1887

Abstract

SUMMARY: Some of the recorded properties of a filterable organism (the PAP organism) isolated by Eaton and colleagues from cases of human primary atypical pneumonia suggest that it may be related biologically to the Mycoplasma (pleuropneumonia-like) group. In further investigation of this possibility now reported it was found that the organic gold salt, sodium aurothiomalate, which is known to inhibit certain mycoplasmas, would also inhibit infection with the PAP organism in the hamster and chick embryo lung. Some accepted viruses of a similar order of size to the PAP organism —namely, Nigg’s pneumonitis virus of mice (psittacosis group), three strains of influenza virus A, vaccinia and variola viruses—were not inhibited by sodium aurothiomalate. On the other hand, grey lung virus of mice, an organism with some properties resembling those of the PAP organism, was strongly inhibited. Diethyl ether and the antibiotic kanamycin sulphate both inhibited the growth of the PAP organism in chick embryo lung. An intensified Giemsa-staining method revealed small red-purple coccobacillary bodies (later called elementary bodies, EB) in the lungs of chick embryos infected with three different strains of PAP organism isolated, respectively, in 1944, 1954 and 1960 in different parts of the United States. The EB were not seen in uninfected chick embryo lungs. The EB and the antigen of the PAP organism stained by the fluorescent antibody technique occupied essentially the same position in relation to the mesobronchial epithelial cells of chick embryo lung. The formation of both was suppressed in parallel by treatment of inoculum or eggs with diethyl ether, kanamycin sulphate or sodium aurothiomalate. There was a good but not absolute correlation between the presence or absence of EB and antigen in experiments on the growth or survival of the PAP organism in chick embryos, in cell-free media, and in titrations in eggs.

Loading

Article metrics loading...

/content/journal/micro/10.1099/00221287-29-2-271
1962-10-01
2024-04-20
Loading full text...

Full text loading...

/deliver/fulltext/micro/29/2/mic-29-2-271.html?itemId=/content/journal/micro/10.1099/00221287-29-2-271&mimeType=html&fmt=ahah

