Ascaris Lumbricoides, Roundworm, Causative Agent Of
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Gastrointestinal Helminthic Parasites of Habituated Wild Chimpanzees
Aus dem Institut für Parasitologie und Tropenveterinärmedizin des Fachbereichs Veterinärmedizin der Freien Universität Berlin Gastrointestinal helminthic parasites of habituated wild chimpanzees (Pan troglodytes verus) in the Taï NP, Côte d’Ivoire − including characterization of cultured helminth developmental stages using genetic markers Inaugural-Dissertation zur Erlangung des Grades eines Doktors der Veterinärmedizin an der Freien Universität Berlin vorgelegt von Sonja Metzger Tierärztin aus München Berlin 2014 Journal-Nr.: 3727 Gedruckt mit Genehmigung des Fachbereichs Veterinärmedizin der Freien Universität Berlin Dekan: Univ.-Prof. Dr. Jürgen Zentek Erster Gutachter: Univ.-Prof. Dr. Georg von Samson-Himmelstjerna Zweiter Gutachter: Univ.-Prof. Dr. Heribert Hofer Dritter Gutachter: Univ.-Prof. Dr. Achim Gruber Deskriptoren (nach CAB-Thesaurus): chimpanzees, helminths, host parasite relationships, fecal examination, characterization, developmental stages, ribosomal RNA, mitochondrial DNA Tag der Promotion: 10.06.2015 Contents I INTRODUCTION ---------------------------------------------------- 1- 4 I.1 Background 1- 3 I.2 Study objectives 4 II LITERATURE OVERVIEW --------------------------------------- 5- 37 II.1 Taï National Park 5- 7 II.1.1 Location and climate 5- 6 II.1.2 Vegetation and fauna 6 II.1.3 Human pressure and impact on the park 7 II.2 Chimpanzees 7- 12 II.2.1 Status 7 II.2.2 Group sizes and composition 7- 9 II.2.3 Territories and ranging behavior 9 II.2.4 Diet and hunting behavior 9- 10 II.2.5 Contact with humans 10 II.2.6 -
Free-Living Marine Nematodes from San Antonio Bay (Río Negro, Argentina)
A peer-reviewed open-access journal ZooKeys 574: 43–55Free-living (2016) marine nematodes from San Antonio Bay (Río Negro, Argentina) 43 doi: 10.3897/zookeys.574.7222 DATA PAPER http://zookeys.pensoft.net Launched to accelerate biodiversity research Free-living marine nematodes from San Antonio Bay (Río Negro, Argentina) Gabriela Villares1, Virginia Lo Russo1, Catalina Pastor de Ward1, Viviana Milano2, Lidia Miyashiro3, Renato Mazzanti3 1 Laboratorio de Meiobentos LAMEIMA-CENPAT-CONICET, Boulevard Brown 2915, U9120ACF, Puerto Madryn, Argentina 2 Universidad Nacional de la Patagonia San Juan Bosco, sede Puerto Madryn. Boulevard Brown 3051, U9120ACF, Puerto Madryn, Argentina 3Centro de Cómputos CENPAT-CONICET, Boulevard Brown 2915, U9120ACF, Puerto Madryn, Argentina Corresponding author: Gabriela Villares ([email protected]) Academic editor: H-P Fagerholm | Received 18 November 2015 | Accepted 11 February 2016 | Published 28 March 2016 http://zoobank.org/3E8B6DD5-51FA-499D-AA94-6D426D5B1913 Citation: Villares G, Lo Russo V, Pastor de Ward C, Milano V, Miyashiro L, Mazzanti R (2016) Free-living marine nematodes from San Antonio Bay (Río Negro, Argentina). ZooKeys 574: 43–55. doi: 10.3897/zookeys.574.7222 Abstract The dataset of free-living marine nematodes of San Antonio Bay is based on sediment samples collected in February 2009 during doctoral theses funded by CONICET grants. A total of 36 samples has been taken at three locations in the San Antonio Bay, Santa Cruz Province, Argentina on the coastal littoral at three tidal levels. This presents a unique and important collection for benthic biodiversity assessment of Patagonian nematodes as this area remains one of the least known regions. -
The Influence of Human Settlements on Gastrointestinal Helminths of Wild Monkey Populations in Their Natural Habitat
