Classification and Nomenclature of Human Parasites Lynne S
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Coccidiosis in Chickens Maurice Pitesky DVM, MPVM, ACPVM, University of California Cooperative Extension, UC Davis School of Veterinary Medicine
Coccidiosis in Chickens Maurice Pitesky DVM, MPVM, ACPVM, University of California Cooperative Extension, UC Davis School of Veterinary Medicine Understanding the basics of common poultry diseases are essential for poultry owners primarily because knowledge of common poultry diseases gives owners the tools to treat and prevent future outbreaks of disease. Avian intestinal coccidiosis is a ubiquitous protozoal gastrointestinal (GI) parasite (i.e. microscopic single celled organism) which primarily affects young chickens. Clinical signs include mucoid or bloody diarrhea, dehydration, anemia, listlessness, ruffled feathers, suboptimal growth and death. In addition, in laying hens coccidiosis is commonly associated with a drop in egg production. In chickens there are nine different types of coccidia. It is important to realize that all coccidia are not created equally. Specifically, clinical disease is dependent on which species of coccidia are present and in what quantities they are present. Consequently, the presence of a few coccidial eggs or oocysts may not justify a diagnosis of clinical disease. These differences and subtilties can be difficult for poultry owners who may want to simply know if there chickens have coccidia. In addition, control of coccidia can be difficult in backyard flocks because of the presence of mixed aged flocks. In mixed aged flocks, older apparently ‘healthy’ chickens can shed coccidial oocysts in their feces and subsequently infect younger chicks. The following article is designed to educate backyard poultry owners about relevant aspects of the biology and epidemiology of coccidiosis in order to facilitate control and if necessary treatment of infections. Bio 101 of Coccidiosis: Coccidiosis refers to protozoa (i.e. -
Basal Body Structure and Composition in the Apicomplexans Toxoplasma and Plasmodium Maria E
Francia et al. Cilia (2016) 5:3 DOI 10.1186/s13630-016-0025-5 Cilia REVIEW Open Access Basal body structure and composition in the apicomplexans Toxoplasma and Plasmodium Maria E. Francia1* , Jean‑Francois Dubremetz2 and Naomi S. Morrissette3 Abstract The phylum Apicomplexa encompasses numerous important human and animal disease-causing parasites, includ‑ ing the Plasmodium species, and Toxoplasma gondii, causative agents of malaria and toxoplasmosis, respectively. Apicomplexans proliferate by asexual replication and can also undergo sexual recombination. Most life cycle stages of the parasite lack flagella; these structures only appear on male gametes. Although male gametes (microgametes) assemble a typical 9 2 axoneme, the structure of the templating basal body is poorly defined. Moreover, the rela‑ tionship between asexual+ stage centrioles and microgamete basal bodies remains unclear. While asexual stages of Plasmodium lack defined centriole structures, the asexual stages of Toxoplasma and closely related coccidian api‑ complexans contain centrioles that consist of nine singlet microtubules and a central tubule. There are relatively few ultra-structural images of Toxoplasma microgametes, which only develop in cat intestinal epithelium. Only a subset of these include sections through the basal body: to date, none have unambiguously captured organization of the basal body structure. Moreover, it is unclear whether this basal body is derived from pre-existing asexual stage centrioles or is synthesized de novo. Basal bodies in Plasmodium microgametes are thought to be synthesized de novo, and their assembly remains ill-defined. Apicomplexan genomes harbor genes encoding δ- and ε-tubulin homologs, potentially enabling these parasites to assemble a typical triplet basal body structure. -
Balantidium Coli
