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Metabolic changes of the host-pathogen environment in a Cryptosporidium infection

https://doi.org/10.1101/145979
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Outgoing claims: the papers this work cites, builds on, or argues with.

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MR metabolomics of fecal extracts: applications in the study of bowel diseases
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Hypoxanthine, Guanine, Xanthine Phosphoribosyltransferase Activity inCryptosporidium parvum
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Cryptosporidium parvum oocyst viability and behaviour of the residual body during the excystation process
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Synthesis of glutamine, glycine and 10-formyl tetrahydrofolate is coregulated with purine biosynthesis in Saccharomyces cerevisiae
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Role of taurine supplementation to prevent exercise-induced oxidative stress in healthy young men
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Effects of taurine on gut microbiota and metabolism in mice
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1H NMR-based metabonomic assessment of probiotic effects in a colitis mouse model
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Treatment of Cryptosporidium: What We Know, Gaps, and the Way Forward
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Inhibition of the purified and reconstituted calcium pump of erythrocytes by μM levels of dids and nap‐taurine
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Intestinal function and injury in acquired immunodeficiency syndrome—related cryptosporidiosis
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Ileal and jejunal absorptive function in patients with AIDS and enterococcidial infection
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Antioxidant role and subcellular location of hypotaurine and taurine in human neutrophils
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Molecular Epidemiology of Human Cryptosporidiosis
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Phylogenomics of the Intracellular Parasite Mikrocytos mackini Reveals Evidence for a Mitosome in Rhizaria
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Molecular epidemiology of Cryptosporidium in humans and cattle in The Netherlands
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Evolution of Cryptosporidium in vitro culture
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In vitro culture systems for the study of apicomplexan parasites in farm animals
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Continuous culture of Cryptosporidium parvum using hollow fiber technology
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A cell culture platform for Cryptosporidium that enables long-term cultivation and new tools for the systematic investigation of its biology
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The application of LC–NMR and LC–MS for the separation and rapid structure elucidation of an unknown impurity in 5-aminosalicylic acid
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Development of an untargeted metabolomics method for the analysis of human faecal samples using Cryptosporidium-infected samples
inferredcites →https://doi.org/10.1016/s0021-9258(18)96535-xopenalex-snapshot
δ-Aminolevulinic Acid Synthetase
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Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the Global Enteric Multicenter Study, GEMS): a prospective, case-control study
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Cryptosporidiosis-an overview
inferredcites →https://doi.org/10.1016/s1937-6448(10)81005-6openalex-snapshot
Metabolic Pathways in the Apicoplast of Apicomplexa
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Dissection of the hierarchy and synergism of the bile derived signal on Cryptosporidium parvum excystation and infectivity
inferredcites →https://doi.org/10.1017/s0950268814000673openalex-snapshot
Approaches to the detection of very small, common, and easily missed outbreaks that together contribute substantially to human Cryptosporidium infection
inferredcites →https://doi.org/10.1021/acsinfecdis.6b00094openalex-snapshot
