Early detection of bean infection by Pseudomonas syringae in asymptomatic leaf areas using chlorophyll fluorescence imaging

Chlorophyll fluorescence imaging has been used to analyse the response elicited in Phaseolus vulgaris after inoculation with Pseudomonas syringae pv. phaseolicola 1448A (compatible interaction) and P. syringae pv. tomato DC3000 (incompatible interaction). With the aim of modulating timing of symptom development, different cell densities were used to inoculate bean plants and the population dynamics of both bacterial strains was followed within the leaf tissue. Fluorescence quenching analysis was carried out and images of the different chlorophyll fluorescence parameters were obtained for infected as well as control plants at different timepoints post-infection. Among the different parameters analysed, we observed that non-photochemical quenching maximised the differences between the compatible and the incompatible interaction before the appearance of visual symptom. A decrease in non-photochemical quenching, evident in both infiltrated and non-infiltrated leaf areas, was observed in P. syringae pv. phaseolicola-infected plants as compared with corresponding values from controls and P. syringae pv. tomato-infected plants. No photoinhibitory damage was detected, as the maximum photosystem II quantum yield remained stable during the infection period analysed.

[1]  Ryan A. Rapp,et al.  A pseudomonas syringae pv. tomato DC3000 Hrp (Type III secretion) deletion mutant expressing the Hrp system of bean pathogen P. syringae pv. syringae 61 retains normal host specificity for tomato. , 2003, Molecular plant-microbe interactions : MPMI.

[2]  O. Björkman,et al.  Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origins , 1987, Planta.

[3]  V. Repka Chlorophyll-Deficient Mutant in Oak (Quercus petraea L.) Displays an Accelerated Hypersensitive-Like Cell Death and an Enhanced Resistance to Powdery Mildew Disease , 2002, Photosynthetica.

[4]  S. S. Hirano,et al.  Bacteria in the Leaf Ecosystem with Emphasis onPseudomonas syringae—a Pathogen, Ice Nucleus, and Epiphyte , 2000, Microbiology and Molecular Biology Reviews.

[5]  Ladislav Nedbal,et al.  Visualization of dynamics of plant-pathogen interaction by novel combination of chlorophyll fluorescence imaging and statistical analysis: differential effects of virulent and avirulent strains of P. syringae and of oxylipins on A. thaliana. , 2007, Journal of experimental botany.

[6]  M. Vandeven,et al.  Imaging viral infection: studies on Nicotiana benthamiana plants infected with the pepper mild mottle tobamovirus , 2007, Photosynthesis Research.

[7]  Sharon A. Robinson,et al.  Concepts of plant biotic stress. Some insights into the stress physiology of virus‐infected plants, from the perspective of photosynthesis , 1997 .

[8]  H. Aronsson,et al.  POR - import and membrane association of a key element in chloroplast development. , 2003, Physiologia plantarum.

[9]  BJ Staskawicz,et al.  Molecular genetics of plant disease resistance , 1995, Science.

[10]  D. Cuppels Generation and Characterization of Tn5 Insertion Mutations in Pseudomonas syringae pv. tomato , 1986, Applied and environmental microbiology.

[11]  M. Barón,et al.  Changes in photosynthetic metabolism induced by tobamovirus infection in Nicotiana benthamiana studied in vivo by thermoluminescence. , 2007, The New phytologist.

[12]  Mihai Aldea,et al.  Expression profiling soybean response to Pseudomonas syringae reveals new defense-related genes and rapid HR-specific downregulation of photosynthesis. , 2005, Molecular plant-microbe interactions : MPMI.

[13]  T. Roitsch,et al.  Complex regulation of gene expression, photosynthesis and sugar levels by pathogen infection in tomato , 2004 .

[14]  M. Barón,et al.  Proteomic analysis of the oxygen‐evolving complex of photosystem II under biotec stress: Studies on Nicotiana benthamiana infected with tobamoviruses , 2004, Proteomics.

[15]  Hur-Song Chang,et al.  Quantitative Nature of Arabidopsis Responses during Compatible and Incompatible Interactions with the Bacterial Pathogen Pseudomonas syringae Online version contains Web-only data. Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.007591. , 2003, The Plant Cell Online.

[16]  S. Rolfe,et al.  Infection of Arabidopsis thaliana leaves with Albugo candida (white blister rust) causes a reprogramming of host metabolism. , 2000, Molecular plant pathology.

[17]  M. Barón,et al.  Inhibition of photosynthesis by viral infection : Effect on PSII structure and function , 2000 .

[18]  C. R. Ireland,et al.  The relationship between carbon dioxide fixation and chlorophyll a fluorescence during induction of photosynthesis in maize leaves at different temperatures and carbon dioxide concentrations , 1984, Planta.

[19]  K. Matous,et al.  Case study of combinatorial imaging: What protocol and what chlorophyll fluorescence image to use when visualizing infection of Arabidopsis thaliana by Pseudomonas syringae? , 2007, Photosynthesis Research.

[20]  P. Mullineaux,et al.  Light perception in plant disease defence signalling. , 2003, Current opinion in plant biology.

[21]  Murray Grant,et al.  Type III effectors orchestrate a complex interplay between transcriptional networks to modify basal defence responses during pathogenesis and resistance. , 2006, The Plant journal : for cell and molecular biology.

[22]  D. Van Der Straeten,et al.  Robotized thermal and chlorophyll fluorescence imaging of pepper mild mottle virus infection in Nicotiana benthamiana. , 2006, Plant & cell physiology.

[23]  J. R. Wood,et al.  Avirulence genes from Pseudomonas syringae pathovars phaseolicola and pisi confer specificity towards both host and non-host species☆ , 1992 .

[24]  T. Roitsch,et al.  Infection with virulent and avirulent P. syringae strains differentially affects photosynthesis and sink metabolism in Arabidopsis leaves , 2006, Planta.

[25]  S. Rolfe,et al.  Photosynthesis in localised regions of oat leaves infected with crown rust (Puccinia coronata): quantitative imaging of chlorophyll fluorescence , 1996, Planta.

[26]  L. Šindelář,et al.  Photosynthesis in leaves of Nicotiana tabacum L. infected with tobacco mosaic virus , 2005, Photosynthetica.

[27]  A. Bent,et al.  Identification of Pseudomonas syringae pathogens of Arabidopsis and a bacterial locus determining avirulence on both Arabidopsis and soybean. , 1991, The Plant cell.

[28]  L. Nedbal,et al.  Plant response to destruxins visualized by imaging of chlorophyll fluorescence , 2003 .

[29]  Alexandra M. E. Jones,et al.  Modifications to the Arabidopsis Defense Proteome Occur Prior to Significant Transcriptional Change in Response to Inoculation with Pseudomonas syringae1[W][OA] , 2006, Plant Physiology.

[30]  B. Genty,et al.  Inhibition of photosynthesis by Colletotrichum lindemuthianum in bean leaves determined by chlorophyll fluorescence imaging , 2001 .

[31]  C. Osmond,et al.  Infection with Phloem Limited Abutilon Mosaic Virus Causes Localized Carbohydrate Accumulation in Leaves of Abutilon striatum: Relationships to Symptom Development and Effects on Chlorophyll Fluorescence Quenching During Photosynthetic Induction , 2000 .

[32]  Jonathan D. G. Jones,et al.  The plant immune system , 2006, Nature.

[33]  Ladislav Nedbal,et al.  Kinetic imaging of chlorophyll fluorescence using modulated light , 2004, Photosynthesis Research.