Review Article Nematodes of Birds of Armenia
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Checklist of Helminths from Lizards and Amphisbaenians (Reptilia, Squamata) of South America Ticle R A
The Journal of Venomous Animals and Toxins including Tropical Diseases ISSN 1678-9199 | 2010 | volume 16 | issue 4 | pages 543-572 Checklist of helminths from lizards and amphisbaenians (Reptilia, Squamata) of South America TICLE R A Ávila RW (1), Silva RJ (1) EVIEW R (1) Department of Parasitology, Botucatu Biosciences Institute, São Paulo State University (UNESP – Univ Estadual Paulista), Botucatu, São Paulo State, Brazil. Abstract: A comprehensive and up to date summary of the literature on the helminth parasites of lizards and amphisbaenians from South America is herein presented. One-hundred eighteen lizard species from twelve countries were reported in the literature harboring a total of 155 helminth species, being none acanthocephalans, 15 cestodes, 20 trematodes and 111 nematodes. Of these, one record was from Chile and French Guiana, three from Colombia, three from Uruguay, eight from Bolivia, nine from Surinam, 13 from Paraguay, 12 from Venezuela, 27 from Ecuador, 17 from Argentina, 39 from Peru and 103 from Brazil. The present list provides host, geographical distribution (with the respective biome, when possible), site of infection and references from the parasites. A systematic parasite-host list is also provided. Key words: Cestoda, Nematoda, Trematoda, Squamata, neotropical. INTRODUCTION The present checklist summarizes the diversity of helminths from lizards and amphisbaenians Parasitological studies on helminths that of South America, providing a host-parasite list infect squamates (particularly lizards) in South with localities and biomes. America had recent increased in the past few years, with many new records of hosts and/or STUDIED REGIONS localities and description of several new species (1-3). -
Giardiasis Importance Giardiasis, a Gastrointestinal Disease Characterized by Acute Or Chronic Diarrhea, Is Caused by Protozoan Parasites in the Genus Giardia
Giardiasis Importance Giardiasis, a gastrointestinal disease characterized by acute or chronic diarrhea, is caused by protozoan parasites in the genus Giardia. Giardia duodenalis is the major Giardia Enteritis, species found in mammals, and the only species known to cause illness in humans. This Lambliasis, organism is carried in the intestinal tract of many animals and people, with clinical signs Beaver Fever developing in some individuals, but many others remaining asymptomatic. In addition to diarrhea, the presence of G. duodenalis can result in malabsorption; some studies have implicated this organism in decreased growth in some infected children and Last Updated: December 2012 possibly decreased productivity in young livestock. Outbreaks are occasionally reported in people, as the result of mass exposure to contaminated water or food, or direct contact with infected individuals (e.g., in child care centers). People are considered to be the most important reservoir hosts for human giardiasis. The predominant genetic types of G. duodenalis usually differ in humans and domesticated animals (livestock and pets), and zoonotic transmission is currently thought to be of minor significance in causing human illness. Nevertheless, there is evidence that certain isolates may sometimes be shared, and some genetic types of G. duodenalis (assemblages A and B) should be considered potentially zoonotic. Etiology The protozoan genus Giardia (Family Giardiidae, order Giardiida) contains at least six species that infect animals and/or humans. In most mammals, giardiasis is caused by Giardia duodenalis, which is also called G. intestinalis. Both names are in current use, although the validity of the name G. intestinalis depends on the interpretation of the International Code of Zoological Nomenclature. -
Gastrointestinal Helminths of Two Populations of Wild Pigeons
