Mycorrhization alleviates benzo[a]pyrene-induced oxidative stress in an in vitro chicory root model.
Identifieur interne : 002829 ( Main/Exploration ); précédent : 002828; suivant : 002830Mycorrhization alleviates benzo[a]pyrene-induced oxidative stress in an in vitro chicory root model.
Auteurs : Djouher Debiane [France] ; Guillaume Garçon ; Anthony Verdin ; Joël Fontaine ; Roger Durand ; Pirouz Shirali ; Anne Grandmougin-Ferjani ; Anissa Lounès-Hadj SahraouiSource :
- Phytochemistry [ 1873-3700 ]
Descripteurs français
- KwdFr :
- Benzo[a]pyrène (toxicité), Chicorée (effets des médicaments et des substances chimiques), Désoxyguanosine (analogues et dérivés), Désoxyguanosine (biosynthèse), Glomeromycota (croissance et développement), Malonaldéhyde (métabolisme), Mycorhizes (physiologie), Protéines végétales (MeSH), Racines de plante (effets des médicaments et des substances chimiques), Stress oxydatif (MeSH), Superoxide dismutase (métabolisme).
- MESH :
- analogues et dérivés : Désoxyguanosine.
- biosynthèse : Désoxyguanosine.
- croissance et développement : Glomeromycota.
- effets des médicaments et des substances chimiques : Chicorée, Racines de plante.
- métabolisme : Malonaldéhyde, Superoxide dismutase.
- physiologie : Mycorhizes.
- toxicité : Benzo[a]pyrène.
- Protéines végétales, Stress oxydatif.
English descriptors
- KwdEn :
- 8-Hydroxy-2'-Deoxyguanosine (MeSH), Benzo(a)pyrene (toxicity), Chicory (drug effects), Deoxyguanosine (analogs & derivatives), Deoxyguanosine (biosynthesis), Glomeromycota (growth & development), Malondialdehyde (metabolism), Mycorrhizae (physiology), Oxidative Stress (MeSH), Plant Proteins (MeSH), Plant Roots (drug effects), Superoxide Dismutase (metabolism).
- MESH :
- chemical , analogs & derivatives : Deoxyguanosine.
- chemical , biosynthesis : Deoxyguanosine.
- chemical , metabolism : Malondialdehyde, Superoxide Dismutase.
- chemical , toxicity : Benzo(a)pyrene.
- chemical : 8-Hydroxy-2'-Deoxyguanosine, Plant Proteins.
- drug effects : Chicory, Plant Roots.
- growth & development : Glomeromycota.
- physiology : Mycorrhizae.
- Oxidative Stress.
Abstract
Among chemicals that are widely spread both in terrestrial and aquatic ecosystems, benzo[a]pyrene is a major source of concern. However, little is known about its adverse effects on plants, as well as about the role of mycorrhization in protection of plant grown in benzo[a]pyrene-polluted conditions. Hence, to contribute to a better understanding of the adverse effects of polycyclic aromatic hydrocarbons on the partners of mycorrhizal symbiotic association, benzo[a]pyrene-induced oxidative stress was studied in transformed Cichorium intybus roots grown in vitro and colonized or not by Glomus intraradices. The arbuscular mycorrhizal fungus development (colonization, extraradical hyphae length, and spore formation) was significantly reduced in response to increasing concentrations of benzo[a]pyrene (35-280 microM). The higher length of arbuscular mycorrhizal roots, compared to non-arbuscular mycorrhizal roots following benzo[a]pyrene exposure, pointed out a lower toxicity of benzo[a]pyrene in arbuscular mycorrhizal roots, thereby suggesting protection of the roots by mycorrhization. Accordingly, in benzo[a]pyrene-exposed arbuscular mycorrhizal roots, statistically significant decreases were observed in malondialdehyde concentration and 8-hydroxy-2'-desoxyguanosine formation. The higher superoxide dismutase activity detected in mycorrhizal chicory roots could explain the benzo[a]pyrene tolerance of the colonized roots. Taken together, these results support an essential role of mycorrhizal fungi in protecting plants submitted to polycyclic aromatic hydrocarbon, notably by reducing polycyclic aromatic hydrocarbon-induced oxidative stress damage.
