Abstract
The plant cell wall responds dynamically during interaction with various pathogens. Upon recognition of “nonself” components, plant cells deploy a variety of immune responses including cell wall fortification. Callose, a β-(1, 3)-D-glucan polymer, is a component of the material deposited at the site of infection between the plasma membrane and the preexisting cell wall that is hypothesized to serve as a physical barrier and platform for directed antimicrobial compound deposition. The defense-associated function of callose deposition is supported by its induction during pathogen-associated molecular patterns (PAMP)-triggered immunity (PTI) and its inhibition by defense suppressing virulence effectors. Thus, callose deposition is a commonly monitored read-out in plant defense. This protocol describes the use of aniline blue staining and fluorescent microscopy to measure callose deposition in bacteria-infected or elicitor-challenged Arabidopsis leaf tissues.
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Jin, L., & Mackey, D. M. (2017). Measuring callose deposition, an indicator of cell wall reinforcement, during bacterial infection in Arabidopsis. In Methods in Molecular Biology (Vol. 1578, pp. 195–205). Humana Press Inc. https://doi.org/10.1007/978-1-4939-6859-6_16
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