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An Intestinal Gregarine of Nothria Conchylega (Polychaeta, Onuphidae)
Journal of Invertebrate Pathology 104 (2010) 172–179 Contents lists available at ScienceDirect Journal of Invertebrate Pathology journal homepage: www.elsevier.com/locate/jip Description of Trichotokara nothriae n. gen. et sp. (Apicomplexa, Lecudinidae) – An intestinal gregarine of Nothria conchylega (Polychaeta, Onuphidae) Sonja Rueckert *, Brian S. Leander Canadian Institute for Advanced Research, Program in Integrated Microbial Biodiversity, Departments of Botany and Zoology, University of British Columbia, #3529 – 6270 University Blvd., Vancouver, BC, Canada V6T 1Z4 article info abstract Article history: The trophozoites of a novel gregarine apicomplexan, Trichotokara nothriae n. gen. et sp., were isolated and Received 12 November 2009 characterized from the intestines of the onuphid tubeworm Nothria conchylega (Polychaeta), collected at Accepted 11 March 2010 20 m depth from the North-eastern Pacific Coast. The trophozoites were 50–155 lm long with a mid-cell Available online 23 March 2010 indentation that formed two prominent bulges (anterior bulge, 14–48 lm wide; posterior bulge, 15– 55 lm wide). Scanning electron microscopy (SEM) demonstrated that approximately 400 densely packed, Keywords: longitudinal epicytic folds (5 folds/lm) inscribe the surface of the trophozoites, and a prominently elon- Alveolata gated mucron (14–60 lm long and 6–12 lm wide) was covered with hair-like projections (mean length, Apicomplexa 1.97 m; mean width, 0.2 m at the base). Although a septum occurred at the junction between the cell Lecudinidae l l Lecudina proper and the mucron in most trophozoites, light microscopy (LM) demonstrated that the cell proper Parasite extended into the core of the mucron as a thin prolongation. -
Feline Immune Response to Infection with Cytauxzoon Felis and The
FELINE IMMUNE RESPONSE TO INFECTION WITH CYTAUXZOON FELIS AND THE ROLE OF CD18 IN THE PATHOGENESIS OF CYTAUXZOONOSIS by KARELMA FRONTERA-ACEVEDO (Under the Direction of Kaori Sakamoto) ABSTRACT Cytauxzoonosis is a highly fatal, hemoprotozoal disease of cats in the Mid-Western, Mid- Atlantic, and Southeastern United States, caused by Cytauxzoon felis. Although the causative agent has been recognized since 1976, no study has profiled the immune response of infected cats, there is no definitive cure, and C. felis has not been successfully maintained in cell cultures in vitro, thwarting research efforts. One of the main histopathologic characteristics of this disease is the presence of giant, infected, intravascular macrophages, many of which are adhered to the vascular endothelium. The main goals of this project are: 1) to characterize the feline immune response to C. felis; 2) to develop a cell culture system in order to study C. felis in vitro; and 3) to determine whether CD18 plays a role in the pathogenesis of cytauxzoonosis. INDEX WORDS: Cat, Cytauxzoon felis, pathogenesis, protozoal disease, veterinary pathology FELINE IMMUNE RESPONSE TO INFECTION WITH CYTAUXZOON FELIS AND THE ROLE OF CD18 IN THE PATHOGENESIS OF CYTAUXZOONOSIS by KARELMA FRONTERA-ACEVEDO BS, University of Florida, 2004 DVM, Louisiana State University, 2008 A Dissertation Submitted to the Graduate Faculty of The University of Georgia in Partial Fulfillment of the Requirements for the Degree DOCTOR OF PHILOSOPHY ATHENS, GEORGIA 2013 © 2013 Karelma Frontera-Acevedo All -
Proceedings of the Helminthological Society of Washington 49(2) 1982
