Insecticide Resistance Questions to answer: What is resistance?

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Insecticide Resistance Questions to answer: What is resistance? How prevalent is resistance; what are some important examples? How is resistance identified and measured? What biological mechanisms confer resistance? How can resistance be managed? (Or Can resistance be managed?)

References http://pesticidestewardship.org/resistance/insecticide/pages/ InsecticideResistance.aspx http://en.wikipedia.org/wiki/pesticide_resistance

Keep in mind throughout this lecture: In resistance, pre-existing mechanisms are selected by insecticide use; this drives the evolution of resistant forms. Populations, not species become resistant. Individuals are born "resistant;" immunity does not develop. Resistance results from selection pressure. Managing resistance to conventional insecticides almost always depends upon minimizing pesticide use. Insecticide resistance is not the same as tolerance (though this terminology is always debated). Low-level resistance is still resistance, not tolerance. Species-wide abilities to survive particular insecticides are tolerance, not resistance. (Aphids are not killed by the insecticide carbaryl (Sevin) they did NOT develop resistance as a result of selection pressure by repeated use of this insecticide; they always have been tolerant to this insecticide.)

How prevalent / how important is resistance? Resistance has been documented... to every major group of insecticides in more than 500 insect and mite species roughly 56% are crop pests 37 % are med/vet pests 5 % are beneficial species

Resistance is most common in... Diptera (34% of resistant species) including house fly, horn fly, and many mosquitoes Lepidoptera (15%) Mites (14%) Coleoptera (13%) Homoptera (Hemiptera: Homoptera) (11%)

Examples include: Western corn rootworm to cyclodienes (organochlorines) (not to any of the soil insecticides commonly used in the last 30 years Why not?) Indianmeal moth to malathion and Bacillus thuringiensis Red flour beetle to malathion Horn fly to pyrethroids House fly to many insecticides Diamondback moth to many insecticides Greenhouse whitefly to many insecticides Tobacco budworm (Heliothis virscens) to many insecticides Colorado potato beetle to many insecticides Anopholes mosquitoes to many insecticides Codling moth to the organophosphates Imidan and Guthion Corn earworm (Helicoverpa zea) to pyrethroids (And there are MANY more)

Resistance causes pesticide failures that lead to...

Resistance triggers new pesticide development, especially for niche market products Colorado potato beetle for cryolite (an old abrasive), rotenone, and then neonicotinoids (when they were just a niche-market product) Diamondback moth for widespread use of Bacillus thuringiensis (before resistance to it as well) and then other new insecticides German cockroach for bait stations that use fungal pathogens, also hydroprene Codling moth Altacor, Assail, Delegate, and Rimon all follow the failures of Imidan and Guthion

Resistance is identified / measured in bioassays...

What allows insects to survive high doses of insecticides? There are 4 broad categories of resistance mechanisms:

Behavioral resistance A shift in behavior avoids exposure to insecticides. Examples are controversial do they represent shifts in the genetics of behavior or just survival for long enough (because of changes in metabolic activity or target-site resistance) to exhibit avoidance behaviors that always existed? Examples: red flour beetle, cockroaches, and horn fly to pyrethroids.

Reduced penetration usually provides low levels of resistance, most useful where increased metabolism (metabolic resistance) provides internal detoxification). The PEN gene in house flies confers cross resistance to different insecticides; similar genes appear to exist in other species. Examples are known from house fly, certain mosquitoes, tobacco budworm, and others.

Metabolic resistance: Detoxification mechanisms exist in insects anyway... nonspecific enzymes break down toxic, lipophilic (fat-loving) compounds into less toxic (usually) more soluble compounds for excretion. Why don't all insects detoxify compounds equally? Production of unnecessary enzymes is an energy expenditure. As a result, resistant individuals may be less "fit" than susceptible counterparts in the absence of the pesticide. Recessive genes for greater detoxification action are maintained "without cost" for the species' benefit. Realize that although we may have named an enzyme DDT dehydrochlorinase or aldrin epoxidase, these enzymes had (have) other functions as well.

