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1.
Protist ; 174(1): 125929, 2023 02.
Article in English | MEDLINE | ID: mdl-36455480

ABSTRACT

Biological soil crusts (BSC) are associations of different macro and microorganisms and aggregated soil particles located on the surface of soils in many different habitats. BSC harbour a diverse and complex community of ciliates and testate amoebae. These phagotrophic protists play an important role in C and N recycling in soil ecosystems but have not been frequently studied in BSC. In this context, the effects of three increasing N inputs on ciliates and testate amoebae in crusts from a semi-arid Mediterranean ecosystem were evaluated. A field experiment with artificial N-deposition was designed to mimic the effects caused by anthropogenic N depositions. The results have shown that the protist populations of these semi-arid Mediterranean environments have lower species richness than other soil environments. The increase in N produces a net loss of diversity in the populations studied and shifts in the community structure. It has also been shown that some ciliates and testate amoebae, due to their population responses to increased N concentrations, could potentially be used as bio-indicators of N contamination in these BSCs.


Subject(s)
Amoeba , Ecosystem , Soil Microbiology , Amoeba/physiology , Soil
2.
Microb Ecol ; 80(1): 248, 2020 Jul.
Article in English | MEDLINE | ID: mdl-31873774

ABSTRACT

The original version of this article contained an erratum of omission in the Acknowledgments section.

3.
Microb Ecol ; 79(4): 882-897, 2020 May.
Article in English | MEDLINE | ID: mdl-31796996

ABSTRACT

Rain fed granite rock basins are ancient geological landforms of worldwide distribution and structural simplicity. They support habitats that can switch quickly from terrestrial to aquatic along the year. Diversity of animals and plants, and the connexion between communities in different basins have been widely explored in these habitats, but hardly any research has been carried out on microorganisms. The aim of this study is to provide the first insights on the diversity of eukaryotic microbial communities from these environments. Due to the ephemeral nature of these aquatic environments, we predict that the granitic basins should host a high proportion of dormant microeukaryotes. Based on an environmental DNA diversity survey, we reveal diverse communities with representatives of all major eukaryotic taxonomic supergroups, mainly composed of a diverse pool of low abundance OTUs. Basin communities were very distinctive, with alpha and beta diversity patterns non-related to basin size or spatial distance respectively. Dissimilarity between basins was mainly characterised by turnover of OTUs. The strong microbial eukaryotic heterogeneity observed among the basins may be explained by a complex combination of deterministic factors (diverging environment in the basins), spatial constraints, and randomness including founder effects. Most interestingly, communities contain organisms that cannot coexist at the same time because of incompatible metabolic requirements, thus suggesting the existence of a pool of dormant organisms whose activity varies along with the changing environment. These organisms accumulate in the pools, which turns granitic rock into high biodiversity microbial islands whose conservation and study deserve further attention.


Subject(s)
Eukaryota/physiology , Geologic Sediments/microbiology , Geologic Sediments/parasitology , Silicon Dioxide , Eukaryota/isolation & purification , Microbiota , Mycobiome , Rain , Spain
4.
J Eukaryot Microbiol ; 64(4): 539-554, 2017 07.
Article in English | MEDLINE | ID: mdl-28061024

ABSTRACT

Recent advances in molecular technology have revolutionized research on all aspects of the biology of organisms, including ciliates, and created unprecedented opportunities for pursuing a more integrative approach to investigations of biodiversity. However, this goal is complicated by large gaps and inconsistencies that still exist in the foundation of basic information about biodiversity of ciliates. The present paper reviews issues relating to the taxonomy of ciliates and presents specific recommendations for best practice in the observation and documentation of their biodiversity. This effort stems from a workshop that explored ways to implement six Grand Challenges proposed by the International Research Coordination Network for Biodiversity of Ciliates (IRCN-BC). As part of its commitment to strengthening the knowledge base that supports research on biodiversity of ciliates, the IRCN-BC proposes to populate The Ciliate Guide, an online database, with biodiversity-related data and metadata to create a resource that will facilitate accurate taxonomic identifications and promote sharing of data.


