Transformation of an Australian Cotton Cultivar: Prospects for Cotton Improvement Through Genetic Engineering

1991 ◽  
Vol 18 (5) ◽  
pp. 481 ◽  
Author(s):  
YL Cousins ◽  
BR Lyon ◽  
DJ Llewellyn

Somatic embryogenesis and regeneration of whole plants is a highly genotype-dependent process in cotton. We have identified at least one highly regenerable Australian cultivar, Siokra 1-3, which is a sister line to the current major variety being grown in Australia. A number of plants have been regenerated and although some are showing abnormal pollen development, most can produce fertile seed when selfed or crossed with a normal pollen donor. Agrobacterium tumefaciens has been used to efficiently produce fertile transgenic Siokra 1-3 plants expressing novel genes such as the bacterial neomycin phosphotransferase or the β-glucuronidase. This is the first example of the transformation of an elite commercial cultivar. Critical factors in the transformation are the use of a supervirulent disarmed Ti-plasmid with a binary transformation vector, and a highly regenerable genotype of cotton. Bacterial concentration at the time of infection, tissue age, kanamycin selection regime, and co-cultivation support and media composition all have an influence on transformation efficiency and were optimised in our protocol. The ability to transform an elite Australian cultivar of cotton paves the way for agronomic improvements through genetic engineering. We have concentrated on increasing the tolerance of Australian cotton to the herbicide 2,4-D (to protect it from spray drift damage from adjacent cereal crops), and increasing its tolerance to insect pests, such as Helicoverpa armigera, using BT-toxin genes, protease inhibitors and other novel insect resistance genes.

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Matthew J. Byrne ◽  
Matthew G. Iadanza ◽  
Marcos Arribas Perez ◽  
Daniel P. Maskell ◽  
Rachel M. George ◽  
...  

AbstractInsect pests are a major cause of crop losses worldwide, with an estimated economic cost of $470 billion annually. Biotechnological tools have been introduced to control such insects without the need for chemical pesticides; for instance, the development of transgenic plants harbouring genes encoding insecticidal proteins. The Vip3 (vegetative insecticidal protein 3) family proteins from Bacillus thuringiensis convey toxicity to species within the Lepidoptera, and have wide potential applications in commercial agriculture. Vip3 proteins are proposed to exert their insecticidal activity through pore formation, though to date there is no mechanistic description of how this occurs on the membrane. Here we present cryo-EM structures of a Vip3 family toxin in both inactive and activated forms in conjunction with structural and functional data on toxin–membrane interactions. Together these data demonstrate that activated Vip3Bc1 complex is able to insert into membranes in a highly efficient manner, indicating that receptor binding is the likely driver of Vip3 specificity.


2021 ◽  
Author(s):  
Martin Raspor ◽  
Aleksandar Cingel

Significant limitations in potato production are crop loss due to the damage made by insect pests, and the cost of enormous amount of chemicals, harmful to humans and environment, extensively used in their control. As an alternative, development of genetically modified potato offered possibility for pest management in a more sustainable, environmentally friendly way. Over the past 30 years introduction of pest resistance traits progressed from a single gene to multiple stacked events and from Bt-toxin expression to expression of proteins from non-Bt sources, dsRNA and their combination, while advances in molecular biology have brought “cleaner” gene manipulation technologies. However, together with benefits any new technology also bears its risks, and there are still a range of unanswered questions and concerns about long-term impact of genetically modified crops – that with knowledge and precautionary approaches can be avoided or mitigated. Sustainability of genetically modified crops for pest control largely depends on the willingness to gain and implement such knowledge.


2021 ◽  
Vol 17 (AAEBSSD) ◽  
pp. 326-330
Author(s):  
Omprakash ◽  
Aparna ◽  
Bapsila Loitongbam ◽  
S. K. Bairwa ◽  
Kailash Chandra

Gene stacking is the process of addition of two or more gene of interest into a single plant. The combination or stacking of different traits or genes in plants is rapidly gaining popularity in biotech crop production. The new evolved trait is known as stacked trait and the crop is known as biotech stacked or simply stacked. This can be accomplished in many ways, one of which is gene pyramiding. Biotech stacks give crops a larger genetic and agronomic boost, allowing them to perform better in challenging farming situations. Biotech stacks are designed to increase productivity by overcoming biotic and abiotic challenges like as insect pests, diseases, weeds, and environmental stress. This review will explain about the gene stacking principle, the need for biotech stacking, and the many gene stacking methods.


