Laboratoire de Microbiologie Signaux et Micro-Environnement, Université de Rouen, Evreux, France.
BMC Microbiol. 2012 Sep 29;12:223. doi: 10.1186/1471-2180-12-223.
Pseudomonas fluorescens biovar I MFN1032 is a clinical isolate able to grow at 37°C. This strain displays secretion-mediated hemolytic activity involving phospholipase C and cyclolipopeptides, and a cell-associated hemolytic activity distinct from the secreted hemolytic activity. Cell-associated hemolysis is independent of biosurfactant production and remains in a gacA mutant. Disruption of the hrpU-like operon (the basal part of type III secretion system from rhizospheric strains) suppresses this activity. We hypothesized that this phenotype could reflect evolution of an ancestral mechanism involved in the survival of this species in its natural niche. In this study, we evaluated the hrpU-like operon's contribution to other virulence mechanisms using a panel of Pseudomonas strains from various sources.
We found that MFN1032 inhibited the growth of the amoebae Dictyostelium discoideum and that this inhibition involved the hrpU-like operon and was absent in a gacA mutant. MFN1032 was capable of causing macrophage lysis, if the hrpU-like operon was intact, and this cytotoxicity remained in a gacA mutant. Cell-associated hemolytic activity and macrophage necrosis were found in other P. fluorescens clinical isolates, but not in biocontrol P. fluorescens strains harbouring hrpU-like operon. The growth of Dictyostelium discoideum was inhibited to a different extent by P. fluorescens strains without correlation between this inhibition and hrpU-like operon sequences.
In P. fluorescens MFN1032, the basal part of type III secretion system plays a role in D. discoideum growth inhibition and macrophage necrosis. The inhibition of D. discoideum growth is dependent on the GacS/GacA system, while cell-associated hemolytic activity and macrophage lysis are not. Virulence against eukaryotic cells based on the hrpU-like operon may be more than just a stochastic evolution of a conserved system dedicated to survival in competition with natural predators such as amoebae. It may also mean that there are some important modifications of other type III secretion system components, which remain unknown. Cell-associated hemolysis might be a good indicator of the virulence of Pseudomonas fluorescens strain.
荧光假单胞菌生物变种 I MFN1032 是一种能够在 37°C 下生长的临床分离株。该菌株表现出涉及磷脂酶 C 和环脂肽的分泌介导的溶血活性,以及与分泌的溶血活性不同的细胞相关的溶血活性。细胞相关的溶血活性与生物表面活性剂的产生无关,并存在于 gacA 突变体中。hrpU 样操纵子(根际菌株 III 型分泌系统的基本部分)的破坏抑制了这种活性。我们假设这种表型可能反映了该物种在其自然栖息地中生存的祖先机制的进化。在这项研究中,我们使用来自各种来源的一系列假单胞菌菌株评估了 hrpU 样操纵子对其他毒力机制的贡献。
我们发现 MFN1032 抑制变形虫 Dictyostelium discoideum 的生长,这种抑制涉及 hrpU 样操纵子,并且在 gacA 突变体中不存在。如果 hrpU 样操纵子完整,MFN1032 能够导致巨噬细胞裂解,并且这种细胞毒性在 gacA 突变体中仍然存在。在其他荧光假单胞菌临床分离株中发现了细胞相关的溶血活性和巨噬细胞坏死,但在携带 hrpU 样操纵子的生物防治荧光假单胞菌菌株中则没有。变形虫生长受到荧光假单胞菌菌株的不同程度抑制,但这种抑制与 hrpU 样操纵子序列之间没有相关性。
在荧光假单胞菌 MFN1032 中,III 型分泌系统的基本部分在 D. discoideum 的生长抑制和巨噬细胞坏死中起作用。D. discoideum 的生长抑制依赖于 GacS/GacA 系统,而细胞相关的溶血活性和巨噬细胞裂解则不依赖于该系统。基于 hrpU 样操纵子的对真核细胞的毒力可能不仅仅是一种针对与变形虫等自然捕食者竞争中生存的保守系统的随机进化。这也可能意味着其他 III 型分泌系统组件发生了一些重要的修改,这些修改仍然未知。细胞相关的溶血活性可能是荧光假单胞菌菌株毒力的一个很好的指标。