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Diversity and Distribution of Eukaryotic Microbes in and Around a Brine Pool Adjacent to the Thuwal Cold Seeps in the Red Sea

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2014 Feb 28
PMID 24575081
Citations 10
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Abstract

A hypoxic/suboxic brine pool at a depth of about 850 m was discovered near the Thuwal cold seeps in the Red Sea. Filled with high concentrations of hydrogen sulfide and ammonia, such a brine pool might limit the spread of eukaryotic organisms. Here, we compared the communities of the eukaryotic microbes in a microbial mat, sediments and water samples distributed in 7 sites within and adjacent to the brine pool. Taxonomic classification of the pyrosequenced 18S rRNA amplicon reads showed that fungi highly similar to the species identified along the Arabic coast were almost ubiquitous in the water and sediment samples, supporting their wide distribution in various environments. The microbial mat displayed the highest species diversity and contained grazers and a considerable percentage of unclassified species. Phylogeny-based methods revealed novel lineages representing a majority of the reads from the interface between the sea water and brine pool. Phylogenetic relationships with more reference sequences suggest that the lineages were affiliated with novel Alveolata and Euglenozoa inhabiting the interface where chemosynthetic prokaryotes are highly proliferative due to the strong chemocline and halocline. The brine sediments harbored abundant species highly similar to invertebrate gregarine parasites identified in different oxygen-depleted sediments. Therefore, the present findings support the uniqueness of some microbial eukaryotic groups in this cold seep brine system.

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References
1.
Marande W, Lopez-Garcia P, Moreira D . Eukaryotic diversity and phylogeny using small- and large-subunit ribosomal RNA genes from environmental samples. Environ Microbiol. 2009; 11(12):3179-88. DOI: 10.1111/j.1462-2920.2009.02023.x. View

2.
Pawlowski J, Christen R, Lecroq B, Bachar D, Shahbazkia H, Amaral-Zettler L . Eukaryotic richness in the abyss: insights from pyrotag sequencing. PLoS One. 2011; 6(4):e18169. PMC: 3070721. DOI: 10.1371/journal.pone.0018169. View

3.
Orsi W, Biddle J, Edgcomb V . Deep sequencing of subseafloor eukaryotic rRNA reveals active Fungi across marine subsurface provinces. PLoS One. 2013; 8(2):e56335. PMC: 3572030. DOI: 10.1371/journal.pone.0056335. View

4.
Reeder J, Knight R . Rapidly denoising pyrosequencing amplicon reads by exploiting rank-abundance distributions. Nat Methods. 2010; 7(9):668-9. PMC: 2945879. DOI: 10.1038/nmeth0910-668b. View

5.
Simpson A, Roger A . The real 'kingdoms' of eukaryotes. Curr Biol. 2004; 14(17):R693-6. DOI: 10.1016/j.cub.2004.08.038. View