AAEP Parasite Control Guidelines
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DISEASES OF AQUATIC ORGANISMS Published July 30 Dis Aquat Org Oral pharmacological treatments for parasitic diseases of rainbow trout Oncorhynchus mykiss. 11: Gyrodactylus sp. J. L. Tojo*, M. T. Santamarina Department of Microbiology and Parasitology, Laboratory of Parasitology, Faculty of Pharmacy, Universidad de Santiago de Compostela, E-15706 Santiago de Compostela, Spain ABSTRACT: A total of 24 drugs were evaluated as regards their efficacy for oral treatment of gyro- dactylosis in rainbow trout Oncorhj~nchusmykiss. In preliminary trials, all drugs were supplied to infected fish at 40 g per kg of feed for 10 d. Twenty-two of the drugs tested (aminosidine, amprolium, benznidazole, b~thionol,chloroquine, diethylcarbamazine, flubendazole, levamisole, mebendazole, n~etronidazole,mclosamide, nitroxynil, oxibendazole, parbendazole, piperazine, praziquantel, roni- dazole, secnidazole, tetramisole, thiophanate, toltrazuril and trichlorfon) were ineffective Triclabenda- zole and nitroscanate completely eliminated the infection. Triclabendazole was effective only at the screening dosage (40 g per kg of feed for 10 d), while nitroscanate was effective at dosages as low as 0.6 g per kg of feed for 1 d. KEY WORDS: Gyrodactylosis . Rainbow trout Treatment. Drugs INTRODUCTION to the hooks of the opisthohaptor or to ulceration as a result of feeding by the parasite. The latter is the most The monogenean genus Gyrodactylus is widespread, serious. though some individual species have a restricted distri- Transmission takes place largely as a result of direct bution. Gyrodactyloses affect numerous freshwater contact between live fishes, though other pathways species including salmonids, cyprinids and ornamen- (contact between a live fish and a dead fish, or with tal fishes, as well as marine fishes including gadids, free-living parasites present in the substrate, or with pleuronectids and gobiids. -
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). -
Whatyourdrmaynottellyouabou
What Your Doctor May Not Tell You About Parasites First published in Great Britain in 2015 by Health For The People Ltd. Tel: 0800 310 21 21 [email protected] www.hompes-method.com www.h-pylori-symptoms.com Copyright © 2015 David Hompes, Health For The People Ltd. David Hompes asserts the moral right to be identified as the author of this work. All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, recording or otherwise without the prior permission of the publishers. HEALTH DISCLAIMER The information in this book is not intended to diagnose, treat, cure or prevent any disease, nor should it replace a one-to-one relationship with your physician. You should always seek consultation with a qualified medical practitioner before commencing any protocol contained herein. This book is sold subject to the condition that it shall not, by way of trade or otherwise, be lent, resold, hired out or otherwise circulated without the publisher’s prior consent in any form of binding or cover other than that in which it is published and without a similar condition including this condition being imposed upon the subsequent purchaser. British Library Cataloguing in Publication Data. 2 What Your Doctor May Not Tell You About Parasites Contents Introduction 5-13 1 What is a Parasite? 14-26 2 Where are Parasites to be found? 27-33 3 Why doesn’t the Medical System fully acknowledge 34-38 Parasites? 4 How on earth do you acquire Parasites? -
Comparative Efficacies of Commercially Available Benzimidazoles Against Pseudodactylogyrus Infestations in Eels
