Evidence map›Paper›PMID 17502390›Full record

ArticleInfection and immunity2007

Protective role of Bacillus anthracis exosporium in macrophage-mediated killing by nitric oxide.

John Weaver, Tae Jin Kang, Kimberly W Raines, Guan-Liang Cao, Stephen Hibbs, Pei Tsai, Les Baillie, Gerald M Rosen, Alan S Cross

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Insights into the Structure and Protein Composition ofInternational journal of molecular sciences · 2022
    Article
  4. Review
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  6. Article
  7. TheMicrobiology spectrum · 2019
    Review
  8. Article
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  11. Article
  12. Article
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  17. Review
  18. Article
  19. Surface architecture of endospores of the Bacillus cereus/anthracis/thuringiensis family at the subnanometer scale.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  20. 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 3 institutions in 2 countries.

John WeaverCenter for Vaccine Development, Department of Medicine, University of Maryland School of Medicine, 685 W. Baltimore Street, Baltimore, MD 21201, USA.
Tae Jin Kang
Kimberly W Raines
Guan-Liang Cao
Stephen Hibbs
Pei Tsai
Les Baillie
Gerald M Rosen
Alan S Cross
Biotechnology Institute · USCardiff University · GBUniversity of Maryland, Baltimore · US

Funding

Vaccine strategy for broad spectrum protection agains non-typhoidal salmonellU54AI057168 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI BUSHMAN, FREDERIC D · 2003 to 2013
$91.5M
Very Low Frequency EPR Imaging in Vivo Phisiology P41 EB02034P41EB002034 · NIBIB · UNIVERSITY OF CHICAGO · PI HALPERN, HOWARD J · 2003 to 2017
$16.1M
NIAID NIH HHS U54 AI 057168NIAID NIH HHS U54 AI057168NIBIB NIH HHS EB 2034NIBIB NIH HHS P41 EB002034
6 · The paper itself

Abstract

The ability of the endospore-forming, gram-positive bacterium Bacillus anthracis to survive in activated macrophages is key to its germination and survival. In a previous publication, we discovered that exposure of primary murine macrophages to B. anthracis endospores upregulated NOS 2 concomitant with an .NO-dependent bactericidal response. Since NOS 2 also generates O(2).(-), experiments were designed to determine whether NOS 2 formed peroxynitrite (ONOO(-)) from the reaction of .NO with O(2).(-) and if so, was ONOO(-) microbicidal toward B. anthracis. Our findings suggest that ONOO(-) was formed upon macrophage infection by B. anthracis endospores; however, ONOO(-) does not appear to exhibit microbicidal activity toward this bacterium. In contrast, the exosporium of B. anthracis, which exhibits arginase activity, protected B. anthracis from macrophage-mediated killing by decreasing .NO levels in the macrophage. Thus, the ability of B. anthracis to subvert .NO production has important implications in the control of B. anthracis-induced infection.

Indexed as

Microbial ViabilityAnimalsAnti-Bacterial AgentsBacillus anthracisCells, CulturedMacrophages, PeritonealMiceNitric OxidePeroxynitrous AcidReactive Oxygen SpeciesSpores, BacterialAnti-Bacterial AgentsNitric OxidePeroxynitrous AcidReactive Oxygen Species

Identifiers

PMID17502390
PMCPMC1951973
OpenAlexW2149718558

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.