Method for mosquito control

Information

  • Patent Grant
  • 12201109
  • Patent Number
    12,201,109
  • Date Filed
    Thursday, March 23, 2023
    2 years ago
  • Date Issued
    Tuesday, January 21, 2025
    2 months ago
  • Inventors
  • Examiners
    • Lankford; Blaine
    • Van Buren; Lauren K
    Agents
    • Weyer, Esq.; Stephen J.
    • Stites & Harbison, PLLC
Abstract
A method for mosquito control is provided in the form of mosquito larvicide carrying insects which can be introduced in a mosquito population to thereby control the mosquito population. The larvicide carrier insects may include artificially generated adult insect carriers of a mosquito larvicide in which the mosquito larvicide has minimal impact on the adult insect carrier and which mosquito larvicide affects juvenile mosquito survival or interferes with metamorphosis of juvenile mosquitoes to adulthood. The larvicide carrier insects may be either male or female and may include mosquitoes and non-mosquito insects.
Description
FIELD OF THE INVENTION

The present invention relates to a method and a formulation for mosquito control and, in particular, a method and a formulation for mosquito control which includes, but is not limited to, using mosquitoes or other insects for delivering agents, e.g., insecticides such as a larvicide, to an insect population to thereby control the insect population.


BACKGROUND OF THE INVENTION

Malaria, dengue and dengue haemorrhagic fever, West Nile Virus (WNV) and other encephalites, human African trypanosomiasis (HAT), human filariasis, dog heartworm and other pathogens important to animals are on the increase. These diseases are transmitted via insects and, in particular, mosquitoes. Methods for controlling mosquito populations include the use of pesticides and vector control methods.


Existing insecticidal control methods rely upon field technicians, who fail to find and treat many breeding sites, which can be numerous, cryptic and inaccessible. Additional methods consist of area-wide treatment via airplane or wind-assisted dispersal from truck-mounted foggers. Unfortunately, the latter fail to treat many breeding sites and are complicated by variable environmental conditions. Barrera et al., “Population Dynamics of Aedes aegypti and Dengue as Influenced by Weather and Human Behavior in San Juan, Puerto Rico,” PLoS Neglected Tropical Diseases, 5:e1378, 2011, describing the effects of various breeding sites on disease.


Surveys of natural and artificial water containers demonstrate mosquitoes and other arthropods to be highly efficient in finding, inhabiting and laying eggs in variously sized, cryptic water pools, including tree holes and gutters high above ground level.


One prior formulation or method for treating mosquito populations includes the use of dissemination stations which are deployed in a target environment. The dissemination stations may be laced with a pesticide, including, but not limited to, a juvenile hormone analog. The dissemination station may include a box or other structure which attracts female mosquitoes. The mosquitoes enter the dissemination station, become exposed to the pesticide or hormone, and carry that hormone back to affect other mosquitoes by mating. An example of this mosquito control is described in the article by Devine et al., entitled “Using adult mosquitoes to transfer insecticides to Aedes aegypti larval habitats,” PNAS, vol. 106, no. 28, Jul. 14, 2009.


In tests of another dissemination station, researchers showed that males in the wild that acquire the pesticide from a station can transfer the pesticide to females during copulation. The females receiving pesticide particles via venereal transfer were then shown to cause a significant inhibition of emergence in larval bioassays. This was reported in the article by Gaugler et al, entitled “An autodissemination station for the transfer of an insect growth regulator to mosquito oviposition sites,” Med. Vet. Entomol. 2011.


In view of continuing mosquito problems, as noted, additional tools are required to control mosquitoes that are important as nuisance pests and disease vectors.


SUMMARY OF THE INVENTION

The present invention is directed to a novel, self-delivering, insecticidal formulations and delivery techniques. The formulations, in one form, are larvicide treated insects, such as male mosquitoes. The insecticidal formulations can control medically important mosquitoes. These medically important mosquitoes include mosquitoes having an economic or medical importance to animal or human health. Medically important mosquitoes include those listed in the Appendix to this disclosure.


One aspect of the present formulations and delivery techniques relates to a new larvicide treatment for males, as a formulation which can be used to control a mosquito population. The formulation can be generated by exposing adult insects, such as mosquitoes and, in particular, male mosquitoes, to a pesticide, such as a juvenile hormone which affects juvenile survival or interferes with metamorphosis of juvenile mosquitoes and has relatively little impact on adult mosquitoes. Advantageously, the adult insects are exposed to the pesticide in a controlled, factory environment. The factory-reared or captured from the wild adult insects which have been exposed to the pesticide are referred to as direct treated individuals (DTI). The DTI are then released into an environment in which one wishes to control the mosquito population. The DTI control a mosquito population by interacting with untreated individuals (e.g., mating), such that the pesticide, e.g., a larvicide, is communicated to other individuals (known as Indirectly Treated Individuals; (ITI)).


In specific further embodiments, the control method uses compounds that affect immature/juvenile stages (eggs, larvae, pupae) more than adults. A list of larvicidal compounds is maintained at the IR-4 Public Health Pesticides Database. Examples of compounds include (1) insect growth regulators such as juvenile hormone mimics or analogs, including methoprene, pyriproxyfen (PPF), and (2) Microbial larvicides, such as Bacillus thuringiensis and Bacillus sphaericus, herein incorporated by reference. Exemplary compounds are provided in Tables 1-3, below, in the Detailed Description section.


The present invention, in one form thereof, relates to a method for insect control. The method includes introducing insects which carry one or more insecticides comprising at least one larvicide, to an insect population, to thereby control the insect population. In one specific embodiment, the insects are adult males and the method further includes exposing the adult male insects to a pesticide which affects juvenile survival or interferes with metamorphosis of juvenile insects to adulthood, and which pesticide has little impact on adult insects.


In one further, specific embodiment, the insect population is a mosquito population. Further, the juvenile active insecticide (i.e. larvicide) may be within a chemical class (Table 1) or biological class (Table 2). Examples within the chemical class include insect growth regulators, such as juvenile hormone analogs or compounds which mimic juvenile hormones. For example, the larvicide may be pyriproxyfen or methoprene. Examples within the biological class include viruses, bacteria, protozoa, fungi and crustacean organisms or toxic compounds that they produce.


