Parasitology
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Balantidium Coli
GLOBAL WATER PATHOGEN PROJECT PART THREE. SPECIFIC EXCRETED PATHOGENS: ENVIRONMENTAL AND EPIDEMIOLOGY ASPECTS BALANTIDIUM COLI Francisco Ponce-Gordo Complutense University Madrid, Spain Kateřina Jirků-Pomajbíková Institute of Parasitology Biology Centre, ASCR, v.v.i. Budweis, Czech Republic Copyright: This publication is available in Open Access under the Attribution-ShareAlike 3.0 IGO (CC-BY-SA 3.0 IGO) license (http://creativecommons.org/licenses/by-sa/3.0/igo). By using the content of this publication, the users accept to be bound by the terms of use of the UNESCO Open Access Repository (http://www.unesco.org/openaccess/terms-use-ccbysa-en). Disclaimer: The designations employed and the presentation of material throughout this publication do not imply the expression of any opinion whatsoever on the part of UNESCO concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. The ideas and opinions expressed in this publication are those of the authors; they are not necessarily those of UNESCO and do not commit the Organization. Citation: Ponce-Gordo, F., Jirků-Pomajbíková, K. 2017. Balantidium coli. In: J.B. Rose and B. Jiménez-Cisneros, (eds) Global Water Pathogens Project. http://www.waterpathogens.org (R. Fayer and W. Jakubowski, (eds) Part 3 Protists) http://www.waterpathogens.org/book/balantidium-coli Michigan State University, E. Lansing, MI, UNESCO. Acknowledgements: K.R.L. Young, Project Design editor; Website Design (http://www.agroknow.com) Published: January 15, 2015, 11:50 am, Updated: October 18, 2017, 5:43 pm Balantidium coli Summary 1.1.1 Global distribution Balantidium coli is reported worldwide although it is To date, Balantidium coli is the only ciliate protozoan more common in temperate and tropical regions (Areán and reported to infect the gastrointestinal track of humans. -
New Zealand's Genetic Diversity
1.13 NEW ZEALAND’S GENETIC DIVERSITY NEW ZEALAND’S GENETIC DIVERSITY Dennis P. Gordon National Institute of Water and Atmospheric Research, Private Bag 14901, Kilbirnie, Wellington 6022, New Zealand ABSTRACT: The known genetic diversity represented by the New Zealand biota is reviewed and summarised, largely based on a recently published New Zealand inventory of biodiversity. All kingdoms and eukaryote phyla are covered, updated to refl ect the latest phylogenetic view of Eukaryota. The total known biota comprises a nominal 57 406 species (c. 48 640 described). Subtraction of the 4889 naturalised-alien species gives a biota of 52 517 native species. A minimum (the status of a number of the unnamed species is uncertain) of 27 380 (52%) of these species are endemic (cf. 26% for Fungi, 38% for all marine species, 46% for marine Animalia, 68% for all Animalia, 78% for vascular plants and 91% for terrestrial Animalia). In passing, examples are given both of the roles of the major taxa in providing ecosystem services and of the use of genetic resources in the New Zealand economy. Key words: Animalia, Chromista, freshwater, Fungi, genetic diversity, marine, New Zealand, Prokaryota, Protozoa, terrestrial. INTRODUCTION Article 10b of the CBD calls for signatories to ‘Adopt The original brief for this chapter was to review New Zealand’s measures relating to the use of biological resources [i.e. genetic genetic resources. The OECD defi nition of genetic resources resources] to avoid or minimize adverse impacts on biological is ‘genetic material of plants, animals or micro-organisms of diversity [e.g. genetic diversity]’ (my parentheses). -
The Intestinal Protozoa
The Intestinal Protozoa A. Introduction 1. The Phylum Protozoa is classified into four major subdivisions according to the methods of locomotion and reproduction. a. The amoebae (Superclass Sarcodina, Class Rhizopodea move by means of pseudopodia and reproduce exclusively by asexual binary division. b. The flagellates (Superclass Mastigophora, Class Zoomasitgophorea) typically move by long, whiplike flagella and reproduce by binary fission. c. The ciliates (Subphylum Ciliophora, Class Ciliata) are propelled by rows of cilia that beat with a synchronized wavelike motion. d. The sporozoans (Subphylum Sporozoa) lack specialized organelles of motility but have a unique type of life cycle, alternating between sexual and asexual reproductive cycles (alternation of generations). e. Number of species - there are about 45,000 protozoan species; around 8000 are parasitic, and around 25 species are important to humans. 