Report of a Case of Staphylococcus Aureus Infection of Skin After Scuba Diving
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Photoinhibition and Photoprotection in Symbiotic Dinoflagellates from Reef-Building Corals
MARINE ECOLOGY PROGRESS SERIES Vol. 183: 73-86.1999 Published July 6 Mar Ecol Prog Ser 1 Photoinhibition and photoprotection in symbiotic dinoflagellates from reef-building corals Ove Hoegh-Guldberg*, Ross J. Jones School of Biological Sciences, Building A08. The University of Sydney, New South Wales 2006. Australia ABSTRACT: Pulse-amplitude-modulation fluorometry and oxygen respirometry were used to investi- gate die1 photosynthetic responses by symbiotic dnoflagellates to light levels in summer and winter on a high latitude coral reef. The symbiotic dinoflagellates from 2 species of reef-building coral (Porites cylindnca and Stylophora pistillata) showed photoinhibitory decreases in the ratio of variable (F,) to maximal (F,) fluorescence (F,/F,,,) as early as 09:00 h on both summer and winter days on the reefs associated wlth One Tree Island (23" 30'S, 1.52" 06' E; Great Barrier Reef, Australia). This was due to decreases in maximum, F,, and to a smaller extent minimum, F,, chlorophyll fluorescence. Complete recovery took 4 to 6 h and began to occur as soon as light levels fell each day. Chlorophyll fluorescence quenching analysis of corals measured during the early afternoon revealed classic regulation of photo- system I1 (PSII) efficiency through non-photochemical quenching (NPQ). These results appear to be similar to data collected for other algae and higher plants, suggesting involvement of the xanthophyll cycle of symbiotic dinoflagellates in regulating the quantum efficiency of PSII. The ability of symbiotic dinoflagellates to develop significant NPQ, however, depended strongly on when the symbiotic dinoflagellates were studied. Whereas symbiotic dinoflagellates from corals in the early afternoon showed a significant capacity to regulate the efficiency of PSII using NPQ, those sampled before sun- rise had a slower and much reduced capacity, suggesting that elements of the xanthophyll cycle are suppressed prior to sunrise. -
The Distribution of Mycosporine-Like Amino Acids (Maas) and the Phylogenetic Identity of Symbiotic Dinoflagellates in Cnidarian
Journal of Experimental Marine Biology and Ecology 337 (2006) 131–146 www.elsevier.com/locate/jembe The distribution of mycosporine-like amino acids (MAAs) and the phylogenetic identity of symbiotic dinoflagellates in cnidarian hosts from the Mexican Caribbean ⁎ Anastazia T. Banaszak a, , Maria Guadalupe Barba Santos a, Todd C. LaJeunesse b, Michael P. Lesser c a Unidad Académica Puerto Morelos, Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México, Apartado Postal 1152, Cancún, Quintana Roo, 77500, Mexico b Department of Biology, Florida International University, University Park Campus, Miami, Florida, 33199, USA c Department of Zoology and Center for Marine Biology, University of New Hampshire, Durham, New Hampshire, 03824, USA Received 22 May 2006; accepted 10 June 2006 Abstract A survey of 54 species of symbiotic cnidarians that included hydrozoan corals, anemones, gorgonians and scleractinian corals was conducted in the Mexican Caribbean for the presence of mycosporine-like amino acids (MAAs) in the host as well as the Symbio- dinium fractions. The host fractions contained relatively simple MAA profiles, all harbouring between one and three MAAs, principally mycosporine-glycine followed by shinorine and porphyra-334 in smaller amounts. Symbiodinium populations were identified to sub-generic levels using PCR-DGGE analysis of the Internal Transcribed Spacer 2 (ITS2) region. Regardless of clade identity, all Symbiodinium extracts contained MAAs, in contrast to the pattern that has been found in cultures of Symbiodinium, where clade A symbionts produced MAAs whereas clade B, C, D, and E symbionts did not. Under natural conditions between one and four MAAs were identified in the symbiont fractions, mycosporine-glycine (λmax =310 nm), shinorine (λmax =334 nm), porphyra-334 (λmax =334 nm) and palythine (λmax =320 nm). -
