Acanthocephalan Infestation in Fishes –A Review
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Review of Acanthocephala (Hemiptera: Heteroptera: Coreidae) of America North of Mexico with a Key to Species
Zootaxa 2835: 30–40 (2011) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2011 · Magnolia Press ISSN 1175-5334 (online edition) Review of Acanthocephala (Hemiptera: Heteroptera: Coreidae) of America north of Mexico with a key to species J. E. McPHERSON1, RICHARD J. PACKAUSKAS2, ROBERT W. SITES3, STEVEN J. TAYLOR4, C. SCOTT BUNDY5, JEFFREY D. BRADSHAW6 & PAULA LEVIN MITCHELL7 1Department of Zoology, Southern Illinois University, Carbondale, Illinois 62901, USA. E-mail: [email protected] 2Department of Biological Sciences, Fort Hays State University, Hays, Kansas 67601, USA. E-mail: [email protected] 3Enns Entomology Museum, Division of Plant Sciences, University of Missouri, Columbia, Missouri 65211, USA. E-mail: [email protected] 4Illinois Natural History Survey, University of Illinois at Urbana-Champaign, Illinois 61820, USA. E-mail: [email protected] 5Department of Entomology, Plant Pathology, & Weed Science, New Mexico State University, Las Cruces, New Mexico 88003, USA. E-mail: [email protected] 6Department of Entomology, University of Nebraska-Lincoln, Panhandle Research & Extension Center, Scottsbluff, Nebraska 69361, USA. E-mail: [email protected] 7Department of Biology, Winthrop University, Rock Hill, South Carolina 29733, USA. E-mail: [email protected] Abstract A review of Acanthocephala of America north of Mexico is presented with an updated key to species. A. confraterna is considered a junior synonym of A. terminalis, thus reducing the number of known species in this region from five to four. New state and country records are presented. Key words: Coreidae, Coreinae, Acanthocephalini, Acanthocephala, North America, review, synonymy, key, distribution Introduction The genus Acanthocephala Laporte currently is represented in America north of Mexico by five species: Acan- thocephala (Acanthocephala) declivis (Say), A. -
Platyhelminthes, Nemertea, and "Aschelminthes" - A
BIOLOGICAL SCIENCE FUNDAMENTALS AND SYSTEMATICS – Vol. III - Platyhelminthes, Nemertea, and "Aschelminthes" - A. Schmidt-Rhaesa PLATYHELMINTHES, NEMERTEA, AND “ASCHELMINTHES” A. Schmidt-Rhaesa University of Bielefeld, Germany Keywords: Platyhelminthes, Nemertea, Gnathifera, Gnathostomulida, Micrognathozoa, Rotifera, Acanthocephala, Cycliophora, Nemathelminthes, Gastrotricha, Nematoda, Nematomorpha, Priapulida, Kinorhyncha, Loricifera Contents 1. Introduction 2. General Morphology 3. Platyhelminthes, the Flatworms 4. Nemertea (Nemertini), the Ribbon Worms 5. “Aschelminthes” 5.1. Gnathifera 5.1.1. Gnathostomulida 5.1.2. Micrognathozoa (Limnognathia maerski) 5.1.3. Rotifera 5.1.4. Acanthocephala 5.1.5. Cycliophora (Symbion pandora) 5.2. Nemathelminthes 5.2.1. Gastrotricha 5.2.2. Nematoda, the Roundworms 5.2.3. Nematomorpha, the Horsehair Worms 5.2.4. Priapulida 5.2.5. Kinorhyncha 5.2.6. Loricifera Acknowledgements Glossary Bibliography Biographical Sketch Summary UNESCO – EOLSS This chapter provides information on several basal bilaterian groups: flatworms, nemerteans, Gnathifera,SAMPLE and Nemathelminthes. CHAPTERS These include species-rich taxa such as Nematoda and Platyhelminthes, and as taxa with few or even only one species, such as Micrognathozoa (Limnognathia maerski) and Cycliophora (Symbion pandora). All Acanthocephala and subgroups of Platyhelminthes and Nematoda, are parasites that often exhibit complex life cycles. Most of the taxa described are marine, but some have also invaded freshwater or the terrestrial environment. “Aschelminthes” are not a natural group, instead, two taxa have been recognized that were earlier summarized under this name. Gnathifera include taxa with a conspicuous jaw apparatus such as Gnathostomulida, Micrognathozoa, and Rotifera. Although they do not possess a jaw apparatus, Acanthocephala also belong to Gnathifera due to their epidermal structure. ©Encyclopedia of Life Support Systems (EOLSS) BIOLOGICAL SCIENCE FUNDAMENTALS AND SYSTEMATICS – Vol. -
