CONICAL FLUKES in RUMINANTS Dr. JH Vorster, Bvsc, Mmedvet(Path)
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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. -
Biliary Obstruction Caused by the Liver Fluke, Fasciola Hepatica
CME Practice CMAJ Cases Biliary obstruction caused by the liver fluke, Fasciola hepatica Takuya Ishikawa MD PhD, Vanessa Meier-Stephenson MD PhD, Steven J. Heitman MD MSc Competing interests: None 20-year-old previously healthy man declared. presented to hospital with a two-day This article has been peer A history of right upper quadrant pain reviewed. and vomiting. Nine months earlier, he had The authors have obtained immigrated to Canada from Sudan, but he had patient consent. also lived in Djibouti and Ethiopia. Four Correspondence to: months before he presented to hospital, he Steven Heitman, received a diagnosis of tuberculous lymphade- [email protected] nitis and a four-drug course of tuberculosis CMAJ 2016. DOI:10.1503 treatment was started. However, he was non- /cmaj.150696 adherent after only two months of treatment. In addition, results from screening tests at that time showed evidence of schistosomiasis for Figure 1: A flat, leaf-shaped, brown worm emerg- which he was prescribed praziquantel. ing from the common bile duct of a 20-year-old On examination, he was alert and without man with abdominal pain. jaundice or scleral icterus. He had right upper quadrant tenderness on abdominal examination, ter of 1.1 cm. A computed tomography scan of but there were no palpable masses. The remain- the abdomen also showed prominence of the der of his examination was unremarkable. Labo- common bile duct, but no calcified stone was ratory test results showed elevated liver enzymes identified (Appendix 1). A hepatobiliary imino- (aspartate transaminase 133 [normal < 40] U/L, diacetic acid scan suggested distal obstruction in alanine transaminase 217 [normal < 41] U/L, the common bile duct. -
Classificação E Morfologia De Platelmintos Em Medicina Veterinária
UNIVERSIDADE FEDERAL RURAL DO RIO DE JANEIRO INSTITUTO DE VETERINÁRIA CLASSIFICAÇÃO E MORFOLOGIA DE PLATELMINTOS EM MEDICINA VETERINÁRIA: TREMATÓDEOS SEROPÉDICA 2016 PREFÁCIO Este material didático foi produzido como parte do projeto intitulado “Desenvolvimento e produção de material didático para o ensino de Parasitologia Animal na Universidade Federal Rural do Rio de Janeiro: atualização e modernização”. Este projeto foi financiado pela Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ) Processo 2010.6030/2014-28 e coordenado pela professora Maria de Lurdes Azevedo Rodrigues (IV/DPA). SUMÁRIO Caracterização morfológica de endoparasitos de filos do reino Animalia 03 A. Filo Nemathelminthes 03 B. Filo Acanthocephala 03 C. Filo Platyhelminthes 03 Caracterização morfológica de endoparasitos do filo Platyhelminthes 03 C.1. Superclasse Cercomeridea 03 1. Classe Trematoda 03 1.1. Subclasse Digenea 03 1.1.1. Ordem Paramphistomida 03 A.1.Família Paramphistomidae 04 A. 1.1. Gênero Paramphistomum 04 Espécie Paramphistomum cervi 04 A.1.2. Gênero Cotylophoron 04 Espécie Cotylophoron cotylophorum 04 1.1.2. Ordem Echinostomatida 05 A. Superfamília Cyclocoeloidea 05 A.1. Família Cyclocoelidae 05 A.1.1.Gênero Typhlocoelum 05 Espécie Typhlocoelum cucumerinum 05 A.2. Família Fasciolidaea 06 A.2.1. Gênero Fasciola 06 Espécie Fasciola hepatica 06 A.3. Família Echinostomatidae 07 A.3.1. Gênero Echinostoma 07 Espécie Echinostoma revolutum 07 A.4. Família Eucotylidae 08 A.4.1. Gênero Tanaisia 08 Espécie Tanaisia bragai 08 1.1.3. Ordem Diplostomida 09 A. Superfamília Schistosomatoidea 09 A.1. Família Schistosomatidae 09 A.1.1. Gênero Schistosoma 09 Espécie Schistosoma mansoni 09 B. -
Imaging Parasitic Diseases
