National Repository of Grey Literature 3 records found  Search took 0.01 seconds. 
Optimized biological method for the detection of sensitivity of red clover varieties to white clover mosaic virus (WClMV) and red clover mottle virus (RCMV) infection in the climatic conditions of the Czech Republic
Jakešová, H. ; Fránová, Jana
Red clover is a very important leguminous plant used in crop rotations on arable land, in temporary as well as permanent clover and grass stands. The persistence of clovers is negatively influenced by pests and diseases that attack the root and shoot parts of the plant. In the course of studies into the presence of viral diseases (2007–2011), the most frequently detected viruses were White clover mosaic virus, (WClMV, genus Potexvirus, family Alphaflexiviridae) and Red clover mottle virus (RCMV, genus Comovirus, family Secoviridae). The two viruses were observed in populations of clover throughout the Czech Republic. RCMV significantly reduced the yield and stand persistence of red clover. Given that no direct protection has yet been developed against the viruses, plant breeding directed to enhancing resistance to both WClMV and RCMV offers good prospects. Both viruses are mechanically transmissible.
Purification of white clover mosaic virus, antiserum production and IgG isolation for serological detection of virus by ELISA
KOLÁŘOVÁ, Klára
White clover mosaic virus (WClMV) virions were purified using a modified method of Wetter (1960). Antisera were produced by rabbit immunisation and virus-specific polyclonal antibodies were obtained. Suitable conditions were optimised for serological detection of virus by DAS-ELISA and compared with a commercial kit.
Identification of filamentous virus which infected red clover (\kur{Trifolium pratense})
BEČKOVÁ, Martina
Samples of red clover plants characteristic with dwarf growth were investigated with transmission electron microscopy. Most frequent virus particles observed there were filamentous ones of 300 to 800 nm long. Nucleic acid was isolated, transcribed and amplified using PCR with potexvirus- and potyvirus-specific primers 353G1, 353G2 (Petrzik, K., unpublished data), P9502, P0502 (Revers et al., 1999) and Poty2/P4 (Gibbs and Mackenzie, 1997). Successful amplification with potexvirus-specific primers, sequencing and comparison with GenBank sequences revealed White clover mosaic virus (WClMV) there. Coat protein gene of this virus was obtained with amplification and compared with complete sequence of WClMV from GenBank. O-strain of WClMV was identified.

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