Evidence map›Paper›PMID 24866806›Full record

ArticleInfection and immunity2014

Inflammatory effects of Edwardsiella ictaluri lipopolysaccharide modifications in catfish gut.

Javier Santander, Jacquelyn Kilbourne, Jie-Yeun Park, Taylor Martin, Amanda Loh, Ignacia Diaz, Robert Rojas, Cristopher Segovia, Dale DeNardo, Roy Curtiss

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 20 citations in OpenAlex.

  1. Frontiers in immunology · 2019
    Article
  2. Effects of Vitamin DFrontiers in immunology · 2019
    Article
  3. Article
  4. Review
  5. 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

10 authors at 2 institutions in 2 countries.

Javier SantanderCenter for Infectious Diseases and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, Arizona, USA Microbial Pathogenesis and Vaccinology Laboratory, Nucleus for Microbiology and Immunity, Faculty of Sciences, Universidad Mayor, Huechuraba, Chile School of Life Sciences, Arizona State University, Tempe, Arizona, USA javier.santander@umayor.cl.
Jacquelyn KilbourneCenter for Infectious Diseases and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
Jie-Yeun ParkCenter for Infectious Diseases and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, Arizona, USA.
Taylor MartinCenter for Infectious Diseases and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, Arizona, USA School of Life Sciences, Arizona State University, Tempe, Arizona, USA.
Amanda LohCenter for Infectious Diseases and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, Arizona, USA School of Life Sciences, Arizona State University, Tempe, Arizona, USA.
Ignacia DiazCenter for Infectious Diseases and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, Arizona, USA Microbial Pathogenesis and Vaccinology Laboratory, Nucleus for Microbiology and Immunity, Faculty of Sciences, Universidad Mayor, Huechuraba, Chile Department of Physics, Master Program in Nanoscience, Arizona State University, Tempe, Arizona, USA.
Robert RojasMucosal Immunity Laboratory, Nucleus for Microbiology and Immunity, Faculty of Sciences, Universidad Mayor, Huechuraba, Chile.
Cristopher SegoviaMicrobial Pathogenesis and Vaccinology Laboratory, Nucleus for Microbiology and Immunity, Faculty of Sciences, Universidad Mayor, Huechuraba, Chile.
Dale DeNardoSchool of Life Sciences, Arizona State University, Tempe, Arizona, USA.
Roy CurtissCenter for Infectious Diseases and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, Arizona, USA School of Life Sciences, Arizona State University, Tempe, Arizona, USA.
Arizona State University · USUniversidad Mayor · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial lipopolysaccharides (LPS) are structural components of the outer membranes of Gram-negative bacteria and also are potent inducers of inflammation in mammals. Higher vertebrates are extremely sensitive to LPS, but lower vertebrates, like fish, are resistant to their systemic toxic effects. However, the effects of LPS on the fish intestinal mucosa remain unknown. Edwardsiella ictaluri is a primitive member of the Enterobacteriaceae family that causes enteric septicemia in channel catfish (Ictalurus punctatus). E. ictaluri infects and colonizes deep lymphoid tissues upon oral or immersion infection. Both gut and olfactory organs are the primary sites of invasion. At the systemic level, E. ictaluri pathogenesis is relatively well characterized, but our knowledge about E. ictaluri intestinal interaction is limited. Recently, we observed that E. ictaluri oligo-polysaccharide (O-PS) LPS mutants have differential effects on the intestinal epithelia of orally inoculated catfish. Here we evaluate the effects of E. ictaluri O-PS LPS mutants by using a novel catfish intestinal loop model and compare it to the rabbit ileal loop model inoculated with Salmonella enterica serovar Typhimurium LPS. We found evident differences in rabbit ileal loop and catfish ileal loop responses to E. ictaluri and S. Typhimurium LPS. We determined that catfish respond to E. ictaluri LPS but not to S. Typhimurium LPS. We also determined that E. ictaluri inhibits cytokine production and induces disruption of the intestinal fish epithelia in an O-PS-dependent fashion. The E. ictaluri wild type and ΔwibT LPS mutant caused intestinal tissue damage and inhibited proinflammatory cytokine synthesis, in contrast to E. ictaluri Δgne and Δugd LPS mutants. We concluded that the E. ictaluri O-PS subunits play a major role during pathogenesis, since they influence the recognition of the LPS by the intestinal mucosal immune system of the catfish. The LPS structure of E. ictaluri mutants is needed to understand the mechanism of interaction.

Indexed as

AnimalsCatfishesEdwardsiella ictaluriGastrointestinal TractInflammationIntestinal MucosaLipopolysaccharidesMutationLipopolysaccharides

Identifiers

PMID24866806
PMCPMC4136215
OpenAlexW2117700646

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.