DOI: 10.1016/j.phytochem.2009.07.002
PubMed: 19758666
Affiliations:
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sort="Grandmougin Ferjani, Anne" uniqKey="Grandmougin Ferjani A" first="Anne" last="Grandmougin-Ferjani">Anne Grandmougin-Ferjani</name></author><author><name sortKey="Lounes Hadj Sahraoui, Anissa" sort="Lounes Hadj Sahraoui, Anissa" uniqKey="Lounes Hadj Sahraoui A" first="Anissa" last="Lounès-Hadj Sahraoui">Anissa Lounès-Hadj Sahraoui</name></author></analytic><series><title level="j">Phytochemistry</title><idno type="eISSN">1873-3700</idno></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>8-Hydroxy-2'-Deoxyguanosine (MeSH)</term><term>Benzo(a)pyrene (toxicity)</term><term>Chicory (drug effects)</term><term>Deoxyguanosine (analogs & derivatives)</term><term>Deoxyguanosine (biosynthesis)</term><term>Glomeromycota (growth & development)</term><term>Malondialdehyde (metabolism)</term><term>Mycorrhizae (physiology)</term><term>Oxidative Stress (MeSH)</term><term>Plant Proteins (MeSH)</term><term>Plant Roots (drug effects)</term><term>Superoxide Dismutase (metabolism)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Benzo[a]pyrène (toxicité)</term><term>Chicorée (effets des médicaments et des substances chimiques)</term><term>Désoxyguanosine (analogues et dérivés)</term><term>Désoxyguanosine (biosynthèse)</term><term>Glomeromycota (croissance et développement)</term><term>Malonaldéhyde (métabolisme)</term><term>Mycorhizes (physiologie)</term><term>Protéines végétales (MeSH)</term><term>Racines de plante (effets des médicaments et des substances chimiques)</term><term>Stress oxydatif (MeSH)</term><term>Superoxide dismutase (métabolisme)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analogs & derivatives" xml:lang="en"><term>Deoxyguanosine</term></keywords><keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Deoxyguanosine</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Malondialdehyde</term><term>Superoxide Dismutase</term></keywords><keywords scheme="MESH" type="chemical" qualifier="toxicity" xml:lang="en"><term>Benzo(a)pyrene</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>8-Hydroxy-2'-Deoxyguanosine</term><term>Plant Proteins</term></keywords><keywords scheme="MESH" qualifier="analogues et dérivés" xml:lang="fr"><term>Désoxyguanosine</term></keywords><keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>Désoxyguanosine</term></keywords><keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr"><term>Glomeromycota</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Chicory</term><term>Plant Roots</term></keywords><keywords scheme="MESH" qualifier="effets des médicaments et des substances chimiques" xml:lang="fr"><term>Chicorée</term><term>Racines de plante</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Glomeromycota</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Malonaldéhyde</term><term>Superoxide dismutase</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Mycorhizes</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Mycorrhizae</term></keywords><keywords scheme="MESH" qualifier="toxicité" xml:lang="fr"><term>Benzo[a]pyrène</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Oxidative Stress</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Protéines végétales</term><term>Stress oxydatif</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Among chemicals that are widely spread both in terrestrial and aquatic ecosystems, benzo[a]pyrene is a major source of concern. However, little is known about its adverse effects on plants, as well as about the role of mycorrhization in protection of plant grown in benzo[a]pyrene-polluted conditions. Hence, to contribute to a better understanding of the adverse effects of polycyclic aromatic hydrocarbons on the partners of mycorrhizal symbiotic association, benzo[a]pyrene-induced oxidative stress was studied in transformed Cichorium intybus roots grown in vitro and colonized or not by Glomus intraradices. The arbuscular mycorrhizal fungus development (colonization, extraradical hyphae length, and spore formation) was significantly reduced in response to increasing concentrations of