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Occurrence of common bacterial blight on mungbean ( Vigna radiata ) in Iran caused by Xanthomonas axonopodis pv. phaseoli
Author(s) -
Osdaghi Ebrahim
Publication year - 2014
Publication title -
new disease reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.184
H-Index - 4
ISSN - 2044-0588
DOI - 10.5197/j.2044-0588.2014.030.009
Subject(s) - vigna , nutrient agar , biology , microbiology and biotechnology , potato dextrose agar , inoculation , spots , horticulture , agar , botany , bacteria , genetics
During the summer of 2011 and 2012, several mungbean (Vigna radiata) fields with suspected bacterial disease symptoms were observed in Southwest Iran (Khuzestan province: Shushtar, Dezfoul, Andimeshk, Mollasani and Gotvand Counties). High incidence of the disease was observed, with some fields in Shushtar and Gotvand (North Khuzestan) fully destroyed in 2011 and incidence up to 70% in 2012. Symptoms included irregular necrotic spots surrounded by a thin chlorotic and watersoaked halo that developed into leaf blight (Fig. 1). Symptom-bearing leaves were surface sterilised by dipping in 1% sodium hypochlorite for two minutes, lesion margins were macerated in distilled water and the resulting suspension was streaked onto nutrient agar (NA) and incubated at 27°C. Yellow, circular and raised bacterial colonies consistently appeared after 48 h (Fig. 2). Five representative bacterial strains (Xapk1-5) were selected and subjected to biochemical and molecular identification. All yellow pigmented isolates were Gram negative rods, appearing mucoid on yeast dextrose chalk agar and had oxidative but not fermentative metabolism; and all hydrolysed gelatin, starch, aesculin and casein, produced acid from arabinose and hydrogen sulphide from cysteine. They were also positive for catalase and lecithinase. All isolates were negative for the presence of pectinase, oxidase, arginine dihydrolase and nitrate reductase. Xanthomonas axonopodis pv. phaseoli (Xap)-specific PCR primers (X4c: 5’-GGCAACACCCGATCCCTAAACAGG-3' and X4e: 5’-CGCCGGAAGCACGATCCTCGAAG-3') were used to confirm the identity of the isolates (Audy et al., 1994). The Xap-19 isolate of Xap provided by the Department of Plant Pathology, Tarbiat Modares

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