Insights Imaging (2017) 8:101–125 DOI 10.1007/s13244-016-0525-2 REVIEW Unexpected hosts: imaging parasitic diseases Pablo Rodríguez Carnero1 & Paula Hernández Mateo2 & Susana Martín-Garre2 & Ángela García Pérez3 & Lourdes del Campo1 Received: 8 June 2016 /Revised: 8 September 2016 /Accepted: 28 September 2016 /Published online: 23 November 2016 # The Author(s) 2016. This article is published with open access at Springerlink.com Abstract Radiologists seldom encounter parasitic dis- • Some parasitic diseases are still endemic in certain regions eases in their daily practice in most of Europe, although in Europe. the incidence of these diseases is increasing due to mi- • Parasitic diseases can have complex life cycles often involv- gration and tourism from/to endemic areas. Moreover, ing different hosts. some parasitic diseases are still endemic in certain • Prompt diagnosis and treatment is essential for patient man- European regions, and immunocompromised individuals agement in parasitic diseases. also pose a higher risk of developing these conditions. • Radiologists should be able to recognise and suspect the This article reviews and summarises the imaging find- most relevant parasitic diseases. ings of some of the most important and frequent human parasitic diseases, including information about the para- Keywords Parasitic diseases . Radiology . Ultrasound . site’s life cycle, pathophysiology, clinical findings, diag- Multidetector computed tomography . Magnetic resonance nosis, and treatment. We include malaria, amoebiasis, imaging toxoplasmosis, trypanosomiasis, leishmaniasis, echino- coccosis, cysticercosis, clonorchiasis, schistosomiasis, fascioliasis, ascariasis, anisakiasis, dracunculiasis, and Introduction strongyloidiasis. The aim of this review is to help radi- ologists when dealing with these diseases or in cases Parasites are organisms that live in another organism at the where they are suspected. -
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). -
Nigella Sativaseed Extract Affected Tegument and Internal Organs of Trematode Paramphistomum Cervi
Advances in Animal and Veterinary Sciences Research Article Nigella sativa Seed Extract Affected Tegument and Internal Organs of Trematode Paramphistomum cervi 1* 2 3 MUHAMMAD HAMBAL , HENNI VANDA , SITI RANI AYUTI 1Veterinary Parasitology Department, Faculty of Veterinary Medicine, Universitas Syiah Kuala 23111, Indonesia; 2Veterinary Pharmacology Department, Faculty of Veterinary Medicine, Universitas Syiah Kuala 23111, Indonesia; 3Veterinary Biochemistry Department, Faculty of Veterinary Medicine, Universitas Syiah Kuala 23111, Indonesia. Abstract | Paramphistomum cervi infects ruminants and wildlife with significant economic losses. Anthelmintic resis- tance and high cost of treatment could be resolved by using traditional herbs to replace synthetic drugs. Nigella sativa is one of the alternative plants to treat paramphistomiasis. This study aimed to investigate the efficacy of N. sativa seed extract towards adult Paramphistomum flukes in vitro. The flukes were divided into six groups, consisted of ten flukes each, and soaked in 5% (T1), 10% (T2), 25% (T3), 40% (T4) N. sativa extract, in PBS (C0) as the negative control, and also in albendazole (C1) as the positive control. The motility and mortality time of flukes were recorded, and the dead flukes were further prepared for histopathology observation. The results revealed that treatment and control groups were significantly different (p<0.05). The most effective concentration was 40% N. sativa (T4), followed by T3, T2, and T1. N. sativa extract had stronger effect than albendazole towards P. cervi in vitro. In term of histological findings, the flukes in T3 and T4 showed disintegration and breaking of tegument, and necrose of parenchyma cells, while in T1 and T2, the tegument was still intact. -
Paramphistomum Spp in Irish Livestock
HERD HEALTH < FOCUS Paramphistomum spp in Irish livestock A previously unidentified Paramphistomum spp, has now been identified in sheep flocks and deer herds; Sharon Magnier, ruminant technical adviser, MSD Animal Health, looks at the impact this will have in Irish livestock In the past, paramphistomosis (infection with rumen fluke) species of rumen fluke that has been identified in cattle is was not considered to be a significant parasitic disease Calicophoron daubneyi. in cattle in Europe. However, over the past few years the prevalence of rumen fluke has increased sharply and clinically CLINICAL SIGNS significant outbreaks have been reported in several European The immature stages of the fluke in the duodenum cause countries, including countries with a temperate climate, such