeted detection of known and novel pathogens in carcass-associated microbial communities ("necrobiome"), with portable platforms supporting field-based surveillance. Integrating carcass-based surveillance into One Health frameworks through interdisciplinary collaboration among ecologists, epidemiologists, and data scientists offers a proactive approach to early outbreak detection, improved pandemic preparedness, and ecosystem health monitoring. Given the projected increase in climate-driven mortality events, incorporating carcass-scavenger networks into disease surveillance strategies is a valuable and under-utilised complement to existing approaches, enhancing our ability to monitor and mitigate emerging infectious diseases.

Indexed as

carriongenomicinfectious diseaseriskscavengingspillover

Identifiers

PMID41394910
PMCPMC12699599

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.