Shifts in mycorrhizal fungi during the evolution of autotrophy to mycoheterotrophy in Cymbidium (Orchidaceae).
Identifieur interne : 001F23 ( Main/Corpus ); précédent : 001F22; suivant : 001F24Shifts in mycorrhizal fungi during the evolution of autotrophy to mycoheterotrophy in Cymbidium (Orchidaceae).
Auteurs : Yuki Ogura-Tsujita ; Jun Yokoyama ; Kazumitsu Miyoshi ; Tomohisa YukawaSource :
- American journal of botany [ 1537-2197 ] ; 2012.
English descriptors
- KwdEn :
- MESH :
- genetics : Mycorrhizae, Orchidaceae.
- isolation & purification : Mycorrhizae.
- microbiology : Orchidaceae.
- Autotrophic Processes, Biological Evolution, Heterotrophic Processes, Species Specificity, Symbiosis.
Abstract
PREMISE OF THE STUDY
Mycoheterotrophic plants, which completely depend upon mycorrhizal fungi for their nutrient supply, have unusual associations with fungal partners. The processes involved in shifts in fungal associations during cladogenesis of plant partners from autotrophy to mycoheterotrophy have not been demonstrated using a robust phylogenetic framework.
METHODS
Consequences of a mycorrhizal shift were examined in Cymbidium (Orchidaceae) using achlorophyllous and sister chlorophyllous species. Fungal associates of the two achlorophyllous mycoheterotrophs (C. macrorhizon and C. aberrans), their close relatives, the chlorophyllous mixotrophs (C. goeringii and C. lancifolium) and an outgroup, the chlorophyllous autotroph C. dayanum, were identified by internal transcribed spacers of the nuclear ribosomal DNA sequences.
KEY RESULTS
Molecular identification of mycorrhizal fungi revealed: (1) the outgroup autotroph is predominantly dependent on saprobic Tulasnellaceae, (2) the mixotrophs associate with the Tulasnellaceae and ectomycorrhizal groups including the Sebacinales, Russulaceae, Thelephoraceae and Clavulinaceae, and (3) the two mycoheterotrophs are mostly specialized with ectomycorrhizal Sebacinales.
CONCLUSION
Fungal partners in Cymbidium have shifted from saprobic to ectomycorrhizal fungi via a phase of coexistence of both nutritional types of fungi. These three phases correspond to the evolution from autotrophy to mycoheterotrophy via mixotrophy in Cymbidium. We demonstrate that shifts in mycorrhizal fungi correlate with the evolution of nutritional modes in plants. Furthermore, gradual shifts in fungal partners through a phase of coexistence of different types of mycobionts may play a crucial role in the evolution of mycoheterotrophic plants.
DOI: 10.3732/ajb.1100464
PubMed: 22763355
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pubmed:22763355Le document en format XML
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<author><name sortKey="Ogura Tsujita, Yuki" sort="Ogura Tsujita, Yuki" uniqKey="Ogura Tsujita Y" first="Yuki" last="Ogura-Tsujita">Yuki Ogura-Tsujita</name>
<affiliation><nlm:affiliation>Tsukuba Botanical Garden, National Museum of Nature and Science, Tsukuba, Japan. oguyttjita@gmail.com</nlm:affiliation>
</affiliation>
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<author><name sortKey="Yokoyama, Jun" sort="Yokoyama, Jun" uniqKey="Yokoyama J" first="Jun" last="Yokoyama">Jun Yokoyama</name>
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<author><name sortKey="Miyoshi, Kazumitsu" sort="Miyoshi, Kazumitsu" uniqKey="Miyoshi K" first="Kazumitsu" last="Miyoshi">Kazumitsu Miyoshi</name>
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<author><name sortKey="Yukawa, Tomohisa" sort="Yukawa, Tomohisa" uniqKey="Yukawa T" first="Tomohisa" last="Yukawa">Tomohisa Yukawa</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Shifts in mycorrhizal fungi during the evolution of autotrophy to mycoheterotrophy in Cymbidium (Orchidaceae).</title>
<author><name sortKey="Ogura Tsujita, Yuki" sort="Ogura Tsujita, Yuki" uniqKey="Ogura Tsujita Y" first="Yuki" last="Ogura-Tsujita">Yuki Ogura-Tsujita</name>
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<author><name sortKey="Yokoyama, Jun" sort="Yokoyama, Jun" uniqKey="Yokoyama J" first="Jun" last="Yokoyama">Jun Yokoyama</name>
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<author><name sortKey="Miyoshi, Kazumitsu" sort="Miyoshi, Kazumitsu" uniqKey="Miyoshi K" first="Kazumitsu" last="Miyoshi">Kazumitsu Miyoshi</name>
