Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1949 Jun 30;90(1):85–96. doi: 10.1084/jem.90.1.85

THE INHIBITION OF SURFACE PHAGOCYTOSIS BY THE CAPSULAR "SLIME LAYER" OF PNEUMOCOCCUS TYPE III

W Barry Wood Jr 1, Mary Ruth Smith 1
PMCID: PMC2135934  PMID: 18152341

Abstract

Five strains of type III pneumococcus have been shown to possess wide capsular slime layers during the logarithmic phase of growth in serum broth. The slime layer stains metachromatically with methylene blue and can be visualized under the electron microscope as a fuzzy halo which extends well beyond the surace of the capsule proper and causes centrifugates of the organism to be of extremely large volume. This outer capsular structure is most readily demonstrated in vivo and in nutrient broth containing glucose and serum. It disappears from the surface of the cell with aging of the culture, and is easily removed by dilute alkali, alcohol, and heat. Exposure of slime-covered type III pneumococci to homologous antibody and to type III polysaccharidase reveals that the slime layer contains the same type-specific polysaccharide that is present in the rest of the capsule. From a type III strain producing a prominent slime layer an intermediate mutant has been isolated which forms small non-mucoid colonies on blood agar and possesses a relatively small capsule with a barely discernible slime layer. The wide slime layer protects virulent type III pneumococci from surface phagocytosis. Whenever the type III cells lose their broad slime layer, whether from aging of the culture, from mutation, from exposure to injurious chemicals, or from the action of type III polysaccharidase, they become susceptible to phagocytosis by the surface mechanism. Once phagocyted the type III pneumococci are promptly destroyed, even in the absence of antibodies.

Full Text

The Full Text of this article is available as a PDF (878.9 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Blake F. G., Trask J. D. Pneumococcus Variants Intermediate between the S and R Forms. J Bacteriol. 1933 Mar;25(3):289–307. doi: 10.1128/jb.25.3.289-307.1933. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Dawson M. H. THE INTERCONVERTIBILITY OF "R" AND "S" FORMS OF PNEUMOCOCCUS. J Exp Med. 1928 Mar 31;47(4):577–591. doi: 10.1084/jem.47.4.577. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Enders J. F., Shaffer M. F., Wu C. J. STUDIES ON NATURAL IMMUNITY TO PNEUMOCOCCUS TYPE III : III. CORRELATION OF THE BEHAVIOR IN VIVO OF PNEUMOCOCCI TYPE III VARYING IN THEIR VIRULENCE FOR RABBITS WITH CERTAIN DIFFERENCES OBSERVED IN VITRO. J Exp Med. 1936 Jul 31;64(2):307–330. doi: 10.1084/jem.64.2.307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Heidelberger M., Kendall F. E., Scherp H. W. THE SPECIFIC POLYSACCHARIDES OF TYPES I, II, AND III PNEUMOCOCCUS : A REVISION OF METHODS AND DATA. J Exp Med. 1936 Sep 30;64(4):559–572. doi: 10.1084/jem.64.4.559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Macleod C. M., Krauss M. R. STEPWISE INTRATYPE TRANSFORMATION OF PNEUMOCOCCUS FROM R TO S BY WAY OF A VARIANT INTERMEDIATE IN CAPSULAR POLYSACCHARIDE PRODUCTION. J Exp Med. 1947 Nov 30;86(6):439–452. doi: 10.1084/jem.86.6.439. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Mudd S., Heinmets F., Anderson T. F. Bacterial Morphology as Shown by the Electron Microscope: VI. Capsule, Cell-Wall and Inner Protoplasm of Pneumococcus, Type III. J Bacteriol. 1943 Aug;46(2):205–211. doi: 10.1128/jb.46.2.205-211.1943. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Paul J. R. Pneumococcus Variants: I. Intermediate Forms and the Influence of Environment in Their Production During In-vitro S to R and R to S Transitions. J Bacteriol. 1934 Jul;28(1):45–67. doi: 10.1128/jb.28.1.45-67.1934. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Sabin A. B., Feldman H. A. Dyes as Microchemical Indicators of a New Immunity Phenomenon Affecting a Protozoon Parasite (Toxoplasma). Science. 1948 Dec 10;108(2815):660–663. doi: 10.1126/science.108.2815.660. [DOI] [PubMed] [Google Scholar]
  9. Shaffer M. F., Enders J. F., Wu C. J. STUDIES ON NATURAL IMMUNITY TO PNEUMOCOCCUS TYPE III : II. CERTAIN DISTINGUISHING PROPERTIES OF TWO STRAINS OF PNEUMOCOCCUS TYPE III VARYING IN THEIR VIRULENCE FOR RABBITS, AND THE REAPPEARANCE OF THESE PROPERTIES FOLLOWING R-->S RECONVERSION OF THEIR RESPECTIVE ROUGH DERIVATIVES. J Exp Med. 1936 Jul 31;64(2):281–305. doi: 10.1084/jem.64.2.281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Smith M. R., Wood W. B. STUDIES ON THE MECHANISM OF RECOVERY IN PNEUMONIA DUE TO FRIEDLADER'S BACILLUS : III. THE ROLE OF "SURFACE PHAGOCYTOSIS" IN THE DESTRUCTION OF THE MICROORGANISMS IN THE LUNG. J Exp Med. 1947 Aug 31;86(3):257–266. doi: 10.1084/jem.86.3.257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Wood W. B., Jr, Smith M. R. Intercellular Surface Phagocytosis. Science. 1947 Jul 25;106(2743):86–87. doi: 10.1126/science.106.2743.86. [DOI] [PubMed] [Google Scholar]
  12. Wood W. B., Smith M. R., Watson B. STUDIES ON THE MECHANISM OF RECOVERY IN PNEUMOCOCCAL PNEUMONIA : IV. THE MECHANISM OF PHAGOCYTOSIS IN THE ABSENCE OF ANTIBODY. J Exp Med. 1946 Sep 30;84(4):387–402. doi: 10.1084/jem.84.4.387. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES