Evidence map›Paper›PMID 39885107›Full record

ArticleImmunologic research2025

Amphibian cellular immune response to chytridiomycosis at metamorphic climax.

Josephine E Humphries, Allan Hicks, Chantal Lanctôt, Hamish McCallum, David Newell, Laura F Grogan

Abstract read
In one paragraph

Article in Immunologic research, 2025. 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
–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

3 citing papers in PubMed.

  1. Advancing the study of microbial symbionts of amphibians and reptiles.Frontiers in amphibian and reptile science · 2026
    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

6 authors.

Josephine E HumphriesSchool of Environment and Science, Griffith University, Southport, QLD, 4222, Australia. Josephine.humphries@outlook.com.ORCID http://orcid.org/0000-0001-9094-3982
Allan HicksSchool of Pharmacy and Medical Sciences, Griffith University, Southport, QLD, 4222, Australia.
Chantal LanctôtSchool of Environment and Science, Griffith University, Southport, QLD, 4222, Australia.
Hamish McCallumCentre for Planetary Health and Food Security, Griffith University, Southport, QLD, 4222, Australia.
David NewellFaculty of Science and Engineering, Southern Cross University, Lismore, NSW, 2480, Australia.
Laura F GroganSchool of Environment and Science, Griffith University, Southport, QLD, 4222, Australia.

Funding

ARC Discovery Early Career Researcher Award DE180101286Australian Research Council DP180101415
6 · The paper itself

Abstract

The fungal disease chytridiomycosis (caused by Batrachochytrium dendrobatidis [Bd]) is a primary contributor to amphibian declines. The frog metamorphic stages, characterised by extensive physiological reorganisation and energy expenditure, have heightened susceptibility to Bd. However, little is known about how these metamorphic stages respond immunologically to Bd infection. In this study, we examined Bd infection and the cellular immune response of Mixophyes fleayi at Gosner stages 40, 42 and 45, using blood smears and skin and liver histology. Although proportional differences were observed, the impact of Bd exposure appeared negligible prior to Gosner stage 45 (onset of morbidity), with no significant differences observed in absolute leukocyte counts for blood or liver samples between control and Bd-exposed groups at Gosner stages 40 and 42. Animals exhibiting clinical signs at Gosner stage 45 demonstrated significant elevation in liver leukocyte counts, blood neutrophil and monocyte counts and neutrophil-to-lymphocyte ratios. These findings are reminiscent of the amplified inflammatory response characteristic of immunopathology in clinically infected amphibians. Interestingly, a subset of exposed animals that had apparently cleared infections at Gosner stage 45 had similar blood leukocyte counts but reduced liver leukocyte counts compared to naïve controls. This could be a consequence of prior cellular consumption during pathogen removal or effective immune regulation via anti-inflammatory protective feedback mechanisms. We recommend targeted gene expression analyses (e.g. immunomodulatory cytokines) to establish the mechanisms responsible for the varied immune expression and infection outcomes across metamorphosis.

Indexed as

AnuraBatrachochytriumChytridiomycotaMycosesAnimalsImmunity, CellularLeukocyte CountLiverSkinAmphibianBatrachochytrium dendrobatidisDiseaseHistologyImmune cellsMetamorphosis

Identifiers

PMID39885107
PMCPMC11782352

What Socratic 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 Socratic graph.