S. Jock et al., Screening of ornamental plants from the Botanic Gardens of Melbourne and Adelaide for the occurrence of Erwinia amylovora, AUSTRALAS P, 29(2), 2000, pp. 120-128
Host plants of Erwinia amylovora in the Royal Botanic Gardens of Melbourne
(RBGM) and the Adelaide Botanic Gardens (ABG) were inspected for symptoms o
f fire blight including dieback, and shoot and stem cankers. Forty five sym
ptomatic plants were sampled and concurrently tested for the presence of E,
amylovora at the Institute for Horticultural Development, Victoria; Macqua
rie University, New South Wales; and the Max Planck Institute, Germany. At
Max Planck, E. amylovora was isolated from wood samples from a Cotoneaster
(Ag0002) and a Sorbus sorbus (Ag0034) from RBGM, and from a soft agar cultu
re of bacteria isolated in Australia from Ag0002 and forwarded to Germany.
Wood samples from ABG tested negative. Identification was confirmed by test
s on selective media, by polymerase chain reaction assays, and by reactions
on tobacco, pear slices and juvenile apple plants. The patterns obtained b
y pulsed field gel electrophoresis of the strains isolated from Australian
samples in Germany and New Zealand were identical with each other and with
strains of E. amylovora from Central Europe, New Zealand and with the Engli
sh standard strain Ea595. However, the German and New Zealand strains of E.
amylovora isolated from Australian wood samples differed in the size of th
e short DNA sequence repeat within the amplified plasmid pEA29 fragment. Ex
haustive attempts in both Australian laboratories to isolate E, amylovora b
y similar test protocols from wood samples from RBGM and ABG were unsuccess
ful. Extensive surveys since the original outbreak have not detected the di
sease or the pathogen.