Sexual attraction pheromone of tribolium castaneum and insect control device

Abstract
A sexual attraction pheromone exclusively obtained from Tribolium castaneum male insects, a method to obtain said pheromone and a device useful for controlling insects in grain silos are disclosed. The device comprises an outer shell, a membrane impregnated with the sexual attraction pheromone and a nucleus containing an insecticide formulation comprising effective amount of an isolated microsclerotia of Beauveria bassiana and an agronomically acceptable carrier.
Description
TECHNICAL FIELD

The present invention relates to an insect sexual attraction pheromone and to a device useful for controlling pests, in particular insects, in grain silos. The device comprises an outer shell, a membrane impregnated with a sexual attraction pheromone extracted from Tribolium castaneum males and an interior region comprising insecticide formulation.


BACKGROUND

Insect control devices with a “lure and trap” mechanism often include a luring composition, such as an aggregation pheromone, to attract insects, as well as an insecticide formulation or other pest control compounds. Several of these compounds may require carefully controlled conditions in order to activate the biological mechanisms involved in the insecticidal effect. For example, bioinsecticides based on dormant forms of several entomopathogenic fungi may be activated under adequate humidity conditions. These conditions may be obtained through the aggregation of a certain number of insects in the vicinity of these dormant forms. When the adequate conditions are met, the dormant forms activate, and the insecticidal effect is achieved. A sexual attraction pheromone, which targets only insects of a certain sex, can be advantageously used to achieve these controlled conditions.


4,8-dimethyldecanal, also known as tribolure, is an aggregation pheromone of Tribolium castaneum. Although it has been mistakenly reported as a “sexual pheromone”, it has been found that this molecule attracts both male and female insects, therefore not constituting a true sexual pheromone.


There is therefore a need to provide a sexual pheromone of Tribolium castaneum useful for insect control devices employing a luring composition.


SUMMARY OF THE INVENTION

In a first aspect, an object of the present invention is an isolated sexual attraction pheromone of Tribolium castaneum that is exclusively obtained from male insects. The pheromone has an average molecular weight of approximately 210 g/mol, a molecular formula of C14H26O and a chemical structure having only one degree of unsaturation and a terminal carbonyl group.


In a second aspect, an object of the present invention is a method to obtain an isolated sexual attraction pheromone from a plurality of male insects, comprising the steps of:

    • placing the plurality of male insects in an airtight container comprising a solid support,
    • placing and maintaining the container on a stove to generate volatile organic compounds,
    • separating the plurality of male insects from the solid support,
    • extracting the volatile organic compounds from the solid support using solid-phase microextraction fibers, and
    • isolating of the pheromone from the volatile organic compounds by capillary gas chromatography.


In a preferred embodiment of the second aspect, said solid support is selected from filter paper and a feed medium comprising flour. Preferably, the feed medium comprises about 30 g of flour.


In another preferred embodiment of the second aspect, the container is maintained on a stove for a period of approximately one month.


In a third aspect, it as an object of the present invention an insect control device comprising:

    • an outer shell comprising a plurality of orifices,
    • a central membrane impregnated with a luring composition, and
    • an interior region comprising an insecticide formulation.


In a fourth aspect, it as an object of the present invention an insect control device comprising:

    • an outer shell comprising a plurality of orifices,
    • a central membrane impregnated with the isolated sexual attraction pheromone of Tribolium castaneum of the first aspect of the invention, and
    • an interior region comprising an insecticide formulation.


In preferred embodiments of the third and fourth aspects, said membrane is comprised in a capsule attached to the outer shell.


In preferred embodiments of the third and fourth aspects, said capsule further comprises a conical surface. Preferably, said conical surface has a smooth, polished and shining surface.


In further preferred embodiments of the third and fourth aspects, the insecticide formulation comprises an effective amount of isolated microsclerotia of Beauveria bassiana and an agronomically acceptable carrier. Such microsclerotia are described in U.S. patent application No. 62/815,541, the contents of which are incorporated by reference herein.