The influence of human settlements on gastrointestinal helminths of wild monkey populations in their natural habitat Zur Erlangung des akademischen Grades eines DOKTORS DER NATURWISSENSCHAFTEN (Dr. rer. nat.) Fakultät für Chemie und Biowissenschaften Karlsruher Institut für Technologie (KIT) – Universitätsbereich genehmigte DISSERTATION von Dipl. Biol. Alexandra Mücke geboren in Germersheim Dekan: Prof. Dr. Martin Bastmeyer Referent: Prof. Dr. Horst F. Taraschewski 1. Korreferent: Prof. Dr. Eckhard W. Heymann 2. Korreferent: Prof. Dr. Doris Wedlich Tag der mündlichen Prüfung: 16.12.2011 To Maya Index of Contents I Index of Contents Index of Tables ..............................................................................................III Index of Figures............................................................................................. IV Abstract .......................................................................................................... VI Zusammenfassung........................................................................................VII Introduction ......................................................................................................1 1.1 Why study primate parasites?...................................................................................2 1.2 Objectives of the study and thesis outline ................................................................4 Literature Review.............................................................................................7 2.1 Parasites -
Guide to the Parasites of Fishes of Canada Part V: Nematoda
Wilfrid Laurier University Scholars Commons @ Laurier Biology Faculty Publications Biology 2016 ZOOTAXA: Guide to the Parasites of Fishes of Canada Part V: Nematoda Hisao P. Arai Pacific Biological Station John W. Smith Wilfrid Laurier University Follow this and additional works at: https://scholars.wlu.ca/biol_faculty Part of the Biology Commons, and the Marine Biology Commons Recommended Citation Arai, Hisao P., and John W. Smith. Zootaxa: Guide to the Parasites of Fishes of Canada Part V: Nematoda. Magnolia Press, 2016. This Book is brought to you for free and open access by the Biology at Scholars Commons @ Laurier. It has been accepted for inclusion in Biology Faculty Publications by an authorized administrator of Scholars Commons @ Laurier. For more information, please contact [email protected]. Zootaxa 4185 (1): 001–274 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Monograph ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4185.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:0D054EDD-9CDC-4D16-A8B2-F1EBBDAD6E09 ZOOTAXA 4185 Guide to the Parasites of Fishes of Canada Part V: Nematoda HISAO P. ARAI3, 5 & JOHN W. SMITH4 3Pacific Biological Station, Nanaimo, British Columbia V9R 5K6 4Department of Biology, Wilfrid Laurier University, Waterloo, Ontario N2L 3C5. E-mail: [email protected] 5Deceased Magnolia Press Auckland, New Zealand Accepted by K. DAVIES (Initially edited by M.D.B. BURT & D.F. McALPINE): 5 Apr. 2016; published: 8 Nov. 2016 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 HISAO P. ARAI & JOHN W. -
Ahead of Print Online Version Phylogenetic Relationships of Some
Ahead of print online version FOLIA PARASITOLOGICA 58[2]: 135–148, 2011 © Institute of Parasitology, Biology Centre ASCR ISSN 0015-5683 (print), ISSN 1803-6465 (online) http://www.paru.cas.cz/folia/ Phylogenetic relationships of some spirurine nematodes (Nematoda: Chromadorea: Rhabditida: Spirurina) parasitic in fishes inferred from SSU rRNA gene sequences Eva Černotíková1,2, Aleš Horák1 and František Moravec1 1 Institute of Parasitology, Biology Centre of the Academy of Sciences of the Czech Republic, Branišovská 31, 370 05 České Budějovice, Czech Republic; 2 Faculty of Science, University of South Bohemia, Branišovská 31, 370 05 České Budějovice, Czech Republic Abstract: Small subunit rRNA sequences were obtained from 38 representatives mainly of the nematode orders Spirurida (Camalla- nidae, Cystidicolidae, Daniconematidae, Philometridae, Physalopteridae, Rhabdochonidae, Skrjabillanidae) and, in part, Ascaridida (Anisakidae, Cucullanidae, Quimperiidae). The examined nematodes are predominantly parasites of fishes. Their analyses provided well-supported trees allowing the study of phylogenetic relationships among some spirurine nematodes. The present results support the placement of Cucullanidae at the base of the suborder Spirurina and, based