The present invention, in another form thereof, relates to a formulation for insect control which comprises an artificially generated adult insect carrier of a larvicide. The larvicide has minimal impact on the adult insect and the larvicide interferes with metamorphosis of juvenile insects to adulthood. In one specific formulation, the adult insect is a male mosquito and in an alternative form, the larvicide is pyriproxyfen, methoprene and microbial larvicides, including, but not limited to, Bacillus thuringiensis and Bacillus sphaericus.


The present invention, in one specific form is directed to a method for insect control that includes rearing insects in a laboratory or artificially controlled environment. A mosquito larvicide is applied to an exterior surface of the insects in a laboratory or controlled environment to produce insects which carry the mosquito larvicide. When the larvicide carrying insects are released to a mosquito population in the wild, the larvicide carrying insects control the mosquito insect population. The method in one specific further form includes releasing the larvicide carrying insects to a mosquito insect population in the wild to thereby control the mosquito insect population.


The method in one further specific form includes the larvicide carrying insects being non-mosquito insects. Alternatively, the insects can be female insects including female mosquitoes that have been altered to have limited ability to procreate, vector disease or bite.


As an alternative to non-mosquito insects or female mosquito insects as mosquito larvicide carrying insects, the insects can be male insects including male mosquitoes.


In yet a further alternative form, the method of applying one or more mosquito larvicide includes applying a larvicide coating to the surface of the insects, while the insects are in a controlled environment via (i) dusting with a powder, granular or otherwise solid larvicide directly at the insects or (ii) spraying with a liquid insecticide containing the one or more larvicide directed at the insects, wherein the one or more mosquito larvicide has minimal impact on the insects to which the larvicide is applied and which larvicide affects juvenile mosquito survival or interferes with metamorphoses of juvenile mosquito insects to adulthood.


In one specific form the larvicide applied to the insects is sufficient so that when the larvicide coated insects are released from the controlled environment into an environment with an indigenous mosquito population, the larvicide coated insects are effective to deliver a sufficient amount of larvicide to other insects or indigenous spawning sites to affect juvenile mosquito survival or interfere with metamorphoses of juvenile mosquitoes to adulthood, thereby controlling the indigenous mosquito population.


The present invention in one further form thereof is specifically directed to larvicide coated insects which are produced by any of the aforementioned methods described above.


The present invention in yet another further form is directed to insect carriers of mosquito larvicides produced by a method that includes applying a larvicide coating to surfaces of a population of suitable adult insects in a laboratory or controlled environment. The suitable insects are selected from the group consisting of non-mosquito insects, male mosquitoes, and female mosquitoes altered to have limited ability to procreate, vector disease or bite. The coating is applied via dusting with a powder, granular or otherwise solid insecticide directed at the insects or spraying with a liquid insecticide directed at the population of insects. The dusting or spraying produces larvicide coated insects. The insecticide comprises at least one larvicide and the insecticide has minimal impact on the suitable insects and which larvicide affects juvenile mosquito survival or interferes with metamorphoses of juvenile mosquitoes to adulthood. The larvicide coating applied to the insects is sufficient so that when the larvicide coated insects are released from the controlled environment and introduced into an environment with an indigenous mosquito population, the larvicide coated insects are effective to deliver a sufficient amount of larvicide to other insects' indigenous spawning site to affect juvenile mosquito survival or interfere with metamorphose of juvenile mosquitoes to adulthood, thereby controlling the indigenous mosquito population.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a graph showing survival of treated (black) and untreated (white) adults, with bars showing standard deviation, in accordance with the present invention.



FIG. 2 is a photograph showing larvicide coated mosquitoes.



FIG. 3 is a table with photographs showing mosquitoes with larvicide coating.





DETAILED DESCRIPTION

The present invention is directed to a method and a formulation for mosquito control. The formulation, in one advantageous form, is larvicide treated males. The treated males are generated from medically important adult male mosquitoes obtained via factory-rearing or captured from the wild. As a demonstration of the chemical class of juvenile active insecticides (Table 1), the adult male mosquitoes are exposed to a larvicide, such as pyriproxyfen (PPF), advantageously in a controlled laboratory or factory environment. PPF is a juvenile hormone mimic which interferes with metamorphosis of juvenile mosquitoes and has relatively little impact on adult mosquitoes. Thus, PPF is commonly used as a mosquito larvicide, but is not used as an adulticide.


The treated males are subsequently referred to as the Direct Treated Individuals (DTI), and this is the insecticidal formulation. The DTI are released into areas with indigenous conspecifics. Male mosquitoes do not blood feed or transmit disease. Accordingly, male mosquitoes provide unique advantages in the present control method as couriers of the larvicide. The DTI interact with untreated individuals (e.g., mating), such that PPF is communicated to the other individuals to produce Indirectly Treated Individuals (ITI). The PPF is delivered by both the DTI and ITI in the wild/in the environment, into the breeding areas, where the PPF accumulates to lethal doses and acts as a larvicide. It is noted that the PPF would impact additional mosquito species that share the same breeding site, providing control of additional mosquito species.


In an alternative control method, female mosquitoes can be used as the DTI. However, female mosquitoes blood feed and can vector disease. The use of female mosquitoes are applicable when the females are incapacitated prior to deployment in the environment and the females have limited procreation ability, bite and vector diseases.


In a further alternative method, other larvicidal active ingredients can be used which include, but are not limited to, compounds that affect juvenile survival or affect immature/juvenile stages of development (eggs, larvae, pupae) more than adults. A list of larvicidal compounds is maintained at the IR-4 Public Health Pesticides Database. Examples of compounds include (1) insect growth regulators such as juvenile hormone mimics or analogs, including methoprene, pyriproxyfen (PPF), and (2) Microbial larvicides, such as Bacillus thuringiensis and Bacillus sphaericus. Tables 1-3 provide abridged, exemplary lists of suitable compounds.









TABLE 1





Juvenile Active Insecticide - Chemical*

















Azadirachtin



Diflubenzuron



Methoprene



Neem Oil (Azadirachta indica)



Novaluron



Pyriproxyfen



S-Methoprene



S-Hydropene



Temephos







*A list of Public Health Pesticides is maintained at the IR-4 Public Health Pesticides Database













TABLE 2





Juvenile Active Insecticide - Biological*


















Ascogregarine spp.





