
Public Release: March 2006
Mutation in a Single Gene Switches a Fungus-Grass Symbiosis from Mutualistic
to Antagonistic
In research reported this month in The Plant Cell, scientists highlight a novel
role for reactive oxygen species (ROS) in a symbiotic association between a
filamentous fungus (Epichloë festucae) and a grass (Lolium perenne). They
isolated the fungal gene responsible for the production of ROS and found that
disruption of this gene causes the fungus to become pathogenic rather than beneficial.
The authors propose that the function of ROS in this association is to control
the growth of the fungus within the plant. A surprising result of this work
is that the mutation of only one gene was required to switch a symbiotic association
from a beneficial to an antagonistic one.
Contact: Beatrice Grabowski
beatrice@aspb.org
301-251-0560 ext 121
American Society of Plant Biologists
Full release.
THE PLANT CELL http://www.plantcell.org
Contacts:
Barry Scott
Massey University
New Zealand
d.b.scott@massey.ac.nz
(64) 6-350-5688

Mutation in a Single Gene Switches a Fungus-Grass Symbiosis
from Mutualistic to Antagonistic
Research Highlights a Novel Role for Reactive Oxygen Species in the Fungus-Grass
Symbiotic Relationship
A symbiotic relationship is one in which two organisms of different species
interact in ways that profoundly affect their livelihoods and reproductive success.
Such interactions range from mutually beneficial to antagonistic and are considered
to be of major ecological and evolutionary importance in shaping plant and animal
communities. Examples of beneficial symbioses include the microbes that live
in the guts of herbivorous mammals like cows and help to digest cellulose, ants
that protect plants from herbivores, and the fig wasps that pollinate fig trees
by depositing their eggs in the fig flowers, which their larvae then feed on.
Plants participate in numerous symbiotic associations. Examples include the
nitrogen-fixing bacteria that live in plant roots, the fungus-alga association
that makes up lichens, and grasses and endophytic fungi (fungi that live inside
the leaves, stems, and other structures of the plant).
Fungal endophytes in the genus Epichloë form symbiotic associations with
many grasses. Studies have shown that Epichloë endophytes can result in
enhanced biomass production, seed production, and root growth of the grass plants
as well as improved recovery after drought compared to plants without endophytes.
Like other endophytes, the symbioses of grass species with Epichloë fungi
can be mutualistic or antagonistic or both. In the beneficial interactions,
Epichloë endophytes are strictly limited in their intercellular growth
throughout the plant. The growth of the endophyte is synchronized with that
of the grass; fungal hyphae grow actively in expanding leaves but cease to grow
as the leaf matures.
Aiko Tanaka, Daigo Takemotot and Barry Scott at the Centre for Functional Genomics
at Massey University in New Zealand; Michael Christensen at the Grasslands Research
Centre, also in New Zealand, and Pyoyun Park at the Graduate School of Science
and Technology at Kobe University, Japan, studied the interaction of the fungal
endophyte Epichloë festucae and its host, perennial ryegrass, Lolium perenne.
As a result, they discovered a novel role for reactive oxygen species (ROS)
in regulating the mutualistic interaction between E. festucae and its grass
host.
Tanaka et al. used a forward genetics approach to create mutants of the endophyte
that would be unable to establish or maintain a mutualistic relationship with
perennial ryegrass. They inserted foreign DNA randomly into the genome of Epichloë
festucae, resulting in a population of fungal strains having disruptions in
different genes throughout the fungal genome. From this collection they isolated
a mutant that is unable to synchronize its growth with that of the plant host.
Plants infected with the mutant fungus showed stunted growth, premature senescence,
and death, whereas those infected with the wild-type fungus exhibited their
usual growth pattern. This was accompanied by a dramatic increase in fungal
endophyte growth within the plant compared with plants inoculated with wild-type
fungus. The fungal hyphae of the wild type fungus showed limited branching and
were mostly oriented parallel fo the intercellular spaces of the leaf. On the
other hand, the hyphae of the mutant fungus showed extensive colonization of
the leaf-similar to a pathogenic infection. As a result, the biomass of the
mutant fungus increased significantly compared to wild type. Thus a mutualistic
interaction became an antagonistic one with the mutation of a single gene.
Tanaka et al. then went on identify and sequence the fungal gene responsible
for the mutant phenotype. They determined that the foreign DNA had disrupted
a fungal gene, called noxA, which encodes an enzyme that catalyzes the conversion
of molecular oxygen to superoxide. The altered symbiotic phenotype is due to
a mutation (caused by the insertion of a segment of foreign DNA) in the E. festucae
noxA gene.
NADPH oxidase catalyzes the production of ROS or superoxides by transferring
electrons from NADPH (a ubiquitous electron donor in nature) to molecular oxygen,
with secondary generation of hydrogen peroxide. Superoxides are unstable and
highly reactive molecules that can be extremely destructive in biological systems
and have been implicated, for example, as causal agents in cancer formation.
For this reason, antioxidants, which destroy superoxides are recommended as
cancer prevention measures. However, in this case ROS appear to be part of the
arsenal that plants use to protect themselves, as NADPH oxidase enzymes generate
superoxides in response to pathogen colonization.
Tanaka et al. looked at the production of the ROS hydrogen peroxide (H2O2)
in plants infected with wild type and mutant E. festucae by electron microscopy.
Cerium perhydroxides, which are formed by a reaction with H2O2, were detected
in actively growing tissue of plants with wild type fungus but rarely in the
same tissue of plants with mutant fungus. These results confirmed that it is
the fungus, not the plant, that is mainly responsible for ROS production.
The authors proposed that ROS produced by the endophyte NoxA enzyme in the
plant negatively regulates the growth of the fungus, preventing excessive colonization
of the host. Thus, the ROS act as a brake on the growth of the fungus, preventing
it from becoming pathogenic and allowing it to maintain a beneficial, mutualistic
symbiosis with the plant. When this gene is disrupted, the growth of the fungus
is uncontrolled and the association becomes pathogenic. This study has highlighted
a previously unknown role for ROS in maintaining a mutualistic symbiosis between
endophytic fungi and plants and shown that the mutation of the fungal noxA gene
can switch the symbiosis from beneficial to antagonistic.
###
The authors of this study are Aiko Tanaka, Daigo Takemoto, and Barry Scott of
the Centre for Functional Genomics, Institute of Molecular BioSciences, Massey
University, New Zealand; Michael J. Christensen, AgResearch, Grasslands Research
Centre, Palmerston North, New Zealand; and Pyoyun Park, Graduate School of Science
and Technology, Kobe University, Japan.
###
The research paper cited in this report is available at the following link:
http://www.aspb.org/pressreleases/TPC039263.pdf
The Plant Cell (http://www.plantcell.org/)
is published by the American Society of Plant Biologists. For more information
about ASPB, please visit http://www.aspb.org/.
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