![Chondrostereum purpureum fruiting bodies have a white upper surface while the lower, spore-producing surface is light-brown to purple to reddish. Photo from a birch stump, Helsinki, Finland (collection Miettinen 19107). [Photo credit: Otto Miettinen]](/public/Chopur1/DSC_6563+Chonpur.jpg)
In the "1KFG: Deep Sequencing of Ecologically-relevant Dikarya"
project (CSP1974), we are sequencing keystone lineages of
plant-interacting fungi and saprophytic fungi that are of special
ecological importance for understanding terrestrial ecosystems. In
addition, comparative genome analysis with saprotrophic,
mycorrhizal and pathogenic fungi will provide new insights into the
specific and conserved adaptations associated with each fungal
lifestyle.
Chondrostereum purpureum
Chondrostereum purpureum is a wood-inhabiting
basidiomycete with stereoid fruiting bodies, i.e. caps with a
smooth hymenial surface. It belongs to the Agaricales, in
Cyphellaceae (Vizzini et al. 2022). The species is a fast-growing
pioneer wood decomposer on various angiosperm wood, and can attack
living trees through wounds (Rayner and Boddy 1988). After initial
dominance and only limited wood decay, it gets replaced in a few
years by other wood decomposing basidiomycetes. In fruit trees,
particulary of Rosaceae, it causes so-called silver leaf disease
(van Zoeren and McManus 2021).
C. purpureum is widely distributed in temperate and
boreal regions of Eurasia and North America, and is also found in
New Zealand. It shows considerable genetic variation, but no
evidence of reproductive barriers has been found nor is the genetic
variation structured by geography or host tree (Ramsfield et al.
1996; Becker et al. 2004; Hamberg et al. 2018).
Due to its pathogenic ability, researchers in Canada and Europe
have developed a method to use it as a biocontrol agent preventing
growth of unwanted deciduous tree sprouts after logging or forest
clearance. Stumps of deciduous trees and saplings are treated with
Chondrostereum, which kills them in a year or two, while
uncut trees (and conifers) are not affected (Wall 1990; Becker et
al. 2005; Hamberg et al. 2021). Its pathogenic mechanism has been
studied, though it is not fully understood - polygalacturonases,
laccases and peroxidase activities are associated with the
infection (Hamberg et al. 2021).
Reina et al. (2019) published a genome of C. purpureum
based on a German strain originating from birch wood. Based on the
enzymatic profile, they concluded the species is a white-rot
fungus. Laccases in particular are numerous. The genomes of this
commercially and ecologically important fungus can be used to study
pathogenecity, intraspecific genetic variation, as well as
evolution of wood decomposition.
The current genome is based on a polysporic culture OMC 1767 from
boreal central Finland (Jyväskylä), where the species
fruited on a recently girdled, dead aspen (Populus
tremula) tree (herbarium collection Miettinen 22148.1, http://id.luomus.fi/HA.H6014639).
Researchers who wish to publish analyses using data from
unpublished CSP genomes are respectfully required to contact the PI
and JGI to avoid potential conflicts on data use and coordinate
other publications with the CSP master paper(s).
References
- Becker E, Shamoun SF, Hintz WE (2005) Efficacy and environmental fate of Chondrostereum purpureum used as a biological control for red alder (Alnus rubra). Biological Control 33 (3):269-277. doi:10.1016/j.biocontrol.2005.02.013
- Becker EM, Bastide PY, Hintz WE (2004) A retrotransposon-like element and its occurrence in British Columbia populations of Chondrostereum purpureum. Fungal Genet Biol 41 (10):921-929. doi:10.1016/j.fgb.2004.07.001
- Hamberg L, de la Bastide P, Hintz W, Shamoun SF, Brandtberg M, Hantula J (2018) Interfertility and genetic variability among European and North American isolates of the basidiomycete fungus Chondrostereum purpureum. Fungal Biol 122 (7):659-667. doi:10.1016/j.funbio.2018.03.009
- Hamberg L, Saksa T, Hantula J (2021) Role and function of Chondrostereum purpureum in biocontrol of trees. Applied microbiology and biotechnology 105 (2):431-440. doi:10.1007/s00253-020-11053-5
- Ramsfield TD, Becker EM, Rathlef SM, Tang Y, Hintz WE, Vrain TC, Shamoun SF (1996) Geographic variation of Chondrostereum purpureum detected by polymorphisms in the ribosomal DNA. 74 (12):1919-1929. doi:10.1139/b96-229
- Rayner ADM, Boddy L (1988) Fungal decomposition of wood: it's biology and ecology. John Wiley & Sons, Chichester, New York
- Reina R, Kellner H, Hess J, Jehmlich N, García-Romera I, Aranda E, Hofrichter M, Liers C (2019) Genome and secretome of Chondrostereum purpureum correspond to saprotrophic and phytopathogenic life styles. PloS one 14 (3):e0212769. doi:10.1371/journal.pone.0212769
- van Zoeren J, McManus P (2021) Silver Leaf. University of Wisconsin-Madison. https://pddc.wisc.edu/2019/03/05/silver-leaf/. Accessed Dec 4 2022
- Vizzini A, Consiglio G, Marchetti M, Borovička J, Campo E, Cooper J, Lebeuf R, Ševčíková H (2022) New data in Porotheleaceae and Cyphellaceae: epitypification of Prunulus scabripes Murrill, the status of Mycopan Redhead, Moncalvo & Vilgalys and a new combination in Pleurella Horak emend. Mycol Prog 21 (4). doi:10.1007/s11557-022-01795-z
- Wall RE (1990) The fungus Chondrostereum purpureum as a silvicide to control stump sprouting in hardwoods. Northern Journal of Applied Forestry 7 (1):17-19. doi:10.1093/njaf/7.1.17