on the position of the genus Philonema (subfamily Philoneminae) forming a sister group to Skrjabillanidae (thus Philoneminae should be elevated to Philonemidae), the paraphyly of the Philometridae. Comparison of a large number of sequences of representatives of the latter family supports the paraphyly of the genera Philometra, Philometroides and Dentiphilometra. The validity of the newly included genera Afrophilometra and Carangi- nema is not supported. These results indicate geographical isolation has not been the cause of speciation in this parasite group and no coevolution with fish hosts is apparent. On the contrary, the group of South-American species ofAlinema , Nilonema and Rumai is placed in an independent branch, thus markedly separated from other family members. -
Nematodes in Aquatic Environments Adaptations and Survival Strategies
Biodiversity Journal , 2012, 3 (1): 13-40 Nematodes in aquatic environments: adaptations and survival strategies Qudsia Tahseen Nematode Research Laboratory, Department of Zoology, Aligarh Muslim University, Aligarh-202002, India; e-mail: [email protected]. ABSTRACT Nematodes are found in all substrata and sediment types with fairly large number of species that are of considerable ecological importance. Despite their simple body organization, they are the most complex forms with many metabolic and developmental processes comparable to higher taxa. Phylum Nematoda represents a diverse array of taxa present in subterranean environment. It is due to the formative constraints to which these individuals are exposed in the interstitial system of medium and coarse sediments that they show pertinent characteristic features to survive successfully in aquatic environments. They represent great degree of mor - phological adaptations including those associated with cuticle, sensilla, pseudocoelomic in - clusions, stoma, pharynx and tail. Their life cycles as well as development seem to be entrained to the environment type. Besides exhibiting feeding adaptations according to the substrata and sediment type and the kind of food available, the aquatic nematodes tend to wi - thstand various stresses by undergoing cryobiosis, osmobiosis, anoxybiosis as well as thio - biosis involving sulphide detoxification mechanism. KEY WORDS Adaptations; fresh water nematodes; marine nematodes; morphology; ecology; development. Received 24.01.2012; accepted 23.02.2012; -
Redalyc.First Record of Intestinal Parasites in a Wild Population Of
Revista Brasileira de Parasitologia Veterinária ISSN: 0103-846X [email protected] Colégio Brasileiro de Parasitologia Veterinária Brasil Srbek-Araujo, Ana Carolina; Costa Santos, Juliana Lúcia; Medeiros de Almeida, Viviane; Pezzi Guimarães, Marcos; Garcia Chiarello, Adriano First record of intestinal parasites in a wild population of jaguar in the Brazilian Atlantic Forest Revista Brasileira de Parasitologia Veterinária, vol. 23, núm. 3, julio-septiembre, 2014, pp. 393-398 Colégio Brasileiro de Parasitologia Veterinária Jaboticabal, Brasil Available in: http://www.redalyc.org/articulo.oa?id=397841493016 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Research note Braz. J. Vet. Parasitol., Jaboticabal, v. 23, n. 3, p. 393-398, jul.-set. 2014 ISSN 0103-846X (Print) / ISSN 1984-2961 (Electronic) Doi: http://dx.doi.org/10.1590/S1984-29612014065 First record of intestinal parasites in a wild population of jaguar in the Brazilian Atlantic Forest Primeiros registros de parasitos intestinais em uma população silvestre de onça-pintada na Mata Atlântica Brasileira Ana Carolina Srbek-Araujo1,2*; Juliana Lúcia Costa Santos3; Viviane Medeiros de Almeida3; Marcos Pezzi Guimarães3; Adriano Garcia Chiarello4 1Programa de Pós-graduação em Ecologia de Ecossistemas, Universidade Vila Velha – UVV, Vila Velha, ES, -
Proteomic Insights Into the Biology of the Most Important Foodborne Parasites in Europe
