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Gene expression analysis in Musa acuminata during compatible interactions with Meloidogyne incognita.

Identifieur interne : 000088 ( Main/Exploration ); précédent : 000087; suivant : 000089

Gene expression analysis in Musa acuminata during compatible interactions with Meloidogyne incognita.

Auteurs : Nancy Eunice Ni O Casta Eda [Brésil] ; Gabriel Sergio Costa Alves [Brésil] ; Rosane Mansan Almeida [Brésil] ; Edson Perito Amorim [Brésil] ; Claudia Fortes Ferreira [Brésil] ; Roberto Coiti Togawa [Brésil] ; Marcos Mota Do Carmo Costa [Brésil] ; Priscila Grynberg [Brésil] ; Jansen Rodrigo Pereira Santos [États-Unis] ; Juvenil Enrique Cares [Brésil] ; Robert Neil Gerard Miller [Brésil]

Source :

RBID : pubmed:28130221

Descripteurs français

English descriptors

Abstract

Background and Aims

Endoparasitic root-knot nematodes (RKNs) ( Meloidogyne spp.) cause considerable losses in banana ( Musa spp.), with Meloidogyne incognita a predominant species in Cavendish sub-group bananas. This study investigates the root transcriptome in Musa acuminata genotypes 4297-06 (AA) and Cavendish Grande Naine (CAV; AAA) during early compatible interactions with M. incognita .

Methods

Roots were analysed by brightfield light microscopy over a 35 d period to examine nematode penetration and morphological cell transformation. RNA samples were extracted 3, 7 and 10 days after inoculation (DAI) with nematode J2 juveniles, and cDNA libraries were sequenced using lllumina HiSeq technology. Sequences were mapped to the M. acuminata ssp. malaccensis var. Pahang genome sequence, differentially expressed genes (DEGs) identified and transcript representation determined by gene set enrichment and pathway mapping.

Key Results

Microscopic analysis revealed a life cycle of M. incognita completing in 24 d in CAV and 27 d in 4279-06. Comparable numbers of DEGs were up- and downregulated in each genotype, with potential involvement of many in early host defence responses involving reactive oxygen species and jasmonate/ethylene signalling. DEGs revealed concomitant auxin metabolism and cell wall modification processes likely to be involved in giant cell formation. Notable transcripts related to host defence included those coding for leucine-rich repeat receptor-like serine/threonine-protein kinases, peroxidases, thaumatin-like pathogenesis-related proteins, and DREB, ERF, MYB, NAC and WRKY transcription factors. Transcripts related to giant cell development included indole acetic acid-amido synthetase GH3.8 genes, involved in auxin metabolism, as well as genes encoding expansins and hydrolases, involved in cell wall modification.

Conclusions

Expression analysis in M. acuminata during compatible interactions with RKNs provides insights into genes modulated during infection and giant cell formation. Increased understanding of both defence responses to limit parasitism during compatible interactions and effector-targeted host genes in this complex interaction will facilitate the development of genetic improvement measures for RKNs.


DOI: 10.1093/aob/mcw272
PubMed: 28130221
PubMed Central: PMC5604581


Affiliations:


