Infectious in vivo Transcripts from a Full-length Clone of Soybean mosaic virus Strain G5H

An infectious full-length clone of Soybean mosaic virus (SMV) strain G5H was constructed under the control of the cauliflower mosaic virus 35S promoter. The cloned SMV G5H established infections upon simple rubinoculation of soybean leaves with intact plasmid DNA. We demonstrated that this SMV G5H i...

Full description

Saved in:
Bibliographic Details
Published inThe plant pathology journal Vol. 25; no. 1; pp. 54 - 61
Main Authors Seo, J.K. (Seoul National University, Seoul, Republic of Korea), Lee, H.G. (Seoul National University, Seoul, Republic of Korea), Choi, H.S. (National Institute of Agricultural Science and Technology, RDA, Suwon, Republic of Korea), Lee, S.H. (National Institute of Agricultural Science and Technology, RDA, Suwon, Republic of Korea), Kim, K.H. (Seoul National University, Seoul, Republic of Korea), E-mail: kookkim@snu.ac.kr
Format Journal Article
LanguageEnglish
Published 한국식물병리학회 01.03.2009
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:An infectious full-length clone of Soybean mosaic virus (SMV) strain G5H was constructed under the control of the cauliflower mosaic virus 35S promoter. The cloned SMV G5H established infections upon simple rubinoculation of soybean leaves with intact plasmid DNA. We demonstrated that this SMV G5H infectious DNA clone caused typical characteristic symptoms and virulence of SMV strain G5H in twelve tested soybean cultivars. Soybean cultivars Lee74, Somyungkong and Sowonkong developed systemic mosaic symptom while Kwanggyo, Taekwangkong, Hwangkeumkong and Geumjeongkong-1 showed systemic necrosis. In contrast, Geumjeongkong-2, Jinpumkong-2, L29, V94-5152 and Ogden showed resistant response against SMV-G5H infection. We also determined full-length sequence of cloned SMV-G5H. The phyogenetic analyses reveal that SMV-G5H is most closely related to SMV-G5, and support that SMV-G5H might be derived from SMV-G5 by recombination rather than mutation.
Bibliography:H01
2009004638
G704-000528.2009.25.1.008
ISSN:1598-2254
2093-9280
DOI:10.5423/PPJ.2009.25.1.054