Abstract:
This work investigated the production of the biocontrol agents: Penicillium
oxalicum to control Fusarium oxysporum f.sp. Iycopersici in the rhizosphere; and
Epicoccum nigrum and Penicillium frequentans to control Monilinia laxa in the
phyllosphere. Ecophysiological studies were carried out to categorise different
inoculum types, and to test their biocontrol efficacy.
A method was developed for the induction of submerged conidiation of
P.oxalicum for the first time. This was achieved by transferring 24 h cultures to a
nitrogen free medium, and further stimulated by a high C:N ratio with 20 mM
calcium. Optimum submerged conidial concentrations obtained were 35x10
6
spores mr1. The hydrophobicity of submerged and aerial conidia of P.oxalicum
was similar. However, different results were obtained depending on the method
used. Appearance of both spore types under the SEM was similar in size and
shape. However, submerged spores were covered by a filamentous matrix,
absent in aerial ones. Viability of aerial and submerged P.oxalicum spores was
higher than 80% after 27 weeks, when stored fresh at either 4 or 25°C, but aerial
spores survived slightly better. Freeze-drying severely affected viability,
especially of submerged spores. Aerial spores effectively colonised sterile soil in
tomato seedbeds with water potentials in the range 1-7 (-MPa), and this was
further favoured by the addition of nutrients. Aerial conidia of P.oxalicum applied
to seedbeds were able to significantly (P<0.05) reduce Fusarium wilt of tomato at
concentrations as low as 6x10
4
spores mr
1
substratum, indicating that the amount
of the antagonist needed is not a limiting factor for the practical application of this
antagoniSt. Aerial spores were slightly more effective than submerged ones in the
control of the disease. However, mycelium was ineffective. Coating of tomato
seeds with formulations of aerial spores of P.oxalicum in alginate or methyl
cellulose significantly (P<0.05) enhanced the growth promotion effect of the
antagonist in vitro, which may be related to the ability of the fungus to control the
disease.
E.nigrum spores were produced by solid fermentation on wheat grains at
different water activities (aw). Maximum levels of sporulation (7-11x10
6
spores g-1
grain) were obtained at high aw (0.996) or reduced aw (0.98) adjusted with a mixture glycerol/water. E.nigrum and P.frequentans were both produced in culture
medium at reduced aw, to improve their ecological competence in the
phyllosphere and therefore their biocontrol ability. E.nigrum produced at reduced
aw showed improved germ tube extension and in some cases colony growth rate
when placed on medium at reduced aw, showing water stress tolerance of such
modified inocula. Furthermore, such inocula showed an enhanced ability to
compete with the pathogen, M.laxa, at reduced aw, shown by a higher Niche
Overlap Index (the proportion of the carbon compounds utilised by M.laxa that
were also utilised by E.nigrum). E.nigrum spores produced at reduced aw had
improved survival when stored fresh at 4 or 25°C. Freeze-drying severely affected
the viability of both spore types (produced at high or reduced aw).
E.nigrum and P.frequentans produced at reduced aw accumulated low
molecular weight polyols as compatible solutes. Improvement of biocontrol of
peach twig blight was obtained in the case of E.nigrum, which is more sensitive to
conditions of low water availability than the xerotolerant P.frequentans. However,
both fungi accumulated glycerol as the main compatible solute, indicating that
different accumulation mechanisms may be responsible for the different tolerance
to low water availability. Glycerol was also the main compatible solute in E.nigrum
spores produced by solid fermentation at reduced aw. E.nigrum produced at high
or reduced aw was also able to control brown rot of cherries, under optimum
conditions for the development of the disease.
The results presented in this work show that the conditions during the
production of biocontrol agents are critical in determining their efficacy.
Therefore, when developing mass-production systems it is necessary to aim not
only for high propagule numbers but also for inoculum quality, defined by
parameters such as ecological competence or survival during storage.