References

  1. Andrewes C. H., King H., van den Ende M. 1943; Chemotherapeutic experiments with the viruses of influenza A, lymphogranuloma and vaccinia. J. Path. Bad 55:173
    [Google Scholar]
  2. Andrewes C. H., Glover R. E. 1945; Grey lung virus: an agent pathogenic for mice and other rodents. Brit. J. exp. Path 26:379
    [Google Scholar]
  3. Andrewes C. H., Niven J. S. F. 1953; Action of arsenicals on infection of mice with grey lung virus. J. Path. Bad 66:565
    [Google Scholar]
  4. Bauer D. J. 1958; Chemotherapeutic effect of compounds of copper, rhodium and certain other metals in mice infected with neurovaccinia and ectromelia viruses. Brit. J. exp. Path 39:480
    [Google Scholar]
  5. Betts A. O. 1952; Respiratory diseases of pigs. V. Some clinical and epidemiological aspects of virus pneumonia of pigs. Vet. Rec 64:283
    [Google Scholar]
  6. Bridre J., Donatien A., Hilbert D. 1928; Le stovarsol, speciflque de l’agalaxie contagieuse du mouton et de la chevre. C.R. Acad. Sci., Paris 187:262
    [Google Scholar]
  7. Burnet F. M. 1936; Influenza virus in the developing egg. 1. Changes associated with the development of an egg-passage strain of virus Brit. J. exp. Path 17:282
    [Google Scholar]
  8. Chanock R. M., Fox H. H., James W. D., Bloom H. H., Mufson M. A. 1960; Growth of laboratory and naturally occurring strains of Eaton agent in monkey kidney tissue culture. Proc. Soc. exp. Biol., N.Y 105:371
    [Google Scholar]
  9. Chanock R. M., Mufson M. A., Bloom H. H., James W. D., Fox H. H., Kingston J. R. 1961; Eaton agent pneumonia. J. Amer. med. Ass 175:213S
    [Google Scholar]
  10. Chanock R. M., Hayflick L., Barile M. F. 1962; Growth on artificial medium of an agent associated with atypical pneumonia and its identification as a PPLO. Proc. nat. Acad. Sci., Wash 48:41
    [Google Scholar]
  11. Clyde W. A., Denny F. W., Dingle J. H. 1960; Fluorescent stainable antibodies to the Eaton agent in human primary atypical pneumonia transmission studies. J. Lab. clin. Med 56:799
    [Google Scholar]
  12. Clyde W. A. 1961; Demonstration of Eaton’s Agent in Tissue Culture. Proc. Soc. exp. Biol, N. Y 107:715
    [Google Scholar]
  13. Cook M. K., Chanock R. M., Fox H. H., Huebner R. J., Buescher E. L., Johnson R. T. 1960; Role of Eaton agent in disease of lower respiratory tract. Evidence for infection in adults Brit. med. J i:905
    [Google Scholar]
  14. Donald H. B., Liu C. 1959; Cytological studies of chick embryo cells infected with the virus of primary atypical pneumonia. Virology 9:24
    [Google Scholar]
  15. Eaton M. D., Meiklejohn G., van Herick W. 1944; Studies on the etiology of primary atypical pneumonia. A filterable agent transmissible to cotton rats, hamsters and chick embryos J. exp. Med 79:649
    [Google Scholar]
  16. Eaton M. D., Meiklejohn G., van Herick W., Corey M. 1945; Studies on the etiology of primary atypical pneumonia. II. Properties of the virus isolated and propagated in chick embryos. J. exp. Med 82:317
    [Google Scholar]
  17. Eaton M. D. 1950a Virus pneumonia and pneumonitis viruses of man and animals
    [Google Scholar]
  18. Handbuch d. Virusforschung. p 87 Ed. by Doerr R., Hallauer C. Vienna: Springer;
    [Google Scholar]
  19. Eaton M. D. 1950b; Action of aureomycin and chloromycetin on the virus of primary atypical pneumonia. Proc. Soc. exp. Biol., N.Y 73:24
    [Google Scholar]
  20. Eaton M. D. 1954–55; Effect of some newer antibiotics on the agent of primary atypical pneumonia. In Antibiotics Annual 1954–55 p 1046 Ed. by Welch H., Marti-Ibanez F. New York: Medical Encyclopedia, Inc;
    [Google Scholar]
  21. Eaton M. D., Liu C. 1957; Studies on sensitivity to streptomycin of the atypical pneumonia agent. J. Bad 74:784
    [Google Scholar]
  22. Eaton M. D., Perry M. E., Gocke I. M. 1957; Effect of nitro-compounds and aldehyde semicarbazones on virus of primary atypical pneumonia. Proc. Soc. exp. Biol., N.Y 77:422
    [Google Scholar]
  23. Edward D. G. F. 1947; Catarrh of the upper respiratory tract in mice and its association with pleuropneumonia-like organisms. J. Path. Bact 59:209
    [Google Scholar]
