Mlinar Zdenko, Kostelac Deni, Kovaček Ivančica, Klobučar Ana, Tešić Vanja, Prahin Vedran, Frece Jadranka
Andrija Štampar Teaching Institute of Public Health, Mirogojska cesta 16, 10000 Zagreb, Croatia.
Faculty of Food Technology and Biotechnology, University of Zagreb, Pierottijeva ulica 6, 10000 Zagreb, Croatia.
Food Technol Biotechnol. 2023 Jun;61(2):250-258. doi: 10.17113/ftb.61.02.23.8018.
While it is clear that SARS CoV-2 coronavirus is the primary respiratory virus, there are no entirely clarified ways of transmission. Foodborne transmission has remained an unexplained path. Therefore, the goals of this paper are to examine and present an assessment of the most appropriate of the four selected kits for RNA extraction for the testing and detection of SARS-CoV-2 on food packaging surfaces, food surfaces, and in food. This will enable to indicate the possibility of infection through contact or direct food consumption.
Finding the best technique is vital as RNA extraction is one of the essential elements in detecting SARS-CoV-2. This was achieved through an experiment with four commercial kits following the original manufacturers' protocols, and with a modification of the original protocols that included the use of ethanol and isopropanol. The selected kit was used for RNA extraction from the swabs of packaging surfaces, food surface, and ready-to-eat food samples. The coronavirus was then identified using real-time reverse transcription-polymerase chain reaction (RT-PCR) assays to determine whether the SARS-CoV-2 virus or viral particles are present in the food chain with the overall purpose of demonstrating the possibility that food can contribute as a vehicle for the transmission of the virus.
The findings of this investigation made the most effective extraction kit and protocol stand out. The results of the applicability of the kit indicated a significant share of positive samples of viral SARS-CoV-2 virus particles on surfaces from the environment where infected persons with 'silent' COVID-19 infection, with mild symptoms or no symptoms, were present. However, according to the findings of the second part of the study, the virus was not detected on the examined samples of food packaging surfaces, food surfaces, and food.
The presented results distinguished one of the most suitable protocols for isolating RNA from environmental surface samples. The main contribution of the study is in the presentation of the results, that is, the examination of samples that are primarily related to the food chain, food packaging, food surfaces, and ready-to-eat food. The results of this study could also be helpful for further determination of the potential of food as a vector for the transmission of coronaviruses.
虽然很明显严重急性呼吸综合征冠状病毒2(SARS-CoV-2)是主要的呼吸道病毒,但尚无完全明确的传播途径。经食物传播仍是一条未得到解释的途径。因此,本文的目标是检验并评估四种选定的用于从食品包装表面、食品表面及食品中提取RNA以检测SARS-CoV-2的试剂盒中最合适的一种。这将有助于指出通过接触或直接食用食物而感染的可能性。
由于RNA提取是检测SARS-CoV-2的关键要素之一,找到最佳技术至关重要。这是通过按照原始制造商的方案使用四种商业试剂盒进行实验实现的,并且对原始方案进行了修改,包括使用乙醇和异丙醇。选定的试剂盒用于从包装表面、食品表面和即食食品样本的拭子中提取RNA。然后使用实时逆转录-聚合酶链反应(RT-PCR)检测来鉴定冠状病毒,以确定SARS-CoV-2病毒或病毒颗粒是否存在于食物链中,其总体目的是证明食物作为病毒传播载体的可能性。
本研究结果使最有效的提取试剂盒和方案脱颖而出。该试剂盒适用性的结果表明,在存在“无症状”新冠病毒感染、症状轻微或无症状的感染者的环境表面上,有相当比例的样本检测出SARS-CoV-2病毒颗粒呈阳性。然而,根据研究第二部分的结果,在所检测的食品包装表面、食品表面和食品样本中未检测到该病毒。
所呈现的结果区分出了从环境表面样本中分离RNA的最合适方案之一。该研究的主要贡献在于结果的呈现,即对主要与食物链、食品包装、食品表面和即食食品相关的样本进行检测。本研究结果也可能有助于进一步确定食物作为冠状病毒传播载体的可能性。