In yet further preferred embodiments of the third and fourth aspects, the interior region is located in a lower portion of the device.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 shows a chromatograph with the main components of male Tribolium castaneum extracts.



FIG. 2 shows the attraction of female insects to a paper impregnated with the sexual pheromone of the present invention.



FIGS. 3 to 6 show embodiments of the insect control device of the present invention as well as its individual components.



FIG. 7 shows the results of the use of the insect control device of the present invention in a laboratory-scale silo containing 5 kg of wheat.



FIG. 8 shows the results of the use of the insect control device of the present invention in a pilot-plant scale silo containing 20 kg of wheat.





DETAILED DESCRIPTION OF THE INVENTION

The present invention will be described in detail below, with reference to the figures and examples, which are included only for the purpose of illustrating the invention and are not to be construed as limiting thereof.


The term “approximately” as used herein when referring to a measurable value means that it comprises variations of ±10% from the specified amount.


As used herein, the terms “comprises”, “has” and “includes” and their conjugations mean “including but not limited to”.


The sexual pheromone of the present invention is biosynthesized exclusively by male Tribolium castaneum insects and thus constitutes a true sexual pheromone, as opposed to those of the prior art.


The insect control device of the present invention operates by a “lure and trap” mechanism. In an embodiment, insects are attracted and aggregate into the inside of the device, by crawling through the orifices of the outer shell. In an embodiment of the device, when a certain number of insects has entered the device, the resulting humidity conditions activate a bioinsecticide formulation. In the case of bioinsecticides comprising microsclerotia, adequate humidity conditions will cause the proliferation of conidia from the microsclerotia.


In this manner, the initial charge of bioinsecticide can be activated several times and in response to the entrance and exit of insects into the device.


Alternatively, when a single insect or a lower number of insects enter the device, they become impregnated with a bioinsecticide in dormant form (i.e. microsclerotia). This form will yield a large number of conidia when the humidity conditions are met, for example in the insects' nests.


EXAMPLES

1) Extraction of Tribolium castaneum Sexual Pheromone


Insects


Specimens of pest insects of stored grains, Tribolium castaneum, were employed. The insects were bred in 500 mL glass jars covered with a fine cloth net and kept in a breeding chamber at 27±2° C. and 70±5% relative humidity, with a light: darkness photoperiod of 12 h/12 h.


The insects were fed a mixed diet of wheat flour (85%), brewer's yeast (5%), wheat germ (5%) and skimmed milk powder (5%).


During the pupa stage, males and females were separated taking into account the morphological differences of both sexes and were kept in the diet until adult molting, thus obtaining virgin insects.


For the extraction of the pheromone of Tribolium castaneum, pools of 200 male insects were employed, which were placed in individual 200 mL containers with 30 grs of flour and kept in the stove in the above-mentioned conditions for a period of 1 month. Finally, the insects were separated, and 90 grs of flour were placed in 250 mL Erlenmeyer flasks sealed with a Teflon lid with a septum to aid the extraction of volatile organic compounds (VOCs).


Extraction in Solid Phase


The VOCs released by Tribolium castaneum males were extracted from the head space of the Erlenmeyer flasks containing the flour using solid-phase microextraction fibers (SPME) of intermediate polarity composed of polydimethylsiloxane/divinylbenzene and the sample was taken for 60 minutes at room temperature (in a temperature range of 25 to 30° C.).



FIG. 1 shows the main components of the VOCs released by male and female Tribolium castaneum, including defense pheromones (benzoquinones) and aggregate pheromones (4,8-dimethyldecanal). The detector signal corresponding to the sexual pheromone of the present invention is only present in male insects.


