Evidence map›Paper›PMID 21371137›Full record

ArticleMolecular microbiology2011

Two capsular polysaccharides enable Bacillus cereus G9241 to cause anthrax-like disease.

So-Young Oh, Jonathan M Budzik, Gabriella Garufi, Olaf Schneewind

Abstract read
In one paragraph

Article in Molecular microbiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
–field-weighted citation impact
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

48 citing papers in PubMed.

  1. Article
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  6. Review
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  8. Pathogenicity and Genomic Characterization of a Novel Genospecies,International journal of molecular sciences · 2023
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  19. Characterization ofFrontiers in microbiology · 2020
    Article
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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.

So-Young OhDepartment of Microbiology, University of Chicago, Chicago, IL 60637, USA.
Jonathan M Budzik
Gabriella Garufi
Olaf Schneewind

Funding

Vaccines and Therapies Against BotulismU54AI057153 · NIAID · UNIVERSITY OF CHICAGO · PI SHUMAN, HOWARD A · 2003 to 2013
$87.6M
MEDICAL SCIENTIST TRAININGT32GM007281 · NIGMS · UNIVERSITY OF CHICAGO · PI CLARK, MARCUS RAMSAY · 1985 to 2022
$32.1M
Surface Proteins of Gram-Positive BacteriaR01AI038897 · NIAID · UNIVERSITY OF CHICAGO · PI MISSIAKAS, DOMINIQUE M. · 1996 to 2024
$8.9M
Surface Proteins of Bacillus anthracisR01AI069227 · NIAID · UNIVERSITY OF CHICAGO · PI Dominique Missiakas · 2007 to 2026
$6.5M
Surface Proteins of Bacillus anthracisR37AI069227 · NIAID · UNIVERSITY OF CHICAGO · PI SCHNEEWIND, OLAF · 2017 to 2018
$809k
NIAID NIH HHS R01 AI038897NIAID NIH HHS R01 AI069227NIAID NIH HHS R37 AI069227NIAID NIH HHS U54 AI057153NIGMS NIH HHS T32 GM007281
6 · The paper itself

Abstract

Bacillus cereus G9241 causes an anthrax-like respiratory illness in humans; however, the molecular mechanisms of disease pathogenesis are not known. Genome sequencing identified two putative virulence plasmids proposed to provide for anthrax toxin (pBCXO1) and/or capsule expression (pBC218). We report here that B. cereus G9241 causes anthrax-like disease in immune-competent mice, which is dependent on each of the two virulence plasmids. pBCXO1 encodes pagA1, the homologue of anthrax protective antigen, as well as hasACB, providing for hyaluronic acid capsule formation, two traits that each contribute to disease pathogenesis. pBC218 harbours bpsX-H, B. cereus exo-polysaccharide, which produce a second capsule. During infection, B. cereus G9241 elaborates both hasACB and bpsX-H capsules, which together are essential for the establishment of anthrax-like disease and the resistance of bacilli to phagocytosis. A single nucleotide deletion causes premature termination of hasA translation in Bacillus anthracis, which is known to escape phagocytic killing by its pXO2 encoded poly-d-γ-glutamic acid (PDGA) capsule. Thus, multiple different gene clusters endow pathogenic bacilli with capsular material, provide for escape from innate host immune responses and aid in establishing the pathogenesis of anthrax-like disease.

Indexed as

PlasmidsAnimalsAnthraxBacillus cereusGram-Positive Bacterial InfectionsImmune EvasionMiceMice, Inbred C57BLMultigene FamilyPhagocytosisPolysaccharides, BacterialSurvival AnalysisVirulenceVirulence FactorsPolysaccharides, BacterialVirulence Factors

Identifiers

PMID21371137
PMCPMC3538873

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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.