I , , _ / ,' "T '- "/-_ J, . _. Volume 49 Jrily 1982;} Nufnber,2 \~-.\ .•'.' ''•-,- -• ;- - S "• . v-T /7, ' V. >= v.-"' " - . f "-< "'• '-.' '" J; PROCEEDINGS -. .-.•, • "*-. -. The Helmifltliological Society Washington :- ' ; "- ' A^siBmiohnua/ /ourna/ of research devofedVfp ^He/miiithoibgy and , a// branches of Parasi'fology in part by the ; r r;Brqytpn H.yRansom Memorial /Trust Fond TA'&'- -s^^>~J ••..''/'""', ':vSj ''--//;i -^v Subscription ^$18X)0 a Volume; Foreign, $19.00 AMIN, ,OwARr M. Adult Trematodes (Digenea) from Lake'Fishes ;6f Southeastern;Wisconsin, A with a Key to;Species ofvthe Genus Crleptdottomu/rt firwm, 1900 in-North America '_'.C-_~i-, 196- '•}AMIN, OMAR M. Two larval Trematodes'^Strigeoide^y^f fishes iri/Southeastern Wiscpnsin .:._ 207 AIMIN, OMARM. Description of Larval Acanthoctphajus parksidei Amin, 1975 (Acanthocephala: I A Echinorhynchidae) from Its iSopod Intermediate Host—i'.i.—_i.;—;-__-..-_-__-.—J....... 235 AMIN, PAIARM."and DONAL G.'My/ER. 'Paracreptbtrematina\timi gen.;et sp. inov. (Digenea: -. v Allocreadiidae) frohi-the Mudminnow, Umbra limi '.:'-._.2i_i-..__.^^.^i.., _— -____i_xS185 BAKER, M.i R. ,'On Two'Nevy Nie;matode Parasites (TnchOstrongyloidea: Molineidae) from f— , Amphibians;and Reptiles (...^d.-. -—._..-l.H— --^_./——.—.—.j- ^::l.._.___i__ 252 CAMPBELL, RONALD A:, STEVEN J- CORREIA, AND ;RIGHA»PTL. HAEPRJGH., A ,New Mbnor : • \ ^genean/and Cestode from'jthe Deep-Sea Fish, Macrourus berglax Lacepede, ;1802,' from jHe Flemish 'Cap off Newfoundland -u—— :.^..——u—^—-—^—y——i——~--———::-—:^ 169 vCAMPBELL, .RoNALp A. AND JOHN V.-^GARTNER, JR. "'Pistarta eutypharyifgis gen.\et sp. 'n.' , (', (Ceystoda: Pseudophyllidea)_from/;the Bathypelagic Gulper .Eel, ~Eurypharynx-pelecanoides ^.Vaillant, 1882, withiComments on Host arid Parasite Ecology -.:^-_r-::--—i—---_—L——I. -
Biology of Marine Fungi 20130420 151718.Pdf
Progress in Molecular and Subcellular Biology Series Editors Werner E.G. Mu¨ller Philippe Jeanteur, Robert E. Rhoads, Ðurðica Ugarkovic´, Ma´rcio Reis Custo´dio 53 Volumes Published in the Series Progress in Molecular Subseries: and Subcellular Biology Marine Molecular Biotechnology Volume 36 Volume 37 Viruses and Apoptosis Sponges (Porifera) C. Alonso (Ed.) W.E.G. Mu¨ller (Ed.) Volume 38 Volume 39 Epigenetics and Chromatin Echinodermata Ph. Jeanteur (Ed.) V. Matranga (Ed.) Volume 40 Volume 42 Developmental Biology of Neoplastic Antifouling Compounds Growth N. Fusetani and A.S. Clare (Eds.) A. Macieira-Coelho (Ed.) Volume 43 Volume 41 Molluscs Molecular Basis of Symbiosis G. Cimino and M. Gavagnin (Eds.) J. Overmann (Ed.) Volume 46 Volume 44 Marine Toxins as Research Tools Alternative Splicing and Disease N. Fusetani and W. Kem (Eds.) Ph. Jeanlevr (Ed.) Volume 47 Volume 45 Biosilica in Evolution, Morphogenesis, Asymmetric Cell Division and Nanobiotechnology A. Macieira Coelho (Ed.) W.E.G. Mu¨ller and M.A. Grachev (Eds.) Volume 48 Volume 52 Centromere Molecular Biomineralization Ðurdica- Ugarkovic´ (Ed.) W.E.G. Mu¨ller (Ed.) Volume 49 Volume 53 Aestivation Biology of Marine Fungi C.A. Navas and J.E. Carvalho (Eds.) C. Raghukumar (Ed.) Volume 50 miRNA Regulation of the Translational Machinery R.E. Rhoads (Ed.) Volume 51 Long Non-Coding RNAs Ðurdica- Ugarkovic (Ed.) Chandralata Raghukumar Editor Biology of Marine Fungi Editor Dr. Chandralata Raghukumar National Institute of Oceanography Marine Biotechnology Laboratory Dona Paula 403004 Panjim India [email protected] ISSN 0079-6484 ISBN 978-3-642-23341-8 e-ISBN 978-3-642-23342-5 DOI 10.1007/978-3-642-23342-5 Springer Heidelberg Dordrecht London New York Library of Congress Control Number: 2011943185 # Springer-Verlag Berlin Heidelberg 2012 This work is subject to copyright. -
