Elimination of TSWV from Impatiens hawkerii Bull. and regeneration of virus-free plant
Full Text
Reprint PDF

Keywords

meristem culture
New Guinea Impatiens
Tomato spotted wilt virus
virus- free plants

How to Cite

1.
Milošević S, Subotić A, Bulajić A, Djekić I, Jevremović S, Vučurović A, Krstić B. Elimination of TSWV from Impatiens hawkerii Bull. and regeneration of virus-free plant. Electron. J. Biotechnol. [Internet]. 2011 Jan. 18 [cited 2024 Sep. 18];14(1). Available from: https://preprints.pucv.cl/index.php/ejbiotechnology/article/view/v14n1-5

Abstract

The possibility for obtaining virus free plants from Impatiens hawkerii Bull. shoots infectedwith Tomato spotted wilt virus (TSWV) through meristem-tip culture was examined. TSWV presence in I. hawkerii plants was detected by DAS-ELISA and RT-PCR and identification of the virus was confirmed by sequencing one of the chosen isolate (GenBank Accesion CQ132190). Meristem-tip explants (0.3-1.5 mm) from virus-infected shoots are cultured on MS media supplemented with different concentrations of the cytokinins, CPPU or TDZ (0.01-1.0 µM), respectively. Using this system, a large number of in vitro shoots could be produced from a single explant. Also, cytokinins showed a stimulatory effect on the length, fresh and dry weights of the newly formed shoots. Plant pigments content in I. hawkerii shoots increased significantly in the presence of cytokinins. Rooting of shoots was spontaneous on the same media. Rooted plantlets were transferred to soil where 97% successfully acclimatized. By DAS-ELISA and RT-PCR, 80% of the in vitro plantlets were shown to be a virus-free. Considering these, the present protocol seems to be an efficient method for in vitro generation of virus-free I. hawkerii plantlets by meristem tip cultures.

Full Text
Reprint PDF

Upon acceptance of an article by the journal, authors will be asked to transfer the copyright to Electronic Journal of Biotechnology, which is committed to maintain the electronic access to the journal and to administer a policy of fair control and ensure the widest possible dissemination of the information. The author can use the article for academic purposes, stating clearly the following: "Published in Electronic Journal of Biotechnology at DOI:10.2225/volXX-issueX-fulltext-XX".

The Copyright Transfer Agreement must be submitted as a signed scanned copy to biotec@ucv.cl. All authors must send a copy of this document.