利用流式细胞术,通过荧光报告基因组合对生防假单胞菌在谷物上的根定植和抗真菌基因表达进行同时监测。
Combination of fluorescent reporters for simultaneous monitoring of root colonization and antifungal gene expression by a biocontrol pseudomonad on cereals with flow cytometry.
机构信息
Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland.
出版信息
Mol Plant Microbe Interact. 2010 Jul;23(7):949-61. doi: 10.1094/MPMI-23-7-0949.
Some root-associated pseudomonads sustain plant growth by suppressing root diseases caused by pathogenic fungi. We investigated to which extent select cereal cultivars influence expression of relevant biocontrol traits (i.e., root colonization efficacy and antifungal activity) in Pseudomonas fluorescens CHA0. In this representative plant-beneficial bacterium, the antifungal metabolites 2,4-diacetylphloroglucinol (DAPG), pyrrolnitrin (PRN), pyoluteorin (PLT), and hydrogen cyanide (HCN) are required for biocontrol. To monitor host plant effects on the expression of biosynthetic genes for these compounds on roots, we developed fluorescent dual-color reporters suited for flow cytometric analysis using fluorescence-activated cell sorting (FACS). In the dual-label strains, the constitutively expressed red fluorescent protein mCherry served as a cell tag and marker for root colonization, whereas reporter fusions based on the green fluorescent protein allowed simultaneous recording of antifungal gene expression within the same cell. FACS analysis revealed that expression of DAPG and PRN biosynthetic genes was promoted in a cereal rhizosphere, whereas expression of PLT and HCN biosynthetic genes was markedly less sustained. When analyzing the response of the bacterial reporters on roots of a selection of wheat, spelt, and triticale cultivars, we were able to detect subtle species- and cultivar-dependent differences in colonization and DAPG and HCN gene expression levels. The expression of these biocontrol traits was particularly favored on roots of one spelt cultivar, suggesting that a careful choice of pseudomonad-cereal combinations might be beneficial to biocontrol. Our approach may be useful for selective single-cell level analysis of plant effects in other bacteria-root interactions.
一些与根共生的假单胞菌通过抑制由致病真菌引起的根病来维持植物生长。我们研究了特定的谷类品种在多大程度上影响荧光假单胞菌 CHA0 中相关生物防治特性(即根定殖效力和抗真菌活性)的表达。在这种代表性的植物有益细菌中,抗真菌代谢物 2,4-二乙酰基邻苯二酚(DAPG)、吡咯并菌素(PRN)、吡咯并[1,2-α]嘧啶(PLT)和氰化氢(HCN)是生物防治所必需的。为了监测宿主植物对这些化合物生物合成基因在根上表达的影响,我们开发了荧光双标记报告基因,适合使用荧光激活细胞分选(FACS)进行流式细胞术分析。在双标记菌株中,组成型表达的红色荧光蛋白 mCherry 作为细胞标记和根定殖的标记,而基于绿色荧光蛋白的报告基因融合允许在同一细胞内同时记录抗真菌基因的表达。FACS 分析表明,DAPG 和 PRN 生物合成基因的表达在谷类根际中得到促进,而 PLT 和 HCN 生物合成基因的表达则明显减少。当分析细菌报告基因在一系列小麦、斯佩尔特小麦和黑小麦品种根系上的反应时,我们能够检测到定殖和 DAPG 和 HCN 基因表达水平上微妙的种间和品种间差异。这些生物防治特性的表达在一种斯佩尔特小麦品种的根上特别受到青睐,这表明谨慎选择假单胞菌-谷类组合可能有益于生物防治。我们的方法可用于在其他细菌-根相互作用中进行选择性的单细胞水平分析植物的影响。