Evidence map›Paper›PMID 25964473›Full record

ArticleInfection and immunity2015

The Human Antimicrobial Protein Calgranulin C Participates in Control of Helicobacter pylori Growth and Regulation of Virulence.

Kathryn P Haley, Alberto G Delgado, M Blanca Piazuelo, Brittany L Mortensen, Pelayo Correa, Steven M Damo, Walter J Chazin, Eric P Skaar, Jennifer A Gaddy

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
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  6. Article
  7. Pathogenic role of S100 proteins in psoriasis.Frontiers in immunology · 2023
    Review
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  20. Calcium Regulates S100A12 Zinc Sequestration by Limiting Structural Variations.Chembiochem : a European journal of chemical biology · 2020
    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 2 institutions in 1 country.

Kathryn P HaleyDepartment of Medicine, Vanderbilt University, Nashville, Tennessee, USA.
Alberto G DelgadoDepartment of Medicine, Vanderbilt University, Nashville, Tennessee, USA.
M Blanca PiazueloDepartment of Medicine, Vanderbilt University, Nashville, Tennessee, USA.
Brittany L MortensenDepartment of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Pelayo CorreaDepartment of Medicine, Vanderbilt University, Nashville, Tennessee, USA Department of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Steven M DamoDepartments of Biochemistry and Chemistry, Vanderbilt University, Nashville, Tennessee, USA Center for Structural Biology, Vanderbilt University, Nashville, Tennessee, USA Department of Life and Physical Sciences, Fisk University, Nashville, Tennessee, USA.
Walter J ChazinDepartments of Biochemistry and Chemistry, Vanderbilt University, Nashville, Tennessee, USA Center for Structural Biology, Vanderbilt University, Nashville, Tennessee, USA.
Eric P SkaarVeterans Affairs Tennessee Valley Healthcare Services, Nashville, Tennessee, USA Department of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
Jennifer A GaddyVeterans Affairs Tennessee Valley Healthcare Services, Nashville, Tennessee, USA Department of Medicine, Vanderbilt University, Nashville, Tennessee, USA jennifer.a.gaddy@vanderbilt.edu.
Vanderbilt University · USVA Tennessee Valley Healthcare System · US

Funding

VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Project 3 - Molecular Signatures of Gastric Carcinogenesis in the Host Response to H. pyloriP01CA028842 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WILSON, KEITH T. · 1985 to 2019
$15.8M
Host-mediated zinc sequestration during Acinetobacter baumannii infectionR01AI101171 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI WALTER J. CHAZIN, DAVID P. GIEDROC · 2013 to 2026
$8.2M
MOLECULAR BIOPHYSICS TRAINING PROGRAM AT VANDERBILTT32GM008320 · NIGMS · VANDERBILT UNIVERSITY · PI CHAZIN, WALTER J. · 1989 to 2023
$7.9M
Childhood Infections Research ProgramT32AI095202 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI JAMES E CASSAT · 2011 to 2026
$4.2M
Elucidating the A. baumannii response to calprotectin-mediated zinc starvationF32AI108192 · NIAID · VANDERBILT UNIVERSITY · PI NAIRN, BRITTANY LYNNE · 2013 to 2014
$102k
Regulation of Helicobacter pylori pili encoded by the cag pathogenicity islandIK2BX001701 · VA · VETERANS HEALTH ADMINISTRATION · PI GADDY, JENNIFER A · 2013 to 2017
–
BLRD VA IK2 BX001701NCATS NIH HHS 2 UL1TR000445-06NCATS NIH HHS UL1 TR000445NCI NIH HHS P01 CA028842NCRR NIH HHS UL1 RR024975NCRR NIH HHS UL1 RR024975-01NIAID NIH HHS F32 AI108192NIAID NIH HHS R01 AI101171NIAID NIH HHS T32 AI095202NIAID NIH HHS T32-AI095202NIDDK NIH HHS P30 DK058404NIDDK NIH HHS P30DK058404NIGMS NIH HHS T32 GM008320
6 · The paper itself

Abstract

During infectious processes, antimicrobial proteins are produced by both epithelial cells and innate immune cells. Some of these antimicrobial molecules function by targeting transition metals and sequestering these metals in a process referred to as "nutritional immunity." This chelation strategy ultimately starves invading pathogens, limiting their growth within the vertebrate host. Recent evidence suggests that these metal-binding antimicrobial molecules have the capacity to affect bacterial virulence, including toxin secretion systems. Our previous work showed that the S100A8/S100A9 heterodimer (calprotectin, or calgranulin A/B) binds zinc and represses the elaboration of the H. pylori cag type IV secretion system (T4SS). However, there are several other S100 proteins that are produced in response to infection. We hypothesized that the zinc-binding protein S100A12 (calgranulin C) is induced in response to H. pylori infection and also plays a role in controlling H. pylori growth and virulence. To test this, we analyzed gastric biopsy specimens from H. pylori-positive and -negative patients for S100A12 expression. These assays showed that S100A12 is induced in response to H. pylori infection and inhibits bacterial growth and viability in vitro by binding nutrient zinc. Furthermore, the data establish that the zinc-binding activity of the S100A12 protein represses the activity of the cag T4SS, as evidenced by the gastric cell "hummingbird" phenotype, interleukin 8 (IL-8) secretion, and CagA translocation assays. In addition, high-resolution field emission gun scanning electron microscopy (FEG-SEM) was used to demonstrate that S100A12 represses biogenesis of the cag T4SS. Together with our previous work, these data reveal that multiple S100 proteins can repress the elaboration of an oncogenic bacterial surface organelle.

Indexed as

AdultBiopsyGastric MucosaHelicobacter InfectionsHelicobacter pyloriHumansMicrobial ViabilityMicroscopy, Electron, ScanningS100A12 ProteinS100 ProteinsVirulenceZincS100A12 ProteinS100A12 protein, humanS100 ProteinsZinc

Identifiers

PMID25964473
PMCPMC4468547
OpenAlexW1960988776

What OpenQuestion holds

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Registered trials

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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.