Establishment and Characterization of Insect Cell Lines from 10 Lepidopteran Species
In Vitro Cell. Dev. Biol.ÐAnimal 37:367±373, June 2001 q 2001 Society for In Vitro Biology 1071-2690/01 $10.00+0.00 ESTABLISHMENT AND CHARACTERIZATION OF INSECT CELL LINES FROM 10 LEPIDOPTERAN SPECIES CYNTHIA L. GOODMAN,1 GALAL N. EL SAYED, ARTHUR H. MCINTOSH, JAMES J. GRASELA, AND BRAD STILES Biological Control of Insects Research Laboratory (BCIRL), U.S. Department of Agriculture (USDA),2 Agricultural Research Service (ARS), Columbia, Missouri 65203-3535 (C. L. G., A. H. M., J. J. G.), Department of Entomology, University of Missouri, Columbia, Missouri 65211 (G. N. E.), and BASF Agro Research (formerly American Cyanamid Co., Agricultural Research Div.), P.O. Box 400, Princeton, New Jersey 08540 (B. S.) (Received 27 December 2000; accepted 16 March 2001) SUMMARY Cell lines from selected lepidopteran species were established for the overall purpose of use in baculovirus production. A total of 36 new cell lines from 10 lepidopteran species were generated, including cell lines from a pyralid, the European corn borer, Ostrinia nubilalis, a plutellid, the diamondback moth, Plutella xylostella, as well as eight noctuids: the black cutworm, Agrotis ipsilon, the celery looper, Anagrapha falcifera, the velvetbean caterpillar, Anticarsia gemmatalis, the corn earworm, Helicoverpa zea, the tobacco budworm, Heliothis virescens, the beet armyworm, Spodoptera exigua, the fall armyworm, Spodoptera frugiperda, and the cabbage looper, Trichoplusia ni. Tissues used for cell line establishment included fat bodies, ovaries, testes, or whole embryos/larvae/pupae. All the cell lines were subcultured numerous times, characterized by isoenzyme analysis and/or deoxyribonucleic acid ampli®cation ®ngerprinting using polymerase chain reaction, and stored in liquid nitrogen.
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