Switchable Nitroproteome States of Phytophthora infestans Biology and Pathobiology.
Identifieur interne : 000378 ( Main/Exploration ); précédent : 000377; suivant : 000379Switchable Nitroproteome States of Phytophthora infestans Biology and Pathobiology.
Auteurs : Karolina Izbia Ska [Pologne] ; Jolanta Floryszak-Wieczorek [Pologne] ; Joanna Gajewska [Pologne] ; Jarosław Gzyl [Pologne] ; Tomasz Jelonek [Pologne] ; Magdalena Arasimowicz-Jelonek [Pologne]Source :
- Frontiers in microbiology [ 1664-302X ] ; 2019.
Abstract
The study demonstrates protein tyrosine nitration as a functional post-translational modification (PTM) in biology and pathobiology of the oomycete Phytophthora infestans (Mont.) de Bary, the most harmful pathogen of potato (Solanum tuberosum L.). Using two P. infestans isolates differing in their virulence toward potato cv. Sarpo Mira we found that the pathogen generates reactive nitrogen species (RNS) in hyphae and mature sporangia growing under in vitro and in planta conditions. However, acceleration of peroxynitrite formation and elevation of the nitrated protein pool within pathogen structures were observed mainly during the avr P. infestans MP 946-potato interaction. Importantly, the nitroproteome profiles varied for the pathogen virulence pattern and comparative analysis revealed that vr MP 977 P. infestans represented a much more diverse quality spectrum of nitrated proteins. Abundance profiles of nitrated proteins that were up- or downregulated were substantially different also between the analyzed growth phases. Briefly, in planta growth of avr and vr P. infestans was accompanied by exclusive nitration of proteins involved in energy metabolism, signal transduction and pathogenesis. Importantly, the P. infestans-potato interaction indicated cytosolic RXLRs and Crinklers effectors as potential sensors of RNS. Taken together, we explored the first plant pathogen nitroproteome. The results present new insights into RNS metabolism in P. infestans indicating protein nitration as an integral part of pathogen biology, dynamically modified during its offensive strategy. Thus, the nitroproteome should be considered as a flexible element of the oomycete developmental and adaptive mechanism to different micro-environments, including host cells.
DOI: 10.3389/fmicb.2019.01516
PubMed: 31379758
PubMed Central: PMC6647872
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Poznań</wicri:regionArea><wicri:noRegion>Poznań</wicri:noRegion></affiliation></author><author><name sortKey="Floryszak Wieczorek, Jolanta" sort="Floryszak Wieczorek, Jolanta" uniqKey="Floryszak Wieczorek J" first="Jolanta" last="Floryszak-Wieczorek">Jolanta Floryszak-Wieczorek</name><affiliation wicri:level="1"><nlm:affiliation>Department of Plant Physiology, Faculty of Horticulture and Landscape Architecture, Poznań University of Life Sciences, Poznań, Poland.</nlm:affiliation><country xml:lang="fr">Pologne</country><wicri:regionArea>Department of Plant Physiology, Faculty of Horticulture and Landscape Architecture, Poznań University of Life Sciences, Poznań</wicri:regionArea><wicri:noRegion>Poznań</wicri:noRegion></affiliation></author><author><name sortKey="Gajewska, Joanna" sort="Gajewska, Joanna" uniqKey="Gajewska J" first="Joanna" last="Gajewska">Joanna Gajewska</name><affiliation wicri:level="1"><nlm:affiliation>Department of Plant Ecophysiology, Faculty of Biology, Adam Mickiewicz University in Poznań, Poznań, Poland.</nlm:affiliation><country xml:lang="fr">Pologne</country><wicri:regionArea>Department of Plant Ecophysiology, Faculty of Biology, Adam Mickiewicz University in Poznań, Poznań</wicri:regionArea><wicri:noRegion>Poznań</wicri:noRegion></affiliation></author><author><name sortKey="Gzyl, Jaroslaw" sort="Gzyl, Jaroslaw" uniqKey="Gzyl J" first="Jarosław" last="Gzyl">Jarosław Gzyl</name><affiliation wicri:level="1"><nlm:affiliation>Department of Plant Ecophysiology, Faculty of Biology, Adam Mickiewicz University in Poznań, Poznań, Poland.</nlm:affiliation><country xml:lang="fr">Pologne</country><wicri:regionArea>Department of Plant Ecophysiology, Faculty of Biology, Adam Mickiewicz University in Poznań, Poznań</wicri:regionArea><wicri:noRegion>Poznań</wicri:noRegion></affiliation></author><author><name sortKey="Jelonek, Tomasz" sort="Jelonek, Tomasz" uniqKey="Jelonek T" first="Tomasz" last="Jelonek">Tomasz Jelonek</name><affiliation wicri:level="1"><nlm:affiliation>Department of Forest Utilization, Faculty of Forestry, Poznań University of Life Sciences, Poznań, Poland.