1887

Abstract

Strain PYAN-1 (T = type strain), which was isolated from a pupal gut of the firefly beetle , and strains PIMN-1 and PIPN-2, which were isolated from guts of adult and fireflies, respectively, were demonstrated to be sterol-requiring mollicutes. Cells of the three strains were shown by electron and dark-field microscopy to be small, pleomorphic, nonhelical, nonmotile bodies surrounded by single membranes. No evidence of a cell wall was observed, and the organisms were not susceptible to 500 U of penicillin per ml. The three strains grew rapidly in SP-4 broth medium. Strains PIMN-1 and PIPN-2 grew in medium supplemented with bovine serum fraction, but strain PYAN-1 did not. All three strains grew on solid media when the cultures were incubated aerobically, but only strains PYAN-1 and PIPN-2 formed colonies when anaerobic conditions were employed. The three strains catabolized glucose but hydrolyzed neither arginine nor urea. All of the strains grew at temperatures of 18 to 32°C; strains PYAN-1 and PIMN-1 also grew at 10°C. The optimal temperature for growth for strains PYAN-1 and PIPN-2 was 30°C; strain PIMN-1 grew equally well at 30 or 32°C. None of the three strains grew at 37°C. The genome sizes of strains PYAN-1, PIMN-1, and PIPN-2 were about 527 (478 to 589), 570 (480 to 630), and 762 (635 to 871) megadaltons, respectively. The guanine-plus-cytosine contents of the DNAs of the strains, as determined by buoyant density, thermal denaturation, and high-performance liquid chromatography methods, were as follows: 27.4, 30.2, and 27.5 mol%, respectively, for strain PYAN-1; 28.8, 31.2, and 29.2 mol%, respectively, for strain PIMN-1; and 28.4, 30.4, and 31.2 mol%, respectively, for strain PIPN-2. All three strains were serologically unrelated to the type strains of previously established species (including ), to each other, and to 15 other unclassified sterol-requiring strains isolated from animals, plants, and insects. Along with , these three organisms represent an unusual cluster of strains belonging to the genus isolated from insects. Strain PYAN-1 (= ATCC 49194) is the type strain of sp. nov.; strain PIMN-1 (= ATCC 49195) is the type strain of sp. nov.; and strain PIPN-2 (= ATCC 49196) is the type strain of sp. nov.

Loading

Article metrics loading...

/content/journal/ijsem/10.1099/00207713-40-2-160
1990-04-01
2024-04-16
Loading full text...

Full text loading...

/deliver/fulltext/ijsem/40/2/ijsem-40-2-160.html?itemId=/content/journal/ijsem/10.1099/00207713-40-2-160&mimeType=html&fmt=ahah