2013 ◽  
Vol 66 ◽  
pp. 386-386
Author(s):  
R. Gardner-Gee

Sulphur is mainly used as a fungicide but is known to have insecticidal properties against some insect pests A series of laboratory studies was conducted to assess its effect on the tomato potato psyllid (Bactericera cockerelli; TPP) a recently established pest species in New Zealand that transmits the bacterium Candidatus Liberibacter solanacearum (Lso) Short assays (8805; 24 h) using dipped leaves indicated that fresh sulphur residues had no discernible impact on TPP settlement patterns or onleaf behaviour However longer assays (8805; 72 h) using whole plants indicated that sulphur residues can disrupt egglaying behaviour but the effect was dependent on the assay design In 72 h choice assays TPP laid fewer eggs on plants sprayed with sulphur compared with control plants In nochoice assays sulphur residues did not consistently reduce egglaying Together these results suggest that sulphur may slow the buildup of TPP populations within crops by deterring egglaying However the lack of repellence or antifeeding properties means that sulphur treatments alone may not be sufficient to prevent the transmission of Lso by TPP


1992 ◽  
Vol 1 (3) ◽  
pp. 323-338 ◽  
Author(s):  
S. Mohan Jain ◽  
Christian Oker-Blom ◽  
Eija Pehu ◽  
R. J. Newton

Advances in gene transfer technologies have enabled the production of both monocot and dicot transgenic plants. With the biolistic method, genes can be transferred in recalcitrant crop plants and forest trees, independent of their genotype. Inexpensive methods for both stable and transient gene transfers - ultrasonication, direct DNA insertion during imbibition using somatic embryos, and silicon carbide fibres - have been developed. The frequency of Agrobacterium-mediated transformation rates of cloned genes can be enhanced in plant cells. The analysis of molecular markers (RFLPs, RAPDs, DNA fingerprints) can accomplish the characterization, gene mapping and identification and certification and patent protection of cultivars. With PCR, selective amplification of a specific DNA segment from a small amount of an organism’s total DNA can be used toidentify transgenic cultivars. The expression of a target gene can be inhibited with antisense RNA. So far, a limited number of genes have been identified and cloned with genetic engineering. With specific gene transfers, many goals such as biological control of insect pests and fungi, male sterility, virus resistance, improving seed protein, and production of transgenic plants as “bioreactors” can be accomplished. T-DNA mutagenesis may lead to learning more about the genetic control of plant development and morphogenesis, and isolation of useful mutants. Before genetic engineering becomes a reliable tool of plant breeding, more attention is needed to explore: (a) new plant genetic resources in order toidentify and clone new genes, (b) fate of selective and scorable marker genes, and (c) field evaluation of transgenes in transgenic plants.


2019 ◽  
Vol 112 (4) ◽  
pp. 1695-1704 ◽  
Author(s):  
Scott H Graham ◽  
Fred M Musser ◽  
Alana L Jacobson ◽  
Anitha Chitturi ◽  
Beverly Catchot ◽  
...  

Abstract Thrips (Thysanoptera: Thripidae) and tarnished plant bug, Lygus lineolaris (Hemiptera: Miridae), are among the most important insect pests of cotton, Gosssypium hirsutum, in the mid-southern United States. These pests are currently managed primarily by insecticides; however, a new Bt toxin, Cry51Aa2.834_16 is under evaluation for control of thrips and tarnished plant bug. Experiments were conducted to evaluate the behavioral response of thrips and tarnished plant bug to Bt Cry51Aa2.834_16. Adult thrips avoided Bt Cry51Aa2.834_16 cotton in field choice tests and in separate field tests of Bt and non-Bt cotton not treated with insecticides. In a greenhouse choice test, approximately twice as many adult thrips and eggs were found on non-Bt compared with Bt Cry51Aa2.834_16 cotton. Similarly, in a field test of nontreated Bt Cry51Aa2.834_16 and non-Bt cotton, 68% of adult thrips collected were found on non-Bt cotton. In cotton that was not sprayed with insecticides, Bt Cry51Aa2.834_16 did not affect the distribution of tarnished plant bug within the canopy, although more square and flower injury was caused by tarnished plant bug in non-Bt cotton. Adult tarnished plant bug exhibited a nonpreference for diet containing lyophilized Bt Cry51Aa2.834_16 leaves and for excised Bt Cry51Aa2.834_16 squares in choice tests with non-Bt squares. The behavioral responses of these pests when exposed to this new Bt toxin will play a key role in the efficacy and potential resistance management strategies if this new technology is incorporated in an overall cotton insect pest management system.


