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Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants
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| Zeitschriftentitel: | Plant Biotechnology Journal |
|---|---|
| Personen und Körperschaften: | , , , , , , , |
| In: | Plant Biotechnology Journal, 15, 2017, 10, S. 1346-1357 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
Wiley
|
| Schlagwörter: |
| author_facet |
Liu, Caixiang Du, Ba Hao, Fuhua Lei, Hehua Wan, Qianfen He, Guangcun Wang, Yulan Tang, Huiru Liu, Caixiang Du, Ba Hao, Fuhua Lei, Hehua Wan, Qianfen He, Guangcun Wang, Yulan Tang, Huiru |
|---|---|
| author |
Liu, Caixiang Du, Ba Hao, Fuhua Lei, Hehua Wan, Qianfen He, Guangcun Wang, Yulan Tang, Huiru |
| spellingShingle |
Liu, Caixiang Du, Ba Hao, Fuhua Lei, Hehua Wan, Qianfen He, Guangcun Wang, Yulan Tang, Huiru Plant Biotechnology Journal Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants Plant Science Agronomy and Crop Science Biotechnology |
| author_sort |
liu, caixiang |
| spelling |
Liu, Caixiang Du, Ba Hao, Fuhua Lei, Hehua Wan, Qianfen He, Guangcun Wang, Yulan Tang, Huiru 1467-7644 1467-7652 Wiley Plant Science Agronomy and Crop Science Biotechnology http://dx.doi.org/10.1111/pbi.12721 <jats:title>Summary</jats:title><jats:p>Brown planthopper (<jats:italic>Nilaparvata lugens</jats:italic> Stål, <jats:styled-content style="fixed-case">BPH</jats:styled-content>) causes huge economic losses in rice‐growing regions, and new strategies for combating <jats:styled-content style="fixed-case">BPH</jats:styled-content> are required. To understand how <jats:styled-content style="fixed-case">BPH</jats:styled-content>s respond towards <jats:styled-content style="fixed-case">BPH</jats:styled-content>‐resistant plants, we systematically analysed the metabolic differences between <jats:styled-content style="fixed-case">BPH</jats:styled-content>s feeding on the resistant and susceptible plants using <jats:styled-content style="fixed-case">NMR</jats:styled-content> and <jats:styled-content style="fixed-case">GC</jats:styled-content>‐<jats:styled-content style="fixed-case">FID</jats:styled-content>/<jats:styled-content style="fixed-case">MS</jats:styled-content>. We also measured the expression of some related genes involving glycolysis and biosyntheses of trehalose, amino acids, chitin and fatty acids using real‐time <jats:styled-content style="fixed-case">PCR</jats:styled-content>. <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabonome was dominated by more than 60 metabolites including fatty acids, amino acids, carbohydrates, nucleosides/nucleotides and <jats:styled-content style="fixed-case">TCA</jats:styled-content> cycle intermediates. After initial 12 h, <jats:styled-content style="fixed-case">BPH</jats:styled-content>s feeding on the resistant plants had lower levels of amino acids, glucose, fatty acids and <jats:styled-content style="fixed-case">TCA</jats:styled-content> cycle intermediates than on the susceptible ones. The levels of these metabolites recovered after 24 h feeding. This accompanied with increased level in trehalose, choline metabolites and nucleosides/nucleotides compared with <jats:styled-content style="fixed-case">BPH</jats:styled-content> feeding on the susceptible plants. Decreased levels of <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabolites at the early feeding probably resulted from less <jats:styled-content style="fixed-case">BPH</jats:styled-content> uptakes of sap from resistant plants and recovery of <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabolites at the later stage probably resulted from their adaptation to the adverse environment with their increased hopping frequency to ingest more sap together with contributions from yeast‐like symbionts in <jats:styled-content style="fixed-case">BPH</jats:styled-content>s. Throughout 96 h, <jats:styled-content style="fixed-case">BPH</jats:styled-content> feeding on the resistant plants showed significant up‐regulation of chitin synthase catalysing biosynthesis of chitin for insect exoskeleton, peritrophic membrane lining gut and tracheae. These findings provided useful metabolic information for understanding the <jats:styled-content style="fixed-case">BPH</jats:styled-content>–rice interactions and perhaps for developing new <jats:styled-content style="fixed-case">BPH</jats:styled-content>‐combating strategies.</jats:p> Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants Plant Biotechnology Journal |
| doi_str_mv |
10.1111/pbi.12721 |
| facet_avail |
Online Free |
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Biologie Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft Technik |
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ElectronicArticle |
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| imprint |
Wiley, 2017 |
| imprint_str_mv |
Wiley, 2017 |
| issn |
1467-7644 1467-7652 |
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1467-7644 1467-7652 |
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English |
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liu2017dynamicmetabolicresponsesofbrownplanthopperstowardssusceptibleandresistantriceplants |
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2017 |
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Wiley |
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ai |
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Plant Biotechnology Journal |
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49 |
| title |
Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_unstemmed |
Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_full |
Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_fullStr |
Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_full_unstemmed |
Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_short |
Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_sort |
dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| topic |
Plant Science Agronomy and Crop Science Biotechnology |
| url |
http://dx.doi.org/10.1111/pbi.12721 |
| publishDate |
2017 |
| physical |
1346-1357 |
| description |
<jats:title>Summary</jats:title><jats:p>Brown planthopper (<jats:italic>Nilaparvata lugens</jats:italic> Stål, <jats:styled-content style="fixed-case">BPH</jats:styled-content>) causes huge economic losses in rice‐growing regions, and new strategies for combating <jats:styled-content style="fixed-case">BPH</jats:styled-content> are required. To understand how <jats:styled-content style="fixed-case">BPH</jats:styled-content>s respond towards <jats:styled-content style="fixed-case">BPH</jats:styled-content>‐resistant plants, we systematically analysed the metabolic differences between <jats:styled-content style="fixed-case">BPH</jats:styled-content>s feeding on the resistant and susceptible plants using <jats:styled-content style="fixed-case">NMR</jats:styled-content> and <jats:styled-content style="fixed-case">GC</jats:styled-content>‐<jats:styled-content style="fixed-case">FID</jats:styled-content>/<jats:styled-content style="fixed-case">MS</jats:styled-content>. We also measured the expression of some related genes involving glycolysis and biosyntheses of trehalose, amino acids, chitin and fatty acids using real‐time <jats:styled-content style="fixed-case">PCR</jats:styled-content>. <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabonome was dominated by more than 60 metabolites including fatty acids, amino acids, carbohydrates, nucleosides/nucleotides and <jats:styled-content style="fixed-case">TCA</jats:styled-content> cycle intermediates. After initial 12 h, <jats:styled-content style="fixed-case">BPH</jats:styled-content>s feeding on the resistant plants had lower levels of amino acids, glucose, fatty acids and <jats:styled-content style="fixed-case">TCA</jats:styled-content> cycle intermediates than on the susceptible ones. The levels of these metabolites recovered after 24 h feeding. This accompanied with increased level in trehalose, choline metabolites and nucleosides/nucleotides compared with <jats:styled-content style="fixed-case">BPH</jats:styled-content> feeding on the susceptible plants. Decreased levels of <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabolites at the early feeding probably resulted from less <jats:styled-content style="fixed-case">BPH</jats:styled-content> uptakes of sap from resistant plants and recovery of <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabolites at the later stage probably resulted from their adaptation to the adverse environment with their increased hopping frequency to ingest more sap together with contributions from yeast‐like symbionts in <jats:styled-content style="fixed-case">BPH</jats:styled-content>s. Throughout 96 h, <jats:styled-content style="fixed-case">BPH</jats:styled-content> feeding on the resistant plants showed significant up‐regulation of chitin synthase catalysing biosynthesis of chitin for insect exoskeleton, peritrophic membrane lining gut and tracheae. These findings provided useful metabolic information for understanding the <jats:styled-content style="fixed-case">BPH</jats:styled-content>–rice interactions and perhaps for developing new <jats:styled-content style="fixed-case">BPH</jats:styled-content>‐combating strategies.</jats:p> |
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| description | <jats:title>Summary</jats:title><jats:p>Brown planthopper (<jats:italic>Nilaparvata lugens</jats:italic> Stål, <jats:styled-content style="fixed-case">BPH</jats:styled-content>) causes huge economic losses in rice‐growing regions, and new strategies for combating <jats:styled-content style="fixed-case">BPH</jats:styled-content> are required. To understand how <jats:styled-content style="fixed-case">BPH</jats:styled-content>s respond towards <jats:styled-content style="fixed-case">BPH</jats:styled-content>‐resistant plants, we systematically analysed the metabolic differences between <jats:styled-content style="fixed-case">BPH</jats:styled-content>s feeding on the resistant and susceptible plants using <jats:styled-content style="fixed-case">NMR</jats:styled-content> and <jats:styled-content style="fixed-case">GC</jats:styled-content>‐<jats:styled-content style="fixed-case">FID</jats:styled-content>/<jats:styled-content style="fixed-case">MS</jats:styled-content>. We also measured the expression of some related genes involving glycolysis and biosyntheses of trehalose, amino acids, chitin and fatty acids using real‐time <jats:styled-content style="fixed-case">PCR</jats:styled-content>. <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabonome was dominated by more than 60 metabolites including fatty acids, amino acids, carbohydrates, nucleosides/nucleotides and <jats:styled-content style="fixed-case">TCA</jats:styled-content> cycle intermediates. After initial 12 h, <jats:styled-content style="fixed-case">BPH</jats:styled-content>s feeding on the resistant plants had lower levels of amino acids, glucose, fatty acids and <jats:styled-content style="fixed-case">TCA</jats:styled-content> cycle intermediates than on the susceptible ones. The levels of these metabolites recovered after 24 h feeding. This accompanied with increased level in trehalose, choline metabolites and nucleosides/nucleotides compared with <jats:styled-content style="fixed-case">BPH</jats:styled-content> feeding on the susceptible plants. Decreased levels of <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabolites at the early feeding probably resulted from less <jats:styled-content style="fixed-case">BPH</jats:styled-content> uptakes of sap from resistant plants and recovery of <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabolites at the later stage probably resulted from their adaptation to the adverse environment with their increased hopping frequency to ingest more sap together with contributions from yeast‐like symbionts in <jats:styled-content style="fixed-case">BPH</jats:styled-content>s. Throughout 96 h, <jats:styled-content style="fixed-case">BPH</jats:styled-content> feeding on the resistant plants showed significant up‐regulation of chitin synthase catalysing biosynthesis of chitin for insect exoskeleton, peritrophic membrane lining gut and tracheae. These findings provided useful metabolic information for understanding the <jats:styled-content style="fixed-case">BPH</jats:styled-content>–rice interactions and perhaps for developing new <jats:styled-content style="fixed-case">BPH</jats:styled-content>‐combating strategies.</jats:p> |
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| spelling | Liu, Caixiang Du, Ba Hao, Fuhua Lei, Hehua Wan, Qianfen He, Guangcun Wang, Yulan Tang, Huiru 1467-7644 1467-7652 Wiley Plant Science Agronomy and Crop Science Biotechnology http://dx.doi.org/10.1111/pbi.12721 <jats:title>Summary</jats:title><jats:p>Brown planthopper (<jats:italic>Nilaparvata lugens</jats:italic> Stål, <jats:styled-content style="fixed-case">BPH</jats:styled-content>) causes huge economic losses in rice‐growing regions, and new strategies for combating <jats:styled-content style="fixed-case">BPH</jats:styled-content> are required. To understand how <jats:styled-content style="fixed-case">BPH</jats:styled-content>s respond towards <jats:styled-content style="fixed-case">BPH</jats:styled-content>‐resistant plants, we systematically analysed the metabolic differences between <jats:styled-content style="fixed-case">BPH</jats:styled-content>s feeding on the resistant and susceptible plants using <jats:styled-content style="fixed-case">NMR</jats:styled-content> and <jats:styled-content style="fixed-case">GC</jats:styled-content>‐<jats:styled-content style="fixed-case">FID</jats:styled-content>/<jats:styled-content style="fixed-case">MS</jats:styled-content>. We also measured the expression of some related genes involving glycolysis and biosyntheses of trehalose, amino acids, chitin and fatty acids using real‐time <jats:styled-content style="fixed-case">PCR</jats:styled-content>. <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabonome was dominated by more than 60 metabolites including fatty acids, amino acids, carbohydrates, nucleosides/nucleotides and <jats:styled-content style="fixed-case">TCA</jats:styled-content> cycle intermediates. After initial 12 h, <jats:styled-content style="fixed-case">BPH</jats:styled-content>s feeding on the resistant plants had lower levels of amino acids, glucose, fatty acids and <jats:styled-content style="fixed-case">TCA</jats:styled-content> cycle intermediates than on the susceptible ones. The levels of these metabolites recovered after 24 h feeding. This accompanied with increased level in trehalose, choline metabolites and nucleosides/nucleotides compared with <jats:styled-content style="fixed-case">BPH</jats:styled-content> feeding on the susceptible plants. Decreased levels of <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabolites at the early feeding probably resulted from less <jats:styled-content style="fixed-case">BPH</jats:styled-content> uptakes of sap from resistant plants and recovery of <jats:styled-content style="fixed-case">BPH</jats:styled-content> metabolites at the later stage probably resulted from their adaptation to the adverse environment with their increased hopping frequency to ingest more sap together with contributions from yeast‐like symbionts in <jats:styled-content style="fixed-case">BPH</jats:styled-content>s. Throughout 96 h, <jats:styled-content style="fixed-case">BPH</jats:styled-content> feeding on the resistant plants showed significant up‐regulation of chitin synthase catalysing biosynthesis of chitin for insect exoskeleton, peritrophic membrane lining gut and tracheae. These findings provided useful metabolic information for understanding the <jats:styled-content style="fixed-case">BPH</jats:styled-content>–rice interactions and perhaps for developing new <jats:styled-content style="fixed-case">BPH</jats:styled-content>‐combating strategies.</jats:p> Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants Plant Biotechnology Journal |
| spellingShingle | Liu, Caixiang, Du, Ba, Hao, Fuhua, Lei, Hehua, Wan, Qianfen, He, Guangcun, Wang, Yulan, Tang, Huiru, Plant Biotechnology Journal, Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants, Plant Science, Agronomy and Crop Science, Biotechnology |
| title | Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_full | Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_fullStr | Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_full_unstemmed | Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_short | Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_sort | dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| title_unstemmed | Dynamic metabolic responses of brown planthoppers towards susceptible and resistant rice plants |
| topic | Plant Science, Agronomy and Crop Science, Biotechnology |
| url | http://dx.doi.org/10.1111/pbi.12721 |