benzo[a]pyrene (35-280 microM). The higher length of arbuscular mycorrhizal roots, compared to non-arbuscular mycorrhizal roots following benzo[a]pyrene exposure, pointed out a lower toxicity of benzo[a]pyrene in arbuscular mycorrhizal roots, thereby suggesting protection of the roots by mycorrhization. Accordingly, in benzo[a]pyrene-exposed arbuscular mycorrhizal roots, statistically significant decreases were observed in malondialdehyde concentration and 8-hydroxy-2'-desoxyguanosine formation. The higher superoxide dismutase activity detected in mycorrhizal chicory roots could explain the benzo[a]pyrene tolerance of the colonized roots. Taken together, these results support an essential role of mycorrhizal fungi in protecting plants submitted to polycyclic aromatic hydrocarbon, notably by reducing polycyclic aromatic hydrocarbon-induced oxidative stress damage.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">19758666</PMID><DateCompleted><Year>2010</Year><Month>01</Month><Day>13</Day></DateCompleted><DateRevised><Year>2019</Year><Month>12</Month><Day>10</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1873-3700</ISSN><JournalIssue CitedMedium="Internet"><Volume>70</Volume><Issue>11-12</Issue><PubDate><MedlineDate>2009 Jul-Aug</MedlineDate></PubDate></JournalIssue><Title>Phytochemistry</Title><ISOAbbreviation>Phytochemistry</ISOAbbreviation></Journal><ArticleTitle>Mycorrhization alleviates benzo[a]pyrene-induced oxidative stress in an in vitro chicory root model.</ArticleTitle><Pagination><MedlinePgn>1421-7</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.phytochem.2009.07.002</ELocationID><Abstract><AbstractText>Among chemicals that are widely spread both in terrestrial and aquatic ecosystems, benzo[a]pyrene is a major source of concern. However, little is known about its adverse effects on plants, as well as about the role of mycorrhization in protection of plant grown in benzo[a]pyrene-polluted conditions. Hence, to contribute to a better understanding of the adverse effects of polycyclic aromatic hydrocarbons on the partners of mycorrhizal symbiotic association, benzo[a]pyrene-induced oxidative stress was studied in transformed Cichorium intybus roots grown in vitro and colonized or not by Glomus intraradices. The arbuscular mycorrhizal fungus development (colonization, extraradical hyphae length, and spore formation) was significantly reduced in response to increasing concentrations of benzo[a]pyrene (35-280 microM). The higher length of arbuscular mycorrhizal roots, compared to non-arbuscular mycorrhizal roots following benzo[a]pyrene exposure, pointed out a lower toxicity of benzo[a]pyrene in arbuscular mycorrhizal roots, thereby suggesting protection of the roots by mycorrhization. Accordingly, in benzo[a]pyrene-exposed arbuscular mycorrhizal roots, statistically significant decreases were observed in malondialdehyde concentration and 8-hydroxy-2'-desoxyguanosine formation. The higher superoxide dismutase activity detected in mycorrhizal chicory roots could explain the benzo[a]pyrene tolerance of the colonized roots. Taken together, these results support an essential role of mycorrhizal fungi in protecting plants submitted to polycyclic aromatic hydrocarbon, notably by reducing polycyclic aromatic hydrocarbon-induced oxidative stress damage.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Debiane</LastName><ForeName>Djouher</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Univ Lille Nord de France, F-59000 Lille, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Garçon</LastName><ForeName>Guillaume</ForeName><Initials>G</Initials></Author><Author ValidYN="Y"><LastName>Verdin</LastName><ForeName>Anthony</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Fontaine</LastName><ForeName>Joël</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Durand</LastName><ForeName>Roger</ForeName><Initials>R</Initials></Author><Author ValidYN="Y"><LastName>Shirali</LastName><ForeName>Pirouz</ForeName><Initials>P</Initials></Author><Author ValidYN="Y"><LastName>Grandmougin-Ferjani</LastName><ForeName>Anne</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Lounès-Hadj