Parasitology International 71 (2019) 56–58
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Coinfection of Schistosoma (Trematoda) with Bacteria, Protozoa and Helminths
CHAPTER 1 Coinfection of Schistosoma (Trematoda) with Bacteria, Protozoa and Helminths ,† ‡ Amy Abruzzi* and Bernard Fried Contents 1.1. Introduction 3 1.2. Coinfection of Species of Schistosoma and Plasmodium 4 1.2.1. Animal studies 21 1.2.2. Human studies 23 1.3. Coinfection of Schistosoma Species with Protozoans other than in the Genus Plasmodium 24 1.3.1. Leishmania 32 1.3.2. Toxoplasma 32 1.3.3. Entamoeba 34 1.3.4. Trypanosoma 35 1.4. Coinfection of Schistosoma Species with Salmonella 36 1.4.1. Animal studies 36 1.4.2. Human studies 42 1.5. Coinfection of Schistosoma Species with Bacteria other than Salmonella 43 1.5.1. Mycobacterium 43 1.5.2. Helicobacter pylori 49 1.5.3. Staphylococcus aureus 50 1.6. Coinfection of Schistosoma and Fasciola Species 50 1.6.1. Animal studies 57 1.6.2. Human studies 58 * Skillman Library, Lafayette College, Easton, Pennsylvania, USA { Epidemiology, University of Medicine and Dentistry of New Jersey (UMDNJ), Piscataway, New Jersey, USA { Department of Biology, Lafayette College, Easton, Pennsylvania, USA Advances in Parasitology, Volume 77 # 2011 Elsevier Ltd. ISSN 0065-308X, DOI: 10.1016/B978-0-12-391429-3.00005-8 All rights reserved. 1 2 Amy Abruzzi and Bernard Fried 1.7. Coinfection of Schistosoma Species and Helminths other than the Genus Fasciola 59 1.7.1. Echinostoma 59 1.7.2. Hookworm 70 1.7.3. Trichuris 70 1.7.4. Ascaris 71 1.7.5. Strongyloides and Trichostrongyloides 72 1.7.6. Filarids 73 1.8. Concluding Remarks 74 References 75 Abstract This review examines coinfection of selected species of Schisto- soma with bacteria, protozoa and helminths and focuses on the effects of the coinfection on the hosts. -
Helminth Parasites (Trematoda, Cestoda, Nematoda, Acanthocephala) of Herpetofauna from Southeastern Oklahoma: New Host and Geographic Records
125 Helminth Parasites (Trematoda, Cestoda, Nematoda, Acanthocephala) of Herpetofauna from Southeastern Oklahoma: New Host and Geographic Records Chris T. McAllister Science and Mathematics Division, Eastern Oklahoma State College, Idabel, OK 74745 Charles R. Bursey Department of Biology, Pennsylvania State University-Shenango, Sharon, PA 16146 Matthew B. Connior Life Sciences, Northwest Arkansas Community College, Bentonville, AR 72712 Abstract: Between May 2013 and September 2015, two amphibian and eight reptilian species/ subspecies were collected from Atoka (n = 1) and McCurtain (n = 31) counties, Oklahoma, and examined for helminth parasites. Twelve helminths, including a monogenean, six digeneans, a cestode, three nematodes and two acanthocephalans was found to be infecting these hosts. We document nine new host and three new distributional records for these helminths. Although we provide new records, additional surveys are needed for some of the 257 species of amphibians and reptiles of the state, particularly those in the western and panhandle regions who remain to be examined for helminths. ©2015 Oklahoma Academy of Science Introduction Methods In the last two decades, several papers from Between May 2013 and September 2015, our laboratories have appeared in the literature 11 Sequoyah slimy salamander (Plethodon that has helped increase our knowledge of sequoyah), nine Blanchard’s cricket frog the helminth parasites of Oklahoma’s diverse (Acris blanchardii), two eastern cooter herpetofauna (McAllister and Bursey 2004, (Pseudemys concinna concinna), two common 2007, 2012; McAllister et al. 1995, 2002, snapping turtle (Chelydra serpentina), two 2005, 2010, 2011, 2013, 2014a, b, c; Bonett Mississippi mud turtle (Kinosternon subrubrum et al. 2011). However, there still remains a hippocrepis), two western cottonmouth lack of information on helminths of some of (Agkistrodon piscivorus leucostoma), one the 257 species of amphibians and reptiles southern black racer (Coluber constrictor of the state (Sievert and Sievert 2011). -
Waterborne Zoonotic Helminthiases Suwannee Nithiuthaia,*, Malinee T