Molecular Investigation of the Cnidarian-Dinoflagellate Symbiosis
AN ABSTRACT OF THE DISSERTATION OF Laura Lynn Hauck for the degree of Doctor of Philosophy in Zoology presented on March 20, 2007. Title: Molecular Investigation of the Cnidarian-dinoflagellate Symbiosis and the Identification of Genes Differentially Expressed during Bleaching in the Coral Montipora capitata. Abstract approved: _________________________________________ Virginia M. Weis Cnidarians, such as anemones and corals, engage in an intracellular symbiosis with photosynthetic dinoflagellates. Corals form both the trophic and structural foundation of reef ecosystems. Despite their environmental importance, little is known about the molecular basis of this symbiosis. In this dissertation we explored the cnidarian- dinoflagellate symbiosis from two perspectives: 1) by examining the gene, CnidEF, which was thought to be induced during symbiosis, and 2) by profiling the gene expression patterns of a coral during the break down of symbiosis, which is called bleaching. The first chapter characterizes a novel EF-hand cDNA, CnidEF, from the anemone Anthopleura elegantissima. CnidEF was found to contain two EF-hand motifs. A combination of bioinformatic and molecular phylogenetic analyses were used to compare CnidEF to EF-hand proteins in other organisms. The closest homologues identified from these analyses were a luciferin binding protein involved in the bioluminescence of the anthozoan Renilla reniformis, and a sarcoplasmic calcium- binding protein involved in fluorescence of the annelid worm Nereis diversicolor. Northern blot analysis refuted link of the regulation of this gene to the symbiotic state. The second and third chapters of this dissertation are devoted to identifying those genes that are induced or repressed as a function of coral bleaching. In the first of these two studies we created a 2,304 feature custom DNA microarray platform from a cDNA subtracted library made from experimentally bleached Montipora capitata, which was then used for high-throughput screening of the subtracted library. -
Bioactivity of Venom Extracted from the Sea Anemone Anthopleura Asiatica (Cnidaria: Anthozoa): Toxicity and Histopathological Studies
International Journal of Fisheries and Aquaculture Vol. 4(4), pp. 71-76, 9 March, 2012 Available online at http://www.academicjournals.org/IJFA DOI: 10.5897/IJFA11.019 ISSN 2006-9839 ©2012 Academic Journals Full Length Research Paper Bioactivity of venom extracted from the sea anemone Anthopleura asiatica (Cnidaria: Anthozoa): Toxicity and Histopathological studies Ramkumar S.1*, Arun Sudhagar S.2 and Venkateshvaran K. 1 1Fisheries Resources, Harvest and Post Harvest Division, Central Institute of Fisheries Education, Mumbai, India. 2Aquatic Environment and Health Management Division, Central Institute of Fisheries Education, Mumbai, India. Accepted 21 October, 2011 The bioactivity of the venom from a locally available sea anemone, Anthopleura asiatica collected from the Mumbai coast was studied. The crude venom from sixty sea anemones (Sixty numbers) was extracted in aqueous medium. The protein content of the crude venom was 4.3459±0.027 mg/ml. The crude venom was found to be lethal at 1ml when injected intra-peritoneal to kasuali strain male albino mice (20±2 g). The crude venom was partially purified by anion exchange chromatography using a step- wise gradient of 0.1-1.0M NaCl and 10 fractions each of 15 ml, F1 – F10 were collected. Fractions F8, F9 and F10 exhibited lethality to mice, upon envenomation. The symptoms of toxicity observed in the mice indicated that the venom affected the central nervous, cardiovascular and urinary systems. Histopathological study revealed accumulation of polymorphic nuclear cells with necrosis in brain, hemolysis in heart, occlusion with hemolysed blood in kidney and necrosis, vacuolation with pleomorphic nuclear material and hemolysis in liver. -
