Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1992 Mar;58(3):1011–1018. doi: 10.1128/aem.58.3.1011-1018.1992

Comparative Study of 35 Bacteriophages of Lactobacillus helveticus: Morphology and Host Range

Laurent Séchaud 1, Micheline Rousseau 1, Blandine Fayard 1, Maria Luisa Callegari 1,, Pascal Quénée 1, Jean-Pierre Accolas 1,*
PMCID: PMC195370  PMID: 16348661

Abstract

This survey included 23 phages isolated from cheese whey and 12 temperate phages induced with mitomycin from their lysogenic host strains. All of the phages had an isometric head and a tail with a contractile sheath. In addition, short-tailed (160-nm-long) and long-tailed (260-nm-long) phages were distinguished. Short-tailed phages were by far the most widespread in French cheese factories (32 of the 35 phages studied). The study of phage relationships enabled two large groups of strains to be distinguished: those not or slightly sensitive to phages and those very sensitive to phages. There was an obvious relationship in the first group between phage sensitivity (or resistance) and the geographic origin of the strains. The second group contained primarily strains from large international collections and those isolated from commercial starters. The relationships among short-tailed phages, either temperate or isolated as lytic, suggest that lysogenic strains could be the major source of phages in French cheese factories.

Full text

PDF
1011

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bradley D. E. Ultrastructure of bacteriophage and bacteriocins. Bacteriol Rev. 1967 Dec;31(4):230–314. doi: 10.1128/br.31.4.230-314.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Classification and nomenclature of viruses. Fourth report of the International Committee on Taxonomy of Viruses. Intervirology. 1982;17(1-3):1–199. doi: 10.1159/000149278. [DOI] [PubMed] [Google Scholar]
  3. Cluzel P. J., Veaux M., Rousseau M., Accolas J. P. Evidence for temperate bacteriophages in two strains of Lactobacillus bulgaricus. J Dairy Res. 1987 Aug;54(3):397–405. doi: 10.1017/s0022029900025577. [DOI] [PubMed] [Google Scholar]
  4. DEKLERK H. C., COETZEE J. N., FOURIE J. T. THE FINE STRUCTURE OF LACTOBACILLUS BACTERIOPHAGES. J Gen Microbiol. 1965 Jan;38:35–38. doi: 10.1099/00221287-38-1-35. [DOI] [PubMed] [Google Scholar]
  5. Joerger M. C., Klaenhammer T. R. Characterization and purification of helveticin J and evidence for a chromosomally determined bacteriocin produced by Lactobacillus helveticus 481. J Bacteriol. 1986 Aug;167(2):439–446. doi: 10.1128/jb.167.2.439-446.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Lahbib-Mansais Y., Mata M., Ritzenthaler P. Molecular taxonomy of Lactobacillus phages. Biochimie. 1988 Mar;70(3):429–435. doi: 10.1016/0300-9084(88)90217-9. [DOI] [PubMed] [Google Scholar]
  7. Sechaud L., Cluzel P. J., Rousseau M., Baumgartner A., Accolas J. P. Bacteriophages of lactobacilli. Biochimie. 1988 Mar;70(3):401–410. doi: 10.1016/0300-9084(88)90214-3. [DOI] [PubMed] [Google Scholar]
  8. Sozzi T., Watanabe K., Stetter K., Smiley M. Bacteriophages of the genus Lactobacillus. Intervirology. 1981;16(3):129–135. doi: 10.1159/000149259. [DOI] [PubMed] [Google Scholar]
  9. de Klerk H. C., Hugo N. Phage-like structures from Lactobacillus acidophilus. J Gen Virol. 1970 Sep;8(3):231–234. doi: 10.1099/0022-1317-8-3-231. [DOI] [PubMed] [Google Scholar]
  10. de Los Reyes-Gavilán C. G., Limsowtin G. K., Séchaud L., Veaux M., Accolas J. P. Evidence for a Plasmid-Linked Restriction-Modification System in Lactobacillus helveticus. Appl Environ Microbiol. 1990 Nov;56(11):3412–3419. doi: 10.1128/aem.56.11.3412-3419.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES