Be Aware of Schistosomiasis
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Schistosomiasis
MODULE \ Schistosomiasis For the Ethiopian Health Center Team Laikemariam Kassa; Anteneh Omer; Wutet Tafesse; Tadele Taye; Fekadu Kebebew, M.D.; and Abdi Beker Haramaya University In collaboration with the Ethiopia Public Health Training Initiative, The Carter Center, the Ethiopia Ministry of Health, and the Ethiopia Ministry of Education January 2005 Funded under USAID Cooperative Agreement No. 663-A-00-00-0358-00. Produced in collaboration with the Ethiopia Public Health Training Initiative, The Carter Center, the Ethiopia Ministry of Health, and the Ethiopia Ministry of Education. Important Guidelines for Printing and Photocopying Limited permission is granted free of charge to print or photocopy all pages of this publication for educational, not-for-profit use by health care workers, students or faculty. All copies must retain all author credits and copyright notices included in the original document. Under no circumstances is it permissible to sell or distribute on a commercial basis, or to claim authorship of, copies of material reproduced from this publication. ©2005 by Laikemariam Kassa, Anteneh Omer, Wutet Tafesse, Tadele Taye, Fekadu Kebebew, and Abdi Beker All rights reserved. Except as expressly provided above, no part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system, without written permission of the author or authors. This material is intended for educational use only by practicing health care workers or students and faculty in a health care field. ACKNOWLEDGMENTS The authors are grateful to The Carter Center and its staffs for the financial, material, and moral support without which it would have been impossible to develop this module. -
First Morphogenetic Analysis of Parasite Eggs from Schistosomiasis
First morphogenetic analysis of parasite eggs from Schistosomiasis haematobium infected sub-Saharan migrants in Spain and proposal for a new standardised study methodology Marta Reguera-Gomez, M Valero, M Carmen Oliver-Chiva, Alejandra de Elias-Escribano, Patricio Artigas, M Cabeza-Barrera, Joaquín Salas-Coronas, Jérôme Boissier, Santiago Mas-Coma, M Dolores Bargues To cite this version: Marta Reguera-Gomez, M Valero, M Carmen Oliver-Chiva, Alejandra de Elias-Escribano, Patricio Artigas, et al.. First morphogenetic analysis of parasite eggs from Schistosomiasis haematobium infected sub-Saharan migrants in Spain and proposal for a new standardised study methodology. Acta Tropica, Elsevier, 2021, 223, pp.106075. 10.1016/j.actatropica.2021.106075. hal-03332420 HAL Id: hal-03332420 https://hal.archives-ouvertes.fr/hal-03332420 Submitted on 2 Sep 2021 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. First morphogenetic analysis of parasite eggs from Schistosomiasis haematobium infected sub-Saharan migrants in Spain and proposal for a new standardised study methodology Marta Reguera-Gomez a, M. Adela Valero a,*, M. Carmen Oliver-Chiva a, Alejandra de Elias-Escribano a, Patricio Artigas a, M. Isabel Cabeza-Barrera b, Joaquín Salas- Coronas b, Jérôme Boissierc, Santiago Mas-Coma a, M. -
Pocket Guide to Clinical Microbiology
4TH EDITION Pocket Guide to Clinical Microbiology Christopher D. Doern 4TH EDITION POCKET GUIDE TO Clinical Microbiology 4TH EDITION POCKET GUIDE TO Clinical Microbiology Christopher D. Doern, PhD, D(ABMM) Assistant Professor, Pathology Director of Clinical Microbiology Virginia Commonwealth University Health System Medical College of Virginia Campus Washington, DC Copyright © 2018 Amer i can Society for Microbiology. All rights re served. No part of this publi ca tion may be re pro duced or trans mit ted in whole or in part or re used in any form or by any means, elec tronic or me chan i cal, in clud ing pho to copy ing and re cord ing, or by any in for ma tion stor age and re trieval sys tem, with out per mis sion in writ ing from the pub lish er. Disclaimer: To the best of the pub lish er’s knowl edge, this pub li ca tion pro vi des in for ma tion con cern ing the sub ject mat ter cov ered that is ac cu rate as of the date of pub li ca tion. The pub lisher is not pro vid ing le gal, med i cal, or other pro fes sional ser vices. Any ref er ence herein to any spe cific com mer cial prod ucts, pro ce dures, or ser vices by trade name, trade mark, man u fac turer, or oth er wise does not con sti tute or im ply en dorse ment, rec om men da tion, or fa vored sta tus by the Ameri can Society for Microbiology (ASM). -
Schistosoma-Associated Salmonella Resist Antibiotics Via Specific Fimbrial