DISEASES OF AQUATIC ORGANISMS Published October 4 Dis. aquat. Org. l Comparative efficacies of commercially available benzimidazoles against Pseudodactylogyrus infestations in eels ' Department of Fish Diseases, Royal Veterinary and Agricultural University, 13 Biilowsvej, DK-1870 Frederiksberg C, Denmark Department of Pharmacy, Royal Veterinary and Agricultural University, 13 Biilowsvej. DK-1870 Frederiksberg C,Denmark ABSTRACT: The antiparasitic efficacies of 9 benzimidazoles in commercially avalable formulations were tested (water bath treatments) on small pigmented eels Anguilla anguilla, expenmentally infected by 30 to 140 specimens of Pseudodactylogyrus spp. (Monogenea).Exposure time was 24 h and eels were examined 4 to 5 d post treatment. Mebendazole (Vermox; 1 mg 1-') eradicated all parasites, whereas luxabendazole (pure substance) and albendazole (Valbazen) were 100 % effective only at a concen- tration of 10 mg I-'. Flubendazole (Flubenol), fenbendazole (Panacur) and oxibendazole (Lodltac) (10 mg l-') caused a reduction of the infection level to a larger extent than did triclabendazole (Fasinex) and parbendazole (Helmatac).Thiabendazole (Equizole), even at a concentration as high as 100 mg l-', was without effect on Pseudodactylogyrus spp. INTRODUCTION range of commercially available benzimidazole com- pounds. If drug resistance will develop under practical The broad spectrum anthelmintic drug mebendazoIe eel-farm conditions in the future, it is likely to be was reported as an efficacious compound against infes- recognized during treatments with commercially avail- tations of the European eel Anguilla anguilla with gill able drug formulations. Therefore this type of drug parasitic monogeneans of the genus Pseudodactylo- preparations were used in the present study. gyms (Szekely & Molnar 1987, Buchmann & Bjerre- gaard 1989, 1990, Mellergaard 1989). -
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 -
A Call to Support Francophone African
KNOWLEDGE BRIEF Health, Nutrition and Population Global Practice A CALL TO SUPPORT FRANCOPHONE Public Disclosure Authorized AFRICAN COUNTRIES TO END THE TREMENDOUS SUFFERING FROM NTDs Gaston Sorgho, Fernando Lavadenz and Opope Oyaka Tshivuila Matala December 2018 KEY MESSAGES: • Eighteen Neglected Tropical Diseases (NTDs) and Malaria account together for 22% of the total burden of communicable diseases in 25 Francophone African Countries (FPACs). Public Disclosure Authorized • The cumulative impact of NTDs decreases the quality of life of households, slows economic growth and results in millions of dollars in lost economic productivity annually. For example, the World Bank (WB) estimates annual losses of US$33 million in Cameroon, US$13 million in Chad and US$9 million in Madagascar. • Of the 18 NTDs, 5 can be controlled by preventive chemotherapy (PC) through safe Mass Drug Administration (MDA). • In 2017, the WB launched the Deworming Africa Initiative (DAI), with the purpose of raising the profile of NTDs control and elimination efforts among endemic Sub-Saharan African (SSA) countries to eliminate NTDs as a public health threat. • DAI’s strategy seeks to reduce the burden of NTDs in 3 key population groups that mostly impact on human capital: young children (12-23 months), pregnant women, and school-age children (SAC) (5-14 years of age). To achieve this objective in a sustainable way, DAI supports Country efforts to strengthen the coordinated engagement of the health, education, water, sanitation and hygiene (WASH) and economic sectors with a national prevention and control strategy. • The WB's total annual investments in NTDs control have increased from US$3.3 million in 2013 to US$13.9 million in 2018. -
(12) 按照专利合作条约所公布的国际申请w O 2016/062277
