Succession of indigenous Pseudomonas spp. and actinomycetes on barley roots affected by the antagonistic strain Pseudomonas fluorescens DR54 and the fungicide imazalil
L. Thirup et al., Succession of indigenous Pseudomonas spp. and actinomycetes on barley roots affected by the antagonistic strain Pseudomonas fluorescens DR54 and the fungicide imazalil, APPL ENVIR, 67(3), 2001, pp. 1147-1153
In recent years, the interest in the use of bacteria for biological control
of plant-pathogenic fungi has increased. We studied the possible side effe
cts of coating barley seeds with the antagonistic strain Pseudomonas fluore
scens DR54 or a commercial fungicide, imazalil, This was done by monitoring
the number of indigenous Pseudomonas organisms and actinomycetes on barley
roots during growth in soil, harvest after 50 days, and subsequent decompo
sition. Bacteria were enumerated by traditional plate spreading on Gould's
S1 agar (Pseudomonas) and as filamentous colonies on Winogradsky agar (acti
nomycetes) and by two quantitative competitive PCR assays. For this we deve
loped an assay targeting Streptomyces and closely related genera, DR54 cons
tituted more than 75% of the Pseudomonas population at the root base during
the first 21 days but decreased to less than 10% at day 50, DR54 was not s
uccessful in colonizing root tips, Initially, DR54 affected the number of i
ndigenous Pseudomonas organisms negatively, whereas imazalil affected Pseud
omonas numbers positively, but the effects were transient, Although plate c
ounts were considerably lower than the number of DNA copies, the two method
s correlated well for Pseudomonas during plant growth, but after plant harv
est Pseudomonas-specific DNA copy numbers decreased while plate counts were
in the same magnitude as before. Hence, Pseudomonas was 10-fold more cultu
rable in a decomposition environment than in the rhizosphere, The abundance
of actinomycetes was unaffected by DR54 or imazalil amendments, and CFU an
d quantitative PCR results correlated throughout the experiment. The abunda
nce of actinomycetes increased gradually, mostly in numbers of DNA copies,
confirming their role in colonizing old roots.