Oxalic Acid Metabolism Contributes to Full Virulence and Pycnidial Development in the Poplar Canker Fungus Cytospora chrysosperma.
Identifieur interne : 000230 ( Main/Exploration ); précédent : 000229; suivant : 000231Oxalic Acid Metabolism Contributes to Full Virulence and Pycnidial Development in the Poplar Canker Fungus Cytospora chrysosperma.
Auteurs : Yuanyuan Wang [République populaire de Chine] ; Yonglin Wang [République populaire de Chine]Source :
- Phytopathology [ 0031-949X ] ; 2020.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical : Oxalic Acid.
- Ascomycota, Plant Diseases, Populus, Virulence.
Abstract
Poplar Cytospora canker, which is mainly caused by Cytospora chrysosperma, is one of the most destructive and widespread tree diseases worldwide. Although oxalic acid (OA) is demonstrated as an important virulence determinant in several necrotrophic fungi, specific functions of OA during pathogenesis remain controversial. Here, we identified three genes (CcOah, CcOdc1, and CcOdc2) directly involved in OA biosynthesis and catabolism in C. chrysosperma. We demonstrated that CcOah is required for OA biogenesis. All three genes were found to be highly upregulated during early infection stages of the poplar stem. The deletion of any of the three genes led to an obvious reduction of pycnidial production but no abnormality of hyphal growth and morphology. Furthermore, the individual deletion strain exhibited significantly limited lesion sizes on poplar twigs and leaves. Exogenous application of OA or citric acid can complement the virulence defects of ΔCcOah and ΔCcOdc1 strains. We further found that the ΔCcOah strain strongly promoted reactive oxygen species burst of poplar leaves during infection. Finally, induced secretion of OA was observed by monitoring color change of the plates after poplar stem extracts were added in the cultures; however, we failed to quantify OA concentration by high-performance liquid chromatography. Taken together, the present results provide insights into the function of OA acting as an important virulence factor of C. chrysosperma.
DOI: 10.1094/PHYTO-10-19-0381-R
PubMed: 32154765
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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<author><name sortKey="Wang, Yuanyuan" sort="Wang, Yuanyuan" uniqKey="Wang Y" first="Yuanyuan" last="Wang">Yuanyuan Wang</name>
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<author><name sortKey="Wang, Yonglin" sort="Wang, Yonglin" uniqKey="Wang Y" first="Yonglin" last="Wang">Yonglin Wang</name>
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<term>Oxalic Acid (MeSH)</term>
<term>Plant Diseases (MeSH)</term>
<term>Populus (MeSH)</term>
<term>Virulence (MeSH)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Acide oxalique (MeSH)</term>
<term>Ascomycota (MeSH)</term>
<term>Maladies des plantes (MeSH)</term>
<term>Populus (MeSH)</term>
<term>Virulence (MeSH)</term>
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<term>Plant Diseases</term>
<term>Populus</term>
<term>Virulence</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Acide oxalique</term>
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<front><div type="abstract" xml:lang="en">Poplar Cytospora canker, which is mainly caused by <i>Cytospora chrysosperma</i>
, is one of the most destructive and widespread tree diseases worldwide. Although oxalic acid (OA) is demonstrated as an important virulence determinant in several necrotrophic fungi, specific functions of OA during pathogenesis remain controversial. Here, we identified three genes (<i>CcOah</i>
, <i>CcOdc1,</i>
and <i>CcOdc2</i>
) directly involved in OA biosynthesis and catabolism in <i>C. chrysosperma</i>
. We demonstrated that <i>CcOah</i>
is required for OA biogenesis. All three genes were found to be highly upregulated during early infection stages of the poplar stem. The deletion of any of the three genes led to an obvious reduction of pycnidial production but no abnormality of hyphal growth and morphology. Furthermore, the individual deletion strain exhibited significantly limited lesion sizes on poplar twigs and leaves. Exogenous application of OA or citric acid can complement the virulence defects of Δ<i>CcOah</i>
and Δ<i>CcOdc1</i>
strains. We further found that the Δ<i>CcOah</i>
strain strongly promoted reactive oxygen species burst of poplar leaves during infection. Finally, induced secretion of OA was observed by monitoring color change of the plates after poplar stem extracts were added in the cultures; however, we failed to quantify OA concentration by high-performance liquid chromatography. Taken together, the present results provide insights into the function of OA acting as an important virulence factor of <i>C. chrysosperma</i>
.</div>
</front>
</TEI>
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<ArticleTitle>Oxalic Acid Metabolism Contributes to Full Virulence and Pycnidial Development in the Poplar Canker Fungus <i>Cytospora chrysosperma</i>
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<Abstract><AbstractText>Poplar Cytospora canker, which is mainly caused by <i>Cytospora chrysosperma</i>
, is one of the most destructive and widespread tree diseases worldwide. Although oxalic acid (OA) is demonstrated as an important virulence determinant in several necrotrophic fungi, specific functions of OA during pathogenesis remain controversial. Here, we identified three genes (<i>CcOah</i>
, <i>CcOdc1,</i>
and <i>CcOdc2</i>
) directly involved in OA biosynthesis and catabolism in <i>C. chrysosperma</i>
. We demonstrated that <i>CcOah</i>
is required for OA biogenesis. All three genes were found to be highly upregulated during early infection stages of the poplar stem. The deletion of any of the three genes led to an obvious reduction of pycnidial production but no abnormality of hyphal growth and morphology. Furthermore, the individual deletion strain exhibited significantly limited lesion sizes on poplar twigs and leaves. Exogenous application of OA or citric acid can complement the virulence defects of Δ<i>CcOah</i>
and Δ<i>CcOdc1</i>
strains. We further found that the Δ<i>CcOah</i>
strain strongly promoted reactive oxygen species burst of poplar leaves during infection. Finally, induced secretion of OA was observed by monitoring color change of the plates after poplar stem extracts were added in the cultures; however, we failed to quantify OA concentration by high-performance liquid chromatography. Taken together, the present results provide insights into the function of OA acting as an important virulence factor of <i>C. chrysosperma</i>
.</AbstractText>
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