Peng Yu-Chih, Lu ChienYi, Li Guoqing, Eichenbaum Zehava, Lu Chung-Dar
Department of Biology, Georgia State University, Atlanta, GA, 30303, USA.
Department of Biomedical and Nutritional Sciences, UMass Lowell, Lowell, MA, 01854, USA.
Mol Microbiol. 2017 Jun;104(6):1037-1051. doi: 10.1111/mmi.13678. Epub 2017 Apr 12.
Growth of Pseudomonas aeruginosa on spermine requires a functional γ-glutamylpolyamine synthetase PauA2. Not only subjected to growth inhibition by spermine, the pauA2 mutant became more sensitive to β-lactam antibiotics in human serum. To explore PauA2 as a potential target of drug development, suppressors of the pauA2 mutant, which alleviated toxicity, were isolated from selection plates containing spermine. These suppressors share common phenotypic changes including delayed growth rate, retarded swarming motility, and pyocyanin overproduction. Genome resequencing of a representative suppressor revealed a unique C T mutation at the phoU gene that results in Ser Leu substitution and a constitutive expression of the Pho regulon. Identical phenotypes were also observed in a ΔpauA2ΔphoU double knockout mutant and complemented by the wild-type phoU gene. Accumulation of polyphosphate granules and spermine resistance in the suppressor were reversed concomitantly when expressing exopolyphosphatase PPX from a recombinant plasmid, or by the introduction of deletion alleles in pstS pstC for phosphate uptake, phoB for Pho regulation, and ppk for polyphosphate synthesis. In conclusion, this study identifies polyphosphate accumulation due to an activated Pho regulon and phosphate uptake by the phoU mutation as a potential protection mechanism against spermine toxicity.
铜绿假单胞菌在精胺上的生长需要功能性的γ-谷氨酰多胺合成酶PauA2。不仅受到精胺的生长抑制,pauA2突变体在人血清中对β-内酰胺类抗生素变得更加敏感。为了探索PauA2作为药物开发的潜在靶点,从含有精胺的选择平板中分离出减轻毒性的pauA2突变体的抑制子。这些抑制子具有共同的表型变化,包括生长速率延迟、群体运动迟缓以及绿脓菌素过量产生。对一个代表性抑制子的基因组重测序揭示了phoU基因处一个独特的C→T突变,该突变导致丝氨酸→亮氨酸替代以及Pho调节子的组成型表达。在ΔpauA2ΔphoU双敲除突变体中也观察到相同的表型,并且由野生型phoU基因互补。当从重组质粒表达胞外多磷酸酶PPX,或者通过在pstS、pstC(用于磷酸盐摄取)、phoB(用于Pho调节)和ppk(用于多磷酸盐合成)中引入缺失等位基因时,抑制子中多磷酸盐颗粒的积累和对精胺的抗性会同时逆转。总之,本研究确定由于Pho调节子激活导致的多磷酸盐积累以及phoU突变引起的磷酸盐摄取是对抗精胺毒性的一种潜在保护机制。