Literature DB >> 4289811

Metabolic changes in nicotinamide adenine dinucleotide in response to anthrax toxin.

I Gray, L J Archer.   

Abstract

Bacillus anthracis produces a toxin both in vitro and in vivo which, when injected intravenously into rats, brings about the death of the animals accompanied by gross pulmonary edema. Lung tissue removed prior to death showed, in vitro, a 30% reduction in overall oxidative metabolism (Q(o2)), whereas the nicotinamide adenine dinucleotide (NAD)-independent succinic dehydrogenase remained unaffected. The NAD concentration in the lungs of injected animals was reduced by 50%. Upon addition of NAD, the Q(o2) of lung tissue from injected animals rose to control values. At 45 min after toxin injection, the serum lactate concentration began to rise, showing about a 3.5-fold increase over controls after 75 min. No changes occurred in the pyruvate concentration. These changes may be explained by increased use of the pyruvate for glycolytic energy production with further loss of NAD. Additional experiments with liver, spleen, kidney, and brain tissues showed that the toxin-induced reduction of Q(o2) is an effect specific for lung tissue. Brain tissue showed a significant increase in oxidative metabolism upon the addition of the toxin, whereas the other tissues remained unaffected. It is suggested that a principal effect of the toxin is to inhibit, in lung tissue, the regeneration of NAD in the respiratory chain.

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Year:  1967        PMID: 4289811      PMCID: PMC314964          DOI: 10.1128/jb.93.1.36-39.1967

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  12 in total

1.  Purification of factor I and recognition of a third factor of the anthrax toxin.

Authors:  J L STANLEY; H SMITH
Journal:  J Gen Microbiol       Date:  1961-09

2.  The three factors of anthrax toxin: their immunogenicity and lack of demonstrable enzymic activity.

Authors:  J L STANLEY; H SMITH
Journal:  J Gen Microbiol       Date:  1963-05

3.  Production of toxin in vitro by Bacillus anthracis and its spearation into two components.

Authors:  C B THORNE; D M MOLNAR; R E STRANGE
Journal:  J Bacteriol       Date:  1960-03       Impact factor: 3.490

4.  Mechanism of action of the toxin of Bacillus anthracis. I. Effect in vivo on some blood serum components.

Authors:  M W SLEIN; G F LOGAN
Journal:  J Bacteriol       Date:  1960-07       Impact factor: 3.490

5.  Production in vitro of the toxin of Bacillus anthracis previously recognized in vivo.

Authors:  P W HARRIS-SMITH; H SMITH; J KEPPIE
Journal:  J Gen Microbiol       Date:  1958-08

6.  Pathophysiological investigations into the terminal course of experimental anthrax in the rabbit.

Authors:  B K NORDBERG; C G SCHMITERLOW; H J HANSEN
Journal:  Acta Pathol Microbiol Scand       Date:  1961

7.  The pathogenesis of the lethal effect of anthrax toxin in the rat.

Authors:  F A Beall; F G Dalldorf
Journal:  J Infect Dis       Date:  1966-06       Impact factor: 5.226

8.  Pathophysiology of anthrax.

Authors:  F Klein; J S Walker; D F Fitzpatrick; R E Lincoln; B G Mahlandt; W I Jones; J P Dobbs; K J Hendrix
Journal:  J Infect Dis       Date:  1966-04       Impact factor: 5.226

9.  The chemical basis of the virulence of Bacillus anthracis. V. The specific toxin produced by B. Anthracis in vivo.

Authors:  H SMITH; J KEPPIE; J L STANLEY
Journal:  Br J Exp Pathol       Date:  1955-10

10.  QUANTITATIVE ASSAY FOR CRUDE ANTHRAX TOXINS.

Authors:  B W HAINES; F KLEIN; R E LINCOLN
Journal:  J Bacteriol       Date:  1965-01       Impact factor: 3.490

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  1 in total

1.  Mechanisms of pathogenesis in Listeria monocytogenes infection. V. Early imbalance in host energy metabolism during experimental listeriosis.

Authors:  R E McCallum; C P Sword
Journal:  Infect Immun       Date:  1972-06       Impact factor: 3.441

  1 in total

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