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Lampyridae (Coleoptera): A plethora of mollicute associations

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Abstract

Beetles (Coleoptera) harbor many species ofAcholeplasma andSpiroplasma (division Tenericutes, class Mollicutes). Mollicutes were isolated from guts and/or hemocoels of firefly beetles (Lampyridae) from the United States (Maryland and West Virginia), Ecuador, and Tobago. Firefly beetles were frequent hosts for the group XIV spiroplasma, isolated from Ellychnia corrusca, and the group XIX spiroplasma, isolated fromPhoturis spp. The most unusual feature of the firefly-mollicute association is the carriage of four Mycoplasma species. Recent phylogenetic studies indicate that these species are members of a clade that includes a vertebrate pathogen,Mycoplasma mycoides. The high rate of occurrence ofMycoplasma species (which are, otherwise, infrequent in insects) in lampyrid beetles suggests that the association is significant. The unusual light-producing physiology of lampyrids (which is dependent on large pools of energy) and the production of large amounts of cardenolides from cholesterol (a critical growth factor for many mollicutes) may favor colonization by mollicutes.

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References

  1. Abalain-Colloc ML, Williamson DL, Bonnet F, Bové JM, Whitcomb RF, Tully JG, Chastel C (1990) Classification of spiroplasma group XVI. IOM Lett 1:553

    Google Scholar 

  2. Blum MS, Sannasi A (1974) Reflex bleeding in the lampyridPhotinus pyralis: Defensive function. J Insect Physiol 20:451–460

    Article  Google Scholar 

  3. Bové JM, Carle P, Gamier M, Laigret F, Renaudin J, Saillard C (1989) Molecular and cellular biology of spiroplasmas. In: Whitcomb RF, Tully JG (eds) The mycoplasmas, vol 5. Academic Press, New York, pp 244–364

    Google Scholar 

  4. Buschman LL (1984) Larval biology and ecology ofPhoturis fireflies (Lampyridae: Coleoptera) in northcentral Florida. J Kansas Entomol Soc 57:7–16

    Google Scholar 

  5. Chang C-J (1989) Nutrition and cultivation of spiroplasmas. In: Whitcomb RF, Tully JG (eds) The mycoplasmas, vol 5. Spiroplasmas, acholeplasmas, and mycoplasmas of plants and arthropods. Academic Press, New York, pp 201–241

    Google Scholar 

  6. Chastel C, Devan B, Le Goff F, Simitzis-Le Flohic AM, Gruffaz R, Kerdraon G, Gilot B (1987) Mosquito spiroplasmas from France and their ecology. Isr J Med Sci 23:683–686

    PubMed  CAS  Google Scholar 

  7. Clark TB (1982) Spiroplasmas: Diversity of arthropod reservoirs and host-parasite relationships. Science 217:57–59

    PubMed  Google Scholar 

  8. Clark TB, Peterson RV, Whitcomb RF, Henegar RB, Hackett KJ, Tully JG (1984) Spiroplasmas in the Tabanidae. Isr J Med Sci 20:1002–1005

    PubMed  CAS  Google Scholar 

  9. Clark TB, Whitcomb RF, Tully JG, Mouches C, Saillard C, Bové JM, Wróblewski H, Carle P, Rose DL, Henegar RB, Williamson DL (1985)Spiroplasma melliferum, a new species from the honeybee (Apis mellifera). Int J Syst Bacteriol 35:296–308

    CAS  Google Scholar 

  10. Clark TB, Tully JG, Rose DL, Henegar R, Whitcomb RF (1986) Acholeplasmas and similar nonsterol-requiring mollicutes from insects: Missing link in microbial ecology. Curr Microbiol 13:11–16

    Article  Google Scholar 

  11. Clark TB, Henegar RB, Rosen L, Hackett KJ, Whitcomb RF, Lowry JE, Saillard C, Bové JM, Tully JG, Williamson DL (1987) New spiroplasmas from insects and flowers: Isolation, ecology, and host association. Isr J Med Sci 23:687–690

