Monera and Protista
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Unfolding the Secrets of Coral–Algal Symbiosis
The ISME Journal (2015) 9, 844–856 & 2015 International Society for Microbial Ecology All rights reserved 1751-7362/15 www.nature.com/ismej ORIGINAL ARTICLE Unfolding the secrets of coral–algal symbiosis Nedeljka Rosic1, Edmund Yew Siang Ling2, Chon-Kit Kenneth Chan3, Hong Ching Lee4, Paulina Kaniewska1,5,DavidEdwards3,6,7,SophieDove1,8 and Ove Hoegh-Guldberg1,8,9 1School of Biological Sciences, The University of Queensland, St Lucia, Queensland, Australia; 2University of Queensland Centre for Clinical Research, The University of Queensland, Herston, Queensland, Australia; 3School of Agriculture and Food Sciences, The University of Queensland, St Lucia, Queensland, Australia; 4The Kinghorn Cancer Centre, Garvan Institute of Medical Research, Sydney, New South Wales, Australia; 5Australian Institute of Marine Science, Townsville, Queensland, Australia; 6School of Plant Biology, University of Western Australia, Perth, Western Australia, Australia; 7Australian Centre for Plant Functional Genomics, The University of Queensland, St Lucia, Queensland, Australia; 8ARC Centre of Excellence for Coral Reef Studies, The University of Queensland, St Lucia, Queensland, Australia and 9Global Change Institute and ARC Centre of Excellence for Coral Reef Studies, The University of Queensland, St Lucia, Queensland, Australia Dinoflagellates from the genus Symbiodinium form a mutualistic symbiotic relationship with reef- building corals. Here we applied massively parallel Illumina sequencing to assess genetic similarity and diversity among four phylogenetically diverse dinoflagellate clades (A, B, C and D) that are commonly associated with corals. We obtained more than 30 000 predicted genes for each Symbiodinium clade, with a majority of the aligned transcripts corresponding to sequence data sets of symbiotic dinoflagellates and o2% of sequences having bacterial or other foreign origin. -
Growth and Grazing Rates of the Herbivorous Dinoflagellate Gymnodinium Sp
MARINE ECOLOGY PROGRESS SERIES Published December 16 Mar. Ecol. Prog. Ser. Growth and grazing rates of the herbivorous dinoflagellate Gymnodinium sp. from the open subarctic Pacific Ocean Suzanne L. Strom' School of Oceanography WB-10, University of Washington. Seattle. Washington 98195, USA ABSTRACT: Growth, grazing and cell volume of the small heterotroph~cdinoflagellate Gyrnnodin~um sp. Isolated from the open subarctic Pacific Ocean were measured as a funct~onof food concentration using 2 phytoplankton food species. Growth and lngestlon rates increased asymptotically with Increas- ing phytoplankon food levels, as did grazer cell volume; rates at representative oceanic food levels were high but below maxima. Clearance rates decreased with lncreaslng food levels when Isochrysis galbana was the food source; they increased ~vithlncreaslng food levels when Synechococcus sp. was the food source. There was apparently a grazlng threshold for Ingestion of Synechococcus: below an initial Synechococcus concentration of 20 pgC 1.' ingestion rates on this alga were very low, while above this initial concentratlon Synechococcus was grazed preferent~ally Gross growth efficiency varied between 0.03 and 0.53 (mean 0.21) and was highest at low food concentrations. Results support the hypothesis that heterotrophic d~noflagellatesmay contribute to controlling population increases of small, rap~dly-grow~ngphytoplankton specles even at low oceanic phytoplankton concentrations. INTRODUCTION as Gymnodinium and Gyrodinium is difficult or impos- sible using older preservation and microscopy tech- Heterotrophic dinoflagellates can be a significant niques; experimental emphasis has been on more component of the microzooplankton in marine waters. easily recognizable and collectable microzooplankton In the oceanic realm, Lessard (1984) and Shapiro et al. -
The Planktonic Protist Interactome: Where Do We Stand After a Century of Research?
