Message - 7th IAL Symposium
Message - 7th IAL Symposium
Message - 7th IAL Symposium
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Lichen: from genome to ecosystem in a changing world<br />
1I-O<br />
(1I-O3) Submission ID: <strong>IAL</strong>0276-00001<br />
MICROB<strong>IAL</strong> COMMUNITY IN ANTARCTIC LICHENS<br />
Park C.H. 1 , Kim K. 2 , Chun J. 3 , Jeong G. 3 , Hong S. 1<br />
1 Division of Polar Life Science, Korea Polar Research Institute, Incheon, Korea<br />
2 Korean Bioinformation Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Korea<br />
3 School of Biological Science, Seoul National University, Seoul,Korea<br />
Lichens are symbiotic association of fungal (mycobiont) and photosynthetic algal or cyanobacterial<br />
(photobiont) partners. Contribution of the two major partners has been well known, but composition and role<br />
of other components of lichen ecosystems has not been evaluated carefully. Recently, microbial community in<br />
the lichen thalli has been revealed by cultivation of microorganisms, FISH imaging, and sequence analyses. It<br />
was also suggested that bacteria, archaea and microfungi associated with lichens (microbiont) have important<br />
roles in lichen ecosystem by biodiversity and meta-proteome analyses. In the current study, microbial community<br />
composition in Cladonia, Umbilicaria, Usnea, and 3 crustose lichens from King George Island, Antarctica<br />
was analyzed by pyrosequencing of bacterial 16S rDNA, eukaryotic LSU rDNA, and algal ITS region of nuc<br />
rDNA. Proteobacteria, Acidobacteria, Actinobacteria, and Bacteroidetes in bacterial community and Dothideomycetes,<br />
Eurotiomycetes and Lecanoromycetes in lichen-associated fungal community were the major phyla<br />
in the Antactic lichen ecosystems. Microbial phylotype composition from the same or related lichen species<br />
were more closely related than those of different lichen species. Sequencing results of LSU and ITS regions of<br />
nuclear rDNA and plastid 16S rDNA of algal species indicated that each lichen thalli contain diverse photobionts.<br />
In most cases a major photobiont constituted higher than 97% of total photobiont community, but in some cases,<br />
the second major photobiont comprised upto 20% of total photobiont community. These results imply that lichen<br />
thalli is a complex ecosystem composed of lichenized fungi, diverse photobionts and microbionts such as bacteria<br />
and microfungi. It also suggests that studies for all partners of lichens are required to understand ecology<br />
and physiology of lichens.<br />
(1I-O4) Submission ID: <strong>IAL</strong>0124-00001<br />
THE MICROBIOME OF LICHENS: STRUCTURAL AND BIOGEOGRAPHIC DIVERSITY<br />
Berg G. 1 , Cardinale M. 1 , Grube M. 2<br />
1 Institute of Environmental Biotechnology, University of Technology, Graz, Austria<br />
2 Institute of Plant Sciences, Karl-Franzens University, Graz, Austria<br />
Lichens are traditionally considered as mutualisms between fungi and photoautotrophic species. New<br />
molecular and microscopic techniques revealed progress in the understanding of the lichen-associated microbiome.<br />
Our research during the last years revealed lichens as mini-ecosystems, which harbour highly abundant<br />
and diverse bacterial communities [1]. The analyses of samples from three lichen species (Cladonia arbuscula,<br />
Lecanora polytropa and Umbilicaria cylindrica) from alpine environments by a polyphasic approach showed<br />
biofilm-like structures and a high degree of species specificity [2]. Lichen-associated microbial communities consist<br />
of diverse taxonomic groups. The majority of bacteria in growing parts belong to Alphaproteobacteria [3] but<br />
there are also diverse new phylogenetic lineages as well as new species [4]. As an important driver of bacterial<br />
community the age of the thallus parts was identified: the younger growing parts of the lichens hosted bacterial<br />
communities that significantly differ from those of the older/senescing portions at the basis of the thalli. The<br />
substrate type and, to a lower extent, the exposition to the sun also affected the bacterial community structures<br />
significantly [3]. Moreover, the structure of the bacterial community was influenced by biogeographic aspects.<br />
The variation of the always dominant Alpaproteobacteria correlated with geography, whereas this effect could<br />
not be observed for Burkholderia or functional genes for nitrogen fixation (nif).<br />
2