The Fall Armyworm Spodoptera frugiperda Utilizes Specific UDP-Glycosyltransferases to Inactivate Maize Defensive Benzoxazinoids.
The Fall Armyworm Spodoptera frugiperda Utilizes Specific UDP-Glycosyltransferases to Inactivate Maize Defensive Benzoxazinoids.
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DOI:
10.3389/fphys.2020.604754
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发表时间:
2020
影响因子:
4
通讯作者:
Vassão DG
中科院分区:
文献类型:
--
作者:
Israni B;Wouters FC;Luck K;Seibel E;Ahn SJ;Paetz C;Reinert M;Vogel H;Erb M;Heckel DG;Gershenzon J;Vassão DG
The relationship between plants and insects is continuously evolving, and many insects rely on biochemical strategies to mitigate the effects of toxic chemicals in their food plants, allowing them to feed on well-defended plants. Spodoptera frugiperda, the fall armyworm (FAW), accepts a number of plants as hosts, and has particular success on plants of the Poaceae family such as maize, despite their benzoxazinoid (BXD) defenses. BXDs stored as inert glucosides are converted into toxic aglucones by plant glucosidases upon herbivory. DIMBOA, the main BXD aglucone released by maize leaves, can be stereoselectively re-glucosylated by UDP-glycosyltransferases (UGTs) in the insect gut, rendering it non-toxic. Here, we identify UGTs involved in BXD detoxification by FAW larvae and examine how RNAi-mediated manipulation of the larval glucosylation capacity toward the major maize BXD, DIMBOA, affects larval growth. Our findings highlight the involvement of members of two major UGT families, UGT33 and UGT40, in the glycosylation of BXDs. Most of the BXD excretion in the frass occurs in the form of glucosylated products. Furthermore, the DIMBOA-associated activity was enriched in the gut tissue, with a single conserved UGT33 enzyme (SfUGT33F28) being dedicated to DIMBOA re-glucosylation in the FAW gut. The knock-down of its encoding gene reduces larval performance in a strain-specific manner. This study thus reveals that a single UGT enzyme is responsible for detoxification of the major maize-defensive BXD in this pest insect.
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影响因子:
1.5
作者:
Dumas P;Legeai F;Lemaitre C;Scaon E;Orsucci M;Labadie K;Gimenez S;Clamens AL;Henri H;Vavre F;Aury JM;Fournier P;Kergoat GJ;d'Alençon E
通讯作者:
d'Alençon E
影响因子:
56.9
作者:
Frey, M;Chomet, P;Gierl, A
通讯作者:
Gierl, A
影响因子:
3.8
作者:
Ahn, Seung-Joon;Vogel, Heiko;Heckel, David G.
通讯作者:
Heckel, David G.
影响因子:
3.8
作者:
AHMAD, SA;HOPKINS, TL
通讯作者:
HOPKINS, TL
影响因子:
2.3
作者:
CAMPOS, F;ATKINSON, J;TIMMINS, G
通讯作者:
TIMMINS, G