Evidence map›Paper›PMID 18936179›Full record

ArticleInfection and immunity2009

The mechanism of Bacillus anthracis intracellular germination requires multiple and highly diverse genetic loci.

Soumitra Barua, Matthew McKevitt, Kevin DeGiusti, Elaine E Hamm, Jason Larabee, Salika Shakir, Katie Bryant, Theresa M Koehler, Steven R Blanke, David Dyer and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

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  10. Bacillus anthracis physiology and genetics.Molecular aspects of medicine · 2009
    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

12 authors at 3 institutions in 1 country.

Soumitra BaruaDepartment of Microbiology and Immunology, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104, USA.
Matthew McKevitt
Kevin DeGiusti
Elaine E Hamm
Jason Larabee
Salika Shakir
Katie Bryant
Theresa M Koehler
Steven R Blanke
David Dyer
Allison Gillaspy
Jimmy D Ballard
University of Oklahoma Health Sciences Center · USThe University of Texas Health Science Center at Houston · USUniversity of Illinois Urbana-Champaign · US

Funding

WRCE Nonhuman Primate CoreU54AI057156 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI WALKER, DAVID H · 2003 to 2013
$102.6M
VIRULENCE GENE EXPRESSION BY BACILLUS ANTHRACISR01AI033537 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KOEHLER, THERESA M. · 1998 to 2020
$5.4M
CONTROL OF PROTECTIVE ANTIGEN SYNTHESIS BY B ANTHRACISR29AI033537 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KOEHLER, THERESA M. · 1993 to 1997
–
NIAID NIH HHS AI33537NIAID NIH HHS R01 AI033537NIAID NIH HHS U54 AI057156NIAID NIH HHS U54AI057156
6 · The paper itself

Abstract

In an effort to better understand the mechanisms by which Bacillus anthracis establishes disease, experiments were undertaken to identify the genes essential for intracellular germination. Eighteen diverse genetic loci were identified via an enrichment protocol using a transposon-mutated library of B. anthracis spores, which was screened for mutants delayed in intracellular germination. Fourteen transposon mutants were identified in genes not previously associated with B. anthracis germination and included disruption of factors involved in membrane transport, transcriptional regulation, and intracellular signaling. Four mutants contained transposon insertions in gerHA, gerHB, gerHC, and pagA, respectively, each of which has been previously associated with germination or survival of B. anthracis within macrophages. Strain MIGD101 (named for macrophage intracellular germination defective 101) was of particular interest, since this mutant contained a transposon insertion in an intergenic region between BAs2807 and BAs2808, and was the most highly represented mutant in the enrichment. Analysis of B. anthracis MIGD101 by confocal microscopy and differential heat sensitivity following macrophage infection revealed ungerminated spores within the cell. Moreover, B. anthracis MIGD101 was attenuated in cell killing relative to the parent strain. Further experimental analysis found that B. anthracis MIGD101 was defective in five known B. anthracis germination pathways, supporting a mechanism wherein the intergenic region between BAs2807 and BAs2808 has a global affect on germination of this pathogen. Collectively, these findings provide insight into the mechanisms supporting B. anthracis germination within host cells.

Indexed as

AnimalsBacillus anthracisBacterial ProteinsCell LineCell SurvivalColony Count, MicrobialDNA Transposable ElementsGene OrderGenes, BacterialMacrophagesMiceMutagenesis, InsertionalSpores, BacterialVirulenceVirulence FactorsBacterial ProteinsDNA Transposable ElementsVirulence Factors

Identifiers

PMID18936179
PMCPMC2612280
OpenAlexW2096240968

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.