GLOBAL WATER PATHOGEN PROJECT PART THREE. SPECIFIC EXCRETED PATHOGENS: ENVIRONMENTAL AND EPIDEMIOLOGY ASPECTS BALANTIDIUM COLI Francisco Ponce-Gordo Complutense University Madrid, Spain Kateřina Jirků-Pomajbíková Institute of Parasitology Biology Centre, ASCR, v.v.i. Budweis, Czech Republic Copyright: This publication is available in Open Access under the Attribution-ShareAlike 3.0 IGO (CC-BY-SA 3.0 IGO) license (http://creativecommons.org/licenses/by-sa/3.0/igo). By using the content of this publication, the users accept to be bound by the terms of use of the UNESCO Open Access Repository (http://www.unesco.org/openaccess/terms-use-ccbysa-en). Disclaimer: The designations employed and the presentation of material throughout this publication do not imply the expression of any opinion whatsoever on the part of UNESCO concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. The ideas and opinions expressed in this publication are those of the authors; they are not necessarily those of UNESCO and do not commit the Organization. Citation: Ponce-Gordo, F., Jirků-Pomajbíková, K. 2017. Balantidium coli. In: J.B. Rose and B. Jiménez-Cisneros, (eds) Global Water Pathogens Project. http://www.waterpathogens.org (R. Fayer and W. Jakubowski, (eds) Part 3 Protists) http://www.waterpathogens.org/book/balantidium-coli Michigan State University, E. Lansing, MI, UNESCO. Acknowledgements: K.R.L. Young, Project Design editor; Website Design (http://www.agroknow.com) Published: January 15, 2015, 11:50 am, Updated: October 18, 2017, 5:43 pm Balantidium coli Summary 1.1.1 Global distribution Balantidium coli is reported worldwide although it is To date, Balantidium coli is the only ciliate protozoan more common in temperate and tropical regions (Areán and reported to infect the gastrointestinal track of humans. -
The Functional Parasitic Worm Secretome: Mapping the Place of Onchocerca Volvulus Excretory Secretory Products
pathogens Review The Functional Parasitic Worm Secretome: Mapping the Place of Onchocerca volvulus Excretory Secretory Products Luc Vanhamme 1,*, Jacob Souopgui 1 , Stephen Ghogomu 2 and Ferdinand Ngale Njume 1,2 1 Department of Molecular Biology, Institute of Biology and Molecular Medicine, IBMM, Université Libre de Bruxelles, Rue des Professeurs Jeener et Brachet 12, 6041 Gosselies, Belgium; [email protected] (J.S.); [email protected] (F.N.N.) 2 Molecular and Cell Biology Laboratory, Biotechnology Unit, University of Buea, Buea P.O Box 63, Cameroon; [email protected] * Correspondence: [email protected] Received: 28 October 2020; Accepted: 18 November 2020; Published: 23 November 2020 Abstract: Nematodes constitute a very successful phylum, especially in terms of parasitism. Inside their mammalian hosts, parasitic nematodes mainly dwell in the digestive tract (geohelminths) or in the vascular system (filariae). One of their main characteristics is their long sojourn inside the body where they are accessible to the immune system. Several strategies are used by parasites in order to counteract the immune attacks. One of them is the expression of molecules interfering with the function of the immune system. Excretory-secretory products (ESPs) pertain to this category. This is, however, not their only biological function, as they seem also involved in other mechanisms such as pathogenicity or parasitic cycle (molting, for example). Wewill mainly focus on filariae ESPs with an emphasis on data available regarding Onchocerca volvulus, but we will also refer to a few relevant/illustrative examples related to other worm categories when necessary (geohelminth nematodes, trematodes or cestodes). -
Exposure to Parasitic Protists and Helminths Changes the Intestinal Community Structure Of
