Plants coexist with diverse microorganisms, and their interactions have resulted in coevolution. Higher plants have immune systems with two different levels to resist pathogen invasion and multiplication. The gene-for-gene concept characterizes genetic control by plant resistance gene products and pathogen avirulence proteins, which are pathogen-secreted effectors that manipulate host processes in favour of the pathogen (Goehre & Robatzek, 2008; Gouveia et al., 2017; Wang et al., 2019); their direct or indirect molecular interactions initiate effector-triggered immunity (ETI), which is essential to conventional race-specific resistance breeding programmes (Peng et al., 2018). Moreover, microbial-originated invariant structures, known as microbial-associated molecular patterns (MAMPs), are able to activate pattern-triggered immunity (PTI) in various cultivars of numerous species, resulting in the elicitation of plant stomatal closure and disease resistance (Boller & He, 2009; Chisholm et al., 2006). Chitin is a polymer of N-acetyl-d-glucosamine that can be obtained from natural sources, such as arthropod exoskeletons or fungal cell walls. It is a PTI inducer that elicits stomatal closure and disease resistance, and has been applied to control crop disease (Liu et al.,