2. Diagnosis - must learn to differentiate between the harmless and the medically important. This is most often based upon the morphology of respective organisms. 3. Transmission - mostly person-to-person, via fecal-oral route; fecally contaminated food or water important (organisms remain viable for around 30 days in cool moist environment with few bacteria; other means of transmission include sexual, insects, animals (zoonoses). B. Structures 1. trophozoite - the motile vegetative stage; multiplies via binary fission; colonizes host. 2. cyst - the inactive, non-motile, infective stage; survives the environment due to the presence of a cyst wall. 3. nuclear structure - important in the identification of organisms and species differentiation. 4. diagnostic features a. size - helpful in identifying organisms; must have calibrated objectives on the microscope in order to measure accurately. -
Wda 2016 Conference Proceedi
The 65th International Conference of the Wildlife Disease Association July 31 August 5, 2016 Cortland, New York Sustainable Wildlife: Health Matters! Hosted by at Greek Peak Mountain Resort Cortland, New York, USA 4 Wildlife Disease Association Table of Contents Welcome from the Conference Committee 6 Conference Committee Members 7 WDA Officers 8 Plenary Speakers 9 The 2016 Carlton Herman Fund Speaker 11 Sponsors 12 Events & Meetings 15 Pre-conference Workshops 17 Program 21 Poster Sessions 34 Abstracts 40 Exhibitors 249 Index 256 65th Annual International Conference 5 Welcome from the Conference Committee Welcome to beautiful central New York, the 65th International Conference of the Wildlife Disease Association, and the 2016 Annual Meeting of the American Association of Wildlife Veterinarians. We have planned an exciting scientific program and have lots of networking and learning opportunities in store this week. There will be a break mid-week to allow time to socialize with new and old friends and take in some of the adventures the area has to offer. global challenges and opportunities in managing wildlife health issues with our excellent slate of plenary speakers. In addition, we have three special sessions: How Risk Communication Research in Wildlife Disease Management Contributes to Wildlife Trust Administration, Chelonian Diseases and Conservation, and Vaccines for Conservation. This meeting would not have been possible without the contributions of numerous people and institutions. We are grateful to Cornell University for in-kind and financial support for this event. The Atkinson Center for a Sustainable Future, College of Veterinary Medicine, Department of Population Medicine and Diagnostic Sciences, Animal Health Diagnostic Center, and Lab of Ornithology have all been integral parts of making this meeting a success. -
A KEY to the COMMON PARASITIC PROTOZOANS of NORTH AMERICAN FISHES Thomas L. Wellborn, Jr. and Wilmer A. Rogers Zoology-Ent
. A KEY to the COMMON PARASITIC PROTOZOANS of NORTH AMERICAN FISHES Thomas L. Wellborn, Jr. and Wilmer A. Rogers Zoology-Entomology Department Series Fisheries No. 4 AGRICULTURAL EXPERIMENT STATION AUBURN UNIVERSITY E. V. Smith, Director March 1966 Auburn, Alabama (Revised June 1970) A KEY TO THE COMMON PARASITIC PROTOZOANS 1 OF NORTH AMERICAN FISHES Thomas L. Wellborn, Jr. 2/— and Wilmer A. Rogers 3/— Private, state, and federal fish husbandry industries suffer great losses each year because of disease and parasites. The parasitic protozoans included in this key are the ones most commonly associated with fish mortalities. A total of 23 genera of parasitic protozoans may be identified by use of this key. The fish protozoan parasites are responsible for a large part of the mortalities that occur at fish hatcheries each year. This is because they are capable of building up tremendous populations within relatively short periods of time, and some are capable of causing extreme damage to fish. Proper treatment and control of the diseases caused by the various protozoans are impossible without knowing their identity. This key will be helpful to fishery workers in identifying the more common genera. It must be remembered, however, that a microscope and knowledge of its use are absolute prerequisites for identifying protozoans. Certain parasitic protozoans cannot be identified below the rank of Order - without use of special techniques; therefore, all known genera are not included in the herein reported key. Protozoans belonging to such Orders should be sent to a specialist for identification. 1/ Supported in part by Southeastern Cooperative Fish Parasite and Disease Project (Fish Restoration Funds). -