Supplementary Table S1 18Jan 2021
Supplementary Table S1. Accurate scientific names of plant pathogenic fungi and secondary barcodes. Below is a list of the most important plant pathogenic fungi including Oomycetes with their accurate scientific names and synonyms. These scientific names include the results of the change to one scientific name for fungi. For additional information including plant hosts and localities worldwide as well as references consult the USDA-ARS U.S. National Fungus Collections (http://nt.ars- grin.gov/fungaldatabases/). Secondary barcodes, where available, are listed in superscript between round parentheses after generic names. The secondary barcodes listed here do not represent all known available loci for a given genus. Always consult recent literature for which primers and loci are required to resolve your species of interest. Also keep in mind that not all barcodes are available for all species of a genus and that not all species/genera listed below are known from sequence data. GENERA AND SPECIES NAME AND SYNONYMYS DISEASE SECONDARY BARCODES1 Kingdom Fungi Ascomycota Dothideomycetes Asterinales Asterinaceae Thyrinula(CHS-1, TEF1, TUB2) Thyrinula eucalypti (Cooke & Massee) H.J. Swart 1988 Target spot or corky spot of Eucalyptus Leptostromella eucalypti Cooke & Massee 1891 Thyrinula eucalyptina Petr. & Syd. 1924 Target spot or corky spot of Eucalyptus Lembosiopsis eucalyptina Petr. & Syd. 1924 Aulographum eucalypti Cooke & Massee 1889 Aulographina eucalypti (Cooke & Massee) Arx & E. Müll. 1960 Lembosiopsis australiensis Hansf. 1954 Botryosphaeriales Botryosphaeriaceae Botryosphaeria(TEF1, TUB2) Botryosphaeria dothidea (Moug.) Ces. & De Not. 1863 Canker, stem blight, dieback, fruit rot on Fusicoccum Sphaeria dothidea Moug. 1823 diverse hosts Fusicoccum aesculi Corda 1829 Phyllosticta divergens Sacc. 1891 Sphaeria coronillae Desm. -
Highly Rearranged Mitochondrial Genome in Nycteria Parasites (Haemosporidia) from Bats
Highly rearranged mitochondrial genome in Nycteria parasites (Haemosporidia) from bats Gregory Karadjiana,1,2, Alexandre Hassaninb,1, Benjamin Saintpierrec, Guy-Crispin Gembu Tungalunad, Frederic Arieye, Francisco J. Ayalaf,3, Irene Landaua, and Linda Duvala,3 aUnité Molécules de Communication et Adaptation des Microorganismes (UMR 7245), Sorbonne Universités, Muséum National d’Histoire Naturelle, CNRS, CP52, 75005 Paris, France; bInstitut de Systématique, Evolution, Biodiversité (UMR 7205), Sorbonne Universités, Muséum National d’Histoire Naturelle, CNRS, Université Pierre et Marie Curie, CP51, 75005 Paris, France; cUnité de Génétique et Génomique des Insectes Vecteurs (CNRS URA3012), Département de Parasites et Insectes Vecteurs, Institut Pasteur, 75015 Paris, France; dFaculté des Sciences, Université de Kisangani, BP 2012 Kisangani, Democratic Republic of Congo; eLaboratoire de Biologie Cellulaire Comparative des Apicomplexes, Faculté de Médicine, Université Paris Descartes, Inserm U1016, CNRS UMR 8104, Cochin Institute, 75014 Paris, France; and fDepartment of Ecology and Evolutionary Biology, University of California, Irvine, CA 92697 Contributed by Francisco J. Ayala, July 6, 2016 (sent for review March 18, 2016; reviewed by Sargis Aghayan and Georges Snounou) Haemosporidia parasites have mostly and abundantly been de- and this lack of knowledge limits the understanding of the scribed using mitochondrial genes, and in particular cytochrome evolutionary history of Haemosporidia, in particular their b (cytb). Failure to amplify the mitochondrial cytb gene of Nycteria basal diversification. parasites isolated from Nycteridae bats has been recently reported. Nycteria parasites have been primarily described, based on Bats are hosts to a diverse and profuse array of Haemosporidia traditional taxonomy, in African insectivorous bats of two fami- parasites that remain largely unstudied. -