foods Review Proteomic Insights into the Biology of the Most Important Foodborne Parasites in Europe Robert Stryi ´nski 1,* , El˙zbietaŁopie ´nska-Biernat 1 and Mónica Carrera 2,* 1 Department of Biochemistry, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, 10-719 Olsztyn, Poland; [email protected] 2 Department of Food Technology, Marine Research Institute (IIM), Spanish National Research Council (CSIC), 36-208 Vigo, Spain * Correspondence: [email protected] (R.S.); [email protected] (M.C.) Received: 18 August 2020; Accepted: 27 September 2020; Published: 3 October 2020 Abstract: Foodborne parasitoses compared with bacterial and viral-caused diseases seem to be neglected, and their unrecognition is a serious issue. Parasitic diseases transmitted by food are currently becoming more common. Constantly changing eating habits, new culinary trends, and easier access to food make foodborne parasites’ transmission effortless, and the increase in the diagnosis of foodborne parasitic diseases in noted worldwide. This work presents the applications of numerous proteomic methods into the studies on foodborne parasites and their possible use in targeted diagnostics. Potential directions for the future are also provided. Keywords: foodborne parasite; food; proteomics; biomarker; liquid chromatography-tandem mass spectrometry (LC-MS/MS) 1. Introduction Foodborne parasites (FBPs) are becoming recognized as serious pathogens that are considered neglect in relation to bacteria and viruses that can be transmitted by food [1]. The mode of infection is usually by eating the host of the parasite as human food. Many of these organisms are spread through food products like uncooked fish and mollusks; raw meat; raw vegetables or fresh water plants contaminated with human or animal excrement. -
Origin and Evolution of the Notch Signalling Pathway: an Overview from Eukaryotic Genomes
Origin and evolution of the Notch signalling pathway: an overview from eukaryotic genomes. Eve Gazave, Pascal Lapébie, Gemma S Richards, Frédéric Brunet, Alexander V Ereskovsky, Bernard M Degnan, Carole Borchiellini, Michel Vervoort, Emmanuelle Renard To cite this version: Eve Gazave, Pascal Lapébie, Gemma S Richards, Frédéric Brunet, Alexander V Ereskovsky, et al.. Origin and evolution of the Notch signalling pathway: an overview from eukaryotic genomes.. BMC Evolutionary Biology, BioMed Central, 2009, 9 (1), pp.249. 10.1186/1471-2148-9-249. hal-00493284 HAL Id: hal-00493284 https://hal.archives-ouvertes.fr/hal-00493284 Submitted on 2 May 2019 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. BMC Evolutionary Biology BioMed Central Research article Open Access Origin and evolution of the Notch signalling pathway: an overview from eukaryotic genomes Eve Gazave1, Pascal Lapébie1, Gemma S Richards2, Frédéric Brunet3, Alexander V Ereskovsky1,4, Bernard M Degnan2, Carole Borchiellini1, Michel Vervoort5,6 and Emmanuelle Renard*1 Address: 1Aix-Marseille -
(Stsm) Scientific Report
SHORT TERM SCIENTIFIC MISSION (STSM) SCIENTIFIC REPORT This report is submitted for approval by the STSM applicant to the STSM coordinator Action number: CA15219-45333 STSM title: Free-living marine nematodes from the eastern Mediterranean deep sea - connecting COI and 18S rRNA barcodes to structure and function STSM start and end date: 06/02/2020 to 18/3/2020 (short than the planned two months due to the Co-Vid 19 virus pandemic) Grantee name: Zoya Garbuzov PURPOSE OF THE STSM: My Ph.D. thesis is devoted to the population ecology of free-living nematodes inhabiting deep-sea soft substrates of the Mediterranean Levantine Basin. The success of the study largely depends on my ability to accurately identify collected nematodes at the species level, essential for appropriate environmental analysis. Morphological identification of nematodes at the species level is fraught with difficulties, mainly because of their relatively simple body shape and the absence of distinctive morphological characters. Therefore, a combination of morphological identification to genus level and the use of molecular markers to reach species identification is assumed to provide a better distinction of species in this difficult to identify group. My STSM host, Dr. Nikolaos Lampadariou, is an experienced taxonomist and nematode ecologist. In addition, I will have access to the molecular laboratory of Dr. Panagiotis Kasapidis. Both researchers are based at the Hellenic Center for Marine Research (HCMR) in Crete and this STSM is aimed at combining morphological taxonomy, under the supervision of Dr. Lampadariou, with my recently acquired experience in nematode molecular taxonomy for relating molecular identifiers to nematode morphology. -
