Evidence map›Paper›PMID 26046527›Full record

ArticlePloS one2015

Quantitative Proteomics of an Amphibian Pathogen, Batrachochytrium dendrobatidis, following Exposure to Thyroid Hormone.

Jose Thekkiniath, Masoud Zabet-Moghaddam, Kameswara Rao Kottapalli, Mithun R Pasham, Susan San Francisco, Michael San Francisco

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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.

Jose ThekkiniathDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT, 06520, United States of America.
Masoud Zabet-MoghaddamCenter for Biotechnology and Genomics, Texas Tech University, Lubbock, TX, 79402-3132, United States of America.
Kameswara Rao KottapalliCenter for Biotechnology and Genomics, Texas Tech University, Lubbock, TX, 79402-3132, United States of America.
Mithun R PashamDepartment of Cell Biology and Pediatrics, Harvard Medical School, Boston, MA, 02115, United States of America, and Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA, 02115, United States of America.
Susan San FranciscoCenter for Biotechnology and Genomics, Texas Tech University, Lubbock, TX, 79402-3132, United States of America; Department of Biological Sciences, Texas Tech University, Lubbock, TX, 79409-3131, United States of America.
Michael San FranciscoDepartment of Biological Sciences, Texas Tech University, Lubbock, TX, 79409-3131, United States of America.
Texas Tech University · USHarvard University · USYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Batrachochytrium dendrobatidis (Bd), a chytrid fungus, has increasingly been implicated as a major factor in the worldwide decline of amphibian populations. The fungus causes chytridiomycosis in susceptible species leading to massive die-offs of adult amphibians. Although Bd infects the keratinized mouthparts of tadpoles and negatively affects foraging behavior, these infections are non-lethal. An important morphogen controlling amphibian metamorphosis is thyroid hormone (T3). Tadpoles may be infected with Bd and the fungus may be exposed to T3 during metamorphosis. We hypothesize that exposure of Bd to T3 may induce the expression of factors associated with host colonization and pathogenicity. We utilized a proteomics approach to better understand the dynamics of the Bd-T3 interaction. Using liquid chromatography-mass spectrometry (LC-MS), we generated a data set of a large number of cytoplasmic and membrane proteins following exposure of Bd to T3. From these data, we identified a total of 263 proteins whose expression was significantly changed following T3 exposure. We provide evidence for expression of an array of proteins that may play key roles in both genomic and non-genomic actions of T3 in Bd. Additionally, our proteomics study shows an increase in several proteins including proteases and a class of uncommon crinkler and crinkler-like effector proteins suggesting their importance in Bd pathogenicity as well as those involved in metabolism and energy transfer, protein fate, transport and stress responses. This approach provides insights into the mechanistic basis of the Bd-amphibian interaction following T3 exposure.

Indexed as

ProteomicsAnimalsAnuraBiological TransportCarbohydrate MetabolismChromatography, High Pressure LiquidChytridiomycotaElectrophoresisFungal ProteinsHeat-Shock ProteinsLipid MetabolismMitochondriaPeptidesTandem Mass SpectrometryTriiodothyronineTrypsinFungal ProteinsHeat-Shock ProteinsPeptidesTriiodothyronineTrypsin

Identifiers

PMID26046527
PMCPMC4457425
OpenAlexW1900176936

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.