Sea Anemone (Cnidaria, Anthozoa, Actiniaria) Toxins: an Overview
Mar. Drugs 2012, 10, 1812-1851; doi:10.3390/md10081812 OPEN ACCESS Marine Drugs ISSN 1660-3397 www.mdpi.com/journal/marinedrugs Review Sea Anemone (Cnidaria, Anthozoa, Actiniaria) Toxins: An Overview Bárbara Frazão 1,2, Vitor Vasconcelos 1,2 and Agostinho Antunes 1,2,* 1 CIMAR/CIIMAR, Centro Interdisciplinar de Investigação Marinha e Ambiental, Universidade do Porto, Rua dos Bragas 177, 4050-123 Porto, Portugal; E-Mails: [email protected] (B.F.); [email protected] (V.V.) 2 Departamento de Biologia, Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre, 4169-007 Porto, Portugal * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +351-22-340-1813; Fax: +351-22-339-0608. Received: 31 May 2012; in revised form: 9 July 2012 / Accepted: 25 July 2012 / Published: 22 August 2012 Abstract: The Cnidaria phylum includes organisms that are among the most venomous animals. The Anthozoa class includes sea anemones, hard corals, soft corals and sea pens. The composition of cnidarian venoms is not known in detail, but they appear to contain a variety of compounds. Currently around 250 of those compounds have been identified (peptides, proteins, enzymes and proteinase inhibitors) and non-proteinaceous substances (purines, quaternary ammonium compounds, biogenic amines and betaines), but very few genes encoding toxins were described and only a few related protein three-dimensional structures are available. Toxins are used for prey acquisition, but also to deter potential predators (with neurotoxicity and cardiotoxicity effects) and even to fight territorial disputes. Cnidaria toxins have been identified on the nematocysts located on the tentacles, acrorhagi and acontia, and in the mucous coat that covers the animal body. -
New Geographic Distribution Records for Northeastern Atlantic Species from Peniche and Berlengas Archipelago
SHORT COMMUNICATION New geographic distribution records for Northeastern Atlantic species from Peniche and Berlengas Archipelago NUNO VASCO RODRIGUES Rodrigues, N.V. 2012. New geographic distribution records for Northeastern Atlantic species. Arquipelago. Life and Marine Sciences 29: 63-66. Nuno V. Rodrigues (email: [email protected]), GIRM – Marine Resources Research Group, Polytechnic Institute of Leiria, Campus 4, Santuário Nª Sª dos Remédios, PT-2520-641 Peniche, Portugal. INTRODUCTION CNIDARIA: ACTINIARIA During SCUBA dives and intertidal surveys car- Alicia mirabilis Johnson, 1861 ried out in 2006 and 2007 at Peniche and the Ber- This species occurs in the Eastern Atlantic, from lengas Archipelago (Portugal), undertaken as part the Canary Islands (Ocaña 1994), Azores (Wirtz of a research project with the objective of et al. 2003) and Madeira (Wirtz 1995) to the Por- publishing an underwater marine guide, a photo- tuguese continental coast as far north as Cascais graphic register of several species not yet (Wirtz & Debelius 2004). It was very recently recorded for the area was produced. recorded in Senegal (Wirtz 2011). A. mirabilis is Subsequent identification and bibliographic also common in the western Mediterranean research confirmed that these records were made (Ocaña et al. 2000) and has been recorded in the beyond the previously known geographic distri- Adriatic Sea (Kruzic et al. 2002) and Aegean Sea bution boundaries for each of the species men- (Katsanevakis & Thessalou-Legaki 2007). In the tioned here. Western Atlantic, it is known from Florida and the Bahamas to Brazil (Humann 1992; Zamponi et al. 1998). MATERIAL & METHODS This species was observed in Peniche (39º21.64'N 9º25.28'W) while diving at about 17 Most of the records were made by underwater meters depth over rocky substrate (Fig. -
