A Biologically Active Analog of the Sex Pheromone of the Emerald Ash Borer, Agrilus planipennis

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• 作者：P. J. Silk ; K. Ryall ; P. Mayo ; D. I. MaGee ; G. Leclair…
• 关键词：Dodecan ; 12 ; olide ; (3Z) ; dodecen ; 12 ; olide ; Lactone pheromone ; Agrilus planipennis ; Analog ; Buprestidae ; Invasive insect
• 刊名：Journal of Chemical Ecology
• 出版年：2015
• 出版时间：March 2015
• 年：2015
• 卷：41
• 期：3
• 页码：294-302
• 全文大小：538 KB
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• 作者单位：P. J. Silk (1)
  K. Ryall (2)
  P. Mayo (1)
  D. I. MaGee (3)
  G. Leclair (1)
  J. Fidgen (2)
  R. Lavallee (4)
  J. Price (1)
  J. McConaghy (1)
  
  1. Canadian Forest Service - Atlantic Forestry Centre, Natural Resources Canada, 1350 Regent Street, Fredericton, NB, E3B 5P7, Canada
  2. Canadian Forest Service - Great Lakes Forestry Centre, Natural Resources Canada, 1219 Queen Street East, Sault Ste. Marie, ON, P6A 2E5, Canada
  3. Department of Chemistry, University of New Brunswick, Fredericton, NB, E3B 6E2, Canada
  4. Ressources Naturelles Canada/ Natural Resources Canada, Service Canadien des For锚ts/Canadian Forest Service, CP 10380 Succ Sainte-Foy, Succ. Ste-Foy 1055 du PEPS, PO Box 10380, Qu茅bec, QC, G1V 4C7, Canada
  
• 刊物主题：Ecology; Biochemistry, general; Entomology; Biological Microscopy; Agriculture;
• 出版者：Springer US
• ISSN：1573-1561

文摘

The emerald ash borer, Agrilus planipennis (Coleoptera: Buprestidae) (EAB), is an invasive species causing unprecedented levels of mortality to ash trees in its introduced range. The female-produced sex pheromone of EAB has been shown to contain the macrocyclic lactone (3Z)-dodecen-12-olide. This compound and its geometrical isomer, (3E)-dodecen-12-olide, have been demonstrated previously to be EAG active and, in combination with a host-derived green leaf volatile, (3Z)-hexenol, to be attractive to male EAB in green prism traps deployed in the ash tree canopy. In the current study, we show that the saturated analog, dodecan-12-olide, is similarly active, eliciting an antennal response and significant attraction of EAB in both olfactometer and trapping bioassays in green traps with (3Z)-hexenol. Conformational modeling of the three lactones reveals that their energies and shapes are very similar, suggesting they might share a common receptor in EAB antennae. These findings provide new insight into the pheromone ecology of this species, highlighting the apparent plasticity in response of adults to the pheromone and its analog. Both of the unsaturated isomers are costly to synthesize, involving multistep, low-yielding processes. The saturated analog can be made cheaply, in high yield, and on large scale via Mitsunobu esterification of a saturated 蠅-hydroxy acid or more simply by Baeyer-Villiger oxidation of commercially available cyclododecanone. The analog can thus provide an inexpensive option as a lure for detection surveys as well as for possible mitigation purposes, such as mating disruption.