Bacillus sphaericus





Bacillus thuringiensis israelensis




Baculoviruses




Copepoda spp.





Densovirinae spp.





Lagenidium giganteum





Microsporida spp.




Spinosad



Spinosyn







*A list of Public Health Pesticides is maintained at the IR-4 Public Health Pesticides Database













TABLE 3





Public Health Pesticides from the IR-4 Database*

















(−)-cis-Permethrin
Cyfluthrin
Oil of Basil, African Blue




(Ocimum kilimandscharicum ×





basilicum)



(−)-trans-Permethrin
Cyhalothrin
Oil of Basil, Dwarf Bush




(Ocimum basilicum var.





minimum)



(+)-cis-Permethrin
Cyhalothrin, epimer R157836
Oil of Basil, Greek Bush




(Ocimum minimum)


(±)-cis,trans-Deltamethrin
Cyhalothrin, Total
Oil of Basil, Greek Column



(Cyhalothrin-L + R157836
(Ocimum × citriodorum



epimer)
‘Lesbos’)


(1R)-Alpha-Pinene
Cypermethrin
Oil of Basil, Lemon (Ocimum





americanum)



(1R)-Permethrin
Cyphenothrin
Oil of Basil, Sweet (Ocimum





basilicum)



(1R)-Resmethrin
DDD, o, p
Oil of Basil, Thai Lemon




(Ocimum × citriodorum)


(1R,cis) Phenothrin
DDD, other related
Oil of Bay Laurel (Laurus





nobilis)



(1R,trans) Phenothrin
DDD, p, p′
Oil of Cajeput (Melaleuca





leucadendra)



(1S)-Alpha-Pinene
DDE
Oil of Cassumunar Ginger




(Zingiber montanum)


(1S)-Permethrin
DDE, o, p
Oil of Fishpoison (Tephrosia





purpurea)



(E)-Beta-Caryophyllene
DDT
Oil of Ginger (Zingiber





officinale)



1,1-dichloro-2,2-bis-(4-ethyl-
DDT, o, p′
Oil of Gurjun Balsam


phenyl) ethane

(Dipterocarpus turbinatus




balsam)


1,8-Cineole
DDT, p, p′
Oil of Lemon Eucalyptus




(Corymbia citriodora)


1H-Pyrazole-3-carboxamide,
DDVP
Oil of Lemon Mint


5-amino-1-[2,6-dichloro-4-

(Monarda citriodora)


(trifluoromethyl)phenyl]-4-


[(trifluoromethyl)sulfinyl]


1-Naphthol
DDVP, other related
Oil of Melaleuca




(Melaleuca spp.)


1-Octen-3-ol
DEET
Oil of Myrcia




(Myrcia spp.)


2-(2-(p-(diisobutyl) phenoxy)
Deltamethrin
Oil of Nutmeg (Myristica


ethoxy) ethyl dimethyl


fragrans)



ammonium chloride


2-butyl-2-ethyl-1,3-
Deltamethrin (includes
Oil of Palmarosa


propanediol
parent Tralomethrin)
(Cymbopogon martinii)


2-Hydroxyethyl Octyl Sulfide
Deltamethrin (isomer
Orange Oil



unspecified)
(Citrus sinensis)


2-Isopropyl-4-methyl-6-
Deltamethrin, other related
Oregano Oil


hydroxypyrimidine

(Origanum vulgare)


2-Pyrroline-3-carbonitrile, 2-
Desmethyl Malathion
Ortho-Phenylphenol


(p-chlorophenyl)-5-hydroxy-


4-oxo-5-


3,7-dimethyl-6-octen-1-ol
Desulfinyl Fipronil
Ortho-Phenylphenol, Sodium


acetate

Salt


3,7-dimethyl-6-octen-1-ol
Desulfinylfipronil Amide
Oviposition Attractant A


acetate


3-Phenoxybenzoic Acid
Diatomaceous Earth
Oviposition Attractant B


4-Fluoro-3-phenoxybenzoic
Diatomaceous Earth, other
Oviposition Attractant C


acid
related


Absinth Wormwood
Diazinon
Oviposition Attractant D


(Artemisia absinthium)


Absinthin
Diazoxon
Oxymatrine


Acepromazine
Dibutyl Phthalate
Paracress Oil




(Spilanthes acmella)


Acetaminophen
Didecyl Dimethyl Ammonium
P-Cymene



Chloride


Acetamiprid
Dieldrin
Penfluron


Acetic Acid
Diethyl Phosphate
Pennyroyal Oil (American




False Pennyroyal, Hedeoma





pulegioides)



AI3-35765
Diethylthio Phosphate
Peppermint




(Mentha × piperita)


AI3-37220
Diflubenzuron
Peppermint Oil




(Mentha × piperita)


Alkyl Dimethyl Benzyl
Dihydro Abietyl Alcohol
Permethrin


Ammonium Chloride


(60% C14, 25% C12, 15% C16)


Alkyl Dimethyl Benzyl
Dihydro-5-heptyl-2(3H)-
Permethrin, other related


Ammonium Chloride
furanone


(60% C14, 30% C16, 5% C12,


5% C18)


Alkyl Dimethylethyl Benzyl
Dihydro-5-pentyl-2(3H)-
Phenothrin


Ammonium Chloride
furanone


(50% C12, 30% C14, 17% C16,


3% C18)


Alkyl Dimethylethyl Benzyl
Dimethyl Phosphate
Phenothrin, other related


Ammonium Chloride


(68% C12, 32% C14)


Allethrin
Dimethyldithio Phosphate
Picaridin


Allethrin II
Dimethylthio Phosphate
Pine Oil (Pinus pinea = Stone




Pine)


Allethrins
Dinotefuran
Pine Oil (Pinus spp.)


Allicin
Dipropyl Isocinchomeronate
Pine Oil (Pinus sylvestris =



(2,5 isomer)
Scots Pine)


Allyl Caproate
Dipropyl Isocinchomeronate
Pine Tar Oil (Pinus spp.)



