Aula 3 Giardia E Crypto 2020

Total Page:16

File Type:pdf, Size:1020Kb

Aula 3 Giardia E Crypto 2020 DISCIPLINA PARASITOLOGIA 2020 20 de fevereiro GIARDÍASE E CRIPTOSPORIDIOSE Docente: Profa. Dra. Juliana Q. Reimão • PROTOZOÁRIOS INTESTINAIS • Mais comuns em imunocompetentes • Entamoeba histolytica e Giardia duodenalis • Emergentes e Oportunistas • Causam doença principalmente em imunocomprometidos • Foram recentemente caracterizados como patógenos humanos • Cryptosporidium parvum e Cryptosporidium hominis GIARDÍASE Giardíase • Generalidades • Infecção causada por parasitas flagelados que se prendem à parede do intestino delgado provocando diarreia e desconforto abdominal. • Agente etiológico • Giardia duodenalis • (= Giardia lamblia e Giardia intestinalis) • Parasita monoxênico eurixeno • Exige apenas um hospedeiro • Variedade de hospedeiros vertebrados • Homem e alguns animais • Mamíferos, aves e répteis • Formas de vida • Trofozoíto e cisto Epidemiologia Precárias • 200 milhões de indivíduos sintomáticos condições de higiene, educação • 500 mil casos/ano sanitária e • Distribuição mundial alimentação • Parasita intestinal mais comum em países desenvolvidos Morfologia • Trofozoíto • Corpo piriforme Núcleo Flagelo Disco • Simetria bilateral suctorial • 2 núcleos • 4 pares flagelo Corpo Flagelo basal • 1 disco suctorial • Corpo basal = aparelho de Golgi Flagelo Flagelo • Axóstilo = feixe de microtúbulos Morfologia • Trofozoíto • Achatamento dorsoventral • Disco suctorial • Adesão ao epitélio intestinal Vista dorsal Vista lateral Morfologia • Cisto • Oval • Núcleo e corpo basais duplicados • Cada cisto produz 2 trofozoítos Núcleos Corpo basal • Forma de resistência Parede cística • Viáveis na água por até 3 meses • Resistentes ao processo de cloração da água • São eliminados nas fezes → milhões/dia Ciclo de vida Trofozoítos Cistos Ciclo de vida • Cães e gatos podem ser fontes de infecção → eliminam cistos! • Sua importância como reservatórios não é clara Aspectos clínicos • Em imunocompetentes • Em geral é assintomático • Diarreia • Manifestação mais comum (90% casos) • 2 a 4 semanas • Raramente contém sangue • Esteatorreia • Presença de gordura nas fezes • Desconforto abdominal/cólicas • Náuseas e vômitos • Perda de peso • Autolimitada ou recorrente • Em imunodeprimidos • A infecção pode ser grave, com longa duração (> 7 semanas) Patogenia • Efeito citotóxico • Células epiteliais • Destruição das vilosidades • Contato com a margem dos discos suctoriais Patogenia vilos cripta microvilosidades enterócito Atrofia de vilos e hiperplasia das criptas Mucosa normal Mucosa alterada Patogenia • Consequências do parasitismo Disco suctorial • Redução da produção de enzimas (ex. lactase) • Redução da absorção de carboidratos, gorduras e vitaminas • Inflamação da mucosa e apoptose dos enterócitos • Aumento da secreção de cloretos → acúmulo de líquidos no lúmen intestinal Disco suctorial Vilosidades Patogenia Virulência das cepas Número de cistos ingeridos Infecção assintomática Síndrome da má absorção Idade Estado imune do hospedeiro Exposição prévia ao parasito Diagnóstico • Parasitológico • Exame de fezes (EPF) • Sensibilidade • 1 amostra: 60 a 80% • 3 amostras: 90% • Menos usados • Aspiração intestinal • Biópsia duodenal • Sorológico • ELISA, RIFI, hemaglutinação indireta • Molecular cisto trofozoíto • PCR Reação de imunofluorescência indireta (RIFI) Teste imunoenzimático (ELISA) Teste de aglutinação PCR Tratamento • Nitroimidazóis Metronidazol secnidazol tinidazol metronidazol Medicamento Adulto Criança Secnidazol 2g, VO, dose única 30 mg/kg, dose única Tinidazol 2 