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African Journal of Biotechnology

     
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  Afr. J. Biotechnol.

  Vol. 8 No. 19

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  Mohammadi MR
 
Hajieghrari R



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African Journal of Biotechnology Vol. 8 (20), pp. 5271-5274, 19 October 2009

ISSN 1684-5315  © 2009 Academic Journals  

 

 

Full Length Research Paper

 

Sugarcane mosaic virus: The causal agent of mosaic disease on sorghum (Sorghum bicolor L.) in Tehran province of Iran

 

Mohammad Reza Mohammadi1,2 and Behzad Hajieghrari3*

 

1Department of Plant Protection, Faculty of Agriculture, Islamic Azad University Branch Varamin, Varamin, Iran.

2Institute of Tropical Agriculture, University Putra Malaysia (UPM), Serdang, Selangor, Malaysia.

3Department of Plant Production, Moghan Junior College of Agriculture, University of Mohaghegh – Ardabili, Ardabil, Iran.

 

*Corresponding author. E-mail: bhajieghrari@uma.ac.ir. Tel: +989143186861.

Fax: +984527463417.

 

Accepted 23 February, 2009

 

   Abstract

 

During disease diagnosing studies on sorghum fields in Tehran province, Iran through vegetation period in 2005 - 2006, 75 sorghum expressing virus-associated symptoms including mosaic, leaf-redding and necrosis were collected. The virus was inoculated mechanically to Sweet corn (Zea mays cv. Pars403) and grain sorghum (Sorghum bicolor cv. Kimia). The virus specifically was reacted in Double Antibody Sandwich-Enzyme Linked Immunosorbent Assay (DAS-ELISA) and Dot Immunobinding Assay (DIBA). Also relative molecular mass of virus coat protein was calculated using a densitometer via sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) to determine electrophoretic mobility compared with protein standards. The virus reacted with anti SCMV polyclonal IgG antiserum and was detected with Goat anti-Rabbit IgG alkaline phosphatase conjugate. The total nucleic acids were subjected to reverse transcription-polymerase chain reaction (RT-PCR) using SCMV degenerate and specific primers. Sugarcane mosaic virus (SCMV) was detected in all collected samples. The capsid protein was evaluated approximately 37 kDa in size. Amplification product (approximately 900 bp) was obtained from the collected and inoculated plants but not from healthy plants. This may confirm the presence of SCMV in the symptom-expressing plants.

 

Key words: SCMV, Sorghum bicolor, DAS-ELIZA, DIBA, SDS-PAGE, RT-PCR.

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