clinical disease including enteritis with diarrhoea anorexia as Ireland.1 Since 2012 cases of clinical paramphistomosis, dehydration and increased thirst.3 Youngstock are more severe enough to cause mortalities have been reported in vulnerable than older cattle and infection has been both cattle and sheep.1 associated with high mortality in this group. LIFE CYCLE RUMEN FLUKE IN SHEEP The life cycle of rumen fluke has similarities to liver fluke in A recent study in Irish sheep flocks into the prevalence and that it is indirect, involving the mud snail (Galba truncatula) risk factors associated with rumen fluke demonstrated an as the intermediate host. Encysted fluke (metacercariae) on exceptionally high true flock prevalence of 85.7%.1 This is pasture are ingested by grazing ruminants. The cyst wall is considerably higher than the prevalence reported in other digested releasing immature fluke larvae into the duodenum. -
The Mitochondrial Genome of Paramphistomum Cervi (Digenea), the First Representative for the Family Paramphistomidae
The Mitochondrial Genome of Paramphistomum cervi (Digenea), the First Representative for the Family Paramphistomidae Hong-Bin Yan1., Xing-Ye Wang1,4., Zhong-Zi Lou1,LiLi1, David Blair2, Hong Yin1, Jin-Zhong Cai3, Xue-Ling Dai1, Meng-Tong Lei3, Xing-Quan Zhu1, Xue-Peng Cai1*, Wan-Zhong Jia1* 1 State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Key Laboratory of Veterinary Public Health of Agriculture Ministry, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, Gansu Province, PR China, 2 School of Marine and Tropical Biology, James Cook University, Queensland, Australia, 3 Laboratory of Plateau Veterinary Parasitology, Veterinary Research Institute, Qinghai Academy of Animal Science and Veterinary Medicine, Xining, Qinghai Province, PR China, 4 College of Veterinary Medicine, Northwest A&F University, Yangling, Shanxi Province, PR China Abstract We determined the complete mitochondrial DNA (mtDNA) sequence of a fluke, Paramphistomum cervi (Digenea: Paramphistomidae). This genome (14,014 bp) is slightly larger than that of Clonorchis sinensis (13,875 bp), but smaller than those of other digenean species. The mt genome of P. cervi contains 12 protein-coding genes, 22 transfer RNA genes, 2 ribosomal RNA genes and 2 non-coding regions (NCRs), a complement consistent with those of other digeneans. The arrangement of protein-coding and ribosomal RNA genes in the P. cervi mitochondrial genome is identical to that of other digeneans except for a group of Schistosoma species that exhibit a derived arrangement. The positions of some transfer RNA genes differ. Bayesian phylogenetic analyses, based on concatenated nucleotide sequences and amino-acid sequences of the 12 protein-coding genes, placed P. -
Chronic Wasting Due to Liver and Rumen Flukes in Sheep
animals Review Chronic Wasting Due to Liver and Rumen Flukes in Sheep Alexandra Kahl 1,*, Georg von Samson-Himmelstjerna 1, Jürgen Krücken 1 and Martin Ganter 2 1 Institute for Parasitology and Tropical Veterinary Medicine, Freie Universität Berlin, Robert-von-Ostertag-Str. 7-13, 14163 Berlin, Germany; [email protected] (G.v.S.-H.); [email protected] (J.K.) 2 Clinic for Swine and Small Ruminants, Forensic Medicine and Ambulatory Service, University of Veterinary Medicine Hannover, Foundation, Bischofsholer Damm 15, 30173 Hannover, Germany; [email protected] * Correspondence: [email protected] Simple Summary: Chronic wasting in sheep is often related to parasitic infections, especially to infections with several species of trematodes. Trematodes, or “flukes”, are endoparasites, which infect different organs of their hosts (often sheep, goats and cattle, but other grazing animals as well as carnivores and birds are also at risk of infection). The body of an adult fluke has two suckers for adhesion to the host’s internal organ surface and for feeding purposes. Flukes cause harm to the animals by subsisting on host body tissues or fluids such as blood, and by initiating mechanical damage that leads to impaired vital organ functions. The development of these parasites is dependent on the occurrence of intermediate hosts during the life cycle of the fluke species. These intermediate hosts are often invertebrate species such as various snails and ants. This manuscript provides an insight into the distribution, morphology, life cycle, pathology and clinical symptoms caused by infections of liver and rumen flukes in sheep. -