1995 ◽  
Vol 30 (1) ◽  
pp. 29-42 ◽  
Author(s):  
Robert R. Farrar ◽  
Richard L. Ridgway

To help improve control of insect pests with microbial insecticides, we investigated the interactions of four commercial, nutrient-based phagostimulants (Pheast [AgriSense], Coax [CCT Corp.], Gusto [Atochem North America, Inc.], and Entice [Custom Chemicides] with Bacillus thuringiensis Berliner and four lepidopterous insect pests (gypsy moth, Lymantria dispar [L.] [Lymantriidae]; corn earworm, Helicoverpa zea [Boddie] [Noctuidae]; European corn borer, Ostrinia nubilalis [Hübner] [Pyralidae]; and diamondback moth, Plutella xylostella [L.] [Plutellidae]). Comparisons were made of treated foliage in Petri dishes in the laboratory and of sprayed whole plants in a greenhouse. In general, phagostimulants increased mortality of all species tested, but no consistent differences among phagostimulants were found for any species. Food consumption was generally lower on the treatments that contained phagostimulants causing the highest rates of mortality, possibly as a result of more rapid ingestion of a lethal dose on these treatments. Reduced rates of feeding by insects on treatments with B. thuringiensis alone were seen, probably due in part to intoxication and, possibly, to behavioral effects as well. Indications of potentially significant interactions between host plants and both B. thuringiensis and phagostimulants also were seen.


2014 ◽  
Vol 20 (4) ◽  
Author(s):  
Adane Abraham

Genetic engineering (GE) technologies can contribute to improve crop productivity and quality in Ethiopia. Adoption of commercialized insect resistance and herbicide tolerance technologies can help to protect major crops such as cotton, maize, sorghum and small cereals from their main insect pests or prevent heavy weed-inflicted loss. Moreover, key production constraints such as  bacterial wilt of enset, late blight of potato, drought stress on crops like maize and wheat, lodging resistance on tef as well as low nutritive quality of native crops like enset and grasspea can be addressed by strengthening domestic GE research capacity and international collaboration. Cognizant of this potential, the Ethiopian government has made significant investment in modern biotechnology capacity building in the last decade. There has also been specific interest by cotton sector to boost its productivity by adopting insect resistance (Bt) technologies. However, the GE regulatory system based on the existing biosafety law is so stringent that it is not possible for the country to access useful technologies from abroad as well as initiate domestic GE research. Consequently, no GE experiment is approved so far, leaving the country at risk of missing out on the global GE revolution. To catch up and  harness the benefits of GE technologies, the country needs to create conducive regulatory environment, strengthen domestic GE capacity and devise a farsighted strategy.


Toxins ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 186 ◽  
Author(s):  
Ling Wang ◽  
Yuemin Ma ◽  
Xueqin Guo ◽  
Peng Wan ◽  
Kaiyu Liu ◽  
...  

Insecticidal proteins from Bacillus thuringiensis (Bt) are widely used to control insect pests, but their efficacy is reduced when pests evolve resistance. We report on a novel allele (r16) of the cadherin gene (PgCad1) in pink bollworm (Pectinophora gossypiella) associated with resistance to Bt toxin Cry1Ac, which is produced by transgenic cotton. The r16 allele isolated from a field population in China has 1545 base pairs of a degenerate transposon inserted in exon 20 of PgCad1, which generates a mis-spliced transcript containing a premature stop codon. A strain homozygous for r16 had 300-fold resistance to Cry1Ac, 2.6-fold cross-resistance to Cry2Ab, and completed its life cycle on transgenic Bt cotton producing Cry1Ac. Inheritance of Cry1Ac resistance was recessive and tightly linked with r16. Compared with transfected insect cells expressing wild-type PgCad1, cells expressing r16 were less susceptible to Cry1Ac. Recombinant cadherin protein was transported to the cell membrane in cells transfected with the wild-type PgCad1 allele, but not in cells transfected with r16. Cadherin occurred on brush border membrane vesicles (BBMVs) in the midgut of susceptible larvae, but not resistant larvae. These results imply that the r16 allele mediates Cry1Ac resistance in pink bollworm by interfering with the localization of cadherin.


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