g, VO, dose única - 15 mg/kg/dia 250 mg, VO, 2 vezes Metronidazol (máximo de 250 mg), VO, ao dia por 5 dias dividida em 2 tomadas, por 5 dias • Controle de cura: • 3 exame de fezes (1 por semana) Prevenção e controle • Principais veículos • Água e alimentos crus • Pessoas infectadas • Vetores mecânicos • Moscas e baratas • Moluscos bivalves • Profilaxia • Fervura da água • Saneamento básico • Educação sanitária • Tratamento • Manipuladores de alimentos • Creches e asilos CRIPTOSPORIDIOSE Coccídios intestinais • Generalidades • Parasitas intracelulares obrigatórios • Possuem semelhanças com os apicomplexos • Parasitas monoxênicos • Exigem apenas um hospedeiro • Criptosporidiose • Cryptosporidium hominis • Cryptosporidium parvum • Ciclosporíase • Cyclospora cayetanensis • Cistoisosporíase • Cystoisospora belli Importância • Emergentes • Recentemente descritos como patogênicos • Avanço nas técnicas diagnósticas • Globalização • Alteração HIV positivo • Do meio ambiente (%) • Dos hábitos alimentares HIV negativo • Oportunistas Prevalência • Indivíduos imunossuprimidos Cyclospora Cryptosporidium Cystoisospora • Aumento crescente de incidência cayetanensis parvum belli Criptosporidiose • Importância • Segunda causa de morte por diarreia em crianças no mundo • 30 a 50% das mortes até 5 anos de idade • Consequências letais em imunodeprimidos Epidemiologia • Cosmopolita • Mais frequente em países em desenvolvimento • Prevalência de 0,5 a 10% → subestimada • Crianças 1 a 5 anos • Em Fortaleza: uma pesquisa mostrou que todas as crianças avaliadas apresentavam anticorpos contra C. parvum → exposição prévia ao parasito • AIDS • Prevalência de até 50% • Surtos de transmissão hídrica • Ex.: Milwaukee (EUA): 400 infectados e 100 mortes Aspectos biológicos • Parasito intracelular • Apresenta fusão com a membrana do enterócito • Forma um vacúolo parasitóforo • Extracitoplasmático • Se localiza fora do citoplasma da célula hospedeira • Localização epicelular • Sobrevive em biofilmes • Ambiente aquático • Habitat • Intestino delgado Ciclo de vida Ingestão ou inalação RESERVATÓRIOS de oocistos Cryptosporidium parvum Cryptosporidium Liberação de hominis oocistos nas fezes Ciclo de vida Merogonia Esporozoíto Ingestão ou Meronte tipo I inalação Trofozoíto Meio exterior Auto-infecção Merozoíto Oocisto esporulado parede espessa Oocisto esporulado Microgameta Meronte tipo II parede fina Macrogameta Merozoítos Zigoto Esporogonia Gametogonia Patogenia • Alterações histológicas • Invadem as células epiteliais do intestino • Não atingem as camadas mais profundas da mucosa • Causam atrofia das vilosidades e inflamação • Redução da absorção • Redução da produção de enzimas • Diarreia Oocistos de Cryptosporidium sp. na mucosa intestinal Aspectos clínicos • Em imunocompetentes • Sintomas ausentes ou autolimitados • Diarreia aquosa • Vômitos • Dores abdominais • Perda de peso • Em imunocomprometidos • Diarreia grave, com várias evacuações/dia • Evolução crônica ou fulminante • Perda diária de mais de 20 litros de líquido Cryptosporidium sp. Diagnóstico laboratorial Às bactérias que possuem esta propriedade • Exame parasitológico de fezes (EPF) • Encontro de oocistos Oocistos • Visualização microscópica a fresco nas fezes • Coloração de Ziehl-Neelsen • Coloração usada para microrganismos EPF, coloração de Ziehl-Neelsen álcool-ácido resistentes • Outros exames • Pesquisa de antígenos nas fezes • PCR de fezes • Biópsia ou aspirado intestinal Trofozoítos nas células epiteliais Biópsia intestinal Tratamento • Nitazoxanida • Bem tolerado, com poucos efeitos colaterais • Ação contra outros patógenos intestinais • Pouco efetivo em imunocomprometidos • Cuidados gerais • Hidratação • Tratamento sintomático • Tratamento antiviral em pacientes HIV+ • Restauração da imunidade Os oocistos • São resistentes ao cloro e à maioria Prevenção dos desinfetantes • Viáveis por vários meses no ambiente • Medidas de prevenção • São sensíveis: • Saneamento básico • À altas temperaturas (60 °C) • Educação sanitária • Ao congelamento e à dessecação • Ao H O • Filtração ou fervura da água 2 2 • Controle de contaminação ambiental com fezes • Evitar contato direto com animais infectados • Evitar o consumo de moluscos bivalves crus (ex. ostras) Curiosidades • Se uma pessoa com criptosporidiose defeca na piscina: • 50 milhões de oocistos por mL de fezes x 150 mL fezes = 7.5 bilhões de oocistos na piscina • Em uma piscina padrão de 25 x 12 m (450 m3) teria uma média de 20.000 oocistos por litro = 20 oocistos/mL • Uma criança de 6-18 anos em média ingere 37 mL da água da piscina = 740 oocistos • Alto risco: • Áreas recreacionais com contami- nação por esgoto humano ou animal • Água de irrigação Dúvidas? [email protected] Vídeos relacionados • Surto de diarreia deixa 95 mortos em Pernambuco: • https://www.youtube.com/watch?v=6hZym-EJ5SA • Vídeo Criptosporidium (Monsters inside me – Discovery Channel) • https://www.youtube.com/watch?v=7Rfu235rT6A Discussão de caso clínico Paciente com diarreia crônica • Objetivos a serem atingidos neste estudo: • Identificar os modos de transmissão, os sinais clínicos e os exames diagnósticos empregados no diagnóstico da giardíase e criptosporidiose; • Correlacionar o ciclo biológico do parasito com as principais áreas do corpo humano que podem ser afetadas por este parasitismo; • Conhecer o tratamento e as medidas profiláticas a serem empregadas frente a estas parasitoses; • Discutir informações relevantes com o grupo de estudo e investigar os processos patológicos observados neste caso. Socrative Salas JULIANA2020 e GATTI7970.
Recommended publications
  • Interactions Between Cryptosporidium Parvum and the Intestinal Ecosystem
    Interactions between Cryptosporidium parvum and the Intestinal Ecosystem Thesis by Olga Douvropoulou In Partial Fulfillment of the Requirements For the Degree of Master of Science King Abdullah University of Science and Technology Thuwal, Kingdom of Saudi Arabia April, 2017 2 EXAMINATION COMMITTEE PAGE The thesis of Olga Douvropoulou is approved by the examination committee. Committee Chairperson: Professor Arnab Pain Committee Co-Chair: Professor Giovanni Widmer Committee Members: Professor Takashi Gojobori, Professor Peiying Hong 3 © April, 2017 Olga Douvropoulou All Rights Reserved 4 ABSTRACT Interactions between Cryptosporidium parvum and the Intestinal Ecosystem Olga Douvropoulou Cryptosporidium parvum is an apicomplexan protozoan parasite commonly causing diarrhea, particularly in infants in developing countries. The research challenges faced in the development of therapies against Cryptosporidium slow down the process of drug discovery. However, advancement of knowledge towards the interactions of the intestinal ecosystem and the parasite could provide alternative approaches to tackle the disease. Under this perspective, the primary focus of this work was to study interactions between Cryptosporidium parvum and the intestinal ecosystem in a mouse model. Mice were treated with antibiotics with different activity spectra and the resulted perturbation of the native gut microbiota was identified by microbiome studies. In particular, 16S amplicon sequencing and Whole Genome Sequencing (WGS) were used to determine the bacterial composition