Acanthocephala: Rhadinorhynchidae) from the Red Porgy Pagrus Pagrus (Teleostei: Sparidae) of the Red Sea, Egypt: a Morphological Study
Acta Parasitologica Globalis 9 (3): 133-140 2018 ISSN 2079-2018 © IDOSI Publications, 2018 DOI: 10.5829/idosi.apg.2018.133.140 Serrasentis Sagittifer Linton, 1889 (Acanthocephala: Rhadinorhynchidae) from the Red Porgy Pagrus pagrus (Teleostei: Sparidae) of the Red Sea, Egypt: A Morphological Study 11Nahed Saed, Mahrashan Abdel-Gawad, 2Sahar El-Ganainy, 21Manal Ahmed, Kareem Morsy and 3Asmaa Adel 1Zoology Department, Faculty of Science, Cairo University, Cairo, Egypt 2Zoology Department, Faculty of Science, Minia University, Minya, Egypt 3Zoology Department, Faculty of Science, South Valley University, Qena, Egypt Abstract: In the present study, an acanthocephalan parasite was recovered from the intestine of the red porgy Pagrus pagrus (Sparidae) captured from water locations along the Red Sea at Hurghada coasts, Egypt. The parasite was observed attached to the wall of the host intestine by an armed proboscis equipped by recurved hooks. 14 out of 40 fish specimens (35.0%) were found to be infected during winter season only. The mean intensity ranged from 4-10 parasites/infected fish. The recovered worms were creamy white, elongated with narrow posterior end. Light and scanning electron microscopy showed that the parasite has distinctive rows of spines (combs) on the ventral surface. Body was 3.55±0.02 (3.33-3.58) mm long. Width at the base of probocis was 0.10±0.02 (0.08-0.12) mm. Proboscis club-shaped with a broad anterior end, euipped by longitudinal rows of hooks, each with 15-19 of curved hooks. Neck smooth, the double-walled receptacle was attached to the proboscis wall. Trunk was spinose anteriorly, spines arranged in 7-10 collar rows, each was equipped with 15-18 spines. -
Luth Wfu 0248D 10922.Pdf
SCALE-DEPENDENT VARIATION IN MOLECULAR AND ECOLOGICAL PATTERNS OF INFECTION FOR ENDOHELMINTHS FROM CENTRARCHID FISHES BY KYLE E. LUTH A Dissertation Submitted to the Graduate Faculty of WAKE FOREST UNIVERSITY GRADAUTE SCHOOL OF ARTS AND SCIENCES in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY Biology May 2016 Winston-Salem, North Carolina Approved By: Gerald W. Esch, Ph.D., Advisor Michael V. K. Sukhdeo, Ph.D., Chair T. Michael Anderson, Ph.D. Herman E. Eure, Ph.D. Erik C. Johnson, Ph.D. Clifford W. Zeyl, Ph.D. ACKNOWLEDGEMENTS First and foremost, I would like to thank my PI, Dr. Gerald Esch, for all of the insight, all of the discussions, all of the critiques (not criticisms) of my works, and for the rides to campus when the North Carolina weather decided to drop rain on my stubborn head. The numerous lively debates, exchanges of ideas, voicing of opinions (whether solicited or not), and unerring support, even in the face of my somewhat atypical balance of service work and dissertation work, will not soon be forgotten. I would also like to acknowledge and thank the former Master, and now Doctor, Michael Zimmermann; friend, lab mate, and collecting trip shotgun rider extraordinaire. Although his need of SPF 100 sunscreen often put our collecting trips over budget, I could not have asked for a more enjoyable, easy-going, and hard-working person to spend nearly 2 months and 25,000 miles of fishing filled days and raccoon, gnat, and entrail-filled nights. You are a welcome camping guest any time, especially if you do as good of a job attracting scorpions and ants to yourself (and away from me) as you did on our trips. -
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). -
Appendix: Bioinspired Parasite Details
