DNA SeqUeNCINg ANAlySIS Of AfRICAN Xanthomonas oryzae pv. oryzae vIRUleNCe geNe (aXaVrg) DNA MARkeR

Onasanya, A. and Ekperigin, M.M. and Onasanya, R.O. and Obafemi, T.O. and Ogundipe, A.T. and Ojo, A.A. and Ingelbrecht, I. (2018) DNA SeqUeNCINg ANAlySIS Of AfRICAN Xanthomonas oryzae pv. oryzae vIRUleNCe geNe (aXaVrg) DNA MARkeR. Scientia agriculturae bohemica, 49 (2). pp. 78-86.

Text [18059430 - Scientia Agriculturae Bohemica] DNA Sequencing Analysis of African Xanthomonas oryzae pv. oryzae Virulence Gene (AXaVrg) DNA Marker.pdf Download (1MB)

Abstract

Global rice production is constrained by bacterial leaf blight (BLB) disease caused by Xanthomonas oryzae pv. oryzae (Xoo). BLB disease incidence in West Africa was between 70–85% and yield loss in farmers’ fields was in the range of 50–90% from 2005 to 2010. In the present study, African Xoo virulence gene OPP-172000 DNA marker was identified and purified using randomly amplified polymorphic DNA polymerase chain reaction (RAPD-PCR) products from 50 Xoo isolates. Genomic DNA of 50 Xoo isolates were analyzed using OPP-17 primer in RAPD-PCR during which African Xoo virulence gene OPP-172000 DNA marker was identified, purified, cloned, and sequenced. Cloning and DNA sequencing of African Xoo virulence gene OPP-172000 DNA generated a 1953 bp nucleotide sequence consequently tagged as AXaVrg-1953. BLAST homologous analysis of the AXaVrg-1953 sequence provides comprehensive identification of the type II secretion genes and secreted proteins, type III secretion genes and secreted proteins in African Xoo virulence gene. Phylogenetic unweighted pairgroup method arithmetic (UPGMA) analysis revealed the African AXaVrg-1953 sequence was distinct from the other Xoo virulence gene sequences from China, Japan, Korea, Germany, and the United States. This information is potentially useful for effective management of BLB disease in West Africa. Bacterial leaf blight, Operon primer, RAPD-PCR products, Xoo virulence gene DNA marker, cloning, Secreted proteins, BLAST, West Africa

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