Troccap-Feline-Endo-Guidelines
Disclaimer The guidelines presented in this booklet were independently developed by members of the Tropical Council for Companion Animal Parasites Ltd. These best-practice guidelines are based on evidence-based, peer reviewed, published scientific literature. The authors of these guidelines have made considerable efforts to ensure the information upon which they are based is accurate and up-to-date. Individual circumstances must be taken into account where appropriate when following the recommendations in these guidelines. Sponsors The Tropical Council for Companion Animal Parasites Ltd. wish to acknowledge the kind donations of our sponsors for facilitating the publication of these freely available guidelines. Contents General considerations and recommendations .......................................................... 1 Diagnosis ................................................................................................................ 1 Treatment ............................................................................................................... 1 Prevention and control ............................................................................................ 1 Public health considerations ................................................................................... 2 Gastrointestinal Parasites .......................................................................................... 3 Ascarids (Toxocara spp., Toxascaris leonina) ........................................................ 3 Hookworms (Ancylostoma -
Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes
University of Rhode Island DigitalCommons@URI Biological Sciences Faculty Publications Biological Sciences 9-26-2018 Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes Christopher E. Lane Et Al Follow this and additional works at: https://digitalcommons.uri.edu/bio_facpubs Journal of Eukaryotic Microbiology ISSN 1066-5234 ORIGINAL ARTICLE Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes Sina M. Adla,* , David Bassb,c , Christopher E. Laned, Julius Lukese,f , Conrad L. Schochg, Alexey Smirnovh, Sabine Agathai, Cedric Berneyj , Matthew W. Brownk,l, Fabien Burkim,PacoCardenas n , Ivan Cepi cka o, Lyudmila Chistyakovap, Javier del Campoq, Micah Dunthornr,s , Bente Edvardsent , Yana Eglitu, Laure Guillouv, Vladimır Hamplw, Aaron A. Heissx, Mona Hoppenrathy, Timothy Y. Jamesz, Anna Karn- kowskaaa, Sergey Karpovh,ab, Eunsoo Kimx, Martin Koliskoe, Alexander Kudryavtsevh,ab, Daniel J.G. Lahrac, Enrique Laraad,ae , Line Le Gallaf , Denis H. Lynnag,ah , David G. Mannai,aj, Ramon Massanaq, Edward A.D. Mitchellad,ak , Christine Morrowal, Jong Soo Parkam , Jan W. Pawlowskian, Martha J. Powellao, Daniel J. Richterap, Sonja Rueckertaq, Lora Shadwickar, Satoshi Shimanoas, Frederick W. Spiegelar, Guifre Torruellaat , Noha Youssefau, Vasily Zlatogurskyh,av & Qianqian Zhangaw a Department of Soil Sciences, College of Agriculture and Bioresources, University of Saskatchewan, Saskatoon, S7N 5A8, SK, Canada b Department of Life Sciences, The Natural History Museum, Cromwell Road, London, SW7 5BD, United Kingdom -
Iipcr Assay List 2020.Xlsx
