Influence of infected cell growth state on bacteriophage reactivation levels

Citation
Dr. Kadavy et al., Influence of infected cell growth state on bacteriophage reactivation levels, APPL ENVIR, 66(12), 2000, pp. 5206-5212
Citations number
33
Categorie Soggetti
Biology,Microbiology
Journal title
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
ISSN journal
00992240 → ACNP
Volume
66
Issue
12
Year of publication
2000
Pages
5206 - 5212
Database
ISI
SICI code
0099-2240(200012)66:12<5206:IOICGS>2.0.ZU;2-X
Abstract
Reactivation of W-C-inactivated Pseudomonas aeruginosa bacteriophages D3C3, F116, G101, and UNL-1 was quantified in host cells infected during the exp onential phase, during the stationary phase, and after starvation (1 day, 1 and 5 weeks) under conditions designed to detect dark repair and photoreac tivation. Our experiments revealed that while the photoreactivation capacit y of stationary-phase or starved cells remained about the same as that of e xponential-phase cells, in some cases their capacity to support dark repair of UV-inactivated bacteriophages increased over 10-fold, This enhanced rea ctivation capacity was correlated with the ca, 30-fold-greater W-C resistan ce of P, aeruginosa host cells that were in the stationary phase or exposed to starvation conditions prior to irradiation. The dark repair capacity of P, aeruginosa cells that were infected while they were starved for prolong ed periods depended on the bacteriophage examined. For bacteriophage D3C3 t his dark repair capacity declined with prolonged starvation, while for bact eriophage G101 the dark repair capacity continued to increase when cells we re starved for 24 h or 1 week prior to infection. For G101, the reactivatio n potentials were 16-, 18-, 10-, and 3-fold at starvation intervals of 1 da y, 1 week, 5 weeks, and 1.5 years, respectively; Exclusive use of exponenti al-phase cells to quantify bacteriophage reactivation should detect only a fraction of the true phage reactivation potential.