Veterinary Parasitology 126 (2004) 167–193 www.elsevier.com/locate/vetpar Review Waterborne zoonotic helminthiases Suwannee Nithiuthaia,*, Malinee T. Anantaphrutib, Jitra Waikagulb, Alvin Gajadharc aDepartment of Pathology, Faculty of Veterinary Science, Chulalongkorn University, Henri Dunant Road, Patumwan, Bangkok 10330, Thailand bDepartment of Helminthology, Faculty of Tropical Medicine, Mahidol University, Ratchawithi Road, Bangkok 10400, Thailand cCentre for Animal Parasitology, Canadian Food Inspection Agency, Saskatoon Laboratory, Saskatoon, Sask., Canada S7N 2R3 Abstract This review deals with waterborne zoonotic helminths, many of which are opportunistic parasites spreading directly from animals to man or man to animals through water that is either ingested or that contains forms capable of skin penetration. Disease severity ranges from being rapidly fatal to low- grade chronic infections that may be asymptomatic for many years. The most significant zoonotic waterborne helminthic diseases are either snail-mediated, copepod-mediated or transmitted by faecal-contaminated water. Snail-mediated helminthiases described here are caused by digenetic trematodes that undergo complex life cycles involving various species of aquatic snails. These diseases include schistosomiasis, cercarial dermatitis, fascioliasis and fasciolopsiasis. The primary copepod-mediated helminthiases are sparganosis, gnathostomiasis and dracunculiasis, and the major faecal-contaminated water helminthiases are cysticercosis, hydatid disease and larva migrans. Generally, only parasites whose infective stages can be transmitted directly by water are discussed in this article. Although many do not require a water environment in which to complete their life cycle, their infective stages can certainly be distributed and acquired directly through water. Transmission via the external environment is necessary for many helminth parasites, with water and faecal contamination being important considerations. -
REVEALING BIOTIC DIVERSITY: HOW DO COMPLEX ENVIRONMENTS INFLUENCE HUMAN SCHISTOSOMIASIS in a HYPERENDEMIC AREA Martina R
University of New Mexico UNM Digital Repository Biology ETDs Electronic Theses and Dissertations Spring 5-9-2018 REVEALING BIOTIC DIVERSITY: HOW DO COMPLEX ENVIRONMENTS INFLUENCE HUMAN SCHISTOSOMIASIS IN A HYPERENDEMIC AREA Martina R. Laidemitt Follow this and additional works at: https://digitalrepository.unm.edu/biol_etds Recommended Citation Laidemitt, Martina R.. "REVEALING BIOTIC DIVERSITY: HOW DO COMPLEX ENVIRONMENTS INFLUENCE HUMAN SCHISTOSOMIASIS IN A HYPERENDEMIC AREA." (2018). https://digitalrepository.unm.edu/biol_etds/279 This Dissertation is brought to you for free and open access by the Electronic Theses and Dissertations at UNM Digital Repository. It has been accepted for inclusion in Biology ETDs by an authorized administrator of UNM Digital Repository. For more information, please contact [email protected]. Martina Rose Laidemitt Candidate Department of Biology Department This dissertation is approved, and it is acceptable in quality and form for publication: Approved by the Dissertation Committee: Dr. Eric S. Loker, Chairperson Dr. Jennifer A. Rudgers Dr. Stephen A. Stricker Dr. Michelle L. Steinauer Dr. William E. Secor i REVEALING BIOTIC DIVERSITY: HOW DO COMPLEX ENVIRONMENTS INFLUENCE HUMAN SCHISTOSOMIASIS IN A HYPERENDEMIC AREA By Martina R. Laidemitt B.S. Biology, University of Wisconsin- La Crosse, 2011 DISSERT ATION Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Biology The University of New Mexico Albuquerque, New Mexico July 2018 ii ACKNOWLEDGEMENTS I thank my major advisor, Dr. Eric Samuel Loker who has provided me unlimited support over the past six years. His knowledge and pursuit of parasitology is something I will always admire. I would like to thank my coauthors for all their support and hard work, particularly Dr. -
Endemicity of Opisthorchis Viverrini Liver Flukes, Vietnam, 2011–2012
LETTERS Endemicity of for species identification of Opisthor- A total of 4 fish species were in- chis fluke metacercariae 7( ). fected with O. viverrini metacercariae Opisthorchis Fish were collected from Tuy (online Technical Appendix Table 1, viverrini Liver Hoa City and from the districts of Hoa wwwnc.cdc.gov/EID/article/20/1/13- Flukes, Vietnam, Xuan Dong, Tuy An, and Song Hinh; 0168-Techapp1.pdf). Metacercariae these 3 districts are areas of large prevalence was highest (28.1%) 2011–2012 aquaculture production of freshwater among crucian carp (Carasius aura- To the Editor: Fishborne zoo- fish. Fresh fish from ponds, rice fields, tus). Specific identification was con- notic trematodes are highly prevalent rivers, and swamps were purchased at