A Review of Toxins from Cnidaria
marine drugs Review A Review of Toxins from Cnidaria Isabella D’Ambra 1,* and Chiara Lauritano 2 1 Integrative Marine Ecology Department, Stazione Zoologica Anton Dohrn, Villa Comunale, 80121 Napoli, Italy 2 Marine Biotechnology Department, Stazione Zoologica Anton Dohrn, Villa Comunale, 80121 Napoli, Italy; [email protected] * Correspondence: [email protected]; Tel.: +39-081-5833201 Received: 4 August 2020; Accepted: 30 September 2020; Published: 6 October 2020 Abstract: Cnidarians have been known since ancient times for the painful stings they induce to humans. The effects of the stings range from skin irritation to cardiotoxicity and can result in death of human beings. The noxious effects of cnidarian venoms have stimulated the definition of their composition and their activity. Despite this interest, only a limited number of compounds extracted from cnidarian venoms have been identified and defined in detail. Venoms extracted from Anthozoa are likely the most studied, while venoms from Cubozoa attract research interests due to their lethal effects on humans. The investigation of cnidarian venoms has benefited in very recent times by the application of omics approaches. In this review, we propose an updated synopsis of the toxins identified in the venoms of the main classes of Cnidaria (Hydrozoa, Scyphozoa, Cubozoa, Staurozoa and Anthozoa). We have attempted to consider most of the available information, including a summary of the most recent results from omics and biotechnological studies, with the aim to define the state of the art in the field and provide a background for future research. Keywords: venom; phospholipase; metalloproteinases; ion channels; transcriptomics; proteomics; biotechnological applications 1. -
Aquatic Microalgae As Potential Sources of Uv-Screening Compounds
Philippine Journal of Science 139 (1): 5-16, June 2010 ISSN 0031 - 7683 Aquatic Microalgae As Potential Sources Of Uv-Screening Compounds Maribel L. Dionisio-Sese Institute of Biological Sciences, College of Arts and Sciences, University of the Philippines Los Baños, College, Laguna 4031, Philippines Microalgae are a polyphyletic and biochemically diverse assemblage of chlorophyll a-containing microorganisms capable of oxygenic photosynthesis that are predominantly found in aquatic environments with observed high levels of ultraviolet (UV) radiation. Certain microalgae produce organic metabolites, such as sporopollenin, scytonemin and mycosporine-like amino acids, to protect themselves from UV radiation while allowing visible radiation involved in photosynthesis to pass through. Sporopollenin, an acetolysis-resistant inert biopolymer usually observed in plant pollens and spores, was detected in the cell wall of some UV-tolerant chlorophytes. Scytonemin, a yellow-brown lipid-soluble dimeric pigment, was found in the extracellular polysaccharide sheath of some cyanobacteria. Mycosporine- like amino acids, which belong to a family of water-soluble compounds, were reported in several free-living cyanobacteria, chlorophytes, haptophytes, diatoms, and dinoflagellates, as well as in several marine invertebrate-microalgal symbiotic associations. Their capacity to intercept UV radiation and dissipate its energy as heat without the formation of radical intermediates makes these microalgal compounds potential sources of protection from UV and photo-oxidative stress. Key Words: microalgae, mycosporine-like amino acids, scytonemin, sporopollenin, UV-absorbing/ screening compounds, UV photoprotection INTRODUCTION the high UV transparency of clear tropical ocean water. In high latitudes, enhanced UV radiation due to stratospheric Microalgae refers to a polyphyletic and biochemically ozone depletion is also a major stress factor for many diverse assemblage of chlorophyll-a containing organisms. -