bioRxiv preprint doi: https://doi.org/10.1101/587352; this version posted May 2, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Bjorbækmo et al., 23.03.2019 – preprint copy - BioRxiv The planktonic protist interactome: where do we stand after a century of research? Marit F. Markussen Bjorbækmo1*, Andreas Evenstad1* and Line Lieblein Røsæg1*, Anders K. Krabberød1**, and Ramiro Logares2,1** 1 University of Oslo, Department of Biosciences, Section for Genetics and Evolutionary Biology (Evogene), Blindernv. 31, N- 0316 Oslo, Norway 2 Institut de Ciències del Mar (CSIC), Passeig Marítim de la Barceloneta, 37-49, ES-08003, Barcelona, Catalonia, Spain * The three authors contributed equally ** Corresponding authors: Ramiro Logares: Institute of Marine Sciences (ICM-CSIC), Passeig Marítim de la Barceloneta 37-49, 08003, Barcelona, Catalonia, Spain. Phone: 34-93-2309500; Fax: 34-93-2309555. [email protected] Anders K. Krabberød: University of Oslo, Department of Biosciences, Section for Genetics and Evolutionary Biology (Evogene), Blindernv. 31, N-0316 Oslo, Norway. Phone +47 22845986, Fax: +47 22854726. [email protected] Abstract Microbial interactions are crucial for Earth ecosystem function, yet our knowledge about them is limited and has so far mainly existed as scattered records. Here, we have surveyed the literature involving planktonic protist interactions and gathered the information in a manually curated Protist Interaction DAtabase (PIDA). In total, we have registered ~2,500 ecological interactions from ~500 publications, spanning the last 150 years. -
(Alveolata) As Inferred from Hsp90 and Actin Phylogenies1
J. Phycol. 40, 341–350 (2004) r 2004 Phycological Society of America DOI: 10.1111/j.1529-8817.2004.03129.x EARLY EVOLUTIONARY HISTORY OF DINOFLAGELLATES AND APICOMPLEXANS (ALVEOLATA) AS INFERRED FROM HSP90 AND ACTIN PHYLOGENIES1 Brian S. Leander2 and Patrick J. Keeling Canadian Institute for Advanced Research, Program in Evolutionary Biology, Departments of Botany and Zoology, University of British Columbia, Vancouver, British Columbia, Canada Three extremely diverse groups of unicellular The Alveolata is one of the most biologically diverse eukaryotes comprise the Alveolata: ciliates, dino- supergroups of eukaryotic microorganisms, consisting flagellates, and apicomplexans. The vast phenotypic of ciliates, dinoflagellates, apicomplexans, and several distances between the three groups along with the minor lineages. Although molecular phylogenies un- enigmatic distribution of plastids and the economic equivocally support the monophyly of alveolates, and medical importance of several representative members of the group share only a few derived species (e.g. Plasmodium, Toxoplasma, Perkinsus, and morphological features, such as distinctive patterns of Pfiesteria) have stimulated a great deal of specula- cortical vesicles (syn. alveoli or amphiesmal vesicles) tion on the early evolutionary history of alveolates. subtending the plasma membrane and presumptive A robust phylogenetic framework for alveolate pinocytotic structures, called ‘‘micropores’’ (Cavalier- diversity will provide the context necessary for Smith 1993, Siddall et al. 1997, Patterson -
Short Term in Vitro Culture of Cryptocaryon Irritans, a Protozoan Parasite of Marine Fishes
魚 病 研 究 Fish Pathology,39(4),175-181,2004.12 2004 The Japanese Society of Fish Pathology Short Term in vitro Culture of Cryptocaryon irritans, a Protozoan Parasite of Marine Fishes Apolinario V. Yambot1,3 and Yen-Ling Song1,2* 1Institute of Zoology, National Taiwan University, Taipei 106, Taiwan, ROC 2Department of Life Science , National Taiwan University, Taipei 106, Taiwan, ROC3 Present address: College of Fisheries-Freshwater Aquaculture Center , Central Luzon State University, Philippines (Received March 19, 2004) ABSTRACT--Attempts were made to cultivate Cryptocaryon irritans in vitro at 23-25℃. Attachment of theronts and subsequent enlargement into trophonts were achieved in two experi ments using strips of trypticase soy agar (TSA, supplemented with 3% NaCl) as an attachment substrate in filtered seawater. In the third experiment, transformation of theronts into trophonts was achieved in an enriched liquid medium composed of 50% filtered seawater, 30% Leibovitz L-15 and 20% fetal calf serum without attachment onto the TSA. Sizes (mean ±SD) of the trophonts, 114.6 ± 57.9 μm to 295.9 ± 130 μm, were from a recorded size range (50 to 700 μm) of the parasite in vivo. Although only limited numbers of theronts (0.28-1.71%) transformed into trophonts, these results showed that the in vitro culture of C. irritans is potentially feasible as evidenced by the enlargement of the trophonts within the in vivo size range using either a solid medium as an attach ment substrate or a liquid medium without attachment. There is a need, however, to determine essential factors that influence the transformation of the trophonts into viable tomonts capable of producing theronts. -