firmed by morphologic appearance of in many Asian communities (1,2). Al- local markets from April 2011 through adult worms recovered from hamsters though presence of the liver flukeClo - March 2012. The fish sellers provided (Figure) and PCR and sequence anal- norchis sinensis is well documented information about the source of the ysis of the partial metacercarial CO1 in Vietnam (3), evidence of the pres- fish (e.g., type of water body). Fish gene, amplified by CO1-OV-Hap- ence of the more common liver fluke were transported live with mechani- F&R primers (7). Infected fish origi- of Southeast Asia, Opisthorchis viver- cal aeration to the Research Institute nated predominantly from so-called rini, is only circumstantial. Surveys of for Aquaculture No. 3 in Nha Trang, wild water (i.e., swamps, rice fields, human fecal samples have frequently where they were examined for meta- rivers). -
WHO CC Web Fac.Farm V.Ingles
WHO COLLABORATING CENTRE ON FASCIOLIASIS AND ITS SNAIL VECTORS Reference of the World Health Organization (WHO/OMS): WHO CC SPA-37 Date of Nomination: 31 of March of 2011 Last update of the contents of this website: 28 of January of 2014 DESIGNATED CENTRE: Human Parasitic Disease Unit (Unidad de Parasitología Sanitaria) Departamento de Parasitología Facultad de Farmacia Universidad de Valencia Av. Vicent Andres Estelles s/n 46100 Burjassot - Valencia Spain DESIGNATED DIRECTOR OF THE CENTRE: Prof. Dr. Dr. Honoris Causa SANTIAGO MAS-COMA Parasitology Chairman WHO RESPONSIBLE OFFICER: Dr. DIRK ENGELS Coordinator, Preventive Chemotherapy and Transmission Control (HTM/NTD/PCT) (appointed as the new Director of the Department of Control of Neglected Tropical Diseases from 1 May 2014) Department of Control of Neglected Tropical Diseases (NTD) World Health Organization WHO Headquarters Avenue Appia No. 20 1211 Geneva 27 Switzerland RESEARCH GROUPS, LEADERS AND ACTIVITIES The Research Team designated as WHO CC comprises the following three Research Groups, Leaders and respective endorsed tasks: A) Research Group on (a) Epidemiology and (b) Control: Group Leader (research responsible): Prof. Dr. Dr. Honoris Causa SANTIAGO MAS-COMA Parasitology Chairman (Email: S. [email protected]) Activities: - Studies on the disease epidemiology in human fascioliasis endemic areas of Latin America, Europe, Africa and Asia - Implementation and follow up of disease control interventions against fascioliasis in human endemic areas B) Research Group on c) Transmission and d) Vectors: Group Leader (research responsible): Prof. Dra. MARIA DOLORES BARGUES Parasitology Chairwoman (Email: [email protected]) Activities: - Molecular, genetic and malacological characterization of lymnaeid snails - Studies on the transmission characteristics of human fascioliasis and the human infection ways in human fascioliasis endemic areas C) Research Group on e) Diagnostics and f) Immunopathology: Group Leader (research responsible): Prof. -
Diplomarbeit
DIPLOMARBEIT Titel der Diplomarbeit „Microscopic and molecular analyses on digenean trematodes in red deer (Cervus elaphus)“ Verfasserin Kerstin Liesinger angestrebter akademischer Grad Magistra der Naturwissenschaften (Mag.rer.nat.) Wien, 2011 Studienkennzahl lt. Studienblatt: A 442 Studienrichtung lt. Studienblatt: Diplomstudium Anthropologie Betreuerin / Betreuer: Univ.-Doz. Mag. Dr. Julia Walochnik Contents 1 ABBREVIATIONS ......................................................................................................................... 7 2 INTRODUCTION ........................................................................................................................... 9 2.1 History ..................................................................................................................................... 9 2.1.1 History of helminths ........................................................................................................ 9 2.1.2 History of trematodes .................................................................................................... 11 2.1.2.1 Fasciolidae ................................................................................................................. 12 2.1.2.2 Paramphistomidae ..................................................................................................... 13 2.1.2.3 Dicrocoeliidae ........................................................................................................... 14 2.1.3 Nomenclature ............................................................................................................... -
