Aula 3 Giardia E Crypto 2020
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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 -
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. -
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. -
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. -
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. -
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 -
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. -
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. -
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. -
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. -
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. -
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.