Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection
Summary Plant diseases are an important threat to food production. While major pathogenicity determinants required for disease have been extensively studied, less is known on how pathogens thrive during host colonization, especially at early infection stages. Here, we used randomly barcoded‐transpos...
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Veröffentlicht in: | The New phytologist 2022-10, Vol.236 (1), p.235-248 |
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creator | Luneau, Julien S. Baudin, Maël Quiroz Monnens, Thomas Carrère, Sébastien Bouchez, Olivier Jardinaud, Marie‐Françoise Gris, Carine François, Jonas Ray, Jayashree Torralba, Babil Arlat, Matthieu Lewis, Jennifer D. Lauber, Emmanuelle Deutschbauer, Adam M. Noël, Laurent D. Boulanger, Alice |
description | Summary
Plant diseases are an important threat to food production. While major pathogenicity determinants required for disease have been extensively studied, less is known on how pathogens thrive during host colonization, especially at early infection stages.
Here, we used randomly barcoded‐transposon insertion site sequencing (RB‐TnSeq) to perform a genome‐wide screen and identify key bacterial fitness determinants of the vascular pathogen Xanthomonas campestris pv campestris (Xcc) during infection of the cauliflower host plant (Brassica oleracea). This high‐throughput analysis was conducted in hydathodes, the natural entry site of Xcc, in xylem sap and in synthetic media.
Xcc did not face a strong bottleneck during hydathode infection. In total, 181 genes important for fitness were identified in plant‐associated environments with functional enrichment in genes involved in metabolism but only few genes previously known to be involved in virulence. The biological relevance of 12 genes was independently confirmed by phenotyping single mutants. Notably, we show that XC_3388, a protein with no known function (DUF1631), plays a key role in the adaptation and virulence of Xcc possibly through c‐di‐GMP‐mediated regulation.
This study revealed yet unsuspected social behaviors adopted by Xcc individuals when confined inside hydathodes at early infection stages. |
doi_str_mv | 10.1111/nph.18313 |
format | Article |
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Plant diseases are an important threat to food production. While major pathogenicity determinants required for disease have been extensively studied, less is known on how pathogens thrive during host colonization, especially at early infection stages.
Here, we used randomly barcoded‐transposon insertion site sequencing (RB‐TnSeq) to perform a genome‐wide screen and identify key bacterial fitness determinants of the vascular pathogen Xanthomonas campestris pv campestris (Xcc) during infection of the cauliflower host plant (Brassica oleracea). This high‐throughput analysis was conducted in hydathodes, the natural entry site of Xcc, in xylem sap and in synthetic media.
Xcc did not face a strong bottleneck during hydathode infection. In total, 181 genes important for fitness were identified in plant‐associated environments with functional enrichment in genes involved in metabolism but only few genes previously known to be involved in virulence. The biological relevance of 12 genes was independently confirmed by phenotyping single mutants. Notably, we show that XC_3388, a protein with no known function (DUF1631), plays a key role in the adaptation and virulence of Xcc possibly through c‐di‐GMP‐mediated regulation.
This study revealed yet unsuspected social behaviors adopted by Xcc individuals when confined inside hydathodes at early infection stages.</description><identifier>ISSN: 0028-646X</identifier><identifier>EISSN: 1469-8137</identifier><identifier>DOI: 10.1111/nph.18313</identifier><identifier>PMID: 35706385</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Bacteriology ; Biochemistry, Molecular Biology ; Brassica ; Brassica oleracea ; Colonization ; Enrichment ; Fitness ; Food production ; Genes ; Genomes ; Genomics ; Host plants ; hydathodes ; Infections ; Life Sciences ; Metabolism ; Microbiology and Parasitology ; Pathogenicity ; Pathogens ; Phenotyping ; Phytopathology and phytopharmacy ; Plant bacterial diseases ; Plant diseases ; Plants ; RB‐TnSeq ; Social behavior ; Vegetal Biology ; Virulence ; Wide screen ; Xanthomonas ; Xanthomonas campestris ; Xylem</subject><ispartof>The New phytologist, 2022-10, Vol.236 (1), p.235-248</ispartof><rights>2022 The Authors. © 2022 New Phytologist Foundation.