A regulatory role for Staphylococcus aureus toxin–antitoxin system PemIKSa

被引:0
作者
Michal Bukowski
Robert Lyzen
Weronika M. Helbin
Emilia Bonar
Agnieszka Szalewska-Palasz
Grzegorz Wegrzyn
Grzegorz Dubin
Adam Dubin
Benedykt Wladyka
机构
[1] Faculty of Biochemistry,Department of Analytical Biochemistry
[2] Biophysics and Biotechnology,Department of Molecular Biology
[3] Jagiellonian University,Department of Microbiology
[4] Gronostajowa 7,undefined
[5] 30-387 Krakow,undefined
[6] Poland,undefined
[7] University of Gdansk,undefined
[8] Wita Stwosza 59,undefined
[9] 80-308 Gdansk,undefined
[10] Poland,undefined
[11] Faculty of Biochemistry,undefined
[12] Biophysics and Biotechnology,undefined
[13] Jagiellonian University,undefined
[14] Gronostajowa 7,undefined
[15] 30-387 Krakow,undefined
[16] Poland,undefined
[17] Malopolska Centre of Biotechnology,undefined
[18] Gronostajowa 7,undefined
[19] 30-387 Krakow,undefined
[20] Poland,undefined
来源
Nature Communications | / 4卷
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摘要
Toxin–antitoxin systems were shown to be involved in plasmid maintenance when they were initially discovered, but other roles have been demonstrated since. Here we identify and characterize a novel toxin–antitoxin system (pemIKSa) located on Staphylococcus aureus plasmid pCH91. The toxin (PemKSa) is a sequence-specific endoribonuclease recognizing the tetrad sequence U↓AUU, and the antitoxin (PemISa) inhibits toxin activity by physical interaction. Although the toxin–antitoxin system is responsible for stable plasmid maintenance our data suggest the participation of pemIKSa in global regulation of staphylococcal virulence by alteration of the translation of large pools of genes. We propose a common mechanism of reversible activation of toxin–antitoxin systems based on antitoxin transcript resistance to toxin cleavage. Elucidation of this mechanism is particularly interesting because reversible activation is a prerequisite for the proposed general regulatory role of toxin–antitoxin systems.
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