Pusillus Poseidon's Guide to Protozoa
Pusillus Poseidon’s guide to PROTOZOA GENERAL NOTES ABOUT PROTOZOANS Protozoa are also called protists. The word “protist” is the more general term and includes all types of single-celled eukaryotes, whereas “protozoa” is more often used to describe the protists that are animal-like (as opposed to plant-like or fungi-like). Protists are measured using units called microns. There are 1000 microns in one millimeter. A millimeter is the smallest unit on a metric ruler and can be estimated with your fingers: The traditional way of classifying protists is by the way they look (morphology), by the way they move (mo- tility), and how and what they eat. This gives us terms such as ciliates, flagellates, ameboids, and all those colors of algae. Recently, the classification system has been overhauled and has become immensely complicated. (Infor- mation about DNA is now the primary consideration for classification, rather than how a creature looks or acts.) If you research these creatures on Wikipedia, you will see this new system being used. Bear in mind, however, that the categories are constantly shifting as we learn more and more about protist DNA. Here is a visual overview that might help you understand the wide range of similarities and differences. Some organisms fit into more than one category and some don’t fit well into any category. Always remember that classification is an artificial construct made by humans. The organisms don’t know anything about it and they don’t care what we think! CILIATES Eats anything smaller than Blepharisma looks slightly pink because it Blepharisma itself, even smaller Bleph- makes a red pigment that senses light (simi- arismas. -
Protistology an International Journal Vol
Protistology An International Journal Vol. 10, Number 2, 2016 ___________________________________________________________________________________ CONTENTS INTERNATIONAL SCIENTIFIC FORUM «PROTIST–2016» Yuri Mazei (Vice-Chairman) Welcome Address 2 Organizing Committee 3 Organizers and Sponsors 4 Abstracts 5 Author Index 94 Forum “PROTIST-2016” June 6–10, 2016 Moscow, Russia Website: http://onlinereg.ru/protist-2016 WELCOME ADDRESS Dear colleagues! Republic) entitled “Diplonemids – new kids on the block”. The third lecture will be given by Alexey The Forum “PROTIST–2016” aims at gathering Smirnov (Saint Petersburg State University, Russia): the researchers in all protistological fields, from “Phylogeny, diversity, and evolution of Amoebozoa: molecular biology to ecology, to stimulate cross- new findings and new problems”. Then Sandra disciplinary interactions and establish long-term Baldauf (Uppsala University, Sweden) will make a international scientific cooperation. The conference plenary presentation “The search for the eukaryote will cover a wide range of fundamental and applied root, now you see it now you don’t”, and the fifth topics in Protistology, with the major focus on plenary lecture “Protist-based methods for assessing evolution and phylogeny, taxonomy, systematics and marine water quality” will be made by Alan Warren DNA barcoding, genomics and molecular biology, (Natural History Museum, United Kingdom). cell biology, organismal biology, parasitology, diversity and biogeography, ecology of soil and There will be two symposia sponsored by ISoP: aquatic protists, bioindicators and palaeoecology. “Integrative co-evolution between mitochondria and their hosts” organized by Sergio A. Muñoz- The Forum is organized jointly by the International Gómez, Claudio H. Slamovits, and Andrew J. Society of Protistologists (ISoP), International Roger, and “Protists of Marine Sediments” orga- Society for Evolutionary Protistology (ISEP), nized by Jun Gong and Virginia Edgcomb. -