Analyses of Compact Trichinella Kinomes Reveal a MOS-Like Protein Kinase with a Unique N-Terminal Domain
G3: Genes|Genomes|Genetics Early Online, published on July 13, 2016 as doi:10.1534/g3.116.032961 G3 Genes | Genomes | Genetics R1_23_06_16 (~ 5500 words) Analyses of Compact Trichinella Kinomes Reveal a MOS-like Protein Kinase with a Unique N-terminal Domain Andreas J. Stroehlein*, Neil D. Young*, Pasi K. Korhonen*, Bill C.H. Chang*,†, Paul W. Sternberg‡, Giuseppe La Rosa§, Edoardo Pozio§ and Robin B. Gasser*,1 *Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, Victoria 3010, Australia †Yourgene Bioscience, Shu-Lin District, New Taipei City 23863, Taiwan ‡HHMI and Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, California 91125, USA §Istituto Superiore di Sanità, 00161 Rome, Italy 1Corresponding author: Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Corner of Flemington Road & Park Drive, Parkville, Victoria 3010, Australia. E- mail: [email protected] Abbreviations AGC, protein kinases A, G and C, and other nucleoside-regulated kinases; aPK, atypical protein kinase; CAMK, Ca2+/calmodulin-dependent kinase; CK1, casein kinase 1; CMGC, cyclin-dependent kinases (CDKs), mitogen-activated protein kinases (MAPKs), glycogen synthase kinases (GSKs) and CDK-like kinases; ePK, eukaryotic protein kinase; KEGG, Kyoto Encyclopedia of Genes and Genomes; MLKL, mixed-lineage kinase domain-like protein; MOS, v-mos Moloney murine sarcoma viral oncogene homolog; RGC, receptor guanylate cyclase; STE, MAPK cascade kinases; TK, tyrosine kinase; TKL, tyrosine kinase-like kinase; TTBK, tau-tubulin kinase. 1 © The Author(s) 2013. Published by the Genetics Society of America. G3 Genes | Genomes | Genetics R1_23_06_16 (~ 5500 words) ABSTRACT Parasitic worms of the genus Trichinella (phylum Nematoda; class Enoplea) represent a complex of at least twelve taxa that infect a range of different host animals, including humans, around the world. -
Ascaris Lumbricoides
Vivek Dixit ASCARIS LUMBRICOIDES Kingdom: Animalia Phylum: Nematoda Class: Chromadorea Order: Ascaridida Family: Ascarididae Genus: Ascaris Species: A. lumbricoides Ascaris lumbricoides The number of people in the world with Ascaris is probably second only to those infected with the pinworm, Enterobius vermicularis. Ascaris was well known in Roman times as Lumbricus teres (confused with the common earthworm) and has probably been infecting humans for thousands of years. It is prevalent in moist, warm climates, but can also survive in the temperate zones. Ascaris species are very large (adult females: 20 to 35 cm; adult males: 15 to 30 cm) nematodes (roundworms) that parasitize the human intestine. A. lumbricoides is the primary species involved in human infections globally. The adult worms are cylindrical, with a tapering anterior end. They are the largest of the common nematode parasites of humans; females measure 20 to 35 cm long and the males are 15 to 31 cm long, with a curved posterior end. Also, the three well developed lips are characteristic of this group. Infection in humans is acquired through ingestion of the embryonated eggs from contaminated soil. On ingestion, the eggs hatch in the stomach and duodenum, where the larvae actively penetrate the intestinal wall; they are then carried to the right heart via the hepatic portal circulation. Then the larvae are carried into the pulmonary circulation, where they are filtered out by the capillaries. After approximately 10 days in the lung, the larvae break into the alveoli, migrate via the bronchi until they reach the trachea and pharynx, and are then swallowed.