Isolation of the Sexual Pheromone by Capillary Gas Chromatography


The VOCs extracted by SPME were analyzed and isolated by capillary gas chromatography (CGC). A Hewlett Packard 6850 gas chromatograph with a DB-5 non-polar capillary column was used. The injector was operated in splitless mode at 250° C., He gas was used as a carrier at constant flow rate of 1.5 mL/min, the furnace temperature was programmed at 40° C. for 0 min, 50° C./min at 100° C., 4° C./min at 220° C., with a retention time of 5 min at the final temperature. The flame ionization detector (FID) temperature was set to 280° C. This equipment is fitted with a microcontrol valve that allowed part of the analyzed sample to be diverted to the outside of the chromatograph, which is coupled with a transfer line maintaining the temperature of the column at 220° C. The fraction of interest was collected in a 4 mL flask at 0° C. The purity of the compound was verified using a Hewlett Packard 6890 chromatograph equipped with an infernal Zebron-5HT capillary column (30 m×0.25 mm I.D., F.T. 0.25 μm, Phenomenex, USA), in the above-mentioned conditions. The CGC was operated coupled to an Agilent 5975C VL mass selective detector (MSD). The MSD was operated in SCAN mode with a mass range of 35 to 650 u.m.a.; in electronic impact mode at 70 eV; transfer line at 320° C.; ionization chamber temperature at 230° C. and quadrupole at 150° C. The MSD was operated in SCAN mode with a mass range of 35 to 650 u.m.a.; in electronic impact mode at 70 eV; transfer line at 320° C.; ionization chamber temperature at 230° C. and quadrupole at 150° C.


Characterization of the Sexual Pheromone


Preliminary mass spectrometry analysis revealed a molecular weight of 210 g/mol, a twelve-carbon unsaturated backbone and at least one methyl-branch.


Further analysis provided a molecular formula of C14H26O and a chemical structure having only one degree of unsaturation and a terminal carbonyl group.



FIG. 2 shows the attraction of female insects to a paper impregnated with a solution comprising the extracted male pheromone.


2) Insect Control Device



FIGS. 3 to 6 show different configurations of the device of the present invention, representing exemplary and non-limiting embodiments of the device and/or individual components thereof.


The device (1) of the present invention comprises an outer capsule (2) and an inner capsule (3). An interior region (4) of the inner capsule (3), comprising an insecticide formulation, is the compartment defined by inner capsule (3). The capsules are coupled to each other by shape correspondence and are arranged concentrically. In this manner, the insect which is crawling in the interior of the device (1) is forced to go through the inner capsule (3) in order to reach the interior region (4) comprising the insecticide.


The outer capsule (2) defines the outer shell of the device, which is provided with a plurality of orifices (6), so that insects may crawl into or out of the device.


The inner capsule (3) comprises an entrance zone (8) which is an entrance to the interior region (4) and may also comprise other orifices (6), when configured as an “open inner capsule”. An open inner capsule allows the insect to freely crawl about it, entering and exiting the inner capsule without being retained. A closed inner capsule, i.e. an inner capsule without orifices other than the entrance zone, allows the insect to remain contained inside the inner capsule; this can be achieved by providing a conical or a cylindrical surface (9) inside the inner capsule. Once in contact with the smooth, polished and shining surface conical or cylindrical surface (9), the insects will remain trapped inside, since they will not be able to crawl up the surface (9). In this manner, insects remain in the interior of the inner capsule (3) until they are removed or liberated.


The closing of the device is ensured by flexible fasteners (11) provided in the inner and outer capsules, thus obtaining semi-permanent couplings.


The interior region (4) of the device of the present invention comprises a membrane (12), located inside the interior region (4) and impregnated with a substance acting as a lure mechanism. For example, the isolated sexual pheromone of the present invention may be used. Due to its central location, the membrane will generate an adequate concentration gradient of the substance in the surrounding air by diffusion and natural convection, thus promoting the luring effect.


Insecticides that may be used for the interior region comprise bioinsecticides, such as dormant forms as antipathogenic fungi, such as Beauveria bassiana microsclerotia. Since these dormant forms require controlling humidity conditions in order to ensure a controlled release, their combination with the sexual pheromone of the present invention, which only attracts female insects, is advantageous to achieve a controlled and efficient release of an insecticide formulation.


