Abstract
Transduction has been shown to play a significant role in the transfer of plasmid and chromosomal DNA in aquatic ecosystems. Such ecosystems contain a multitude of environmental factors, any one of which may influence the transduction process. It was the purpose of this study to show how one of these factors, particulate matter, affects the frequency of transduction. In situ transduction rates were measured in lake water microcosms containing either high or low concentrations of particulate matter. The microcosms were incubated in a freshwater lake in central Oklahoma. Transduction frequencies were found to be enhanced as much as 100-fold in the presence of particulates. Our results suggest that aggregations of bacteriophages and bacterial cells are stimulated by the presence of these suspended particulates. This aggregation increases the probability of progeny phages and transducing particles finding and infecting new host cells. Consequently, both phage production and transduction frequencies increase in the presence of particulate matter.
Full Text
The Full Text of this article is available as a PDF (571.5 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- 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]
- Harvey R. W., Young L. Y. Enumeration of particle-bound and unattached respiring bacteria in the salt marsh environment. Appl Environ Microbiol. 1980 Jul;40(1):156–160. doi: 10.1128/aem.40.1.156-160.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hedges R. W., Jacoby G. A. Compatibility and molecular properties of plasmid Rms 149 in Pseudomonas aeruginosa and Escherichia coli. Plasmid. 1980 Jan;3(1):1–6. doi: 10.1016/s0147-619x(80)90029-3. [DOI] [PubMed] [Google Scholar]
- Iriberri J., Unanue M., Barcina I., Egea L. Seasonal variation in population density and heterotrophic activity of attached and free-living bacteria in coastal waters. Appl Environ Microbiol. 1987 Oct;53(10):2308–2314. doi: 10.1128/aem.53.10.2308-2314.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller R. V., Ku C. M. Characterization of Pseudomonas aeruginosa mutants deficient in the establishment of lysogeny. J Bacteriol. 1978 Jun;134(3):875–883. doi: 10.1128/jb.134.3.875-883.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller R. V., Pemberton J. M., Clark A. J. Prophage F116: evidence for extrachromosomal location in Pseudomonas aeruginosa strain PAO. J Virol. 1977 Jun;22(3):844–847. doi: 10.1128/jvi.22.3.844-847.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller R. V., Pemberton J. M., Richards K. E. F116, D3 and G101: temperate bacteriophages of Pseudomonas aeruginosa. Virology. 1974 Jun;59(2):566–569. doi: 10.1016/0042-6822(74)90466-8. [DOI] [PubMed] [Google Scholar]
- Morrison W. D., Miller R. V., Sayler G. S. Frequency of F116-mediated transduction of Pseudomonas aeruginosa in a freshwater environment. Appl Environ Microbiol. 1978 Nov;36(5):724–730. doi: 10.1128/aem.36.5.724-730.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- O'Morchoe S. B., Ogunseitan O., Sayler G. S., Miller R. V. Conjugal transfer of R68.45 and FP5 between Pseudomonas aeruginosa strains in a freshwater environment. Appl Environ Microbiol. 1988 Aug;54(8):1923–1929. doi: 10.1128/aem.54.8.1923-1929.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rella M., Haas D. Resistance of Pseudomonas aeruginosa PAO to nalidixic acid and low levels of beta-lactam antibiotics: mapping of chromosomal genes. Antimicrob Agents Chemother. 1982 Aug;22(2):242–249. doi: 10.1128/aac.22.2.242. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ripp S., Ogunseitan O. A., Miller R. V. Transduction of a freshwater microbial community by a new Pseudomonas aeruginosa generalized transducing phage, UT1. Mol Ecol. 1994 Apr;3(2):121–126. doi: 10.1111/j.1365-294x.1994.tb00112.x. [DOI] [PubMed] [Google Scholar]
- Saye D. J., Ogunseitan O. A., Sayler G. S., Miller R. V. Transduction of linked chromosomal genes between Pseudomonas aeruginosa strains during incubation in situ in a freshwater habitat. Appl Environ Microbiol. 1990 Jan;56(1):140–145. doi: 10.1128/aem.56.1.140-145.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Saye D. J., Ogunseitan O., Sayler G. S., Miller R. V. Potential for transduction of plasmids in a natural freshwater environment: effect of plasmid donor concentration and a natural microbial community on transduction in Pseudomonas aeruginosa. Appl Environ Microbiol. 1987 May;53(5):987–995. doi: 10.1128/aem.53.5.987-995.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stotzky G. Influence of clay minerals on microorganisms. 3. Effect of particle size, cation exchange capacity, and surface area on bacteria. Can J Microbiol. 1966 Dec;12(6):1235–1246. doi: 10.1139/m66-165. [DOI] [PubMed] [Google Scholar]
- Stotzky G., Rem L. T. Influence of clay minerals on microorganisms. I. Montmorillonite and kaolinite on bacteria. Can J Microbiol. 1966 Jun;12(3):547–563. doi: 10.1139/m66-078. [DOI] [PubMed] [Google Scholar]
