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Genetic nature, stability, and improved virulence of hybrids from protoplast fusion in Beauveria

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Abstract

Genetic improvement of two different strains of the entomopathogenic fungus Beauveria bassiana for more effective control of Ostrinia nubilalis and Leptinotarsa decemlineata was obtained by crosses with the insecticidal toxin-producing strain Beauveria sulfurescens. Protoplast fusion between diauxotrophic mutants resulted in the recovery of some stable prototrophic fusion products. The low levels of virulence of the wild type strain B. bassiana 28 isolated originally from L. decemlineata were enhanced both on L. decemlineata and O. nubilalis for one of the hybrids obtained (FP 8) from the cross B. bassiana 28 × B. sulfurescens 2. Fusion product 25 obtained from the cross between B. sulfurescens and the highly pathogenic strain B. bassiana 147 showed a three-day reduction in the LT50 towards O. nubilalis. Southern blot hybridization with nine probe-enzyme combinations were conducted on genomic DNAs from the original wild strains, parental mutant strains, and fusion products. Additive banding patterns or unique banding pattern of either parental strain was observed in five hybrids, indicating their status as recombinant and/or partially diploïd. Combination of RFLP markers indicative of both parental genomes was never observed with fusion product FP 25. The stability of the virulence following passage through insect-host and stability of molecular structure for the fusion products FP 8 and FP 25 suggest that asexual genetic recombination by protoplast fusion may provide an attractive method for the genetic improvement of biocontrol efficiency in entomopathogenic fungi.

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Authors and Affiliations

  1. Station de Recherches de Lutte biologique, INRA, La Minière 78285, Guyancourt Cedex, France

    Y. Couteaudier, M. Viaud & G. Riba

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  1. Y. Couteaudier
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  2. M. Viaud
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  3. G. Riba
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Couteaudier, Y., Viaud, M. & Riba, G. Genetic nature, stability, and improved virulence of hybrids from protoplast fusion in Beauveria . Microb Ecol 32, 1–10 (1996). https://doi.org/10.1007/BF00170102

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  • DOI: https://doi.org/10.1007/BF00170102

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