Evidence map›Paper›PMID 26388860›Full record

ArticleFrontiers in microbiology2015

Nitric oxide as a regulator of B. anthracis pathogenicity.

Taissia G Popova, Allison Teunis, Haley Vaseghi, Weidong Zhou, Virginia Espina, Lance A Liotta, Serguei G Popov

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

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  8. Adaptation inFrontiers in microbiology · 2016
    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

7 authors at 1 institution in 1 country.

Taissia G PopovaNational Center for Biodefense and Infectious Disease, College of Science, George Mason University, Manassas, VA USA ; Center for Applied Proteomics and Molecular Medicine, College of Science, George Mason University, Manassas, VA USA.
Allison TeunisCenter for Applied Proteomics and Molecular Medicine, College of Science, George Mason University, Manassas, VA USA.
Haley VaseghiUniversity of North Carolina at Chapel Hill, Chapel Hill, NC USA.
Weidong ZhouCenter for Applied Proteomics and Molecular Medicine, College of Science, George Mason University, Manassas, VA USA.
Virginia EspinaCenter for Applied Proteomics and Molecular Medicine, College of Science, George Mason University, Manassas, VA USA.
Lance A LiottaCenter for Applied Proteomics and Molecular Medicine, College of Science, George Mason University, Manassas, VA USA.
Serguei G PopovNational Center for Biodefense and Infectious Disease, College of Science, George Mason University, Manassas, VA USA.
University of North Carolina at Chapel Hill · US

Funding

Microparticle Capture-Based Analysis of Lymph Node ProteomeR21AI099851 · NIAID · GEORGE MASON UNIVERSITY · PI ESPINA, VIRGINIA ANNE, LIOTTA, LANCE ALLEN · 2013 to 2014
$405k
NIAID NIH HHS R21 AI099851
6 · The paper itself

Abstract

Nitric oxide (NO) is a key physiological regulator in eukaryotic and prokaryotic organisms. It can cause a variety of biological effects by reacting with its targets or/and indirectly inducing oxidative stress. NO can also be produced by bacteria including the pathogenic Bacillus anthracis; however, its role in the infectious process only begins to emerge. NO incapacitates macrophages by S-nitrosylating the intracellular proteins and protects B. anthracis from oxidative stress. It is also implicated in the formation of toxic peroxynitrite. In this study we further assessed the effects of B. anthracis NO produced by the NO synthase (bNOS) on bacterial metabolism and host cells in experiments with the bNOS knockout Sterne strain. The mutation abrogated accumulation of nitrite and nitrate as tracer products of NO in the culture medium and markedly attenuated growth in both aerobic and microaerobic conditions. The regulatory role of NO was also suggested by the abnormally high rate of nitrate denitrification by the mutant in the presence of oxygen. Anaerobic regulation mediated by NO was reflected in reduced fermentation of glucose by the mutant correlating with the reduced toxicity of bacteria toward host cells in culture. The toxic effect of NO required permeabilization of the target cells as well as the activity of fermentation-derived metabolite in the conditions of reduced pH. The host cells demonstrated increased phosphorylation of major survivor protein kinase AKT correlating with reduced toxicity of the mutant in comparison with Sterne. Our global proteomic analysis of lymph from the lymph nodes of infected mice harboring bacteria revealed numerous changes in the pattern and levels of proteins associated with the activity of bNOS influencing key cell physiological processes relevant to energy metabolism, growth, signal transduction, stress response, septic shock, and homeostasis. This is the first in vivo observation of the bacterial NO effect on the lymphatic system.

Indexed as

anthraxlymph nodenitric oxidenitric oxide synthaseproteome

Identifiers

PMID26388860
PMCPMC4557104
OpenAlexW1852318297

What OpenQuestion holds

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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.