Barnhill et al. Parasites & Vectors 2011, 4:123 http://www.parasitesandvectors.com/content/4/1/123 RESEARCH Open Access Schistosoma-associated Salmonella resist antibiotics via specific fimbrial attachments to the flatworm Alison E Barnhill, Ekaterina Novozhilova, Tim A Day* and Steve A Carlson Abstract Background: Schistosomes are parasitic helminths that infect humans through dermo-invasion while in contaminated water. Salmonella are also a common water-borne human pathogen that infects the gastrointestinal tract via the oral route. Both pathogens eventually enter the systemic circulation as part of their respective disease processes. Concurrent Schistosoma-Salmonella infections are common and are complicated by the bacteria adhering to adult schistosomes present in the mesenteric vasculature. This interaction provides a refuge in which the bacterium can putatively evade antibiotic therapy and anthelmintic monotherapy can lead to a massive release of occult Salmonella. Results: Using a novel antibiotic protection assay, our results reveal that Schistosoma-associated Salmonella are refractory to eight different antibiotics commonly used to treat salmonellosis. The efficacy of these antibiotics was decreased by a factor of 4 to 16 due to this association. Salmonella binding to schistosomes occurs via a specific fimbrial protein (FimH) present on the surface on the bacterium. This same fimbrial protein confers the ability of Salmonella to bind to mammalian cells. Conclusions: Salmonella can evade certain antibiotics by binding to Schistosoma. As a result, effective bactericidal concentrations of antibiotics are unfortunately above the achievable therapeutic levels of the drugs in co-infected individuals. Salmonella-Schistosoma binding is analogous to the adherence of Salmonella to cells lining the mammalian intestine. -
Evolution of the Schistosomes (Digenea: Schistosomatoidea): the Origin of Dioecy and Colonization of the Venous System
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications from the Harold W. Manter Laboratory of Parasitology Parasitology, Harold W. Manter Laboratory of 12-1997 Evolution of the Schistosomes (Digenea: Schistosomatoidea): The Origin of Dioecy and Colonization of the Venous System Thomas R. Platt St. Mary's College Daniel R. Brooks University of Toronto, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/parasitologyfacpubs Part of the Parasitology Commons Platt, Thomas R. and Brooks, Daniel R., "Evolution of the Schistosomes (Digenea: Schistosomatoidea): The Origin of Dioecy and Colonization of the Venous System" (1997). Faculty Publications from the Harold W. Manter Laboratory of Parasitology. 229. https://digitalcommons.unl.edu/parasitologyfacpubs/229 This Article is brought to you for free and open access by the Parasitology, Harold W. Manter Laboratory of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Publications from the Harold W. Manter Laboratory of Parasitology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. J. Parasitol., 83(6), 1997 p. 1035-1044 ? American Society of Parasitologists 1997 EVOLUTIONOF THE SCHISTOSOMES(DIGENEA: SCHISTOSOMATOIDEA): THE ORIGINOF DIOECYAND COLONIZATIONOF THE VENOUS SYSTEM Thomas R. Platt and Daniel R. Brookst Department of Biology, Saint Mary's College, Notre Dame, Indiana 46556 ABSTRACT: Trematodesof the family Schistosomatidaeare -
Neglected Tropical Diseases
Neglected Tropical Diseases David Mabey London School of Hygiene & Tropical Medicine Disease Control strategy Elimination target Schistosomiasis MDA, health education, sanitation, snail control Yes (in some countries) Onchocerciasis MDA, (vector control) Yes (in Americas) Lymphatic filariasis MDA, vector control Yes (as a PH problem) Trachoma MDA, water and sanitation, health education Yes (as a PH problem) Yaws MDA Yes Soil transmitted helminths MDA No Guinea worm Safe water, health education Yes African trypanosomiasis Case finding and treatment, (vector control) Yes (T.b. gambiense) Visceral leishmaniasis Case finding and treatment Yes (subcontinent) Leprosy Case finding and treatment Yes Cysticercosis Sanitation, meat inspection, vaccination of pigs No Echinococcosis Abattoir control, treatment of dogs, education No Fascioliasis Treatment of sheep, health education No Chagas disease Vector control, blood screening Yes (some countries) Buruli ulcer Case finding and treatment No Rabies Vaccination of dogs, health education No Dengue Vector control No 35 year old English man • Unwell for 3 days • Fever • Cough • Itchy rash • Holiday in Malawi for 2 weeks • Returned 5 weeks ago • What else would you like to know? Travel History is important Where exactly has the patient been? • Which countries? • Rural or urban? • Dates of travel, when did symptoms begin? What exactly has the patient been doing? • New sexual partner(s)? • Fresh water contact? • Exposure to sick people? Immunisations before travel? Malaria prophylaxis? Any other medication -
Lecture 18 Feb 24 Shisto.Pdf
