Christine Becker, Christof B Steingass, Heiko Vogel, Annette Reineke
{"title":"改变你的饮食:二氧化碳、植物物候和基因型如何改变葡萄品质,并影响食草昆虫的生产性能和幼虫转录组。","authors":"Christine Becker, Christof B Steingass, Heiko Vogel, Annette Reineke","doi":"10.1111/mec.17636","DOIUrl":null,"url":null,"abstract":"<p><p>Herbivorous insects need to cope with changing host plant biochemistry caused by abiotic and biotic impacts, to meet their dietary requirements. Larvae of the multivoltine European grapevine moth Lobesia botrana, one of the main insect pests in viticulture, feed on both flowers and berries. The nutritional value and defence compounds of these organs are changing with plant phenology and are affected by climate change which may accordingly alter plant-insect interactions. Here, we assessed the impacts of future elevated atmospheric CO<sub>2</sub> concentrations on the host plant quality of different grapevine organs and the larval performance and the transcriptome of L. botrana. Using the Geisenheim VineyardFACE facility, where 'Riesling' and 'Cabernet Sauvignon' were cultivated in the field under ambient or elevated (ca. + 20%) atmospheric CO<sub>2</sub> concentrations, we found that nutrient (amino acids and sugars) and defence compound (phenolic compounds) concentrations of inflorescences and ripening berries differed strongly due to plant phenology and less due to cultivar and CO<sub>2</sub> concentration. Assessing global gene expression after feeding on the respective organs, we found that larval transcriptomic plasticity largely mirrored the plant biochemical plasticity. Larval relative growth rate differed between treatments in a plant phenology-dependent manner. Grape berries contained higher amino acid concentrations and altered phenolics profiles after larval feeding. In the near future, the grapevine-L. botrana interaction will probably change less because of elevated CO<sub>2</sub> concentrations than it does currently during one season. Changes associated with plant phenology, however, may be relevant for contemporary pest management.</p>","PeriodicalId":210,"journal":{"name":"Molecular Ecology","volume":" ","pages":"e17636"},"PeriodicalIF":4.5000,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Change Your Diet: How CO<sub>2</sub>, Plant Phenology and Genotype Alter Grapevine Quality and Affect Performance and Larval Transcriptome of an Insect Herbivore.\",\"authors\":\"Christine Becker, Christof B Steingass, Heiko Vogel, Annette Reineke\",\"doi\":\"10.1111/mec.17636\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Herbivorous insects need to cope with changing host plant biochemistry caused by abiotic and biotic impacts, to meet their dietary requirements. Larvae of the multivoltine European grapevine moth Lobesia botrana, one of the main insect pests in viticulture, feed on both flowers and berries. The nutritional value and defence compounds of these organs are changing with plant phenology and are affected by climate change which may accordingly alter plant-insect interactions. Here, we assessed the impacts of future elevated atmospheric CO<sub>2</sub> concentrations on the host plant quality of different grapevine organs and the larval performance and the transcriptome of L. botrana. Using the Geisenheim VineyardFACE facility, where 'Riesling' and 'Cabernet Sauvignon' were cultivated in the field under ambient or elevated (ca. + 20%) atmospheric CO<sub>2</sub> concentrations, we found that nutrient (amino acids and sugars) and defence compound (phenolic compounds) concentrations of inflorescences and ripening berries differed strongly due to plant phenology and less due to cultivar and CO<sub>2</sub> concentration. Assessing global gene expression after feeding on the respective organs, we found that larval transcriptomic plasticity largely mirrored the plant biochemical plasticity. Larval relative growth rate differed between treatments in a plant phenology-dependent manner. Grape berries contained higher amino acid concentrations and altered phenolics profiles after larval feeding. In the near future, the grapevine-L. botrana interaction will probably change less because of elevated CO<sub>2</sub> concentrations than it does currently during one season. 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Change Your Diet: How CO2, Plant Phenology and Genotype Alter Grapevine Quality and Affect Performance and Larval Transcriptome of an Insect Herbivore.
Herbivorous insects need to cope with changing host plant biochemistry caused by abiotic and biotic impacts, to meet their dietary requirements. Larvae of the multivoltine European grapevine moth Lobesia botrana, one of the main insect pests in viticulture, feed on both flowers and berries. The nutritional value and defence compounds of these organs are changing with plant phenology and are affected by climate change which may accordingly alter plant-insect interactions. Here, we assessed the impacts of future elevated atmospheric CO2 concentrations on the host plant quality of different grapevine organs and the larval performance and the transcriptome of L. botrana. Using the Geisenheim VineyardFACE facility, where 'Riesling' and 'Cabernet Sauvignon' were cultivated in the field under ambient or elevated (ca. + 20%) atmospheric CO2 concentrations, we found that nutrient (amino acids and sugars) and defence compound (phenolic compounds) concentrations of inflorescences and ripening berries differed strongly due to plant phenology and less due to cultivar and CO2 concentration. Assessing global gene expression after feeding on the respective organs, we found that larval transcriptomic plasticity largely mirrored the plant biochemical plasticity. Larval relative growth rate differed between treatments in a plant phenology-dependent manner. Grape berries contained higher amino acid concentrations and altered phenolics profiles after larval feeding. In the near future, the grapevine-L. botrana interaction will probably change less because of elevated CO2 concentrations than it does currently during one season. Changes associated with plant phenology, however, may be relevant for contemporary pest management.
期刊介绍:
Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include:
* population structure and phylogeography
* reproductive strategies
* relatedness and kin selection
* sex allocation
* population genetic theory
* analytical methods development
* conservation genetics
* speciation genetics
* microbial biodiversity
* evolutionary dynamics of QTLs
* ecological interactions
* molecular adaptation and environmental genomics
* impact of genetically modified organisms