Original Article Braz. J. Vet. Parasitol., Jaboticabal, v. 26, n. 4, p. 446-450, oct.-dec. 2017 ISSN 0103-846X (Print) / ISSN 1984-2961 (Electronic) Doi: http://dx.doi.org/10.1590/S1984-29612017071 Gastrointestinal helminths of two populations of wild pigeons (Columba livia) in Brazil Helmintos gastrointestinais de duas populações de pombos de vida livre (Columba livia) no Brasil Frederico Fontanelli Vaz1; Lidiane Aparecida Firmino da Silva2; Vivian Lindmayer Ferreira1; Reinaldo José da Silva2; Tânia Freitas Raso1* 1 Departamento de Patologia Veterinária, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo – USP, São Paulo, SP, Brasil 2 Departamento de Parasitologia, Instituto de Biociências, Universidade Estadual Paulista – UNESP, Botucatu, SP, Brasil Received July 2, 2017 Accepted November 8, 2017 Abstract The present study analyzed gastrointestinal helminth communities in 265 wild pigeons Columba( livia) living in the municipalities of São Paulo and Tatuí, state of São Paulo, Brazil, over a one-year period. The birds were caught next to grain storage warehouses and were necropsied. A total of 790 parasites comprising one nematode species and one cestode genus were recovered from 110 pigeons, thus yielding an overall prevalence of 41.5%, mean intensity of infection of 7.2 ± 1.6 (range 1-144) and discrepancy index of 0.855. Only 15 pigeons (5.7%) presented mixed infection. The helminths isolated from the birds were Ascaridia columbae (Ascaridiidae) and Raillietina sp. (Davaineidae). The birds’ weights differed according to sex but this did not influence the intensity of infection. The overall prevalence and intensity of infection did not differ between the sexes, but the prevalence was higher among the birds from Tatuí (47.8%). -
Tinamiformes – Falconiformes
LIST OF THE 2,008 BIRD SPECIES (WITH SCIENTIFIC AND ENGLISH NAMES) KNOWN FROM THE A.O.U. CHECK-LIST AREA. Notes: "(A)" = accidental/casualin A.O.U. area; "(H)" -- recordedin A.O.U. area only from Hawaii; "(I)" = introducedinto A.O.U. area; "(N)" = has not bred in A.O.U. area but occursregularly as nonbreedingvisitor; "?" precedingname = extinct. TINAMIFORMES TINAMIDAE Tinamus major Great Tinamou. Nothocercusbonapartei Highland Tinamou. Crypturellus soui Little Tinamou. Crypturelluscinnamomeus Thicket Tinamou. Crypturellusboucardi Slaty-breastedTinamou. Crypturellus kerriae Choco Tinamou. GAVIIFORMES GAVIIDAE Gavia stellata Red-throated Loon. Gavia arctica Arctic Loon. Gavia pacifica Pacific Loon. Gavia immer Common Loon. Gavia adamsii Yellow-billed Loon. PODICIPEDIFORMES PODICIPEDIDAE Tachybaptusdominicus Least Grebe. Podilymbuspodiceps Pied-billed Grebe. ?Podilymbusgigas Atitlan Grebe. Podicepsauritus Horned Grebe. Podicepsgrisegena Red-neckedGrebe. Podicepsnigricollis Eared Grebe. Aechmophorusoccidentalis Western Grebe. Aechmophorusclarkii Clark's Grebe. PROCELLARIIFORMES DIOMEDEIDAE Thalassarchechlororhynchos Yellow-nosed Albatross. (A) Thalassarchecauta Shy Albatross.(A) Thalassarchemelanophris Black-browed Albatross. (A) Phoebetriapalpebrata Light-mantled Albatross. (A) Diomedea exulans WanderingAlbatross. (A) Phoebastriaimmutabilis Laysan Albatross. Phoebastrianigripes Black-lootedAlbatross. Phoebastriaalbatrus Short-tailedAlbatross. (N) PROCELLARIIDAE Fulmarus glacialis Northern Fulmar. Pterodroma neglecta KermadecPetrel. (A) Pterodroma -
Diptera: Muscidae) Due to Habronema Muscae (Nematoda: Habronematidae
©2017 Institute of Parasitology, SAS, Košice DOI 10.1515/helm-2017-0029 HELMINTHOLOGIA, 54, 3: 225 – 230, 2017 Preimaginal mortality of Musca domestica (Diptera: Muscidae) due to Habronema muscae (Nematoda: Habronematidae) R. K. SCHUSTER Central Veterinary Research Laboratory, PO Box 597, Dubai, United Arab Emirates, E-mail: [email protected] Article info Summary Received December 29, 2016 In order to study the damage of Habronema muscae (Carter, 1861) on its intermediate host, Mus- Accepted April 24, 2017 ca domestica Linnaeus, 1758, fl y larval feeding experiments were carried out. For this, a defi ned number of praeimaginal stages of M. domestica was transferred in daily intervals (from day 0 to day 10) on faecal samples of a naturally infected horse harboring 269 adult H. muscae in its stomach. The development of M. domestica was monitored until imagines appeared. Harvested pupae were measured and weighted and the success of infection was studied by counting 3rd stage nematode larvae in freshly hatched fl ies. In addition, time of pupation and duration of the whole development of the fl ies was noticed. Pupation, hatching and preimaginal mortality rates were calculated and the number of nematode larvae in freshly hatched fl ies was counted. Adult fl ies harboured up to 60 Habronema larvae. Lower pupal volumes and weights, lower pupation rates and higher preimaginal mortality rates were found in experimental groups with long exposure to parasite eggs compared to experimental groups with short exposure or to the uninfected control groups. Maggots of the former groups pupated earlier and fl y imagines occurred earlier. These fi ndings clearly showed a negative impact of H. -
