Denayer Sarah, Matthijs Sandra, Cornelis Pierre
Laboratory of Microbial Interactions, Department of Molecular and Cellular Interactions, VIB, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium.
J Bacteriol. 2007 Nov;189(21):7663-8. doi: 10.1128/JB.00992-07. Epub 2007 Aug 24.
Soluble (S-type) pyocins are Pseudomonas aeruginosa bacteriocins that kill nonimmune P. aeruginosa strains via a specific receptor. The genes coding for pyocin Sa (consisting of a killing protein and an immunity protein) were cloned and expressed in Escherichia coli. Sequence analysis revealed that Sa is identical to pyocin S2. Seventy-nine strains of P. aeruginosa were tested for their sensitivity to pyocins S1, S2, and S3, and their ferripyoverdine receptors were typed by multiplex PCR. No strain was found to be sensitive to both S2 and S3, suggesting that the receptors for these two pyocins cannot coexist in one strain. As expected, all S3-sensitive strains had the type II ferripyoverdine receptor fpvA gene, confirming our previous reports. S1 killed strains irrespective of the type of ferripyoverdine receptor they produced. All S2-sensitive strains had the type I fpvA gene, and the inactivation of type I fpvA in an S2-sensitive strain conferred resistance to the S2 pyocin. Accordingly, complementation with type I fpvA in trans restored sensitivity to S2. Some S2-resistant type I fpvA-positive strains were detected, the majority (all but five) of which had the S1-S2 immunity gene. Comparison of type I fpvA sequences from immunity gene-negative S2-sensitive and S2-resistant strains revealed only a valine-to-isoleucine substitution at position 46 of type I FpvA. However, both type I fpvA genes conferred the capacity for type I pyoverdine utilization and sensitivity to S2. When these two type I fpvA genes were introduced into strain 7NSK2 carrying mutations in type II fpvA (encoding the type II pyoverdine receptor) and fpvB (encoding the alternative type I receptor), growth in the presence of type I pyoverdine was observed and the strain became sensitive to S2. We also found that type I pyoverdine could signal type II pyoverdine production via the type I FpvA receptor in 7NSK2.
可溶性(S型)绿脓菌素是铜绿假单胞菌的细菌素,可通过特定受体杀死非免疫性铜绿假单胞菌菌株。编码绿脓菌素Sa(由杀伤蛋白和免疫蛋白组成)的基因被克隆并在大肠杆菌中表达。序列分析表明,Sa与绿脓菌素S2相同。对79株铜绿假单胞菌进行了对绿脓菌素S1、S2和S3的敏感性测试,并通过多重PCR对其铁载体绿脓菌素受体进行分型。未发现有菌株对S2和S3均敏感,这表明这两种绿脓菌素的受体不能在同一菌株中共存。正如预期的那样,所有对S3敏感的菌株都具有II型铁载体绿脓菌素受体fpvA基因,证实了我们之前的报道。S1可杀死菌株,无论它们产生何种类型的铁载体绿脓菌素受体。所有对S2敏感的菌株都具有I型fpvA基因,并且在对S2敏感的菌株中I型fpvA的失活赋予了对S2绿脓菌素的抗性。因此,通过反式互补I型fpvA可恢复对S2的敏感性。检测到一些对S2耐药的I型fpvA阳性菌株,其中大多数(除5株外)具有S1-S2免疫基因。对来自免疫基因阴性的S2敏感和S2耐药菌株的I型fpvA序列进行比较,发现在I型FpvA的第46位仅存在缬氨酸到异亮氨酸的取代。然而,这两个I型fpvA基因都赋予了利用I型绿脓菌素的能力和对S2的敏感性。当将这两个I型fpvA基因导入在II型fpvA(编码II型绿脓菌素受体)和fpvB(编码替代I型受体)中携带突变的7NSK2菌株时,观察到在I型绿脓菌素存在下的生长,并且该菌株对S2变得敏感。我们还发现,I型绿脓菌素可通过7NSK2中的I型FpvA受体向II型绿脓菌素的产生发出信号。