A Machine Vision System for Tracking Population Behavior of Zooplankton
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Twenty Thousand Parasites Under The
ADVERTIMENT. Lʼaccés als continguts dʼaquesta tesi queda condicionat a lʼacceptació de les condicions dʼús establertes per la següent llicència Creative Commons: http://cat.creativecommons.org/?page_id=184 ADVERTENCIA. El acceso a los contenidos de esta tesis queda condicionado a la aceptación de las condiciones de uso establecidas por la siguiente licencia Creative Commons: http://es.creativecommons.org/blog/licencias/ WARNING. The access to the contents of this doctoral thesis it is limited to the acceptance of the use conditions set by the following Creative Commons license: https://creativecommons.org/licenses/?lang=en Departament de Biologia Animal, Biologia Vegetal i Ecologia Tesis Doctoral Twenty thousand parasites under the sea: a multidisciplinary approach to parasite communities of deep-dwelling fishes from the slopes of the Balearic Sea (NW Mediterranean) Tesis doctoral presentada por Sara Maria Dallarés Villar para optar al título de Doctora en Acuicultura bajo la dirección de la Dra. Maite Carrassón López de Letona, del Dr. Francesc Padrós Bover y de la Dra. Montserrat Solé Rovira. La presente tesis se ha inscrito en el programa de doctorado en Acuicultura, con mención de calidad, de la Universitat Autònoma de Barcelona. Los directores Maite Carrassón Francesc Padrós Montserrat Solé López de Letona Bover Rovira Universitat Autònoma de Universitat Autònoma de Institut de Ciències Barcelona Barcelona del Mar (CSIC) La tutora La doctoranda Maite Carrassón Sara Maria López de Letona Dallarés Villar Universitat Autònoma de Barcelona Bellaterra, diciembre de 2016 ACKNOWLEDGEMENTS Cuando miro atrás, al comienzo de esta tesis, me doy cuenta de cuán enriquecedora e importante ha sido para mí esta etapa, a todos los niveles. -
Catching the Complexity of Salmon-Louse Interactions
Fish and Shellfish Immunology 90 (2019) 199–209 Contents lists available at ScienceDirect Fish and Shellfish Immunology journal homepage: www.elsevier.com/locate/fsi Full length article Catching the complexity of salmon-louse interactions T ∗ Cristian Gallardo-Escáratea, , Valentina Valenzuela-Muñoza, Gustavo Núñez-Acuñaa, Crisleri Carreraa, Ana Teresa Gonçalvesa, Diego Valenzuela-Mirandaa, Bárbara P. Benaventea, Steven Robertsb a Interdisciplinary Center for Aquaculture Research, Laboratory of Biotechnology and Aquatic Genomics, Department of Oceanography, Universidad de Concepción, Concepción, Chile b School of Aquatic and Fishery Sciences (SAFS), University of Washington, Seattle, USA ABSTRACT The study of host-parasite relationships is an integral part of the immunology of aquatic species, where the complexity of both organisms has to be overlayed with the lifecycle stages of the parasite and immunological status of the host. A deep understanding of how the parasite survives in its host and how they display molecular mechanisms to face the immune system can be applied for novel parasite control strategies. This review highlights current knowledge about salmon and sea louse, two key aquatic animals for aquaculture research worldwide. With the aim to catch the complexity of the salmon-louse interactions, molecular information gleaned through genomic studies are presented. The host recognition system and the chemosensory receptors found in sea lice reveal complex molecular components, that in turn, can be disrupted through specific molecules such as non-coding RNAs. 1. Introduction worldwide the most studied sea lice species are Lepeophtheirus salmonis and Caligus rogercresseyi [8–10]. Annually the salmon industry presents Host-parasite interactions are a complex relationship where one estimated losses of US $ 480 million, representing between 4 and 10% organism benefits the other and often where there is a negative impact of production costs [10]. -
