1887

Abstract

Abstract

Twenty mollicute strains isolated primarily from insect hosts were characterized and arranged into eight new species in the genus Morphological examination of the organisms by electron and dark-field microscopic techniques revealed that the cells of each strain were small, nonhelical, nonmotile, pleomorphic, and coccoid and that each cell was surrounded by a single cytoplasmic membrane with no evidence of a cell wall. Although the new mollicutes grew well in media containing horse or fetal bovine serum, growth in serum-free or cholesterol-free medium occurred only when the medium contained 0.04% polyoxyethylene sorbitan (Tween 80). The optimum temperature for growth was usually 30°C, but multiplication generally occurred over a temperature range of 10 to 32°C. All strains catabolized glucose. Most strains did not hydrolyze arginine or urea, although three related strains isolated from fireflies (the strain PUPA-2 [T = type strain] group) did hydrolyze arginine. The genome sizes ranged from 825 to 930 kbp, and the DNA base compositions (guanine-plus-cytosine contents) ranged from 26.5 to 31.6 mol%. The proposed type strains of the eight new species were not serologically related to the type strains of four other species, five species, 11 species, and 100 species and subspecies. Strain PS-1 (= ATCC 49582) is the type strain of sp. nov., strain PUPA-2 (= ATCC 49581) is the type strain sp. nov., strain YJS (= ATCC 43706) is the type strain of sp. nov., strain CHPA-2 (= ATCC 49578) is the type strain of sp. nov., strain ELCA-2 (= ATCC 49579) is the type strain of sp. nov., strain GRUA-1 (= ATCC 49580) is the type strain of sp. nov., strain BARC 779 (= ATCC 49583) is the type strain of sp. nov., and strain BARC 857 (= ATCC 49584) is the type strain of sp. nov.

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1994-10-01
2024-04-20
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References