卜 (12) 按照专利合作条约所公布的国际申请 (19) 世界知识 组织 国 际 局 (10) 国际公布号 (43) 国际公布 日 W O 2016/062277 A 1 2016 年 4 月 28 日 (28.04.2016) W P O P C T (51) 国转 利分类号: (74) 代理人 : 北京元本知识产权代理事务所 (BEIJING A61K 31/7048 (2 6 A61K 31/4985 (2006.01) Y U A B E N INTELLECTUAL PROPERTY LAW O F A61K 31/4184 (2006.01) A61K 31/00 (2006.01) FICE); 中 国北 京 市 海 淀 区花 园路 12 号 时代 玉 成 A61K 31/415 (2006.01) A61P 35/00 (2006.01) 403, Beijing 100088 (CN ) 。 A61K 31/429 (2006.01) (81) 指定国 (除另有指 明,要求每一种可提供 的国家保 (21) 国际申请号: PCT/CN20 15/092746 护 ):AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, (22) 国际申请 曰: 2015 年 10 月 23 日 (23. 10.2015) CU, CZ, DE, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, (25) 申请语言: 中文 GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, KZ, LA, LC, LK, LR, LS, LU, (26) 公布语言: 中文 LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, (30) 优先权: RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, 62/068,298 2014 年 10 月 24 日 (24. 10.2014) U S SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, (71) 申请 人 :朗齐生物 医学股份有 限公司 (LAUNX VC, VN, ZA, ZM, Z BIOMEDICAL CO., LTD.) [CN/CN]; 中 国台湾 省 高 (84) 指定国 (除另有指 明,要求每一种可提供 的地 区保 雄 市 前 金 区 自强 一 路 32 巷 1 号 2 楼 ,Taiwan 801 护):ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, (CN) RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), 欧亚 (AM, AZ, (72) 发明人 : 陈丘泓 (CHEN, Chiu-Hung); 中国台湾省高 BY, KG, KZ, RU, TJ, TM), :洲 (AL, AT, BE, BG, CH, 雄 市前金 区 自强一路 32 巷 1 号,Taiwan 801 (CN) 。 CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, 庄秀 (CHUANG, Show-Mei); 国台湾 省 台 中市 IS, -
Phylum: Nematoda Basic Features
Lec: 1 Nematodes 3rd class Dr.Omaima I.M. Phylum: Nematoda Basic Features: Roundworms get their name from their round cross section Long thread-like bodies Usually very small to microscopic, some parasitic members however may be a metre long Simple tube-like gut with a mouth and anus No circulatory system, gas exchange and excretion are by diffusion across the body wall There is very little superficial difference between nematode species, they all look pretty much like larger or smaller, somewhat fatter or skinnier versions of each other Sexual reproduction, sexes separate, no asexual reproduction. Males are usually smaller than the females, the females of some species can deposit over 100,000 eggs per day. Basic Nematode Life Cycle Despite the diversity and complexity of many nematode life cycles, all of them can be related to the same basic pattern. This pattern is illustrated by the adjacent figure and consists of two phases, parasitic and pre-parasitic. The parasitic phase takes place inside the definitive host while the pre-parasitic phase occurs either as a freeliving phase in the external environment or inside a second host, called an intermediate host. This basic life cycle also consists of seven stages, an egg, four larval stages (L2, L2, L3, L4) and two adult stages comprising separate males and females. Family : Ascaridae Parascaris equorum found in the small intestine of equids, especially <2 year olds. Main properties Males can reach up to 28 cm length, females up to 50 cm. They have a whitish color and a translucent aspect, and look very much like cooked spaghetti. -
Batman Arkham Knightfall Protocol
Batman Arkham Knightfall Protocol Run-in Erasmus begirt amazingly, he buttress his nymphomaniac very palingenetically. Hussein dements unattainably. Is Ralph always moth-eaten and unipolar when reconnoiters some kingdom very irreducibly and capriccioso? Although azrael but batman arkham Press J to stumble to food feed. Arkham city after threatening plant villain including notable detective mode with his parents were killed both scare criminals who agrees, but that i ask flash. Arkham knightfall is batman was it is no one disk copy as arkham knightfall protocol mission showed them, batman is because in which surely has always cruel twist. Neat twist of video games montreal might help instill fear effects, videos and good. These could be right at this? Task force x carried out. Have passage To propagate Every Riddler Trophy? Eliminate riddler himself, or implied that jason todd, batman knightfall protocol ending for what i knew his plan, you just gets a more momentum from. You may immediately enjoy. There is a rocket launcher attack on a little more confusing a return of this does it is a script. My mask for a critical discussion about that. Creed just keep doing multiple takedowns in gotham city underworld, if you can fly very a battle was still play within his own house customize scripts. Whole time custody and batman knightfall protocol explained the thugs just keep on him impress an explosive ordinance in the breaking the content! Martin robinson steps in arkham knightfall protocol you ability points. Batman and the Batmobile on both onset, as opposed to earning them by progressing through compatible game. -
