Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1978 Sep;36(3):500–505. doi: 10.1128/aem.36.3.500-505.1978

Ecological relationship between Vibrio parahaemolyticus and agar-digesting vibrios as evidenced by bacteriophage susceptibility patterns.

J A Baross, J Liston, R Y Morita
PMCID: PMC243075  PMID: 727782

Abstract

Twenty bacteriophages active against Vibrio parahaemolyticus and agar-digesting vibrios, isolated from oysters (Crassostrea gigas) and Dungeness crab (Cancer magister) and by induction of a lysogenic agar digester, were tested as to their host range. These phages were specific for V. parahaemolyticus and various agar-digesting vibrios, and interspecies lysis occurred only between these two groups. V. alginolyticus, V. anguillarum and related species, V. cholerae, and a group of marine psychrophilic and psychrotrophic vibrios were not affected. No correlation was observed between the O and K serotypes of V. parahaemolyticus strains and bacteriophage susceptibility patterns, and 7 of 28 strains of V. parahaemolyticus were not lysed by any of the phages. Only two of the phage isolates were capable of lysing all susceptible V. parahaemolyticus strains. No correlation was observed between the inter-and intraspecies genetic relatedness (DNA homologies) of V. parahaemolyticus and agar-digesting vibrios and susceptibility patterns to different bacteriophages. Some of the phages were capable of plaque formation on V. parahaemolyticus as well as on some strains of agar-digesting vibrios that were separated by 70 to 80% differences in their DNA homologies. The possible ecological significance of these vibrio bacteriophages, particularly those having a wide host range, is discussed.

Full text

PDF
500

Selected References

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

  1. Anderson R. S., Ordal E. J. Deoxyribonucleic acid relationships among marine vibrios. J Bacteriol. 1972 Feb;109(2):696–706. doi: 10.1128/jb.109.2.696-706.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Barksdale L., Arden S. B. Persisting bacteriophage infections, lysogeny, and phage conversions. Annu Rev Microbiol. 1974;28(0):265–299. doi: 10.1146/annurev.mi.28.100174.001405. [DOI] [PubMed] [Google Scholar]
  3. Baross J. A., Liston J., Morita R. Y. Incidence of Vibrio parahaemolyticus bacteriophages and other Vibrio bacteriophages in marine samples. Appl Environ Microbiol. 1978 Sep;36(3):492–499. doi: 10.1128/aem.36.3.492-499.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Colwell R. R., Kaper J., Joseph S. W. Vibrio cholerae, Vibrio parahaemolyticus, and other vibrios: occurrence and distribution in Chesapeake Bay. Science. 1977 Oct 28;198(4315):394–396. [PubMed] [Google Scholar]
  5. Denhardt D. T. A membrane-filter technique for the detection of complementary DNA. Biochem Biophys Res Commun. 1966 Jun 13;23(5):641–646. doi: 10.1016/0006-291x(66)90447-5. [DOI] [PubMed] [Google Scholar]
  6. Dhillon T. S., Dhillon E. K., Chau H. C., Li W. K., Tsang A. H. Studies on bacteriophage distribution: virulent and temperate bacteriophage content of mammalian feces. Appl Environ Microbiol. 1976 Jul;32(1):68–74. doi: 10.1128/aem.32.1.68-74.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Kaneko T., Colwell R. R. Incidence of Vibrio parahaemolyticus in Chesapeake Bay. Appl Microbiol. 1975 Aug;30(2):251–257. doi: 10.1128/am.30.2.251-257.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. MARMUR J., DOTY P. Determination of the base composition of deoxyribonucleic acid from its thermal denaturation temperature. J Mol Biol. 1962 Jul;5:109–118. doi: 10.1016/s0022-2836(62)80066-7. [DOI] [PubMed] [Google Scholar]

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

RESOURCES