Non-Invasive, Bioluminescence-Based Visualisation and Quantification of Bacterial Infections in Arabidopsis Over Time

被引:1
作者
Taks, Nanne W. [1 ]
Batstra, Mathijs D. [2 ]
Kortekaas, Ronald F. [2 ]
Stevens, Floris D. [1 ]
Pfeilmeier, Sebastian [1 ]
van den Burg, Harrold A. [1 ,3 ]
机构
[1] Univ Amsterdam, Fac Sci, Swammerdam Inst Life Sci, Mol Plant Pathol, Amsterdam, Netherlands
[2] Univ Amsterdam, Fac Sci, Technol Ctr FNWI, Amsterdam, Netherlands
[3] Rijk Zwaan Zaadteelt Zaadhandel BV, Burgemeester Crezeelaan 40, De Lier, Netherlands
关键词
<fixed-case>Arabidopsis thaliana</fixed-case>; automated image analysis; bioluminescence; non-invasive phenotyping; phytopathogenic bacteria; plant resistance; <fixed-case>Xanthomonas campestris</fixed-case>; CAMPESTRIS PV. CAMPESTRIS; PSEUDOMONAS-SYRINGAE; PHOTORHABDUS-LUMINESCENS; GENES; EFFECTOR; IMMUNITY; CHROMOSOMES; HYDATHODES; RESISTANCE; INSERTION;
D O I
10.1111/mpp.70055
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Plant-pathogenic bacteria colonise their hosts using various strategies, exploiting both natural openings and wounds in leaves and roots. The vascular pathogen Xanthomonas campestris pv. campestris (Xcc) enters its host through hydathodes, organs at the leaf margin involved in guttation. Subsequently, Xcc breaches the hydathode-xylem barrier and progresses into the xylem vessels causing systemic disease. To elucidate the mechanisms that underpin the different stages of an Xcc infection, a need exists to image bacterial progression in planta in a non-invasive manner. Here, we describe a phenotyping setup and Python image analysis pipeline for capturing 16 independent Xcc infections in Arabidopsis thaliana plants in parallel over time. The setup combines an RGB camera for imaging disease symptoms and an ultrasensitive CCD camera for monitoring bacterial progression inside leaves using bioluminescence. The method reliably quantified bacterial growth in planta for two bacterial species, that is, vascular Xcc and the mesophyll pathogen Pseudomonas syringae pv. tomato (Pst). The camera resolution allowed Xcc imaging already in the hydathodes, yielding reproducible data for the first stages prior to the systemic infection. Data obtained through the image analysis pipeline was robust and validated findings from other bioluminescence imaging methods, while requiring fewer samples. Moreover, bioluminescence was reliably detected within 5 min, offering a significant time advantage over our previously reported method with light-sensitive films. Thus, this method is suitable to quantify the resistance level of a large number of Arabidopsis thaliana accessions and mutant lines to different bacterial strains in a non-invasive manner for phenotypic screenings.
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页数:11
相关论文
共 43 条
[1]   AN IMPROVED TN7-BASED SYSTEM FOR THE SINGLE-COPY INSERTION OF CLONED GENES INTO CHROMOSOMES OF GRAM-NEGATIVE BACTERIA [J].
BAO, Y ;
LIES, DP ;
FU, H ;
ROBERTS, GP .
GENE, 1991, 109 (01) :167-168
[2]  
Bradski G. A., 2000, OpenCV. Dr Dobbs J. Softw. Tools, P3
[3]   Immunity at Cauliflower Hydathodes Controls Systemic Infection by Xanthomonas campestris pv campestris [J].
Cerutti, Aude ;
Jauneau, Alain ;
Auriac, Marie-Christine ;
Lauber, Emmanuelle ;
Martinez, Yves ;
Chiarenza, Serge ;
Leonhardt, Nathalie ;
Berthome, Richard ;
Noel, Laurent D. .
PLANT PHYSIOLOGY, 2017, 174 (02) :700-716
[4]   A 10-min method for preparation of highly electrocompetent Pseudomonas aeruginosa cells:: Application for DNA fragment transfer between chromosomes and plasmid transformation [J].
Choi, KH ;
Kumar, A ;
Schweizer, HP .
JOURNAL OF MICROBIOLOGICAL METHODS, 2006, 64 (03) :391-397
[5]   Mini-Tn7 insertion in bacteria with single attTn7 sites:: example Pseudomonas aeruginosa [J].
Choi, Kyoung-Hee ;
Schweizer, Herbert P. .
NATURE PROTOCOLS, 2006, 1 (01) :153-161
[6]   Quantitative Resistance: More Than Just Perception of a Pathogen [J].
Corwin, Jason A. ;
Kliebenstein, Daniel J. .
PLANT CELL, 2017, 29 (04) :655-665
[7]   Cladosporium fulvum Effectors: Weapons in the Arms Race with Tomato [J].
de Wit, Pierre J. G. M. .
ANNUAL REVIEW OF PHYTOPATHOLOGY, VOL 54, 2016, 54 :1-23
[8]   Structure-function analysis of the Fusarium oxysporum Avr2 effector allows uncoupling of its immune-suppressing activity from recognition [J].
Di, Xiaotang ;
Cao, Lingxue ;
Hughes, Richard K. ;
Tintor, Nico ;
Banfield, Mark J. ;
Takken, Frank L. W. .
NEW PHYTOLOGIST, 2017, 216 (03) :897-914
[9]   Multiple Candidate Effectors from the Oomycete Pathogen Hyaloperonospora arabidopsidis Suppress Host Plant Immunity [J].
Fabro, Georgina ;
Steinbrenner, Jens ;
Coates, Mary ;
Ishaque, Naveed ;
Baxter, Laura ;
Studholme, David J. ;
Koerner, Evelyn ;
Allen, Rebecca L. ;
Piquerez, Sophie J. M. ;
Rougon-Cardoso, Alejandra ;
Greenshields, David ;
Lei, Rita ;
Badel, Jorge L. ;
Caillaud, Marie-Cecile ;
Sohn, Kee-Hoon ;
Van den Ackerveken, Guido ;
Parker, Jane E. ;
Beynon, Jim ;
Jones, Jonathan D. G. .
PLOS PATHOGENS, 2011, 7 (11)
[10]   High-throughput quantitative luminescence assay of the growth in planta of Pseudomonas syringae chromosomally tagged with Photorhabdus luminescens luxCDABE [J].
Fan, Jun ;
Crooks, Casey ;
Lamb, Chris .
PLANT JOURNAL, 2008, 53 (02) :393-399