</rights><rights>This article is protected by copyright. All rights reserved.</rights><rights>2022. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Attribution - NonCommercial</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4223-f6713934e058ecc5fbf4668eba292bcb29e4a09e70761f54db67fc712c14d9df3</citedby><cites>FETCH-LOGICAL-c4223-f6713934e058ecc5fbf4668eba292bcb29e4a09e70761f54db67fc712c14d9df3</cites><orcidid>0000-0002-0110-1423 ; 0000-0001-6245-8920 ; 0000-0001-5918-9547 ; 0000-0001-5933-4476 ; 0000-0002-2348-0778 ; 0000-0003-1112-8723 ; 0000-0001-8103-3813 ; 0000-0001-6196-4856 ; 0000-0002-7255-0058 ; 0000-0001-8290-7527 ; 0000-0003-4337-8292 ; 0000-0002-1917-3468 ; 0000-0003-3172-0150</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fnph.18313$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fnph.18313$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35706385$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03744702$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Luneau, Julien S.</creatorcontrib><creatorcontrib>Baudin, Maël</creatorcontrib><creatorcontrib>Quiroz Monnens, Thomas</creatorcontrib><creatorcontrib>Carrère, Sébastien</creatorcontrib><creatorcontrib>Bouchez, Olivier</creatorcontrib><creatorcontrib>Jardinaud, Marie‐Françoise</creatorcontrib><creatorcontrib>Gris, Carine</creatorcontrib><creatorcontrib>François, Jonas</creatorcontrib><creatorcontrib>Ray, Jayashree</creatorcontrib><creatorcontrib>Torralba, Babil</creatorcontrib><creatorcontrib>Arlat, Matthieu</creatorcontrib><creatorcontrib>Lewis, Jennifer D.</creatorcontrib><creatorcontrib>Lauber, Emmanuelle</creatorcontrib><creatorcontrib>Deutschbauer, Adam M.</creatorcontrib><creatorcontrib>Noël, Laurent D.</creatorcontrib><creatorcontrib>Boulanger, Alice</creatorcontrib><title>Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection</title><title>The New phytologist</title><addtitle>New Phytol</addtitle><description>Summary
Plant diseases are an important threat to food production. While major pathogenicity determinants required for disease have been extensively studied, less is known on how pathogens thrive during host colonization, especially at early infection stages.
Here, we used randomly barcoded‐transposon insertion site sequencing (RB‐TnSeq) to perform a genome‐wide screen and identify key bacterial fitness determinants of the vascular pathogen Xanthomonas campestris pv campestris (Xcc) during infection of the cauliflower host plant (Brassica oleracea). This high‐throughput analysis was conducted in hydathodes, the natural entry site of Xcc, in xylem sap and in synthetic media.
Xcc did not face a strong bottleneck during hydathode infection. In total, 181 genes important for fitness were identified in plant‐associated environments with functional enrichment in genes involved in metabolism but only few genes previously known to be involved in virulence. The biological relevance of 12 genes was independently confirmed by phenotyping single mutants. Notably, we show that XC_3388, a protein with no known function (DUF1631), plays a key role in the adaptation and virulence of Xcc possibly through c‐di‐GMP‐mediated regulation.
This study revealed yet unsuspected social behaviors adopted by Xcc individuals when confined inside hydathodes at early infection stages.