植物病理学与微生物学杂志

抽象的

Relationship of Luteovirus and PAV-Barley Yellow Dwarf Virus

Hoda MA Waziri*, Hala A Amin, KE Saker, AM Soliman

Barley Yellow Dwarf Virus (BYDV-PAV) isolated from Wheat plants grown in Egypt has been characterized. Two coding regions of the Barley Yellow Dwarf Virus (BYDV-PAV) isolate for the polymerase gene (P1) located in Open Reading Frame (ORF1) and Coat Protein gene (CP) located in Open Reading Frame (ORF3) was targeted. Two sets of specific primers were designed according to of BYDV-PAV isolate in Genbank. The DNA fragments of ORF1and ORF3 of an Egyptian isolate of BYDV-PAV were cloned and sequenced. The sequence contained a full-length ORF1 coding for the viral polymerase gene (P1). It comprises 910 knot in length encodes a predicted polypeptide chain of 303 amino acids with an M(r) of 34.67. On the other hand, the sequence data for the ORF3 coding for the viral coat protein revealed that it was 603 bp in length encodes a predicted protein 200 amino acids, with molecular weight of 21.96 KDa. However, the phylogenetic homology tree based on the multiple sequence alignments of the Egyptian isolate Egy-Wz with those isolates available in NCBI GenBank revealed that the polymerase gene (P1) shared 76.5%-99% and 71.6%-93.2% sequence identities at amino acid and nucleotide levels with the 05GG2 , PAV 014 and PAV014, PAV-Aus isolates respectively. On the other hand, the coat protein gene (CP) showed 85.1% -99.5% and 89.7%-99.2% sequence similarity with two isolates 06KM14 and 05GG2 at the amino acid and nucleotide level, respectively.