bioRxiv preprint doi: https://doi.org/10.1101/717165; this version posted July 28, 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. 1 Title: Exposure to parasitic protists and helminths changes the intestinal community structure of 2 bacterial microbiota but not of eukaryotes in a cohort of mother-child binomial from a semi-rural 3 setting in Mexico 4 Running title: Parasites affect intestinal microbiome 5 Oswaldo Partida-Rodriguez1,2, Miriam Nieves-Ramirez1,2, Isabelle Laforest-Lapointe3,4, Eric Brown2, 6 Laura Parfrey5,6, Lisa Reynolds2, Alicia Valadez-Salazar1, Lisa Thorson2, Patricia Morán1, Enrique 7 Gonzalez1, Edgar Rascon1, Ulises Magaña1, Eric Hernandez1, Liliana Rojas-V1, Javier Torres7, Marie 8 Claire Arrieta2,3,4*, Cecilia Ximenez1*#, Brett Finlay2,8,9* 9 * Senior authors, contributed equally. 10 1Laboratorio de Inmunología del Departamento de Medicina Experimental, UNAM, Mexico City, Mexico 11 2Michael Smith Laboratories, Department of Microbiology & Immunology, University of British 12 Columbia, Vancouver, British Columbia, Canada 13 3Department of Physiology & Pharmacology, University of Calgary, Calgary, Alberta, Canada 14 4Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada 15 5Department of Zoology, University of British Columbia, Vancouver, British Columbia, Canada 16 6Department of Botany, University -
Baylisascariasis
Baylisascariasis Importance Baylisascaris procyonis, an intestinal nematode of raccoons, can cause severe neurological and ocular signs when its larvae migrate in humans, other mammals and birds. Although clinical cases seem to be rare in people, most reported cases have been Last Updated: December 2013 serious and difficult to treat. Severe disease has also been reported in other mammals and birds. Other species of Baylisascaris, particularly B. melis of European badgers and B. columnaris of skunks, can also cause neural and ocular larva migrans in animals, and are potential human pathogens. Etiology Baylisascariasis is caused by intestinal nematodes (family Ascarididae) in the genus Baylisascaris. The three most pathogenic species are Baylisascaris procyonis, B. melis and B. columnaris. The larvae of these three species can cause extensive damage in intermediate/paratenic hosts: they migrate extensively, continue to grow considerably within these hosts, and sometimes invade the CNS or the eye. Their larvae are very similar in appearance, which can make it very difficult to identify the causative agent in some clinical cases. Other species of Baylisascaris including B. transfuga, B. devos, B. schroeder and B. tasmaniensis may also cause larva migrans. In general, the latter organisms are smaller and tend to invade the muscles, intestines and mesentery; however, B. transfuga has been shown to cause ocular and neural larva migrans in some animals. Species Affected Raccoons (Procyon lotor) are usually the definitive hosts for B. procyonis. Other species known to serve as definitive hosts include dogs (which can be both definitive and intermediate hosts) and kinkajous. Coatimundis and ringtails, which are closely related to kinkajous, might also be able to harbor B. -
Combination Anthelmintic Treatment for Persistent Ancylostoma Caninum Ova Shedding in Greyhounds
CASE SERIES Combination Anthelmintic Treatment for Persistent Ancylostoma caninum Ova Shedding in Greyhounds Lindie B. Hess, BS, Laurie M. Millward, DVM, Adam Rudinsky DVM, Emily Vincent, BS, Antoinette Marsh, PhD ABSTRACT Ancylostoma caninum is a nematode of the canine gastrointestinal tract commonly referred to as hookworm. This study involved eight privately owned adult greyhounds presenting with persistent A. caninum ova shedding despite previous deworming treatments. The dogs received a combination treatment protocol comprising topical moxidectin, followed by pyrantel/febantel/praziquantel within 24 hr. At 7–10 days posttreatment, a fecal examination monitored for parasite ova. Dogs remained on the monthly combination treatment protocol until they ceased shedding detectable ova. The dogs then received only the monthly topical moxidectin maintenance treatment. The dogs