Temperate phages promote colicin‐dependent fitness of S almonella enterica serovar T yphimurium

Bacteria employ bacteriocins for interference competition in microbial ecosystems. Colicin Ib ( ColIb ), a pore‐forming bacteriocin, confers a significant fitness benefit to S almonella enterica serovar T yphimurium ( S .   Tm ) in competition against commensal E scherichia coli in the gut. ColIb is...

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Veröffentlicht in:Environmental microbiology 2016-05, Vol.18 (5), p.1591-1603
Hauptverfasser: Nedialkova, Lubov P., Sidstedt, Maja, Koeppel, Martin B., Spriewald, Stefanie, Ring, Diana, Gerlach, Roman G., Bossi, Lionello, Stecher, Bärbel
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Sprache:eng
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Zusammenfassung:Bacteria employ bacteriocins for interference competition in microbial ecosystems. Colicin Ib ( ColIb ), a pore‐forming bacteriocin, confers a significant fitness benefit to S almonella enterica serovar T yphimurium ( S .   Tm ) in competition against commensal E scherichia coli in the gut. ColIb is released from S . Tm into the environment, where it kills susceptible competitors. However, colicin‐specific release proteins, as they are known for other colicins, have not been identified in case of ColIb . Thus, its release mechanism has remained unclear. In the current study, we have established a new link between ColIb release and lysis activity of temperate, lambdoid phages. By the use of phage‐cured S .   Tm mutant strains, we show that the presence of temperate phages and their lysis genes is necessary and sufficient for release of active ColIb into the culture supernatant. Furthermore, phage‐mediated lysis significantly enhanced S .   Tm fitness in competition against a ColIb ‐susceptible competitor. Finally, transduction with the lambdoid phage 933W rescued the defect of E . coli strain MG1655 with respect to ColIb release. In conclusion, ColIb is released from bacteria in the course of phage lysis. Our data reveal a new mechanism for colicin release and point out a novel function of temperate phages in enhancing colicin‐dependent bacterial fitness.
ISSN:1462-2912
1462-2920
DOI:10.1111/1462-2920.13077