Piscirickettsia Salmonis and the Sea Louse Caligus Rogercresseyi
Disease Resistance in Atlantic Salmon (Salmo salar): Coinfection of the Intracellular Bacterial Pathogen Piscirickettsia salmonis and the Sea Louse Caligus rogercresseyi Jean Paul Lhorente1, Jose´ A. Gallardo2*, Beatriz Villanueva3, Marı´a J. Caraban˜ o3, Roberto Neira1,4 1 Aquainnovo S.A, Puerto Montt, Chile, 2 Pontificia Universidad Cato´lica de Valparaı´so, Valparaı´so, Chile, 3 Departamento de Mejora Gene´tica Animal, INIA, Madrid, Spain, 4 Departamento de Produccio´n Animal, Facultad de Ciencias Agrono´micas, Universidad de Chile, Santiago, Chile Abstract Background: Naturally occurring coinfections of pathogens have been reported in salmonids, but their consequences on disease resistance are unclear. We hypothesized that 1) coinfection of Caligus rogercresseyi reduces the resistance of Atlantic salmon to Piscirickettsia salmonis; and 2) coinfection resistance is a heritable trait that does not correlate with resistance to a single infection. Methodology: In total, 1,634 pedigreed Atlantic salmon were exposed to a single infection (SI) of P. salmonis (primary pathogen) or coinfection with C. rogercresseyi (secondary pathogen). Low and high level of coinfection were evaluated (LC = 44 copepodites per fish; HC = 88 copepodites per fish). Survival and quantitative genetic analyses were performed to determine the resistance to the single infection and coinfections. Main Findings: C. rogercresseyi significantly increased the mortality in fish infected with P. salmonis (SI mortality = 251/545; LC mortality = 544/544 and HC mortality = 545/545). Heritability estimates for resistance to P. salmonis were similar and of 2 2 2 medium magnitude in all treatments (h SI = 0.2360.07; h LC = 0.1760.08; h HC = 0.2460.07). A large and significant genetic correlation with regard to resistance was observed between coinfection treatments (rg LC-HC = 0.9960.01) but not between the single and coinfection treatments (rg SI-LC = 20.1460.33; rg SI-HC = 0.3260.34). -
Host-Parasite Interaction of Atlantic Salmon (Salmo Salar) and the Ectoparasite Neoparamoeba Perurans in Amoebic Gill Disease
ORIGINAL RESEARCH published: 31 May 2021 doi: 10.3389/fimmu.2021.672700 Host-Parasite Interaction of Atlantic salmon (Salmo salar) and the Ectoparasite Neoparamoeba perurans in Amoebic Gill Disease † Natasha A. Botwright 1*, Amin R. Mohamed 1 , Joel Slinger 2, Paula C. Lima 1 and James W. Wynne 3 1 Livestock and Aquaculture, CSIRO Agriculture and Food, St Lucia, QLD, Australia, 2 Livestock and Aquaculture, CSIRO Agriculture and Food, Woorim, QLD, Australia, 3 Livestock and Aquaculture, CSIRO Agriculture and Food, Hobart, TAS, Australia Marine farmed Atlantic salmon (Salmo salar) are susceptible to recurrent amoebic gill disease Edited by: (AGD) caused by the ectoparasite Neoparamoeba perurans over the growout production Samuel A. M. Martin, University of Aberdeen, cycle. The parasite elicits a highly localized response within the gill epithelium resulting in United Kingdom multifocal mucoid patches at the site of parasite attachment. This host-parasite response Reviewed by: drives a complex immune reaction, which remains poorly understood. To generate a model Diego Robledo, for host-parasite interaction during pathogenesis of AGD in Atlantic salmon the local (gill) and University of Edinburgh, United Kingdom systemic transcriptomic response in the host, and the parasite during AGD pathogenesis was Maria K. Dahle, explored. A dual RNA-seq approach together with differential gene expression and system- Norwegian Veterinary Institute (NVI), Norway wide statistical analyses of gene and transcription factor networks was employed. A multi- *Correspondence: tissue transcriptomic data set was generated from the gill (including both lesioned and non- Natasha A. Botwright lesioned tissue), head kidney and spleen tissues naïve and AGD-affected Atlantic salmon [email protected] sourced from an in vivo AGD challenge trial. -