remained in the study for 5–14 mo with periodical fecal examinations performed. During the study, three dogs reverted to positive fecal ova status, with two being associated with client noncompliance. Reinstitution of the combination treatment protocol resulted in no detectable ova. Use of monthly doses of combination pyrantel, febantel and moxidectin appears to be an effective treatment for nonresponsive or persistent A. caninum ova shedding. Follow-up fecal examinations were important for verifying the presence or absence of ova shedding despite the use of anthelmintic treatment. Limitations of the current study include small sample size, inclusion of only privately owned greyhounds, and client compliance with fecal collection and animal care. (JAmAnimHospAssoc2019; 55:---–---. DOI 10.5326/ JAAHA-MS-6904) Introduction include the following: moxidectina,b, milbemycin oximec, fenben- Ancylostoma caninum is a nematode of the canine gastrointestinal dazoled, and/or pyrantel-containing productse,f. -
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 -
New Zealand's Genetic Diversity
1.13 NEW ZEALAND’S GENETIC DIVERSITY NEW ZEALAND’S GENETIC DIVERSITY Dennis P. Gordon National Institute of Water and Atmospheric Research, Private Bag 14901, Kilbirnie, Wellington 6022, New Zealand ABSTRACT: The known genetic diversity represented by the New Zealand biota is reviewed and summarised, largely based on a recently published New Zealand inventory of biodiversity. All kingdoms and eukaryote phyla are covered, updated to refl ect the latest phylogenetic view of Eukaryota. The total known biota comprises a nominal 57 406 species (c. 48 640 described). Subtraction of the 4889 naturalised-alien species gives a biota of 52 517 native species. A minimum (the status of a number of the unnamed species is uncertain) of 27 380 (52%) of these species are endemic (cf. 26% for Fungi, 38% for all marine species, 46% for marine Animalia, 68% for all Animalia, 78% for vascular plants and 91% for terrestrial Animalia). In passing, examples are given both of the roles of the major taxa in providing ecosystem services and of the use of genetic resources in the New Zealand economy. Key words: Animalia, Chromista, freshwater, Fungi, genetic diversity, marine, New Zealand, Prokaryota, Protozoa, terrestrial. INTRODUCTION Article 10b of the CBD calls for signatories to ‘Adopt The original brief for this chapter was to review New Zealand’s measures relating to the use of biological resources [i.e. genetic genetic resources. The OECD defi nition of genetic resources resources] to avoid or minimize adverse impacts on biological is ‘genetic material of plants, animals or micro-organisms of diversity [e.g. genetic diversity]’ (my parentheses). -
Proceedings of the Helminthological Society of Washington 51(2) 1984
Volume 51 July 1984 PROCEEDINGS ^ of of Washington '- f, V-i -: ;fx A semiannual journal of research devoted to Helminthohgy and all branches of Parasitology Supported in part by the -•>"""- v, H. Ransom Memorial 'Tryst Fund : CONTENTS -j<:'.:,! •</••• VV V,:'I,,--.. Y~v MEASURES, LENA N., AND Roy C. ANDERSON. Hybridization of Obeliscoides cuniculi r\ XGraybill, 1923) Graybill, ,1924 jand Obeliscoides,cuniculi multistriatus Measures and Anderson, 1983 .........:....... .., :....„......!"......... _ x. iXJ-v- 179 YATES, JON A., AND ROBERT C. LOWRIE, JR. Development of Yatesia hydrochoerus "•! (Nematoda: Filarioidea) to the Infective Stage in-Ixqdid Ticks r... 187 HUIZINGA, HARRY W., AND WILLARD O. GRANATH, JR. -Seasonal ^prevalence of. Chandlerellaquiscali (Onehocercidae: Filarioidea) in Braih, of the Common Grackle " '~. (Quiscdlus quisculd versicolor) '.'.. ;:,„..;.......„.;....• :..: „'.:„.'.J_^.4-~-~-~-<-.ii -, **-. 191 ^PLATT, THOMAS R. Evolution of the Elaphostrongylinae (Nematoda: Metastrongy- X. lojdfea: Protostrongylidae) Parasites of Cervids,(Mammalia) ...,., v.. 196 PLATT, THOMAS R., AND W. JM. SAMUEL. Modex of Entry of First-Stage Larvae ofr _^ ^ Parelaphostrongylus odocoilei^Nematoda: vMefastrongyloidea) into Four Species of Terrestrial Gastropods .....:;.. ....^:...... ./:... .; _.... ..,.....;. .-: 205 THRELFALL, WILLIAM, AND JUAN CARVAJAL. Heliconema pjammobatidus sp. n. (Nematoda: Physalbpteridae) from a Skate,> Psammobatis lima (Chondrichthyes: ; ''•• \^ Rajidae), Taken in Chile _... .„ ;,.....„.......„..,.......;. ,...^.J::...^..,....:.....~L.:....., -
