Gunasekera T S, Sundin G W
Center for Microbial Ecology and Department of Plant Pathology, Michigan State University, East Lansing, MI 48824, USA.
J Appl Microbiol. 2006 May;100(5):1073-83. doi: 10.1111/j.1365-2672.2006.02841.x.
To assess the role of DNA repair and photoreactivation in the solar radiation survival of the plant pathogen and leaf surface epiphyte Pseudomonas syringae pv. syringae (Pss).
Mutants of Pss B728a, with insertional mutations within the nucleotide excision repair gene uvrA, photolyase gene phr, or uvrA phr double mutants, were constructed to examine the importance of individual repair mechanisms in solar UV radiation (UVR) survival. The survival of either the uvrA mutant or the phr mutant was reduced by approx. 10(2)-fold following exposure to a dose of 4.5 kJ m(-2) solar UVB (290-320 nm wavelengths) while the uvrA phr double mutant was reduced >10(6)-fold by the same dose. We constructed a transcriptional fusion between the Pss recA promoter and gfp to examine the induction of the SOS response in wild-type and mutant strains. Initiation of the recA mediated SOS response was more rapid and peaked at higher levels in mutant strains suggesting both increased DNA damage in mutant strains and also that photoreactivation and nucleotide excision repair remove DNA damage as it is incurred which is reflected in a delay of recA expression. Visualization of expression of B728a cells containing the recA::gfp reporter on UVB-irradiated bean leaves highlighted the movement of cells to intercellular spaces over time and that SOS induction was detectable when leaves were irradiated 48 h following leaf inoculation.
This study indicated that solar UVB is detrimental to Pss B728a, DNA repair mechanisms play an important role in strain survival and expression of the SOS regulon on leaf surfaces contributes to survival of UVR-exposed cells during plant colonization.
This work links previous laboratory-based UVR analyses with solar UVB dose-response analyses and highlights the role of photoreactivation in delaying induction of the SOS response following solar irradiation. Knowledge of population dynamics following direct solar irradiation will enhance our understanding of the biology of Pss in the phyllosphere.
评估DNA修复和光复活作用在植物病原体及叶表面附生菌丁香假单胞菌丁香致病变种(Pss)的太阳辐射存活中的作用。
构建了Pss B728a的突变体,其核苷酸切除修复基因uvrA、光解酶基因phr内存在插入突变,或为uvrA phr双突变体,以研究个体修复机制在太阳紫外线辐射(UVR)存活中的重要性。uvrA突变体或phr突变体在暴露于4.5 kJ m(-2)的太阳UVB(波长290 - 320 nm)剂量后,存活率降低约10(2)倍,而uvrA phr双突变体在相同剂量下存活率降低>10(6)倍。我们构建了Pss recA启动子与gfp之间的转录融合体,以检测野生型和突变株中SOS应答的诱导情况。recA介导的SOS应答在突变株中启动更快且峰值更高,这表明突变株中DNA损伤增加,同时光复活和核苷酸切除修复在DNA损伤发生时就将其去除,这反映在recA表达的延迟上。对含recA::gfp报告基因的B728a细胞在UVB照射的菜豆叶片上的表达进行可视化分析,突出了细胞随时间向细胞间隙移动的情况,并且在叶片接种48 h后照射叶片时可检测到SOS诱导。
本研究表明太阳UVB对Pss B728a有害,DNA修复机制在菌株存活中起重要作用,叶表面SOS调节子的表达有助于植物定殖过程中暴露于UVR的细胞存活。
这项工作将先前基于实验室的UVR分析与太阳UVB剂量反应分析联系起来,突出了光复活在延迟太阳照射后SOS应答诱导中的作用。对直接太阳照射后种群动态的了解将增强我们对叶际中Pss生物学的理解。