Enhancing the resilience of transgenic cotton for insect resistance

Author(s):  
Mohsin Shad ◽  
Aneela Yasmeen ◽  
Saira Azam ◽  
Allah Bakhsh ◽  
Ayesha Latif ◽  
...  
2019 ◽  
Vol 61 (9) ◽  
pp. 663-673 ◽  
Author(s):  
Mahrukh Zubair ◽  
Ayesha Latif ◽  
Abdul Qayyum Rao ◽  
Saira Azam ◽  
Naila Shahid ◽  
...  

2013 ◽  
Vol 110 (15) ◽  
pp. 5806-5811 ◽  
Author(s):  
T. Brevault ◽  
S. Heuberger ◽  
M. Zhang ◽  
C. Ellers-Kirk ◽  
X. Ni ◽  
...  

2001 ◽  
Vol 94 (2) ◽  
pp. 315-325 ◽  
Author(s):  
Yves Carrière ◽  
Timothy J. Dennehy ◽  
Brent Pedersen ◽  
Shirley Haller ◽  
Christa Ellers-Kirk ◽  
...  

2017 ◽  
Vol 15 (9) ◽  
pp. 1204-1213 ◽  
Author(s):  
Mi Ni ◽  
Wei Ma ◽  
Xiaofang Wang ◽  
Meijing Gao ◽  
Yan Dai ◽  
...  

2020 ◽  
Author(s):  
Peng He ◽  
Shuyin Wu ◽  
Lili Tian ◽  
Xiaoli Hu ◽  
Shufen Chang ◽  
...  

Abstract Background: Cotton is a major fiber crop in the world that can be severely infested by pests in agricultural fields. Identifying new insect-resistance genes and increasing expression of known insect-resistance genes are imperative in cultivated cotton. Galanthus nivalis agglutinin, a type of plant lectin that is reportedly toxic towards Homoptera sap-sucking pests when administered in their artificial diet or when fed transgenic plant material expressing the gene. The natural GNA gene is mainly expressed in monocotyledons instead of in dicotyledons, thus modification of the gene is necessary to effectively express the GNA gene in transgenic cotton. Results: We report the artificial synthesis of a modified GNA gene (ASGNA), via codon augmentation, and its insertion into Arabidopsis thaliana and cotton to test its efficacy as an insect-resistance gene against cotton aphids and Plutella xylostella. The level of ASGNA expression in transgenic plants was determined by the enzyme-linked immunosorbent assay (ELISA), and the amount of ASGNA among transgenic plants reached approximately 6.5 μg/g fresh weight. A feeding bioassay showed that survival and reproductive rates of aphids fed transgenic tissues were significantly lower than those fed wild type tissues. Likewise, larvae mortality of P. xylostella fed with transgenic plants showed significantly increased levels. Similar results were recorded of aphids feeding on cotton cotyledons with transient expression of ASGNA. Conclusions: Altogether, results show that ASGNA exhibited high insecticidal activity towards sap-sucking insects and is a promising candidate gene to improve insect resistance in cotton and other dicot plants.


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 526d-526
Author(s):  
M. Freeman ◽  
C. Walters ◽  
M.A. Thorpe ◽  
T. Gradziel

Almond, as with other stone fruit, possesses a highly lignified endocarp or shell. The dominant hard-shelled trait (D-) is positively associated with greater resistant to insect infestation than nuts expressing the paper-shelled (dd) trait. Hard-shelled genotypes have undesirable effects, including a lower kernel meat-to-nut crack-out ratio, greater kernel damage during mechanical shelling, and a reduction in plant energy available to kernel development. Histogenic analysis shows that the almond endocarp, unlike peach, has a tri-partite structure. Insect feeding studies have subsequently demonstrated that the inner endocarp layer, which is similar in both hard and paper-shelled types, is the most important structural barrier to insect infestation. Shell-seal integrity and X-ray studies have confirmed that discontinuities at the inner endocarp suture seal are the primary, though not the sole site of entry for insect pests. Paper-shelled almond selections with highly lignified and well-sealed inner endocarps show resistance levels comparable to hard shelled types but with crack-out ratios 30% to 40% higher. Pseudo-paper-shelled types have also been selected, in which a highly lignified outer endocarp is formed, but is retained by the fruit hull at dehiscence. An understanding of endocarp morphology and development is thus important in breeding for insect resistance as well as the commercial utilization of both kernel and hull.


2021 ◽  
Vol 9 (1) ◽  
pp. 140
Author(s):  
Ruying Wang ◽  
Simin Luo ◽  
Bruce B. Clarke ◽  
Faith C. Belanger

Strong creeping red fescue (Festuca rubra subsp. rubra) is a commercially important low-maintenance turfgrass and is often naturally infected with the fungal endophyte Epichloë festucae. Epichloë spp. are endophytes of several cool-season grass species, often conferring insect resistance to the grass hosts due to the production of toxic alkaloids. In addition to insect resistance, a unique feature of the strong creeping red fescue/E. festucae symbiosis is the endophyte-mediated disease resistance to the fungal pathogen Clarireedia jacksonii, the causal agent of dollar spot disease. Such disease resistance is not a general feature of other grass/ Epichloë interactions. E. festucae isolates infecting red fescue have an antifungal protein gene Efe-afpA, whereas most other Epichloë spp. do not have a similar gene. The uniqueness of this gene suggests it may, therefore, be a component of the unique disease resistance seen in endophyte-infected red fescue. Here, we report the generation of CRISPR-Cas9 Efe-afpA gene knockouts with the goal of determining if absence of the protein in endophyte-infected Festuca rubra leads to disease susceptibility. However, it was not possible to infect plants with the knockout isolates, although infection was possible with the wild type E. festucae and with complemented isolates. This raises the interesting possibility that, in addition to having antifungal activity, the protein is required for the symbiotic interaction. The antifungal protein is a small secreted protein with high expression in planta relative to its expression in culture, all characteristics consistent with effector proteins. If Efe-AfpA is an effector protein it must be specific to certain interactions, since most Epichloë spp. do not have such a gene in their genomes.


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