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Exogenous N‐acyl‐homoserine lactones enhance the expression of flagella of Pseudomonas syringae and activate defence responses in plants

Summary In order to cope with pathogens, plants have evolved sophisticated mechanisms to sense pathogenic attacks and to induce defence responses. The N‐acyl‐homoserine lactone (AHL)‐mediated quorum sensing in bacteria regulates diverse physiological processes, including those involved in pathogenic...

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Published in:Molecular plant pathology 2018-01, Vol.19 (1), p.104-115
Main Authors: Cheng, Feifei, Ma, Anzhou, Zhuang, Guoqiang, Fray, Rupert G.
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container_title Molecular plant pathology
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creator Cheng, Feifei
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description Summary In order to cope with pathogens, plants have evolved sophisticated mechanisms to sense pathogenic attacks and to induce defence responses. The N‐acyl‐homoserine lactone (AHL)‐mediated quorum sensing in bacteria regulates diverse physiological processes, including those involved in pathogenicity. In this work, we study the interactions between AHL‐producing transgenic tobacco plants and Pseudomonas syringae pv. tabaci 11528 (P. syringae 11528). Both a reduced incidence of disease and decrease in the growth of P. syringae 11528 were observed in AHL‐producing plants compared with wild‐type plants. The present data indicate that plant‐produced AHLs enhance disease resistance against this pathogen. Subsequent RNA‐sequencing analysis showed that the exogenous addition of AHLs up‐regulated the expression of P. syringae 11528 genes for flagella production. Expression levels of plant defence genes in AHL‐producing and wild‐type plants were determined by quantitative real‐time polymerase chain reaction. These data showed that plant‐produced AHLs activated a wide spectrum of defence responses in plants following inoculation, including the oxidative burst, hypersensitive response, cell wall strengthening, and the production of certain metabolites. These results demonstrate that exogenous AHLs alter the gene expression patterns of pathogens, and plant‐produced AHLs either directly or indirectly enhance plant local immunity during the early stage of plant infection.
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The N‐acyl‐homoserine lactone (AHL)‐mediated quorum sensing in bacteria regulates diverse physiological processes, including those involved in pathogenicity. In this work, we study the interactions between AHL‐producing transgenic tobacco plants and Pseudomonas syringae pv. tabaci 11528 (P. syringae 11528). Both a reduced incidence of disease and decrease in the growth of P. syringae 11528 were observed in AHL‐producing plants compared with wild‐type plants. The present data indicate that plant‐produced AHLs enhance disease resistance against this pathogen. Subsequent RNA‐sequencing analysis showed that the exogenous addition of AHLs up‐regulated the expression of P. syringae 11528 genes for flagella production. Expression levels of plant defence genes in AHL‐producing and wild‐type plants were determined by quantitative real‐time polymerase chain reaction. These data showed that plant‐produced AHLs activated a wide spectrum of defence responses in plants following inoculation, including the oxidative burst, hypersensitive response, cell wall strengthening, and the production of certain metabolites. 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The N‐acyl‐homoserine lactone (AHL)‐mediated quorum sensing in bacteria regulates diverse physiological processes, including those involved in pathogenicity. In this work, we study the interactions between AHL‐producing transgenic tobacco plants and Pseudomonas syringae pv. tabaci 11528 (P. syringae 11528). Both a reduced incidence of disease and decrease in the growth of P. syringae 11528 were observed in AHL‐producing plants compared with wild‐type plants. The present data indicate that plant‐produced AHLs enhance disease resistance against this pathogen. Subsequent RNA‐sequencing analysis showed that the exogenous addition of AHLs up‐regulated the expression of P. syringae 11528 genes for flagella production. Expression levels of plant defence genes in AHL‐producing and wild‐type plants were determined by quantitative real‐time polymerase chain reaction. 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These results demonstrate that exogenous AHLs alter the gene expression patterns of pathogens, and plant‐produced AHLs either directly or indirectly enhance plant local immunity during the early stage of plant infection.</description><subject>Bacteria</subject><subject>Cell walls</subject><subject>defence responses</subject><subject>disease incidence</subject><subject>Disease resistance</subject><subject>Flagella</subject><subject>flagellum</subject><subject>Gene expression</subject><subject>gene expression regulation</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>Homoserine lactones</subject><subject>Hypersensitive response</subject><subject>Immunity</subject><subject>Inoculation</subject><subject>Lactones</subject><subject>Metabolites</subject><subject>N-Acyl homoserine lactone</subject><subject>N‐acyl‐homoserine lactones, Pseudomonas syringae pv. tabaci 11528</subject><subject>Original</subject><subject>Pathogenicity</subject><subject>Pathogens</subject><subject>Plant diseases</subject><subject>Polymerase chain reaction</subject><subject>Pseudomonas</subject><subject>Pseudomonas syringae</subject><subject>Pseudomonas syringae pv. tabaci</subject><subject>quantitative polymerase chain reaction</subject><subject>Quorum sensing</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Tobacco</subject><subject>Transgenic plants</subject><subject>virulence</subject><issn>1464-6722</issn><issn>1364-3703</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kc1u1DAQxy1ERT_gwBtY4gKHbf2R2MkFCVUFKpWyBzhbTjLZdeXYwU5K98YDcOgz8iSdsBUSSPgyI_k_v5n_DCEvOTvl-M6GcTzlomTiCTniUhUrqZl8inmBudJCHJLjnG8Y47oW5TNyKLQuFWfiiPy8uIsbCHHO9PrXj3vb7jyGbRxihuQCUG_bKQbIFMLWhhbotAUKd2OCnF0MNPa093YD3tslX2eYO6wONtO8Q8LGArWho4hxt3YC2kEPCwcBYwwZyS7Q0dsw5efkoLc-w4vHeEK-vr_4cv5xdfX5w-X5u6tVW2glVgCWdaqxuu9ACynLggn0JjoFaLBqaiVKodpGshpEJaCuu5JVDaiyt6UCJk_I2z13nJsBuhbClKw3Y3KDTTsTrTN__wS3NZt4a5SS2EAg4PUjIMVvM-TJDC63yw4C4CqNwIEqrXi19Hr1j_QmzimgPcNrXdRCSVah6s1e1aaYc4L-zzCcmeXGBm9sft8YtWd77XfnYfd_ofm0Xu8rHgAJuawD</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Cheng, Feifei</creator><creator>Ma, Anzhou</creator><creator>Zhuang, Guoqiang</creator><creator>Fray, Rupert G.</creator><general>John Wiley &amp; 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ispartof Molecular plant pathology, 2018-01, Vol.19 (1), p.104-115
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source Open Access: Wiley-Blackwell Open Access Journals
subjects Bacteria
Cell walls
defence responses
disease incidence
Disease resistance
Flagella
flagellum
Gene expression
gene expression regulation
Gene sequencing
Genes
Homoserine lactones
Hypersensitive response
Immunity
Inoculation
Lactones
Metabolites
N-Acyl homoserine lactone
N‐acyl‐homoserine lactones, Pseudomonas syringae pv. tabaci 11528
Original
Pathogenicity
Pathogens
Plant diseases
Polymerase chain reaction
Pseudomonas
Pseudomonas syringae
Pseudomonas syringae pv. tabaci
quantitative polymerase chain reaction
Quorum sensing
Ribonucleic acid
RNA
Tobacco
Transgenic plants
virulence
title Exogenous N‐acyl‐homoserine lactones enhance the expression of flagella of Pseudomonas syringae and activate defence responses in plants
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