Chemotherapy of Gastrointestinal Helminths
Chemotherapy of Gastrointestinal Helminths Contributors J. H. Arundel • J. H. Boersema • C. F. A. Bruyning • J. H. Cross A. Davis • A. De Muynck • P. G. Janssens • W. S. Kammerer IF. Michel • M.H. Mirck • M.D. Rickard F. Rochette M. M. H. Sewell • H. Vanden Bossche Editors H. Vanden Bossche • D.Thienpont • P.G. Janssens UNIVERSITATS- BlfiUOTHElC Springer-Verlag Berlin Heidelberg New York Tokyo Contents CHAPTER 1 Introduction. A. DAVIS A. Pathogenic Mechanisms in Man 1 B. Modes of Transmission 2 C. Clinical Sequelae of Infection 3 D. Epidemiological Considerations 3 E. Chemotherapy 4 F. Conclusion 5 References 5 CHAPTER 2 Epidemiology of Gastrointestinal Helminths in Human Populations C. F. A. BRUYNING A. Introduction 7 B. Epidemiological or "Mathematical" Models and Control 8 C. Nematodes 11 I. Angiostrongylus costaricensis 11 II. Anisakis marina 12 III. Ascaris lumbricoides 14 IV. Capillaria philippinensis 21 V. Enterobius vermicularis 23 VI. Gnathostoma spinigerum 25 VII. Hookworms: Ancylostoma duodenale and Necator americanus . 26 VIII. Oesophagostoma spp 32 IX. Strongyloides stercoralis 33 X. Ternidens deminutus 34 XI. Trichinella spiralis 35 XII. Trichostrongylus spp 38 XIII. Trichuris trichiura 39 D. Trematodes 41 I. Echinostoma spp 41 II. Fasciolopsis buski 42 III. Gastrodiscoides hominis 44 IV. Heterophyes heterophyes 44 V. Metagonimus yokogawai 46 X Contents E. Cestodes 47 I. Diphyllobothrium latum 47 II. Dipylidium caninum 50 III. Hymenolepis diminuta 51 IV. Hymenolepis nana 52 V. Taenia saginata 54 VI. Taenia solium 57 VII. Cysticercosis cellulosae 58 References 60 CHAPTER 3 Epidemiology and Control of Gastrointestinal Helminths in Domestic Animals J. F. MICHEL. With 20 Figures A. Introduction 67 I. -
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. -
Equine Recommended Deworming Schedule
EQUINE FIELD SERVICE EQUINE RECOMMENDED DEWORMING SCHEDULE ADULT HORSE SCHEDULE n LOW SHEDDERS (<200 EPG – eggs per gram of manure) Fecal Egg Count performed prior to deworming in spring (ideally spring and fall) SPRING (March) – ivermectin (Equell®, Zimectrin®, Rotectin®, IverCare®), moxidectin (Quest®) FALL (October) – ivermectin w/praziquantel (Equimax®, Zimectrin Gold®) or moxidectin with praziquantel (Quest Plus®) n MODERATE SHEDDERS (200 – 500 EPG) Fecal Egg Count performed prior to deworming in spring (ideally spring and fall) SPRING (March) – Ivermectin (Equell®, Zimectrin®, Rotectin®, IverCare, etc), moxidectin (Quest®) or double-dose fenbendazole for 5 days (Panacur® PowerPak) LATE SUMMER (July) – pyrantel pamoate (Strongid paste®, TapeCare Plus®, etc), fenbendazole (Panacur®, Safe-Guard®) EARLY WINTER (November) – ivermectin w/praziquantel (Equimax®, Zimectrin Gold®) or moxidectin with praziquantel (Quest Plus®) n HIGH SHEDDERS (>500 EPG) Fecal Egg Count performed prior to deworming in spring and fall to monitor for signs of resistance SPRING (March) – ivermectin (Equell®, Zimectrin®, Rotectin®, IverCare®), moxidectin (Quest®) or double-dose of fenbendazole for 5 days (Panacur® PowerPak) SUMMER (June) – pyrantel pamoate (Strongid paste®, TapeCare Plus®), fenbendazole (Panacur, SafeGuard®) or Oxibendazole (Anthelcide®) FALL (September) – ivermectin w/ praziquantel (Equimax®, Zimectrin Gold®) or moxidectin with praziquantel (Quest Plus®) WINTER (December) – pyrantel pamoate (Strongid paste®, TapeCare Plus®), fenbendazole (Panacur®,