TY - JOUR
T1 - Metabolism, penetration, and partitioning of [14C]aldrin in aldrin-resistant and susceptible corn rootworms
AU - Siegfried, Blair D.
AU - Mullin, Christopher Albert
N1 - Funding Information:
We are grateful for support from the U.S.D.A. (82-CRSR-2-2057 and 87-CRSR-2-2977) and the Pennsylvania Agricultural Experiment Station (Journal Series No. 8272) for this investigation. The technical assistance of W. R. Wenerick and S. L. Everett for insect collection and maintenance is much appreciated.
Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1990/2
Y1 - 1990/2
N2 - The mechanisms responsible for 300-fold higher levels of aldrin resistance in western corn rootworms relative to the closely related and sympatric northern corn rootworm were investigated. In vivo metabolism of [14C]aldrin by the resistant and susceptible rootworms proceeds similarly with a rapid conversion to its epoxide, dieldrin, which accounted for approximately 60% of the recovered dose in both species. Western corn rootworms exhibited 40% slower penetration and 40% greater excretion than aldrin-susceptible northern corn rootworms, but such differences alone are unlikely to account for overall susceptibility differences. Both species showed similar in vitro rates of aldrin metabolism within nervous tissue; however, western corn rootworm formed more aldrin trans-diol relative to dieldrin than northern corn rootworm. Aldrin trans-diol formation from aldrin in the central nervous system was much higher than its rate of production in the whole rootworm body. Western corn rootworms displayed low levels of cross-resistance to picrotoxinin, a compound thought to share a similar target site with cyclodiene insecticides, but such results are insufficient to ascribe resistance differences solely to target site insensitivity. It is proposed that the joint action of decreased penetration, increased excretion, increased detoxification at the nerve site, and mild nerve insensitivity are responsible for aldrin resistance in western corn rootworm. The possible influence of reduced alternative host plant feeding of the western compared to northern species on resistance mechanisms, particularly nerve site factors, are discussed.
AB - The mechanisms responsible for 300-fold higher levels of aldrin resistance in western corn rootworms relative to the closely related and sympatric northern corn rootworm were investigated. In vivo metabolism of [14C]aldrin by the resistant and susceptible rootworms proceeds similarly with a rapid conversion to its epoxide, dieldrin, which accounted for approximately 60% of the recovered dose in both species. Western corn rootworms exhibited 40% slower penetration and 40% greater excretion than aldrin-susceptible northern corn rootworms, but such differences alone are unlikely to account for overall susceptibility differences. Both species showed similar in vitro rates of aldrin metabolism within nervous tissue; however, western corn rootworm formed more aldrin trans-diol relative to dieldrin than northern corn rootworm. Aldrin trans-diol formation from aldrin in the central nervous system was much higher than its rate of production in the whole rootworm body. Western corn rootworms displayed low levels of cross-resistance to picrotoxinin, a compound thought to share a similar target site with cyclodiene insecticides, but such results are insufficient to ascribe resistance differences solely to target site insensitivity. It is proposed that the joint action of decreased penetration, increased excretion, increased detoxification at the nerve site, and mild nerve insensitivity are responsible for aldrin resistance in western corn rootworm. The possible influence of reduced alternative host plant feeding of the western compared to northern species on resistance mechanisms, particularly nerve site factors, are discussed.
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U2 - 10.1016/0048-3575(90)90005-M
DO - 10.1016/0048-3575(90)90005-M
M3 - Article
AN - SCOPUS:0025364775
SN - 0048-3575
VL - 36
SP - 135
EP - 146
JO - Pesticide Biochemistry and Physiology
JF - Pesticide Biochemistry and Physiology
IS - 2
ER -