3) Use of the Insect Control Device in a Laboratory Scale Silo



FIG. 7 illustrates the attraction effect of a luring composition comprising the isolated sexual pheromone of the present invention obtained from Tribolium castaneum male insects in two laboratory-scale silo containing 5 kg of wheat of the Audaz variety.


Two sets of experiments were carried out: each set consisted of a “control” silo, containing an insect control device without any luring composition, and an “attraction” silo, containing the insect control device of the present invention, i.e. with a luring composition comprising the isolated sexual attraction pheromone of male Tribolium castaneum.


The left hand side of FIG. 7 shows the results for the distributions of insects for different positions inside the control and model silos containing Sitophilus sp insects. It can be seen that for the control species Sitophilus sp., both the control and the attraction silos have equivalent insect distributions.


The right hand side FIG. 7 shows the corresponding results for silos containing Tribolium castaneum insects. In this case, it is observed that this species is distributed such that the number of insects closer to the insect control device is higher, which illustrates the successful and specific attraction of Tribolium castaneum insects using the luring composition of the present invention.


4) Use of the Insect Control Device in a Pilot-Plant Scale Silo


The insect control device was further tested in pilot-plant scale silos containing 200 kg of wheat of the Audaz variety.


Two experiments were carried out: the first in a “control” silo, containing six insect control devices, each one without any luring composition, and the second in an “attraction” silo, containing six insect control devices of the present invention, i.e. each one with a luring composition comprising the isolated sexual attraction pheromone of male Tribolium castaneum.



FIG. 8 shows the results for the distributions of insects for different positions inside the control and model silos containing Tribolium castaneum insects. The graph in FIG. 8 represents the percentage of insects found in different areas of the silo, as defined by three radial sections in the silo, corresponding to 0 cm, 15 cm and 25 measured from the center of the silo, as well as 8 longitudinal sections from the bottom of the silo to the loading surface.


When comparing the obtained results for the distribution of female Tribolium castaneum insects, it can be observed that the insects are attracted to the part of the “attraction” silo containing the insect control devices, as evidenced by the distribution in the right hand side of the graph in FIG. 8, and compared to the distribution in the left hand side of the graph in FIG. 8, corresponding to the experiment in the “control” silo (i.e. insect control devices without any luring composition).