GeneReach Biotechnology Corp. Human Aquaculture Companion animal Livestock Diseases Emerging Human Shrimp Fish Canine Feline Equine Bovine Poultry Swine Ruminant Diseases Diseases AHPND/EMS Aeromonas Anaplasma Bartonella Anaplasma Bovine Actinobacillus Bluetongue Bacillus ALV-J C. difficile Plasmid salmonicida platys henselae phagocytophilum Leukemia Virus Pleuropneumonia Virus anthracis PL3 AHPND/EMS Carp Edema Bordetella Bovine Papular Avian Influenza Africa Swine Fever Bacillus Babesia gibsoni EAV Brucella abortus Chagas Disease Toxin 1 Virus (CEV) bronchiseptica Stomatitis Virus H9 Virus anthracis pXO1 Candidatus Baculovirus Flavobacterium Bordetella Bovine Avian Brachyspira Brucella Bacillus Chikungunya Mycoplasma EHV-1 penaei psychrophilum bronchiseptica Tuberculosis metapneumovirus hyodysenteriae melitensis anthracis pXO2 virus haemominutum Candidatus Avian Reovirus IRIDO- Canine Adeno Brucella Chlamydia CMNV Mycoplasma EHV-3 Brucella abortus (Asia & America Chlamydia psittaci Brucella spp. Megalocytivirus Virus 2 abortus psittaci turicensis regions only) Crimean-Congo Crimean–Congo IRIDO- Chlamydophila Chicken infectious Brucella EHP Canine Babesia EHV-4 Brucella spp. CSFV Hemorrhagic hemorrhagic Ranaviruses felis anemia virus melitensis Fever fever Canine Influenza Duck Virus IHHNV ISAV Cytauxzoon felis EIAV BVDV-1 FMDV FMDV Brucella spp. Dengue Virus Virus Enteritis Virus Fowl adenovirus Infectious Canine Filariasis (Brugia IMNV KHV D. immitis Influenza H3N8 BVDV-2 (Pan Adv, type 4, JEV Bovine Chagas disease Leishmaniasis spp.) -
Emerging Human Babesiosis with “Ground Zero” in North America
microorganisms Review Emerging Human Babesiosis with “Ground Zero” in North America Yi Yang 1, Jevan Christie 2, Liza Köster 3 , Aifang Du 1,* and Chaoqun Yao 4,* 1 Department of Veterinary Medicine, College of Animal Sciences, Zhejiang Provincial Key Laboratory of Preventive Veterinary Medicine, Zhejiang University, Hangzhou 310058, China; [email protected] 2 The Animal Hospital, Murdoch University, 90 South Street, Murdoch, WA 6150, Australia; [email protected] 3 Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Tennessee, 2407 River Drive, Knoxville, TN 37996, USA; [email protected] 4 Department of Biomedical Sciences and One Health Center for Zoonoses and Tropical Veterinary Medicine, Ross University School of Veterinary Medicine, Basseterre 00334, Saint Kitts and Nevis * Correspondence: [email protected] (A.D.); [email protected] (C.Y.) Abstract: The first case of human babesiosis was reported in the literature in 1957. The clinical disease has sporadically occurred as rare case reports in North America and Europe in the subsequent decades. Since the new millennium, especially in the last decade, many more cases have apparently appeared not only in these regions but also in Asia, South America, and Africa. More than 20,000 cases of human babesiosis have been reported in North America alone. In several cross-sectional surveys, exposure to Babesia spp. has been demonstrated within urban and rural human populations with clinical babesiosis reported in both immunocompromised and immunocompetent humans. This review serves to highlight the widespread distribution of these tick-borne pathogens in humans, their tick vectors in readily accessible environments such as parks and recreational areas, and their Citation: Yang, Y.; Christie, J.; Köster, phylogenetic relationships. -
Abstracts and Presenter Biographical Information Oral Presentations
