Vše

Co hledáte?

Vše
Projekty
Výsledky výzkumu
Subjekty

Rychlé hledání

  • Projekty podpořené TA ČR
  • Významné projekty
  • Projekty s nejvyšší státní podporou
  • Aktuálně běžící projekty

Chytré vyhledávání

  • Takto najdu konkrétní +slovo
  • Takto z výsledků -slovo zcela vynechám
  • “Takto můžu najít celou frázi”

Development of multiplex tool for detection of pathogenic agents in food and environment

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F18%3AN0000077" target="_blank" >RIV/00027162:_____/18:N0000077 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00216224:14310/18:00106012

  • Výsledek na webu

    <a href="http://www.eavld2018.org/images/files/EAVLD_2018-Abstract_book.pdf" target="_blank" >http://www.eavld2018.org/images/files/EAVLD_2018-Abstract_book.pdf</a>

  • DOI - Digital Object Identifier

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Development of multiplex tool for detection of pathogenic agents in food and environment

  • Popis výsledku v původním jazyce

    5th Congress of the European Association of Veterinary Laboratory Diagnostics, MCE BUSINESS Conference Centre, Brussels, Belgium, 14. – 17.10.2018 – presentation. Microbiological safety of food and environment is currently a highly discussed topic. Detection of pathogenic agents in most cases relies on protocols using real time PCR (qPCR). qPCR, providing sensitive and specific detection, is still generally considered as a gold standard. However, qPCR has a significant drawback. There is not enough fluorescent dyes to create sufficiently robust systems for detection of larger number of targets. For this purpose, the xMAP® technology based method is being developed. The method uses two DNA probes for every target. One of them carries specific TAG sequence. These probes are linked together in presence of target DNA. Universal primer binding sequences at the ends of probes allow amplification of ligated probes. One of the two primers used for amplification is labelled. Detection of amplified probes uses sets of magnetic beads with unique absorption spectrum which are covered by anti-TAG sequences. Amplified probes are thus bound by their specific TAG sequence to complementary anti-TAG sequence on appropriate beads. Signal from beads is eventually read by MAGPIX® instrument. The developed method provides unique tool with potential to make routine analysis of various samples much more robust (up to 50 targets in one reaction), less laborious, less expensive and time consuming. Until now, several systems comprising human and veterinary pathogens have been developed (e.g. Campylobacter jejuni, Listeria monocytogenes, Salmonella enterica, Escherichia coli, Giardia lamblia, Taenia saginata, Norovirus, hepatitis A virus, hepatitis E virus). Validation of those systems and development of other targets is underway.

  • Název v anglickém jazyce

    Development of multiplex tool for detection of pathogenic agents in food and environment

  • Popis výsledku anglicky

    5th Congress of the European Association of Veterinary Laboratory Diagnostics, MCE BUSINESS Conference Centre, Brussels, Belgium, 14. – 17.10.2018 – presentation. Microbiological safety of food and environment is currently a highly discussed topic. Detection of pathogenic agents in most cases relies on protocols using real time PCR (qPCR). qPCR, providing sensitive and specific detection, is still generally considered as a gold standard. However, qPCR has a significant drawback. There is not enough fluorescent dyes to create sufficiently robust systems for detection of larger number of targets. For this purpose, the xMAP® technology based method is being developed. The method uses two DNA probes for every target. One of them carries specific TAG sequence. These probes are linked together in presence of target DNA. Universal primer binding sequences at the ends of probes allow amplification of ligated probes. One of the two primers used for amplification is labelled. Detection of amplified probes uses sets of magnetic beads with unique absorption spectrum which are covered by anti-TAG sequences. Amplified probes are thus bound by their specific TAG sequence to complementary anti-TAG sequence on appropriate beads. Signal from beads is eventually read by MAGPIX® instrument. The developed method provides unique tool with potential to make routine analysis of various samples much more robust (up to 50 targets in one reaction), less laborious, less expensive and time consuming. Until now, several systems comprising human and veterinary pathogens have been developed (e.g. Campylobacter jejuni, Listeria monocytogenes, Salmonella enterica, Escherichia coli, Giardia lamblia, Taenia saginata, Norovirus, hepatitis A virus, hepatitis E virus). Validation of those systems and development of other targets is underway.

Klasifikace

  • Druh

    O - Ostatní výsledky

  • CEP obor

  • OECD FORD obor

    10606 - Microbiology

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/VI20152020044" target="_blank" >VI20152020044: Multiplexní xMAP technologie pro komplexní detekci patogenních agens významných z pohledu zajištění ochrany zdraví lidí a zvířat</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2018

  • Kód důvěrnosti údajů

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