Digeneans: All life cycles involve a mollusc and a vertebrate All life cycles are similar but different All life cycles are a variation of one theme. Adult-egg-miracidium-[black box of sprorocyst/rediae] Cercariae leave snail (usually): 1) penetrate host (definitive or intermediate) 2) encyst on vegetation Among human parasitic diseases, schistosomiasis (sometimes called bilharziasis) ranks second behind malaria in terms of socio-economic and public health importance in tropical and subtropical areas. The disease is endemic in 74 developing countries, infecting more than 200 million people in rural agricultural and peri-urban areas. Of these, 20 million suffer severe consequences from the disease and 120 million are symptomatic. In many areas, schistosomiasis infects a large proportion of under-14 children. An estimated 500-600 million people worldwide are at risk from the disease Globally, about 120 million of the 200 million infected people are estimated to be symptomatic, and 20 million are thought to suffer severe consequences of the infection. Yearly, 20,000 deaths are estimated to be associated with schistosomiasis. This mortality is mostly due to bladder cancer or renal failure associated with urinary schistosomiasis and to liver fibrosis and portal hypertension associated with intestinal schistosomiasis. Biogeography The major forms of human schistosomiasis are caused by five species of water- borne flatworm, or blood flukes, called schistosomes: Schistosoma mansoni causes intestinal schistosomiasis and is prevalent in 52 countries and territories of Africa, Caribbean, the Eastern Mediterranean and South America Schistosoma japonicum/Schistosoma mekongi cause intestinal schistosomiasis and are prevalent in 7 African countries and the Pacific region Schistosoma intercalatum is found in ten African countries Schistosoma haematobium causes urinary schistosomiasis and affects 54 countries in Africa and the Eastern Mediterranean. -
Recent Progress in the Development of Liver Fluke and Blood Fluke Vaccines
Review Recent Progress in the Development of Liver Fluke and Blood Fluke Vaccines Donald P. McManus Molecular Parasitology Laboratory, Infectious Diseases Program, QIMR Berghofer Medical Research Institute, Brisbane 4006, Australia; [email protected]; Tel.: +61-(41)-8744006 Received: 24 August 2020; Accepted: 18 September 2020; Published: 22 September 2020 Abstract: Liver flukes (Fasciola spp., Opisthorchis spp., Clonorchis sinensis) and blood flukes (Schistosoma spp.) are parasitic helminths causing neglected tropical diseases that result in substantial morbidity afflicting millions globally. Affecting the world’s poorest people, fasciolosis, opisthorchiasis, clonorchiasis and schistosomiasis cause severe disability; hinder growth, productivity and cognitive development; and can end in death. Children are often disproportionately affected. F. hepatica and F. gigantica are also the most important trematode flukes parasitising ruminants and cause substantial economic losses annually. Mass drug administration (MDA) programs for the control of these liver and blood fluke infections are in place in a number of countries but treatment coverage is often low, re-infection rates are high and drug compliance and effectiveness can vary. Furthermore, the spectre of drug resistance is ever-present, so MDA is not effective or sustainable long term. Vaccination would provide an invaluable tool to achieve lasting control leading to elimination. This review summarises the status currently of vaccine development, identifies some of the major scientific targets for progression and briefly discusses future innovations that may provide effective protective immunity against these helminth parasites and the diseases they cause. Keywords: Fasciola; Opisthorchis; Clonorchis; Schistosoma; fasciolosis; opisthorchiasis; clonorchiasis; schistosomiasis; vaccine; vaccination 1. Introduction This article provides an overview of recent progress in the development of vaccines against digenetic trematodes which parasitise the liver (Fasciola hepatica, F. -
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 -
Be Aware of Schistosomiasis | 2015 1 Fig