    PubMed  CAS  Google Scholar 

  12. Cottew GS, Yeats FR (1982) Mycoplasmas and mites in the ears of clinically normal goats. Austr J Vet Sci 59:77–81

    CAS  Google Scholar 

  13. Crowson RA (1981) The biology of the Coleoptera. Academic Press, New York

    Google Scholar 

  14. Edward DG (1947) A selective medium for pleuropneumonia-like organisms. J Gen Microbiol 1:238–243

    CAS  PubMed  Google Scholar 

  15. Eisner T, Wiemer DF, Haynes LW, Meinwald J (1978) Lucibufagins: Defensive steroids from the firefliesPhotinus ignitus andP. marginellus (Coleoptera: Lampyridae). Proc Natl Acad Sci USA 75:905–908

    Article  PubMed  CAS  Google Scholar 

  16. French FE, Whitcomb RF, Tully JG, Hackett KJ, Clark EA, Henegar RB, Rose DL (1990) Tabanid spiroplasmas of the southeast USA: New groups, and correlation with host life history strategy. Art Zbl (Suppl) 20:919–921

    Google Scholar 

  17. Goetz M, Wiemer DF, Haynes LW, Meinwald J, Eisner T (1979) Lucibufagines. Partie III. Oxo-11- et oxo-12-bufalines, steroides defensifs des lampyresPhotinus ignitus etP. marginellus (Coleoptera: Lampyridae). Helv Chim Acta 62:1396–1400

    Article  CAS  Google Scholar 

  18. Hackett KJ (1990) Evolutionary considerations—Arthropod and plant mollicutes. Art Zbl (Suppl) 20:345–351

    Google Scholar 

  19. Hackett KJ, Clark TB (1989) Ecology of spiroplasmas. In: Whitcomb RF, Tully JG (eds) The mycoplasmas, vol 5. Spiroplasmas, acholeplasmas, and mycoplasmas of plants and arthropods. Academic Press, New York, pp 113–200

    Google Scholar 

  20. Hackett KJ, Lynn DE (1985) Cultivation of a fastidious spiroplasma. Science 230:825–827

    PubMed  Google Scholar 

  21. Hackett KJ, Lynn DE, Whitcomb RF (1989) Spiroplasmas and other mollicutes: Possible application to control of plant pests. In: Roberts DW, Granados RR (eds) Symposium on biotechnology, biological pesticides and novel plant-pest resistance for insect pest management. Boyce Thomson Institute, Ithaca, NY

    Google Scholar 

  22. Hackett KJ, Whitcomb RF, Henegar RB, Wagner AG, Clark EA, Tully JG, Green F, McKay WH, Santini P, Rose DL, Anderson JJ, Lynn DE (1990) Mollicute diversity in arthropod hosts. Art Zbl (Suppl) 20:441–454

    Google Scholar 

  23. Int Comm Syst Bacteriol, Subcomm Taxon Mollicutes (1979) Proposal of minimal standards for descriptions of new species of the classMollicutes. Int J Syst Bacteriol 29:172–180

    Google Scholar 

  24. Lloyd J (1966) Studies on the flash communication system inPhotinus fireflies. Univ Mich Mus Zool Misc Pub 130

  25. Lloyd J (1984) Occurrence of aggressive mimicry in fireflies. Flor Entomol 67:368–376

    Google Scholar 

  26. Markham P, Clark TB, Whitcomb (1983) Culture media for spiroplasmas from arthropods. In: Tully JG, Razin S (eds) Methods in mycoplasmology, vol 2. Academic Press, New York, pp 217–223

    Google Scholar 

  27. McCoy RE, Basham HG, Tully JG, Rose DL, Carle P, Bové JM (1984)Acholeplasma florum: A new species isolated from plants. Int J Syst Bacteriol 34:11–15

    CAS  Google Scholar 

  28. Meinwald J, Wiemer DF, Eisner T (1979) Lucibufagins. 2. Esters of 12-oxo-2β,5β,11α-tri-hydroxybufalin, the major defensive steroids of the fireflyPhotinus pyralis (Coleoptera: Lampyridae). J Am Chem Soc 101:3055–3060

    Article  CAS  Google Scholar 

  29. Razin S, Tully JG (1970) Cholesterol requirements of mycoplasmas. J Bacteriol 102:306–310

    PubMed  CAS  Google Scholar 

  30. Razin S, Tully JG (eds) (1983) Methods in mycoplasmology, vol 1. Academic Press, New York

    Google Scholar 

  31. Shaikh AA, Stevens C, Johnson WE, Tang AY, Cody RM (1987) Isolation of spiroplasmas from three species of mosquitoes and partial characterizationin vitro. Isr J Med Sci 23:503