A p p e n d i x : B i o i n s p i r e d P a r a s i t e Details Internal Parasites: Endoparasites Biological endoparasites live inside a hosts’ body. In farms, biological parasites infect, hurt, and even kill animals, hurting a farming business. This book is look- ing for inspiration from biology to prevent or treat business “disease.” In business, there are many opportunities for inoculation and treatment. Brain Jackers—Acanthocephala— Thorny-Headed Worms Thorny-headed worms are rare in humans, and also cause disease in birds, amphibians, and reptiles. They are called thorny-headed because they use a bio- logical lancet to pierce and hold onto the stomach walls of the host (Wikipedia, 2013). Their lifecycle includes invertebrates, fish, lizards, birds, and mammals. In one stage of their lifecycle, they “brain jack” a small crustacean eaten by ducks. Just as inner-city drivers are subject to “car-jacking,” this parasite actually redi- rects the crustacean’s dominant behavior from staying away from light to actively seeking it—where ducks may be more likely to eat them, and where the parasite reproduces (Wikipedia, 2013). Alaskan Inuit have a zest for raw fish and that contributes to their increased incidence of Acanthocephala infection compared with other groups of people (Roberts & Janovy, 2009, p. 506). Prevention and Treatment for Acanthocephala Endoscopic and X-ray examinations detect Acanthocephala because their eggs are not passed through feces (Mehlhorn, 2008, p. 25). Controlling the spread of rodents, as well as protecting and cooking food prevents infection. -
Smaller Protostome Phyla: Rotifera, Gastrotricha, Nematomorpha & Acanthocephala Bio 1413: General Zoology Lab (Ziser, 2008) [Exercise 10B] Lab Activities: 1
Smaller Protostome Phyla: Rotifera, Gastrotricha, Nematomorpha & Acanthocephala Bio 1413: General Zoology Lab (Ziser, 2008) [Exercise 10B] Lab Activities: 1. Rotifers (p167) slide: Rotifers, wm • Examine prepared slide of a rotifer and be able to identify the following structures: corona, foot, mastax, digestive tract, reproductive tract • Attempt to locate and to identify living rotifers from the water samples provided • Recognize and identify rotifers on illustrations and be able to identify to Phylum 2. Gastrotrichs (p167) slide: Gastrotrichs, wm • Observe living specimens (if available) and note their appearance and movement • examine prepared slides of a gastrotrich and identify: mouth, pharynx, adhesive gland, scales 3. Nematomorpha (p168) preserved: horsehair worms • examine living and/or preserved horsehair worms as available and be able to recognize them and distinguish them from other “wormlike” phyla 4. Acanthocephala (p168) • examine preserved specimens and slides as available and be able to recognize them and distinguish them from other “wormlike” phyla eg. Macracanthorhynchus preserved: Macracanthorhynchus this animal is parasitic in the intestine of pigs, the larvae develop in beetle grubs which are eaten by pigs to complete its life cycle eg. examine the prepared slide slide: acanthoceophala, wm identify the following: retractable proboscis with hooks, proboscis receptacle, ligament sac Notebook Suggestions: Describe the kinds of movement seen in live rotifers and compare to the movement seen in roundworms; is it similar? Diagram some of the variety of rotifers in samples and illustrations; what characteristics do all share; how do each differ If living gastrotrichs are available, describe how their movement differs from that of rotifers. Can you identify any organs on the gastrotrich Describe the similarities and differences between acanthocephala and nematomorpha make a diagram of the general life cycle of a horsehair worm and an acanthocephalan. -
The Life Cycle of the Parasite Pomphorhynchus Tereticollis in Reference to 0+ Cyprinids and the Intermediate Host Gammarus Spp in the UK