Sahraoui</LastName><ForeName>Anissa</ForeName><Initials>A</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2009</Year><Month>09</Month><Day>14</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Phytochemistry</MedlineTA><NlmUniqueID>0151434</NlmUniqueID><ISSNLinking>0031-9422</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010940">Plant Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>3417WMA06D</RegistryNumber><NameOfSubstance UI="D001564">Benzo(a)pyrene</NameOfSubstance></Chemical><Chemical><RegistryNumber>4Y8F71G49Q</RegistryNumber><NameOfSubstance UI="D008315">Malondialdehyde</NameOfSubstance></Chemical><Chemical><RegistryNumber>88847-89-6</RegistryNumber><NameOfSubstance UI="D000080242">8-Hydroxy-2'-Deoxyguanosine</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.15.1.1</RegistryNumber><NameOfSubstance UI="D013482">Superoxide Dismutase</NameOfSubstance></Chemical><Chemical><RegistryNumber>G9481N71RO</RegistryNumber><NameOfSubstance UI="D003849">Deoxyguanosine</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000080242" MajorTopicYN="N">8-Hydroxy-2'-Deoxyguanosine</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001564" MajorTopicYN="N">Benzo(a)pyrene</DescriptorName><QualifierName UI="Q000633" MajorTopicYN="Y">toxicity</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018651" MajorTopicYN="N">Chicory</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003849" MajorTopicYN="N">Deoxyguanosine</DescriptorName><QualifierName UI="Q000031" MajorTopicYN="N">analogs & derivatives</QualifierName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D055137" MajorTopicYN="N">Glomeromycota</DescriptorName><QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008315" MajorTopicYN="N">Malondialdehyde</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018384" MajorTopicYN="Y">Oxidative Stress</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018517" MajorTopicYN="N">Plant Roots</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013482" MajorTopicYN="N">Superoxide Dismutase</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2009</Year><Month>01</Month><Day>23</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2009</Year><Month>06</Month><Day>25</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2009</Year><Month>07</Month><Day>01</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2009</Year><Month>9</Month><Day>18</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2009</Year><Month>9</Month><Day>18</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2010</Year><Month>1</Month><Day>14</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">19758666</ArticleId><ArticleId IdType="pii">S0031-9422(09)00276-3</ArticleId><ArticleId IdType="doi">10.1016/j.phytochem.2009.07.002</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>France</li></country><region><li>Hauts-de-France</li><li>Nord-Pas-de-Calais</li></region><settlement><li>Lille</li></settlement></list><tree><noCountry><name sortKey="Durand, Roger" sort="Durand, Roger" uniqKey="Durand R" first="Roger" last="Durand">Roger Durand</name><name sortKey="Fontaine, Joel" sort="Fontaine, Joel" uniqKey="Fontaine J" first="Joël" last="Fontaine">Joël Fontaine</name><name sortKey="Garcon, Guillaume" sort="Garcon, Guillaume" uniqKey="Garcon G" first="Guillaume" last="Garçon">Guillaume Garçon</name><name sortKey="Grandmougin Ferjani, Anne" sort="Grandmougin Ferjani, Anne" uniqKey="Grandmougin Ferjani A" first="Anne" last="Grandmougin-Ferjani">Anne Grandmougin-Ferjani</name><name sortKey="Lounes Hadj Sahraoui, Anissa" sort="Lounes Hadj Sahraoui, Anissa" uniqKey="Lounes Hadj Sahraoui A" first="Anissa" last="Lounès-Hadj Sahraoui">Anissa Lounès-Hadj Sahraoui</name><name sortKey="Shirali, Pirouz" sort="Shirali, Pirouz" uniqKey="Shirali P" first="Pirouz" last="Shirali">Pirouz Shirali</name><name sortKey="Verdin, Anthony" sort="Verdin, Anthony" uniqKey="Verdin A" first="Anthony" last="Verdin">Anthony Verdin</name></noCountry><country name="France"><region name="Hauts-de-France"><name sortKey="Debiane, Djouher" sort="Debiane, Djouher" uniqKey="Debiane D" first="Djouher" 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