Endocrine regulation of de novo aggregation pheromone biosynthesis in the pine engraver, Ips pini (Say) (Coleoptera: Scolytidae)

1998 ◽  
Vol 28 (9) ◽  
pp. 705-715 ◽  
Author(s):  
Julie A. Tillman ◽  
Glenn L. Holbrook ◽  
Paul L. Dallara ◽  
Coby Schal ◽  
David L. Wood ◽  
...  
2009 ◽  
Vol 141 (2) ◽  
pp. 158-160 ◽  
Author(s):  
Therese M. Poland ◽  
Deepa S. Pureswaran ◽  
Tina M. Ciaramitaro ◽  
John H. Borden

AbstractIn field experiments at three sites in Michigan and Ohio we tested the activity of 1-octen-3-ol in combination with ipsdienol, the aggregation pheromone of the pine engraver, Ips pini (Say). When 1-octen-3-ol was added to funnel traps baited with ipsdienol, significantly fewer beetles of either sex were captured than in traps baited with ipsdienol alone. This result suggests that the compound is potentially repellent and interrupts the response of beetles to their aggregation pheromone, and is consistent with previous reports of its inhibition of aggregation behaviour in other bark beetles.


2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
John A. Byers ◽  
Göran Birgersson

A paradigm developed in the 1970s thatIpsbark beetles biosynthesize their aggregation pheromone components ipsenol and ipsdienol by hydroxylating myrcene, a host tree monoterpene. Similarly, hostα-pinene was hydroxylated to a third pheromone componentcis-verbenol. In 1990, however, we reported that amounts of ipsenol and ipsdienol produced by maleIps paraconfusus(Coleoptera: Scolytinae) feeding in five host pine species were nearly the same, even though no detectable myrcene precursor was detected in one of these pines (Pinus sabiniana). Subsequent research showed ipsenol and ipsdienol are also biosynthesized from smaller precursors such as acetate and mevalonate, and thisde novopathway is the major one, while host tree myrcene conversion by the beetle is the minor one. We report concentrations of myrcene,α-pinene and other major monoterpenes in five pine hosts (Pinus ponderosa,P. lambertiana,P. jeffreyi,P. sabiniana, andP. contorta) ofI. paraconfusus. A scheme for biosynthesis of ipsdienol and ipsenol from myrcene and possible metabolites such as ipsenone is presented. Mass spectra and quantities of ipsenone are reported and its possible role in biosynthesis of aggregation pheromone. Coevolution of bark beetles and host trees is discussed in relation to pheromone biosynthesis, host plant selection/suitability, and plant resistance.


2002 ◽  
Vol 89 (2) ◽  
pp. 79-83 ◽  
Author(s):  
Gregory M. Hall ◽  
Claus Tittiger ◽  
Gracie L. Andrews ◽  
Grant S. Mastick ◽  
Marilyn Kuenzli ◽  
...  

2018 ◽  
Vol 115 (37) ◽  
pp. E8634-E8641 ◽  
Author(s):  
Jason Lancaster ◽  
Ashot Khrimian ◽  
Sharon Young ◽  
Bryan Lehner ◽  
Katrin Luck ◽  
...  

Insects use a diverse array of specialized terpene metabolites as pheromones in intraspecific interactions. In contrast to plants and microbes, which employ enzymes called terpene synthases (TPSs) to synthesize terpene metabolites, limited information from few species is available about the enzymatic mechanisms underlying terpene pheromone biosynthesis in insects. Several stink bugs (Hemiptera: Pentatomidae), among them severe agricultural pests, release 15-carbon sesquiterpenes with a bisabolene skeleton as sex or aggregation pheromones. The harlequin bug, Murgantia histrionica, a specialist pest of crucifers, uses two stereoisomers of 10,11-epoxy-1-bisabolen-3-ol as a male-released aggregation pheromone called murgantiol. We show that MhTPS (MhIDS-1), an enzyme unrelated to plant and microbial TPSs but with similarity to trans-isoprenyl diphosphate synthases (IDS) of the core terpene biosynthetic pathway, catalyzes the formation of (1S,6S,7R)-1,10-bisaboladien-1-ol (sesquipiperitol) as a terpene intermediate in murgantiol biosynthesis. Sesquipiperitol, a so-far-unknown compound in animals, also occurs in plants, indicating convergent evolution in the biosynthesis of this sesquiterpene. RNAi-mediated knockdown of MhTPS mRNA confirmed the role of MhTPS in murgantiol biosynthesis. MhTPS expression is highly specific to tissues lining the cuticle of the abdominal sternites of mature males. Phylogenetic analysis suggests that MhTPS is derived from a trans-IDS progenitor and diverged from bona fide trans-IDS proteins including MhIDS-2, which functions as an (E,E)-farnesyl diphosphate (FPP) synthase. Structure-guided mutagenesis revealed several residues critical to MhTPS and MhFPPS activity. The emergence of an IDS-like protein with TPS activity in M. histrionica demonstrates that de novo terpene biosynthesis evolved in the Hemiptera in an adaptation for intraspecific communication.


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