(3,5 isomer)


Allyl Isothiocyanate
Dipropylene Glycol
Pinene


Alpha-Cypermethrin
d-Limonene
Piperine


Alpha-lonone
d-Phenothrin
Piperonyl Butoxide


Alpha-Pinene
Dried Blood
Piperonyl Butoxide,




technical, other related


Alpha-Terpinene
d-trans-Beta-Cypermethrin
Pirimiphos-Methyl


Aluminum Phosphide
Esfenvalerate
PMD (p-Menthane-3,8-diol)


Amitraz
Ester Gum
Potassium Laurate




Potassium Salts of Fatty


Ammonium Bicarbonate
Estragole
Acids


Ammonium Fluosilicate
Etofenprox
Potassium Sorbate


Anabasine

Eucalyptus Oil (Eucalyptus

Prallethrin



spp.)


Anabsinthine
Eugenol
Propoxur


Andiroba Oil (Carapa
Eugenyl Acetate
Propoxur Phenol



guianensis)



Andiroba Oil (Carapa
Extract of Piper spp.
Propoxur, other related



procera)



Andiroba, African (Carapa
Extracts of Common Juniper
Putrescent Whole Egg Solids



procera)

(Juniperus communis)


Andiroba, American (Carapa
Fenchyl Acetate
Pyrethrin I



guianensis)



Anethole
Fenitrothion
Pyrethrin II


Anise (Pimpinella anisum)
Fennel (Foeniculum vulgaris)
Pyrethrins


Aniseed Oil (Pimpinella
Fennel Oil (Foeniculum
Pyrethrins and Pyrethroids,



anisum)


vulgaris)

manufg. Residues


Atrazine
Fenoxycarb
Pyrethrins, other related


Avermectin
Fenthion
Pyrethrum


Azadirachtin
Fenthion Oxon
Pyrethrum Marc


Azadirachtin A
Fenthion Sulfone
Pyrethrum Powder other




than Pyrethrins



Bacillus sphaericus

Fenthion Sulfoxide
Pyriproxyfen



Bacillus sphaericus, serotype


Ferula hermonis

Pyrrole-2-carboxylic acid, 3-


H-5A5B, strain 2362

bromo-5-(p-chlorophenyl)-4-




cyano-




Pyrrole-2-carboxylic acid, 5-



Bacillus thuringiensis


Ferula hermonis Oil

(p-chlorophenyl)-4-cyano-



israelensis


(metabolite of AC 303268)



Bacillus thuringiensis

Finger Root Oil

Quassia




israelensis, serotype H-14

(Boesenbergia pandurata)



Bacillus thuringiensis

Fipronil
Quassin



israelensis, strain AM 65-52




Bacillus thuringiensis

Fipronil Sulfone
R-(−)-1-Octen-3-ol



israelensis, strain BK, solids,



spores, and insecticidal


toxins, ATCC number 35646



Bacillus thuringiensis

Fipronil Sulfoxide
Red Cedar Chips (Juniperus



israelensis, strain BMP 144



virginiana)




Bacillus thuringiensis

Fragrance Orange 418228
Resmethrin



israelensis, strain EG2215




Bacillus thuringiensis

Gamma-Cyhalothrin
Resmethrin, other related



israelensis, strain IPS-78




Bacillus thuringiensis

Garlic (Allium sativum)
Rhodojaponin-III



israelensis, strain SA3A



Balsam Fir Oil (Abies
Garlic Chives Oil (Allium
Rose Oil (Rosa spp.)



balsamea)


tuberosum)



Basil, Holy (Ocimum
Garlic Oil (Allium sativum)
Rosemary (Rosmarinus



tenuiflorum)



officinalis)



Bendiocarb
Geraniol
Rosemary Oil (Rosmarinus





officinalis)



Benzyl Benzoate
Geranium Oil (Pelargonium
Rosmanol




graveolens)



Bergamot Oil (Citrus
Glyphosate, Isopropylamine
Rosmaridiphenol



aurantium bergamia)

Salt


Beta-Alanine
Hexaflumuron
Rosmarinic Acid


Beta-Caryophyllene
Hydroprene
Rotenone


Beta-Cyfluthrin
Hydroxyethyl Octyl Sulfide,
R-Pyriproxyfen



other related


Beta-Cypermethrin
Imidacloprid
R-Tetramethrin


Beta-Cypermethrin ([(1R)-
Imidacloprid Guanidine
Rue Oil


1a(S*),3a] isomer)

(Ruta chalepensis)


Beta-Cypermethrin ([(1R)-
Imidacloprid Olefin
Ryania


1a(S*),3b] isomer)


Beta-Cypermethrin ([(1S)-
Imidacloprid Olefinic-
Ryanodine


1a((R*),3a] isomer)
Guanidine


Beta-Cypermethrin ([(1S)-
Imidacloprid Urea
S-(+)-1-Octen-3-ol


1a(R*),3b] isomer)


Beta-Myrcene
Imiprothrin
Sabinene


Beta-Pinene
Indian Privet Tree Oil (Vitex
Sabinene




negundo)



Betulinic Acid
Ionone
Sage Oil (Salvia officinalis)


Bifenthrin
IR3535 (Ethyl
Sassafras Oil (Sassafras



Butylacetylaminopropionate)

albidum)



Billy-Goat Weed Oil
Isomalathion

Schoenocaubn officinale



(Ageratum conyzoides)


Bioallethrin = d-trans-


Allethrin
Isopropyl Alcohol
S-Citronellol


Biopermethrin
Japanese Mint Oil (Mentha
Sesame (Sesamum indicum)




arvensis)



Bioresmethrin
Jasmolin I
Sesame Oil (Sesamum





indicum)



Bitter Orange Oil (Citrus
Jasmolin II
Sesamin



aurantium)



Blend of Oils: of Lemongrass,
Kerosene
Sesamolin


of Citronella, of Orange, of


Bergamot; Geraniol, lonone


Alpha, Methyl Salicylate and


Allylisothioc


Boric Acid
L-(+)-Lactic acid
S-Hydroprene


Borneol
Lactic Acid
Silica Gel


Bornyl Acetate

Lagenidium giganteum

Silver Sagebrush




(Artemisia cana)


Bromine

Lagenidium giganteum

Silver Sagebrush Oil



(California strain)
(Artemisia cana)


Butane
Lambda-Cyhalothrin
S-Methoprene


Butoxy Poly Propylene Glycol
Lambda-Cyhalothrin R ester
Sodium Chloride


Caffeic Acid
Lambda-Cyhalothrin S ester
Sodium Lauryl Sulfate


Camphene
Lambda-Cyhalothrin total
Solvent Naphtha




(Petroleum), Light Aromatic


Camphor
Lauryl Sulfate
Soybean Oil (Glycine max)


Camphor Octanane
Lavender Oil (Lavendula
Spinosad




angustifolia)



Canada Balsam
Leaves of Eucalyptus
Spinosyn A



(Eucalyptus spp.)


