Evidence map›Paper›PMID 24841130›Full record

ArticleG3 (Bethesda, Md.)2014

Fighting a losing battle: vigorous immune response countered by pathogen suppression of host defenses in the chytridiomycosis-susceptible frog Atelopus zeteki.

Amy R Ellison, Anna E Savage, Grace V DiRenzo, Penny Langhammer, Karen R Lips, Kelly R Zamudio

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
9.5field-weighted citation impact, top 2% 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

51 citing papers in PubMed, 106 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Amphibian (Journal of fungi (Basel, Switzerland) · 2025
    Article
  5. Article
  6. Evolutionary ecology of host competence after a chytrid outbreak in a naive amphibian community.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. The amphibian complement system and chytridiomycosis.Journal of experimental zoology. Part A, Ecological and integrative physiology · 2020
    Review
  16. Article
  17. Immunological Aspects of Chytridiomycosis.Journal of fungi (Basel, Switzerland) · 2020
    Review
  18. Article
  19. Article
  20. 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 at 3 institutions in 1 country.

Amy R EllisonDepartment of Ecology and Evolutionary Biology, Cornell University, Ithaca, New York 14853 are35@cornell.edu.
Anna E SavageDepartment of Ecology and Evolutionary Biology, Cornell University, Ithaca, New York 14853 Center for Conservation and Evolutionary Genetics, Smithsonian Institution, Washington, DC 20013.
Grace V DiRenzoDepartment of Biology, University of Maryland, College Park, Maryland 20742.
Penny LanghammerSchool of Life Sciences, Arizona State University, Tempe, Arizona 85287.
Karen R LipsDepartment of Biology, University of Maryland, College Park, Maryland 20742.
Kelly R ZamudioDepartment of Ecology and Evolutionary Biology, Cornell University, Ithaca, New York 14853.
Cornell University · USUniversity of Maryland, College Park · USArizona State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The emergence of the disease chytridiomycosis caused by the chytrid fungus Batrachochytrium dendrobatidis (Bd) has been implicated in dramatic global amphibian declines. Although many species have undergone catastrophic declines and/or extinctions, others appear to be unaffected or persist at reduced frequencies after Bd outbreaks. The reasons behind this variance in disease outcomes are poorly understood: differences in host immune responses have been proposed, yet previous studies suggest a lack of robust immune responses to Bd in susceptible species. Here, we sequenced transcriptomes from clutch-mates of a highly susceptible amphibian, Atelopus zeteki, with different infection histories. We found significant changes in expression of numerous genes involved in innate and inflammatory responses in infected frogs despite high susceptibility to chytridiomycosis. We show evidence of acquired immune responses generated against Bd, including increased expression of immunoglobulins and major histocompatibility complex genes. In addition, fungal-killing genes had significantly greater expression in frogs previously exposed to Bd compared with Bd-naïve frogs, including chitinase and serine-type proteases. However, our results appear to confirm recent in vitro evidence of immune suppression by Bd, demonstrated by decreased expression of lymphocyte genes in the spleen of infected compared with control frogs. We propose susceptibility to chytridiomycosis is not due to lack of Bd-specific immune responses but instead is caused by failure of those responses to be effective. Ineffective immune pathway activation and timing of antibody production are discussed as potential mechanisms. However, in light of our findings, suppression of key immune responses by Bd is likely an important factor in the lethality of this fungus.

Indexed as

Adaptive ImmunityAnimalsBufonidaeChitinasesChytridiomycotaDisease SusceptibilityImmunity, InnateMycosesSequence Analysis, RNASerine ProteasesTranscriptomeChitinasesSerine Proteasesacquired immunityAtelopus zetekiBatrachochytrium dendrobatidiscomplex geneticscomplex immunitygenetics of immunityimmunogenomicsimmunosuppressioninfectioninnate immunityresistancetolerance

Identifiers

PMID24841130
PMCPMC4455776
OpenAlexW2115019334

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.