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Determination of African swine fever virus viability in meat during long-term storage and sous-vide cooking using cell culture and real-time PCR combined with palladium compound pre-treatment methods

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F23%3AN0000010" target="_blank" >RIV/00027162:_____/23:N0000010 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://actavet.vfu.cz/92/1/0053/" target="_blank" >https://actavet.vfu.cz/92/1/0053/</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2754/avb202392010053" target="_blank" >10.2754/avb202392010053</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Determination of African swine fever virus viability in meat during long-term storage and sous-vide cooking using cell culture and real-time PCR combined with palladium compound pre-treatment methods

  • Popis výsledku v původním jazyce

    African swine fever virus is causative agent of an acute and highly contagious disease affecting domestic and wild members of the family Suidae. The virus can be transmitted by direct contact among infected animals or via a contaminated environment or feed. Since the contaminated meat or products thereof have been characterised as the most probable vehicle in several outbreaks, the aim of present study was to define viability of the virus in meat under conditions of freezing and chilling (-25 °C and 6 °C) and low temperature cooking (55 °C for 2.5 hours and for 1 hour). Two independent methods were employed; cell culture as a reference and real-time polymerase chain reaction combined with palladium compounds (BB-PdCl2 and PdCl2COD) pre-treatment as an alternative method. Obtained results demonstrated minimal decrease in infectious virus titter during the storage at -25 °C and remaining dose of viruses in meat stored at 6 °C for 14 months that can cause a disease after ingestion. The result obtained by both methods applied on samples corresponded to each other. In contrast, results related to the virus persistence during thermal-treated meat indicated that its stability is much lower than previously thought; the infectious viruses were not detected after the treatment at 55 °C for 1 hour by infectivity assay. The observed difference of one order of magnitude of virus detected using palladium compounds pre-treatment suggests presence of intact rather than infectious viruses. The better suitability of PdCl2COD than BB-PdCl2 pre-treatment was demonstrated.

  • Název v anglickém jazyce

    Determination of African swine fever virus viability in meat during long-term storage and sous-vide cooking using cell culture and real-time PCR combined with palladium compound pre-treatment methods

  • Popis výsledku anglicky

    African swine fever virus is causative agent of an acute and highly contagious disease affecting domestic and wild members of the family Suidae. The virus can be transmitted by direct contact among infected animals or via a contaminated environment or feed. Since the contaminated meat or products thereof have been characterised as the most probable vehicle in several outbreaks, the aim of present study was to define viability of the virus in meat under conditions of freezing and chilling (-25 °C and 6 °C) and low temperature cooking (55 °C for 2.5 hours and for 1 hour). Two independent methods were employed; cell culture as a reference and real-time polymerase chain reaction combined with palladium compounds (BB-PdCl2 and PdCl2COD) pre-treatment as an alternative method. Obtained results demonstrated minimal decrease in infectious virus titter during the storage at -25 °C and remaining dose of viruses in meat stored at 6 °C for 14 months that can cause a disease after ingestion. The result obtained by both methods applied on samples corresponded to each other. In contrast, results related to the virus persistence during thermal-treated meat indicated that its stability is much lower than previously thought; the infectious viruses were not detected after the treatment at 55 °C for 1 hour by infectivity assay. The observed difference of one order of magnitude of virus detected using palladium compounds pre-treatment suggests presence of intact rather than infectious viruses. The better suitability of PdCl2COD than BB-PdCl2 pre-treatment was demonstrated.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10607 - Virology

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/QK1920113" target="_blank" >QK1920113: Virus afrického moru prasat v mase a masných výrobcích – metody detekce a studium perzistence</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2023

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    Acta Veterinaria Brno

  • ISSN

    0001-7213

  • e-ISSN

    1801-7576

  • Svazek periodika

    92

  • Číslo periodika v rámci svazku

    1

  • Stát vydavatele periodika

    CZ - Česká republika

  • Počet stran výsledku

    7

  • Strana od-do

    53-59

  • Kód UT WoS článku

    000933978400008

  • EID výsledku v databázi Scopus

    2-s2.0-85147815938