Proceedings of the United States National Museum
— THE ADAPTIVE MODIFICATIONS AND THE TAXONOMIC VALUE OF THE TONGUE IN BIRDS By Leon L. Gardner, Of the United States Army Medical Corps Since the work of Lucas 1 there has been little systematic investiga- tion on the tongues of birds, and with the exception of an occasional description the subject has been largely neglected. It is in the hope of reopening interest in the subject that this paper is written. As is well known the tongue is an exceptionally variable organ in the Class Aves, as is to be expected from the fact that it is so inti- mately related with the birds' most important problem, that of obtaining food. For this function it must serve as a probe or spear (woodpeckers and nuthatches), a sieve (ducks), a capillary tube (sunbirds and hummers), a brush (Trichoglossidae), a rasp (vul- tures, hawks, and owls), as a barbed organ to hold slippery prey (penguins), as a finger (parrots and sparrows), and perhaps as a tactile organ in long-billed birds, such as sandpipers, herons, and the like. The material upon which this paper is based is the very extensive alcoholic collection of birds in the United States National Museum, Washington, D. C, for the use of which and for his abundant aid in numberless ways I am very much indebted to Dr. Charles W. Richmond, associate curator of the Division of Birds. To Dr. Alexander Wetmore, assistant secretary in charge of the United States National Museum, I wish to express my thanks for his kind assistance in reviewing the paper and for his help in its preparation. -
Parasites of the Neotropic Cormorant Nannopterum (Phalacrocorax) Brasilianus (Aves, Phalacrocoracidae) in Chile
Original Article ISSN 1984-2961 (Electronic) www.cbpv.org.br/rbpv Parasites of the Neotropic cormorant Nannopterum (Phalacrocorax) brasilianus (Aves, Phalacrocoracidae) in Chile Parasitos da biguá Nannopterum (Phalacrocorax) brasilianus (Aves, Phalacrocoracidae) do Chile Daniel González-Acuña1* ; Sebastián Llanos-Soto1,2; Pablo Oyarzún-Ruiz1 ; John Mike Kinsella3; Carlos Barrientos4; Richard Thomas1; Armando Cicchino5; Lucila Moreno6 1 Laboratorio de Parásitos y Enfermedades de Fauna Silvestre, Departamento de Ciencia Animal, Facultad de Medicina Veterinaria, Universidad de Concepción, Chillán, Chile 2 Laboratorio de Vida Silvestre, Departamento de Ciencia Animal, Facultad de Medicina Veterinaria, Universidad de Concepción, Chillán, Chile 3 Helm West Lab, Missoula, MT, USA 4 Escuela de Medicina Veterinaria, Universidad Santo Tomás, Concepción, Chile 5 Universidad Nacional de Mar del Plata, Mar del Plata, Argentina 6 Facultad de Ciencias Naturales y Oceanográficas, Universidad de Concepción, Concepción, Chile How to cite: González-Acuña D, Llanos-Soto S, Oyarzún-Ruiz P, Kinsella JM, Barrientos C, Thomas R, et al. Parasites of the Neotropic cormorant Nannopterum (Phalacrocorax) brasilianus (Aves, Phalacrocoracidae) in Chile. Braz J Vet Parasitol 2020; 29(3): e003920. https://doi.org/10.1590/S1984-29612020049 Abstract The Neotropic cormorant Nannopterum (Phalacrocorax) brasilianus (Suliformes: Phalacrocoracidae) is widely distributed in Central and South America. In Chile, information about parasites for this species is limited to helminths and nematodes, and little is known about other parasite groups. This study documents the parasitic fauna present in 80 Neotropic cormorants’ carcasses collected from 2001 to 2008 in Antofagasta, Biobío, and Ñuble regions. Birds were externally inspected for ectoparasites and necropsies were performed to examine digestive and respiratory organs in search of endoparasites. -
(Nematoda: Habronematidae) from the Burchelps Zebras and Hartmann's Mountain Zebras in Southern Africa
