characterizing reca-independent induction of shiga toxin2-encoding phages by edta treatment描述reca-independent感应edta志贺toxin2-encoding噬菌体的治疗.pdfVIP
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characterizing reca-independent induction of shiga toxin2-encoding phages by edta treatment描述reca-independent感应edta志贺toxin2-encoding噬菌体的治疗
Characterizing RecA-Independent Induction of Shiga
toxin2-Encoding Phages by EDTA Treatment
Lejla Imamovic, Maite Muniesa*
Department of Microbiology, University of Barcelona, Barcelona, Spain
Abstract
Background: The bacteriophage life cycle has an important role in Shiga toxin (Stx) expression. The induction of Shiga
toxin-encoding phages (Stx phages) increases toxin production as a result of replication of the phage genome, and phage
lysis of the host cell also provides a means of Stx toxin to exit the cell. Previous studies suggested that prophage induction
might also occur in the absence of SOS response, independently of RecA.
Methodology/Principal Findings: The influence of EDTA on RecA-independent Stx2 phage induction was assessed, in
laboratory lysogens and in EHEC strains carrying Stx2 phages in their genome, by Real-Time PCR. RecA-independent
mechanisms described for phage l induction (RcsA and DsrA) were not involved in Stx2 phage induction. In addition,
mutations in the pathway for the stress response of the bacterial envelope to EDTA did not contribute to Stx2 phage
induction. The effect of EDTA on Stx phage induction is due to its chelating properties, which was also confirmed by the use
of citrate, another chelating agent. Our results indicate that EDTA affects Stx2 phage induction by disruption of the bacterial
outer membrane due to chelation of Mg2+. In all the conditions evaluated, the pH value had a decisive role in Stx2 phage
induction.
Conclusions/Significance: Chelating agents, such as EDTA and citrate, induce Stx phages, which raises concerns due to
their frequent use in food and pharmaceutical products. This study contributes to our understanding of the phenomenon of
induction and release of Stx phages as an important factor in the pathogenicity of Sh
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