</nlm:affiliation><country xml:lang="fr">Pologne</country><wicri:regionArea>Department of Forest Utilization, Faculty of Forestry, Poznań University of Life Sciences, Poznań</wicri:regionArea><wicri:noRegion>Poznań</wicri:noRegion></affiliation></author><author><name sortKey="Arasimowicz Jelonek, Magdalena" sort="Arasimowicz Jelonek, Magdalena" uniqKey="Arasimowicz Jelonek M" first="Magdalena" last="Arasimowicz-Jelonek">Magdalena Arasimowicz-Jelonek</name><affiliation wicri:level="1"><nlm:affiliation>Department of Plant Ecophysiology, Faculty of Biology, Adam Mickiewicz University in Poznań, Poznań, Poland.</nlm:affiliation><country xml:lang="fr">Pologne</country><wicri:regionArea>Department of Plant Ecophysiology, Faculty of Biology, Adam Mickiewicz University in Poznań, Poznań</wicri:regionArea><wicri:noRegion>Poznań</wicri:noRegion></affiliation></author></analytic><series><title level="j">Frontiers in microbiology</title><idno type="ISSN">1664-302X</idno><imprint><date when="2019" type="published">2019</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The study demonstrates protein tyrosine nitration as a functional post-translational modification (PTM) in biology and pathobiology of the oomycete <i>Phytophthora infestans</i> (Mont.) de Bary, the most harmful pathogen of potato (<i>Solanum tuberosum</i> L.). Using two <i>P. infestans</i> isolates differing in their virulence toward potato cv. Sarpo Mira we found that the pathogen generates reactive nitrogen species (RNS) in hyphae and mature sporangia growing under <i>in vitro</i> and <i>in planta</i> conditions. However, acceleration of peroxynitrite formation and elevation of the nitrated protein pool within pathogen structures were observed mainly during the <i>avr P. infestans</i> MP 946-potato interaction. Importantly, the nitroproteome profiles varied for the pathogen virulence pattern and comparative analysis revealed that <i>vr</i> MP 977 <i>P. infestans</i> represented a much more diverse quality spectrum of nitrated proteins. Abundance profiles of nitrated proteins that were up- or downregulated were substantially different also between the analyzed growth phases. Briefly, <i>in planta</i> growth of <i>avr</i> and <i>vr P. infestans</i> was accompanied by exclusive nitration of proteins involved in energy metabolism, signal transduction and pathogenesis. Importantly, the <i>P. infestans-</i>potato interaction indicated cytosolic RXLRs and Crinklers effectors as potential sensors of RNS. Taken together, we explored the first plant pathogen nitroproteome. The results present new insights into RNS metabolism in <i>P. infestans</i> indicating protein nitration as an integral part of pathogen biology, dynamically modified during its offensive strategy. Thus, the nitroproteome should be considered as a flexible element of the oomycete developmental and adaptive mechanism to different micro-environments, including host cells.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">31379758</PMID><DateRevised><Year>2020</Year><Month>10</Month><Day>01</Day></DateRevised><Article PubModel="Electronic-eCollection"><Journal><ISSN IssnType="Print">1664-302X</ISSN><JournalIssue CitedMedium="Print"><Volume>10</Volume><PubDate><Year>2019</Year></PubDate></JournalIssue><Title>Frontiers in microbiology</Title><ISOAbbreviation>Front Microbiol</ISOAbbreviation></Journal><ArticleTitle>Switchable Nitroproteome States of <i>Phytophthora infestans</i> Biology and Pathobiology.</ArticleTitle><Pagination><MedlinePgn>1516</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.3389/fmicb.2019.01516</ELocationID><Abstract><AbstractText>The study demonstrates protein tyrosine nitration as a functional post-translational modification (PTM) in biology and pathobiology of the oomycete <i>Phytophthora infestans</i> (Mont.) de Bary, the most harmful pathogen of potato (<i>Solanum tuberosum</i> L.). Using two <i>P. infestans</i> isolates differing in their virulence toward potato cv. Sarpo Mira we found that the pathogen generates reactive nitrogen species (RNS) in hyphae and mature sporangia growing under <i>in vitro</i> and <i>in planta</i> conditions. However, acceleration of peroxynitrite formation and elevation of the nitrated protein pool within pathogen structures were observed mainly during