TY - JOUR
T1 - Pesticide resistance
T2 - Can we make it a renewable resource?
AU - Pittendrigh, B. R.
AU - Gaffney, P. J.
N1 - Funding Information:
This project is part of the MPRINT program and was supported by Department of Entomology funds. All pictures of #ies given in this paper are reproduced with the permission and copyright of Exploratorium, www.exploratorium.edu. This is publication No. 16466, Purdue University Agricultural Experimental Station, West Lafayette, IN, U.S.A.
PY - 2001/8/21
Y1 - 2001/8/21
N2 - Negative cross-resistance (NCR) occurs when a mutant allele confers (i) resistance to one toxic chemical and (ii) hyper-susceptibility to another. Sequential deployment of NCR toxins is useful for insect control in few situations (Pittendrigh et al., 2000). Using Monte Carlo simulations, we investigated the concurrent use of a pair of NCR toxins to control a hypothetical insect pest population. When the toxins killed more heterozygotes than homozygotes, the resistance allele became either extremely common or rare depending on starting allelic frequency. If the NCR toxins did not kill the two homozygous groups equally, then the toxin with lesser toxicity eventually played a greater role in the control of the pest population. Based on our results, we present an approach for the systematic development of an NCR toxin after the commercial release of the first toxin. First, large-scale screens are performed to find chemicals that kill the resistant homozygous insects, but not the susceptible ones. Chemicals that preferentially kill resistant insects are then tested for toxicity to the heterozygotes. Those highly toxic to both homo- and heterozygotes are given the highest priority for development. This screen can be adapted to identify compounds useful in controlling antibiotic-, herbicide- or fungicide-resistant organisms.
AB - Negative cross-resistance (NCR) occurs when a mutant allele confers (i) resistance to one toxic chemical and (ii) hyper-susceptibility to another. Sequential deployment of NCR toxins is useful for insect control in few situations (Pittendrigh et al., 2000). Using Monte Carlo simulations, we investigated the concurrent use of a pair of NCR toxins to control a hypothetical insect pest population. When the toxins killed more heterozygotes than homozygotes, the resistance allele became either extremely common or rare depending on starting allelic frequency. If the NCR toxins did not kill the two homozygous groups equally, then the toxin with lesser toxicity eventually played a greater role in the control of the pest population. Based on our results, we present an approach for the systematic development of an NCR toxin after the commercial release of the first toxin. First, large-scale screens are performed to find chemicals that kill the resistant homozygous insects, but not the susceptible ones. Chemicals that preferentially kill resistant insects are then tested for toxicity to the heterozygotes. Those highly toxic to both homo- and heterozygotes are given the highest priority for development. This screen can be adapted to identify compounds useful in controlling antibiotic-, herbicide- or fungicide-resistant organisms.
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U2 - 10.1006/jtbi.2001.2359
DO - 10.1006/jtbi.2001.2359
M3 - Article
C2 - 11476620
AN - SCOPUS:0035928852
SN - 0022-5193
VL - 211
SP - 365
EP - 375
JO - Journal of Theoretical Biology
JF - Journal of Theoretical Biology
IS - 4
ER -