Evidence map›Paper›PMID 38355905›Full record

ArticleScientific reports2024

Diversity of selected toll-like receptor genes in cheetahs (Acinonyx jubatus) and African leopards (Panthera pardus pardus).

René Meißner, Prudent Mokgokong, Chantelle Pretorius, Sven Winter, Kim Labuschagne, Antoinette Kotze, Stefan Prost, Petr Horin, Desire Dalton, Pamela A Burger

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

10 authors at 6 institutions in 5 countries.

René MeißnerResearch Institute of Wildlife Ecology, University of Veterinary Medicine, Savoyenstraße 1, 1160, Vienna, Austria.
Prudent MokgokongSouth African National Biodiversity Institute, National Zoological Garden, 232 Boom Street, Pretoria, 0002, South Africa.
Chantelle PretoriusSouth African National Biodiversity Institute, National Zoological Garden, 232 Boom Street, Pretoria, 0002, South Africa.
Sven WinterResearch Institute of Wildlife Ecology, University of Veterinary Medicine, Savoyenstraße 1, 1160, Vienna, Austria.
Kim LabuschagneSouth African National Biodiversity Institute, National Zoological Garden, 232 Boom Street, Pretoria, 0002, South Africa.
Antoinette KotzeSouth African National Biodiversity Institute, National Zoological Garden, 232 Boom Street, Pretoria, 0002, South Africa.
Stefan ProstSouth African National Biodiversity Institute, National Zoological Garden, 232 Boom Street, Pretoria, 0002, South Africa.
Petr HorinDepartment of Animal Genetics, University of Veterinary Sciences, Brno, Czech Republic.
Desire DaltonSouth African National Biodiversity Institute, National Zoological Garden, 232 Boom Street, Pretoria, 0002, South Africa. D.Dalton@tees.ac.uk.
Pamela A BurgerResearch Institute of Wildlife Ecology, University of Veterinary Medicine, Savoyenstraße 1, 1160, Vienna, Austria. pamela.burger@vetmeduni.ac.at.
South African National Biodiversity Institute · ZAUniversity of Veterinary Medicine Vienna · ATNational Zoological Gardens of South Africa · ZAUniversity of Oulu · FIUniversity of the Free State · ZAUniversity of Veterinary Sciences Brno · CZ

Funding

Austrian Science Fund I5081-BAustrian Science Fund FWF I 5081Grantová Agentura České Republiky 21-28637 LÖsterreichische Agentur für Internationale Mobilität und Kooperation in Bildung, Wissenschaft und Forschung ZA02/2019
6 · The paper itself

Abstract

The anthropogenic impact on wildlife is ever increasing. With shrinking habitats, wild populations are being pushed to co-exist in proximity to humans leading to an increased threat of infectious diseases. Therefore, understanding the immune system of a species is key to assess its resilience in a changing environment. The innate immune system (IIS) is the body's first line of defense against pathogens. High variability in IIS genes, like toll-like receptor (TLR) genes, appears to be associated with resistance to infectious diseases. However, few studies have investigated diversity in TLR genes in vulnerable species for conservation. Large predators are threatened globally including leopards and cheetahs, both listed as 'vulnerable' by IUCN. To examine IIS diversity in these sympatric species, we used next-generation-sequencing to compare selected TLR genes in African leopards and cheetahs. Despite differences, both species show some TLR haplotype similarity. Historic cheetahs from all subspecies exhibit greater genetic diversity than modern Southern African cheetahs. The diversity in investigated TLR genes is lower in modern Southern African cheetahs than in African leopards. Compared to historic cheetah data and other subspecies, a more recent population decline might explain the observed genetic impoverishment of TLR genes in modern Southern African cheetahs. However, this may not yet impact the health of this cheetah subspecies.

Indexed as

AcinonyxCommunicable DiseasesPantheraAnimalsAnimals, WildEcosystemHumans

Identifiers

PMID38355905
PMCPMC10866938
OpenAlexW4391810001

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.