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<term>Animals (MeSH)</term>
<term>Gene Expression Profiling (MeSH)</term>
<term>Musa (genetics)</term>
<term>Musa (parasitology)</term>
<term>Plant Diseases (genetics)</term>
<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (metabolism)</term>
<term>Plant Roots (genetics)</term>
<term>Plant Roots (metabolism)</term>
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<term>Analyse de profil d'expression de gènes (MeSH)</term>
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<term>Maladies des plantes (génétique)</term>
<term>Musa (génétique)</term>
<term>Musa (parasitologie)</term>
<term>Protéines végétales (génétique)</term>
<term>Protéines végétales (métabolisme)</term>
<term>Racines de plante (génétique)</term>
<term>Racines de plante (métabolisme)</term>
<term>Transcriptome (MeSH)</term>
<term>Tylenchoidea (physiologie)</term>
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<term>Plant Proteins</term>
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<term>Musa</term>
<term>Plant Diseases</term>
<term>Plant Roots</term>
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<term>Maladies des plantes</term>
<term>Musa</term>
<term>Protéines végétales</term>
<term>Racines de plante</term>
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<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Plant Proteins</term>
<term>Plant Roots</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Protéines végétales</term>
<term>Racines de plante</term>
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<keywords scheme="MESH" qualifier="parasitologie" xml:lang="fr">
<term>Musa</term>
</keywords>
<keywords scheme="MESH" qualifier="parasitology" xml:lang="en">
<term>Musa</term>
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<term>Tylenchoidea</term>
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<term>Tylenchoidea</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Gene Expression Profiling</term>
<term>Transcriptome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Analyse de profil d'expression de gènes</term>
<term>Animaux</term>
<term>Transcriptome</term>
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<p>
<b>Background and Aims</b>
</p>
<p>Endoparasitic root-knot nematodes (RKNs) ( Meloidogyne spp.) cause considerable losses in banana ( Musa spp.), with Meloidogyne incognita a predominant species in Cavendish sub-group bananas. This study investigates the root transcriptome in Musa acuminata genotypes 4297-06 (AA) and Cavendish Grande Naine (CAV; AAA) during early compatible interactions with M. incognita .</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Methods</b>
</p>
<p>Roots were analysed by brightfield light microscopy over a 35 d period to examine nematode penetration and morphological cell transformation. RNA samples were extracted 3, 7 and 10 days after inoculation (DAI) with nematode J2 juveniles, and cDNA libraries were sequenced using lllumina HiSeq technology. Sequences were mapped to the M. acuminata ssp. malaccensis var. Pahang genome sequence, differentially expressed genes (DEGs) identified and transcript representation determined by gene set enrichment and pathway mapping.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Key Results</b>
</p>
<p>Microscopic analysis revealed a life cycle of M. incognita completing in 24 d in CAV and 27 d in 4279-06. Comparable numbers of DEGs were up- and downregulated in each genotype, with potential involvement of many in early host defence responses involving reactive oxygen species and jasmonate/ethylene signalling. DEGs revealed concomitant auxin metabolism and cell wall modification processes likely to be involved in giant cell formation. Notable transcripts related to host defence included those coding for leucine-rich repeat receptor-like serine/threonine-protein kinases, peroxidases, thaumatin-like pathogenesis-related proteins, and DREB, ERF, MYB, NAC and WRKY transcription factors. Transcripts related to giant cell development included indole acetic acid-amido synthetase GH3.8 genes, involved in auxin metabolism, as well as genes encoding expansins and hydrolases, involved in cell wall modification.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Conclusions</b>
</p>
<p>Expression analysis in M. acuminata during compatible interactions with RKNs provides insights into genes modulated during infection and giant cell formation. Increased understanding of both defence responses to limit parasitism during compatible interactions and effector-targeted host genes in this complex interaction will facilitate the development of genetic improvement measures for RKNs.</p>
</div>
</front>
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</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1095-8290</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>119</Volume>
<Issue>5</Issue>
<PubDate>
<Year>2017</Year>
<Month>03</Month>
<Day>01</Day>
</PubDate>
</JournalIssue>
<Title>Annals of botany</Title>
<ISOAbbreviation>Ann Bot</ISOAbbreviation>
</Journal>
<ArticleTitle>Gene expression analysis in Musa acuminata during compatible interactions with Meloidogyne incognita.</ArticleTitle>
<Pagination>
<MedlinePgn>915-930</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1093/aob/mcw272</ELocationID>
<Abstract>
<AbstractText Label="Background and Aims">Endoparasitic root-knot nematodes (RKNs) ( Meloidogyne spp.) cause considerable losses in banana ( Musa spp.), with Meloidogyne incognita a predominant species in Cavendish sub-group bananas. This study investigates the root transcriptome in Musa acuminata genotypes 4297-06 (AA) and Cavendish Grande Naine (CAV; AAA) during early compatible interactions with M. incognita .</AbstractText>
<AbstractText Label="Methods">Roots were analysed by brightfield light microscopy over a 35 d period to examine nematode penetration and morphological cell transformation. RNA samples were extracted 3, 7 and 10 days after inoculation (DAI) with nematode J2 juveniles, and cDNA libraries were sequenced using lllumina HiSeq technology. Sequences were mapped to the M. acuminata ssp. malaccensis var. Pahang genome sequence, differentially expressed genes (DEGs) identified and transcript representation determined by gene set enrichment and pathway mapping.</AbstractText>