Redalyc.Fasciola Hepatica: Epidemiology, Perspectives in The
Semina: Ciências Agrárias ISSN: 1676-546X [email protected] Universidade Estadual de Londrina Brasil Aleixo, Marcos André; França Freitas, Deivid; Hermes Dutra, Leonardo; Malone, John; Freire Martins, Isabella Vilhena; Beltrão Molento, Marcelo Fasciola hepatica: epidemiology, perspectives in the diagnostic and the use of geoprocessing systems for prevalence studie Semina: Ciências Agrárias, vol. 36, núm. 3, mayo-junio, 2015, pp. 1451-1465 Universidade Estadual de Londrina Londrina, Brasil Available in: http://www.redalyc.org/articulo.oa?id=445744148049 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 REVISÃO/REVIEW DOI: 10.5433/1679-0359.2015v36n3p1451 Fasciola hepatica : epidemiology, perspectives in the diagnostic and the use of geoprocessing systems for prevalence studies Fasciola hepatica : epidemiologia, perspectivas no diagnóstico e estudo de prevalência com uso de programas de geoprocessamento Marcos André Aleixo 1; Deivid França Freitas 2; Leonardo Hermes Dutra 1; John Malone 3; Isabella Vilhena Freire Martins 4; Marcelo Beltrão Molento 1, 5* Abstract Fasciola hepatica is a parasite that is located in the liver of ruminants with the possibility to infect horses, pigs and humans. The parasite belongs to the Trematoda class, and it is the agent causing the disease called fasciolosis. This disease occurs mainly in temperate regions where climate favors the development of the organism. These conditions must facilitate the development of the intermediate host, the snail of the genus Lymnaea . The infection in domestic animals can lead to decrease in production and control is made by using triclabendazole. -
Mini-FLOTAC As an Alternative, Non-Invasive Diagnostic Tool For
Catalano et al. Parasites Vectors (2019) 12:439 https://doi.org/10.1186/s13071-019-3613-6 Parasites & Vectors RESEARCH Open Access Mini-FLOTAC as an alternative, non-invasive diagnostic tool for Schistosoma mansoni and other trematode infections in wildlife reservoirs Stefano Catalano1,2* , Amelia Symeou1, Kirsty J. Marsh1, Anna Borlase1,2, Elsa Léger1,2, Cheikh B. Fall3, Mariama Sène4, Nicolas D. Diouf4, Davide Ianniello5, Giuseppe Cringoli5, Laura Rinaldi5, Khalilou Bâ6 and Joanne P. Webster1,2 Abstract Background: Schistosomiasis and food-borne trematodiases are not only of major public health concern, but can also have profound implications for livestock production and wildlife conservation. The zoonotic, multi-host nature of many digenean trematodes is a signifcant challenge for disease control programmes in endemic areas. However, our understanding of the epidemiological role that animal reservoirs, particularly wild hosts, may play in the transmission of zoonotic trematodiases sufers a dearth of information, with few, if any, standardised, reliable diagnostic tests avail- able. We combined qualitative and quantitative data derived from post-mortem examinations, coprological analyses using the Mini-FLOTAC technique, and molecular tools to assess parasite community composition and the validity of non-invasive methods to detect trematode infections in 89 wild Hubert’s multimammate mice (Mastomys huberti) from northern Senegal. Results: Parasites isolated at post-mortem examination were identifed as Plagiorchis sp., Anchitrema sp., Echinostoma caproni, Schistosoma mansoni, and a hybrid between Schistosoma haematobium and Schistosoma bovis. The reports of E. caproni and Anchitrema sp. represent the frst molecularly confrmed identifcations for these trematodes in defni- tive hosts of sub-Saharan Africa. -
Gastrodiscoidiasis, a Plant-Borne Zoonotic Disease Caused by the Intestinal Amphistome Fluke Gastrodiscoides Hominis (Trematoda: Gastrodiscidae)
