Cargando…

Long-term, sustained feeding by Asian citrus psyllid disrupts salicylic acid homeostasis in sweet orange

BACKGROUND: Phloem-feeding insects are known to modulate the salicylic acid (SA) signaling pathway in various plant-insect interaction models. Diaphorina citri is a phloem feeding vector of the deadly phytopathogens, Candidatus Liberibacter americanus and Candidatus Liberibacter asiaticus, and the i...

Descripción completa

Detalles Bibliográficos
Autores principales: Ibanez, Freddy, Suh, Joon Hyuk, Wang, Yu, Stelinski, Lukasz L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852996/
https://www.ncbi.nlm.nih.gov/pubmed/31718546
http://dx.doi.org/10.1186/s12870-019-2114-2
_version_ 1783469963454971904
author Ibanez, Freddy
Suh, Joon Hyuk
Wang, Yu
Stelinski, Lukasz L.
author_facet Ibanez, Freddy
Suh, Joon Hyuk
Wang, Yu
Stelinski, Lukasz L.
author_sort Ibanez, Freddy
collection PubMed
description BACKGROUND: Phloem-feeding insects are known to modulate the salicylic acid (SA) signaling pathway in various plant-insect interaction models. Diaphorina citri is a phloem feeding vector of the deadly phytopathogens, Candidatus Liberibacter americanus and Candidatus Liberibacter asiaticus, and the interactions of D. citri with its host that may modulate plant defenses are not well understood. The objectives of this study were to investigate the molecular mechanisms involved in transcriptional regulation of SA modification and activation of defense-associated responses in sweet orange (Citrus sinensis) exposed to various durations (7-, 14- and 150- days) of continuous feeding by D. citri. RESULTS: We quantified expression of genes involved in SA pathway activation and subsequent modification, as well as, associated SA metabolites (SA methyl ester, 2,3-DHBA, and SA 2-O-β-D-glucoside). NPR1 and PR-1 expression was upregulated in plants exposed to continuous feeding by D. citri for 14 days. Expression of BSMT-like, MES1-like and DMR6-like oxygenase, as well as, accumulation of their respective SA metabolites (SA methyl ester, 2,3-DHBA) was significantly higher in plants exposed to continuous feeding by D. citri for 150 days than in those without D. citri infestation. Concomitantly, expression of UGT74F2-like was significantly downregulated and its metabolite, SA 2-β-D-glucoside, was highly accumulated in trees exposed to 150 d of feeding compared to control trees without D. citri. CONCLUSIONS: D. citri herbivory differentially regulated transcription and SA-metabolite accumulation in citrus leaves, depending on duration of insect feeding. Our results suggest that prolonged and uninterrupted exposure (150 d) of citrus to D. citri feeding suppressed plant immunity and inhibited growth, which may highlight the importance of vector suppression as part of huanglongbing (HLB) management in citrus.
format Online
Article
Text
id pubmed-6852996
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-68529962019-11-21 Long-term, sustained feeding by Asian citrus psyllid disrupts salicylic acid homeostasis in sweet orange Ibanez, Freddy Suh, Joon Hyuk Wang, Yu Stelinski, Lukasz L. BMC Plant Biol Research Article BACKGROUND: Phloem-feeding insects are known to modulate the salicylic acid (SA) signaling pathway in various plant-insect interaction models. Diaphorina citri is a phloem feeding vector of the deadly phytopathogens, Candidatus Liberibacter americanus and Candidatus Liberibacter asiaticus, and the interactions of D. citri with its host that may modulate plant defenses are not well understood. The objectives of this study were to investigate the molecular mechanisms involved in transcriptional regulation of SA modification and activation of defense-associated responses in sweet orange (Citrus sinensis) exposed to various durations (7-, 14- and 150- days) of continuous feeding by D. citri. RESULTS: We quantified expression of genes involved in SA pathway activation and subsequent modification, as well as, associated SA metabolites (SA methyl ester, 2,3-DHBA, and SA 2-O-β-D-glucoside). NPR1 and PR-1 expression was upregulated in plants exposed to continuous feeding by D. citri for 14 days. Expression of BSMT-like, MES1-like and DMR6-like oxygenase, as well as, accumulation of their respective SA metabolites (SA methyl ester, 2,3-DHBA) was significantly higher in plants exposed to continuous feeding by D. citri for 150 days than in those without D. citri infestation. Concomitantly, expression of UGT74F2-like was significantly downregulated and its metabolite, SA 2-β-D-glucoside, was highly accumulated in trees exposed to 150 d of feeding compared to control trees without D. citri. CONCLUSIONS: D. citri herbivory differentially regulated transcription and SA-metabolite accumulation in citrus leaves, depending on duration of insect feeding. Our results suggest that prolonged and uninterrupted exposure (150 d) of citrus to D. citri feeding suppressed plant immunity and inhibited growth, which may highlight the importance of vector suppression as part of huanglongbing (HLB) management in citrus. BioMed Central 2019-11-12 /pmc/articles/PMC6852996/ /pubmed/31718546 http://dx.doi.org/10.1186/s12870-019-2114-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ibanez, Freddy
Suh, Joon Hyuk
Wang, Yu
Stelinski, Lukasz L.
Long-term, sustained feeding by Asian citrus psyllid disrupts salicylic acid homeostasis in sweet orange
title Long-term, sustained feeding by Asian citrus psyllid disrupts salicylic acid homeostasis in sweet orange
title_full Long-term, sustained feeding by Asian citrus psyllid disrupts salicylic acid homeostasis in sweet orange
title_fullStr Long-term, sustained feeding by Asian citrus psyllid disrupts salicylic acid homeostasis in sweet orange
title_full_unstemmed Long-term, sustained feeding by Asian citrus psyllid disrupts salicylic acid homeostasis in sweet orange
title_short Long-term, sustained feeding by Asian citrus psyllid disrupts salicylic acid homeostasis in sweet orange
title_sort long-term, sustained feeding by asian citrus psyllid disrupts salicylic acid homeostasis in sweet orange
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852996/
https://www.ncbi.nlm.nih.gov/pubmed/31718546
http://dx.doi.org/10.1186/s12870-019-2114-2
work_keys_str_mv AT ibanezfreddy longtermsustainedfeedingbyasiancitruspsylliddisruptssalicylicacidhomeostasisinsweetorange
AT suhjoonhyuk longtermsustainedfeedingbyasiancitruspsylliddisruptssalicylicacidhomeostasisinsweetorange
AT wangyu longtermsustainedfeedingbyasiancitruspsylliddisruptssalicylicacidhomeostasisinsweetorange
AT stelinskilukaszl longtermsustainedfeedingbyasiancitruspsylliddisruptssalicylicacidhomeostasisinsweetorange