Subject(s)
Ciliophora/classification , Databases, Factual , Biodiversity , Ciliophora/genetics , Internet , Phylogeny
5.
Proc Biol Sci ; 283(1831)2016 05 25.
Article in English | MEDLINE | ID: mdl-27194700

ABSTRACT

We investigate the effects of trophic lifestyle and two types of major evolutionary transitions in individuality-the endosymbiotic acquisition of organelles and development of multicellularity-on organellar and cellular metabolism and allometry. We develop a quantitative framework linking the size and metabolic scaling of eukaryotic cells to the abundance, size and metabolic scaling of mitochondria and chloroplasts and analyse a newly compiled, unprecedented database representing unicellular and multicellular cells covering diverse phyla and tissues. Irrespective of cellularity, numbers and total volumes of mitochondria scale linearly with cell volume, whereas chloroplasts scale sublinearly and sizes of both organelles remain largely invariant with cell size. Our framework allows us to estimate the metabolic scaling exponents of organelles and cells. Photoautotrophic cells and organelles exhibit photosynthetic scaling exponents always less than one, whereas chemoheterotrophic cells and organelles have steeper respiratory scaling exponents close to one. Multicellularity has no discernible effect on the metabolic scaling of organelles and cells. In contrast, trophic lifestyle has a profound and uniform effect, and our results suggest that endosymbiosis fundamentally altered the metabolic scaling of free-living bacterial ancestors of mitochondria and chloroplasts, from steep ancestral scaling to a shallower scaling in their endosymbiotic descendants.


Subject(s)
Biological Evolution , Chloroplasts/metabolism , Eukaryota/physiology , Mitochondria/metabolism , Symbiosis , Models, Biological
6.
J Eukaryot Microbiol ; 57(2): 159-70, 2010.
Article in English | MEDLINE | ID: mdl-20015186

ABSTRACT

Marine goniomonads have a worldwide distribution but ultrastructural information has not been available so far. An isolate of the heterotrophic marine nanoflagellate Goniomonas (G. aff. amphinema) from North Wales (UK) has been studied, providing information on its morphology and cellular structure using video, electron, laser scanning confocal microscopy (LSCM), and atomic force microscopy. Here, we describe a new feature, a granular area, potentially involved in particle capture and feeding. The binding of the lectin wheat germ agglutinin to the granular area of cells with discharged ejectisomes indicates the adhesive nature of this novel feature. The presence of a microtubular intracellular cytopharynx, apparently also used for feeding, has been revealed by LSCM. The small subunit rRNA gene of the isolate has been sequenced (1,788 bp). Phylogenetic results corroborate significant genetic divergence within the marine members of Goniomonas. This work highlights the need for integrated morphological, ultrastructural, and molecular investigation when describing and studying heterotrophic nanoflagellates.


Subject(s)
Cryptophyta/classification , Cryptophyta/cytology , Seawater/parasitology , Cluster Analysis , Cryptophyta/genetics , Cryptophyta/isolation & purification , DNA, Algal/chemistry , DNA, Algal/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Feeding Behavior , Genes, rRNA , Lectins/metabolism , Microscopy, Atomic Force , Microscopy, Confocal , Microscopy, Electron , Microscopy, Video , Phylogeny , Protein Binding , RNA, Algal/genetics , RNA, Ribosomal, 18S/genetics , Sequence Analysis, DNA , Sequence Homology, Nucleic Acid , Wales , Wheat Germ Agglutinins/metabolism
7.
Curr Microbiol ; 57(1): 45-50, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18392892

ABSTRACT

Planktonic heterotrophic flagellates are ubiquitous eukaryotic microorganisms that play a crucial role in carbon and nutrient fluxes through pelagic food webs. Here we illustrate for the first time a grazing model of planktonic dinoflagellate, Oxyrrhis marina, on the heterotrophic nanoflagellate Goniomonas amphinema, using the DNA-binding fluorescent dye Hoechst 33342. A solution of 1 microg/mL of the fluorochrome allowed viability of the prey for at least 48 hours, provided low fluorescence quenching, and labelled the flagellate without masking the cytoplasm. After 2 hours of contact between the fluorescent prey and the predator, O. marina population had preyed on live G. amphinema at an ingestion rate of 2.2 prey Oxyrrhis (-1) h(-1). Results show that this model is a time-effective and inexpensive approach for the direct observation of heterotrophic flagellate grazing. The fact that prey remain alive while predation occurs, as well as the low rate of quenching, could be of help in studying the fate of real-time trophic interactions between protists in microbial webs.


