Evidence map›Paper›PMID 25391018›Full record

ArticlePloS one2014

Activation of innate immune-response genes in little brown bats (Myotis lucifugus) infected with the fungus Pseudogymnoascus destructans.

Noreen Rapin, Kirk Johns, Lauren Martin, Lisa Warnecke, James M Turner, Trent K Bollinger, Craig K R Willis, Jamie Voyles, Vikram Misra

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
15.7field-weighted citation impact, top 1% 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

20 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Microbiota diversity and anti-Applied and environmental microbiology · 2024
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  15. Article
  16. White-nose syndrome increases torpid metabolic rate and evaporative water loss in hibernating bats.American journal of physiology. Regulatory, integrative and comparative physiology · 2017
    Article
  17. Article
  18. Article
  19. Secondary metabolite arsenal of an opportunistic pathogenic fungus.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    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

9 authors at 3 institutions in 2 countries.

Noreen RapinDepartment of Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Kirk JohnsDepartment of Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Lauren MartinDepartment of Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Lisa WarneckeDepartment of Biology, University of Winnipeg, Winnipeg, Manitoba, Canada.
James M TurnerDepartment of Biology, University of Winnipeg, Winnipeg, Manitoba, Canada.
Trent K BollingerDepartment of Pathology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Craig K R WillisDepartment of Biology, University of Winnipeg, Winnipeg, Manitoba, Canada.
Jamie VoylesDepartment of Biology, New Mexico Tech, Socorro, New Mexico, United States of America.
Vikram MisraDepartment of Microbiology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
University of Saskatchewan · CAUniversity of Winnipeg · CANew Mexico Institute of Mining and Technology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently bats have been associated with the emergence of diseases, both as reservoirs for several new viral diseases in humans and other animals and, in the northern Americas, as hosts for a devastating fungal disease that threatens to drive several bat species to regional extinction. However, despite these catastrophic events little Information is available on bat defences or how they interact with their pathogens. Even less is known about the response of bats to infection during torpor or long-term hibernation. Using tissue samples collected at the termination of an experiment to explore the pathogenesis of White Nose Syndrome in Little Brown Bats, we determined if hibernating bats infected with the fungus Pseudogymnoascus destructans could respond to infection by activating genes responsible for innate immune and stress responses. Lesions due to fungal infection and, in some cases, secondary bacterial infections, were restricted to the skin. However, we were unable to obtain sufficient amounts of RNA from these sites. We therefore examined lungs for response at an epithelial surface not linked to the primary site of infection. We found that bats responded to infection with a significant increase in lungs of transcripts for Cathelicidin (an anti-microbial peptide) as well as the immune modulators tumor necrosis factor alpha and interleukins 10 and 23. In conclusion, hibernating bats can respond to experimental P. destructans infection by activating expression of innate immune response genes.

Indexed as

AnimalsAntimicrobial Cationic PeptidesAscomycotaCathelicidinsChiropteraGene Expression RegulationImmunity, InnateInterleukin-10Interleukin-23LungMycosesReal-Time Polymerase Chain ReactionSkinTumor Necrosis Factor-alphaAntimicrobial Cationic PeptidesCathelicidinsInterleukin-10Interleukin-23Tumor Necrosis Factor-alpha

Identifiers

PMID25391018
PMCPMC4229191
OpenAlexW2082878774

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.