    [Show full text]
  • Exploration of Laboratory Techniques Relating to Cryptosporidium Parvum Propagation, Life Cycle Observation, and Host Immune Responses to Infection
    EXPLORATION OF LABORATORY TECHNIQUES RELATING TO CRYPTOSPORIDIUM PARVUM PROPAGATION, LIFE CYCLE OBSERVATION, AND HOST IMMUNE RESPONSES TO INFECTION A Thesis Submitted to the Graduate Faculty of the North Dakota State University of Agriculture and Applied Science By Cheryl Marie Brown In Partial Fulfillment for the Degree of MASTER OF SCIENCE Major Department: Veterinary and Microbiological Sciences February 2014 Fargo, North Dakota North Dakota State University Graduate School Title EXPLORATION OF LABORATORY TECHNIQUES RELATING TO CRYPTOSPORIDIUM PARVUM PROPAGATION, LIFE CYCLE OBSERVATION, AND HOST IMMUNE RESPONSES TO INFECTION By Cheryl Marie Brown The Supervisory Committee certifies that this disquisition complies with North Dakota State University’s regulations and meets the accepted standards for the degree of MASTER OF SCIENCE SUPERVISORY COMMITTEE: Dr. Jane Schuh Chair Dr. John McEvoy Dr. Carrie Hammer Approved: 4-8-14 Dr. Charlene Wolf-Hall Date Department Chair ii ABSTRACT Cryptosporidium causes cryptosporidiosis, a self-limiting diarrheal disease in healthy people, but causes serious health issues for immunocompromised individuals. Cryptosporidiosis has been observed in humans since the early 1970s and continues to cause public health concerns. Cryptosporidium has a complicated life cycle making laboratory study challenging. This project explores several ways of studying Cryptosporidium parvum, with a goal of applying existing techniques to further understand this life cycle. Utilization of a neonatal mouse model demonstrated laser microdissection as a tool for studying host immune response to infeciton. A cell culture technique developed on FrameSlides™ enables laser microdissection of individual infected cells for further analysis. Finally, the hypothesis that the availability of cells to infect drives the switch from asexual to sexual parasite reproduction was tested by time-series infection.
    [Show full text]
  • Genetic Basis for Virulence Differences of Various Cryptosporidium Parvum Carcinogenic Isolates
    Genetic basis for virulence differences of various Cryptosporidium parvum carcinogenic isolates Christophe Audebert, Franck Bonardi, Ségolène Caboche, Karine Guyot, Hélène Touzet, Sophie Merlin, Nausicaa Gantois, Colette Creusy, Dionigia Meloni, Anthony Mouray, et al. To cite this version: Christophe Audebert, Franck Bonardi, Ségolène Caboche, Karine Guyot, Hélène Touzet, et al.. Ge- netic basis for virulence differences of various Cryptosporidium parvum carcinogenic isolates. Scientific Reports, Nature Publishing Group, 2020, 10 (1), pp.7316. 10.1038/s41598-020-64370-0. inserm- 02873228 HAL Id: inserm-02873228 https://www.hal.inserm.fr/inserm-02873228 Submitted on 18 Jun 2020 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. www.nature.com/scientificreports OPEN Genetic basis for virulence diferences of various Cryptosporidium parvum carcinogenic isolates Christophe Audebert1,2, Franck Bonardi3, Ségolène Caboche 2,4, Karine Guyot4, Hélène Touzet3,5, Sophie Merlin1,2, Nausicaa Gantois4, Colette Creusy6, Dionigia Meloni4, Anthony Mouray7, Eric Viscogliosi4, Gabriela Certad4,8, Sadia Benamrouz-Vanneste4,9 & Magali Chabé 4 ✉ Cryptosporidium parvum is known to cause life-threatening diarrhea in immunocompromised hosts and was also reported to be capable of inducing digestive adenocarcinoma in a rodent model. Interestingly, three carcinogenic isolates of C.