Inventory of Parasitic Copepods and Their Hosts in the Western Wadden Sea in 1968 and 2010
INVENTORY OF PARASITIC COPEPODS AND THEIR HOSTS IN THE WESTERN WADDEN SEA IN 1968 AND 2010 Wouter Koch NNIOZIOZ KKoninklijkoninklijk NNederlandsederlands IInstituutnstituut vvooroor ZZeeonderzoekeeonderzoek INVENTORY OF PARASITIC COPEPODS AND THEIR HOSTS IN THE WESTERN WADDEN SEA IN 1968 AND 2010 Wouter Koch Texel, April 2012 NIOZ Koninklijk Nederlands Instituut voor Zeeonderzoek Cover illustration The parasitic copepod Lernaeenicus sprattae (Sowerby, 1806) on its fish host, the sprat (Sprattus sprattus) Copyright by Hans Hillewaert, licensed under the Creative Commons Attribution-Share Alike 3.0 Unported license; CC-BY-SA-3.0; Wikipedia Contents 1. Summary 6 2. Introduction 7 3. Methods 7 4. Results 8 5. Discussion 9 6. Acknowledgements 10 7. References 10 8. Appendices 12 1. Summary Ectoparasites, attaching mainly to the fins or gills, are a particularly conspicuous part of the parasite fauna of marine fishes. In particular the dominant copepods, have received much interest due to their effects on host populations. However, still little is known on the copepod fauna on fishes for many localities and their temporal stability as long-term observations are largely absent. The aim of this project was two-fold: 1) to deliver a current inventory of ectoparasitic copepods in fishes in the southern Wadden Sea around Texel and 2) to compare the current parasitic copepod fauna with the one from 1968 in the same area, using data published in an internal NIOZ report and additional unpublished original notes. In total, 47 parasite species have been recorded on 52 fish species in the southern Wadden Sea to date. The two copepod species, where quantitative comparisons between 1968 and 2010 were possible for their host, the European flounder (Platichthys flesus), showed different trends: Whereas Acanthochondria cornuta seems not to have altered its infection rate or per host abundance between years, Lepeophtheirus pectoralis has shifted towards infection of smaller hosts, as well as to a stronger increase of per-host abundance with increasing host length. -
Morphological and Phylogenetic Analysis of Caligus Spp Isolated from Lates Calcarifer Cultured in Floating Net Cages in Malaysia
MORPHOLOGICAL AND PHYLOGENETIC ANALYSIS OF CALIGUS SPP ISOLATED FROM LATES CALCARIFER CULTURED IN FLOATING NET CAGES IN MALAYSIA MUHD FAIZUL HELMI BIN AHAMAD HASMI FACULTY OF SCIENCE UNIVERSITY OF MALAYA KUALA LUMPUR 2013 MORPHOLOGICAL AND PHYLOGENETIC ANALYSIS OF CALIGUS SPP ISOLATED FROM LATES CALCARIFER CULTURED IN FLOATING NET CAGES IN MALAYSIA MUHD FAIZUL HELMI BIN AHAMAD HASMI DISSERTATION SUBMITTED IN FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE INSTITUTE OF BIOLOGICAL SCIENCES FACULTY OF SCIENCE UNIVERSITY OF MALAYA KUALA LUMPUR 2013 UNIVERSITI MALAYA ORIGINAL LITERARY WORK DECLARATION Name of Candidate: MUHD FAIZUL HELMI BIN AHAMAD HASMI I/C/Passport No: 850809045109 Regisration/Matric No.: SGR090128 Name of Degree: MASTER OF SCIENCE Title of Project Paper/Research Report/Dissertation/Thesis (“this Work”): “MORPHOLOGICAL AND PHYLOGENETIC ANALYSIS OF CALIGUS SPP ISOLATED FROM LATES CAILCARIFER CULTURED IN FLOATING NET CAGES IN MALAYSIA” Field of Study: MOLECULAR PARASITOLOGY I do solemnly and sincerely declare that: (1) I am the sole author/writer of this Work, (2) This Work is original, (3) Any use of any work in which copyright exists was done by way of fair dealing and for permitted purposes and any excerpt or extract from, or reference to or reproduction of any copyright work has been disclosed expressly and sufficiently and the title of the Work and its authorship have been acknowledged in this Work, (4) I do not have any actual knowledge nor do I ought reasonably to know that the making of this work -
