Literature DB >> 17576098

Ultrastructure and phylogenetic placement within Heterolobosea of the previously unclassified, extremely halophilic heterotrophic flagellate Pleurostomum flabellatum (Ruinen 1938).

Jong S Park1, Alastair G B Simpson, Won J Lee, Byung C Cho.   

Abstract

Although Pleurostomum was described almost a century ago, flagellates assigned to this taxon have been recorded only in very occasional faunistic studies of highly saline habitats, and their phylogenetic position has remained uncertain. We report the cultivation, ultrastructure, and phylogenetic relationships of Pleurostomum flabellatum isolated from a Korean saltern pond of 313 per thousand salinity. This isolate is biflagellated with a cytostomal groove, and is not distinguishable from previous accounts of P. flabellatum from saturated brines in India and Australia. Pleurostomum flabellatum shows ultrastructural features characteristic of many Heterolobosea: (1) a striated rhizoplast, (2) an absence of stacked Golgi bodies, (3) parallel basal bodies and flagella, and (4) a large number of peripheral microtubules supporting a rostrum. 18S rRNA gene phylogenies strongly confirm the affinities of P. flabellatum within Heterolobosea. Furthermore, the 18S rRNA gene of P. flabellatum has the heterolobosean-specific helix 17_1, and a group I intron in the same position as in Acrasis rosea. Within Heterolobosea, the 'amoeboflagellate' genera Naegleria and Willaertia were its closest relatives with high bootstrap support and posterior probability. P. flabellatum was observed only as a flagellate, and never as an amoeba. Since light microscopy and electron microscopy observations indicate that P. flabellatum flagellates are capable both of feeding and division, there might be no amoeba stage. Being morphologically distinct from its closest relatives and phylogenetically distant from other flagellate-only Heterolobosea, P. flabellatum cannot be moved into any previously described heterolobosean genus. Instead, we move Pleurostomum into Heterolobosea, and assign as the type species Pleurostomum salinum Namyslowski 1913, a species that closely resembles P. flabellatum. The optimal temperature for growth of P. flabellatum is 40 degrees C. Interestingly, P. flabellatum grows optimally at 300 per thousand salinity and fails to grow below 200 per thousand salinity, indicating that it is an 'extreme halophile'. The optimal salinity for growth is the highest for any eukaryote examined to date.

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Year:  2007        PMID: 17576098     DOI: 10.1016/j.protis.2007.03.004

Source DB:  PubMed          Journal:  Protist        ISSN: 1434-4610


  16 in total

1.  Microbial eukaryote life in the new hypersaline deep-sea basin Thetis.

Authors:  Alexandra Stock; Hans-Werner Breiner; Maria Pachiadaki; Virginia Edgcomb; Sabine Filker; Violetta La Cono; Michail M Yakimov; Thorsten Stoeck
Journal:  Extremophiles       Date:  2011-10-19       Impact factor: 2.395

2.  Impairment of O-antigen production confers resistance to grazing in a model amoeba-cyanobacterium predator-prey system.

Authors:  Ryan Simkovsky; Emy F Daniels; Karen Tang; Stacey C Huynh; Susan S Golden; Bianca Brahamsha
Journal:  Proc Natl Acad Sci U S A       Date:  2012-09-24       Impact factor: 11.205

3.  Unveiling microbial activities along the halocline of Thetis, a deep-sea hypersaline anoxic basin.

Authors:  Maria G Pachiadaki; Michail M Yakimov; Violetta LaCono; Edward Leadbetter; Virginia Edgcomb
Journal:  ISME J       Date:  2014-06-20       Impact factor: 10.302

4.  Deep sequencing uncovers protistan plankton diversity in the Portuguese Ria Formosa solar saltern ponds.

Authors:  Sabine Filker; Anna Gimmler; Micah Dunthorn; Frédéric Mahé; Thorsten Stoeck
Journal:  Extremophiles       Date:  2014-12-04       Impact factor: 2.395

5.  Effects of different ion compositions on growth of obligately halophilic protozoan Halocafeteria seosinensis.

Authors:  Jong Soo Park
Journal:  Extremophiles       Date:  2011-12-02       Impact factor: 2.395

6.  Gene expression profiling of microbial activities and interactions in sediments under haloclines of E. Mediterranean deep hypersaline anoxic basins.

Authors:  Virginia P Edgcomb; Maria G Pachiadaki; Paraskevi Mara; Konstantinos A Kormas; Edward R Leadbetter; Joan M Bernhard
Journal:  ISME J       Date:  2016-04-19       Impact factor: 10.302

Review 7.  Ciliary transition zone evolution and the root of the eukaryote tree: implications for opisthokont origin and classification of kingdoms Protozoa, Plantae, and Fungi.

Authors:  Thomas Cavalier-Smith
Journal:  Protoplasma       Date:  2021-12-23       Impact factor: 3.186

8.  Microbial life at high salt concentrations: phylogenetic and metabolic diversity.

Authors:  Aharon Oren
Journal:  Saline Systems       Date:  2008-04-15

9.  Heterotrophic protists in hypersaline microbial mats and deep hypersaline basin water columns.

Authors:  Virginia P Edgcomb; Joan M Bernhard
Journal:  Life (Basel)       Date:  2013-05-22

10.  Is there a common water-activity limit for the three domains of life?

Authors:  Andrew Stevenson; Jonathan A Cray; Jim P Williams; Ricardo Santos; Richa Sahay; Nils Neuenkirchen; Colin D McClure; Irene R Grant; Jonathan Dr Houghton; John P Quinn; David J Timson; Satish V Patil; Rekha S Singhal; Josefa Antón; Jan Dijksterhuis; Ailsa D Hocking; Bart Lievens; Drauzio E N Rangel; Mary A Voytek; Nina Gunde-Cimerman; Aharon Oren; Kenneth N Timmis; Terry J McGenity; John E Hallsworth
Journal:  ISME J       Date:  2014-12-12       Impact factor: 10.302

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