Marine Freshwater Research
CSIRO PUBLISHING Marine Freshwater& Research Volume 50,1999 ©CSIRO Australia 1999 A journal for the publication of original contributions in physical oceanography,marine chemistry, marine and estuarine biology and limnology www.publish.csiro.au/journals/mfr All enquiries and manuscripts should be directed to Marine and Freshwater Research CSIROPUBLISHING PO Box 1139 (150 Oxford St) Collingwood Telephone:61 3 9662 7618 Vic. 3066 Facsimile:61 3 9662 7611 Australia Email:[email protected] Published by CSIROPUBLISHING for CSIRO Australia and the Australian Academy of Science © CSIRO 1999 Mar. Freshwater Res., 1999, 50, 839–66 Climate change, coral bleaching and the future of the world’s coral reefs Ove Hoegh-Guldberg School of Biological Sciences, A08, University of Sydney, NSW 2006, Australia. email: [email protected] Abstract. Sea temperatures in many tropical regions have increased by almost 1°C over the past 100 years, and are currently increasing at ~1–2°C per century. Coral bleaching occurs when the thermal tol- erance of corals and their photosynthetic symbionts (zooxanthellae) is exceeded. Mass coral bleaching has occurred in association with episodes of elevated sea temperatures over the past 20 years and involves the loss of the zooxanthellae following chronic photoinhibition. Mass bleaching has resulted in signifi- cant losses of live coral in many parts of the world. This paper considers the biochemical, physiological and ecological perspectives of coral bleaching. It also uses the outputs of four runs from three models of global climate change which simulate changes in sea temperature and hence how the frequency and inten- sity of bleaching events will change over the next 100 years. -
Character Evolution in Light of Phylogenetic Analysis and Taxonomic Revision of the Zooxanthellate Sea Anemone Families Thalassianthidae and Aliciidae
CHARACTER EVOLUTION IN LIGHT OF PHYLOGENETIC ANALYSIS AND TAXONOMIC REVISION OF THE ZOOXANTHELLATE SEA ANEMONE FAMILIES THALASSIANTHIDAE AND ALICIIDAE BY Copyright 2013 ANDREA L. CROWTHER Submitted to the graduate degree program in Ecology and Evolutionary Biology and the Graduate Faculty of the University of Kansas in partial fulfillment of the requirements for the degree of Doctor of Philosophy. ________________________________ Chairperson Daphne G. Fautin ________________________________ Paulyn Cartwright ________________________________ Marymegan Daly ________________________________ Kirsten Jensen ________________________________ William Dentler Date Defended: 25 January 2013 The Dissertation Committee for ANDREA L. CROWTHER certifies that this is the approved version of the following dissertation: CHARACTER EVOLUTION IN LIGHT OF PHYLOGENETIC ANALYSIS AND TAXONOMIC REVISION OF THE ZOOXANTHELLATE SEA ANEMONE FAMILIES THALASSIANTHIDAE AND ALICIIDAE _________________________ Chairperson Daphne G. Fautin Date approved: 15 April 2013 ii ABSTRACT Aliciidae and Thalassianthidae look similar because they possess both morphological features of branched outgrowths and spherical defensive structures, and their identification can be confused because of their similarity. These sea anemones are involved in a symbiosis with zooxanthellae (intracellular photosynthetic algae), which is implicated in the evolution of these morphological structures to increase surface area available for zooxanthellae and to provide protection against predation. Both -
Tentacle Morphological Variation Coincides with Differential Expression of Toxins in Sea Anemones