APPENDIX 1 Classified List of Fishes Mentioned in the Text, with Scientific and Common Names
APPENDIX 1 Classified list of fishes mentioned in the text, with scientific and common names. ___________________________________________________________ Scientific names and classification are from Nelson (1994). Families are listed in the same order as in Nelson (1994), with species names following in alphabetical order. The common names of British fishes mostly follow Wheeler (1978). Common names of foreign fishes are taken from Froese & Pauly (2002). Species in square brackets are referred to in the text but are not found in British waters. Fishes restricted to fresh water are shown in bold type. Fishes ranging from fresh water through brackish water to the sea are underlined; this category includes diadromous fishes that regularly migrate between marine and freshwater environments, spawning either in the sea (catadromous fishes) or in fresh water (anadromous fishes). Not indicated are marine or freshwater fishes that occasionally venture into brackish water. Superclass Agnatha (jawless fishes) Class Myxini (hagfishes)1 Order Myxiniformes Family Myxinidae Myxine glutinosa, hagfish Class Cephalaspidomorphi (lampreys)1 Order Petromyzontiformes Family Petromyzontidae [Ichthyomyzon bdellium, Ohio lamprey] Lampetra fluviatilis, lampern, river lamprey Lampetra planeri, brook lamprey [Lampetra tridentata, Pacific lamprey] Lethenteron camtschaticum, Arctic lamprey] [Lethenteron zanandreai, Po brook lamprey] Petromyzon marinus, lamprey Superclass Gnathostomata (fishes with jaws) Grade Chondrichthiomorphi Class Chondrichthyes (cartilaginous -
Observing Copepods Through a Genomic Lens James E Bron1*, Dagmar Frisch2, Erica Goetze3, Stewart C Johnson4, Carol Eunmi Lee5 and Grace a Wyngaard6
Bron et al. Frontiers in Zoology 2011, 8:22 http://www.frontiersinzoology.com/content/8/1/22 DEBATE Open Access Observing copepods through a genomic lens James E Bron1*, Dagmar Frisch2, Erica Goetze3, Stewart C Johnson4, Carol Eunmi Lee5 and Grace A Wyngaard6 Abstract Background: Copepods outnumber every other multicellular animal group. They are critical components of the world’s freshwater and marine ecosystems, sensitive indicators of local and global climate change, key ecosystem service providers, parasites and predators of economically important aquatic animals and potential vectors of waterborne disease. Copepods sustain the world fisheries that nourish and support human populations. Although genomic tools have transformed many areas of biological and biomedical research, their power to elucidate aspects of the biology, behavior and ecology of copepods has only recently begun to be exploited. Discussion: The extraordinary biological and ecological diversity of the subclass Copepoda provides both unique advantages for addressing key problems in aquatic systems and formidable challenges for developing a focused genomics strategy. This article provides an overview of genomic studies of copepods and discusses strategies for using genomics tools to address key questions at levels extending from individuals to ecosystems. Genomics can, for instance, help to decipher patterns of genome evolution such as those that occur during transitions from free living to symbiotic and parasitic lifestyles and can assist in the identification of genetic mechanisms and accompanying physiological changes associated with adaptation to new or physiologically challenging environments. The adaptive significance of the diversity in genome size and unique mechanisms of genome reorganization during development could similarly be explored. -