the <i>avr P. infestans</i> MP 946-potato interaction. Importantly, the nitroproteome profiles varied for the pathogen virulence pattern and comparative analysis revealed that <i>vr</i> MP 977 <i>P. infestans</i> represented a much more diverse quality spectrum of nitrated proteins. Abundance profiles of nitrated proteins that were up- or downregulated were substantially different also between the analyzed growth phases. Briefly, <i>in planta</i> growth of <i>avr</i> and <i>vr P. infestans</i> was accompanied by exclusive nitration of proteins involved in energy metabolism, signal transduction and pathogenesis. Importantly, the <i>P. infestans-</i>potato interaction indicated cytosolic RXLRs and Crinklers effectors as potential sensors of RNS. Taken together, we explored the first plant pathogen nitroproteome. The results present new insights into RNS metabolism in <i>P. infestans</i> indicating protein nitration as an integral part of pathogen biology, dynamically modified during its offensive strategy. Thus, the nitroproteome should be considered as a flexible element of the oomycete developmental and adaptive mechanism to different micro-environments, including host cells.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Izbiańska</LastName><ForeName>Karolina</ForeName><Initials>K</Initials><AffiliationInfo><Affiliation>Department of Plant Ecophysiology, Faculty of Biology, Adam Mickiewicz University in Poznań, Poznań, Poland.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Floryszak-Wieczorek</LastName><ForeName>Jolanta</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Department of Plant Physiology, Faculty of Horticulture and Landscape Architecture, Poznań University of Life Sciences, Poznań, Poland.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Gajewska</LastName><ForeName>Joanna</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Department of Plant Ecophysiology, Faculty of Biology, Adam Mickiewicz University in Poznań, Poznań, Poland.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Gzyl</LastName><ForeName>Jarosław</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Department of Plant Ecophysiology, Faculty of Biology, Adam Mickiewicz University in Poznań, Poznań, Poland.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Jelonek</LastName><ForeName>Tomasz</ForeName><Initials>T</Initials><AffiliationInfo><Affiliation>Department of Forest Utilization, Faculty of Forestry, Poznań University of Life Sciences, Poznań, Poland.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Arasimowicz-Jelonek</LastName><ForeName>Magdalena</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Department of Plant Ecophysiology, Faculty of Biology, Adam Mickiewicz University in Poznań, Poznań, Poland.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2019</Year><Month>07</Month><Day>16</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Front Microbiol</MedlineTA><NlmUniqueID>101548977</NlmUniqueID><ISSNLinking>1664-302X</ISSNLinking></MedlineJournalInfo><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Phytophthora infestans</Keyword><Keyword MajorTopicYN="N">late blight</Keyword><Keyword MajorTopicYN="N">pathogen offensive strategy</Keyword><Keyword MajorTopicYN="N">peroxynitrite</Keyword><Keyword MajorTopicYN="N">potato</Keyword><Keyword MajorTopicYN="N">protein tyrosine nitration</Keyword><Keyword MajorTopicYN="N">reactive nitrogen species</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate 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Ska</name></noRegion><name sortKey="Arasimowicz Jelonek, Magdalena" sort="Arasimowicz Jelonek, Magdalena" uniqKey="Arasimowicz Jelonek M" first="Magdalena" last="Arasimowicz-Jelonek">Magdalena Arasimowicz-Jelonek</name><name sortKey="Floryszak Wieczorek, Jolanta" sort="Floryszak Wieczorek, Jolanta" uniqKey="Floryszak Wieczorek J" first="Jolanta" last="Floryszak-Wieczorek">Jolanta Floryszak-Wieczorek</name><name sortKey="Gajewska, Joanna" sort="Gajewska, Joanna" uniqKey="Gajewska J" first="Joanna" last="Gajewska">Joanna Gajewska</name><name sortKey="Gzyl, Jaroslaw" sort="Gzyl, Jaroslaw" uniqKey="Gzyl J" first="Jarosław" last="Gzyl">Jarosław Gzyl</name><name sortKey="Jelonek, Tomasz" sort="Jelonek, Tomasz" uniqKey="Jelonek T" first="Tomasz" last="Jelonek">Tomasz Jelonek</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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