Enteric Protozoa in the Developed World: a Public Health Perspective
Enteric Protozoa in the Developed World: a Public Health Perspective Stephanie M. Fletcher,a Damien Stark,b,c John Harkness,b,c and John Ellisa,b The ithree Institute, University of Technology Sydney, Sydney, NSW, Australiaa; School of Medical and Molecular Biosciences, University of Technology Sydney, Sydney, NSW, Australiab; and St. Vincent’s Hospital, Sydney, Division of Microbiology, SydPath, Darlinghurst, NSW, Australiac INTRODUCTION ............................................................................................................................................420 Distribution in Developed Countries .....................................................................................................................421 EPIDEMIOLOGY, DIAGNOSIS, AND TREATMENT ..........................................................................................................421 Cryptosporidium Species..................................................................................................................................421 Dientamoeba fragilis ......................................................................................................................................427 Entamoeba Species.......................................................................................................................................427 Giardia intestinalis.........................................................................................................................................429 Cyclospora cayetanensis...................................................................................................................................430 -
Novel Lineages of Oxymonad Flagellates from the Termite Porotermes Adamsoni (Stolotermitidae): the Genera Oxynympha and Termitim
Protist, Vol. 170, 125683, December 2019 http://www.elsevier.de/protis Published online date 21 October 2019 ORIGINAL PAPER Novel Lineages of Oxymonad Flagellates from the Termite Porotermes adamsoni (Stolotermitidae): the Genera Oxynympha and Termitimonas a,1 b a c b,1 Renate Radek , Katja Meuser , Samet Altinay , Nathan Lo , and Andreas Brune a Evolutionary Biology, Institute for Biology/Zoology, Freie Universität Berlin, 14195 Berlin, Germany b Research Group Insect Gut Microbiology and Symbiosis, Max Planck Institute for Terrestrial Microbiology, 35043 Marburg, Germany c School of Life and Environmental Sciences, The University of Sydney, Sydney, NSW 2006, Australia Submitted January 21, 2019; Accepted October 9, 2019 Monitoring Editor: Alastair Simpson The symbiotic gut flagellates of lower termites form host-specific consortia composed of Parabasalia and Oxymonadida. The analysis of their coevolution with termites is hampered by a lack of informa- tion, particularly on the flagellates colonizing the basal host lineages. To date, there are no reports on the presence of oxymonads in termites of the family Stolotermitidae. We discovered three novel, deep-branching lineages of oxymonads in a member of this family, the damp-wood termite Porotermes adamsoni. One tiny species (6–10 m), Termitimonas travisi, morphologically resembles members of the genus Monocercomonoides, but its SSU rRNA genes are highly dissimilar to recently published sequences of Polymastigidae from cockroaches and vertebrates. A second small species (9–13 m), Oxynympha loricata, has a slight phylogenetic affinity to members of the Saccinobaculidae, which are found exclusively in wood-feeding cockroaches of the genus Cryptocercus, the closest relatives of termites, but shows a combination of morphological features that is unprecedented in any oxymonad family. -
P1891 Trichomonas Vaginalis Lifecycle Revisited
