Ruparčič Matija, Dolinar Marko
Department of Chemistry and Biochemistry, Faculty of Chemistry and Chemical Technology, University of Ljubljana, Večna pot 113, 1000 Ljubljana, Slovenia.
Toxins (Basel). 2025 Jul 22;17(8):360. doi: 10.3390/toxins17080360.
Type I toxin-antitoxin (TA) systems consist of a protein toxin that exerts a cytostatic or cytotoxic effect and an antisense RNA antitoxin that prevents translation of the toxin. Although well studied, type I TA systems have so far only been discovered in bacteria from the phyla Proteobacteria, Firmicutes, and Tenericutes. We hypothesized that type I systems could also be present in Cyanobacteria. Through bioinformatic analysis of the PCC 7806SL genome, we discovered ten putative type I TA loci and characterized six of them experimentally. Two of the six putative type I toxins, BH695_0320 and MsoT1 (BH695_4017), were observed to negatively affect cell growth, with MsoT1 exerting a phenotype similar to SrnB, a known type I toxin. We focused on the MsoT1/MsoA1 TA system and confirmed the expression of MsoT1 and MsoA1 in our assay. Additionally, we found that MsoA1 delays the toxic effects of MsoT1, indicating its role as a cognate antitoxin of MsoT1. Our results suggest that MsoT1/MsoA1 represents a novel candidate type I TA system, the first to be discovered in the Cyanobacteria phylum.
I型毒素-抗毒素(TA)系统由一种发挥细胞生长抑制或细胞毒性作用的蛋白质毒素和一种阻止毒素翻译的反义RNA抗毒素组成。尽管I型TA系统已得到充分研究,但迄今为止仅在变形菌门、厚壁菌门和柔膜菌门的细菌中发现。我们推测I型系统也可能存在于蓝细菌中。通过对PCC 7806SL基因组的生物信息学分析,我们发现了10个假定的I型TA位点,并对其中6个进行了实验表征。观察到6个假定的I型毒素中的两个,即BH695_0320和MsoT1(BH695_4017)对细胞生长有负面影响,其中MsoT1表现出与已知I型毒素SrnB相似的表型。我们聚焦于MsoT1/MsoA1 TA系统,并在我们的实验中证实了MsoT1和MsoA1的表达。此外,我们发现MsoA1可延迟MsoT1的毒性作用,表明其作为MsoT1同源抗毒素的作用。我们的结果表明,MsoT1/MsoA1代表一种新型的I型TA系统候选物,是在蓝细菌门中首次发现的。