Subject(s)
Benzimidazoles/metabolism , Dinoflagellida/cytology , Microscopy, Fluorescence/methods , Plankton/parasitology , Seawater/parasitology , Animals , Dinoflagellida/growth & development , Dinoflagellida/metabolism , Indicators and Reagents/metabolism
8.
Eur J Protistol ; 43(4): 265-79, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17583484

ABSTRACT

New observations on Opisthonecta matiensis Martín-Cereceda et al. [1999. Description of Opisthonecta matiensis n. sp. (Protozoa, Ciliophora), a new peritrich ciliate from wastewater. J. Eukaryot. Microbiol. 46, 283-289] especially the lack of an epistomial membrane, reveal that the species does not belong to the genus Opisthonecta, but to Telotrochidium, the other genus within the family Opisthonectidae Foissner, 1975. The contractile vacuole and the cytopyge are on the dorsal wall of the vestibulum and the trochal band is limited distally and proximally by rows of narrowly spaced pellicular pores. Thus the species is redefined as Telotrochidium matiense nov. comb. The morphological, cortical and nuclear events occurring during conjugation are illustrated, compared with those in other species, and phylogenetically discussed. Invariably, the microconjugants attach to and penetrate the lateral side of the macroconjugants. Nuclear processes are very similar to those reported from other peritrichs. The small subunit rRNA gene (SSU rDNA) is sequenced and the phylogeny within Opisthonectidae and peritrichs examined. T. matiense is more closely related to Epistylis (63% Maximum Parsimony (MP), 85% Maximum Likelihood (ML)) than to any other genus, while another representative of the family, viz., Opisthonecta henneguyi, is closely related to Vorticella microstoma, Astylozoon enriquesi and clone RT3n18 (100% MP, 100% ML). Morphology and gene sequences suggest that Telotrochidium and Opisthonecta have derived from different lineages of stalked peritrichs: Opisthonecta could have arisen from peritrichs with stalk myonemes, while Telotrochidium probably evolved from peritrichs without stalk myonemes.


Subject(s)
Ciliophora/classification , DNA, Ribosomal/genetics , Phylogeny , Animals , Base Sequence , Ciliophora/genetics , Ciliophora/ultrastructure , DNA Primers/chemistry , Microscopy, Electron, Scanning , Molecular Sequence Data , Polymerase Chain Reaction , Species Specificity
9.
FEMS Microbiol Lett ; 265(2): 202-7, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17147765

ABSTRACT

Carbohydrate-protein interactions appear to play an important role in the phagocytosis of microbial prey by free-living protozoa. The present study utilizes FITC-labelled plant lectins to investigate the presence and localization of cell surface glycoconjugates on live and fixed planktonic protists (Dunaliella primolecta, Oxyrrhis marina, Goniomonas amphinema, Paraphysomonas vestita and Euplotes vannus). With live flagellate preparations, lectins primarily bound to external cell surfaces, with minimal internal staining observed. In contrast, cell fixation permeabilized cell membranes, allowing lectins to bind to internal structures, such as nuclear membranes and food vacuoles, interfering with the characterization of cell surface glycoconjugates. The method developed to label cell surface sugar moieties of live planktonic protists successfully overcomes the problems associated with fixation, and thus provides a useful protocol for future studies on protistan cell surface carbohydrate characterization.


Subject(s)
Cell Membrane Structures/chemistry , Ciliophora/chemistry , Eukaryota/chemistry , Glycoconjugates/chemistry , Lectins/metabolism , Plankton/chemistry , Staining and Labeling/methods , Animals , Ciliophora/microbiology , Concanavalin A , Eukaryota/microbiology , Fluorescein-5-isothiocyanate , Plankton/microbiology , Receptors, Concanavalin A/chemistry , Receptors, Mitogen/chemistry , Seawater/microbiology , Wheat Germ Agglutinins
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