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NMR metabolomics reveals effects of Cryptosporidium infections on host cell metabolome

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F19%3A00520226" target="_blank" >RIV/60077344:_____/19:00520226 - isvavai.cz</a>

  • Alternative codes found

    RIV/60076658:12220/19:43900296

  • Result on the web

    <a href="https://gutpathogens.biomedcentral.com/track/pdf/10.1186/s13099-019-0293-x" target="_blank" >https://gutpathogens.biomedcentral.com/track/pdf/10.1186/s13099-019-0293-x</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1186/s13099-019-0293-x" target="_blank" >10.1186/s13099-019-0293-x</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    NMR metabolomics reveals effects of Cryptosporidium infections on host cell metabolome

  • Original language description

    BackgroundCryptosporidium is an important gut microbe whose contributions towards infant and immunocompromise patient mortality rates are steadily increasing. Over the last decade, we have seen the development of various tools and methods for studying Cryptosporidium infection and its interactions with their hosts. One area that is sorely overlooked is the effect infection has on host metabolic processes.ResultsUsing a H-1 nuclear magnetic resonance approach to metabolomics, we have explored the nature of the mouse gut metabolome as well as providing the first insight into the metabolome of an infected cell line. Statistical analysis and predictive modelling demonstrated new understandings of the effects of a Cryptosporidium infection, while verifying the presence of known metabolic changes. Of note is the potential contribution of host derived taurine to the diarrhoeal aspects of the disease previously attributed to a solely parasite-based alteration of the gut environment, in addition to other metabolites involved with host cell catabolism.ConclusionThis approach will spearhead our understanding of the Cryptosporidium-host metabolic exchange and provide novel targets for tackling this deadly parasite.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    40301 - Veterinary science

Result continuities

  • Project

    <a href="/en/project/GA15-01090S" target="_blank" >GA15-01090S: Revealing Cryptosporidium diversity: Linking genetic variation to parasite biology</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2019

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Gut Pathogens

  • ISSN

    1757-4749

  • e-ISSN

  • Volume of the periodical

    11

  • Issue of the periodical within the volume

    APR 3 2019

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    13

  • UT code for WoS article

    000463842900001

  • EID of the result in the Scopus database

    2-s2.0-85063929769