Some Observations Upon Spirostomum Ambiguum (Ehrenberg). Ann Bishop, 31.Sc
Some Observations upon Spirostomum ambiguum (Ehrenberg). By Ann Bishop, 31.Sc, Victoria University, Manchester. With Plates 22 and 23 and 9 Text-figures. CONTENTS. PAGE 1. HISTORICAL 392 2. MATERIAL AND METHODS ....... 393 Fixation 393 Staining 394 Observations on Living Specimens ..... 394 Feeding Methods ........ 395 3. OBSERVATIONS ON THE MORPHOLOGY OF SPIROSTOMUM AMBIGUUM 395 Contractile Vacuole ........ 395 Endoplasm and Nuclei ....... 397 The Micronuclei . • - . • • .399 Abnormalities in the form of the Meganucleus . .401 >i. METHODS OF CULTIVATION 402 5. FOOD CYCLE 406 6. VARIETIES OF SPIROSTOMUM AMBIGUUM 409 7. REPRODUCTION . .41.1 A. Observations on the Growth and Reproduction of Spiro- stomum ambiguum during cultivation . .411 B. Fission 416 C. Conjugation 422 8. LITERATURE .... 431 9. EXPLANATION OF PLATES 22 AND 23 ..... 433 D d 2 392 ANN BISHOP 1. HISTORICAL. THE genus Spirostomurn was first mentioned by Ehrenberg, but no definition nor description was given. Its systematic position and the question of the number and identity of the species contained in it was a subject for discussion for many years. Later, Dujardin (7) gave a very satisfactory description of the genus in the following words : ' Corps cylindrique tres-allonge et tres-flexible, souvent tordu sur lui-meme, couvert cle cils disposes suivant les stries obliques ou en helice de la surface; avec une bouches situee lateralement au dela du milieu, a l'extremite d'une rangee de cils plus forts.' He recognized, however, only S p ir o s t o m um a m b i g u u m as a true species. It is to Dr. Stein (28) that w^e are indebted for a comprehen- sive and beautifully illustrated description of the genus, together with a detailed account of the vicissitudes of nomen- clature through which it had passed since its discovery by Ehrenberg. -
Biologia Celular – Cell Biology
Biologia Celular – Cell Biology BC001 - Structural Basis of the Interaction of a Trypanosoma cruzi Surface Molecule Implicated in Oral Infection with Host Cells and Gastric Mucin CORTEZ, C.*1; YOSHIDA, N.1; BAHIA, D.1; SOBREIRA, T.2 1.UNIFESP, SÃO PAULO, SP, BRASIL; 2.SINCROTRON, CAMPINAS, SP, BRASIL. e-mail:[email protected] Host cell invasion and dissemination within the host are hallmarks of virulence for many pathogenic microorganisms. As concerns Trypanosoma cruzi that causes Chagas disease, the insect vector-derived metacyclic trypomastigotes (MT) initiate infection by invading host cells, and later blood trypomastigotes disseminate to diverse organs and tissues. Studies with MT generated in vitro and tissue culture-derived trypomastigotes (TCT), as counterparts of insect- borne and bloodstream parasites, have implicated members of the gp85/trans-sialidase superfamily, MT gp82 and TCT Tc85-11, in cell invasion and interaction with host factors. Here we analyzed the gp82 structure/function characteristics and compared them with those previously reported for Tc85-11. One of the gp82 sequences identified as a cell binding site consisted of an alpha-helix, which connects the N-terminal beta-propeller domain to the C- terminal beta-sandwich domain where the second binding site is nested. In the gp82 structure model, both sites were exposed at the surface. Unlike gp82, the Tc85-11 cell adhesion sites are located in the N-terminal beta-propeller region. The gp82 sequence corresponding to the epitope for a monoclonal antibody that inhibits MT entry into target cells was exposed on the surface, upstream and contiguous to the alpha-helix. Located downstream and close to the alpha-helix was the gp82 gastric mucin binding site, which plays a central role in oral T. -
Some Considerations for Analyzing Biodiversity Using Integrative