</description><subject>Bacteriology</subject><subject>Biochemistry, Molecular Biology</subject><subject>Brassica</subject><subject>Brassica oleracea</subject><subject>Colonization</subject><subject>Enrichment</subject><subject>Fitness</subject><subject>Food production</subject><subject>Genes</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Host plants</subject><subject>hydathodes</subject><subject>Infections</subject><subject>Life Sciences</subject><subject>Metabolism</subject><subject>Microbiology and Parasitology</subject><subject>Pathogenicity</subject><subject>Pathogens</subject><subject>Phenotyping</subject><subject>Phytopathology and phytopharmacy</subject><subject>Plant bacterial diseases</subject><subject>Plant diseases</subject><subject>Plants</subject><subject>RB‐TnSeq</subject><subject>Social behavior</subject><subject>Vegetal Biology</subject><subject>Virulence</subject><subject>Wide screen</subject><subject>Xanthomonas</subject><subject>Xanthomonas campestris</subject><subject>Xylem</subject><issn>0028-646X</issn><issn>1469-8137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNp1kc2KFDEURoMoTju68AUk4EYXNZO_SqqWw6DTQqMuFGYXUqmb7gxVSZlUOfTOB3DhM_okpu1xBMFACEkO597Lh9BzSs5oWedh2p3RhlP-AK2okG3VUK4eohUhrKmkkNcn6EnON4SQtpbsMTrhtSKSN_UKfb-CEEf4-e3Hre8Blx1m77w1s48BR4ednwPkjHuYIY0-mDBn7AOed4Cvy2UXxxhMxtaME-Q5-Yw7YwvrzYAnU_63EHC_JB-2GEwa9jjPZgv5IJ-GYig2B_ZQ7yl65MyQ4dndeYo-v33z6XJdbT5cvbu82FRWMMYrJxXlLRdA6gasrV3nhJQNdIa1rLMda0EY0oIiSlJXi76TyllFmaWib3vHT9Hro3dnBj0lP5q019F4vb7Y6MMb4UoIRdhXWthXR3ZK8ctSJtSjzxaG0jnEJWsmlaqVkFQV9OU_6E1cUiiTaKZKTjUTLf1b3KaYcwJ33wEl-hCnLnHq33EW9sWdcelG6O_JP_kV4PwI3PoB9v836fcf10flL20nrHg</recordid><startdate>202210</startdate><enddate>202210</enddate><creator>Luneau, Julien S.</creator><creator>Baudin, Maël</creator><creator>Quiroz Monnens, Thomas</creator><creator>Carrère, Sébastien</creator><creator>Bouchez, Olivier</creator><creator>Jardinaud, Marie‐Françoise</creator><creator>Gris, Carine</creator><creator>François, Jonas</creator><creator>Ray, Jayashree</creator><creator>Torralba, Babil</creator><creator>Arlat, Matthieu</creator><creator>Lewis, Jennifer D.</creator><creator>Lauber, Emmanuelle</creator><creator>Deutschbauer, Adam M.</creator><creator>Noël, Laurent D.</creator><creator>Boulanger, Alice</creator><general>Wiley Subscription Services, Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7SN</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-0110-1423</orcidid><orcidid>https://orcid.org/0000-0001-6245-8920</orcidid><orcidid>https://orcid.org/0000-0001-5918-9547</orcidid><orcidid>https://orcid.org/0000-0001-5933-4476</orcidid><orcidid>https://orcid.org/0000-0002-2348-0778</orcidid><orcidid>https://orcid.org/0000-0003-1112-8723</orcidid><orcidid>https://orcid.org/0000-0001-8103-3813</orcidid><orcidid>https://orcid.org/0000-0001-6196-4856</orcidid><orcidid>https://orcid.org/0000-0002-7255-0058</orcidid><orcidid>https://orcid.org/0000-0001-8290-7527</orcidid><orcidid>https://orcid.org/0000-0003-4337-8292</orcidid><orcidid>https://orcid.org/0000-0002-1917-3468</orcidid><orcidid>https://orcid.org/0000-0003-3172-0150</orcidid></search><sort><creationdate>202210</creationdate><title>Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection</title><author>Luneau, Julien S. ; Baudin, Maël ; Quiroz Monnens, Thomas ; Carrère, Sébastien ; Bouchez, Olivier ; Jardinaud, Marie‐Françoise ; Gris, Carine ; François, Jonas ; Ray, Jayashree ; Torralba, Babil ; Arlat, Matthieu ; Lewis, Jennifer D. ; Lauber, Emmanuelle ; Deutschbauer, Adam M. ; Noël, Laurent D. ; Boulanger, Alice</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4223-f6713934e058ecc5fbf4668eba292bcb29e4a09e70761f54db67fc712c14d9df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Bacteriology</topic><topic>Biochemistry, Molecular Biology</topic><topic>Brassica</topic><topic>Brassica oleracea</topic><topic>Colonization</topic><topic>Enrichment</topic><topic>Fitness</topic><topic>Food production</topic><topic>Genes</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Host plants</topic><topic>hydathodes</topic><topic>Infections</topic><topic>Life Sciences</topic><topic>Metabolism</topic><topic>Microbiology and Parasitology</topic><topic>Pathogenicity</topic><topic>Pathogens</topic><topic>Phenotyping</topic><topic>Phytopathology and phytopharmacy</topic><topic>Plant bacterial diseases</topic><topic>Plant diseases</topic><topic>Plants</topic><topic>RB‐TnSeq</topic><topic>Social behavior</topic><topic>Vegetal Biology</topic><topic>Virulence</topic><topic>Wide screen</topic><topic>Xanthomonas</topic><topic>Xanthomonas campestris</topic><topic>Xylem</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luneau, Julien S.