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Research Paper |
grzyn1,3
Department of Molecular Biology, University of Gdansk, K
adki 24, 80-822 Gdansk, Poland1
Division of Genomic Medicine, University of Sheffield Medical School, Beech Hill Road, Sheffield S10 2RX, UK2
Institute of Oceanology, Polish Academy of Sciences,
w. Wojciecha 5, 81-347 Gdynia, Poland3
Author for correspondence: Mark S. Thomas. Tel: +44 114 271 2834. Fax: +44 114 273 9926. e-mail: m.s.thomas{at}shef.ac.uk
It was found that infection of Escherichia coli by bacteriophage
is inhibited in the presence of certain bile salts and carbohydrates when cells are in the OFF state for production of the phase-variable cell surface protein antigen 43 (Ag43). The inhibition of phage growth was found to be due to a significant impairment in the process of phage adsorption. Expression of the gene encoding Ag43 (agn43) from a plasmid or inactivation of the oxyR gene (encoding an activator of genes important for defence against oxidative stress) suppressed this inhibition. A mutation, rpoA341, in the gene encoding the
subunit of RNA polymerase also facilitated phage adsorption in the presence of bile salts and carbohydrates. The rpoA341 mutation promoted efficient production of Ag43 in a genetic background that would otherwise be in the OFF phase for expression of the agn43 gene. Analysis of a reporter gene fusion demonstrated that the promoter for the agn43 gene was more active in the rpoA341 mutant than in the otherwise isogenic rpoA+ strain. The combined inhibitory action of bile salts and carbohydrates on phage adsorption and the abolition of this inhibition by production of Ag43 was not restricted to
, as a similar phenomenon was observed for the coliphages P1 and T4.
Keywords: bacteriophage infection, MacConkey agar, antigen 43, RNA polymerase
subunit, phase switching
Abbreviations: DOC, deoxycholate; PVP, polyvinylpyrrolidone; WSS Wytwórnia Surowic I Szczepionek
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