Agent for Expelling Parasites in Humans, Animals Or Birds
(19) TZZ Z_T (11) EP 2 496 089 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) Int Cl.: of the grant of the patent: A01N 65/00 (2009.01) A01N 65/10 (2009.01) 22.02.2017 Bulletin 2017/08 A61K 36/23 (2006.01) A01P 5/00 (2006.01) (21) Application number: 10803029.7 (86) International application number: PCT/BE2010/000077 (22) Date of filing: 05.11.2010 (87) International publication number: WO 2011/054066 (12.05.2011 Gazette 2011/19) (54) AGENT FOR EXPELLING PARASITES IN HUMANS, ANIMALS OR BIRDS MITTEL ZUR ABWEISUNG VON PARASITEN BEI MENSCHEN, TIEREN ODER VÖGELN AGENT POUR EXPULSER DES PARASITES CHEZ DES HUMAINS, DES ANIMAUX OU DES OISEAUX (84) Designated Contracting States: (56) References cited: AL AT BE BG CH CY CZ DE DK EE ES FI FR GB • RAMADAN NASHWA I ET AL: "The in vitro effect GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO of assafoetida on Trichomonas vaginalis", PL PT RO RS SE SI SK SM TR JOURNAL OF THE EGYPTIAN SOCIETY OF PARASITOLOGY, EGYPTIAN SOCIETY OF (30) Priority: 06.11.2009 BE 200900689 PARAS1TOLOGY, CAIRO, EG, vol. 33, no. 2, 1 August 2003 (2003-08-01) , pages 615-630, (43) Date of publication of application: XP009136264, ISSN: 1110-0583 12.09.2012 Bulletin 2012/37 • DATABASE MEDLINE [Online] US NATIONAL LIBRARY OF MEDICINE (NLM), BETHESDA, MD, (73) Proprietors: US; December 2004 (2004-12), RAMADAN • MEIJS, Maria Wilhelmina NASHWA I ET AL: "Effect of Ferula assafoetida 4852 Hombourg (BE) on experimental murine Schistosoma mansoni • VAESSEN, Jan Jozef infection.", XP002592455, Database accession 4852 Hombourg (BE) no. -
The Intestinal Protozoa
The Intestinal Protozoa A. Introduction 1. The Phylum Protozoa is classified into four major subdivisions according to the methods of locomotion and reproduction. a. The amoebae (Superclass Sarcodina, Class Rhizopodea move by means of pseudopodia and reproduce exclusively by asexual binary division. b. The flagellates (Superclass Mastigophora, Class Zoomasitgophorea) typically move by long, whiplike flagella and reproduce by binary fission. c. The ciliates (Subphylum Ciliophora, Class Ciliata) are propelled by rows of cilia that beat with a synchronized wavelike motion. d. The sporozoans (Subphylum Sporozoa) lack specialized organelles of motility but have a unique type of life cycle, alternating between sexual and asexual reproductive cycles (alternation of generations). e. Number of species - there are about 45,000 protozoan species; around 8000 are parasitic, and around 25 species are important to humans. 2. Diagnosis - must learn to differentiate between the harmless and the medically important. This is most often based upon the morphology of respective organisms. 3. Transmission - mostly person-to-person, via fecal-oral route; fecally contaminated food or water important (organisms remain viable for around 30 days in cool moist environment with few bacteria; other means of transmission include sexual, insects, animals (zoonoses). B. Structures 1. trophozoite - the motile vegetative stage; multiplies via binary fission; colonizes host. 2. cyst - the inactive, non-motile, infective stage; survives the environment due to the presence of a cyst wall. 3. nuclear structure - important in the identification of organisms and species differentiation. 4. diagnostic features a. size - helpful in identifying organisms; must have calibrated objectives on the microscope in order to measure accurately.