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Purification and Serological Studies on Barley Stripe Mosaic Hordevirus

Purification and Serological Studies on Barley Stripe Mosaic Hordevirus

M.A.S. El-Kady1, Om-Hashem M. El-Banna 2, E.A Salama2, Salwa N. Zein1

1 Virus and Phytoplasma Research Department. Plant Pathology Research Institute,
Agricultural Research Center. Giza, Egypt.
 2 Plant Pathology Department, Faculty of Agriculture, Cairo University. Giza, Egypt.

ABSTRACT

Three different procedures of purification were performed to purify a local isolate Of Barley stripe mosaic Hordevirus (BSMV). The 1st procedure was successful in producing relatively high yield of virus preparation 3.7 mg/100 g of barley leaves with adequate purity and one light-scattering zone was round in sucrose density-gradient column. The 2nd and 3rd procedures yielded aggregated virions (2.3 and 7.0 mg/ 100 g of fresh barley leaves, respectively). Electron microscopy of negatively stained purified virus preparation showed rod-shaped particles with dimension of 150x25 nm. The polyclonal antibodies raised against the local isolate of BSMV had a specific titer of 1:2000. Positive reactions were obtained when purified IgG and IgG conjugate with alkaline phosphatase was 1:1000. The prepared antiserum was used detection of BSMV by serological methods i.e., Enzyme-linked immunosorbent assay (ELISA), Dot-blot and tissues-blot immunobinding assays (DBIA and TBIA). The presence of the virus was confirmed in mature seed parts and non-seed parts of the different five barley cultivars tested.

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Journal of Virological Sciences

July

Vol. 3, Iss. 1

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