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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 |
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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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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.</description><identifier>ISSN: 1464-6722</identifier><identifier>EISSN: 1364-3703</identifier><identifier>DOI: 10.1111/mpp.12502</identifier><identifier>PMID: 27756102</identifier><language>eng</language><publisher>Oxford: John Wiley & Sons, Inc</publisher><subject>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</subject><ispartof>Molecular plant pathology, 2018-01, Vol.19 (1), p.104-115</ispartof><rights>2016 BSPP AND JOHN WILEY & SONS LTD</rights><rights>2018 BSPP AND JOHN WILEY & SONS LTD</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4762-eea0d6ba7fde723354020012d6e1798b962526cb309e282e99d508be65fa56e03</citedby><cites>FETCH-LOGICAL-c4762-eea0d6ba7fde723354020012d6e1798b962526cb309e282e99d508be65fa56e03</cites><orcidid>0000-0001-6197-777X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637982/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637982/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,11540,27900,27901,46026,46450,53765,53767</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2Fmpp.12502$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc></links><search><creatorcontrib>Cheng, Feifei</creatorcontrib><creatorcontrib>Ma, Anzhou</creatorcontrib><creatorcontrib>Zhuang, Guoqiang</creatorcontrib><creatorcontrib>Fray, Rupert G.</creatorcontrib><title>Exogenous N‐acyl‐homoserine lactones enhance the expression of flagella of Pseudomonas syringae and activate defence responses in plants</title><title>Molecular plant pathology</title><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.</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 & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6197-777X</orcidid></search><sort><creationdate>201801</creationdate><title>Exogenous N‐acyl‐homoserine lactones enhance the expression of flagella of Pseudomonas syringae and activate defence responses in plants</title><author>Cheng, Feifei ; Ma, Anzhou ; Zhuang, Guoqiang ; Fray, Rupert G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4762-eea0d6ba7fde723354020012d6e1798b962526cb309e282e99d508be65fa56e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Bacteria</topic><topic>Cell walls</topic><topic>defence responses</topic><topic>disease incidence</topic><topic>Disease resistance</topic><topic>Flagella</topic><topic>flagellum</topic><topic>Gene expression</topic><topic>gene expression regulation</topic><topic>Gene sequencing</topic><topic>Genes</topic><topic>Homoserine lactones</topic><topic>Hypersensitive response</topic><topic>Immunity</topic><topic>Inoculation</topic><topic>Lactones</topic><topic>Metabolites</topic><topic>N-Acyl homoserine lactone</topic><topic>N‐acyl‐homoserine lactones, Pseudomonas syringae pv. tabaci 11528</topic><topic>Original</topic><topic>Pathogenicity</topic><topic>Pathogens</topic><topic>Plant diseases</topic><topic>Polymerase chain reaction</topic><topic>Pseudomonas</topic><topic>Pseudomonas syringae</topic><topic>Pseudomonas syringae pv. tabaci</topic><topic>quantitative polymerase chain reaction</topic><topic>Quorum sensing</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Tobacco</topic><topic>Transgenic plants</topic><topic>virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheng, Feifei</creatorcontrib><creatorcontrib>Ma, Anzhou</creatorcontrib><creatorcontrib>Zhuang, Guoqiang</creatorcontrib><creatorcontrib>Fray, Rupert G.</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular plant pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Cheng, Feifei</au><au>Ma, Anzhou</au><au>Zhuang, Guoqiang</au><au>Fray, Rupert G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exogenous N‐acyl‐homoserine lactones enhance the expression of flagella of Pseudomonas syringae and activate defence responses in plants</atitle><jtitle>Molecular plant pathology</jtitle><date>2018-01</date><risdate>2018</risdate><volume>19</volume><issue>1</issue><spage>104</spage><epage>115</epage><pages>104-115</pages><issn>1464-6722</issn><eissn>1364-3703</eissn><abstract>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.</abstract><cop>Oxford</cop><pub>John Wiley & Sons, Inc</pub><pmid>27756102</pmid><doi>10.1111/mpp.12502</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-6197-777X</orcidid><oa>free_for_read</oa></addata></record> |
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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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