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首页> 外文期刊>Applied and Environmental Microbiology >Spontaneous Gac Mutants of Pseudomonas Biological Control Strains: Cheaters or Mutualists?
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Spontaneous Gac Mutants of Pseudomonas Biological Control Strains: Cheaters or Mutualists?

机译:假单胞菌生物控制菌株的自发Gac突变体:骗子还是互惠生?

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Bacteria rely on a range of extracellular metabolites to suppress competitors, gain access to resources, and exploit plant or animal hosts. The GacS/GacA two-component regulatory system positively controls the expression of many of these beneficial external products in pseudomonad bacteria. Natural populations often contain variants with defective Gac systems that do not produce most external products. These mutants benefit from a decreased metabolic load but do not appear to displace the wild type in nature. How could natural selection maintain the wild type in the presence of a mutant with enhanced growth? One hypothesis is that Gac mutants are “cheaters” that do not contribute to the public good, favored within groups but selected against between groups, as groups containing more mutants lose access to ecologically important external products. An alternative hypothesis is that Gac mutants have a mutualistic interaction with the wild type, so that each variant benefits by the presence of the other. In the biocontrol bacterium Pseudomonas chlororaphis strain 30-84, Gac mutants do not produce phenazines, which suppress competitor growth and are critical for biofilm formation. Here, we test the predictions of these alternative hypotheses by quantifying interactions between the wild type and the phenazine- and biofilm-deficient Gac mutant within growing biofilms. We find evidence that the wild type and Gac mutants interact mutualistically in the biofilm context, whereas a phenazine-defective structural mutant does not. Our results suggest that the persistence of alternative Gac phenotypes may be due to the stabilizing role of local mutualistic interactions.
机译:细菌依靠多种细胞外代谢物来抑制竞争者,获得资源并利用动植物宿主。 GacS / GacA两组分调节系统可有效控制假单胞菌中许多有益外部产物的表达。自然种群通常包含具有缺陷Gac系统的变种,这些变种不能产生大多数外部产品。这些突变体受益于降低的代谢负荷,但似乎并未取代自然界中的野生型。在存在生长增强的突变体的情况下,自然选择如何保持野生型?一种假设是,Gac突变体是“骗子”,对公众利益无济于事,在群体内部受到青睐,但在群体之间进行选择,因为包含更多突变体的群体无法获得具有生态重要性的外部产品。另一种假设是,Gac突变体与野生型具有相互的相互作用,因此每个变体均会因另一个变体而受益。在生物控制细菌绿假单胞菌菌株30-84中,Gac突变体不产生吩嗪,吩嗪抑制竞争者的生长并且对生物膜的形成至关重要。在这里,我们通过量化野生型与生长中生物膜内吩嗪和生物膜缺陷型Gac突变体之间的相互作用来测试这些替代假设的预测。我们发现证据表明,野生型和Gac突变体在生物膜环境中相互相互作用,而吩嗪缺陷型结构突变体则没有。我们的研究结果表明,替代性Gac表型的持久性可能是由于本地互惠互动的稳定作用。

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