P1891 Trichomonas vaginalis lifecycle revisited Piotr Kochan1, Agata Pietrzyk2, Alban Vogel*3, Maria Gołębiowska3, Karan Kumar3, Eivind Krågebakk3, Andreas Talgø Lie3, Rebekka Nilsen3, Vilde Strøm3, Michael Zbiegien3, Barbara Papir4, Małgorzata Bulanda5 1Chair of Microbiology, Department of Bacteriology, Microbial Ecology and Parasitology, Kraków, Poland, 2Chair of Microbiology, Head of Parasitology Laboratory, Kraków, , 3School of Medicine in English, Jagiellonian University, Parasitology Research Circle, Kraków, Poland, 4Chair of Microbiology , Parasitology Laboratory, Kraków, , 5Jagiellonian University Medical College, Head of the Chair of Microbiology, Kraków, Poland Background: The World Health Organization (WHO) states there are 1 million new sexually transmitted infections (STI) occurring daily. Among these, Trichomonas vaginalis with over 140 million infected is ranked 4th, just after HBV with over 250 million infected, HPV with over 290 million and HSV ranked 1st with over 500 million infected. Despite the availability of treatment of this protozoan, it’s still prevalent both in the developing and developed countries, although chlamydial infections are on the rise, currently ranked as 5th by WHO. Trichomoniasis is twice as common as gonorrhea (~78 million), almost 4 times more common than HIV infections (~37 million) and 25 times more common than syphilis (~6 million). Trichomonas infection not only facilitates HIV acquisition due to epithelial damage, but also promotes HIV propagation. We aimed to re-evaluate our current knowledge on the lifecycle of Trichomonas vaginalis, including not only its multiplication, but also possible genetic exchange. Materials/methods: The study made use of two strains of Trichomonas vaginalis: reference strain ATCC-PRA-92 and the strain from the Chair of Microbiology of Jagiellonian University Medical College. -
23.3 Groups of Protists
Chapter 23 | Protists 639 cysts that are a protective, resting stage. Depending on habitat of the species, the cysts may be particularly resistant to temperature extremes, desiccation, or low pH. This strategy allows certain protists to “wait out” stressors until their environment becomes more favorable for survival or until they are carried (such as by wind, water, or transport on a larger organism) to a different environment, because cysts exhibit virtually no cellular metabolism. Protist life cycles range from simple to extremely elaborate. Certain parasitic protists have complicated life cycles and must infect different host species at different developmental stages to complete their life cycle. Some protists are unicellular in the haploid form and multicellular in the diploid form, a strategy employed by animals. Other protists have multicellular stages in both haploid and diploid forms, a strategy called alternation of generations, analogous to that used by plants. Habitats Nearly all protists exist in some type of aquatic environment, including freshwater and marine environments, damp soil, and even snow. Several protist species are parasites that infect animals or plants. A few protist species live on dead organisms or their wastes, and contribute to their decay. 23.3 | Groups of Protists By the end of this section, you will be able to do the following: • Describe representative protist organisms from each of the six presently recognized supergroups of eukaryotes • Identify the evolutionary relationships of plants, animals, and fungi within the six presently recognized supergroups of eukaryotes • Identify defining features of protists in each of the six supergroups of eukaryotes. In the span of several decades, the Kingdom Protista has been disassembled because sequence analyses have revealed new genetic (and therefore evolutionary) relationships among these eukaryotes. -
That of a Typical Flagellate. the Flagella May Equally Well Be Called Cilia
ZOOLOGY; KOFOID AND SWEZY 9 FLAGELLATE AFFINITIES OF TRICHONYMPHA BY CHARLES ATWOOD KOFOID AND OLIVE SWEZY ZOOLOGICAL LABORATORY, UNIVERSITY OF CALIFORNIA Communicated by W. M. Wheeler, November 13, 1918 The methods of division among the Protozoa are of fundamental signifi- cance from an evolutionary standpoint. Unlike the Metazoa which present, as a whole, only minor variations in this process in the different taxonomic groups and in the many different types of cells in the body, the Protozoa have evolved many and widely diverse types of mitotic phenomena, which are Fharacteristic of the groups into which the phylum is divided. Some strik- ing confirmation of the value of this as a clue to relationships has been found in recent work along these lines. The genus Trichonympha has, since its discovery in 1877 by Leidy,1 been placed, on the one hand, in the ciliates and, on the other, in the flagellates, and of late in an intermediate position between these two classes, by different investigators. Certain points in its structure would seem to justify each of these assignments. A more critical study of its morphology and especially of its methods of division, however, definitely place it in the flagellates near the Polymastigina. At first glance Trichonympha would undoubtedly be called a ciliate. The body is covered for about two-thirds of its surface with a thick coating of cilia or flagella of varying lengths, which stream out behind the body. It also has a thick, highly differentiated ectoplasm which contains an alveolar layer as well as a complex system of myonemes. -