    [Show full text]
  • Cryptosporidium Hominis N. Sp. (Apicomplexa: Cryptosporidiidae) from Homo Sapiens
    The Journal of Eukaryotic Microbiology Volume 49 November-December 2002 Number 6 J. Eukiiyor rMioohio/.. 49(6). 2002 pp. 433440 0 2002 by the Society oi Protozoologisls Cryptosporidium hominis n. sp. (Apicomplexa: Cryptosporidiidae) from Homo sapiens UNA M. MORGAN-RYAN,” ABBIE FALL; LUCY A. WARD? NAWAL HIJJAWI: IRSHAD SULAIMAN: RONALD FAYER,” R. C. ANDREW THOMPSON,” M. OLSON,’ ALTAF LAL‘ and LIHUA XUOC “Division of Veterinory and Biomedical Sciences, Murdoch University, Murdoch, Western Australia 6150, and bFood Animal Health Research Program and Department of Veterinuq Preveittative Medicine, Ohio Agricultural Research and Development Centre, The Ohio State University, Wooster, Ohio 44691 USA, rind ‘Division of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Public Health Services, U. S. Department of Health and Huniun Services, Atlantu, Georgia 30341. and W. S. Department of Agriculture, Anitnal Waste Pathogen Laboratory, Beltsville, Maryland 20705, und eUniver.~ir)of Calgary., FaculQ of Medicine, Animal Resources Center, Department OJ‘ Gastrointestinal Science, 3330 Hospital DI-NW, Calgary, Albertu 72N 4NI, Canada ABSTRACT. The structure and infectivity of the oocysts of a new species of Cryptosporidiurn from the feces of humans are described. Oocysts are structurally indistinguishable from those of Cr.y~~tos€,oridiunlpurvum. Oocysts of the new species are passed fully sporulated, lack sporocysts, and measure 4.4-5.4 prn (mean = 4.86) X 4.4-5.9 pm (mean = 5.2 prn) with a length to width ratio 1 .&I .09 (mean 1.07) (n = 100). Oocysts were not infectious for ARC Swiss mice. nude mice, Wistat’ rat pups, puppies, kittens or calves, but were infectious to neonatal gnotobiotic pigs.
    [Show full text]
  • High Frequency of Cryptosporidium Hominis Infecting Infants Points to a Potential Anthroponotic Transmission in Maputo, Mozambique
    pathogens Brief Report High Frequency of Cryptosporidium hominis Infecting Infants Points to A Potential Anthroponotic Transmission in Maputo, Mozambique Idalécia Cossa-Moiane 1,2,* , Hermínio Cossa 3, Adilson Fernando Loforte Bauhofer 1,4 , Jorfélia Chilaúle 1, Esperança Lourenço Guimarães 1,4, Diocreciano Matias Bero 1 , Marta Cassocera 1,4, Miguel Bambo 1, Elda Anapakala 1, Assucênio Chissaque 1,4 ,Júlia Sambo 1,4, Jerónimo Souzinho Langa 1, Lena Vânia Manhique-Coutinho 1, Maria Fantinatti 5, Luis António Lopes-Oliveira 5, Alda Maria Da-Cruz 5,6 and Nilsa de Deus 1,7 1 Instituto Nacional de Saúde (INS), EN1, Bairro da Vila–Parcela n◦ 3943, Distrito de Marracuene, Maputo 264, Mozambique; [email protected] (A.F.L.B.); [email protected] (J.C.); [email protected] (E.L.G.); [email protected] (D.M.B.); [email protected] (M.C.); [email protected] (M.B.); [email protected] (E.A.); [email protected] (A.C.); [email protected] (J.S.); [email protected] (J.S.L.); [email protected] (L.V.M.-C.); [email protected] (N.d.D.) 2 Institute of Tropical Medicine, 2000 Antwerp, Belgium 3 Centro de Investigação em Saúde de Manhiça (CISM), Unidade de Pesquisa Social, Manhiça Foundation (Fundação Manhiça, FM), Manhiça 1929, Mozambique; [email protected] Citation: Cossa-Moiane, I.; Cossa, H.; 4 Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, 1349-008 Lisboa, Portugal 5 Bauhofer, A.F.L.; Chilaúle, J.; Laboratório Interdisciplinar de Pesquisas Médicas, Instituto Oswaldo Cruz-FIOCRUZ, Guimarães, E.L.; Bero, D.M.; Rio de Janeiro 22040-360, Brazil; [email protected] (M.F.); [email protected] (L.A.L.-O.); alda@ioc.fiocruz.br (A.M.D.-C.) Cassocera, M.; Bambo, M.; Anapakala, 6 Disciplina de Parasitologia, Faculdade de Ciências Médicas, UERJ/RH, Rio de Janeiro 21040-900, Brazil E.; Chissaque, A.; et al.
