Ulla Kaasalainen

Dr. Ulla Kaasalainen

Finnish Museum of Natural History, University of Helsinki, Helsinki, Uusimaa, Finland
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Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 March 2012 in Proceedings of the National Academy of Sciences
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Journal Article
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UKUlla Kaasalainen
Ulla Kaasalainen
DFDavid P. Fewer
David P. Fewer
JJJouni Jokela
Jouni Jokela
MWMatti Wahlsten
Matti Wahlsten
KSKaarina Sivonen
Kaarina Sivonen
JRJouko Rikkinen
Jouko Rikkinen
Lichens are symbiotic associations between fungi and photosynthetic algae or cyanobacteria. Microcystins are potent toxins that are responsible for the poisoning of both humans and animals. These toxins are mainly associated with aquatic cyanobacterial blooms, but here we show that the cyanobacterial symbionts of terrestrial lichens from all over the world commonly produce microcystins. We screened 803 lichen specimens from five different continents for cyanobacterial toxins by amplifying a part of the gene cluster encoding the enzyme complex responsible for microcystin production and detecting toxins directly from lichen thalli. We found either the biosynthetic genes for making microcystins or the toxin itself in 12% of all analyzed lichen specimens. A plethora of different microcystins was found with over 50 chemical variants, and many of the variants detected have only rarely been reported from free-living cyanobacteria. In addition, high amounts of nodularin, up to 60 μg g −1 , were detected from some lichen thalli. This microcystin analog and potent hepatotoxin has previously been known only from the aquatic bloom-forming genus Nodularia . Our results demonstrate that the production of cyanobacterial hepatotoxins in lichen symbiosis is a global phenomenon and occurs in many different lichen lineages. The very high genetic diversity of the mcyE gene and the chemical diversity of microcystins suggest that lichen symbioses may have been an important environment for diversification of these cyanobacteria.

1 June 2009 in Molecular Plant-Microbe Interactions®
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UKUlla Kaasalainen
Ulla Kaasalainen
JJJouni Jokela
Jouni Jokela
DFDavid Fewer
David Fewer
KSKaarina Sivonen
Kaarina Sivonen
JRJouko Rikkinen
Jouko Rikkinen
We show that the cyanobacterial symbionts of a tripartite cyanolichen can produce hepatotoxic microcystins in situ. Microcystins were detected with high-performance liquid chromatography mass spectrometry both from cephalodia of the tripartite cyanolichen Peltigera leucophlebia and from a symbiotic Nostoc strain isolated from the same lichen specimen. Genetic identities of symbiotic Nostoc strains were studied by amplifying and sequencing the 16S rRNA gene. Also, the presence of the microcystin synthetase gene mcyE was confirmed by sequencing. Three highly toxic microcystins were detected from the lichen specimen. Several different Nostoc 16S rRNA haplotypes were present in the lichen sample but only one was found in the toxin-producing cultures. In culture, the toxin-producing Nostoc strain produced a total of 19 different microcystin variants. In phylogenetic analysis, this cyanobacterium and related strains from the lichen thallus grouped together with a previously known microcystin-producing Nostoc strain and other strains previously isolated from the symbiotic thalloid bryophyte Blasia pusilla. Our finding is the first direct evidence of in situ production of microcystins in lichens or plant–cyanobacterial symbioses. Microcystins may explain why cyanolichens and symbiotic bryophytes are not among the preferred food sources of most animal grazers.

24 April 2017 in Nature Plants
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UKUlla Kaasalainen
Ulla Kaasalainen
ASAlexander R. Schmidt
Alexander R. Schmidt
JRJouko Rikkinen
Jouko Rikkinen

1 March 2011 in The Bryologist
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KFKatja Fedrowitz
Katja Fedrowitz
UKUlla Kaasalainen
Ulla Kaasalainen
JRJouko Rikkinen
Jouko Rikkinen

19 March 2018 in The Lichenologist
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ASAve Suija
Ave Suija
UKUlla Kaasalainen
Ulla Kaasalainen
PKPaul Muigai Kirika
Paul Muigai Kirika
JRJouko Rikkinen
Jouko Rikkinen
During lichenological explorations of tropical montane forests in Kenya, a remarkable new lichenicolous fungus was repeatedly found growing on thalli of the epiphytic tripartite cyanolichen Crocodia cf. clathrata. Molecular phylogenetic analyses placed the fungus within Gomphillaceae (Ostropales, Lecanoromycetes), a family mainly of lichen-symbiotic species in the tropics. The anatomical features (unitunicate, non-amyloid asci and simple, septate paraphyses) as well as the hemiangiocarpic ascoma development confirm its taxonomic affinity. DNA sequence data showed the closest relationship was with Gyalidea fritzei, followed by Corticifraga peltigerae. A monotypic genus, Taitaia, is introduced to incorporate a single species, T. aurea. The new fungus is characterized by aggregated ascomata with yellow margins and salmon red discs developing from a single base.

8 June 2015 in PLOS ONE
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UKUlla Kaasalainen
Ulla Kaasalainen
JHJochen Heinrichs
Jochen Heinrichs
MKMichael Krings
Michael Krings
LMLeena Myllys
Leena Myllys
HGHeinrich Grabenhorst
Heinrich Grabenhorst
ASAlexander R. Schmidt
Alexander R. Schmidt
One of the most important issues in molecular dating studies concerns the incorporation of reliable fossil taxa into the phylogenies reconstructed from DNA sequence variation in extant taxa. Lichens are symbiotic associations between fungi and algae and/or cyanobacteria. Several lichen fossils have been used as minimum age constraints in recent studies concerning the diversification of the Ascomycota. Recent evolutionary studies of Lecanoromycetes, an almost exclusively lichen-forming class in the Ascomycota, have utilized the Eocene amber inclusion Alectoria succinic as a minimum age constraint. However, a re-investigation of the type material revealed that this inclusion in fact represents poorly preserved plant remains, most probably of a root. Consequently, this fossil cannot be used as evidence of the presence of the genus Alectoria (Parmeliaceae, Lecanorales) or any other lichens in the Paleogene. However, newly discovered inclusions from Paleogene Baltic and Bitterfeld amber verify that alectorioid morphologies in lichens were in existence by the Paleogene. The new fossils represent either a lineage within the alectorioid group or belong to the genus Oropogon.