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<author><name sortKey="Yukawa, Tomohisa" sort="Yukawa, Tomohisa" uniqKey="Yukawa T" first="Tomohisa" last="Yukawa">Tomohisa Yukawa</name>
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<series><title level="j">American journal of botany</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Autotrophic Processes (MeSH)</term>
<term>Biological Evolution (MeSH)</term>
<term>Heterotrophic Processes (MeSH)</term>
<term>Mycorrhizae (genetics)</term>
<term>Mycorrhizae (isolation & purification)</term>
<term>Orchidaceae (genetics)</term>
<term>Orchidaceae (microbiology)</term>
<term>Species Specificity (MeSH)</term>
<term>Symbiosis (MeSH)</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Mycorrhizae</term>
<term>Orchidaceae</term>
</keywords>
<keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en"><term>Mycorrhizae</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Orchidaceae</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Autotrophic Processes</term>
<term>Biological Evolution</term>
<term>Heterotrophic Processes</term>
<term>Species Specificity</term>
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<front><div type="abstract" xml:lang="en"><p><b>PREMISE OF THE STUDY</b>
</p>
<p>Mycoheterotrophic plants, which completely depend upon mycorrhizal fungi for their nutrient supply, have unusual associations with fungal partners. The processes involved in shifts in fungal associations during cladogenesis of plant partners from autotrophy to mycoheterotrophy have not been demonstrated using a robust phylogenetic framework.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>METHODS</b>
</p>
<p>Consequences of a mycorrhizal shift were examined in Cymbidium (Orchidaceae) using achlorophyllous and sister chlorophyllous species. Fungal associates of the two achlorophyllous mycoheterotrophs (C. macrorhizon and C. aberrans), their close relatives, the chlorophyllous mixotrophs (C. goeringii and C. lancifolium) and an outgroup, the chlorophyllous autotroph C. dayanum, were identified by internal transcribed spacers of the nuclear ribosomal DNA sequences.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>KEY RESULTS</b>
</p>
<p>Molecular identification of mycorrhizal fungi revealed: (1) the outgroup autotroph is predominantly dependent on saprobic Tulasnellaceae, (2) the mixotrophs associate with the Tulasnellaceae and ectomycorrhizal groups including the Sebacinales, Russulaceae, Thelephoraceae and Clavulinaceae, and (3) the two mycoheterotrophs are mostly specialized with ectomycorrhizal Sebacinales.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>CONCLUSION</b>
</p>
<p>Fungal partners in Cymbidium have shifted from saprobic to ectomycorrhizal fungi via a phase of coexistence of both nutritional types of fungi. These three phases correspond to the evolution from autotrophy to mycoheterotrophy via mixotrophy in Cymbidium. We demonstrate that shifts in mycorrhizal fungi correlate with the evolution of nutritional modes in plants. Furthermore, gradual shifts in fungal partners through a phase of coexistence of different types of mycobionts may play a crucial role in the evolution of mycoheterotrophic plants.</p>
</div>
</front>
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<Abstract><AbstractText Label="PREMISE OF THE STUDY" NlmCategory="OBJECTIVE">Mycoheterotrophic plants, which completely depend upon mycorrhizal fungi for their nutrient supply, have unusual associations with fungal partners. The processes involved in shifts in fungal associations during cladogenesis of plant partners from autotrophy to mycoheterotrophy have not been demonstrated using a robust phylogenetic framework.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Consequences of a mycorrhizal shift were examined in Cymbidium (Orchidaceae) using achlorophyllous and sister chlorophyllous species. Fungal associates of the two achlorophyllous mycoheterotrophs (C. macrorhizon and C. aberrans), their close relatives, the chlorophyllous mixotrophs (C. goeringii and C. lancifolium) and an outgroup, the chlorophyllous autotroph C. dayanum, were identified by internal transcribed spacers of the nuclear ribosomal DNA sequences.</AbstractText>
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