rice stripe disease
Recently Published Documents


TOTAL DOCUMENTS

19
(FIVE YEARS 3)

H-INDEX

8
(FIVE YEARS 0)

2021 ◽  
Vol 118 (30) ◽  
pp. e2103393118
Author(s):  
Yonghuan Ma ◽  
Hong Lu ◽  
Wei Wang ◽  
Jiaming Zhu ◽  
Wan Zhao ◽  
...  

The importin α family belongs to the conserved nuclear transport pathway in eukaryotes. However, the biological functions of importin α in the plasma membrane are still elusive. Here, we report that importin α, as a plasma membrane–associated protein, is exploited by the rice stripe virus (RSV) to enter vector insect cells, especially salivary gland cells. When the expression of three importin α genes was simultaneously knocked down, few virions entered the salivary glands of the small brown planthopper, Laodelphax striatellus. Through hemocoel inoculation of virions, only importin α2 was found to efficiently regulate viral entry into insect salivary-gland cells. Importin α2 bound the nucleocapsid protein of RSV with a relatively high affinity through its importin β–binding (IBB) domain, with a dissociation constant KD of 9.1 μM. Furthermore, importin α2 and its IBB domain showed a distinct distribution in the plasma membrane through binding to heparin in heparan sulfate proteoglycan. When the expression of importin α2 was knocked down in viruliferous planthoppers or in nonviruliferous planthoppers before they acquired virions, the viral transmission efficiency of the vector insects in terms of the viral amount and disease incidence in rice was dramatically decreased. These findings not only reveal the specific function of the importin α family in the plasma membrane utilized by viruses, but also provide a promising target gene in vector insects for manipulation to efficiently control outbreaks of rice stripe disease.


2021 ◽  
Vol 59 (1) ◽  
Author(s):  
Yi Xu ◽  
Shuai Fu ◽  
Xiaorong Tao ◽  
Xueping Zhou

Rice stripe disease caused by Rice stripe virus (RSV) is one of the most devastating plant viruses of rice and causes enormous losses in production. RSV is transmitted from plant to plant by the small brown planthopper ( Laodelphax striatellus) in a circulative–propagative manner. The recent reemergence of this pathogen in East Asia since 2000 has made RSV one of the most studied plant viruses over the past two decades. Extensive studies of RSV have resulted in substantial advances regarding fundamental aspects of the virus infection. Here, we compile and analyze recent information on RSV with a special emphasis on the strategies that RSV has adopted to establish infections. These advances include RSV replication and movement in host plants and the small brown planthopper vector, innate immunity defenses against RSV infection, epidemiology, and recent advances in the management of rice stripe disease. Understanding these issues will facilitate the design of novel antiviral therapies for management and contribute to a more detailed understanding of negative-sense virus–host interactions at the molecular level. Expected final online publication date for the Annual Review of Phytopathology, Volume 59 is August 2021. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.


2020 ◽  
Vol 22 (2) ◽  
pp. 167-173
Author(s):  
Ichiro Nagaoka ◽  
Hideki Sasahara ◽  
Kei Matsushita ◽  
Hideo Maeda ◽  
Akiko Shigemune ◽  
...  

2018 ◽  
Author(s):  
Yao Li ◽  
Danyu Chen ◽  
Jia Hu ◽  
Lu Zhang ◽  
Yin Xiang ◽  
...  

Rice stripe virus (RSV), causal agent of rice stripe disease, is transmitted by the small brown planthopper (SBPH, Laodelphax striatellus) in a persistent manner. The midgut and salivary glands of SBPH are the first and last barriers in viral circulation and transmission, respectively; however, the precise mechanisms used by RSV to cross these organs and re-inoculate rice have not been fully elucidated. We obtained full-length cDNA of L. striatellus α-tubulin 2 (LsTUB) and found that RSV infection increased the level of LsTUB in vivo. Furthermore, LsTUB was shown to bind the RSV nonstructural protein 3 (NS3) in vitro. RNAi was used to reduce LsTUB expression, which caused a significant reduction in RSV titer, NS3 expression, RSV inoculation rates, and transmission to healthy plants. Electrical penetration graphs (EPG) showed that LsTUB knockdown by RNAi did not impact SBPH feeding; therefore, the reduction in RSV inoculation rate was likely caused by the decrease in RSV transmission. These findings suggest that LsTUB mediates the passage of RSV through midgut and salivary glands and leads to successful horizontal transmission.


2018 ◽  
Vol 217 ◽  
pp. 211-217 ◽  
Author(s):  
Takuya Shiba ◽  
Masahiro Hirae ◽  
Yuriko Hayano-Saito ◽  
Yasuo Ohto ◽  
Hiroshi Uematsu ◽  
...  

2013 ◽  
Vol 19 (2) ◽  
pp. 84-89 ◽  
Author(s):  
Byung-Ryun Kim ◽  
Tae-Woo Jeong ◽  
Kwang-Seop Han ◽  
Soo-Sang Hahm ◽  
Young-Jin Kim ◽  
...  
Keyword(s):  

2012 ◽  
Vol 125 (5) ◽  
pp. 1033-1046 ◽  
Author(s):  
Tackmin Kwon ◽  
Jong-Hee Lee ◽  
Soo-Kwon Park ◽  
Un-Ha Hwang ◽  
Jun-Hyun Cho ◽  
...  

Genome ◽  
2011 ◽  
Vol 54 (8) ◽  
pp. 611-619 ◽  
Author(s):  
Baoxiang Wang ◽  
Ling Jiang ◽  
Yingxin Zhang ◽  
Wenwei Zhang ◽  
Qi Wang ◽  
...  

Rice stripe disease, caused by Rice stripe virus (RSV) and transmitted by the small brown planthopper (Laodelphax striatellus Fallen), is one of the most serious viral diseases of rice in temperate East Asian production regions. Prior quantitative trait loci (QTL) mapping has established that Oryza sativa L. subsp. indica ‘IR24’ carries positive alleles at the three loci qSTV3, qSTV7, and qSTV11-i. Here, we report an advanced backcross analysis based on three selected chromosome segment substitution lines (CSSLs), each predicted to carry one of these three QTL. Three sets of BC4F2:3 populations were bred from a cross between the critical CSSL and its recurrent parent Oryza sativa L. subsp. japonica ‘Asominori’. Both qSTV3 and qSTV11-i were detected in their respective population, but qSTV7 was not. An allelic analysis based on a known carrier of the major RSV resistance gene Stvb-i, which is located on chromosome 11, showed that qSTV11-i was not allelic with Stvb-i. A large mapping population was used to delimit the location of qSTV11-i to a 73.6-kb region. The de novo markers developed for this purpose will be useful as marker-assisted selection tools in efforts to introduce qSTV11-i into breeding programmes aiming to improve the level of RSV resistance.


Sign in / Sign up

Export Citation Format

Share Document