    [Show full text]
  • 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
    [Show full text]
  • The Stem Cell Revolution Revealing Protozoan Parasites' Secrets And
    Review The Stem Cell Revolution Revealing Protozoan Parasites’ Secrets and Paving the Way towards Vaccine Development Alena Pance The Wellcome Sanger Institute, Genome Campus, Hinxton Cambridgeshire CB10 1SA, UK; [email protected] Abstract: Protozoan infections are leading causes of morbidity and mortality in humans and some of the most important neglected diseases in the world. Despite relentless efforts devoted to vaccine and drug development, adequate tools to treat and prevent most of these diseases are still lacking. One of the greatest hurdles is the lack of understanding of host–parasite interactions. This gap in our knowledge comes from the fact that these parasites have complex life cycles, during which they infect a variety of specific cell types that are difficult to access or model in vitro. Even in those cases when host cells are readily available, these are generally terminally differentiated and difficult or impossible to manipulate genetically, which prevents assessing the role of human factors in these diseases. The advent of stem cell technology has opened exciting new possibilities to advance our knowledge in this field. The capacity to culture Embryonic Stem Cells, derive Induced Pluripotent Stem Cells from people and the development of protocols for differentiation into an ever-increasing variety of cell types and organoids, together with advances in genome editing, represent a huge resource to finally crack the mysteries protozoan parasites hold and unveil novel targets for prevention and treatment. Keywords: protozoan parasites; stem cells; induced pluripotent stem cells; organoids; vaccines; treatments Citation: Pance, A. The Stem Cell Revolution Revealing Protozoan 1. Introduction Parasites’ Secrets and Paving the Way towards Vaccine Development.
    [Show full text]
  • Cryptosporidium Parvum
    PROTOZOA—life cycles Protozoa Transmitted ;Trophozoites (merozoites, tachyzoites) — active, feeding, via Food (and Water) dividing (+ bradyzoites) ;Cysts — inert transmission form PHR 250 (exception: Toxoplasma) ;Gamonts → zygote → oöcyst (sporozoites) Giardia lamblia Giardiasis (= duodenalis = intestinalis) ;Leading protozoan cause of foodborne and waterborne disease in US ;CDC, ’98−’02: 3 foodborne outbreaks, 119 cases; ’03−’04: 2 waterborne outbreaks, 14 cases ;Spheroid cysts 9–12 µm long Giardia cyst Giardiasis 1 Giardia trophozoite Giardia lamblia ;Incubation 7–10 days; characteristic diarrhea from noninvasive colonization of upper small intestine may persist for weeks if untreated; asymptomatic infections very common. ;Reservoirs: humans, beavers, cattle, and other animals. Giardia lamblia vehicles ;Unfiltered surface water Cryptosporidium parvum (Giardia is fairly resistant to ;Oöcysts from humans, cattle, chlorine) other domestic & wild species ;Drinking water recontaminated (human-specific species: “C. with sewage hominis”) ;Fruits, vegetables, salads, and ;Small (4–6 µm), tough, chlorine- other foods subject to direct or indirect fecal contamination resistant Cryptosporidium parvum Cryptosporidium parvum ;Outbreaks from apple juice ;Largest outbreak of waterborne (cider) 1993 & 1996, and raw disease in history (Milwaukee, milk and a few other food 1993, ca. 403,000 cases, but only vehicles one waterborne U.S. outbreak ;CDC (’98–’02): 4 outreaks, 130 during ’03–’04 cases ;FoodNet (2005): ~8850 cases 2 Cryptosporidium C. parvum, C. hominis hominis ;Incubation ~1 week, profuse diarrhea usually <30 days (shedding 2–6 months); intracellular parasitism; treatment is rehydration. C. parvum oocyst C. parvum excysting Cryptosporidium parvum or C. parvum sporozoites C. hominis 3 C. parvum or C. hominis C. parvum or C. hominis ;Cryptosporidiosis is ;Concern for cryptosporidiosis diagnostic of AIDS in (especially waterborne) is HIV-positive persons & evoking stringent measures in will generally persist the U.S.
