Literature DB >> 631893

Electron microscopic study on phagocytosis of staphylococci by mouse peritoneal macrophages.

K Iwata, Y Kanda, H Yamaguchi.   

Abstract

Macrophages from the mouse peritoneal cavity were examined by electron microscopy at various time intervals up to 24 h after intraperitoneal administration of each of three strains of staphylococci different in virulence for mice: high-virulent, low-virulent, and avirulent strains. After engulfment, avirulent bacteria were highly liable to intracellular digestion, resulting in almost complete degradation within 24 h after injection, whereas high-virulent bacteria were more resistant to digestion, some showing figures suggestive of a dividing process; the gross configuration of most of the ingested bacteria was relatively well preserved over the 24-h period. Time-dependent morphological changes of low-virulent bacteria were intermediate. Among the most distinct cytoplasmic responses to the ingested bacteria was the formation of phagocytic vacuoles around them, the type of which was dependent on the staphylococcal strain infected; ingestion of avirulent bacteria led to formation of vacuoles in which the bacteria were surrounded by a halo of amorphous material of moderate density, which may be the lysosomal content. In contrast, larger vacuoles developed after ingestion of high-virulent bacteria and contained only a small quantity of such amorphous materials. Both types of phagocytic vacuoles were seen around the low-virulent bacteria ingested. Some degenerative changes were found in the macrophages ingesting high- or low-virulent bacteria, but were not in those ingesting avirulent bacteria. Thus, resistance to intracellular degradation, as well as cytotoxicity toward phagocytes of staphylococcal strains, can be correlated with their virulence.

Entities:  

Mesh:

Year:  1978        PMID: 631893      PMCID: PMC414130          DOI: 10.1128/iai.19.2.649-658.1978

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  24 in total

1.  ELECTRON MICROSCOPE OBSERVATIONS OF BRUCELLA ABORTUS GROWN WITHIN MONOCYTES IN VITRO.

Authors:  G KARLSBAD; R W KESSEL; S DE PETRIS; L MONACO
Journal:  J Gen Microbiol       Date:  1964-06

2.  THIN-SECTION ELECTRON MICROGRAPHS OF MONOCYTES INFECTED WITH BRUCELLA SUIS.

Authors:  G R PEARSON; B A FREEMAN; W D HINES
Journal:  J Bacteriol       Date:  1963-11       Impact factor: 3.490

3.  ELECTRON MICROSCOPICAL OBSERVATIONS ON THE PERITONEAL MACROPHAGES OF NORMAL MICE AND MICE IMMUNISED WITH LISTERIA MONOCYTOGENES. II. STRUCTURE OF MACROPHAGES FROM IMMUNE MICE AND EARLY CYTOPLASMIC RESPONSE TO THE PRESENCE OF INGESTED BACTERIA.

Authors:  R J NORTH; G B MACKANESS
Journal:  Br J Exp Pathol       Date:  1963-12

Review 4.  CELLULAR REACTIONS IN INFECTION.

Authors:  E SUTER; H RAMSEIAR
Journal:  Adv Immunol       Date:  1964       Impact factor: 3.543

5.  The eventual intracellular destruction of staphylococci by mononuclear cells.

Authors:  M G SHAYEGANI; F A KAPRAL
Journal:  J Gen Microbiol       Date:  1962-12

6.  Electron microscopic study of phagocytosis of Staphylococcus by human leukocytes.

Authors:  J R GOODMAN; R E MOORE
Journal:  J Bacteriol       Date:  1956-05       Impact factor: 3.490

7.  Further observations on the behavior of staphylococci within human leukocytes.

Authors:  D E ROGERS; M A MELLY
Journal:  J Exp Med       Date:  1960-04-01       Impact factor: 14.307

8.  Determinants of infection in the peritoneal cavity. I. Response to and fate of Staphylococcus aureus and Staphylococcus albus in the mouse.

Authors:  Z A COHN
Journal:  Yale J Biol Med       Date:  1962-08

9.  The distribution of S35-labeled bovine serum albumin in newborn and immunologically tolerant adult rabbits.

Authors:  J S GARVEY; D V EITZMAN; R T SMITH
Journal:  J Exp Med       Date:  1960-09-01       Impact factor: 14.307

10.  The phagocytosis and inactivation of staphylococci by macrophages of normal rabbits.

Authors:  G B MACKANESS
Journal:  J Exp Med       Date:  1960-07-01       Impact factor: 14.307

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  1 in total

1.  Pathogenesis of Campylobacter fetus infections. Failure of encapsulated Campylobacter fetus to bind C3b explains serum and phagocytosis resistance.

Authors:  M J Blaser; P F Smith; J E Repine; K A Joiner
Journal:  J Clin Invest       Date:  1988-05       Impact factor: 14.808

  1 in total

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