Paramphistomum Leydeni) in Finland
Notable seasonal variation observed in the morphology of the reindeer rumen fluke (Paramphistomum leydeni) in Finland Sven Nikander & Seppo Saari Department of Basic Veterinary Sciences (FINPAR), P.O. Box 66, FIN-00014 University of Helsinki, Finland (corresponding author: [email protected]). Abstract: Although numerous Paramphistomum species have been described from the rumen and reticulum of domestic and wild ruminants, information about rumen flukes in reindeer is sparse and their nomenclature is somewhat conflicting. Rumen fluke of reindeer is usually referred to as P. cervi, but P. leydeni and Cotylophoron skriabini are also mentioned in the literature. Here, the surface structures and internal anatomy of rumen flukes from reindeer, as seen by scanning electron microscopy (SEM) and in histological sections under light microscopy, are presented. The aim of the study was to find morphological information to enable identification of rumen flukes in reindeer to species level. In addition, the morphology of rumen flukes collected in winter (winter flukes) was compared with that of flukes collected in summer (summer flukes). Key morphological findings were as follows: the acetabulum of the rumen flukes was of paramphistomum type, the pharynx of liorchis type, and the genital atrium of leydeni type. Both winter and summer flukes shared these morpho- logical features. Based on these findings, it was concluded that rumen flukes of reindeer in Finland belonged to the species P. leydeni. Significant morphological variation was observed when winter and summer flukes were compared. The winter fluke was smaller in size, possessed immature gonads (testes, ovary, uterus), and immature accessory genital glands (Mehlis’ gland, vitelline follicles), and had barely discernible tegumental papillae. -
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 ............................................................................................................... -
Common Helminth Infections of Donkeys and Their Control in Temperate Regions J
EQUINE VETERINARY EDUCATION / AE / SEPTEMBER 2013 461 Review Article Common helminth infections of donkeys and their control in temperate regions J. B. Matthews* and F. A. Burden† Disease Control, Moredun Research Institute, Edinburgh; and †The Donkey Sanctuary, Sidmouth, Devon, UK. *Corresponding author email: [email protected] Keywords: horse; donkey; helminths; anthelmintic resistance Summary management of helminths in donkeys is of general importance Roundworms and flatworms that affect donkeys can cause to their wellbeing and to that of co-grazing animals. disease. All common helminth parasites that affect horses also infect donkeys, so animals that co-graze can act as a source Nematodes that commonly affect donkeys of infection for either species. Of the gastrointestinal nematodes, those belonging to the cyathostomin (small Cyathostomins strongyle) group are the most problematic in UK donkeys. Most In donkey populations in which all animals are administered grazing animals are exposed to these parasites and some anthelmintics on a regular basis, most harbour low burdens of animals will be infected all of their lives. Control is threatened parasitic nematode infections and do not exhibit overt signs of by anthelmintic resistance: resistance to all 3 available disease. As in horses and ponies, the most common parasitic anthelmintic classes has now been recorded in UK donkeys. nematodes are the cyathostomin species. The life cycle of The lungworm, Dictyocaulus arnfieldi, is also problematical, these nematodes is the same as in other equids, with a period particularly when donkeys co-graze with horses. Mature of larval encystment in the large intestinal wall playing an horses are not permissive hosts to the full life cycle of this important role in the epidemiology and pathogenicity of parasite, but develop clinical signs on infection.