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Abstract
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In October and November 2012, white-scaled onions bulbs with necrotic symptoms were collected in the area under cultivation in Khuzestan province. Symptoms were dark spots frequently organised in concentric rings, forming patches of up to 1 cm in diameter (Fig. 1). These spots are made up of stromatic masses formed beneath the cuticle of the host, consisting of intertwining thick-walled mycelial threads in dark green to black stromata, usually only a fraction of a millimetre in diameter and a few to several hundred microns thick. The affected tissue was surface sterilised with sodium hypochlorite (0.8% chlorine) for 30 seconds and dried with sterile paper before small pieces were excised and aseptically transferred to potato dextrose agar (PDA) and water agar (WA) in petri dishes and incubated in the dark at ambient temperature (30 ± 2°C). Isolates grown on PDA, produced acervuli with dark, almost black, 1-3 septate acicular setae having a bulbous base, measuring up to 290 x 8 μm (Fig. 2 A, B). Conidia were hyaline, unicellular, 16-25 x 3-5 μm, slightly falcate, guttulated (Fig. 1 C). A small amount of mycelia was scraped from a seven-day-old culture and the internal spacer region (ITS) of the extracted fungal DNA was amplified with universal primers ITS1 and ITS4. The resulting sequence (509 bp) was submitted to the NCBI GenBank (isolate IRAN2185C, Accession No. KJ458968,). A blast search of ITS sequences revealed that this fungus was Colletotrichum circinans with 100% query coverage with KC790955 and AJ301955 and 99% query coverage with GQ369595. Diseased tissue was cut into 1-2 cm lengths, surface-sterilised, and the original pathogen from onion placed on water agar to recover the fungus. Three isolates of C. circinans were tested for pathogenicity to onion bulbs by artificial inoculation with conidial suspensions (1-2 x 10 conidia/ml) that were prepared from 20-day-old PDA cultures. Sterile distilled water was used as control. Plastic boxes containing the inocul
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