Home LiteratureArticle Details
PMID: 24196310 Published · ppublish English Journal Article

Dynamic interactions ofPseudomonas aeruginosa and bacteriophages in lake water.

Microbial ecology ·Vol. 19 ·No. 2 ·1990-03-00 ·Pages 171-85

Ogunseitan OA, Sayler GS, Miller RV

Abstract

The persistence and interaction between newly isolated strains ofPseudomonas aeruginosa and resident bacteriophages indigenous to a freshwater environment was monitored over 45 days in lake water microcosms. The interaction between susceptible and resistant bacteria with pure phage (UT1) particles or a mixed phage population (M1) was investigated by following temporal changes in host density, phage-to-bacteria ratio (PBR), and the appearance of apparent prophage carriers within the host population. Decay rates of the phage (UT1) ranged from 0.054 hour(-1) in natural water to 0.027 hour(-1) in filtered lake water. About 45% of sensitive bacteria incubated with phase UT1 were pseudolysogenic within 12 hours of incubation in natural lake water. This process was delayed until 72 hours in the steile lake water control, suggesting that host-phage interaction is promoted in the presence of a viable natural microbial community. Phage UT1 appeared to stabilize the density of host bacteria in lake water at a level of 10(4) colony-forming units (cfu) ml(-1). Bacterial coexistence with the mixed phage (M1) population resulted in an oscillating equilibrium with the PBR stabilizing at about 3. The presence of extraneous homoimmune phages appeared to be detrimental to the stability of the pseudolysogens, which were maintained at a lower population density than prophage-free cells in lake water containing the mixed phage (M1) population.

Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ogunseitan O A
Department of Microbiology and The Graduate Program in Ecology, Center for Environmental Biotechnology, University of Tennessee, 37932-2567, Knoxville, Tennessee.
Sayler G S
Miller R V
References (21)
21 references, click to expand
  1. Rapid concentration of bacteriophages from aquatic habitats.
    J Appl Bacteriol. 1977 Jun;42(3):417-21 PMID: 407206
  2. Persisting bacteriophage infections, lysogeny, and phage conversions.
    Annu Rev Microbiol. 1974;28(0):265-99 PMID: 4215366
  3. Fate in model ecosystems of microbial species of potential use in genetic engineering.
    Appl Environ Microbiol. 1982 Sep;44(3):708-14 PMID: 6814361
  4. Application of DNA-DNA colony hybridization to the detection of catabolic genotypes in environmental samples.
    Appl Environ Microbiol. 1985 May;49(5):1295-303 PMID: 4004244
  5. New selective media for enumeration and recovery of fluorescent pseudomonads from various habitats.
    Appl Environ Microbiol. 1985 Jan;49(1):28-32 PMID: 16346705
  6. Frequency of F116-mediated transduction of Pseudomonas aeruginosa in a freshwater environment.
    Appl Environ Microbiol. 1978 Nov;36(5):724-30 PMID: 103503
  7. Minimum bacterial density for bacteriophage replication: implications for significance of bacteriophages in natural ecosystems.
    Appl Environ Microbiol. 1985 Jan;49(1):19-23 PMID: 3156556
  8. Conversion of somatic antigens in Salmonella by phage infection leading to lysis or lysogeny.
    Virology. 1958 Feb;5(1):68-91 PMID: 13519750
  9. Research needs for biotic environmental effects of genetically-engineered microorganisms.
    Recomb DNA Tech Bull. 1984 Mar;7(1):20-30 PMID: 6587444
  10. Coevolution of Escherichia coli and bacteriophages in chemostat culture.
    Science. 1970 May 22;168(3934):992-3 PMID: 4909622
  11. Bacteriocinogeny and lysogeny in the genus Pseudomonas.
    J Gen Microbiol. 1965 Jun;39(3):295-303 PMID: 5864527
  12. The population biology of bacterial viruses: why be temperate.
    Theor Popul Biol. 1984 Aug;26(1):93-117 PMID: 6484871
  13. A regulatory model for steady-state conditions in populations of lysogenic bacteria.
    J Theor Biol. 1968 Jan;18(1):1-8 PMID: 5648881
  14. 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):987-95 PMID: 3111371
  15. Characterization of the Pseudomonas aeruginosa recA gene: the Les- phenotype.
    J Bacteriol. 1988 Feb;170(2):578-82 PMID: 3123459
  16. Medium for the selective isolation of members of the genus Pseudomonas from natural habitats.
    Appl Environ Microbiol. 1977 May;33(5):1222-4 PMID: 879779
  17. Further observations on the change to virulence of bacteriophage-infected a virulent strains of Corynebacterium diphtheria.
    J Bacteriol. 1952 Mar;63(3):407-14 PMID: 14927573
  18. Origin of polysaccharide depolymerase associated with bacteriophage infection.
    J Virol. 1969 Mar;3(3):290-6 PMID: 4976560
  19. Comparative effects of Aroclor 1254 (polychlorinated biphenyls) and phenanthrene on glucose uptake by freshwater microbial populations.
    Appl Environ Microbiol. 1979 May;37(5):878-85 PMID: 114110
  20. Grouping Pseudomonas aeruginosa by lysogenicity and pyocinogenicity.
    J Pathol Bacteriol. 1960 Oct;80:448-50 PMID: 13715403
  21. An ecological study of bacteriophages of Vibrio natriegens.
    Can J Microbiol. 1978 Mar;24(3):321-4 PMID: 647480
Article Info
Journal
Microbial ecology
Abbr.
Microb Ecol
ISSN
0095-3628
Published
1990-03-00
Pages
171-85
Language
English
Region
United States
NLM ID
7500663
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com