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