ABSTRACT
Carnation latent virus (CLV) and Carnation Vein Mottle Virus ( CarVMV ) were of the most important virus affecting carnation plants .The two viruses were detected serologically by DAS-ELISA using specific antibodies . Shoots from plants infected with ( CLV & CarVMV ) which maintained in green house were used for tip culture . Murashige and Skoog medium (MS ) supplemented with (0.2 mg/L BA ) and (Img/l BA and 0.5 mg/L kinetin ) were used for proliferation and micropropagation of the infected shoot clumps respectively. The plantlets were rooted in MS medium supplemented with (1.5 mg/l NAA ) . Plantlets regenerated from meristem measuring 0.1 mm and 0.2 mm yielded (90 and 80 % ) for CLV and (92 and 80 ) for CarVMV virus-free tested plantlets respectively,while larger meristems (0.3 and 0.4 mm ) were not effective . As well as the plantlets survival was (20 , 35 , 65 and 80% ) for meristem measuring( 0.1, 0.2, 0.3and 0.4 mm ) respectively . Where as the exposure of carnation plantlets infected with CLV and CarVMV to three temperature regimes (36 , 38 and 40±1 0c for 3 and 4 weeks ) .1t was found that (38±10c/3weeks ) gave ( 65 and 70 % ) for CLV and CarVMV virustested plantlets respectively and plantlets survival were ( 67 and 40 % ) While ( 38 and 40±1 Oc for 4 weeks ) gave higher precentage of virus —free plantlets but has a negative correlation with the survival of the plants
However , because of better survival rate , the temperature regime 38 Oc/3weeks is recomended for virus —free tested carnation plants.
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