Skip to main content
Log in

A study of five bacteriophages of theMyoviridae family which replicate on different gram-positive bacteria

  • Original Papers
  • Published:
Archives of Virology Aims and scope Submit manuscript

Summary

A comparative study is reported on five phages of theMyoviridae family which propagate onBacillus subtilis, B. thuringiensis, Enterococcus sp.,Lactobacillus plantarum, orStaphylococcus aureus. The phages are morphologically identical and characterized by isometric heads with conspicuous capsomers and by contractile tails with complex base plates. The phages show similar protein profiles, but vary considerably in burst size. Phage DNAs are about 95–166kb in size and are unrelated by DNA-DNA hybridization and restriction endonuclease analysis. Therefore the phages are unrelated at species level. Implications of these data for our understanding of the development of phage species are discussed.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Ackermann H-W, DuBow MS (1987 a) Viruses of prokaryotes. I. General properties of bacteriophages. CRC Press, Boca Raton, pp 179–182

    Google Scholar 

  2. Ackerman H-W, DuBow MS (1987 b) Viruses of prokaryotes. II. Natural groups of bacteriophages. CRC Press, Boca Raton, pp 51–161

    Google Scholar 

  3. Ackermann H-W, DuBow MS, Jarvis AW, Jones LA, Krylov VN, Maniloff J, Rocourt J, Safferman RS, Schneider J, Seldin L, Sozzi T, Stewart PR, Werquin M, Wünsche L (1992) The species concept and its application to tailed phages. Arch Virol 124: 69–82

    Google Scholar 

  4. Ackermann H-W, Greer GG, Rocourt J (1988) Morphology ofBrochothrix thermosphacta phages. Microbios 56: 19–26

    Google Scholar 

  5. Braun V, Hertwig S, Neve H, Geis A, Teuber M (1989) Taxonomic differentiation of bacteriophages ofLactococcus lactis by electron microscopy, DNA-DNA hybridization and protein profiles. J Gen Microbiol 135: 2551–2560

    Google Scholar 

  6. Francki RIB, Fauquet CM, Knudson DL, Brown F (eds) (1991) Classification and nomenclature of viruses. Fifth Report of the International Committee on Taxonomy of Viruses. Springer, Wien New York (Arch Virol [Suppl]2)

    Google Scholar 

  7. Jarvis AW (1978) Serological studies of a host range mutant of a lactic streptococcal bacteriophage. Appl Environ Microbiol 36: 785–789

    Google Scholar 

  8. Jarvis AW, Fitzgerald GF, Mata M, Mercenier A, Neve H, Powell IB, Ronda C, Saxelin M, Teuber M (1991) Species and type phages of lactococcal bacteriophages. Intervirology 32: 2–9

    Google Scholar 

  9. Jarvis AW, Meyer J (1986) Electron microscopic heteroduplex study and restriction endonuclease analysis of the DNA genomes of three lactococcal bacteriophages. Appl Environ Microbiol 51: 1272–1277

    Google Scholar 

  10. Klaenhammer TR, Sanozky RB (1985) Conjugal transfer fromStreptococcus lactis ME 2 of plasmids encoding phage resistance, nisin resistance and lactose-fermenting ability: evidence for a high-frequency conjugative plasmid responsible for abortive infection of virulent bacteriophage. J Gen Microbiol 131: 1531–1541

    Google Scholar 

  11. Korsten KH, Tomkiewicz T, Hausmann R (1979) The strategy of infection as a criterion for phylogenetic relationships of non-coli phage morphologically similar to phage T7. J Gen Microbiol 43: 57–73

    Google Scholar 

  12. Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680–685

    Google Scholar 

  13. London J, Kline K (1973) Aldolase of lactic acid bacteria: a case history in the use of an enzyme as evolutionary marker. Bacteriol Rev 37: 453–478

    Google Scholar 

  14. Ludwig W, Schleifer K-H, Stackebrandt E (1984) 16 S rRNA analysis ofListeria monocytogenes andBrochothrix thermosphacta. FEMS Microbiol Lett 25: 199–204

    Google Scholar 

  15. Luftwig R (1976) An accurate measurement of the catalase crystal period and its use as an internal marker for electron microscopy. J Ultrastruct Res 20: 91–102

    Google Scholar 

  16. Southern EM (1975) Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 98: 503–517

    Google Scholar 

  17. Tikhonenko AS (1970) Ultrastructure of bacterial viruses. Plenum Press, New York, pp 143–145

    Google Scholar 

  18. Twort FW (1915) An investigation on the nature of ultramicroscopic viruses. Lancet 2: 1241

    Google Scholar 

  19. Ward LJH, Jarvis AW (1992) Rapid removal of cesium chloride from DNA obtained from ultracentrifuge gradients. Biotechnics 12: 12

    Google Scholar 

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

    Google Scholar 

  21. Zink R, Loessner MJ (1992) Classification of virulent and temperate bacteriophages ofListeria spp. on the basis of morphology and protein analysis. Appl Environ Microbiol 58: 296–302

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Chairperson

Vice Chairperson of ICTV Bacterial Virus Subcommittee

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jarvis, A.W., Collins, L.J. & Ackermann, H.W. A study of five bacteriophages of theMyoviridae family which replicate on different gram-positive bacteria. Archives of Virology 133, 75–84 (1993). https://doi.org/10.1007/BF01309745

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01309745

Keywords

Navigation