Metabolomic response to huanglongbing: Role of carboxylic compounds in citrus sinensis response to 'candidatus liberibacter asiaticus' and its vector, diaphorina citri

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Abstract

Huanglongbing, a destructive disease of citrus, is caused by the fastidious bacterium 'Candidatus Liberibacter asiaticus' and transmitted by Asian citrus psyllid, Diaphorina citri. The impact of 'Ca. L. asiaticus' infection or D. citri infestation on Valencia sweet orange (Citrus sinensis) leaf metabolites was investigated using gas chromatography mass spectrometry, followed by gene expression analysis for 37 genes involved in jasmonic acid (JA), salicylic acid (SA), and proline-glutamine pathways. The total amino acid abundance increased after 'Ca. L. asiaticus' infection, while the total fatty acids increased dramatically after infestation with D. citri, compared with control plants. Seven amino acids (glycine, L-isoleucine, L-phenylalanine, L-proline, L-serine, L-threonine, and L-tryptophan) and five organic acids (benzoic acid, citric acid, fumaric acid, SA, and succinic acid) increased in 'Ca. L. asiaticus'-infected plants. On the other hand, the abundance of trans-JA and its precursor a-linolenic increased in D. citri-infested plants. Surprisingly, the double attack of both D. citri infestation and 'Ca. L. asiaticus' infection moderated the metabolic changes in all chemical classes studied. In addition, the gene expression analysis supported these results. Based on these findings, we suggest that, although amino acids such as phenylalanine are involved in citrus defense against 'Ca. L. asiaticus' infection through the activation of an SAmediated pathway, fatty acids, especially a-linolenic acid, are involved in defense against D. citri infestation via the induction of a JA-mediated pathway.

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Killiny, N., & Nehela, Y. (2017). Metabolomic response to huanglongbing: Role of carboxylic compounds in citrus sinensis response to “candidatus liberibacter asiaticus” and its vector, diaphorina citri. Molecular Plant-Microbe Interactions, 30(8), 666–678. https://doi.org/10.1094/MPMI-05-17-0106-R

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