Literature DB >> 13278457

The behavior of virulent and avirulent staphylococci in the tissues of normal mice.

J M SMITH, R J DUBOS.   

Abstract

The fate of hemolytic staphylococci injected intravenousiy into albino mice was followed by determining quantitatively the numbers of living organisms present in the various tissues at different intervals of time after infection. Irrespective of the strain of staphylococcus used, most of the organisms disappeared rapidly from the blood, liver, spleen, and kidneys. This was true even when the infective dose consisted of large numbers of virulent, coagulase-positive staphylococci, capable of producing a fatal disease in a high percentage of the infected mice. The initial rate of removal or destruction of staphylococci was particularly high in the lungs and kidneys. In all cases on the other hand, a few living staphylococci persisted in the various organs for several weeks after infection, even when the organisms were non-virulent and coagulase-negative. Although virulent as well as avirulent staphylococci were eliminated extremely rapidly and efficiently from the kidneys during the initial stage of infection, the microorganisms soon began to multiply in this organ, causing abscesses first detected in the cortex. Death of the animals infected with virulent cultures appeared to be due to the destruction of renal tissue by these abscesses. The abscesses caused by the avirulent strains eventually became sterile, and healed. No convincing difference could be recognized amongst seven strains in their resistance to the bactericidal power of the mouse tissues during the initial phase of the infection. In contrast, marked quantitative differences came to light in their subsequent behavior in the kidneys. The multiplication of the coagulase-negative staphylococci in this organ soon came to an end in all animals and never proceeded far enough to result in fatal disease. The staphylococci of a weakly coagulase-positive strain multiplied somewhat more extensively in the kidneys than did the coagulase-negative, but never sufficiently to cause the death of any animal within the period of observation of 1 month. The three coagulase-positive strains tested yielded the largest bacterial population in the kidneys and caused the death of many of the infected animals. These three virulent strains differed quantitatively amongst themselves with regard to both the rapidity and extent of their multiplication in the kidneys and the lethal power of a given infective dose. Taken together, the findings indicate that the hemolytic strains of staphylococci can be arranged in a continuous spectrum according to their ability to cause disease in albino mice. Although virulence for these animals appeared to be correlated with the production of coagulase, it did not seem to depend upon the ability of this substance to interfere with the bactericidal mechanisms of the mouse organs during the early phase of the infection. Virulence manifested itself chiefly by the production in the kidneys of progressive abscesses originating from the few staphylococci which were not destroyed during the initial bactericidal reaction.

Entities:  

Keywords:  MICROCOCCUS PYOGENES

Mesh:

Substances:

Year:  1956        PMID: 13278457      PMCID: PMC2136557          DOI: 10.1084/jem.103.1.87

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  12 in total

1.  A study of 435 strains of Staphylococcus pyogenes with reference to factors which may contribute to pathogenicity.

Authors:  C H LACK; D G WAILLING
Journal:  J Pathol Bacteriol       Date:  1954-10

2.  Pathogenicity of staphylococci; a comparison of alpha-hemolysin production with the coagulase test and clinical observations of virulence.

Authors:  G G JACKSON; H F DOWLING; M H LEPPER
Journal:  N Engl J Med       Date:  1955-06-16       Impact factor: 91.245

3.  Coagulase in reversing antibacterial activity of normal human serum on Micrococcus pyogenes.

Authors:  R D EKSTEDT; W J NUNGESTER
Journal:  Proc Soc Exp Biol Med       Date:  1955-05

4.  Vitamin nutrition of the staphylococci with special reference to their biotin requirements.

Authors:  A C GRETLER; P MUCCIOLO; J B EVANS; C F NIVEN
Journal:  J Bacteriol       Date:  1955-07       Impact factor: 3.490

5.  Origin of penicillin-resistant Staphylococcus pyogenes.

Authors:  J C GOULD
Journal:  Nature       Date:  1955-07-23       Impact factor: 49.962

6.  THE COAGULASE TEST FOR STAPHYLOCOCCI AND ITS CORRELATION WITH THE RESISTANCE OF THE ORGANISMS TO THE BACTERICIDAL ACTION OF HUMAN BLOOD.

Authors:  W W Spink; J J Vivino
Journal:  J Clin Invest       Date:  1942-05       Impact factor: 14.808

7.  Virulence to mice of Staphylococcus pyogenes: its measurement and its relation to certain in vitro properties.

Authors:  F R SELBIE; R D SIMON
Journal:  Br J Exp Pathol       Date:  1952-08

8.  The survival of staphylococci within human leukocytes.

Authors:  D E ROGERS; R TOMPSETT
Journal:  J Exp Med       Date:  1952-02       Impact factor: 14.307

9.  The effect of dinitrophenol and thyroxin on the susceptibility of mice to staphylococcal infections.

Authors:  J M SMITH; R J DUBOS
Journal:  J Exp Med       Date:  1956-01-01       Impact factor: 14.307

10.  Multiplication and survival of tubercle bacilli in the organs of mice.

Authors:  C H PIERCE; R J DUBOS; W B SCHAEFER
Journal:  J Exp Med       Date:  1953-02-01       Impact factor: 14.307

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  44 in total

1.  STUDIES OF STAPHYLOCOCCAL INFECTIONS. I. VIRULENCE OF STAPHYLOCOCCI AND CHARACTERISTICS OF INFECTIONS IN EMBRYONATED EGGS.

Authors:  W R MCCABE
Journal:  J Clin Invest       Date:  1964-11       Impact factor: 14.808

2.  Proteus vulgaris urinary tract infections in rats; treatment with nitrofuran derivatives.

Authors:  D J HOSSACK
Journal:  Br J Pharmacol Chemother       Date:  1962-10

3.  Staphylococcal infections; incidence, environmental and laboratory studies.

Authors:  C P ARTZ; J B GROGAN
Journal:  Ann Surg       Date:  1961-10       Impact factor: 12.969

4.  Studies on staphylococci. II. Effect of coagulase on the virulence of coagulase negative strains.

Authors:  R D EKSTEDT; W W YOTIS
Journal:  J Bacteriol       Date:  1960-10       Impact factor: 3.490

5.  [Experimental animal studies on the problem of natural resistance to bacterial infections. Part I, Induction of staphylococcal sepsis in the white rat after administration of foreign protein].

Authors:  M KIENITZ; W RITZERFELD; R SEBERS
Journal:  Z Hyg Infektionskr       Date:  1960

6.  [Mechanisms of nonspecific infection resistance].

Authors:  D BOHME
Journal:  Klin Wochenschr       Date:  1958-09-15

7.  Increased staphylococcal penicillinase activity accompanying penicillin treatment of experimentally infected mice.

Authors:  L H GERONIMUS; S COHEN
Journal:  J Bacteriol       Date:  1957-10       Impact factor: 3.490

8.  Studies on bacteriemia. I. Mechanisms relating to the persistence of bacteriemia in rabbits following the intravenous injection of staphylococci.

Authors:  D E ROGERS
Journal:  J Exp Med       Date:  1956-06-01       Impact factor: 14.307

9.  Colony spreading in Staphylococcus aureus.

Authors:  Chikara Kaito; Kazuhisa Sekimizu
Journal:  J Bacteriol       Date:  2006-12-28       Impact factor: 3.490

10.  Purification and characterization of Staphylococcus aureus type 8 capsular polysaccharide.

Authors:  J M Fournier; W F Vann; W W Karakawa
Journal:  Infect Immun       Date:  1984-07       Impact factor: 3.441

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