    [Show full text]
  • GLYCAN TRIGGERS of LIFE CYCLE DEVELOPMENT in the APICOMPLEXAN PARASITE CRYPTOSPORIDIUM a Dissertation Submitted to the Graduate
    GLYCAN TRIGGERS OF LIFE CYCLE DEVELOPMENT IN THE APICOMPLEXAN PARASITE CRYPTOSPORIDIUM A Dissertation Submitted to the Graduate Faculty of the North Dakota State University of Agriculture and Applied Science By Adam LeRoy Edwinson In Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY Major Program: Molecular Pathogenesis April 2017 Fargo, North Dakota North Dakota State University Graduate School Title GLYCAN TRIGGERS OF LIFE CYCLE DEVELOPMENT IN THE APICOMPLEXAN PARASITE CRYPTOSPORIDIUM By Adam LeRoy Edwinson The Supervisory Committee certifies that this disquisition complies with North Dakota State University’s regulations and meets the accepted standards for the degree of DOCTOR OF PHILOSOPHY SUPERVISORY COMMITTEE: Dr. John McEvoy Chair Dr. Teresa Bergholz Dr. Eugene Berry Dr. Glenn Dorsam Dr. Mark Clark Approved: 06/06/17 Dr. Peter Bergholz Date Department Chair ABSTRACT Cryptosporidium is an apicomplexan parasite that causes the diarrheal disease cryptosporidiosis, an infection that can become chronic and life threating in immunocompromised and malnourished individuals. Development of novel therapeutic interventions is critical as current treatments are entirely ineffective in treating cryptosporidiosis in populations at the greatest risk for disease. Repeated cycling of host cell invasion and replication by sporozoites results in the rapid amplification of parasite numbers and the pathology associated with the disease. Little is known regarding the factors that promote the switch from invasion to replication of Cryptosporidium, or the mechanisms underlying this change, but identification of replication triggers could provide potential targets for drugs designed to prevent cryptosporidiosis. The focus of this dissertation was to identify potential triggers and the mechanisms underlying the transition from invasive sporozoite to replicative trophozoites in Cryptosporidium.
    [Show full text]
  • Studies in Cryptosporidium
    STUDIES IN CRYPTOSPORIDIUM: MAINTENANCE OF STABLE POPULATIONS THROUGH IN VIVO PROPOGATION AND MOLECULAR DETECTION STRATEGIES DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of the Ohio State University By Norma E. Ramirez, M.P.H. ! ! ! ! The Ohio State University 2005 Dissertation Committee: Approved by Dr. Srinand Sreevatsan, Adviser Dr. Y.M. Saif ______________________________ Dr. Roger W. Stich Adviser Dr. Lucy A. Ward Graduate Program in Veterinary Preventive Medicine ABSTRACT Cryptosporidiosis, an infection caused by several genotypically and phenotypically diverse Cryptosporidium species, is a serious enteric disease of animals and humans worldwide. The current understanding of cryptosporidiosis, transmission, diagnosis, treatment and prevention measures for this disease is discussed. Contaminated water represents the major source of Cryptosporidium infections for humans. Manure from cattle can be a major source of Cryptosporidium oocysts. Oocysts transport to surface water can occur through direct fecal contamination, surface transport from land-applied manure or leaching through the soil to groundwater. Identification of Cryptosporidium species and genotypes facilitates determining the origin of the oocysts and to recognize sources of infection in outbreak situations and the risk factors associated with transmission. Very few studies have applied isolation methods to field samples because of difficulties with detection of oocysts in environmental samples. The objective of this study was to develop an easy method that can be applied to field samples to rapidly detect the presence of Cryptosporidium oocysts and identify their species. A molecular detection system that included an oocyst recovery method combined with spin column DNA extraction, followed by PCR- hybridization for detection and a Real-Time PCR-melting curve analysis for species ii assignment.
