Evidence map›Paper›PMID 35357202›Full record

ArticlemBio2022

The Mechanism of Pertussis Cough Revealed by the Mouse-Coughing Model.

Yukihiro Hiramatsu, Koichiro Suzuki, Takashi Nishida, Naoki Onoda, Takashi Satoh, Shizuo Akira, Masahito Ikawa, Hiroko Ikeda, Junzo Kamei, Sandra Derouiche and 2 more

RetractedErratum issuedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in mBio, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. The diverse landscape of AB5-type toxins.Engineering microbiology · 2023
    Review
  4. DAT, deacylating autotransporter toxin, fromProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Infectious and Inflammatory Pathways to Cough.Annual review of physiology · 2023
    Review
  6. Article
  7. Generating enhanced mucosal immunity againstFrontiers in immunology · 2023
    Article
  8. Article
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 1 country.

Yukihiro HiramatsuDepartment of Molecular Bacteriology, Research Institute for Microbial Diseases, Osaka Universitygrid.136593.b, Suita, Osaka, Japan.ORCID 0000-0002-6340-864X
Koichiro SuzukiDepartment of Molecular Bacteriology, Research Institute for Microbial Diseases, Osaka Universitygrid.136593.b, Suita, Osaka, Japan.
Takashi NishidaDepartment of Molecular Bacteriology, Research Institute for Microbial Diseases, Osaka Universitygrid.136593.b, Suita, Osaka, Japan.
Naoki OnodaDepartment of Molecular Bacteriology, Research Institute for Microbial Diseases, Osaka Universitygrid.136593.b, Suita, Osaka, Japan.
Takashi SatohLaboratory of Host Defense, World Premier Institute Immunology Frontier Research Center, Osaka Universitygrid.136593.b, Suita, Osaka, Japan.
Shizuo AkiraLaboratory of Host Defense, World Premier Institute Immunology Frontier Research Center, Osaka Universitygrid.136593.b, Suita, Osaka, Japan.
Masahito IkawaDepartment of Experimental Genome Research, Research Institute for Microbial Diseases, Osaka Universitygrid.136593.b, Suita, Osaka, Japan.
Hiroko IkedaDepartment of Pathophysiology and Therapeutics, Hoshi University School of Pharmacy and Pharmaceutical Sciences, Tokyo, Japan.
Junzo KameiJuntendo Advanced Research Institute for Health Science, Juntendo Universitygrid.258269.2, Tokyo, Japan.
Sandra DerouicheDivision of Cell Signaling, National Institute for Physiological Sciencesgrid.467811.d, Okazaki, Aichi, Japan.
Makoto TominagaDivision of Cell Signaling, National Institute for Physiological Sciencesgrid.467811.d, Okazaki, Aichi, Japan.
Yasuhiko HoriguchiDepartment of Molecular Bacteriology, Research Institute for Microbial Diseases, Osaka Universitygrid.136593.b, Suita, Osaka, Japan.ORCID 0000-0002-1592-5861
The University of Osaka · JPNational Institutes of Natural Sciences · JPOsaka International University · JPHoshi University · JPJuntendo University · JPKyoto Biken Laboratories (Japan) · JP

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) JP26293096MEXT |Japan Society for the Promotion of Science (JSPS) JP16H06276
6 · The paper itself

Abstract

Pertussis, also known as whooping cough, is a contagious respiratory disease caused by the Gram-negative bacterium Bordetella pertussis. This disease is characterized by severe and uncontrollable coughing, which imposes a significant burden on patients. However, its etiological agent and the mechanism are totally unknown because of a lack of versatile animal models that reproduce the cough. Here, we present a mouse model that reproduces coughing after intranasal inoculation with the bacterium or its components and demonstrate that lipooligosaccharide (LOS), pertussis toxin (PTx), and Vag8 of the bacterium cooperatively function to cause coughing. Bradykinin induced by LOS sensitized a transient receptor potential ion channel, TRPV1, which acts as a sensor to evoke the cough reflex. Vag8 further increased bradykinin levels by inhibiting the C1 esterase inhibitor, the major downregulator of the contact system, which generates bradykinin. PTx inhibits intrinsic negative regulation systems for TRPV1 through the inactivation of G

Indexed as

Whooping CoughAnimalsBordetella pertussisBradykininCoughDisease Models, AnimalHumansMicePertussis ToxinTranscription FactorsBradykininPertussis ToxinTranscription FactorsBordetella pertussisbradykinincoughpertussis toxinTRPV1Vag8

Identifiers

PMID35357202
PMCPMC9040802
OpenAlexW4221126965

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.