<AbstractText Label="Key Results">Microscopic analysis revealed a life cycle of M. incognita completing in 24 d in CAV and 27 d in 4279-06. Comparable numbers of DEGs were up- and downregulated in each genotype, with potential involvement of many in early host defence responses involving reactive oxygen species and jasmonate/ethylene signalling. DEGs revealed concomitant auxin metabolism and cell wall modification processes likely to be involved in giant cell formation. Notable transcripts related to host defence included those coding for leucine-rich repeat receptor-like serine/threonine-protein kinases, peroxidases, thaumatin-like pathogenesis-related proteins, and DREB, ERF, MYB, NAC and WRKY transcription factors. Transcripts related to giant cell development included indole acetic acid-amido synthetase GH3.8 genes, involved in auxin metabolism, as well as genes encoding expansins and hydrolases, involved in cell wall modification.</AbstractText>
<AbstractText Label="Conclusions">Expression analysis in M. acuminata during compatible interactions with RKNs provides insights into genes modulated during infection and giant cell formation. Increased understanding of both defence responses to limit parasitism during compatible interactions and effector-targeted host genes in this complex interaction will facilitate the development of genetic improvement measures for RKNs.</AbstractText>
<CopyrightInformation>© The Author 2017. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oup.com</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Castañeda</LastName>
<ForeName>Nancy Eunice Niño</ForeName>
<Initials>NEN</Initials>
<AffiliationInfo>
<Affiliation>Universidade de Brasília, Instituto de Ciências Biológicas, CEP 70910-900, Brasilia, DF, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Alves</LastName>
<ForeName>Gabriel Sergio Costa</ForeName>
<Initials>GSC</Initials>
<AffiliationInfo>
<Affiliation>Universidade de Brasília, Instituto de Ciências Biológicas, CEP 70910-900, Brasilia, DF, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Almeida</LastName>
<ForeName>Rosane Mansan</ForeName>
<Initials>RM</Initials>
<AffiliationInfo>
<Affiliation>Universidade de Brasília, Instituto de Ciências Biológicas, CEP 70910-900, Brasilia, DF, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Amorim</LastName>
<ForeName>Edson Perito</ForeName>
<Initials>EP</Initials>
<AffiliationInfo>
<Affiliation>Embrapa Cassava and Tropical Fruits, CEP 44380-000, Cruz das Almas, BA, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Fortes Ferreira</LastName>
<ForeName>Claudia</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Embrapa Cassava and Tropical Fruits, CEP 44380-000, Cruz das Almas, BA, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Togawa</LastName>
<ForeName>Roberto Coiti</ForeName>
<Initials>RC</Initials>
<AffiliationInfo>
<Affiliation>Embrapa Recursos Genéticos e Biotecnologia, Parque Estação Biológica, CP 02372, CEP 70770-917, Brasília, DF, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Costa</LastName>
<ForeName>Marcos Mota Do Carmo</ForeName>
<Initials>MMDC</Initials>
<AffiliationInfo>
<Affiliation>Embrapa Recursos Genéticos e Biotecnologia, Parque Estação Biológica, CP 02372, CEP 70770-917, Brasília, DF, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Grynberg</LastName>
<ForeName>Priscila</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>Embrapa Recursos Genéticos e Biotecnologia, Parque Estação Biológica, CP 02372, CEP 70770-917, Brasília, DF, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Santos</LastName>
<ForeName>Jansen Rodrigo Pereira</ForeName>
<Initials>JRP</Initials>
<AffiliationInfo>
<Affiliation>University of California, Department of Nematology, 900 University Avenue, Riverside, CA 92521, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Cares</LastName>
<ForeName>Juvenil Enrique</ForeName>
<Initials>JE</Initials>
<AffiliationInfo>
<Affiliation>Universidade de Brasília, Instituto de Ciências Biológicas, CEP 70910-900, Brasilia, DF, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Miller</LastName>
<ForeName>Robert Neil Gerard</ForeName>
<Initials>RNG</Initials>
<AffiliationInfo>
<Affiliation>Universidade de Brasília, Instituto de Ciências Biológicas, CEP 70910-900, Brasilia, DF, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
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<Country>England</Country>
<MedlineTA>Ann Bot</MedlineTA>
<NlmUniqueID>0372347</NlmUniqueID>
<ISSNLinking>0305-7364</ISSNLinking>
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<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D010940">Plant Proteins</NameOfSubstance>
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<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D020869" MajorTopicYN="N">Gene Expression Profiling</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D028521" MajorTopicYN="N">Musa</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000469" MajorTopicYN="Y">parasitology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010935" MajorTopicYN="N">Plant Diseases</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018517" MajorTopicYN="N">Plant Roots</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D059467" MajorTopicYN="Y">Transcriptome</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D014431" MajorTopicYN="N">Tylenchoidea</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="Y">Meloidogyne incognita</Keyword>
<Keyword MajorTopicYN="Y">Musa acuminata</Keyword>
<Keyword MajorTopicYN="Y">biotic stress</Keyword>
<Keyword MajorTopicYN="Y">monocotyledons</Keyword>
<Keyword MajorTopicYN="Y">root-knot nematode</Keyword>
<Keyword MajorTopicYN="Y">transcriptome</Keyword>
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<Year>2016</Year>
<Month>10</Month>
<Day>31</Day>
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<PubMedPubDate PubStatus="accepted">
<Year>2016</Year>
<Month>12</Month>
<Day>01</Day>
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<li>États-Unis</li>
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<li>Californie</li>
<li>District fédéral (Brésil)</li>
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   |texte=   Gene expression analysis in Musa acuminata during compatible interactions with Meloidogyne incognita.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:28130221" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a ThaumatinV1 

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