  24. Edward D. G. F. 1954; The pleuropneumonia group of organisms: a review, together with some new observations. J. gen. Microbiol 10:27
    [Google Scholar]
  25. Findlay G. M., Mackenzie R. D., MacCallum F. O. 1940; Chemotherapeutic experiments in pleuropneumonia organisms in rodents. Brit. J. exp. Path 21:13
    [Google Scholar]
  26. Fogh J., Hacker C. 1960; Elimination of pleuropneumonia-like organisms from cell cultures. Exp. Cell Res 21:242
    [Google Scholar]
  27. Goodburn G. M., Marmion B. P. 1962; Investigations of the nature of Eaton’s primary atypical pneumonia organism. Proceedings of the Congress on Respiratory Tract Diseases of Virus and Rickettsial Origin, Prague, May 1961 J. Hyg. Epid. Microbiol. Immunol (in the Press)
    [Google Scholar]
  28. Gordon F. B., Quan A. L., Cook M. K., Chanock R. M., Fox H. H. 1960; Growth of the Eaton agent of primary atypical pneumonia in chick entodermal tissue culture. Proc. Soc. exp. Biol., N.Y 105:375
    [Google Scholar]
  29. Gulrajani T. S., Beveridge W. I. B. 1951; Infectious pneumonia of pigs. Nature, Lond 167:856
    [Google Scholar]
  30. Henneguy P. 1891; Cited in Bolles Lee. The Microtomisfs Vade-mecum p 184–370 London (1937): Churchill;
    [Google Scholar]
  31. Jungeblut C. W. 1930 1931 Attempts at chemotherapy in experimental poliomyelitis. Proc. Soc. exp. Biol., N.Y 28:176
    [Google Scholar]
  32. Klieneberger-Nobel E. 1962 Pleuropneumonia-like Organisms (PPLO) Mycoplasma-taceae London: Academic Press;
    [Google Scholar]
  33. Kolmer J. A., Rule A. M. 1933 1934 A note on the chemotherapy of experimental poliomyelitis of monkeys. Proc. Soc. exp. Biol., N.Y 31:50
    [Google Scholar]
  34. Liu C., Eaton M. D., Heyl J. T. 1956; Studies on primary atypical pneumonia. Bull. N.Y. Acad. Med 32:170
    [Google Scholar]
  35. Liu C. 1957; Studies on primary atypical pneumonia. I. Localization, isolation, and cultivation of a virus in chick embryos J. exp. Med 106:455
    [Google Scholar]
  36. Marmion B. P., Goodburn G. M. 1961; Effect of an organic gold salt on Eaton’s primary atypical pneumonia organism and other observations. Nature, Lond 189:247
    [Google Scholar]
  37. Mornet P., Orue J., Marty J. P. 1951; Note sur le traitement de la peri-pneumonie bovine par la penicilline, la streptomycine et certains derives sulfamides. Action com-paree avec le novarsenobenzol Bull. Acad. vd. Fr 24:213
    [Google Scholar]
  38. Morton H. E. 1958; The pleuropneumonia and pleuropneumonia-like organisms. Bacterial and Mycotic Infections of Man pp 563–81 Ed Dubos R. J., 3rd ed. London: Pitman Medical;
    [Google Scholar]
  39. Nigg C., Eaton M. D. 1944; Isolation from normal mice of a pneumotropic virus which forms elementary bodies. J. exp. Med 79:497
    [Google Scholar]
  40. Pearse A. G. E. 1960 Histochemistry, Theoretical and Applied pp 13–24, 2nd ed.. London: Churchill;
    [Google Scholar]
  41. Pollock M. E., Kenny G. E., Syverton J. T. 1960; Isolation and elimination of pleuropneumonia-like organisms from mammalian cell cultures. Proc. Soc. exp. Biol., N.Y 105:10
    [Google Scholar]
  42. Richardson G. M. 1941; Preservation of liquid complement serum. Lancet ii:696
    [Google Scholar]
  43. Sabin A. B., Warren J. 1940; The therapeutic effectiveness of a practically non-toxic new compound (calcium aurothiomalate) in experimental, proliferative, chronic arthritis of mice. Science 92:535
    [Google Scholar]
  44. Taylor R. M., Chialvo R. J. 1942; Simplified technic for inoculating into amniotic sac of chick embryos. Proc. Soc. exp. Biol., N.Y 51:328
    [Google Scholar]
  45. van Herick W., Eaton M. D. 1945; An unidentified pleuropneumonia-like organism isolated during passage in chick embryos. J. Boot 50:47
    [Google Scholar]
  46. Vrolijk H., Verlinde J. D., Braams W. G. 1957; Virus pneumonia (snuffling disease) in laboratory rats and wild rats due to an agent probably related to grey lung virus in mice. Leeuwenhoek ned. Tijdschr 23:173
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/micro/10.1099/00221287-29-2-271
Loading
/content/journal/micro/10.1099/00221287-29-2-271
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error