75 Gastrodiscoidiasis, a plant-borne zoonotic disease caused by the intestinal amphistome fluke Gastrodiscoides hominis (Trematoda: Gastrodiscidae). Mas-Coma, S.; Bargues, M.D. & Valero, M.A. Departamento de Parasitología, Facultad de Farmacia, Universidad de Valencia, Burjassot, Valencia, Spain Received: 25.11.05 Accepted: 10.12.05 Abstract: Gastrodiscoidiasis is an intestinal trematodiasis caused by the only common amphistome of man Gastrodiscoides hominis and transmitted by small freshwater snails of the species Helicorbis coenosus, belonging to the family Planorbidae. Human and animal contamination can take place when swallowing encysted metacercariae, by ingestion of vegetation (aquatic plants) or animal products, such as raw or undercooked crustaceans (crayfish), squid, molluscs, or amphibians (frogs, tadpoles). Pigs appear to be the main animal reservoir of any significance in most endemic areas. Its geographical distribution covers India (including Assam, Bengal, Bihar, Uttar Pradesh, Madhya Pradesh and Orissa), Pakistan, Burma, Thailand, Vietnam, Philippines, China, Kazakstan and Volga Delta in Russia, and has also been reported in African countries such as Zambia and Nigeria. The presence of G. hominis in Africa needs further studies, to confirm that the African amphistome in question is really that species and not a closely related African species, and to ascertain its geographical distribution in this continent. In man, this amphistome fluke causes inflammation of the mucosa of caecum and ascending colon with attendant symptoms of diarrhoea. This infection causes ill health in a large number of persons, and deaths among untreated patients, especially children. Human infection by G. hominis is easily recognisable by finding the characteristic eggs of this amphistome in faeces. -
Praziquantel Treatment in Trematode and Cestode Infections: an Update
Review Article Infection & http://dx.doi.org/10.3947/ic.2013.45.1.32 Infect Chemother 2013;45(1):32-43 Chemotherapy pISSN 2093-2340 · eISSN 2092-6448 Praziquantel Treatment in Trematode and Cestode Infections: An Update Jong-Yil Chai Department of Parasitology and Tropical Medicine, Seoul National University College of Medicine, Seoul, Korea Status and emerging issues in the use of praziquantel for treatment of human trematode and cestode infections are briefly reviewed. Since praziquantel was first introduced as a broadspectrum anthelmintic in 1975, innumerable articles describ- ing its successful use in the treatment of the majority of human-infecting trematodes and cestodes have been published. The target trematode and cestode diseases include schistosomiasis, clonorchiasis and opisthorchiasis, paragonimiasis, het- erophyidiasis, echinostomiasis, fasciolopsiasis, neodiplostomiasis, gymnophalloidiasis, taeniases, diphyllobothriasis, hyme- nolepiasis, and cysticercosis. However, Fasciola hepatica and Fasciola gigantica infections are refractory to praziquantel, for which triclabendazole, an alternative drug, is necessary. In addition, larval cestode infections, particularly hydatid disease and sparganosis, are not successfully treated by praziquantel. The precise mechanism of action of praziquantel is still poorly understood. There are also emerging problems with praziquantel treatment, which include the appearance of drug resis- tance in the treatment of Schistosoma mansoni and possibly Schistosoma japonicum, along with allergic or hypersensitivity -
Addendum A: Antiparasitic Drugs Used for Animals
Addendum A: Antiparasitic Drugs Used for Animals Each product can only be used according to dosages and descriptions given on the leaflet within each package. Table A.1 Selection of drugs against protozoan diseases of dogs and cats (these compounds are not approved in all countries but are often available by import) Dosage (mg/kg Parasites Active compound body weight) Application Isospora species Toltrazuril D: 10.00 1Â per day for 4–5 d; p.o. Toxoplasma gondii Clindamycin D: 12.5 Every 12 h for 2–4 (acute infection) C: 12.5–25 weeks; o. Every 12 h for 2–4 weeks; o. Neospora Clindamycin D: 12.5 2Â per d for 4–8 sp. (systemic + Sulfadiazine/ weeks; o. infection) Trimethoprim Giardia species Fenbendazol D/C: 50.0 1Â per day for 3–5 days; o. Babesia species Imidocarb D: 3–6 Possibly repeat after 12–24 h; s.c. Leishmania species Allopurinol D: 20.0 1Â per day for months up to years; o. Hepatozoon species Imidocarb (I) D: 5.0 (I) + 5.0 (I) 2Â in intervals of + Doxycycline (D) (D) 2 weeks; s.c. plus (D) 2Â per day on 7 days; o. C cat, D dog, d day, kg kilogram, mg milligram, o. orally, s.c. subcutaneously Table A.2 Selection of drugs against nematodes of dogs and cats (unfortunately not effective against a broad spectrum of parasites) Active compounds Trade names Dosage (mg/kg body weight) Application ® Fenbendazole Panacur D: 50.0 for 3 d o. C: 50.0 for 3 d Flubendazole Flubenol® D: 22.0 for 3 d o.