Evidence map›Paper›PMID 30633767›Full record

ArticlePloS one2019

A proteome-wide screen of Campylobacter jejuni using protein microarrays identifies novel and conformational antigens.

Jiayou Liu, Jodi R Parrish, Julie Hines, Linda Mansfield, Russell L Finley

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. 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 32% 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, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Antibody reactive immunomes ofFrontiers in cellular and infection microbiology · 2023
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. NPJ vaccines · 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

5 authors at 2 institutions in 1 country.

Jiayou LiuCenter for Molecular Medicine & Genetics, Wayne State University School of Medicine, Detroit, Michigan, United States of America.
Jodi R ParrishCenter for Molecular Medicine & Genetics, Wayne State University School of Medicine, Detroit, Michigan, United States of America.
Julie HinesCenter for Molecular Medicine & Genetics, Wayne State University School of Medicine, Detroit, Michigan, United States of America.
Linda MansfieldDepartment of Microbiology & Molecular Genetics, Michigan State University, East Lansing, Michigan, United States of America.ORCID 0000-0002-7523-7577
Russell L FinleyCenter for Molecular Medicine & Genetics, Wayne State University School of Medicine, Detroit, Michigan, United States of America.ORCID 0000-0003-1144-6887
Wayne State University · USMichigan United · US

Funding

The Impact of Microbiome Composition, Diversity, and Function on Enteric DiseaseU19AI090872 · NIAID · MICHIGAN STATE UNIVERSITY · PI MANSFIELD, LINDA S. · 2010 to 2014
$7.1M
MRU - Food & Waterborne Diseases Integrated Research NetworkN01AI30058 · NIAID · MICHIGAN STATE UNIVERSITY · 2007 to 2010
$5.1M
Defining the role of the early infant microbiome in mediating allergic outcomes associated with asthma in a mouse modelR21AI121748 · NIAID · MICHIGAN STATE UNIVERSITY · PI EWART, SUSAN L, MANSFIELD, LINDA S. · 2016 to 2017
$426k
NIAID NIH HHS N01 AI030058NIAID NIH HHS N01AI30058NIAID NIH HHS R21 AI121748NIAID NIH HHS U19 AI090872
6 · The paper itself

Abstract

Campylobacter jejuni (C. jejuni) is a foodborne intestinal pathogen and major cause of gastroenteritis worldwide. C. jejuni proteins that are immunogenic have been sought for their potential use in the development of biomarkers, diagnostic assays, or subunit vaccines for humans or livestock. To identify new immunogenic C. jejuni proteins, we used a native protein microarray approach. A protein chip, with over 1400 individually purified GST-tagged C. jejuni proteins, representing over 86% of the proteome, was constructed to screen for antibody titers present in test sera raised against whole C. jejuni cells. Dual detection of GST signals was incorporated as a way of normalizing the variation of protein concentrations contributing to the antibody staining intensities. We detected strong signals to 102 C. jejuni antigens. In addition to antigens recognized by antiserum raised against C. jejuni, parallel experiments were conducted to identify antigens cross-reactive to antiserum raised against various serotypes of E. coli or Salmonella or to healthy human sera. This led to the identification of 34 antigens specifically recognized by the C. jejuni antiserum, only four of which were previously known. The chip approach also allowed identification of conformational antigens. We demonstrate in the case of Cj1621 that antigen signals are lost to denaturing conditions commonly used in other approaches to identify immunogens. Antigens identified in this study include those possessing sequence features indicative of cell surface localization, as well as those that do not. Together, our results indicate that the unbiased chip-based screen can help reveal the full repertoire of host antibodies against microbial proteomes.

Indexed as

AnimalsAntibodies, BacterialAntigens, BacterialBacterial ProteinsCampylobacter InfectionsCampylobacter jejuniCross ReactionsHumansMiceProtein Array AnalysisProtein ConformationProteomeRecombinant Fusion ProteinsSequence Analysis, ProteinAntibodies, BacterialAntigens, BacterialBacterial ProteinsProteomeRecombinant Fusion Proteins

Identifiers

PMID30633767
PMCPMC6329530
OpenAlexW2909652762

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.