Claims
  • 1. An insect control device comprising: an outer shell comprising a plurality of orifices,a membrane impregnated with a luring composition, the luring composition comprising an isolated sexual attraction pheromone of male Tribolium castaneum as the sole luring pheromone, wherein the sexual attraction pheromone of male Tribolium castaneum has a molecular weight of approximately 210 g/mol, a molecular formula of C14H26O and a chemical structure having only one degree of unsaturation and a terminal carbonyl group, andan inner capsule located inside the outer shell, which defines an interior region comprising an insecticide formulation comprising isolated microsclerotia of Beauveria bassiana.
  • 2. The insect control device according to claim 1, wherein said membrane is comprised in a capsule attached to the outer shell.
  • 3. The insect control device according to claim 2, wherein said capsule comprises a conical surface.
  • 4. The insect control device according to claim 1, wherein the insecticide formulation comprises isolated microsclerotia of Beauveria bassiana and an agronomically acceptable carrier.
US Referenced Citations (71)
Number Name Date Kind
1024767 Dempster Apr 1912 A
1540621 Hanson Jun 1925 A
2784520 Johnson Mar 1957 A
4030233 Wunsche Jun 1977 A
4130245 Bryson Dec 1978 A
4244135 Harwoods Jan 1981 A
4251946 Lindley Feb 1981 A
4802303 Floyd, III Feb 1989 A
4813174 Cook Mar 1989 A
4817868 Cook Apr 1989 A
4921703 Higuchi May 1990 A
5069231 Rutherford Dec 1991 A
5070891 Rutherford Dec 1991 A
5189831 Miller Mar 1993 A
5413784 Wright May 1995 A
5452540 Dowd Sep 1995 A
5588250 Chiba Dec 1996 A
5685109 Rimback Nov 1997 A
5737870 Thind Apr 1998 A
5842305 Liao Dec 1998 A
5983558 Las Nov 1999 A
6018905 Lingren Feb 2000 A
6058646 Bishoff May 2000 A
6192621 Fain Feb 2001 B1
6216384 Dickson Apr 2001 B1
6370813 Nelson Apr 2002 B1
6517856 Roe Feb 2003 B1
6637149 Bauer Oct 2003 B1
6796082 Duston Sep 2004 B1
7412797 Hiscox Aug 2008 B1
7694456 Curtis Apr 2010 B1
8418399 Palencia-Adrubau Apr 2013 B2
9179662 Kort Nov 2015 B1
10765101 Willert Sep 2020 B2
20020032980 Nelson Mar 2002 A1
20020061324 Light May 2002 A1
20020112396 Nyberg Aug 2002 A1
20020134004 Gordon Sep 2002 A1
20030070348 Spragins Apr 2003 A1
20040001870 Durand Jan 2004 A1
20040068781 Hill Apr 2004 A1
20040088905 Price May 2004 A1
20040244274 Dellevigne Dec 2004 A1
20050000147 Westphal Jan 2005 A1
20050147634 Plato Jul 2005 A1
20060191189 Mayo Aug 2006 A1
20080196296 Studer Aug 2008 A1
20080245797 Berge Oct 2008 A1
20080302000 Kidder Dec 2008 A1
20090000181 Cink Jan 2009 A1
20100071254 Calkins Mar 2010 A1
20110072712 Black Mar 2011 A1
20110146133 Bunker Jun 2011 A1
20110289822 Duehl Dec 2011 A1
20120246998 Vasudeva Oct 2012 A1
20130091758 Hiley Apr 2013 A1
20140311016 Wang Oct 2014 A1
20150121746 Osinga May 2015 A1
20150164060 Pankowski Jun 2015 A1
20150335003 Zeamer Nov 2015 A1
20150359228 Grasso Dec 2015 A1
20150366210 Olson Dec 2015 A1
20160316726 Birger Nov 2016 A1
20160366870 Leier Dec 2016 A1
20170202199 Patel Jul 2017 A1
20170231211 Kupfer Aug 2017 A1
20180014524 Peterson Jan 2018 A1
20180035657 Ots Feb 2018 A1
20190234895 Smilanich Aug 2019 A1
20200060251 DaSilva Feb 2020 A1
20200344992 Kaye Nov 2020 A1
Foreign Referenced Citations (3)
Number Date Country
2727723 Jan 2010 CA
3030854 Jan 2018 CA
WO-2006045122 Apr 2006 WO
Non-Patent Literature Citations (6)
Entry
“Development of a pheromone trap for monitoring Tribolium castaneum,” M. Mullen. Oct. 1992. Journal of Stored Products Research. vol. 28, issue 4, pp. 245-249. (Year: 1992).
“Aggregation pheromone 4,8-dimethyldecanal and kairomone affect the orientation of Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae) adults” D. Dissanayaka et al. Dec. 2018. Journal of Stored Products Research. vol. 72, pp. 144-149. (Year: 2018).
“Beauvaria plus Microhilum, Tritirachium, and Sporothrix” NA Jul. 28, 2011. ARSEF: USDA-ARS Biological Integrated Pest Management Research. (Year: 2011).
K.W. Francke et al, “Chemical Signalling in Beetles,” Topics in Current Chemistry (2005) vol. 240, pp. 85-166, Germany.
D.L. Faustini et al., “Sexually Dimorphic Setiferous Sex Patch in the Male Red Flour Beetle, Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae): Site of Aggregation Pheromone Production,” Journal of Chemical Ecology, vol. 7, No. 2, 1981, Madison, Wisconsin.
L. Arnaud et al., “Is Dimethyldecanal a Common Aggregation Pheromone of Tribolium Flour Beetles?”, Journal of Chemical Ecology, vol. 28, No. 3, Mar. 2002, Gembloux, Belgium.
Related Publications (1)
Number Date Country
20200281206 A1 Sep 2020 US
Provisional Applications (1)
Number Date Country
62815536 Mar 2019 US