High-Level Resistance to Bacillus thuringiensis Toxin Cry1Ac and Cadherin Genotype in Pink Bollworm

2006 ◽  
Vol 99 (6) ◽  
pp. 2125-2131 ◽  
Author(s):  
Bruce E. Tabashnik ◽  
Robert W. Biggs ◽  
Jeffrey A. Fabrick ◽  
Aaron J. Gassmann ◽  
Timothy J. Dennehy ◽  
...  
2006 ◽  
Vol 99 (6) ◽  
pp. 2125-2131 ◽  
Author(s):  
Bruce E. Tabashnik ◽  
Robert W. Biggs ◽  
Jeffrey A. Fabrick ◽  
Aaron J. Gassmann ◽  
Timothy J. Dennehy ◽  
...  

Toxins ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 246 ◽  
Author(s):  
Xingliang Wang ◽  
Yanjun Xu ◽  
Jianlei Huang ◽  
Wenzhong Jin ◽  
Yihua Yang ◽  
...  

The adoption of transgenic crops expressing Bacillus thuringiensis (Bt) insecticidal crystalline (Cry) proteins has reduced insecticide application, increased yields, and contributed to food safety worldwide. However, the efficacy of transgenic Bt crops is put at risk by the adaptive resistance evolution of target pests. Previous studies indicate that resistance to Bacillus thuringiensis Cry1A and Cry1F toxins was genetically linked with mutations of ATP-binding cassette (ABC) transporter subfamily C gene ABCC2 in at least seven lepidopteran insects. Several strains selected in the laboratory of the Asian corn borer, Ostrinia furnacalis, a destructive pest of corn in Asian Western Pacific countries, developed high levels of resistance to Cry1A and Cry1F toxins. The causality between the O. furnacalis ABCC2 (OfABCC2) gene and resistance to Cry1A and Cry1F toxins remains unknown. Here, we successfully generated a homozygous strain (OfC2-KO) of O. furnacalis with an 8-bp deletion mutation of ABCC2 by the CRISPR/Cas9 approach. The 8-bp deletion mutation results in a frame shift in the open reading frame of transcripts, which produced a predicted protein truncated in the TM4-TM5 loop region. The knockout strain OfC2-KO showed much more than a 300-fold resistance to Cry1Fa, and low levels of resistance to Cry1Ab and Cry1Ac (<10-fold), but no significant effects on the toxicities of Cry1Aa and two chemical insecticides (abamectin and chlorantraniliprole), compared to the background NJ-S strain. Furthermore, we found that the Cry1Fa resistance was autosomal, recessive, and significantly linked with the 8-bp deletion mutation of OfABCC2 in the OfC2-KO strain. In conclusion, in vivo functional investigation demonstrates the causality of the OfABCC2 truncating mutation with high-level resistance to the Cry1Fa toxin in O. furnacalis. Our results suggest that the OfABCC2 protein might be a functional receptor for Cry1Fa and reinforces the association of this gene to the mode of action of the Cry1Fa toxin.


2010 ◽  
Vol 103 (5) ◽  
pp. 1821-1831 ◽  
Author(s):  
Eugene R. Hannon ◽  
Mark S. Sisterson ◽  
S. Patricia Stock ◽  
Yves Carrière ◽  
Bruce E. Tabashnik ◽  
...  

2021 ◽  
Vol 66 (1) ◽  
pp. 121-140
Author(s):  
Juan Luis Jurat-Fuentes ◽  
David G. Heckel ◽  
Juan Ferré

Insecticidal proteins from the bacterium Bacillus thuringiensis ( Bt) are used in sprayable formulations or produced in transgenic crops as the most successful alternatives to synthetic pesticides. The most relevant threat to sustainability of Bt insecticidal proteins (toxins) is the evolution of resistance in target pests. To date, high-level resistance to Bt sprays has been limited to one species in the field and another in commercial greenhouses. In contrast, there are currently seven lepidopteran and one coleopteran species that have evolved practical resistance to transgenic plants producing insecticidal Bt proteins. In this article, we present a review of the current knowledge on mechanisms of resistance to Bt toxins, with emphasis on key resistance genes and field-evolved resistance, to support improvement of Bt technology and its sustainability.


1992 ◽  
Vol 85 (4) ◽  
pp. 1516-1521 ◽  
Author(s):  
Douglas F. Wilson ◽  
Hollis M. Flint ◽  
Randy W. Deaton ◽  
David A. Fischhoff ◽  
Frederick J. Perlak ◽  
...  

2019 ◽  
Vol 19 (28) ◽  
pp. 2554-2566 ◽  
Author(s):  
Aurelio Ortiz ◽  
Estibaliz Sansinenea

Background:: Candida species are in various parts of the human body as commensals. However, they can cause local mucosal infections and, sometimes, systemic infections in which Candida species can spread to all major organs and colonize them. Objective:: For the effective treatment of the mucosal infections and systemic life-threatening fungal diseases, a considerably large number of antifungal drugs have been developed and used for clinical purposes that comprise agents from four main drug classes: the polyenes, azoles, echinocandins, and antimetabolites. Method: : The synthesis of some of these drugs is available, allowing synthetic modification of the molecules to improve the biological activity against Candida species. The synthetic methodology for each compound is reviewed. Results: : The use of these compounds has caused a high-level resistance against these drugs, and therefore, new antifungal substances have been described in the last years. The organic synthesis of the known and new compounds is reported. Conclusion: : This article summarizes the chemistry of the existing agents, both the old drugs and new drugs, in the treatment of infections due to C. albicans, including the synthesis of the existing drugs.


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