Development of strain specific molecular markers for the Sclerotinia minor bioherbicide strain IMI 344141 |
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Authors: | L. Pan G.J. Ash B. Ahn |
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Affiliation: | 1. Department of Plant Science , McGill University , 21,111 Lakeshore Road, Ste-Anne-de-Bellevue, Quebec, Canada , H9X 3V9;2. E.H. Graham Centre for Agricultural Innovation , Charles Sturt University , Locked Bag 588, Wagga Wagga, NSW, 2678, Australia |
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Abstract: | The plant pathogenic fungus, Sclerotinia minor IMI 344141, has been developed as a bioherbicide for broadleaf weed control in turfgrass and a means to differentiate this biocontrol agent from like organisms is required. A strain specific molecular marker was developed to detect and monitor the Sclerotinia minor IMI 344141 bioherbicide strain. The method was based on polymerase chain reaction (PCR) amplification of two sequence-characterized amplified regions (SCAR) primer pairs for a first round PCR, and another two sets of nested primers was used for a second round PCR if higher sensitivity was needed. Sclerotinia minor IMI 344141 was successfully traced from both pure cultures and environmental samples originating from bioherbicide-released field trials. DNA of the S. minor bioherbicide isolate IMI 344141 was detected in the soil 2 months after application, but was not detected in the 3- and 9-month samples after application. When applied as a bioherbicide, S. minor (IMI 344141) did not persist into the following spring season in turf environments. This molecular detection method provides a mechanism to distinguish this isolate from related organisms and a tool to monitor behavior of the biocontrol agent S. minor IMI 344141 in nature, particularly in soil. |
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Keywords: | biocontrol bioherbicide detection mycoherbicide PCR RAPD SCAR Sclerotinia minor turfgrass |
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