Carbaryl
Leech Lime Oil (Citrus
Spinosyn D




hystrix)



Carbon Dioxide
Lemon Oil (Citrus limon)
Spinosyn Factor A




Metabolite


Carnosic Acid
Licareol
Spinosyn Factor D




Metabolite


Carvacrol
Limonene
S-Pyriproxyfen


Caryophyllene
Linalool
Succinic Acid


Cassumunar Ginger Oil
Linalyl Acetate
Sulfoxide


(Zingiber montanum)


Castor Oil (Ricinus
Linseed Oil (Linum
Sulfoxide, other related



communis)


usitatissimum)



Catnip Oil (Nepeta cataria)

Lonchocarpus utilis (Cubé)

Sulfur


Catnip Oil, Refined (Nepeta
Lupinine
Sulfuryl Fluoride



cataria)



Cedarwood Oil (Callitropsis
Magnesium Phosphide
Sweet Gale Oil



nootkatensis = Nootka


(Myrica gale)


Cypress, Alaska Yellow


Cedarwood)


Cedarwood Oil (Cedrus
Malabar (Cinnamomum
Tangerine Oil (Citrus



deodara = Deodar Cedar)


tamala)


reticulata)



Cedarwood Oil (Cedrus spp. =
Malabar Oil (Cinnamomum
Tansy Oil (Tanacetum


True Cedars)

tamala)


vulgare)



Cedarwood Oil (Cupressus
Malaoxon
Tar Oils, from Distillation of



funebris = Chinese Weeping


Wood Tar


Cypress)


Cedarwood Oil (Cupressus
Malathion
Tarragon Oil (Artemisia


spp. = Cypress)


dracunculus)



Cedarwood Oil (Juniper and
Malathion Dicarboxylic Acid
Tarwood Oil


Cypress)

(Laxostylis alata)


Cedarwood Oil (Juniperus
Malic Acid
tau-Fluvalinate



ashei = Ashe's Juniper, Texan



Cedarwood)


Cedarwood Oil (Juniperus
Marigold Oil (Tagetes
Teflubenzuron



macropoda = Pencil Cedar)


minuta)



Cedarwood Oil (Juniperus spp.)
Matrine
Temephos


Cedarwood Oil (Juniperus
Menthone
Temephos Sulfoxide



virginiana = Eastern



Redcedar, Southern


Redcedar)


Cedarwood Oil (Oil of
Metaflumizone
Terpinene


Juniper Tar = Juniperus spp.)


Cedarwood Oil (Thuja
Metarhizium anisopliae
Terpineol



occidentalis = Eastern

Strain F52 Spores


Arborvitae)


Cedarwood Oil (Thuja spp. =
Methoprene
Tetrachlorvinphos, Z-isomer


Arborvitae)


Cedarwood Oil (unspecified)
Methoprene Acid
Tetramethrin


Cedrene
Methyl Anabasine
Tetramethrin, other related


Cedrol
Methyl Bromide
Theta-Cypermethrin


Chevron 100 Neutral Oil
Methyl Cinnamate
Thiamethoxam


Chlordane
Methyl cis-3-(2 2-
Thujone



dichlorovinyl)-2 2-



dimethylcyclopropane-1-



carboxylate


Chlorfenapyr
Methyl Eugenol
Thyme




(Thymus vulgaris)


Chloropicrin
Methyl Nonyl Ketone
Thyme Oil




(Thymus vulgaris)


Chlorpyrifos
Methyl Salicylate
Thymol


Cinerin I
Methyl trans-3-(2 2-
Timur Oil



dichlorovinyl)-2 2-
(Zanthoxylum alatum)



dimethylcyclopropane-1-



carboxylate


Cinerin II
Metofluthrin
Tralomethrin


Cinerins
MGK 264 (N-octyl
trans-3-(2,2-Dichlorovinyl)-



Bicycloheptene
2,2-dimethylcyclopropane



Dicarboximide)
carboxylic acid


Cinnamon
Mineral Oil
Trans-Alpha-Ionone


(Cinnamomum zeylanicum)


Cinnamon Oil
Mineral Oil, Petroleum
Transfluthrin


(Cinnamomum zeylanicum)
Distillates, Solvent Refined



Light


cis-3-(2,2-Dichlorovinyl)-2,2-
Mixture of Citronella Oil,
trans-Ocimene


dimethylcyclopropane
Citrus Oil, Eucalyptus Oil,


carboxylic acid
Pine Oil


cis-Deltamethrin
MMF (Poly (oxy-1,2-
Transpermethrin



ethanediyl), alpha-



isooctadecyl-omega-



hydroxy)


Cismethrin
Mosquito Egg Pheromone
trans-Resmethrin


cis-Permethrin
Mugwort (Artemisia vulgaris)
Trichlorfon


Citral
Mugwort Oil (Artemisia
Triethylene Glycol




vulgaris)



Citric Acid
Mustard Oil (Brassica spp.)
Triflumuron


Citronella
Myrcene
Trifluralin


(Cymbopogon winterianus)


Citronella Oil
Naled
Turmeric Oil (Curcuma


(Cymbopogon winterianus)


aromatica)



Citronellal
Neem Oil (Azadirachta
Uniconizole-P




indica)



Citronellol

Nepeta cataria (Catnip)

Ursolic Acid


Citrus Oil (Citrus spp.)
Nepetalactone
Veratridine


Clove
Nicotine

Verbena Oil



(Syzygium aromaticum)

(Verbena spp.)


Clove Oil
Nonanoic Acid
Verbenone


(Syzygium aromaticum)


CME 13406
Nornicotine
Violet Oil




(Viola odorata)


Coriander Oil
Novaluron
White Pepper


(Coriandrum sativum)

(Piper nigrum)


Coriandrol
Ocimene
Wintergreen Oil




(Gaultheria spp.)



