Evidence map›Paper›PMID 32341116›Full record

ReviewInfection and immunity2020

Neural Immune Communication in the Control of Host-Bacterial Pathogen Interactions in the Gastrointestinal Tract.

Valerie Ramirez, Samantha Swain, Kaitlin Murray, Colin Reardon

Open access · greenAbstract readReview
In one paragraph

Review in Infection and immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Substance P receptor signaling contributes to host maladaptive responses during enteric bacterial infection.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Experimental colitis-induced visceral hypersensitivity is attenuated by GABA treatment in mice.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  5. The enteric nervous system.Physiological reviews · 2023
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
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

4 authors at 1 institution in 1 country.

Valerie RamirezDepartment. of Anatomy, Physiology, and Cell Biology, UC Davis School of Veterinary Medicine, Davis, California, USA.
Samantha SwainDepartment. of Anatomy, Physiology, and Cell Biology, UC Davis School of Veterinary Medicine, Davis, California, USA.
Kaitlin MurrayDepartment. of Anatomy, Physiology, and Cell Biology, UC Davis School of Veterinary Medicine, Davis, California, USA.
Colin ReardonDepartment. of Anatomy, Physiology, and Cell Biology, UC Davis School of Veterinary Medicine, Davis, California, USA creardon@ucdavis.edu.ORCID 0000-0003-2204-8091
University of California, Davis · US

Funding

Coordination of mucosal immune response to enteric bacterial pathogens by nociceptive innervationR01AI150647 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI REARDON, COLIN · 2020 to 2024
$2.4M
Predoctoral Training in Pharmacological SciencesT32GM099608 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HELL, JOHANNES W · 2012 to 2021
$2.2M
Neuro-immune mediated control of mucosal immunityR21AI133116 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI REARDON, COLIN · 2017 to 2018
$417k
NIAID NIH HHS R01 AI150647NIAID NIH HHS R21 AI133116NIGMS NIH HHS T32 GM099608
6 · The paper itself

Abstract

The orchestration of host immune responses to enteric bacterial pathogens is a complex process involving the integration of numerous signals, including from the nervous system. Despite the recent progress in understanding the contribution of neuroimmune interactions in the regulation of inflammation, the mechanisms and effects of this communication during enteric bacterial infection are only beginning to be characterized. As part of this neuroimmune communication, neurons specialized to detect painful or otherwise noxious stimuli can respond to bacterial pathogens. Highlighting the complexity of these systems, the immunological consequences of sensory neuron activation can be either host adaptive or maladaptive, depending on the pathogen and organ system. These are but one of many types of neuroimmune circuits, with the vagus nerve and sympathetic innervation of numerous organs now known to modulate immune cell function and therefore dictate immunological outcomes during health and disease. Here, we review the evidence for neuroimmune communication in response to bacterial pathogens, and then discuss the consequences to host morbidity and mortality during infection of the gastrointestinal tract.

Indexed as

AnimalsCalcitonin Gene-Related PeptideCitrobacterEnteric Nervous SystemEnterobacteriaceae InfectionsGastrointestinal MicrobiomeGastrointestinal TractGene Expression RegulationHost-Pathogen InteractionsHumansNeuroimmunomodulationPathogen-Associated Molecular Pattern MoleculesSensory Receptor CellsToll-Like ReceptorsTRPA1 Cation ChannelTRPV Cation ChannelsCalcitonin Gene-Related PeptidePathogen-Associated Molecular Pattern MoleculesToll-Like ReceptorsTRPA1 Cation ChannelTRPA1 protein, humanTRPV1 protein, humanTRPV Cation Channelscholinergic anti-inflammatory pathwayCitrobacterenteric bacterial pathogensenteric nervous systementeric pathogensgastrointestinal infectiongastrointestinal inflammationhost defenseneuroimmunologysensory neuronsvagus nerve

Identifiers

PMID32341116
PMCPMC7440759
OpenAlexW3018963665

What OpenQuestion holds

Textmetadata
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.