From our Whitepaper Files: Be Aware of > See companion document Schistosomiasis World Schistosomiasis 2015 Edition Risk Chart Canada 67 Mowat Avenue, Suite 036 Toronto, Ontario M6K 3E3 (416) 652-0137 USA 1623 Military Road, #279 Niagara Falls, New York 14304-1745 (716) 754-4883 New Zealand 206 Papanui Road Christchurch 5 www.iamat.org | [email protected] | Twitter @IAMAT_Travel | Facebook IAMATHealth THE HELPFUL DATEBOOK It was clear to him that this young woman must It’s noon, the skies are clear, it is unbearably have spent some time in Africa or the Middle hot and a caravan snakes its way across the East where this type of worm is prevalent. When Sahara. Twenty-eight people on camelback are interviewed she confirmed that she had been heading towards the oasis named El Mamoun. in Africa, participating in one of the excursions They are tourists participating in ‘La Sahari- organized by the club. enne’, a popular excursion conducted twice weekly across the desert of southern Tunisia The young woman did not have cancer at all, by an international travel club. In the bound- but had contracted schistosomiasis while less Sahara, they were living a fascinating swimming in the oasis pond. When investiga- experience, their senses thrilled by the majestic tors began to fear that other members of her grandeur of the desert. After hours of riding, group might also be infected, her date book they reached the oasis and were dazzled to see came to their aid. Many of her companions had Fig. 1 Biomphalaria fresh-water snail. a clear pond fed by a bubbling spring. -
Phylogeny of Seven Bulinus Species Originating from Endemic Areas In
Zein-Eddine et al. BMC Evolutionary Biology (2014) 14:271 DOI 10.1186/s12862-014-0271-3 RESEARCH ARTICLE Open Access Phylogeny of seven Bulinus species originating from endemic areas in three African countries, in relation to the human blood fluke Schistosoma haematobium Rima Zein-Eddine1*, Félicité Flore Djuikwo-Teukeng1,2, Mustafa Al-Jawhari3, Bruno Senghor4, Tine Huyse5 and Gilles Dreyfuss1 Abstract Background: Snails species belonging to the genus Bulinus (Planorbidae) serve as intermediate host for flukes belonging to the genus Schistosoma (Digenea, Platyhelminthes). Despite its importance in the transmission of these parasites, the evolutionary history of this genus is still obscure. In the present study, we used the partial mitochondrial cytochrome oxidase subunit I (cox1) gene, and the nuclear ribosomal ITS, 18S and 28S genes to investigate the haplotype diversity and phylogeny of seven Bulinus species originating from three endemic countries in Africa (Cameroon, Senegal and Egypt). Results: The cox1 region showed much more variation than the ribosomal markers within Bulinus sequences. High levels of genetic diversity were detected at all loci in the seven studied species, with clear segregation between individuals and appearance of different haplotypes, even within same species from the same locality. Sequences clustered into two lineages; (A) groups Bulinus truncatus, B. tropicus, B. globosus and B. umbilicatus; while (B) groups B. forskalii, B. senegalensis and B. camerunensis. Interesting patterns emerge regarding schistosome susceptibility: Bulinus species with lower genetic diversity are predicted to have higher infection prevalence than those with greater diversity in host susceptibility. Conclusion: The results reported in this study are very important since a detailed understanding of the population genetic structure of Bulinus is essential to understand the epidemiology of many schistosome parasites. -
TREMATODES Blood Species
Lecturer : Nerran K.F.AL- Rubaey Practical parasites Lab - 13 - TREMATODES Blood Species : 1- Schistosoma mansoni : Common Name ( Manson, s Blood Fluke) Causes Intestinal Schistosomiasis . 2- Schistosoma japonicum :Common Name ( Blood Fluke ) Causes Intestinal Schistosomiasis . 3- Schistosoma haematobium : Common Name ( Bladder Fluke ) Causes Urinary Schistosomiasis. Eggs : The average Schistosoma eggs is comprised of developed miracidium , these eggs are oval in shape and the presence of lateral or terminal spines distinguishes the egg of one species from the other species . Figure ( 1- 1 ) : Egg of Schistosoma mansoni *It, s have large lateral spine and developed miracidium . 1 PDF created with pdfFactory trial version www.pdffactory.com Figure ( 1- 2 ) : Egg of Schistosoma japonicum *It, s have small lateral spine and developed miracidium . Figure ( 1- 3 ) : Egg of Schistosoma haematobium *It, s have large terminal spine and developed miracidium . Adults : The adults of Schistosoma sp.are the only trematodes that have separate sexes . Unlike the other adult trematode , the Schistosomes are rounder in appearance . Although the typical female measures 2 cm in length and the male measures 1.5 cm in length , the male has the capability to almost completely surround the female during copulation . 2 PDF created with pdfFactory trial version www.pdffactory.com Figure ( 1- 4 ) : Schistosomes in copula. ( The Life cycle of Schistosoma sp.) 3 PDF created with pdfFactory trial version www.pdffactory.com Notes *Diagnostic stage is :egg * Infective stage is : cercaria * Final host is : human * Intermediate is : snail Table ( 1 ): Differentiation between Schistosoma sp. Properties Schistosoma Schistosoma Schistosoma mansoni japonicum haematobium 1- natural habitat Adult live in vein Adult live in vein of Adult live in vein of of large intestine small intestine urinary bladder 2- male (No.