Coriandrum sativum


Ocimum × citriodorum (Thai

Wood Creosote


(Coriander)
Lemon Basil)


Corn Gluten Meal

Ocimum × citriodorum

Wood Tar



‘Lesbos’ (Greek Column Basil)


Corn Oil (Zea mays ssp.

Ocimum americanum

Wormwood Oil (Artemisia



Mays)

(Lemon Basil)

absinthium)




Corymbia citriodora (Lemon


Ocimum basilicum (Sweet

Ylang-ylang Oil



Eucalyptus)

Basil)
(Canagium odoratum)


Cottonseed Oil

Ocimum basilicum var.

Zeta-Cypermethrin


(Gossypium spp.)

minimum (Dwarf Bush Basil)



Coumaphos

Ocimum kilimandscharicum ×

Zinc Metal Strips




basilicum (African Blue Basil)



Cryolite

Ocimum minimum (Greek




Bush Basil)


Cubé Extracts
Oil of Balsam Peru


(Lonchocarpus utilis)
(Myroxylon pereirae)





*A list of Public Health Pesticides is maintained at the IR-4 Public Health Pesticides Database; Version from March 2012






In yet another alternative method, the aforementioned methods can be applied to additional susceptible arthropods, including economically and medically important pests (including animal and human health), where one life stage and/or sex does not cause direct damage.


In other alternative delivery techniques, the present method can be applied using non-targeted, beneficial or non-pest arthropods that utilize the same breeding site as the targeted arthropod. For example, the DTI could be PPF-treated arthropods that come in contact with the targeted insect's breeding sites. As an example, Oytiscidae adults (Predaceous Diving Beetles) could be reared or field collected and treated with PPF to become the DTI. Additional candidate insects that could serve as the DTI include, but are not limited to: Diptera (e.g., Tipulidae, Chironomidae, Psychodidae, Ceratapogonidae, Cecidomyiidae, Syrphidae, Sciaridae, Stratiomyiidae, Phoridae), Coleoptera (e.g., Staphylinidae, Scirtidae, Nitidulidae, Oytiscidae, Noteridae) and Hemiptera (e.g., Pleidae, Belostomatidae, Corixidae, Notonectidae, Nepidae).


An additional benefit of the latter strategy (i.e. non-Culicid DTI) is that the DTI may be easier to rear, larger size (allowing increased levels of PPF), be less affected by the PPF, or have an increased probability of direct contact with the breeding site of the targeted arthropod (i.e. not necessarily rely on transfer of the PPF via mating, improved location of breeding sites).


It is noted that the species of DTI would vary based upon the specific application, habitat and location. For example, the regulatory issues may be simplified if the species used for DTI were indigenous. However, it is noted that there are numerous examples of exotic arthropods being imported for biological control. Furthermore, different DTI species may be more/less appropriate for urban, suburban and rural environments.


Referring to the following examples for exemplary purposes only, but not to limit the scope of the invention in any way, Aedes albopictus were used in experiments from a colony established in 2008 from Lexington, Ky. Callosobrochus maculatus were purchased from Carolina Biological Supply Company (Burlington, N.C.) and maintained on mung beans (Vigna radiata). Rearing and experiments were performed in ambient conditions (˜25° C. ; 80% humidity). Larvae were reared in pans with ˜500 ml water and crushed cat food (Science Diet; Hill's Pet Nutrition, Inc.). Adults were provided with raisins as a sugar source. For line maintenance, females were blood fed by the author.


Sumilary 0.5G was generously provided by Sumitomo Chemical (London, UK). Liquid PPF was purchased from Pest Control Outlet (New Port Richey, Fla.). Bacillus thuringiensis subspecies israelensis technical powder was purchased from HydroToYou (Bell, Calif.). For application, Sumilary granules were crushed into a fine powder and applied using a bellows-type dusting apparatus (J.T. Eaton Insecticidal Duster #530; Do-it-yourself Pest Control, Suwanee, Ga.). Liquid PPF was applied using a standard squirt bottle (WalMart, Lexington, Ky.). Treated adults were held in individualized bags with a raisin as a sucrose source until used in larval bioassays. Larval bioassays were performed in 3 oz. Dixie Cups (Georgia-Pacific, Atlanta, Ga.) containing ten L3 larvae, 20 ml water and crushed cat food.


Referring to methods for the larvicide application to the selected mosquito larvicide carrier insects in powder by dusting or liquid by spraying insects, any application technique known to those skilled in the art can be used. For example, the method disclosed in JP5-320001 (hereinafter incorporated by reference) describes spraying its captured female mosquitoes with a larvicide while the mosquitoes are contained. See JP5-320001, paragraph [0015]. Further, reference is made to the book entitled Mosquito Ecology—Field Sampling Methods, John B. Silver, 2008, Chapter 14 (herein incorporated by reference), which describes dusting target insects which are necessarily contained or confined such as in wire cages with mosquito netting.


As a person skilled in the art will appreciate, flying insects necessarily require confinement during a larvicide application process.


Dusting or spraying insects in a confined space with a larvicide produces a larvicide coating essentially over the entire exterior surface of the target insects. FIG. 2 is a photograph showing the complete larvicide coating of the target insects (mosquitoes in the photograph). It is important to note that portions of the insects' wings, back, abdomen, tarsi (“feet”) and other parts will necessarily be coated.


Adult treatment does not affect survival. Male and female Ae. albopictus treated with pulverized Sumilary showed good survival in laboratory assays, which is indistinguishable from that of untreated control individuals. In an initial assay, 100% survival was observed for adults in both the Sumilary treated (n=8 replications) and untreated control groups (n=2 replications) during a two-day observation period. In a second comparison, adults were monitored for eight days. Similar to the initial experiment, no difference was observed between the treated and control groups. Specifically, a similar average longevity was observed comparing the Sumilary treated (6.3±2.0 days; n=4) and undusted control (7.3 days; n=1) groups. In a third experiment, treated and untreated adults were separated by sex and monitored for eight days. Similar to prior experiments, survival was not observed to differ between the treated and untreated groups (Figure).


In a separate experiment, the survival of beetles (Callosobrochus maculatus) dusted with Sumilary were compared to an undusted control group. In both the treatment and control groups, 100% survival was observed during the four day experiment.