Characterization of the Salmon Louse Lepeophtheirus Salmonis
Marine Genomics xxx (xxxx) xxx–xxx Contents lists available at ScienceDirect Marine Genomics journal homepage: www.elsevier.com/locate/margen Characterization of the salmon louse Lepeophtheirus salmonis miRNome: Sex- biased differences related to the coding and non-coding RNA interplay ⁎ Gustavo Núñez-Acuña, Cristian Gallardo-Escárate Laboratory of Biotechnology and Aquatic Genomics, Interdisciplinary Center for Aquaculture Research (INCAR), University of Concepción, Concepción, Chile ARTICLE INFO ABSTRACT Keywords: The salmon louse Lepeophtheirus salmonis is a marine ectoparasite that has a detrimental impact on salmon farms. miRNAs Genomic knowledge of adult stages is critical to understand the reproductive success and lifecycle completion of Lepeophtheirus salmonis this species. Here, we report a comprehensive characterization of the L. salmonis miRNome with emphasis on the Small RNA sequencing sex-differences of the parasite. Small-RNA sequencing was conducted on males and females, and mRNA-se- Sex differentiation quencing was also conducted to identify miRNA-targets at these stages. Based on bioinformatics analyses, 3101 putative miRNAs were found in L. salmonis, including precursors and variants. The most abundant and over- expressed miRNAs belonged to the bantam, mir-100, mir-1, mir-263a and mir-276 families, while the most differentially expressed mRNAs corresponded to genes related to reproduction and other biological processes involved in cell-differentiation. Target analyses revealed that the most up-regulated miRNAs in males can act by inhibiting the expression of genes related to female differentiation such as vitellogenin genes. Target prediction and expression patterns suggested a pivotal role of miRNAs in the reproductive development of L. salmonis. 1. Introduction inhabit the marine environment. -
Oust the Louse: Leaping Behaviour Removes Sea Lice from Wild Juvenile Sockeye Salmon Oncorhynchus Nerka
Received: 21 March 2018 Accepted: 2 June 2018 DOI: 10.1111/jfb.13684 FISH REGULAR PAPER Oust the louse: leaping behaviour removes sea lice from wild juvenile sockeye salmon Oncorhynchus nerka Emma M. Atkinson1 | Andrew W. Bateman2,3 | Lawrence M. Dill1 | Martin Krkošek3,4 | John D. Reynolds1 | Sean C. Godwin1 1Earth to Ocean Research Group, Department of Biological Sciences, Simon Fraser We conducted a manipulative field experiment to determine whether the leaping behaviour of University, Burnaby, British Columbia, Canada wild juvenile sockeye salmon Oncorhynchus nerka dislodges ectoparasitic sea lice Caligus clem- 2Department of Geography, University of ensi and Lepeophtheirus salmonis by comparing sea-lice abundances between O. nerka juveniles Victoria, Victoria, British Columbia, Canada prevented from leaping and juveniles allowed to leap at a natural frequency. Juvenile O. nerka 3 Salmon Coast Field Station, Simoom Sound, allowed to leap had consistently fewer sea lice after the experiment than fish that were pre- British Columbia, Canada vented from leaping. Combined with past research, these results imply potential costs due to 4Department of Ecology and Evolutionary Biology, University of Toronto, Toronto, parasitism and indicate that the leaping behaviour of juvenile O. nerka does, in fact, dislodge Ontario, Canada sea lice. Correspondence Emma M. Atkinson, Earth to Ocean Research KEYWORDS Group, Department of Biological Sciences, – Simon Fraser University, Burnaby, British aquaculture, host parasite, leaping, louse, sub-lethal effects, trade-offs Columbia, V5A 1S6, Canada. Email: [email protected] Funding information This work was supported by Simon Fraser University, the University of Toronto, V. and D. Bradshaw, a Natural Sciences and Engineering Research Council of Canada (NSERC) Undergraduate Student Research Award (E. -
