Skip to main content

The Family Entomoplasmataceae

  • Reference work entry
  • First Online:
The Prokaryotes

Abstract

The Entomoplasmataceae is a family within the class Mollicutes and the order Entomoplasmatales with two genera, Entomoplasma and Mesoplasma. Originally, many of the strains now within the Entomoplasmataceae were designated as belonging to the genus Mycoplasma or the genus Acholeplasma based on morphological, biological, and metabolic characteristics. In 1993, Tully and colleagues proposed a major revision to the taxonomic classification in which the Order Entomoplasmatales was divided into two families based on cell shape: Entomoplasmatacea for nonhelical bacteria and the Spiroplasmataceae for helical bacteria. The Entomoplasmatacea family was then divided into two genera based on sterol requirement: Entomoplasma for those that required sterol and Mesoplasma for those that did not require sterol, but were able to grow in serum-free medium supplemented with polyoxyethylene sorbitan (PES – normally 0.04 % Tween 80) (Tully et al. Int J Syst Bacteriol 43:378–385, 1993). Subsequent phylogenetic analyses based on 16S rRNA gene sequence consistently showed that the Entomoplasmataceae is a sister clade to, and appears to be derived from, the Spiroplasmatacea lineage and that the genera are distinct phylogenetically. Phylogenetic analyses also clearly show that the two genera do not form distinct clades but are intermixed. For this reason, it is clear that the requirement for sterol is not a characteristic that can be used to distinguish the two genera and thus, it has been proposed that the two genera be combined under the Entomoplasma genus designation (Johansson K-E, Pettersson B (2002) Taxonomy of Mollicutes. In: Razin S, Herrman R (eds) Molecular biology and pathogenicity of mycoplasmas. Kluwer, London, pp 1–29; Gasparich et al. Int J Syst Evol Microbiol 54:893–891, 2004). Currently, there are six Entomoplasma species and eleven Mesoplasma species formally described. They have been isolated from arthropod hosts or plant surfaces (most likely deposited by arthropod hosts) and have not been found to be pathogenic to either host. Species from both genera appear as nonhelical, nonmotile, pleomorphic coccoid cells of various sizes under dark-field microscopic examination, were able to be filtered through 220-nm filters, lacked a cell wall (and thus are resistant to penicillin), and all were chemo-organotropic with the ability to ferment glucose using a PEP-dependent carbohydrate phosphotransferase system. There was variable ability to hydrolyze arginine and none were able to hydrolyze urea. The genome size ranged from 613 to 1,030 kbp, the G+C content ranged from 26.4 to 34.1 mol%, and the growth temperature range was from 10 °C to 37 °C with the common optimal growth temperature being 30 °C. The Entomoplasmataceae family as a whole is understudied with little information available for most species beyond the original description.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 699.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 849.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Bonnet F, Saillard C, Vignault JC, Garnier M, Carle P, Bové JM, Rose DL, Tully JG, Whitcomb RF (1991) Acholeplasma seiffertii ap. nov., a mollicute from plant surfaces. Int J Syst Bacteriol 41:45–49

    Article  Google Scholar 

  • Bové JM, Whitcomb RF, McCoy RE (1983) Culture techniques for spiroplasmas from plants. Methods Mycoplasmol 2:225–234

    Article  Google Scholar 

  • Brown DR, Bradbury JM, Whitcomb RF (2011a) Family I. Entomoplasmataceae Tully, Bové, Laigret and Whitcomb 1993, 380VP. In: Krieg NR, Staley JT, Brown DR, Hedlund BP, Pastor BJ, Ward NL, Ludwig W, Whitman WB (eds) Bergey’s manual of systematic bacteriology, 2nd edn. Springer, New York, p 645

    Google Scholar 

  • Brown DR, Bradbury JM, Whitcomb RF (2011b) Genus I. Entomoplasma Tully, Bové, Laigret and Whitcomb 1993, 379VP. In: Krieg NR, Staley JT, Brown DR, Hedlund BP, Pastor BJ, Ward NL, Ludwig W, Whitman WB (eds) Bergey’s manual of systematic bacteriology, 2nd edn. Springer, New York, pp 646–649

    Google Scholar 

  • Brown DR, Bradbury JM, Whitcomb RF (2011c) Genus II. Mesoplasma Tully, Bové, Laigret and Whitcomb 1993, 380VP. In: Krieg NR, Staley JT, Brown DR, Hedlund BP, Pastor BJ, Ward NL, Ludwig W, Whitman WB (eds) Bergey’s manual of systematic bacteriology, 2nd edn. Springer, New York, pp 649–653

    Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

  • 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 

  • Davis RE, Worley JF, Whitcomb RF, Ishijima T, Steere RL (1972) Helical filaments produced by a mycoplasma-like organism associated with corn stunt disease. Science 176:521–523

    Article  PubMed  Google Scholar 

  • Doi Y, Tersanaka M, Yora K, Assuyama H (1967) Mycoplasma-or PLT group-like microorganisms found in the phloem elements of plants infected with mulberry dwarf, potato witches’ broom, aster yellows or Paulownia witches’ broom. Ann Phytopathol Soc Jpn 33:259–266