    Google Scholar 

  32. Shaikh AA, Johnson WE, Stevens E, Tang AY (1987) The isolation of spiroplasmas from mosquitoes in Macon County, Alabama. J Am Mosquito Contr Assoc 3:289–295

    CAS  Google Scholar 

  33. Shifrine M, Bailey KP, Stone SS (1972) Contagious bovine pleuropneumoniae: Isolation ofMycoplasma mycoides, var.mycoides from ticks collected from infected cattle and infection attempts using these ticks. Bull Epizoot Dis Afr (Spec Issue) 20:43–45

    CAS  Google Scholar 

  34. Tully JG (1989) ClassMollicutes: New perspectives from plant and arthropod studies. In: Whitcomb RF, Tully JG (eds) The mycoplasmas, vol 5. Spiroplasmas, acholeplasmas, and mycoplasmas of plants and arthropods. Academic Press, New York, pp 1–31

    Google Scholar 

  35. Tully JG, Rose DL, Whitcomb RF, Hackett KJ, Clark TB, Henegar RB, Clark E, Carle P, Bové JM (1987) Characterization of some new insect-derived acholeplasmas. Isr J Med Sci 23:699–703

    PubMed  CAS  Google Scholar 

  36. Tully JG, Rose DL, Clark E, Carle P, Bove JM, Henegar RB, Whitcomb RF, Colflesh DE, Williamson DL (1987) Revised group classification of the genusSpiroplasma (ClassMollicutes), with proposed new groups XII to XXIII. Int J Syst Bacteriol 37:357–364

    Google Scholar 

  37. Tully JG, Rose DL, Carle P, Bove JM, Hackett KJ, Whitcomb RF (1988)Acholeplasma entomophilum sp. nov. from gut contents of a wide range of host insects. Int J Syst Bacteriol 38:164–167

    Article  Google Scholar 

  38. Tully JG, Rose DL, Hackett KJ, Whitcomb RF, Carle P, Bové JM, Colflesh DE, Williamson DL (1989)Mycoplasma ellychniae sp. nov., a sterol-requiring mollicute from the firefly beetleEllychnia corrusca. Int J Syst Bacteriol 39:284–289

    CAS  Google Scholar 

  39. Tully JG, Whitcomb RF, Rose DL, Hackett KJ, Clark E, Henegar RB, Carle P, Bové JM (1989) Current insight into the diversity of acholeplasmas. Art Zbl (Suppl) 20:461–467

    Google Scholar 

  40. Weisburg WG, Tully JG, Rose DL, Petzel JP, Oyaizu H, Yang D, Mandelco L, Sechrest J, Lawrence TG, Van Etten J, Maniloff J, Woese CR (1989) A phylogenetic analysis of the mycoplasmas: Basis for their classification. J Bacteriol 171:6455–6467

    PubMed  CAS  Google Scholar 

  41. Whitcomb RF (1983) Culture media for spiroplasmas. In: Razin S, Tully JG (eds) Methods in mycoplasmology, vol 1. Academic Press, New York, pp 147–158

    Google Scholar 

  42. Whitcomb RF, Hackett KJ (1989) An essay on prokaryote diversity. In: Knutson L, Stoner AK (eds) Beltsville symposia in agricultural research 13: Biotic diversity and germplasm preservation, global imperatives. Kluwer Academic, Boston, pp 205–240

    Google Scholar 

  43. Whitcomb RF, Hackett KJ, Tully JG, Clark EA, French FE (1990) Tabanid spiroplasmas as a model for mollicute biogeography. Art Zbl (Suppl) 20:931–933

    Google Scholar 

  44. Williamson DL, Tully JG, Rose DL, Hackett KJ, Henegar R, Carle P, Bové JM, Colflesh DE, Whitcomb RF (1990)Mycoplasma somnilux sp. nov.,Mycoplasma luminosum sp. nov.,Mycoplasma lucivorax sp. nov., new sterol-requiring mollicutes from firefly beetles (Coleoptera: Lampyridae). Int J Syst Bacteriol 40:160–164

    PubMed  CAS  Google Scholar 

  45. Woese CR (1987) Bacterial evolution. Microbiol Rev 51:221–271

    PubMed  CAS  Google Scholar 

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Hackett, K.J., Whitcomb, R.F., Tully, J.G. et al. Lampyridae (Coleoptera): A plethora of mollicute associations. Microb Ecol 23, 181–193 (1992). https://doi.org/10.1007/BF00172639

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