    [Show full text]
  • EVE Man 08-050 Mair V2:Layout 1 17/08/2009 14:28 Page 347
    EVE Man 08-050 Mair v2:Layout 1 17/08/2009 14:28 Page 347 Cryptosporidiosis 347 CRYPTOSPORIDIOSIS T. S. Mair*, N. D. Cohen† and G. R. Pearson‡ Bell Equine Veterinary Clinic, Mereworth, Maidstone, Kent ME18 5GS, UK; †Department of Large Animal Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas 77843-4475, USA; and ‡Department of Clinical Veterinary Science, School of Veterinary Science, Bristol University, Langford House, Langford, Bristol BS40 5DU, UK. Keywords: horse; coccidia; Cryptosporidium parvum; cryptosporidiosis; zoonosis; diarrhoea Summary species: C. andersoni, C. baileyi, C. bovis, C. canis, Cryptosporidium parvum is a coccidian parasite that C. felis, C. galli, C. hominis, C. meleagridis, C. infects the microvilli of intestinal epithelial cells. molnari, C. muris, C. parvum, C. saurophilum, C. Strains that infect horses and cattle can also infect scophthalmi, C. serpentis, C. suis and C. wrairi (Xiao man, and therefore cryptosporidiosis is a zoonotic et al. 2004; Sunnotel et al. 2006). C. hominis (formerly disease. In horses, cryptosporidiosis is most known as the C. parvum human genotype or genotype commonly seen in foals (most frequently 1–4 weeks I) almost exclusively infects man, while C. parvum of age) and is associated with diarrhoea and weight (formerly known as the C. parvum bovine genotype loss. Immunocompromised foals (including foals with or genotype II) infects man, ruminants and other severe combined immunodeficiency syndrome) are animal species (Morgan-Ryan et al. 2002). It is particularly at risk. classically known to be responsible for the majority of the zoonotic cryptosporidial infections. More Introduction recently, other species including C.
    [Show full text]
  • ORIGINAL ARTICLE Mirror of Research in Veterinary Sciences
    ORIGINAL ARTICLE Mirror of Research in Veterinary Sciences and Animals Makawi et al., (2016); 5 (3), 1-7 Mirror of MRVSA/ Research inOpen Veterinary Access Sciences DOAJ and Animals An Incidence of intestinal protozoa infection in sheep, sheep handlers and non-handlers in Wasit Governorate/ Iraq Zainab A. Makawi 1, Mohammed Th. S. Al-Zubaidi 1, Abdulkarim J. Karim 2* 1 Department of Parasitology, 2 Unit of Zoonotic Diseases College of Veterinary Medicine/ University of Baghdad/ Iraq. ARTICLE INFO there are suitable conditions in the intestinal lumen that promote the Received: 25.09.2016 parasite multiplication. This study aimed to investigate the cyst and Revised: 10. 09.2016 trophozoites infection in sheep and handlers. One-hundred eighty Accepted: 12.09.2016 fecal samples from sheep and 50 from handlers, were collected from Publish online: 05.10.2016 three different areas (Al-Hafriya, Al-Suwaira, and Al-Azizia) in _____________________ Wasit governorate. Sheep aged 7-36 months, while handlers were 10- *Corresponding author: 40 years. Fecal samples were examined directly and by staining [email protected] methods to detect intestinal protozoa cysts and trophozoites. Al- _____________________ Suwaira showed highest infection rates, 91.66%, and 87.5%, in sheep and handlers, respectively. Male represented higher infection rates Abstract than female in sheep (90.69%) and handlers (75%). In conclusion, Intestinal protozoa in this study approved the incidence of intestinal protozoa infection in sheep and human usually sheep and sheep handlers. The authors suggest doing another future incriminated in diarrhea, when study in different areas of the Wasit to investigate the prevalence rate of the intestinal protozoa.
    [Show full text]