toxins Article Tentacle Morphological Variation Coincides with Differential Expression of Toxins in Sea Anemones Lauren M. Ashwood 1,* , Michela L. Mitchell 2,3,4,5 , Bruno Madio 6, David A. Hurwood 1,7, Glenn F. King 6,8 , Eivind A. B. Undheim 9,10,11 , Raymond S. Norton 2,12 and Peter J. Prentis 1,7 1 School of Biology and Environmental Science, Faculty of Science, Queensland University of Technology, Brisbane, QLD 4000, Australia; [email protected] (D.A.H.); [email protected] (P.J.P.) 2 Medicinal Chemistry, Monash Institute of Pharmaceutical Sciences, Monash University, 381 Royal Parade, Parkville, VIC 3052, Australia; [email protected] (M.L.M.); [email protected] (R.S.N.) 3 Sciences Department, Museum Victoria, G.P.O. Box 666, Melbourne, VIC 3001, Australia 4 Queensland Museum, P.O. Box 3000, South Brisbane, QLD 4101, Australia 5 Bioinformatics Division, Walter & Eliza Hall Institute of Research, 1G Royal Parade, Parkville, VIC 3052, Australia 6 Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia; [email protected] (B.M.); [email protected] (G.F.K.) 7 Centre for Agriculture and the Bioeconomy, Queensland University of Technology, Brisbane, QLD 4000, Australia 8 ARC Centre for Innovations in Peptide and Protein Science, The University of Queensland, St Lucia, QLD 4072, Australia 9 Centre for Advanced Imaging, The University of Queensland, St Lucia, QLD 4072, Australia; [email protected] 10 Centre for Biodiversity Dynamics, Department of Biology, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway 11 Centre for Ecological and Evolutionary Synthesis, Department of Biosciences, University of Oslo, Blindern, NO-0316 Oslo, Norway Citation: Ashwood, L.M.; Mitchell, 12 ARC Centre for Fragment-Based Design, Monash University, Parkville, VIC 3052, Australia M.L.; Madio, B.; Hurwood, D.A.; * Correspondence: [email protected] King, G.F.; Undheim, E.A.B.; Norton, R.S.; Prentis, P.J. -
Sobre Anêmonas-Do-Mar (Actiniaria) Bo Brasil
Bol. Zool. e Biol. Mar., N.S., n.° 30, pp. 457-468, São Paulo, 1973 SOBRE ANÊMONAS-DO-MAR (ACTINIARIA) BO BRASIL DIVA DINIZ CORRÊA Departamento de Zoologia do Instituto de Biociências da Universidade de São Paulo — Caixa Postal, 20.520 —■ São Paulo — Brasil. RESUMO Este trabalho apresenta uma descrição sumária de 5 espécies de anê- monas-do-mar ainda não conhecidas para a costa brasileira. São elas: Lebrunia danae (Duchassaing & Michelotti, 1860), de Pernambuco, Lebrunia coralligens (Wilson, 1890), da Bahia, Condylactis gigantea (Weinland, 1860), da Bahia, Homostichanthus ãuerdeni Carlgren, 1900, de Espírito Santo e Alicia mirabilis Johnson, 1861, de Pernambuco. ON SEA ANEMONES (ACTINIARIA) FROM BRAZIL ABSTRACT In a first paper, Corrêa (1964) described 10 species of sea ane mones from Brazil, mainly from the coast of São Paulo. Only one of them, Calliactis tricolor (Lesueur, 1817), is mentioned to occur in Ceará State, Northeastern coast of Brazil. Later on, one more spe cies, Actinoporus elegans Duchassaing, 1850, also from São Paulo coast, was described (Corrêa, in press). Of the eleven species included in both papers, six are mostly known from Caribbean waters. Four of the five species described here, Lebrunia danae (Duchas saing & Michelotti, 1860), Lebrunia coralligens (Wilson, 1890), Condy lactis gigantea (Weinland, I860), and Homostichanthus ãuerdeni Carlgren, 1900, are known for Caribbean waters also, now collected in Pernambuco (one species), Bahia (two species) and Espírito Santo (one species). The fifth species, Alicia mirabilis Johnson, 1861, already known from Madeira Island, was found in Pernambuco. INTRODUÇÃO Na sua revisão sistemática das três Ordens de anêmonas-do-mar, Ptichodactiaria, Corallimorpharia e Actiniaria, Carlgren (1949) men ciona apenas 4 espécies da última Ordem conhecidas para o Brasil.