    Article  Google Scholar 

  • Eden-Green S, Tully JG (1979) Isolation of Acholeplasma spp. from coconut palms affected by lethal yellowing disease in Jamaica. Curr Microbiol 2:311–316

    Article  Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

  • Freundt EA, Whitcomb RF, Barile MF, Razin S, Tully JG (1984) Proposal for elevation of the family Acholeplasmataceae to ordinal rank: Acholeplasmatales. Int J Syst Bacteriol 34:346–349

    Article  Google Scholar 

  • Gasparich GE, Whitcomb RF, Dodge D, French FE, Glass J, Williamson DL (2004) The genus Spiroplasma and its non-helical descendents: phylogenetic classification, correlation with phenotype and roots of the Mycoplasma mycoides clade. Int J Syst Evol Microbiol 54:893–918

    Article  PubMed  CAS  Google Scholar 

  • Gros O, Saillard C, Helias C, Le Goff F, Marjolet M, Bové JM, Chastel C (1996) Serological and molecular characterization of Mesoplasma seiffertii strains isolated from hematophagous dipterans in France. Int J Syst Bacteriol 46:112–115

    Article  PubMed  CAS  Google Scholar 

  • Gur E, Sauer RT (2008) Evolution of the ssrA degradation tag in Mycoplasma. Specificity switch to a different protease. Proc Natl Acad Sci USA 106:16113–16118

    Article  Google Scholar 

  • Hill AC, Polak-Vogelzang AA, Angulo AF (1992) Acholeplasma multilocale sp. nov., isolated from a horse and a rabbit. Int J Syst Bacteriol 42:513–517

    Article  PubMed  CAS  Google Scholar 

  • Hong SW, Lee JS, Chung KS (2011) Effect of enzyme producing microorganisms on the biomass of epigeic earthworms (Eisenia fetida) in vermicompost. Bioresour Technol 102:6344–6347

    Article  PubMed  CAS  Google Scholar 

  • Hopfe M, Hegemann JH, Henrich B (2005) HinT proteins and their putative interaction partners Mollicutes and Chlamydiaceae. BMC Microbiol 5:27

    Article  PubMed  PubMed Central  Google Scholar 

  • IRPCM Phytoplasma/Spiroplasma Working Team-Phytoplasma Taxonomy Group (2004) ‘Candidatus Phytoplasma’, a taxon for the wall-less, non-helical prokaryotes that colonize plant phloem and insects. Int J Syst Evol Microbiol 54:1243–1255

    Article  Google Scholar 

  • Johansson K-E, Pettersson B (2002) Taxonomy of Mollicutes. In: Razin S, Herrman R (eds) Molecular biology and pathogenicity of mycoplasmas. Kluwer, London, pp 1–29

    Chapter  Google Scholar 

  • Kim JN, Roth A, Breaker RR (2007) Guanine riboswitch variants from Mesoplasma florum selectively recognize 2′-deoxyguanosine. Proc Natl Acad Sci USA 104:16092–16097

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Knight TF Jr (2004) Reclassification of Mesoplasma pleciae as Acholeplasma pleciae comb. nov. on the basis of 16S rRNA and gyrB gene sequence data. Int J Syst Evol Microbiol 54:1951–1952

    Article  PubMed  CAS  Google Scholar 

  • Markham PG, Clark TB, Whitcomb RF (1983) Culture techniques for spiroplasmas from arthropods. Methods Mycoplasmol 2:217–223

    Article  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Navas-Castillo J, Laigret F, Bové JM (1993) 16SrDNA sequence analysis of Acholeplasma seifertii, a mollicute from plant surfaces, and its transfer Mesoplasma, a new genus in the spiroplasma phylogenetic group. Nucl Acids Res 21:2249

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Pollack JD, Williams MV, Banzon J, Jones MA, Harvey L, Tully JG (1996) Comparative metabolism of Mesoplasma, Entomoplasma, Mycoplasma and Acholeplasma. Int J Syst Bacteriol 46:885–890

    Article  PubMed  CAS  Google Scholar 

  • Razin S, Freundt EA (1984) Class I. Mollicutes Edward and Freundt 1967, 267AL Order I. Mycoplasmatales Freundt 1955, 71AL. In: Krieg NR, Holt JG (eds) Bergey’s manual of systematic bacteriology, vol 1. Williams & Wilkins, Baltimore, pp 740–742

    Google Scholar 

  • Robinson IM, Freundt EA (1987) Proposal for an amended classification of anaerobic Mollicutes. Int J Syst Bacteriol 37:78–81

    Article  Google Scholar 

  • Rose DL, Kocka JP, Somerson NL, Tully JG, Whitcomb RF, Carle P, Bové JM, Colflesh DE, Williamson DL (1990) Mycoplasma lactucae sp. nov., a sterol-requiring mollicute from plant surface. Int J Syst Bacteriol 40:138–142