  1. Aluotto B. B., Wittier R. G., Williams C. O., Faber J. E. 1970; Standardized bacteriologic techniques for characterization of Mycoplasma species. Int. J. Syst. Bacteriol. 20:35–58
    [Google Scholar]
  2. Bonnet F., Saillard C., Vignault J. C., Gamier M., Carle P., Bové J. M., Rose D. L., Tully J. G., Whitcomb R. F. 1991; Acholeplasma seiffertii sp. nov., a mollicute from plant surfaces. Int. J. Syst. Bacteriol. 41:45–49
    [Google Scholar]
  3. Bové J. M., Whitcomb R. F., McCoy R. E. 1983; Culture techniques for spiroplasmas from plants. Methods Mycoplasmol. 2:225–234
    [Google Scholar]
  4. Carle P., Rose D. L., Tully J. G., Bové J. M. 1992; The genome size of spiroplasmas and other mollicutes. IOM Lett. 2:263
    [Google Scholar]
  5. Carle P., Saillard C., Bové J. M. 1983; DNA extraction and purification. Methods Mycoplasmol. 1:295–299
    [Google Scholar]
  6. Carle P., Saillard C., Bové J. M. 1983; Determination of guanine plus cytosine content of DNA. Methods Mycoplasmol. 1:301–308
    [Google Scholar]
  7. 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]
  8. Clyde W. A. Jr. 1983; Growth inhibition tests. Methods Mycoplasmol. 1:405–410
    [Google Scholar]
  9. Eden-Green S., Tully J. G. 1979; Isolation of Acholeplasma spp. from coconut palms affected by lethal yellowing disease in Jamaica. Curr. Microbiol. 2:311–316
    [Google Scholar]
  10. Gardella R. S., Del Giudice R. A. 1983; Hemagglutination, hemadsorption, and hemolysis. Methods Mycoplasmol. 1:379–384
    [Google Scholar]
  11. Gardella R. S., Del Giudice R. A., Tully J. G. 1983; Immunofluorescence. Methods Mycoplasmol. 1:431–439
    [Google Scholar]
  12. Hackett K. J., Clark T. B. 1989; Ecology of spiroplasmas. 113–200 In Whitcomb R. F., Tully J. G. (ed.) The mycoplasmas vol. 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. McCoy R. E., Basham H. G., Tully J. G., Rose D. L., Carle P., Bové J. M. 1984; Acholeplasma florum: a new species isolated from plants. Int. J. Syst. Bacteriol. 34:11–15
    [Google Scholar]
  15. McCoy R. E., Williams D. S., Thomas D. L. 1979 Isolation of mycoplasmas from flowers. 75–80 In McCoy R. E., Su H. (ed.) Proceedings of the Republic of China-United States Cooperative Science Seminar, Symposium Series INational Science CouncilTaipai, Taiwan
    [Google Scholar]
  16. Navas-Castillo J., Laigret F., Hocquellet A., Chang C. J., Bové J. M. 1993; Evidence for a phosphoenolpyruvate-dependent sugar-phosphotransferase system in the mollicute Acholeplasma florum. Biochimie 75:675–679
    [Google Scholar]
  17. Navas-Castillo J., Laigret F., Tully J. G., Bové J. M. 1992; Le mollicute Acholeplasma florum possede un gene du systeme phosphoenolpyruvate sucre-phosphotransferase et il utilise UGA comme codon tryptophane. C. R. Acad. Sci. 315:43–48
    [Google Scholar]
  18. Neimark H.C, Tully J. G., Rose D., Lange C. 1992; Chromosome size polymorphism among mollicutes. IOM Lett. 2:261
    [Google Scholar]
  19. Razin S., Tully J. G. 1970; Cholesterol requirement of mycoplasmas. J. Bacteriol. 102:306–310
    [Google Scholar]
  20. Rose D. L., Kocka J. P., Somerson N. L., Tully J. G., Whitcomb R. F., Carle P., Bové 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]
  21. Rose D. L., Tully J. G., Bové J. M., Whitcomb R. F. 1993; A test for measuring growth responses of mollicutes to serum and polyoxyethylene sorbitan. Int. J. Syst. Bacteriol. 43:527–532
    [Google Scholar]
  22. Senterfit L. B. 1983; Preparation of antigens and antisera. Methods Mycoplasmol. 1:401–404
    [Google Scholar]
  23. Tully J. G. 1983; Reflections on recovery of some fastidious mollicutes with implications of the changing host patterns of these organisms. Yale J. Biol. Med. 56:799–813
    [Google Scholar]
  24. Tully J. G. 1983; Cloning and filtration techniques for mycoplasmas. Methods Mycoplasmol. 1:173–177
    [Google Scholar]
  25. Tully J. G. 1983; Tests for digitonin sensitivity and sterol requirement. Methods Mycoplasmol. 1:355–362
    [Google Scholar]
  26. Tully J. G. 1989; Class Mollicutes: new perspectives from plant and arthropod studies. 1–31 In Whitcomb R. F., Tully J. G. (ed.) The mycoplasmas vol. 5 Academic Press, Inc.; New York:
    [Google Scholar]
  27. Tully J. G., Bové J. M., Laigret F., Whitcomb R. F. 1993; Revised taxonomy of the class Mollicutes: proposed elevation of a monophyletic cluster of arthropod-associated mollicutes to ordinal rank (Entomoplasmatales ord. nov.), with provision for familial rank to separate species with nonhelical morphology (Entomoplas-mataceae fam. nov.) from helical species (Spiroplasmataceae), and emended descriptions of the order Mycoplasmatales, family Mycoplasmataceae. Int. J. Syst. Bacteriol. 43:378–385
    [Google Scholar]
  28. Tully J. G., Rose D. L., Carle P., Bové 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]
  29. Tully J.G, Rose D. L., Hackett K. J., Whitcomb R. F., Carle P., Bové 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]
  30. Tully J. G., Rose D. L., McCoy R. E., Carle P., Bové J. M., Whitcomb R. F., Weisburg W. G. 1989; Mycoplasma melaleucae sp. nov., a sterol-requiring mollicute from flowers of several tropical plants. Int. J. Syst. Bacteriol. 40:143–147
    [Google Scholar]
  31. Tully J. G., Rose D. L., Whitcomb R. F., Hackett K. J., Clark T. B., Henegar R. B., Clark E., Carle P., Bové J. M. 1987; Characterization of some new insect-derived acholeplasmas. Isr. J. Med. Sci. 23:699–703
    [Google Scholar]
  32. Tully J. G., Whitcomb R. F., Rose D. L., Hackett K. J., Clark E., Henegar R. B., Carle P., Bové J. M. 1990; Current insight into the host diversity of acholeplasmas. Zentralbl. Bakteriol. (Suppl.) 20:461–467
    [Google Scholar]
  33. Weisburg W.G, Tully J. G., Rose D. L., Petzel J. P., Oyaizu H., Yang D., Mandelco L., Sechrest J., Lawrence T. G., Van Etten J., Maniloff J., Woese C. R. 1989; A phylogenetic analysis of the mycoplasmas: basis for their classification. J. Bacteriol. 171:6455–6467
    [Google Scholar]
  34. Whitcomb R. F. 1983; Culture media for spiroplasmas. Methods Mycoplasmol. 1:147–158
    [Google Scholar]
  35. Whitcomb R. F., Tully J. G., Rose D. L., Stephens E. B., Barile M. F., Smith A. J., McCoy R. E. 1982; Wall-less prokaryotes from fall flowers in central United States and Maryland. Curr. Microbiol. 7:291–296
    [Google Scholar]
  36. Williamson D. L., Tully J. G., Rose D. L., Hackett K. J., Henegar R., Carle P., Bové J. M., Colflesh D. E., Whitcomb R. F. 1990; Mycoplasma somnilux sp. nov., Mycoplasma luminosum sp. nov., and Mycoplasma lucivorax sp. nov., new sterol-requiring mollicutes from firefly beetles (Coleoptera: Lampyridae). Int. J. Syst. Bacteriol. 40:160–164
    [Google Scholar]
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