</creatorcontrib><creatorcontrib>Baudin, Maël</creatorcontrib><creatorcontrib>Quiroz Monnens, Thomas</creatorcontrib><creatorcontrib>Carrère, Sébastien</creatorcontrib><creatorcontrib>Bouchez, Olivier</creatorcontrib><creatorcontrib>Jardinaud, Marie‐Françoise</creatorcontrib><creatorcontrib>Gris, Carine</creatorcontrib><creatorcontrib>François, Jonas</creatorcontrib><creatorcontrib>Ray, Jayashree</creatorcontrib><creatorcontrib>Torralba, Babil</creatorcontrib><creatorcontrib>Arlat, Matthieu</creatorcontrib><creatorcontrib>Lewis, Jennifer D.</creatorcontrib><creatorcontrib>Lauber, Emmanuelle</creatorcontrib><creatorcontrib>Deutschbauer, Adam M.</creatorcontrib><creatorcontrib>Noël, Laurent D.</creatorcontrib><creatorcontrib>Boulanger, Alice</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>The New phytologist</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luneau, Julien S.</au><au>Baudin, Maël</au><au>Quiroz Monnens, Thomas</au><au>Carrère, Sébastien</au><au>Bouchez, Olivier</au><au>Jardinaud, Marie‐Françoise</au><au>Gris, Carine</au><au>François, Jonas</au><au>Ray, Jayashree</au><au>Torralba, Babil</au><au>Arlat, Matthieu</au><au>Lewis, Jennifer D.</au><au>Lauber, Emmanuelle</au><au>Deutschbauer, Adam M.</au><au>Noël, Laurent D.</au><au>Boulanger, Alice</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection</atitle><jtitle>The New phytologist</jtitle><addtitle>New Phytol</addtitle><date>2022-10</date><risdate>2022</risdate><volume>236</volume><issue>1</issue><spage>235</spage><epage>248</epage><pages>235-248</pages><issn>0028-646X</issn><eissn>1469-8137</eissn><abstract>Summary
Plant diseases are an important threat to food production. While major pathogenicity determinants required for disease have been extensively studied, less is known on how pathogens thrive during host colonization, especially at early infection stages.
Here, we used randomly barcoded‐transposon insertion site sequencing (RB‐TnSeq) to perform a genome‐wide screen and identify key bacterial fitness determinants of the vascular pathogen Xanthomonas campestris pv campestris (Xcc) during infection of the cauliflower host plant (Brassica oleracea). This high‐throughput analysis was conducted in hydathodes, the natural entry site of Xcc, in xylem sap and in synthetic media.
Xcc did not face a strong bottleneck during hydathode infection. In total, 181 genes important for fitness were identified in plant‐associated environments with functional enrichment in genes involved in metabolism but only few genes previously known to be involved in virulence. The biological relevance of 12 genes was independently confirmed by phenotyping single mutants. Notably, we show that XC_3388, a protein with no known function (DUF1631), plays a key role in the adaptation and virulence of Xcc possibly through c‐di‐GMP‐mediated regulation.
This study revealed yet unsuspected social behaviors adopted by Xcc individuals when confined inside hydathodes at early infection stages.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>35706385</pmid><doi>10.1111/nph.18313</doi><tpages>248</tpages><orcidid>https://orcid.org/0000-0002-0110-1423</orcidid><orcidid>https://orcid.org/0000-0001-6245-8920</orcidid><orcidid>https://orcid.org/0000-0001-5918-9547</orcidid><orcidid>https://orcid.org/0000-0001-5933-4476</orcidid><orcidid>https://orcid.org/0000-0002-2348-0778</orcidid><orcidid>https://orcid.org/0000-0003-1112-8723</orcidid><orcidid>https://orcid.org/0000-0001-8103-3813</orcidid><orcidid>https://orcid.org/0000-0001-6196-4856</orcidid><orcidid>https://orcid.org/0000-0002-7255-0058</orcidid><orcidid>https://orcid.org/0000-0001-8290-7527</orcidid><orcidid>https://orcid.org/0000-0003-4337-8292</orcidid><orcidid>https://orcid.org/0000-0002-1917-3468</orcidid><orcidid>https://orcid.org/0000-0003-3172-0150</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bacteriology Biochemistry, Molecular Biology Brassica Brassica oleracea Colonization Enrichment Fitness Food production Genes Genomes Genomics Host plants hydathodes Infections Life Sciences Metabolism Microbiology and Parasitology Pathogenicity Pathogens Phenotyping Phytopathology and phytopharmacy Plant bacterial diseases Plant diseases Plants RB‐TnSeq Social behavior Vegetal Biology Virulence Wide screen Xanthomonas Xanthomonas campestris Xylem |
title | Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection |
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