Antifungal Activities of Volatile Secondary Metabolites of Four Diaporthe Strains Isolated from Catharanthus roseus.
Identifieur interne : 000854 ( Main/Exploration ); précédent : 000853; suivant : 000855Antifungal Activities of Volatile Secondary Metabolites of Four Diaporthe Strains Isolated from Catharanthus roseus.
Auteurs : Dong-Hui Yan [République populaire de Chine] ; Xiaoyu Song [République populaire de Chine] ; Hongchang Li [République populaire de Chine] ; Tushou Luo [République populaire de Chine] ; Guiming Dou [République populaire de Chine] ; Gary Strobel [États-Unis]Source :
- Journal of fungi (Basel, Switzerland) [ 2309-608X ] ; 2018.
Abstract
Four endophytic fungi were isolated from the medicinal plant, Catharanthus roseus, and were identified as Diaporthe spp. with partial translation elongation factor 1-alpha (TEF1), beta-tubulin (TUB), histone H3 (HIS), calmodulin (CAL) genes, and rDNA internal transcribed spacer (ITS) region (TEF1-TUB-HIS--CAL-ITS) multigene phylogeny suggested for species delimitation in the Diaporthe genus. Each fungus produces a unique mixture of volatile organic compounds (VOCs) with an abundant mixture of terpenoids analyzed by headspace solid-phase microextraction (SPME) fiber-GC/MS. These tentatively-detected terpenes included α-muurolene, β-phellandrene, γ-terpinene, and α-thujene, as well as other minor terpenoids, including caryophyllene, patchoulene, cedrene, 2-carene, and thujone. The volatile metabolites of each isolate showed antifungal properties against a wide range of plant pathogenic test fungi and oomycetes, including Alternaria alternata, Botrytis cinerea, Colletotrichum gloeosporioides, Fusarium graminearum, and Phytophthora cinnamomi. The growth inhibition of the pathogens varied between 10% and 60% within 72 h of exposure. To our knowledge, the endophytic Diaporthe-like strains are first reported from Catharanthus roseus. VOCs produced by each strain of the endophytic Diaporthe fungi were unique components with dominant monoterpenes comparing to known Diaporthe fungal VOCs. A discussion is presented on the inhibitive bioactivities of secondary metabolites among endophytic Diaporthe fungi and this medicinal plant.
DOI: 10.3390/jof4020065
PubMed: 29848985
PubMed Central: PMC6023506
Affiliations:
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wicri:level="1"><nlm:affiliation>Research Institute of Forest Ecology, Environment and Protection, Chinese Academy of Forestry, Hai Dian District, Beijing 100091, China. yandh@caf.ac.cn.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Research Institute of Forest Ecology, Environment and Protection, Chinese Academy of Forestry, Hai Dian District, Beijing 100091</wicri:regionArea><placeName><settlement type="city">Pékin</settlement></placeName></affiliation></author><author><name sortKey="Song, Xiaoyu" sort="Song, Xiaoyu" uniqKey="Song X" first="Xiaoyu" last="Song">Xiaoyu Song</name><affiliation wicri:level="1"><nlm:affiliation>Research Institute of Forest Ecology, Environment and Protection, Chinese Academy of Forestry, Hai Dian District, Beijing 100091, China. songxiaoyucaf@gmail.com.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Research Institute of Forest Ecology, Environment and 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type="abstract" xml:lang="en">Four endophytic fungi were isolated from the medicinal plant, <i>Catharanthus roseus</i>, and were identified as <i>Diaporthe</i> spp. with partial translation elongation factor 1-alpha (<i>TEF1</i>), beta-tubulin (<i>TUB</i>), histone H3 (<i>HIS</i>), calmodulin (<i>CAL</i>) genes, and rDNA internal transcribed spacer (ITS) region (<i>TEF1</i>-<i>TUB</i>-<i>HIS</i>--<i>CAL</i>-ITS) multigene phylogeny suggested for species delimitation in the <i>Diaporthe</i> genus. Each fungus produces a unique mixture of volatile organic compounds (VOCs) with an abundant