More on metabolic resistance The enzymes that detoxify pesticides include mono-oxygenases (mixed function oxidases, microsomal oxidases, and cytochrome P-450 dependent oxidases), hydrolases(including esterases), and transferases (glutathione-s- transferase). One can determine if metabolic resistance is at work and what enzymes are involved by using synergists... chemicals that block specific enzymes responsible for specific detoxication steps; piperonyl butoxide (pbo) inhibits mixed function oxidases, triphenyl phosphate (TPP) inhibits carboxylesterase, and S,S,S, tributyl phosphorotrithioate (DEF) inhibits esterases. (Synergists are also used in a few instances to make insecticides work better... PBO in house fly sprays is one example.)

Target Site Insensitivity: The insecticide penetrates the insect cuticle, it is not metabolized more rapidly, but it still does not kill the pest... so the target site is insensitive. Examples: the kdr gene in Diptera reduces sensitivity of sodium channels to chlorinated hydrocarbons and pyrethroids. Altered acetylcholinesterase gives resistance to certain organophosphates in the cattle tick, in the mosquito Aedes albimanus, and in the two-spotted spider mite. Altered binding sites on the gut wall in some Lepidoptera result in resistance to Bacillus thuringiensis.

A single insect may be resistant to more than one insecticide as a result of... Cross-resistance: One mechanism confers resistance to more than one insecticide. Examples include kdr resistance to DDT and pyrethroids in the house fly and certain mosquitoes. Oxidases, hydrolases, etc. may detoxify more than one organophosphate or carbamate. Multiple resistance: More than one mechanism evolves independently in response to selection from different insecticide applications. Examples: Colorado potato beetle, house fly, tobacco budworm, diamondback moth, green peach aphid, and certain Anopheles mosquitoes are resistant by separate mechanisms to 4 or more classes of insecticides. In most instances, resistance to a particular insecticide results from the selection of a single gene. (This conclusion is not universally true.)

Resistance Management tries to maintain the usefulness of an insecticide. attempts to manage target pests after resistance has led to control failures. Managing resistance begins with recognizing the factors that influence resistance development...

Biological factors that favor resistance development:

Operational factors that favor resistance development: Treatments provide prolonged exposure to the insecticide (via frequent sprays, long residual, or controlled releases) Selection pressure is high (high mortality in the treated portion of the population) No refuges exist (for susceptible insects and their genes to survive) Large areas are treated All of the factors listed above intensify selection.

Detecting / monitoring resistance Many papers stress the importance of detecting and monitoring insecticide resistance. Although monitoring can be useful, it is important to determine the exact goal of monitoring and assess whether or not it can be met. Purposes include... explanation of control failures determination of insecticide choice for a single field (field kits) determination of the success of resistance management efforts... have resistance frequencies dropped or stabilized? detection of resistance at an early stage so that management efforts can begin... This approach is a problem because statistical probabilities mean that bioassays must contain very high numbers of insects in order to provide detection before the momentum of resistance development is too great.

After the linear relationship between dose and mortality is known, a diagnostic dose may be used to detect the presence of resistance in the field. 10 100 1000

So... Resistance management must begin before detection efforts confirm that resistance development is underway. What can be done in resistance management?

Resistance management techniques Minimize selection pressure to keep susceptible insects alive... the idea here is that genes for susceptibility are a valuable natural resource that should be maintained. No unnecessary treatments Lowest possible effective rates Shortest effective residual Local instead of area-wide treatments (including spot treatments) Preserve untreated refuges Use other controls whenever possible (cultural practices and host plant resistance)

Kill the developing resistant population High dose strategy (a well-chosen dose to kill rare heterozygotes) Dose must remain high (happens only in transgenics)... what nontarget impacts for broad-spectrum insecticides? Synergists to neutralize resistance (for metabolic resistance) but synergists are unstable in UV light Mixtures or rotations of insecticides... to kill those insects that are developing resistance to one compound by using a different one.

So far, for conventional insecticides, minimizing use is the only strategy really proven to work satisfactorily. Rotations involve no extra cost, so they represent a good idea even if they are unproven. Despite their popularity with pesticide manufacturers and distributors, mixtures and high doses usually involve too many negatives to be practical for delaying insecticide resistance but mixtures can be used to manage multiple pests. This differs in managing insect resistance to transgenic plants.

Managing resistance to transgenic crops