Some considerations for analyzing biodiversity using integrative metagenomics and gene networks Lucie Bittner, Sébastien Halary, Claude Payri, Corinne Cruaud, Bruno de Reviers, Philippe Lopez, Eric Bapteste To cite this version: Lucie Bittner, Sébastien Halary, Claude Payri, Corinne Cruaud, Bruno de Reviers, et al.. Some considerations for analyzing biodiversity using integrative metagenomics and gene networks. Biology Direct, BioMed Central, 2010, 5 (5), pp.47. 10.1186/1745-6150-5-47. hal-02922363 HAL Id: hal-02922363 https://hal.archives-ouvertes.fr/hal-02922363 Submitted on 26 Aug 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Bittner et al. Biology Direct 2010, 5:47 http://www.biology-direct.com/content/5/1/47 HYPOTHESIS Open Access Some considerations for analyzing biodiversity using integrative metagenomics and gene networks Lucie Bittner1†, Sébastien Halary2†, Claude Payri3, Corinne Cruaud4, Bruno de Reviers1, Philippe Lopez2, Eric Bapteste2* Abstract Background: Improving knowledge of biodiversity will benefit conservation biology, enhance bioremediation studies, and could lead to new medical treatments. However there is no standard approach to estimate and to compare the diversity of different environments, or to study its past, and possibly, future evolution. -
Snps Reveal Geographical Population Structure of Corallina Officinalis (Corallinaceae, Rhodophyta)
SNPs reveal geographical population structure of Corallina officinalis (Corallinaceae, Rhodophyta) Chris Yesson1, Amy Jackson2, Steve Russell2, Christopher J. Williamson2,3 and Juliet Brodie2 1 Institute of Zoology, Zoological Society of London, London, UK 2 Natural History Museum, Department of Life Sciences, London, UK 3 Schools of Biological and Geographical Sciences, University of Bristol, Bristol, UK CONTACT: Chris Yesson. Email: [email protected] 1 Abstract We present the first population genetics study of the calcifying coralline alga and ecosystem engineer Corallina officinalis. Eleven novel SNP markers were developed and tested using Kompetitive Allele Specific PCR (KASP) genotyping to assess the population structure based on five sites around the NE Atlantic (Iceland, three UK sites and Spain), spanning a wide latitudinal range of the species’ distribution. We examined population genetic patterns over the region using discriminate analysis of principal components (DAPC). All populations showed significant genetic differentiation, with a marginally insignificant pattern of isolation by distance (IBD) identified. The Icelandic population was most isolated, but still had genotypes in common with the population in Spain. The SNP markers presented here provide useful tools to assess the population connectivity of C. officinalis. This study is amongst the first to use SNPs on macroalgae and represents a significant step towards understanding the population structure of a widespread, habitat forming coralline alga in the NE Atlantic. KEYWORDS Marine red alga; Population genetics; Calcifying macroalga; Corallinales; SNPs; Corallina 2 Introduction Corallina officinalis is a calcified geniculate (i.e. articulated) coralline alga that is wide- spread on rocky shores in the North Atlantic (Guiry & Guiry, 2017; Brodie et al., 2013; Williamson et al., 2016). -
Haeckel's 1866 Tree of Life and the Origin of Eukaryotes
PUBLISHED: 26 JULY 2016 | ARTICLE NUMBER: 16114 | DOI: 10.1038/NMICROBIOL.2016.114 correspondence Haeckel’s 1866 tree of life and the origin of eukaryotes To the Editor — In their Letter describing were summarized under the domain an expanded version of the tree of life, Eukarya, which includes all eukaryotic Hug et al.1 refer to a key publication of micro- and macroorganisms (from amoebae Carl Woese and co-workers2, wherein a to humans). 16S rRNA-phylogenetic scheme of the In chapter 26 entitled ‘Phylogenetic domains Bacteria, Archaea and Eukarya is theses’, Haeckel3 re-interpreted and shown. However, the first three-kingdom supplemented Darwin’s evolutionary tree of life that included microorganisms deductions of 1859. With reference to the was depicted by Ernst Haeckel (pictured simplest protists (bacteria), which form the at around 26 years old) in his General root of his ‘oak tree’ (see Fig. 6 in ref. 5), Morphology of Organisms, a seminal book Haeckel3 concluded that “all organisms that was published one hundred and are the descendants of such autogenous fifty years ago3. Moneren”. Hence, according to this In his Origin of Species, Charles Darwin Haeckelian interpretation of the phylogeny refers to the Linnean two-kingdom of life, the Monera (that is, Bacteria and system, with ‘Animalia’ and ‘Vegetabilia’ Archaea)2 are the progenitors of all more as the only two branches of the living complex living beings on Earth. world. Haeckel3, who was also known This 150-year-old idea is consistent with as the German Darwin4, introduced a recent discoveries and genomic analyses that three-kingdom scheme in which, as a support an archaeal origin of eukaryotes1,8.