The Use of Kernel Density Estimation with a Bio-Physical Model Provides
ORIGINAL RESEARCH published: 30 October 2018 doi: 10.3389/fvets.2018.00269 The Use of Kernel Density Estimation With a Bio-Physical Model Provides a Method to Quantify Connectivity Among Salmon Farms: Spatial Planning and Management With Epidemiological Relevance Danielle L. Cantrell 1*, Erin E. Rees 1,2, Raphael Vanderstichel 1, Jon Grant 3, Edited by: Ramón Filgueira 4 and Crawford W. Revie 1 Saraya Tavornpanich, Norwegian Veterinary Institute, 1 Department of Health Management, Atlantic Veterinary College, University of Prince Edward Island, Charlottetown, PE, Norway Canada, 2 Land and Sea Systems Analysis, Granby, QC, Canada, 3 Department of Oceanography, Dalhousie University, Reviewed by: Halifax, NS, Canada, 4 Marine Affairs Program, Dalhousie University, Halifax, NS, Canada Nabeil Salama, Marine Scotland, United Kingdom Ingrid Askeland Johnsen, Connectivity in an aquatic setting is determined by a combination of hydrodynamic Norwegian Institute of Marine circulation and the biology of the organisms driving linkages. These complex processes Research (IMR), Norway can be simulated in coupled biological-physical models. The physical model refers to Lars Qviller, Norwegian Veterinary Institute, an underlying circulation model defined by spatially-explicit nodes, often incorporating Norway a particle-tracking model. The particles can then be given biological parameters or *Correspondence: behaviors (such as maturity and/or survivability rates, diel vertical migrations, avoidance, Danielle L. Cantrell [email protected] or seeking behaviors). The output of the bio-physical models can then be used to quantify connectivity among the nodes emitting and/or receiving the particles. Here we Specialty section: propose a method that makes use of kernel density estimation (KDE) on the output of This article was submitted to Veterinary Epidemiology and a particle-tracking model, to quantify the infection or infestation pressure (IP) that each Economics, node causes on the surrounding area. -
Parasitic Copepods (Crustacea, Hexanauplia) on Fishes from the Lagoon Flats of Palmyra Atoll, Central Pacific
A peer-reviewed open-access journal ZooKeys 833: 85–106Parasitic (2019) copepods on fishes from the lagoon flats of Palmyra Atoll, Central Pacific 85 doi: 10.3897/zookeys.833.30835 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Parasitic copepods (Crustacea, Hexanauplia) on fishes from the lagoon flats of Palmyra Atoll, Central Pacific Lilia C. Soler-Jiménez1, F. Neptalí Morales-Serna2, Ma. Leopoldina Aguirre- Macedo1,3, John P. McLaughlin3, Alejandra G. Jaramillo3, Jenny C. Shaw3, Anna K. James3, Ryan F. Hechinger3,4, Armand M. Kuris3, Kevin D. Lafferty3,5, Victor M. Vidal-Martínez1,3 1 Laboratorio de Parasitología, Centro de Investigación y de Estudios Avanzados del IPN (CINVESTAV- IPN) Unidad Mérida, Carretera Antigua a Progreso Km. 6, Mérida, Yucatán C.P. 97310, México 2 CONACYT, Centro de Investigación en Alimentación y Desarrollo, Unidad Académica Mazatlán en Acuicultura y Manejo Ambiental, Av. Sábalo Cerritos S/N, Mazatlán 82112, Sinaloa, México 3 Department of Ecology, Evolution and Marine Biology and Marine Science Institute, University of California, Santa Barbara CA 93106, USA 4 Scripps Institution of Oceanography-Marine Biology Research Division, University of California, San Diego, La Jolla, California 92093 USA 5 Western Ecological Research Center, U.S. Geological Survey, Marine Science Institute, University of California, Santa Barbara CA 93106, USA Corresponding author: Victor M. Vidal-Martínez ([email protected]) Academic editor: Danielle Defaye | Received 25 October 2018 |