Real-time <em>In Vivo </em>Recording of <em>Arabidopsis</em> Calcium Signals During Insect Feeding Using a Fluorescent Biosensor
Author(s) -
Thomas R. Vincent,
James Canham,
Masatsugu Toyota,
Marieta Avramova,
Sam T. Mugford,
Simon Gilroy,
Tony Miller,
Saskia A. Hogenhout,
Dale Sanders
Publication year - 2017
Publication title -
journal of visualized experiments
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.596
H-Index - 91
ISSN - 1940-087X
DOI - 10.3791/56142
Subject(s) - calcium , arabidopsis thaliana , biology , arabidopsis , calcium imaging , calcium signaling , insect , microbiology and biotechnology , live cell imaging , biophysics , botany , biochemistry , signal transduction , mutant , chemistry , cell , organic chemistry , gene
Calcium ions are predicted to be key signaling entities during biotic interactions, with calcium signaling forming an established part of the plant defense response to microbial elicitors and to wounding caused by chewing insects, eliciting systemic calcium signals in plants. However, the role of calcium in vivo during biotic stress is still unclear. This protocol describes the use of a genetically-encoded calcium sensor to detect calcium signals in plants during feeding by a hemipteran pest. Hemipterans such as aphids pierce a small number of cells with specialized, elongated sucking mouthparts, making them the ideal tool to study calcium dynamics when a plant is faced with a biotic stress, which is distinct from a wounding response. In addition, fluorescent biosensors are revolutionizing the measurement of signaling molecules in vivo in both animals and plants. Expressing a GFP-based calcium biosensor, GCaMP3, in the model plant Arabidopsis thaliana allows for the real-time imaging of plant calcium dynamics during insect feeding, with a high spatial and temporal resolution. A repeatable and robust assay has been developed using the fluorescence microscopy of detached GCaMP3 leaves, allowing for the continuous measurement of cytosolic calcium dynamics before, during, and after insect feeding. This reveals a highly-localized rapid calcium elevation around the aphid feeding site that occurs within a few minutes. The protocol can be adapted to other biotic stresses, such as additional insect species, while the use of Arabidopsis thaliana allows for the rapid generation of mutants to facilitate the molecular analysis of the phenomenon.
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