Transgenic cotton plants expressingCry1Ac and Cry2Ab, from the soil bacterium Bacillus thuringiensis (Bt), provide effective control of certain lepidopteran pests, however, little is known about the proteins below ground expression. We used ELISA to quantify in vitro expression of the Cry1Ac and Cry2Ab proteins in mucilage, root border cells and root tips in five transgenic cultivars of cotton compared to conventional cultivar Sicot 189. Expression of Cry proteins in roots and border cells of the transgenic cotton cultivars was constitutive and at detectable levels, with Cry1Ac and Cry2Ab protein expression ranging from <20 ppb to >100 pbb. To determine if genetically modified cotton demonstrated simple differences in properties of the root, when compared to an elite parental line (cv. Sicot 189), we enumerated border cells on seedling radicles. Border cell counts of 14 cultivars ranged from 0.2 to 1.1 · 10 4 cells per root tip with an average of 5 · 10 3 border cells. Border cell production in the transgenic cultivars was generally similar to that of both donor and elite parents, the exception being the cultivar Sicot 189, which had substantially more border cells than all of its transgenic derivatives. Comparison of border cell number with varietal disease resistance ranking found a limited relationship (r 2 = 0.65, n = 7) between border cell numbers and the commercial resistance rank against Fusarium wilt of cotton. The implications of differences in cotton cultivar border cell number and root tip expression of Cry proteins for plant-microbe interactions in the rhizosphere and the soil ecosystem are yet to be resolved.
Field studies were conducted over six seasons to determine the critical period for weed control (CPWC) in high-yielding cotton, using common sunflower as a mimic weed. Common sunflower was planted with or after cotton emergence at densities of 1, 2, 5, 10, 20, and 50 plants m−2. Common sunflower was added and removed at approximately 0, 150, 300, 450, 600, 750, and 900 growing degree days (GDD) after planting. Season-long interference resulted in no harvestable cotton at densities of five or more common sunflower plants m−2. High levels of intraspecific and interspecific competition occurred at the highest weed densities, with increases in weed biomass and reductions in crop yield not proportional to the changes in weed density. Using a 5% yield-loss threshold, the CPWC extended from 43 to 615 GDD, and 20 to 1,512 GDD for one and 50 common sunflower plants m−2, respectively. These results highlight the high level of weed control required in high-yielding cotton to ensure crop losses do not exceed the cost of control.
Field studies were conducted over five seasons from 2004 to 2015 to determine the critical period for weed control (CPWC) in high-yielding, irrigated cotton using a competitive mimic grass weed, Japanese millet. Japanese millet was planted with or after cotton emergence at densities of 10, 20, 50, 100, and 200 plants m−2. Japanese millet was added and removed at approximately 0, 150, 300, 450, 600, 750, and 900 degree days of crop growth (GDD). Data were combined over years. Japanese millet competed strongly with cotton, with season-long interference resulting in an 84% reduction in cotton yield with 200 Japanese millet plants m−2. The data were fit to extended Gompertz and logistic curves including weed density as a covariate, allowing a dynamic CPWC to be estimated for densities of 10 to 200 Japanese millet plants m−2. Using a 1% yield-loss threshold, the CPWC commenced at 65 GDD, corresponding to 0 to 7 d after crop emergence (DAE), and ended at 803 GDD, 76 to 98 DAE with 10 Japanese millet plants m−2, and 975 GDD, 90 to 115 DAE with 200 Japanese millet plants m−2. These results highlight the high level of weed control required throughout the cropping season in high-yielding cotton to ensure crop losses do not exceed the cost of weed control.
Genetically modified Bt cotton, expressing the Cry1Ac protein for specific insecticidal activity against economically significant lepidopteran pests, has been available commercially in Australia since 1996. This technology has been improved and superseded by the addition of a second gene, allowing new varieties to express both the Cry1Ac the Cry2Ab proteins. Bt cotton offers several advantages to the grower, mainly through reduced insecticide spray requirements. The environmental benefits of reduced insecticide usage are assessed in this paper using the environmental impact quotient (EIQ). The assessment included consideration of the impact of the expressed transgenic proteins Cry1Ac and Cry2Ab. EIQ values of the Cry1Ac and Cry2Ab proteins were calculated at 9.9 and 7.9, respectively. Bt protein expression, plant biomass, insecticide application records, constituent of active ingredient, and insecticide EIQ values were used to produce an environmental impact (EI) value for insecticide use (kg a.i./ha) for conventional non-GM and single- and 2-gene Bt cotton for the 1997–98 to 2003–04 seasons. Inclusion of the Cry proteins in the assessment increased the EI values for Bt cotton by only 2%. The average insecticide EI value, for 2002–03 and 2003–04 seasons, for conventional cotton was 135 kg a.i./ha, whereas for the 2-gene Bt variety it was only 28 kg a.i./ha. Results of the EI evaluation indicate that, due to changes in insecticidal choice and reduction in usage, there was a reduction of >64% in EI from growing Bt cotton compared with conventional non-GM cotton in Australia.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.