References

  1. Aluotto B. B., Wittier R. G., Williams C. O., Faber J. E. 1970; Standardized bactériologie techniques for characterization of Mycoplasma species. Int. J. Syst. Bacteriol. 20:35–58
    [Google Scholar]
  2. Carle P., Bove J. M. 1983; Genome size determination. Methods Mycoplasmol. 1:309–311
    [Google Scholar]
  3. Carle P., Saillard C., Bové J. M. 1983; DNA extraction and purification. Methods Mycoplasmol. 1:295–299
    [Google Scholar]
  4. Carle P., Saillard C., Bové J. M. 1983; Determination of guanine plus cytosine content of DNA. Methods Mycoplasmol. 1:301–308
    [Google Scholar]
  5. Clark T. B. 1982; Spiroplasmas: diversity of arthropod reservoirs and host-parasite relationships. Science 217:57–59
    [Google Scholar]
  6. Clark T. B., Tully J. G., Rose D. L., Henegar R., Whitcomb R. F. 1986; Acholeplasmas and similar nonsterol-requiring mollicutes from insects: missing link in microbial ecology. Curr. Microbiol. 13:11–16
    [Google Scholar]
  7. Clyde W. A. Jr. 1983; Growth inhibition tests. Methods Mycoplasmol. 1:405–410
    [Google Scholar]
  8. Edward D. G. ff. 1947; A selective medium for pleuropneumonia-like organisms. J. Gen. Microbiol. 1:238–243
    [Google Scholar]
  9. Freundt E. A. 1983; Film and spot production. Methods Mycoplasmol. 1:373–374
    [Google Scholar]
  10. Gardella R. S., Del Giudice R. A. 1983; Hemagglutination, hemadsorption, and hemolysis. Methods Mycoplasmol. 1:379384
    [Google Scholar]
  11. Gardella R. S., Del Giudice R. A., TuUy J. G. 1983; Immunofluorescence. Methods Mycoplasmol. 1:431–439
    [Google Scholar]
  12. Hackett K. J., Clark T. B. 1989 The ecology of spiroplasmas. 113–199 Whitcomb R. F., Tully J. G.ed The mycoplasmas 5 Academic Press; Inc., New York:
    [Google Scholar]
  13. International Committee on Systematic Bacteriology Subcommittee on the Taxonomy of Mollicutes 1979; Proposal of minimal standards for descriptions of new species of the class Mollicutes. Int. J. Syst. Bacteriol. 29:172–180
    [Google Scholar]
  14. Markham P. G., Clark T. B., Whitcomb R. F. 1983; Culture techniques for spiroplasmas from arthropods. Methods Mycoplasmol. 2:217–223
    [Google Scholar]
  15. McCoy R. E., Basham H. G., Tully J. G., Rose D. L., Carle P., Bove J. M. 1984; Acholeplasma florum: a new species isolated from plants. Int. J. Syst. Bacteriol. 34:11–15
    [Google Scholar]
  16. Razin S., Tully J. G. 1970; Cholesterol requirements of mycoplasmas. J. Bacteriol. 102:306–310
    [Google Scholar]
  17. Rose D. L., Kocka J. P., Somerson N. L., Tully J. G., Whitcomb R. F., Carle P., Bove J. M., Colflesh D. E., Williamson D. L. 1990; Mycoplasma lactucae sp. nov., a sterol-requiring mollicute from a plant surface. Int. J. Syst. Bacteriol. 40:138–142
    [Google Scholar]
  18. Tully J. G. 1983; Cloning and filtration techniques for mycoplasmas. Methods Mycoplasmol. 1:173–177
    [Google Scholar]
  19. Tully J. G. 1984 The family Acholeplasmataceae, genus Acholeplasma. 781–787 Krieg N. R., Holt J. M.ed Bergey’s manual of systematic bacteriology 1 The Williams & Wilkins Co.; Baltimore:
    [Google Scholar]
  20. Tully J. G. 1989 Class Mollicutes: new perspectives from plant and arthropod studies. 1–31 Whitcomb R. F., Tully J. G.ed The mycoplasmas 5 Academic Press; Inc., New York:
    [Google Scholar]
  21. Tully J. G., Rose D. L., Carle P., Bove J. M., Hackett K. J., Whitcomb R. F. 1988; Acholeplasma entomophilum sp. nov. from gut contents of a wide range of host insects. Int. j. Syst. Bacteriol. 38:164–167
    [Google Scholar]
  22. Tully J. G., Rose D. L., Hackett K. J., Whitcomb R. F., Carle P., Bove J. M., Colflesh D. E., Williamson D. L. 1989; Mycoplasma ellychniae sp. nov., a sterol-requiring mollicute from the firefly beetle Ellychnia corrusca. Int. J. Syst. Bacteriol. 39:284–289
    [Google Scholar]
  23. Tully J. G., Rose D. L., McCoy R. E., Carle P., Bove J. M., Whitcomb R. F., Weisburg W. G. 1990; Mycoplasma melaleucae sp. nov., a sterol-requiring mollicute from flowers of several tropical plants. Int. J. Syst. Bacteriol. 40:143–147
    [Google Scholar]
  24. Tully J. G., Rose D. L., Whitcomb R. F., Hackett K. J., Clark T. B., Henegar R. B., Clark E., Carle P., Bove J. M. 1987; Characterization of some new insect-derived acholeplasmas. Isr. J. Med. Sci. 23:699–703
    [Google Scholar]
  25. Whitcomb R. F. 1983; Culture media for spiroplasmas. Methods Mycoplasmol. 1:147–158
    [Google Scholar]
  26. Williamson D. L., Tully J. G., Whitcomb R. F. 1989 The genus Spiroplasma. 71–111 Whitcomb R. F., Tully J. G.ed The mycoplasmas 5 Academic Press; Inc., New York:
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/ijsem/10.1099/00207713-40-2-160
Loading
/content/journal/ijsem/10.1099/00207713-40-2-160
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