Degradation of oxalic acid by the mycoparasite C oniothyrium minitans plays an important role in interacting with S clerotinia sclerotiorum
C oniothyrium minitans ( Cm ) is a mycoparasite of the phytopathogenic fungus S clerotinia sclerotiorum ( Ss ). Ss produces a virulence factor oxalic acid ( OA ) which is toxic to plants and also to Cm , and Cm detoxifies OA by degradation. In this study, two oxalate decarboxylase genes, Cmoxdc1 and...
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Veröffentlicht in: | Environmental microbiology 2014-08, Vol.16 (8), p.2591-2610 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | C
oniothyrium minitans
(
Cm
) is a mycoparasite of the phytopathogenic fungus
S
clerotinia sclerotiorum
(
Ss
).
Ss
produces a virulence factor oxalic acid (
OA
) which is toxic to plants and also to
Cm
, and
Cm
detoxifies
OA
by degradation. In this study, two oxalate decarboxylase genes,
Cmoxdc1
and
Cmoxdc2
, were cloned from
Cm
strain Chy‐1.
OA
and low
pH
induced expression of
Cmoxdc1
, but not
Cmoxdc2
.
Cmoxdc1
was partially responsible for
OA
degradation, whereas
Cmoxdc2
had no effect on
OA
degradation. Disruption of
Cmoxdc1
in
Cm
reduced its ability to infect
Ss
in dual cultures where
OA
accumulated. Compared with
Chy
‐1, the
Cmoxdc1
‐disrupted mutants had reduced expression levels of two mycoparasitism‐related genes chitinase (
Cmch1
) and β‐1,3‐glucanase (
Cmg1
), and had no detectable activity of extracellular proteases in the presence of
OA
. On the other hand, the cultural filtrates of the
Cmoxdc1
‐disrupted mutants in
OA
‐amended media showed enhanced antifungal activity, possibly because of increased production of antifungal substances under acidic
pH
condition resulted from reduced
Cmoxdc1
‐
mediated
OA
degradation. This study provides direct genetic evidence of
OA
degradation regulating mycoparasitism and antibiosis of
Cm
against
Ss
, and sheds light on the sophisticated strategies of
Cm
in interacting with metabolically active mycelia and dormant sclerotia of
Ss
. |
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ISSN: | 1462-2912 1462-2920 |
DOI: | 10.1111/1462-2920.12409 |