To assess the larvicidal properties of treated adults, Sumilary dusted adults and undusted control adults were placed individually into bioassay cups with larvae. No adults eclosed from the five assay cups receiving a treated adult; in contrast, high levels of adult eclosion was observed from all four control assay cups that received an untreated adult. Chi square analysis shows the adult eclosion resulting in assays receiving a treated adult to be significantly reduced compared to that in the control group (X2 (1, N=9)=12.37, p<0.0004). The bioassay experiment was repeated in a subsequent, larger experiment, yielding similar results; adult eclosion in the treated group was significantly reduced compared to the control group (X2 (1, N=24)=13.67, p<0.0002).


A similar bioassay was used to assess the larvicidal properties of treated beetles. Similar to the prior results, adult eclosion from assays in the treated beetle group was significantly reduced compared to the control group (X2 (1, N=14)=13.38, p<0.0003).


To examine an additional formulation of PPF, an identical bioassay was performed, but a liquid PPF solution was applied (using the techniques disclosed herein) to mosquito adults, instead of Sumilary dust. Similar to the prior results, adult eclosion in the treated group was significantly reduced compared to the control group (X2 (1, N=14)=16.75, p<0.0001).


To examine an example of the biological class of juvenile active insecticides (Table 2) and different active ingredients, an identical bioassay was performed, but a powder formulation of Bacillus thuringiensis subspecies israelensis technical powder was applied to mosquito adults, using the same method as the Sumilary dust. Similar to the prior results, no difference was observed between the longevity of treated versus untreated adults (X2 (1, N=15)=3.2308, p>0.09). Upon exposing larvae to treat adults, eclosion was significantly reduced compared to the control group (X2 (1, N=28)=15.328, p<0.0001).


The results demonstrate that C. maculatus and A. albopictus adults do not experience reduced survival resulting from direct treatment with the insecticides. Specifically, the survival of treated mosquitoes and beetles did not differ significantly from that of the untreated conspecifics. The results are consistent with the traits required for the proposed application of treated adults as a self-delivering larvicide. Treated adults must survive, disperse and find breeding sites under field conditions. The results of the feasibility assays reported here provide evidence of an advantageous method of mosquito or other arthropod control.


Bioassays characterizing the larvicidal properties of treated adults show significant lethality resulting from the presence of treated mosquitoes and beetles. Similar results were observed for multiple formulations (i.e. dust and liquid) and multiple active ingredients. Furthermore, representative examples from each of the chemical and biological classes (Tables 1 and 2) of juvenile active insecticides have been demonstrated. This is also consistent with those traits required for the proposed application of treated arthropods as a self-delivering insecticide. Specifically, treated arthropods that reach mosquito breeding sites can be expected to impact immature mosquitoes that are present at the site.


Experiment


The following experiment demonstrates the effectiveness of complete larvicide coating on target mosquito larvicide carrier insects.


The following experiment shows how a larvicide coating applied to insects by (1) dusting with a powder and (2) spraying with a liquid. The experiment demonstrates coverage using the spraying and dusting techniques described above.


Prior to the release of mosquitoes (larvicide carrier insects), dusting or liquid spraying techniques were used to treat mosquitoes held in a confined area (e.g. cage): 1) a dusting application using a powder-based formulation and 2) a spray application using a liquid formulation. One group of 1000 mosquitoes was treated with dust. A second group of 1000 mosquitoes was sprayed. And a third group was sprayed with water (negative control). For each application method, 100 individuals from each group were randomly selected and analyzed. The spraying and dusting was done in accordance with the disclosed techniques of the present disclosure.


Each group was analyzed under a UV microscope to assess coverage. Coverage was assessed for the head, thorax, abdomen and legs of each individual. Presence of the larvicide was indicated by fluorescing particles located on each body part (FIG. 3). Results demonstrate the application methods provided a consistent rate of coverage per application method (FIG. 2). The dusting application method resulted in a heavier pesticide load when compared to the liquid application method. However, for both application methods, all body parts analyzed were found to have pesticide particles present for all individuals assessed (Table 4). No fluorescing particles were identified on individuals within the water-treated control group assessed in the study.









TABLE 4







Coverage results of individuals analyzed for the


presence of pesticide following ADAM applications












Application
Individuals
Head
Thorax
Abdomen
Legs
















Method
Analyzed
Present
Absent
Present
Absent
Present
Absent
Present
Absent



















Control
100
0
100
0
100
0
100
0
100


Dusting
100
100
0
100
0
100
0
100
0


Spray
100
100
0
100
0
100
0
100
0









Table 4 shows 100% of the insects sprayed and dusted had their entire head, thorax, abdomen and legs covered with the larvicide.


It will now be clear that the present invention is directed to aw novel formulation and method for treating insect populations, including, but not limited to, mosquito populations. Unlike prior control methods that disseminate a pesticide using dissemination stations, followed by an insect in the wild entering the dissemination station to become treated with the pesticide, the present formulation and method starts with generating insect carriers in an artificial controlled environment or setting. The insect carriers can either be factory-reared or adults captured from the wild. Subsequently, the carriers are released into an environment as the control agent or formulation. Thus, the carriers, i.e. the insects with the pesticide/larvicide, are the formulation for insect control, whereas, in prior methods and formulations, the formulation is a treated dissemination station, not a treated insect.


One of ordinary skill in the art will recognize that the present treatment, which targets insect larvae, offers advantages over prior art techniques of insect control which target adult insects. The present method is a trans-generation insect control technique which targets the next generation of insects, whereas prior techniques target the present generation, i.e. adult insects. For example, Garcia-Munguia et al., “Transmission of Beauveria bassiana from male to female Aedes aegypti mosquitoes,” Parasites & Vectors, 4:24, 2011 is a paper published on Feb. 26, 2011 describing mosquito control of adults and, thus, the paper describes the killing of the present generation of insects. The Garcia-Munguia paper describes using fungus-treated males to deliver insecticidal fungus to adult females. The fungus shortens the female lifespan and reduces fecundity of adult females. This type of approach (using insects to deliver an adulticide) is not particularly novel, and has been used in several important insect species, including examples described in Baverstock et al., “Entomopathogenic fungi and insect behaviour: from unsuspecting hosts to targeted vectors,” Biocontrol, 55:89-102, 2009.