Prevalence of Gastro-Intestinal Parasitic Infections of Cats and Efficacy of Antiparasitics Against These Infections in Mymensingh Sadar, Bangladesh
Bangl. J. Vet. Med. (2020). 18 (2): 65–73 ISSN: 1729-7893 (Print), 2308-0922 (Online) Received: 30-11-2020; Accepted: 30-12-2020 DOI: https://doi.org/10.33109/bjvmjd2020sam1 ORIGINAL ARTICLE Prevalence of gastro-intestinal parasitic infections of cats and efficacy of antiparasitics against these infections in Mymensingh sadar, Bangladesh B. H. Mehedi, A. Nahar, A. K. M. A. Rahman, M. A. Ehsan* Department of Medicine, Bangladesh Agricultural University, Mymensingh 2202. Abstract Background: Gastro-intestinal parasitic infection in cats is a major concern for public health as they have zoonotic importance. The present research was conducted to determine the prevalence of gastro-intestinal parasitic infection in cats and evaluate the efficacy of antiparasitics against these infections in different areas of Mymensingh Sadar between December, 2018 to May, 2019. Methods: The fecal samples were examined by simple sedimentation and stoll’s ova counting method for detection of eggs/cysts/oocysts of parasites. The efficacy of antiparasitics against the parasitic infections in cats was evaluated. Results: The overall prevalence of gastrointestinal parasites was 62.9% (39/62) and the mixed parasitic infection was 20.9% (13/62). The prevalence of Toxocara cati and Ancylostoma tubaeforme infections were 17.7% and 6.5%, respectively. The prevalence of Taenia pisiformis infection was 3.22%. However, the prevalence of Isospora felis, Toxoplasma gondii and Balantidium coli infections were 4.8%, 3.2% and 6.5%. The prevalence of infection was significantly (P<0.008) higher in kitten than that in adult cat. The efficacy of albendazole, fenbendazole against single helminth infection was 100%. -
Catalogue of Protozoan Parasites Recorded in Australia Peter J. O
1 CATALOGUE OF PROTOZOAN PARASITES RECORDED IN AUSTRALIA PETER J. O’DONOGHUE & ROBERT D. ADLARD O’Donoghue, P.J. & Adlard, R.D. 2000 02 29: Catalogue of protozoan parasites recorded in Australia. Memoirs of the Queensland Museum 45(1):1-164. Brisbane. ISSN 0079-8835. Published reports of protozoan species from Australian animals have been compiled into a host- parasite checklist, a parasite-host checklist and a cross-referenced bibliography. Protozoa listed include parasites, commensals and symbionts but free-living species have been excluded. Over 590 protozoan species are listed including amoebae, flagellates, ciliates and ‘sporozoa’ (the latter comprising apicomplexans, microsporans, myxozoans, haplosporidians and paramyxeans). Organisms are recorded in association with some 520 hosts including mammals, marsupials, birds, reptiles, amphibians, fish and invertebrates. Information has been abstracted from over 1,270 scientific publications predating 1999 and all records include taxonomic authorities, synonyms, common names, sites of infection within hosts and geographic locations. Protozoa, parasite checklist, host checklist, bibliography, Australia. Peter J. O’Donoghue, Department of Microbiology and Parasitology, The University of Queensland, St Lucia 4072, Australia; Robert D. Adlard, Protozoa Section, Queensland Museum, PO Box 3300, South Brisbane 4101, Australia; 31 January 2000. CONTENTS the literature for reports relevant to contemporary studies. Such problems could be avoided if all previous HOST-PARASITE CHECKLIST 5 records were consolidated into a single database. Most Mammals 5 researchers currently avail themselves of various Reptiles 21 electronic database and abstracting services but none Amphibians 26 include literature published earlier than 1985 and not all Birds 34 journal titles are covered in their databases. Fish 44 Invertebrates 54 Several catalogues of parasites in Australian PARASITE-HOST CHECKLIST 63 hosts have previously been published.