Characterization of Rhopalosiphum padi takeout-like genes and their role in insecticide susceptibility

2021 ◽  
Vol 171 ◽  
pp. 104725
Author(s):  
Xiong Peng ◽  
Suji Wang ◽  
Lei Huang ◽  
Sha Su ◽  
Maohua Chen
2020 ◽  
Vol 71 (9) ◽  
pp. 2796-2807 ◽  
Author(s):  
Carmen Escudero-Martinez ◽  
Patricia A Rodriguez ◽  
Shan Liu ◽  
Pablo A Santos ◽  
Jennifer Stephens ◽  
...  

Abstract Aphids secrete diverse repertoires of effectors into their hosts to promote the infestation process. While ‘omics’ approaches facilitated the identification and comparison of effector repertoires from a number of aphid species, the functional characterization of these proteins has been limited to dicot (model) plants. The bird cherry-oat aphid Rhopalosiphum padi is a pest of cereal crops, including barley. Here, we extend efforts to characterize aphid effectors with regard to their role in promoting susceptibility to the R. padi–barley interaction. We selected three R. padi effectors based on sequence similarity to previously characterized Myzus persicae effectors and assessed their subcellular localization, expression, and role in promoting plant susceptibility. Expression of R. padi effectors RpC002 and Rp1 in transgenic barley lines enhanced plant susceptibility to R. padi but not M. persicae, for which barley is a poor host. Characterization of Rp1 transgenic barley lines revealed reduced gene expression of plant hormone signalling genes relevant to plant–aphid interactions, indicating that this effector enhances susceptibility by suppressing plant defences in barley. Our data suggest that some aphid effectors specifically function when expressed in host species, and feature activities that benefit their corresponding aphid species.


2019 ◽  
Author(s):  
Carmen Escudero-Martinez ◽  
Patricia A. Rodriguez ◽  
Pablo A. Santos ◽  
Jennifer Stephens ◽  
Jorunn I.B. Bos

AbstractAphids secrete diverse repertoires of effectors into their hosts to promote the infestation process. While “omics”-approaches facilitated the identification and comparison of effector repertoires from a number of aphid species, the functional characterization of these proteins has been limited to dicot (model) plants. The bird cherry-oat aphid Rhopalosiphum padi is a pest of cereal crops, including barley. Here, we extended efforts to characterize aphid effectors with regards to their role in promoting susceptibility to the R. padi-barley interaction. We selected 3 R. padi effectors based on sequences similarity to previously characterized M. persicae effectors and assessed their subcellular localisation, expression, and role in promoting plant susceptibility. Expression of R. padi effectors RpC002 and Rp1 in transgenic barley lines enhanced plant susceptibility to R. padi but not M. persicae, for which barley is a poor host. Characterization of Rp1 transgenic barley lines revealed reduced gene expression of plant hormone signalling genes relevant to plant-aphid interactions, indicating this effector enhances susceptibility by suppressing plant defences in barley. Our data suggests that some aphid effectors specifically function when expressed in host species, and feature activities that benefit their corresponding aphid species.


2018 ◽  
Vol 111 (4) ◽  
pp. 1551-1557 ◽  
Author(s):  
Reihaneh Barati ◽  
Mir Jalil Hejazi ◽  
Seyed Abolghasem Mohammadi

2001 ◽  
Vol 1 (1-2) ◽  
pp. 4-5 ◽  
Author(s):  
Jean-Christophe Simon ◽  
Nathalie Leterme ◽  
François Delmotte ◽  
Olivier Martin ◽  
Arnaud Estoup

Virology ◽  
1981 ◽  
Vol 112 (1) ◽  
pp. 346-349 ◽  
Author(s):  
Cleora J. D'Arcy ◽  
P.A. Burnett ◽  
A.D. Hewings ◽  
Robert M. Goodman

Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


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