mixture of terpenoids analyzed by headspace solid-phase microextraction (SPME) fiber-GC/MS. These tentatively-detected terpenes included α-muurolene, β-phellandrene, γ-terpinene, and α-thujene, as well as other minor terpenoids, including caryophyllene, patchoulene, cedrene, 2-carene, and thujone. The volatile metabolites of each isolate showed antifungal properties against a wide range of plant pathogenic test fungi and oomycetes, including <i>Alternaria alternata</i>, <i>Botrytis cinerea</i>, <i>Colletotrichum gloeosporioides</i>, <i>Fusarium graminearum</i>, and <i>Phytophthora cinnamomi.</i> The growth inhibition of the pathogens varied between 10% and 60% within 72 h of exposure. To our knowledge, the endophytic <i>Diaporthe</i>-like strains are first reported from <i>Catharanthus roseus</i>. VOCs produced by each strain of the endophytic <i>Diaporthe</i> fungi were unique components with dominant monoterpenes comparing to known <i>Diaporthe</i> fungal VOCs. A discussion is presented on the inhibitive bioactivities of secondary metabolites among endophytic <i>Diaporthe</i> fungi and this medicinal plant.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">29848985</PMID><DateRevised><Year>2020</Year><Month>10</Month><Day>01</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">2309-608X</ISSN><JournalIssue CitedMedium="Internet"><Volume>4</Volume><Issue>2</Issue><PubDate><Year>2018</Year><Month>May</Month><Day>30</Day></PubDate></JournalIssue><Title>Journal of fungi (Basel, Switzerland)</Title><ISOAbbreviation>J Fungi (Basel)</ISOAbbreviation></Journal><ArticleTitle>Antifungal Activities of Volatile Secondary Metabolites of Four <i>Diaporthe</i> Strains Isolated from <i>Catharanthus roseus</i>.</ArticleTitle><ELocationID EIdType="pii" ValidYN="Y">E65</ELocationID><ELocationID EIdType="doi" ValidYN="Y">10.3390/jof4020065</ELocationID><Abstract><AbstractText>Four endophytic fungi were isolated from the medicinal plant, <i>Catharanthus roseus</i>, and were identified as <i>Diaporthe</i> spp. with partial translation elongation factor 1-alpha (<i>TEF1</i>), beta-tubulin (<i>TUB</i>), histone H3 (<i>HIS</i>), calmodulin (<i>CAL</i>) genes, and rDNA internal transcribed spacer (ITS) region (<i>TEF1</i>-<i>TUB</i>-<i>HIS</i>--<i>CAL</i>-ITS) multigene phylogeny suggested for species delimitation in the <i>Diaporthe</i> genus. Each fungus produces a unique mixture of volatile organic compounds (VOCs) with an abundant mixture of terpenoids analyzed by headspace solid-phase microextraction (SPME) fiber-GC/MS. These tentatively-detected terpenes included α-muurolene, β-phellandrene, γ-terpinene, and α-thujene, as well as other minor terpenoids, including caryophyllene, patchoulene, cedrene, 2-carene, and thujone. The volatile metabolites of each isolate showed antifungal properties against a wide range of plant pathogenic test fungi and oomycetes, including <i>Alternaria alternata</i>, <i>Botrytis cinerea</i>, <i>Colletotrichum gloeosporioides</i>, <i>Fusarium graminearum</i>, and <i>Phytophthora cinnamomi.</i> The growth inhibition of the pathogens varied between 10% and 60% within 72 h of exposure. To our knowledge, the endophytic <i>Diaporthe</i>-like strains are first reported from <i>Catharanthus roseus</i>. VOCs produced by each strain of the endophytic <i>Diaporthe</i> fungi were unique components with dominant monoterpenes comparing to known <i>Diaporthe</i> fungal VOCs. A discussion is presented on the inhibitive bioactivities of secondary metabolites among endophytic <i>Diaporthe</i> fungi and this medicinal plant.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Yan</LastName><ForeName>Dong-Hui</ForeName><Initials>DH</Initials><AffiliationInfo><Affiliation>Research Institute of Forest Ecology, Environment and Protection, Chinese Academy of Forestry, Hai Dian District, Beijing 100091, China. yandh@caf.ac.cn.