Cryptosporidiosis Drug Discovery: Opportunities and Challenges
inferredcites →https://doi.org/10.1021/pr070340kopenalex-snapshot
Species Variation in the Fecal Metabolome Gives Insight into Differential Gastrointestinal Function
inferredcites →https://doi.org/10.1038/503189aopenalex-snapshot
Parasitic infections: Time to tackle cryptosporidiosis
inferredcites →https://doi.org/10.1039/b927543fopenalex-snapshot
An optimised sample preparation method for NMR-based faecal metabonomic analysis
inferredcites →https://doi.org/10.1039/c6mb00362aopenalex-snapshot
Host metabolic responses to Plasmodium falciparum infections evaluated by 1H NMR metabolomics
inferredcites →https://doi.org/10.1074/jbc.m113.482992openalex-snapshot
Identification and Functional Analysis of the Primary Pantothenate Transporter, PfPAT, of the Human Malaria Parasite Plasmodium falciparum
inferredcites →https://doi.org/10.1093/nar/gkv380openalex-snapshot
MetaboAnalyst 3.0—making metabolomics more meaningful
inferredcites →https://doi.org/10.1097/meg.0000000000000541openalex-snapshot
Long-term outcomes in patients diagnosed with bile-acid diarrhoea
inferredcites →https://doi.org/10.1097/qco.0b013e328357e569openalex-snapshot
Burden of disease from cryptosporidiosis
inferredcites →https://doi.org/10.1099/jmm.0.46251-0openalex-snapshot
Genetic analysis of Cryptosporidium from 2414 humans with diarrhoea in England between 1985 and 2000
inferredcites →https://doi.org/10.1111/j.1365-2249.2008.03599.xopenalex-snapshot
Effect of taurine on oxidative stress and apoptosis-related protein expression in trinitrobenzene sulphonic acid-induced colitis
inferredcites →https://doi.org/10.1111/j.1365-3024.2011.01301.xopenalex-snapshot
Genomics and population biology of Cryptosporidium species
inferredcites →https://doi.org/10.1111/jeu.12272openalex-snapshot
Differential Gene Expression and Protein Localization of Cryptosporidium parvum Fatty Acyl‐CoA Synthetase Isoforms
inferredcites →https://doi.org/10.1111/pim.12115openalex-snapshot
Apicomplexan infections in the gut
inferredcites →https://doi.org/10.1111/zph.12078openalex-snapshot
A Survey of U . S . Obstetrician‐Gynecologists' Clinical and Epidemiological Knowledge of Cryptosporidiosis in Pregnancy
inferredcites →https://doi.org/10.1126/science.1094786openalex-snapshot
Complete Genome Sequence of the Apicomplexan, Cryptosporidium parvum
inferredcites →https://doi.org/10.1128/cmr.00115-13openalex-snapshot
The Evolution of Respiratory Cryptosporidiosis: Evidence for Transmission by Inhalation
inferredcites →https://doi.org/10.1128/cmr.12.4.554openalex-snapshot
New Insights into Human Cryptosporidiosis
inferredcites →https://doi.org/10.1128/iai.00169-06openalex-snapshot
Bile Acids Enhance Invasiveness of Cryptosporidium spp. into Cultured Cells
inferredcites →https://doi.org/10.12816/0006403openalex-snapshot
COMPARATIVE STUDY BETWEEN THE EFFECT OF NITAZOXANIDE AND PAROMOMYCINE IN TREATMENT OF CRYPTOSPORIDIOSIS IN HOSPITALIZED CHILDREN
inferredcites →https://doi.org/10.1371/journal.pone.0077803openalex-snapshot
Metabolomic Profiling of Faecal Extracts from Cryptosporidium parvum Infection in Experimental Mouse Models
inferredcites →https://doi.org/10.1645/0022-3395(2001)087[0997:tuosti]2.0.co;2openalex-snapshot
THE UTILIZATION OF SODIUM TAUROCHOLATE IN EXCYSTATION OFCRYPTOSPORIDIUM PARVUMAND INFECTION OF TISSUE CULTURE
inferredcites →https://doi.org/10.1645/ge-661r.1openalex-snapshot
Failure to Propagate Cryptosporidium spp. in Cell-Free Culture
inferredcites →https://doi.org/10.2307/3283888openalex-snapshot
Simplified Methods for Obtaining Purified Oocysts from Mice and for Growing Cryptosporidium parvum In vitro
inferredcites →https://doi.org/10.2307/3285221openalex-snapshot
The Utilization of Sodium Taurocholate in Excystation of Cryptosporidium parvum and Infection of Tissue Culture
inferredcites →https://doi.org/10.4269/ajtmh.13-0254openalex-snapshot
Cryptosporidiosis in HIV/AIDS Patients in Kenya: Clinical Features, Epidemiology, Molecular Characterization and Antibody Responses
inferredcites →https://doi.org/10.4269/ajtmh.1997.56.637openalex-snapshot
Nitazoxanide in the Treatment of Cryptosporidial Diarrhea and other Intestinal Parasitic Infections Associated with Acquired Immunodeficiency Syndrome in Tropical Africa
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