A method involving ice nucleation for the identification of microorganisms antagonistic to Erwinia amylovora on pear flowers

A method was developed for the rapid selection of antagonists capable of suppressing growth of Erwinia amylovora on pear flowers. The population size of E. amylovora on flowers pretreated with potential antagonists was estimated by a flower-freezing assay. E. amylovora harboring the iceC gene from Pseudomonas syringae on the stable plasmid pVSP61 expressed high levels of ice nucleation activity. The threshold freezing temperature of flowers colonized by the ice nucleation-active (Ice + ) strain of E. amylovora increased linearly with the logarithm of the population size of the pathogen. Bacterial and yeast strains were selected from the predominant microflora of pear flowers and tested for their ability to lower the threshold freezing temperature of flowers subsequently inoculated with the Ice + E. amylovora strain. For each antagonist, the proportion of 20 treated flowers that had frozen was evaluated when approximately 95% of the control (E. amylovora only) had frozen. Among 257 strains tested, 45 (4 yeasts and 41 bacteria) were capable of reducing freezing of inoculated flowers by 70% or more. The reduction in the proportion of pretreated flowers that froze relative to the control for a number of antagonists was correlated (R 2 = 0.61) with reduced E. amylovora population sizes. Over 50% of the antagonistic strains that reduced the proportion of frozen flowers by 50% or more during an initial screening conferred a similar reduction in the number of frozen flowers in a second test. Several strains were more antagonistic to E. amylovora in situ than P. fluorescens strain A506, which is used commercially for biological control of fire blight.

[1]  S. Lindow,et al.  A Biological Sensor for Iron Available to Bacteria in Their Habitats on Plant Surfaces , 1994, Applied and environmental microbiology.

[2]  P. Mcmanus,et al.  Epidemiology and genetic analysis of streptomycin-resistant Erwinia amylovora from Michigan and evaluation of oxytetracycline for control , 1994 .

[3]  S. Lindow,et al.  Bacterial ice nucleation: significance and molecular basis , 1993, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[4]  S. Lindow Novel Method for Identifying Bacterial Mutants with Reduced Epiphytic Fitness , 1993, Applied and environmental microbiology.

[5]  J. Norelli,et al.  Streptomycin-resistant bacteria associated with fire blight infections , 1993 .

[6]  J. Andrews Biological control in the phyllosphere. , 1992, Annual review of phytopathology.

[7]  D. Sigee,et al.  Biological control of fire blight of hawthorn (Crataegus monogyna) with Erwinia herbicola under protected conditions. , 1990 .

[8]  P. W. Steiner Fire blight and its control. , 1990 .

[9]  S. Beer,et al.  Scanning electron microscopy of apple blossoms colonized by Erwinia amylovora and E. herbicola , 1986 .

[10]  S. S. Hirano,et al.  Ice nucleation temperature of individual leaves in relation to population sizes of ice nucleation active bacteria and frost injury. , 1985, Plant physiology.

[11]  S. Lindow,et al.  Bacterial ice nucleation: a factor in frost injury to plants. , 1982, Plant physiology.

[12]  J. P. Blakeman,et al.  Potential for Biological Control of Plant Diseases on the Phylloplane , 1982 .