Development of a cell culture-based method for detecting infectious tick-borne encephalitis virus (TBEV) in milk products

IF 4.5 1区 农林科学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Food microbiology Pub Date : 2024-08-13 DOI:10.1016/j.fm.2024.104619
Catherine Hennechart-Collette , Laure Mathews-Martin , Lisa Fourniol , Audrey Fraisse , Sandra Martin-Latil , Laure Bournez , Gaëlle Gonzalez , Sylvie Perelle
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引用次数: 0

Abstract

Tick-borne encephalitis outbreaks have been reported in Europe after consumption of raw milk products from infected animals. While molecular methods are commonly used in viral foodborne outbreak investigations due to their sensitivity, specificity and rapidity, there are very few methods to detect infectious tick-borne encephalitis virus (TBEV) in milk products for routine use/analyses. To address this gap, we developed a cell culture-based method to detect infectious TBEV in artificially contaminated raw goat milk and raw goat cheese, and evaluated the sensitivity of TBEV infectivity assays. Raw goat milk samples were spiked with TBEV to achieve inoculation levels ranging from 106 to 100 TCID50/mL, and Faisselle and Tomme cheese samples were spiked so their TBEV concentrations ranged from 9.28 × 105 to 9.28 × 101 TCID50 per 2.5g. To detect infectious TBEV, Vero cells were infected by raw goat milk. For cheese samples, after homogenisation and membrane filtration, Vero cells were infected with samples adsorbed on the filter (method A) or with samples eluted from the filter (method B). After 5 days, cytopathic effects (CPEs) were observed and TBEV replication in Vero cells was confirmed by an increase in the number of genome copies/mL that were detected in cell supernatant. Infected Vero cells exhibited CPEs for both milk and cheese samples. Infectious TBEV was detected to 103 TCID50/mL in raw milk samples and to 9.28 × 101 TCID50 from Faisselle samples using both methods A and B. For Tomme samples, method A was able to detect TBEV to 9.28 × 102 TCID50/2.5g and method B to 9.28 × 103 TCID50/2.5g. The number of positive samples detected was slightly higher with method A than with method B. To conclude, this qualitative cell culture-based method can detect infectious TBEV artificially inoculated into raw milk and cheese; it should be further evaluated during foodborne outbreak investigations to detect infectious TBEV from naturally contaminated milk and cheese.

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开发基于细胞培养的检测奶制品中传染性蜱传脑炎病毒(TBEV)的方法
据报道,欧洲曾发生过食用来自受感染动物的生鲜乳制品后爆发蜱传脑炎的事件。虽然分子方法因其灵敏性、特异性和快速性而常用于病毒性食源性疾病爆发的调查,但用于常规用途/分析的检测奶制品中传染性蜱传脑炎病毒(TBEV)的方法却很少。为了填补这一空白,我们开发了一种基于细胞培养的方法来检测人工污染的生山羊奶和生山羊奶酪中的传染性 TBEV,并评估了 TBEV 感染性检测方法的灵敏度。在生山羊奶样品中添加 TBEV 以达到 106 到 100 TCID50/mL 的接种水平,在 Faisselle 和 Tomme 奶酪样品中添加 TBEV 以达到 9.28 × 105 到 9.28 × 101 TCID50 每 2.5g 的接种水平。为了检测传染性 TBEV,用生羊奶感染 Vero 细胞。对于奶酪样品,在均质化和膜过滤后,用吸附在过滤器上的样品(方法 A)或从过滤器上洗脱的样品(方法 B)感染 Vero 细胞。5 天后,观察到细胞病理效应(CPE),细胞上清液中检测到的基因组拷贝数/毫升的增加证实了 TBEV 在 Vero 细胞中的复制。牛奶和奶酪样品中受感染的 Vero 细胞都出现了 CPE。对于 Tomme 样品,方法 A 能够检测到 9.28 × 102 TCID50/2.5g的 TBEV,方法 B 能够检测到 9.28 × 103 TCID50/2.5g的 TBEV。总之,这种基于细胞培养的定性方法可以检测出人工接种到生牛奶和奶酪中的传染性 TBEV;在食源性疾病爆发调查中,应进一步评估该方法,以检测出自然污染的牛奶和奶酪中的传染性 TBEV。
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来源期刊
Food microbiology
Food microbiology 工程技术-生物工程与应用微生物
CiteScore
11.30
自引率
3.80%
发文量
179
审稿时长
44 days
期刊介绍: Food Microbiology publishes original research articles, short communications, review papers, letters, news items and book reviews dealing with all aspects of the microbiology of foods. The editors aim to publish manuscripts of the highest quality which are both relevant and applicable to the broad field covered by the journal. Studies must be novel, have a clear connection to food microbiology, and be of general interest to the international community of food microbiologists. The editors make every effort to ensure rapid and fair reviews, resulting in timely publication of accepted manuscripts.
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