Proc. Helminthol. Soc. Wash. 56(2), 1989, pp. 183-191 Habronema malani sp. n. and Habronema tomasi sp. n. (Nematoda: Habronematidae) from the BurchelPs Zebras and Hartmann's Mountain Zebras in Southern Africa ROSINA C. KRECEK Department of Parasitology, Faculty of Veterinary Science, University of Pretoria, Private Bag X04, Onderstepoort 0110, South Africa ABSTRACT: Habronema malani sp. n. is described from the stomachs of 44 Burchell's zebras, Equus burchelli antiquorum, in the Etosha and Kruger national parks and 6 Hartmann's mountain zebras, Equus zebra hart- mannae, from the Etosha National Park in southern Africa. Habronema tomasi sp. n. is described from the small intestines of 35 Burchell's zebras in the Kruger National Park. Habronema malani is distinguished from other members of the genus by its deep buccal capsule with walls that are narrower anteriorly than posteriorly and have projections in the anterior end; spicule length ratio (right:left) ranging 1:2.3 to 1:3.7; a short, stout, and striated right spicule; and a long and slender left spicule with a pointed projection. Habronema tomasi is differentiated from the other species by buccal capsule walls that are wider anteriorly than posteriorly; a distance between the anterior wall of the buccal capsule and the inner surface of the lateral lips that is almost equal to the buccal capsule depth; an ovejector with spiral-shaped muscles; and a spicule length ratio (right: left) ranging 1:1.5 to 1:2.95. The right spicule of//, tomasi is short and cross striated except at the distal fourth where the tip is flanged. -
Review of Zoonotic Pathogens in Ambient Waters
EPA 822-R-09-002 REVIEW OF ZOONOTIC PATHOGENS IN AMBIENT WATERS U.S. Environmental Protection Agency Office of Water Health and Ecological Criteria Division February 2009 [this page intentionally left blank] U.S. Environmental Protection Agency DISCLAIMER This document has been reviewed in accordance with U.S. Environmental Protection Agency policy and approved for publication. Mention of trade names or commercial products does not constitute endorsement or recommendation for use. February 2009 i [this page intentionally left blank] U.S. Environmental Protection Agency ACKNOWLEDGMENTS Questions concerning this document or its application should be addressed to the EPA Work Assignment Manager: John Ravenscroft USEPA Headquarters Office of Science and Technology, Office of Water 1200 Pennsylvania Avenue, NW Mail Code: 4304T Washington, DC 20460 Phone: 202-566-1101 Email: [email protected] This literature review was managed under EPA Contract EP-C-07-036 to Clancy Environmental Consultants, Inc. The following individuals contributed to the development of the report: Lead writer: Audrey Ichida ICF International Leiran Biton ICF International Alexis Castrovinci ICF International Jennifer Clancy Clancy Environmental Consultants Mary Clark ICF International Elizabeth Dederick ICF International Kelly Hammerle ICF International Walter Jakubowski WaltJay Consulting Margaret McVey ICF International Michelle Moser ICF International Jeffery Rosen Clancy Environmental Consultants Tina Rouse ICF International Jennifer Welham ICF International -
Addendum to the Checklist of the Helminth Parasites of Vertebrates in Costa Rica
Rev. Biol. Trop. 52(2): 355-362, 2004 www.ucr.ac.cr www.ots.ac.cr www.ots.duke.edu Addendum to the Checklist of the helminth parasites of vertebrates in Costa Rica Beatriz Rodríguez-Ortíz1, Luis García-Prieto2, Jonathan Herrera-Vázquez1 & Gerardo Pérez-Ponce de León2 1 Laboratorio de Helmintología, Facultad de Microbiología, Universidad de Costa Rica, San José, Costa Rica, e-mail: [email protected]; [email protected] 2 Laboratorio de Helmintología, Instituto de Biología, UNAM. Ap. Postal 70-153. C.P. 04510, México D.F., e-mail: [email protected]; [email protected] Received 22-II-2004. Corrected 01-III-2004. Accepted 01-III-2004. Abstract: In this work, we present an addendum to the “Checklist of the helminth parasites of vertebrates in Costa Rica” with a parasite-host list as well as a host-parasite list. This addendum updates the available infor- mation on this group of parasites in Costa Rica, since very recently a new input has been made to describe the helminth fauna of vertebrates, particularly at the Área de Conservación de Guanacaste. In this paper, we add 33 records, representing 23 species. This raises the number of helminth species described in vertebrates from Costa Rica to 325, represented by 89 species of digeneans, 23 of monogeneans, 63 of cestodes, 13 of acantho- cephalans, and 137 of nematodes. In total, 133 species of vertebrates have been studied for helminths in Costa Rica (31 species of fishes, 7 amphibians, 18 reptiles, 40 birds, and 37 mammals). Currently, 67 species (20.6 %) have been recorded as new species from Costa Rica and most of them are endemic to particular regions. -