March 2020 The life cycle of the parasite Pomphorhynchus tereticollis in reference to 0+ cyprinids and the intermediate host Gammarus spp in the UK. Matthew J Harris Thesis submitted in partial fulfilment of the requirements of the degree of Master’s By Research Bournemouth University Supervisory team; Iain Green, Robert Britton and Demetra Andreou Acknowledgments I would like to thank all of my supervisors for the support they have given me through the project in regard to their enormous plethora of knowledge. In particular I would like to thank Dr Demetra Andreou as without her support, motivation and can-do attitude I may not have been able to finish this project. It was also Dr Andreou who originally inspired me to purse Parasitological studies and without her inspiration in my undergraduate studies, it is unlikely I would have studied a MRes as parasitology bewilders me like no field I have ever come across. I would also like to thank Dr Catherine Gutman-Roberts for allowing me access to samples that she had previously collected. As well as this, Dr Gutmann-Roberts was always helpful and friendly when questions were directed at her. Finally, I would also like to thank her for the help she gave to me regarding field work. Abstract Pomphorhynchus tereticollis is a recently resurrected parasite species that spans the UK and continental Europe. The parasite is the only Pomphorhynchus spp in the UK and has been researched since the early 1970’s. The species has an indirect life cycle which uses a Gammarus spp as an intermediate host and cyprinids and salmonids as final hosts although the main hosts are Squalis cephalus (S. -
(Crustacea: Amphipoda) and Their Manipulative Acanthocephalan Parasites
Effect of the environment on the interaction between gammarids (Crustacea : Amphipoda) and their manipulative acanthocephalan parasites Sophie Labaude To cite this version: Sophie Labaude. Effect of the environment on the interaction between gammarids (Crustacea :Am- phipoda) and their manipulative acanthocephalan parasites. Symbiosis. Université de Bourgogne, 2016. English. NNT : 2016DIJOS022. tel-01486123 HAL Id: tel-01486123 https://tel.archives-ouvertes.fr/tel-01486123 Submitted on 9 Mar 2017 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. Université de Bourgogne UMR CNRS 6282 Biogéosciences PhD Thesis Thèse pour l’obtention du grade de Docteur de l’Université de Bourgogne Discipline : Sciences de la vie Spécialité : Biologie des populations et écologie Effect of the environment on the interaction between gammarids (Crustacea: Amphipoda) and their manipulative acanthocephalan parasites Sophie Labaude Jury Demetra Andreou, Senior Lecturer, Bournemouth University Examinateur Iain Barber, Senior Lecturer, University of Leicester Rapporteur Jean-Nicolas -
3. Eriyusni Upload
Aceh Journal of Animal Science (2019) 4(2): 61-69 DOI: 10.13170/ajas.4.2.14129 Printed ISSN 2502-9568 Electronic ISSN 2622-8734 SHORT COMMUNICATION Endoparasite worms infestation on Skipjack tuna Katsuwonus pelamis from Sibolga waters, Indonesia Eri Yusni*, Raihan Uliya Faculty of Agriculture, University of North Sumatera, Medan, Indonesia. *Corresponding author’s email: [email protected] Received: 24 July 2019 Accepted: 11 August 2019 ABSTRACT Skipjack tuna Katsuwonus pelamis is one of the commercial species of fishes in Indonesia frequently caught by fishermen in Sibolga waters, North Sumatra Province. There is, however, presently no study conducted on the endoparasites infestation in these fishes. Therefore, the objectives of the present study were to identify endoparasitic worms and examine the intensity level in skipjack tuna K. pelamis from Sibolga waters. Sampling was conducted in Debora Private Fishing Port, Sibolga from 4th to 18th June 2019 and a total of 20 fish samples with weight ranged between 740 g and 1.200 g and length from 37.2 cm to 41.4 cm were analyzed in the study. The identification of the worm was conducted in the laboratory using a stereo microscope. The results showed seven species or genera of worms were found in the intestine and stomach of the fish with varying level of intensity and incidence. For example, Echinorhynchus sp. was found with 100% intestinal and 10% stomach incidences at a total intensity of 8.5; Acanthocephalus sp. with 25% intestinal incidence and 1.6 intensity, Rhadinorhynchus sp. with 25% intestinal and 5% stomach incidences, and 1.5 intensity; Leptorhynchoides sp. -