ABSTRACTS AND PRESENTER BIOGRAPHICAL INFORMATION ORAL PRESENTATIONS Abstracts for oral presentations and biographical information for presenters are listed alphabetically below by presenting author’s last name. Abstracts and biographical information appear unmodified, as submitted by the corresponding authors. Day, time, and room number of presentation are also provided. Abatzoglou, John John Abatzoglou, Assistant Professor of Geography, University of Idaho. Research interests span the weather-climate continuum and both basic and applied scientific questions on past, present and future climate dynamics as well as their influence on wildfire, ecology and agriculture and is a key player in the development of integrated climate scenarios for the Pacific Northwest, US. Oral presentation, Wednesday, 2:30 PM, B114 Will climate change increase the occurrence of megafires in the western United States? The largest wildfires in the western United States account for a substantial portion of annual area burned and are associated with numerous direct and indirect geophysical impacts in addition to commandeering suppression resources and national attention. While substantial prior work has been devoted to understand the influence of climate, and weather on annual area burned, there has been limited effort to identify factors that enable and drive the very largest wildfires, or megafires. We hypothesize that antecedent climate and shorter-term biophysically relevant meteorological variables play an essen- tial role in favoring or deterring historical megafire occurrence identified using the Monitoring Trends in Burn Severity Atlas from 1984-2010. Antecedent climatic factors such as drought and winter and spring temperature were found to vary markedly across geographic areas, whereas regional commonality of prolonged extremely low fuel moisture and high fire danger prior to and immediately following megafire discovery. -
Protista (PDF)
1 = Astasiopsis distortum (Dujardin,1841) Bütschli,1885 South Scandinavian Marine Protoctista ? Dingensia Patterson & Zölffel,1992, in Patterson & Larsen (™ Heteromita angusta Dujardin,1841) Provisional Check-list compiled at the Tjärnö Marine Biological * Taxon incertae sedis. Very similar to Cryptaulax Skuja Laboratory by: Dinomonas Kent,1880 TJÄRNÖLAB. / Hans G. Hansson - 1991-07 - 1997-04-02 * Taxon incertae sedis. Species found in South Scandinavia, as well as from neighbouring areas, chiefly the British Isles, have been considered, as some of them may show to have a slightly more northern distribution, than what is known today. However, species with a typical Lusitanian distribution, with their northern Diphylleia Massart,1920 distribution limit around France or Southern British Isles, have as a rule been omitted here, albeit a few species with probable norhern limits around * Marine? Incertae sedis. the British Isles are listed here until distribution patterns are better known. The compiler would be very grateful for every correction of presumptive lapses and omittances an initiated reader could make. Diplocalium Grassé & Deflandre,1952 (™ Bicosoeca inopinatum ??,1???) * Marine? Incertae sedis. Denotations: (™) = Genotype @ = Associated to * = General note Diplomita Fromentel,1874 (™ Diplomita insignis Fromentel,1874) P.S. This list is a very unfinished manuscript. Chiefly flagellated organisms have yet been considered. This * Marine? Incertae sedis. provisional PDF-file is so far only published as an Intranet file within TMBL:s domain. Diplonema Griessmann,1913, non Berendt,1845 (Diptera), nec Greene,1857 (Coel.) = Isonema ??,1???, non Meek & Worthen,1865 (Mollusca), nec Maas,1909 (Coel.) PROTOCTISTA = Flagellamonas Skvortzow,19?? = Lackeymonas Skvortzow,19?? = Lowymonas Skvortzow,19?? = Milaneziamonas Skvortzow,19?? = Spira Skvortzow,19?? = Teixeiromonas Skvortzow,19?? = PROTISTA = Kolbeana Skvortzow,19?? * Genus incertae sedis.