猪肝肠和腊肠样生猪肉肠制作过程中戊型肝炎病毒灭活的测定。

IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY International journal of food microbiology Pub Date : 2025-02-02 DOI:10.1016/j.ijfoodmicro.2024.111018
Katja Schilling-Loeffler , Dirk Meyer , Alexander Wolff , Jorge Santamaría-Palacios , Felix Reich , Reimar Johne
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引用次数: 0

摘要

人畜共患戊型肝炎病毒(HEV)可引起人类急性和慢性肝炎。家猪是戊肝病毒的主要动物宿主,其肉在戊肝病毒传播中起关键作用。虽然猪肉产品可能含有HEV- rna,但不清楚在其生产过程后是否仍存在传染性HEV。本研究采用新建立的香肠病毒提取方法和人工污染香肠中HEV传染性的定量检测方法,对可涂猪肝香肠和仿萨拉米生猪肉香肠生产过程中HEV灭活情况进行了研究。采用细胞培养适应的HEV基因型3c 47832c菌株污染用于生产香肠的肉类制剂,这些香肠是根据德国常用的配方生产的。根据这些配方,将一定直径的可涂抹肝肠放在70℃的水浴中保温30分钟。因此,将接种了HEV的肝肠制剂装入锥形管中,在70℃的水浴中加热。21分钟后,香肠达到70°C的核心温度,进一步孵育18分钟后采集样品。对于生香肠,将接种了HEV的肉类制剂填充到天然肠衣中,并在18°C和80%相对湿度下腌制香肠。样本采集时间长达21天。从所有样品中提取HEV,分别采用细胞培养和RT-qPCR定量分析感染性病毒和病毒RNA。在肝肠生产过程中,感染性HEV在达到核心温度70℃后立即降低4 log10,并在2 min后(热处理23 min)完全失活(降低4.3 log10)。相比之下,在整个孵育时间内,HEV-RNA的数量仅略有下降(10)。在生香肠制作过程中,感染性HEV在三周的腌制过程中仅略有下降(10),而HEV- rna的数量保持不变。可以得出的结论是,在制作可涂抹肝香肠的过程中,预期的加热制度会导致HEV失活,这表明如果这些香肠生产得当,消费者感染HEV的风险很低。相比之下,在生产类似腊肠的生猪肉香肠时,HEV仅被轻微灭活。因此,如果使用高HEV量的原料生产,生香肠可能含有传染性HEV。病毒RNA检测不能用于预测肉制品中戊肝病毒的传染性。
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Determination of hepatitis E virus inactivation during manufacturing of spreadable pork liver sausage and salami-like raw pork sausage
The zoonotic hepatitis E virus (HEV) can cause acute and chronic hepatitis in humans. Meat from domestic pigs, which represent a major animal reservoir of HEV, plays a key role in HEV transmission. Although pork meat products can contain HEV-RNA, it is unknown whether infectious HEV is still present after their manufacturing process. Here, we used a newly developed method for virus extraction from sausages and a quantitative method for detecting HEV infectivity in artificially contaminated sausages to investigate the HEV inactivation during production of spreadable pork liver sausage and salami-like raw pork sausage.
The cell culture-adapted HEV genotype 3c strain 47832c was used to contaminate meat preparations intended for production of sausages, which were manufactured based on recipes commonly used in Germany. According to these recipes, spreadable liver sausages of a certain diameter are to be held in a water bath at 70 °C for 30 min. Therefore, the HEV inoculated liver sausage preparations were filled into conical tubes and heated in a 70 °C water bath. After 21 min, the sausages reached a core temperature of 70 °C and samples were taken after further incubation for up to 18 min. For the raw sausages, the HEV inoculated meat preparation was filled into natural casings and sausages were cured at 18 °C and 80 % relative humidity. Samples were taken for up to 21 days. HEV was extracted from all samples, which were quantitatively analyzed for infectious virus and viral RNA using cell culture and RT-qPCR, respectively.
During liver sausage production, infectious HEV decreased by four log10 immediately after reaching the core temperature of 70 °C and was completely inactivated (>4.3 log10 decrease) 2 min later (23 min heat treatment). In contrast, the HEV-RNA amount decreased only marginally (<0.6 log10) throughout the whole incubation time. During raw sausage manufacturing, infectious HEV decreased only slightly (<1.3 log10) over three weeks of curing, while the HEV-RNA amount remained unchanged.
It can be concluded that the intended heating regime during production of spreadable liver sausages leads to an inactivation of HEV, indicating a low risk of HEV infection for consumers if these sausages are manufactured properly. In contrast, HEV was only slightly inactivated during production of salami-like raw pork sausage. Therefore, raw sausage can contain infectious HEV if starting material with a high HEV amount was used for production. Viral RNA testing cannot be used to predict infectivity of HEV in meat products.
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来源期刊
International journal of food microbiology
International journal of food microbiology 工程技术-食品科技
CiteScore
10.40
自引率
5.60%
发文量
322
审稿时长
65 days
期刊介绍: The International Journal of Food Microbiology publishes papers dealing with all aspects of food microbiology. Articles must present information that is novel, has high impact and interest, and is of high scientific quality. They should provide scientific or technological advancement in the specific field of interest of the journal and enhance its strong international reputation. Preliminary or confirmatory results as well as contributions not strictly related to food microbiology will not be considered for publication.
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