Transgenic watermelon lines expressing the nucleocapsid gene of Watermelon silver mottle virus and the role of thiamine in reducing hyperhydricity in regenerated shoots

2010 ◽  
Vol 106 (1) ◽  
pp. 21-29 ◽  
Author(s):  
Ying-Chih Huang ◽  
Chu-Hui Chiang ◽  
Chin-Mei Li ◽  
Tsong-Ann Yu
1987 ◽  
Vol 68 (6) ◽  
pp. 1533-1542 ◽  
Author(s):  
H. S. Savithri ◽  
S. K. Munshi ◽  
S. Suryanarayana ◽  
S. Divakar ◽  
M. R. N. Murthy
Keyword(s):  

2001 ◽  
Vol 146 (2) ◽  
pp. 389-394 ◽  
Author(s):  
M. Okuda ◽  
S. Taba ◽  
S. Tsuda ◽  
S. Hidaka ◽  
M. Kameya-Iwaki ◽  
...  

1998 ◽  
Vol 88 (4) ◽  
pp. 351-358 ◽  
Author(s):  
Fang-Hua Chu ◽  
Shyi-Dong Yeh

Double-stranded genomic RNAs (dsRNAs) extracted from Chenopodium quinoa infected with watermelon silver mottle virus (WSMV) were similar to those of tomato spotted wilt virus (TSWV, serogroup I) and impatiens necrotic spot virus (INSV, serogroup III), except that the S dsRNA of WSMV is 0.75 and 0.6 kbp longer than those of TSWV and INSV, respectively. The complete nucleotide sequence of the genomic M RNA of WSMV was determined from cDNA clones generated from separated M dsRNA. The M RNA is 4,880 nucleotides in length with two open reading frames (ORFs) in an ambisense organization. The M RNA-encoded nonstructural (NSm) ORF located on the viral strand encodes a protein of 312 amino acids (35 kDa), and the G1/G2 ORF located on the viral complementary strand encodes a protein of 1,121 amino acids (127.6 kDa). The RNA probe corresponding to the NSm or G1/G2 ORF of WSMV failed to hybridize with the M dsRNAs of TSWV and INSV. Comparison of M and S RNAs of WSMV, TSWV, INSV, and peanut bud necrosis virus (PBNV, serogroup IV) revealed a consensus sequence of eight nucleotides of 5′-AGAGCAAU…-3′ at their 5′ ends and 5′-…AUUGCUCU-3′ at their 3′ ends. The low overall nucleotide identities (56.4 to 56.9%) of the M RNA and the low amino acid identities of the NSm and G1/G2 proteins (30.5 to 40.9%) with those of TSWV and INSV indicate that WSMV belongs to the Tospovirus genus but is phylogenetically distinct from viruses in serogroups I and III. The M RNA of WSMV shares a nucleotide identity of 79.6% with that of PBNV, and the two viruses share 83.4 and 88.7% amino acid identities for their NSm and G1/G2 proteins, respectively. It is concluded that they are two related but distinct species of serogroup IV. In addition to the viral or viral complementary full-length M RNA, two putative RNA messages for the NSm gene and the G1/G2 gene, 1.0 and 3.4 kb, respectively, were detected from the total RNA extracted from WSMV-infected tissue of Nicotiana benthamiana. The 1.0- and 3.4-kb RNAs were also detected in the viral RNAs extracted from purified nucleocapsids, suggesting that the putative messages of the M RNA of WSMV can also be encapsidated by the nucleocapsid protein.


2019 ◽  
Vol 139 ◽  
pp. 470-477 ◽  
Author(s):  
Chunyan Fei ◽  
Lijuan Chen ◽  
Ting Yang ◽  
Wenshan Zou ◽  
Honghui Lin ◽  
...  

Author(s):  

Abstract A new distribution map is provided for Watermelon silver mottle virus. Bunyavirales: Bunyaviridae: Orthotospovirus. Hosts: Cucurbitaceae especially watermelon (Citrullus lanatus), melon (Cucumis melo), tomato (Solanum lycopersicum), Capsicum. Information is given on the geographical distribution in Asia (China, Guangdong, Yunnan, India, Maharashtra, Japan, Kyushu, Ryukyu Archipelago, Taiwan, Thailand).


2005 ◽  
Vol 79 (7) ◽  
pp. 4407-4414 ◽  
Author(s):  
Eugénie Hébrard ◽  
Agnès Pinel-Galzi ◽  
Vincent Catherinot ◽  
Gilles Labesse ◽  
Christophe Brugidou ◽  
...  

ABSTRACT Rice yellow mottle virus is classified in five major serotypes; the molecular diversity of the coat protein (CP) is well established, but the amino acids involved in the recognition by discriminant monoclonal antibodies (MAbs) remain unknown. Reconstruction of a phylogenetic tree and sequence alignment of the CP gene of a sample representative of the continental-large diversity were used to identify 10 serospecific amino acids (i.e., conserved in all isolates belonging to the same serotype and distinct in other serotypes). Positions occupied by serospecific residues were localized on the crystal structure of the CP monomer and on modeled capsomers. Structural, molecular, and serological properties of each serotype were analyzed, and subsequently, hypotheses on the potential role of amino acids in discriminating reactions with antibodies were formulated. The residues 114 and 115 (serospecific of Sr1) and 190 (serospecific of Sr2) were localized on the outer surface of the capsid and might be directly involved in the immunoreactivity with MAb D and MAb A, respectively. In contrast, residues 180 (Sr3) and 178 (Sr5) lay within the inner surface of the capsid. To understand the role of these internal positions in the recognition with the antibodies, two substitutions (T180K and G178D) were introduced in the CP of an infectious clone. These mutations modified the antigenicity with MAb G and MAb E discriminating Sr3 and Sr5, respectively, while the reaction with MAb D remained unaffected. This result suggests an indirect effect of these two internal mutations on local immunostructure while the global structure was maintained.


2015 ◽  
Vol 160 (10) ◽  
pp. 2611-2616 ◽  
Author(s):  
Luis Galipienso ◽  
Carolina Martínez ◽  
Anouk Willemsen ◽  
Ana Alfaro-Férnandez ◽  
Isabel Font-San Ambrosio ◽  
...  

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