Chapter 9 in Biology of the Acanthocephala]
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 1985 Epizootiology: [Chapter 9 in Biology of the Acanthocephala] Brent B. Nickol University of Nebraska - Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/parasitologyfacpubs Part of the Parasitology Commons Nickol, Brent B., "Epizootiology: [Chapter 9 in Biology of the Acanthocephala]" (1985). Faculty Publications from the Harold W. Manter Laboratory of Parasitology. 505. https://digitalcommons.unl.edu/parasitologyfacpubs/505 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. Nickol in Biology of the Acanthocephala (ed. by Crompton & Nickol) Copyright 1985, Cambridge University Press. Used by permission. 9 Epizootiology Brent B. Nickol 9.1 Introduction In practice, epizootiology deals with how parasites spread through host populations, how rapidly the spread occurs and whether or not epizootics result. Prevalence, incidence, factors that permit establishment ofinfection, host response to infection, parasite fecundity and methods of transfer are, therefore, aspects of epizootiology. Indeed, most aspects of a parasite could be related in sorne way to epizootiology, but many ofthese topics are best considered in other contexts. General patterns of transmission, adaptations that facilitate transmission, establishment of infection and occurrence of epizootics are discussed in this chapter. When life cycles are unknown, little progress can be made in under standing the epizootiological aspects ofany group ofparasites. -
Phylum Onychophora
Lab exercise 6: Arthropoda General Zoology Laborarory . Matt Nelson phylum onychophora Velvet worms Once considered to represent a transitional form between annelids and arthropods, the Onychophora (velvet worms) are now generally considered to be sister to the Arthropoda, and are included in chordata the clade Panarthropoda. They are no hemichordata longer considered to be closely related to echinodermata the Annelida. Molecular evidence strongly deuterostomia supports the clade Panarthropoda, platyhelminthes indicating that those characteristics which the velvet worms share with segmented rotifera worms (e.g. unjointed limbs and acanthocephala metanephridia) must be plesiomorphies. lophotrochozoa nemertea mollusca Onychophorans share many annelida synapomorphies with arthropods. Like arthropods, velvet worms possess a chitinous bilateria protostomia exoskeleton that necessitates molting. The nemata ecdysozoa also possess a tracheal system similar to that nematomorpha of insects and myriapods. Onychophorans panarthropoda have an open circulatory system with tardigrada hemocoels and a ventral heart. As in arthropoda arthropods, the fluid-filled hemocoel is the onychophora main body cavity. However, unlike the arthropods, the hemocoel of onychophorans is used as a hydrostatic acoela skeleton. Onychophorans feed mostly on small invertebrates such as insects. These prey items are captured using a special “slime” which is secreted from large slime glands inside the body and expelled through two oral papillae on either side of the mouth. This slime is protein based, sticking to the cuticle of insects, but not to the cuticle of the velvet worm itself. Secreted as a liquid, the slime quickly becomes solid when exposed to air. Once a prey item is captured, an onychophoran feeds much like a spider.