    Article  PubMed  CAS  Google Scholar 

  • Rose DL, Tully JG, Bové JM, Whitcomb RF (1993) A test for measuring growth responses of Mollicutes to serum and polyoxyethylene sorbitan. Int J Syst Bacteriol 43:527–532

    Article  PubMed  CAS  Google Scholar 

  • Saglio P, L’hospital M, Lafleche D, Dupont G, Bové JM, Tully JG, Freundt EA (1973) Spiroplasma citri gen. and sp. n.: a mycoplasmalike organisms associated with “stubborn” disease of citrus. Int J Syst Bacteriol 23:191–204

    Article  CAS  Google Scholar 

  • Toth KF, Harrison N, Sears BB (1994) Phylogenetic relationships among members of the class Mollicutes deduced from rps3 gene sequences. Int J Syst Bacteriol 44:119–124

    Article  PubMed  CAS  Google Scholar 

  • Tully JG (1983) Cloning and filtration techniques for mycoplasmas. Methods Mycoplasmol 1:173–177

    Article  Google Scholar 

  • Tully JG (1984) The family Acholeplasmataceae, genus Acholeplasma. In: Krieg NR, Holt JM (eds) Bergey’s manual of systematic bacteriology, vol 1. Williams & Wilkins, Baltimore, pp 781–787

    Google Scholar 

  • 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 

  • Tully JG, Rose DL, Carle P, Bové 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 

  • 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 beetle Ellychnia corrusca. Int J Syst Bacteriol 39:284–289

    Article  CAS  Google Scholar 

  • Tully JG, Rose DL, McCoy RE, Carle P, Bové JM, Whitcomb RF, Weisburg WG (1990) Mycoplasma melaleucae sp. nov., a sterol-requiring mollicute from flowers of several tropical plants. Int J Syst Bacteriol 40:143–147

    Article  PubMed  CAS  Google Scholar 

  • Tully JG, Bové JM, Laigret F, Whitcomb RF (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 (Entomoplasmatacea fam. nov.) from helical species (Spiroplasmatacea), and emended description of the order Mycoplasmatales, Family Mycoplasmatacea. Int J Syst Bacteriol 43:378–385

    Article  Google Scholar 

  • Tully JG, Whitcomb RF, Hackett KJ, Rose DL, Henegar RB, Bové JM, Carle P, Williamson DL, Clark TB (1994) Taxonomic descriptions of eight new non-sterol-requiring mollicutes assigned to the Genus Mesoplasma. Int J Syst Bacteriol 44:685–693

    Article  PubMed  CAS  Google Scholar 

  • Tully JG, Whitcomb RF, Hackett KJ, Williamson DL, Laigret F, Carle P, Bové JM, Henegar RB, Ellis NM, Dodge DE, Adams J (1998) Entomoplasma freundtii sp. nov., a new species from a green tiger beetle (Coleoptera: Cicindelidae). Int J Syst Bacteriol 48:1197–1204

    Article  PubMed  Google Scholar 

  • Volokhov DV, Neverov AA, George J, Kong H, Liu SX, Anderson C, Davidson MK, Chizhikov V (2007) Genetic analysis of housekeeping genes of members of the genus Acholeplasma: phylogeny and complementary molecular markers to the 16S rRNA gene. Mol Phylogenet Evol 44:699–710

    Article  PubMed  CAS  Google Scholar 

  • Wacker A, Buck J, Mathieu D, Richter C, Wohnert J, Schwalbe H (2011) Structure and dynamics of the deoxyguanosine-sensing riboswitch studies by NMR-spectroscopy. Nucl Acids Res 39:6802–6812

    Article  PubMed  CAS  PubMed Central  Google Scholar 

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

    PubMed  CAS  PubMed Central  Google Scholar 

  • Whitcomb RF (1983) Culture media for spiroplasmas. Methods Mycoplasmol 1:147–158

    Article  Google Scholar 

  • 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, and Mycoplasma lucivorax sp. nov., new sterol-requiring Mollicutes from firefly beetles (Coleoptera: Lampyridae). Int J Syst Bacteriol 40:160–164

    Article  PubMed  CAS  Google Scholar 

  • Woese CR, Maniloff J, Zablen LB (1980) Phologenetic analysis of the mycoplasmas. Proc Natl Acad Sci USA 77:494–498

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Zhang Z, Wang H, Zhu J, Suneethi S, Zheng J (2012) Swine manure vermicomposting via housefly larvae (Musca domestica): the dynamics of biochemical and microbial features. Bioresour Technol 118:563–571

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Gail E. Gasparich .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2014 Springer-Verlag Berlin Heidelberg

About this entry

Cite this entry

Gasparich, G.E. (2014). The Family Entomoplasmataceae . In: Rosenberg, E., DeLong, E.F., Lory, S., Stackebrandt, E., Thompson, F. (eds) The Prokaryotes. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-30120-9_390

Download citation

Publish with us

Policies and ethics