As described above, the present technique uniquely uses factory-treatment of adult insects with a larvicide in which the larvicide is chemical or biological in nature. No prior technique includes the manufacturing of larvicidal-treated insects for trans-generational delivery. Further, unlike prior techniques that treat adults with fungi that kills adults, the present technique merely treats adult males with larvicidal compounds which do not kill the adult males; rather, the treatment delivers the larvicidal compounds in a trans-generational delivery to kill the next generation, i.e. larvae.


Advantages which follow from the present technique include using the adults treated with the larvicide to communicate the larvicide to other adults through the lifespan of the initially treated adult insect. As a result, there is an exponential effect of the present technique which delivers a larvicide using treated adults to transfer the treatment to other adults, rather than prior techniques which kill the adult insect.


Further, the present technique delivers the larvicide by the treated adults into breeding sites where the larvicide can affect and kill thousands of developing, immature mosquitoes. This technique is unlike prior techniques which merely target the adults and, thus, only kill the directly affected adults and not thousands of developing, immature mosquitoes, i.e. a next generation of insects.


In addition, the present technique allows for the treatment of insect breeding sites, including cryptic, i.e. previously unknown, breeding sites which prior insect control techniques do not treat.


Further, the present technique allows one to affect insect populations of the species of a treated insect, as well as other species which share a common breeding site. Since the present technique uses adult insects to deliver a larvicide to a breeding site, the present technique allows for the transmission of a larvicide to breeding sites which may be common among more than one insect species. As a result, the present technique can target the species of the treated insect, as well as insects which share a common breeding site.


In addition, in contrast to adulticide methods, the present larvicide technique allows a pesticide to persist in a breeding site after the treated insect has departed or died.


One additional advantage of the present method is that the agents being disseminated are the insects themselves, as carriers of the insecticide which will directly affect an insect population. Prior formulation and methods require indirect dissemination, in which insects of a population in the wild must first find a dissemination station, acquire an appropriate dose of the insecticide, and then return to the population with the larvicide of a dissemination station in order to have an affect on the insect population.


It will now be clear to one of ordinary skill in the art that the present formulation of pesticide carrier insects and the present method for controlling insect populations based on the present experiments. For example, if the insects have a larval stage, adult insects can be used as carriers of larvicides which have minimal affect on the adult insect, but are lethal to the larvae, thereby controlling the insect population.


While the invention has been described in connection with numerous embodiments, it is to be understood that the specific mechanisms and techniques which have been described are merely illustrative of the principles of the invention, numerous modifications may be made to the methods and apparatus described without departing from the spirit and scope of the invention.

Claims
  • 1. A method for mosquito control, comprising: applying in a laboratory or artificially controlled environment, one or more mosquito larvicides to an exterior surface of adult male mosquitoes, that were reared in a laboratory or artificially controlled environment, to produce larvicide carrying adult male mosquitoes; anddelivering said larvicide carrying adult male mosquitoes for treatment of a mosquito breeding site to thereby control a mosquito population.
  • 2. The method of claim 1, wherein applying one or more mosquito larvicides comprises applying a larvicide coating to the surface of the adult male mosquitoes via (i) dusting with a powder, granular or otherwise solid larvicide directed at the adult male mosquitoes or (ii) spraying with a liquid insecticide containing the one more larvicides directed at the adult male mosquitoes, wherein said the one or more mosquito larvicides has minimal impact on the adult male mosquitoes to which the larvicide is applied and which larvicide affects juvenile male mosquito survival or interferes with metamorphosis of juvenile male mosquito insects to adulthood.
  • 3. The method of claim 2, wherein the larvicide coating applied to the adult male mosquitoes is sufficient so that when the larvicide coated adult male mosquitoes are released from the controlled environment and introduced into an environment with an indigenous mosquito population, the larvicide coated adult male mosquitoes are effective to deliver a sufficient amount of larvicide to an indigenous mosquito spawning or breeding sites to affect juvenile mosquito survival or interfere with metamorphosis of juvenile mosquito insects to adulthood, thereby controlling the indigenous mosquito population.
  • 4. A method for mosquito control, comprising: releasing to a mosquito breeding site, adult male mosquitoes that were reared in a laboratory or artificially controlled environment, said adult male mosquitoes having one or more larvicides applied to an exterior surface of the adult male mosquitoes in a laboratory or artificially controlled environment, to thereby control a mosquito population.
  • 5. The method of claim 4, further comprising applying the one or more mosquito larvicides to an exterior surface of adult male mosquitoes via (i) dusting with a powder, granular or otherwise solid larvicide directed at the adult male mosquitoes or (ii) spraying with a liquid insecticide containing the one more larvicides directed at the adult male mosquitoes, wherein said the one or more mosquito larvicides has minimal impact on the adult male mosquitoes to which the larvicide is applied and which larvicide affects juvenile male mosquito survival or interferes with metamorphosis of juvenile male mosquito insects to adulthood.
  • 6. The method of claim 5, wherein the larvicide coating applied to the adult male mosquitoes is sufficient so that when the larvicide coated adult male mosquitoes are released from the controlled environment and introduced into an environment with an indigenous mosquito population, the larvicide coated adult male mosquitoes are effective to deliver a sufficient amount of larvicide to an indigenous mosquito spawning or breeding sites to affect juvenile mosquito survival or interfere with metamorphosis of juvenile mosquito insects to adulthood, thereby controlling the indigenous mosquito population.
CROSS REFERENCE TO RELATED APPLICATIONS

This is a divisional of U.S. Ser. No. 13/636,889, filed Dec. 19, 2022, which is a § 371 national stage application of PCT/US12/31437, filed Mar. 30, 2012, which claims the benefit of U.S. Provisional Application No. 61/477,781, filed Apr. 21, 2011, all herein incorporated by reference.

US Referenced Citations (1)
Number Name Date Kind
20040200128 Metcalfe Oct 2004 A1
Foreign Referenced Citations (1)
Number Date Country
1993320001 Mar 1993 JP
Related Publications (1)
Number Date Country
20230225311 A1 Jul 2023 US
Provisional Applications (1)
Number Date Country
61477781 Apr 2011 US
Divisions (1)
Number Date Country
Parent 13636889 US
Child 18188854 US