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Song</LastName><ForeName>Xiaoyu</ForeName><Initials>X</Initials><AffiliationInfo><Affiliation>Research Institute of Forest Ecology, Environment and Protection, Chinese Academy of Forestry, Hai Dian District, Beijing 100091, China. songxiaoyucaf@gmail.com.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Li</LastName><ForeName>Hongchang</ForeName><Initials>H</Initials><AffiliationInfo><Affiliation>Research Institute of Forest Ecology, Environment and Protection, Chinese Academy of Forestry, Hai Dian District, Beijing 100091, China. lhc1994224@163.com.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Luo</LastName><ForeName>Tushou</ForeName><Initials>T</Initials><AffiliationInfo><Affiliation>Research Institute of Tropical Forestry, Chinese Academy of Forestry, Tianhe District, Guangzhou 510520, China. luots@126.com.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Dou</LastName><ForeName>Guiming</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>Research Institute of Forest Ecology, Environment and Protection, Chinese Academy of Forestry, Hai Dian District, Beijing 100091, China. dgmgogogo@126.com.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Strobel</LastName><ForeName>Gary</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>Department of Plant Sciences, Montana State University, Bozeman, MT 59717, USA. uplgs@montana.edu.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2018</Year><Month>05</Month><Day>30</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>J Fungi (Basel)</MedlineTA><NlmUniqueID>101671827</NlmUniqueID><ISSNLinking>2309-608X</ISSNLinking></MedlineJournalInfo><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Catharanthus roseus</Keyword><Keyword MajorTopicYN="N">Diaporthe spp.</Keyword><Keyword MajorTopicYN="N">antifungal bioactivity</Keyword><Keyword MajorTopicYN="N">endophytic fungi</Keyword><Keyword MajorTopicYN="N">inhibition</Keyword><Keyword MajorTopicYN="N">pathogens</Keyword><Keyword MajorTopicYN="N">terpene</Keyword><Keyword MajorTopicYN="N">volatile organic compounds (VOCs)</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2018</Year><Month>05</Month><Day>01</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2018</Year><Month>05</Month><Day>25</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2018</Year><Month>05</Month><Day>29</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2018</Year><Month>6</Month><Day>1</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2018</Year><Month>6</Month><Day>1</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2018</Year><Month>6</Month><Day>1</Day><Hour>6</Hour><Minute>1</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">29848985</ArticleId><ArticleId IdType="pii">jof4020065</ArticleId><ArticleId IdType="doi">10.3390/jof4020065</ArticleId><ArticleId 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Chine</li><li>États-Unis</li></country><region><li>Guangdong</li><li>Montana</li></region><settlement><li>Jiangmen</li><li>Pékin</li></settlement></list><tree><country name="République populaire de Chine"><noRegion><name sortKey="Yan, Dong Hui" sort="Yan, Dong Hui" uniqKey="Yan D" first="Dong-Hui" last="Yan">Dong-Hui Yan</name></noRegion><name sortKey="Dou, Guiming" sort="Dou, Guiming" uniqKey="Dou G" first="Guiming" last="Dou">Guiming Dou</name><name sortKey="Li, Hongchang" sort="Li, Hongchang" uniqKey="Li H" first="Hongchang" last="Li">Hongchang Li</name><name sortKey="Luo, Tushou" sort="Luo, Tushou" uniqKey="Luo T" first="Tushou" last="Luo">Tushou Luo</name><name sortKey="Song, Xiaoyu" sort="Song, Xiaoyu" uniqKey="Song X" first="Xiaoyu" last="Song">Xiaoyu Song</name></country><country name="États-Unis"><region name="Montana"><name sortKey="Strobel, Gary" sort="Strobel, Gary" uniqKey="Strobel G" first="Gary" last="Strobel">Gary 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