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Article|23 Dec 2023|OPEN
ABA-CsABI5-CsCalS11 module upregulates Callose deposition of citrus infected with Candidatus Liberibacter asiaticus
Lixiao Yao1 , Xingru Guo1 , Juan Su1 , Qingwen Zhang1 , Mengyao Lian1 , Hao Xue1 , Qiang Li1 , Yongrui He1 , Xiuping Zou1 , Zhen Song1 , and Shanchun Chen,1 ,
1National Citrus Engineering Technology Research Center, Citrus Research Institute, Southwest University, Beibei, Chongqing 400712, China
*Corresponding author. E-mail: songzhen@cric.cn,chenshanchun@cric.cn

Horticulture Research 11,
Article number: uhad276 (2024)
doi: https://doi.org/10.1093/hr/uhad276
Views: 76

Received: 20 Dec 2022
Accepted: 10 Dec 2023
Published online: 23 Dec 2023

Abstract

Huanglongbing (HLB) primarily caused by Candidatus Liberibacter asiaticus (CLas) has been threatening citrus production globally. Under HLB conditions, an excessive accumulation of the polysaccharide callose in citrus phloem occurs, leading to phloem blockage and starch accumulation in leaves. The callose production is controlled by callose synthases (CalS), which have multiple members within plants. However, the knowledge of callose production in the citrus upon infection with CLas is limited. In this study, we firstly identified 11 CalSs in the Citrus sinensis genome through bioinformatics and found the expression pattern of CsCalS11 exhibited a positive correlation with callose deposition in CLas-infected leaves (correlation coefficient of 0.77, P ≤ 0.05). Knockdown of CsCalS11 resulted in a reduction of callose deposition and starch accumulation in CLas-infected citrus. Interestingly, we observed significantly higher concentrations of abscisic acid (ABA) in HLB-infected citrus leaves compared to uninfected ones. Furthermore, the expressions of CsABI5CsPYR, and CsSnRK2 in the ABA pathway substantially increased in citrus leaves upon CLas infection. Additionally, the expression of CsCalS11 was significantly upregulated in citrus leaves following the application of exogenous ABA. We confirmed that CsABI5, a pivotal component of the ABA signaling pathway, regulates CsCalS11 expression by binding to its promoter using yeast one-hybrid assay, dual luciferase assay, and transient expression in citrus leaves. In conclusion, our findings strongly suggest that the CsABI5-CsCalS11 module plays a crucial role in regulating callose deposition through the ABA signaling pathway during CLas infection. The results also revealed new function of the ABA signaling pathway in plants under biotic stress.