YOSHINO-01 65417.Pdf
J.Rakuno Gakuen Univ.,38(2):139~148(2014) Filarial nematodes belonging to the superorders Diplotriaenoidea and Aproctoidea from wild and captive birds in Japan Tomoo YOSHINO웋웦워웗,Natsuki HAM A웍웗,Manabu ONUMA웎웗,Masaoki TAKAGI웏웗, Kei SATO원웗,Shin MATSUI웏웗,Mariko HISAKA웏웗,Tokuma YANAI웑웗,Haruo ITO웒웗, Nobutaka URANO웓웗,Yu ichi OSA웋월웗and웬Mitsuhiko ASAKAW A웋웗 (Accepted 17 January 2014) Introduction Materials and Methods Nematodes belonging to the superorders Di- The nematode specimens were obtained from plotriaenoidea and Aproctoidea parasitize many wild and captive birds,including Turdus naum- orders of birds and sometimes reptiles[24,25]. mani Temminck,1820(15:number of infected These nematodes are found in the air sac,lungs, individuals), Poecile varius (Temminck& orbital cavity,body cavity,abdominal cavity, Schlegel,1845)(2),Parus minor Temminck& subcutaneous tissues and/or under the skin[21]. Schlegel,1848(1),Falco columbarius Linnaeus, Also,they are well known to often cause subcuta- 1758(1),Falco peregrinus Tunstall,1771(2),Ac- neous emphysema,pneumonia and/or air sac- cipiter gentilis (Linnaeus,1758)(2),Lanius buce- culitis,including fatal cases,especially in Fal- phalus Temminck& Schlegel,1845(1),Lanius coniformes[1,7-10,14,15,21,23,26,30,31]. cristatus lucionensis Linnaeus,1766(1),Otus flam- Despite the ir common occurrence throughout the meolus Kaup,1853(1)and Otus sunia Hodgson, world,there have been few reports of 1836(2)between 1995 and 2009 in Japan.They nematodiasis attributed to these two groups in were removed in post mortem examination -
Ahead of Print Online Version Phylogenetic Relationships of Some
Ahead of print online version FOLIA PARASITOLOGICA 58[2]: 135–148, 2011 © Institute of Parasitology, Biology Centre ASCR ISSN 0015-5683 (print), ISSN 1803-6465 (online) http://www.paru.cas.cz/folia/ Phylogenetic relationships of some spirurine nematodes (Nematoda: Chromadorea: Rhabditida: Spirurina) parasitic in fishes inferred from SSU rRNA gene sequences Eva Černotíková1,2, Aleš Horák1 and František Moravec1 1 Institute of Parasitology, Biology Centre of the Academy of Sciences of the Czech Republic, Branišovská 31, 370 05 České Budějovice, Czech Republic; 2 Faculty of Science, University of South Bohemia, Branišovská 31, 370 05 České Budějovice, Czech Republic Abstract: Small subunit rRNA sequences were obtained from 38 representatives mainly of the nematode orders Spirurida (Camalla- nidae, Cystidicolidae, Daniconematidae, Philometridae, Physalopteridae, Rhabdochonidae, Skrjabillanidae) and, in part, Ascaridida (Anisakidae, Cucullanidae, Quimperiidae). The examined nematodes are predominantly parasites of fishes. Their analyses provided well-supported trees allowing the study of phylogenetic relationships among some spirurine nematodes. The present results support the placement of Cucullanidae at the base of the suborder Spirurina and, based on the position of the genus Philonema (subfamily Philoneminae) forming a sister group to Skrjabillanidae (thus Philoneminae should be elevated to Philonemidae), the paraphyly of the Philometridae. Comparison of a large number of sequences of representatives of the latter family supports the paraphyly of the genera Philometra, Philometroides and Dentiphilometra. The validity of the newly included genera Afrophilometra and Carangi- nema is not supported. These results indicate geographical isolation has not been the cause of speciation in this parasite group and no coevolution with fish hosts is apparent. On the contrary, the group of South-American species ofAlinema , Nilonema and Rumai is placed in an independent branch, thus markedly separated from other family members.