Inactivation of Highly Pathogenic Avian Influenza Virus with High-temperature Short Time Continuous Flow Pasteurization and Virus Detection in Bulk Milk Tanks

IF 2.1 4区 农林科学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of food protection Pub Date : 2024-08-21 DOI:10.1016/j.jfp.2024.100349
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Abstract

Infections of dairy cattle with clade 2.3.4.4b H5N1 highly pathogenic avian influenza virus (HPAIV) were reported in March 2024 in the U.S. and viable virus was detected at high levels in raw milk from infected cows. This study aimed to determine the potential quantities of infectious HPAIV in raw milk in affected states where herds were confirmed positive by USDA for HPAIV (and therefore were not representative of the entire population), and to confirm that the commonly used continuous flow pasteurization using the FDA approved 72 °C (161°F) for 15 s conditions for high−temperature short time (HTST) processing, will inactivate the virus. Double-blinded raw milk samples from bulk storage tanks from farms (n = 275) were collected in four affected states. Samples were screened for influenza A using quantitative real-time RT-PCR (qrRT-PCR) of which 158 (57.5%) were positive and were subsequently quantified in embryonating chicken eggs. Thirty-nine qrRT-PCR positive samples (24.8%) were positive for infectious virus with a median titer of 3.5 log10 50% egg infectious doses (EID50) per mL. To closely simulate commercial milk pasteurization processing systems, a pilot-scale continuous flow pasteurizer was used to evaluate HPAIV inactivation in artificially contaminated raw milk using the most common legal conditions in the US: 72 °C (161°F) for 15 s. Among all replicates at two flow rates (n = 5 at 0.5 L/min; n = 4 at 1 L/min), no viable virus was detected. A mean reduction of ≥5.8 ± 0.2 log10 EID50/mL occurred during the heating phase where the milk is brought to 72.5 °C before the holding tube. Estimates from heat-transfer analysis support that standard U.S. continuous flow HTST pasteurization parameters will inactivate >12 log10 EID50/mL of HPAIV, which is ∼9 log10 EID50/mL greater than the median quantity of infectious virus detected in raw milk from bulk storage tank samples. These findings demonstrate that the US milk supply is safe when pasteurized.

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用高温短时间连续流巴氏杀菌法灭活高致病性禽流感病毒以及在散装牛奶罐中检测病毒。
2024 年 3 月,美国报告了奶牛感染 2.3.4.4b 支系 H5N1 高致病性禽流感病毒 (HPAIV)的情况,并在受感染奶牛的生奶中检测到高水平的存活病毒。本研究旨在确定受影响州生奶中传染性 HPAIV 的潜在数量,这些州的牛群已被美国农业部确认为 HPAIV 阳性(因此不能代表整个牛群),并确认常用的连续流巴氏杀菌法(使用 FDA 批准的 72°C (161°F) 15 秒高温短时间 (HTST) 处理条件)可灭活病毒。在四个受影响的州收集了来自农场散装储藏罐的双盲生乳样本(n=275)。使用定量实时 RT-PCR (qrRT-PCR)技术对样本进行甲型流感病毒筛查,其中 158 份样本(57.5%)呈阳性,随后在鸡胚蛋中进行定量检测。39 个 qrRT-PCR 阳性样本(24.8%)的传染性病毒呈阳性,平均滴度为每毫升 3.5 log10 50%鸡蛋感染剂量(EID50)。为了近似模拟商业牛奶巴氏杀菌处理系统,我们使用一台中试规模的连续流巴氏杀菌机,在美国最常见的法定条件下评估人工污染生奶中 HPAIV 的灭活情况:72°C (161°F) 15 秒。在两种流速下(0.5 升/分钟,n=5;1 升/分钟,n=4)的所有重复样品中,均未检测到存活病毒。在加热阶段,牛奶温度升至 72.5 摄氏度,然后进入保温管,平均每毫升 EID50 降低≥5.8 ± 0.2 log10。热传递分析的估计结果表明,标准的美国连续流 HTST 巴氏杀菌参数可灭活 >12 log10 EID50/mL 的高致病性禽流感病毒,这比从散装储奶罐样品中检测到的生乳中传染性病毒的平均数量高出 9 log10 EID50/mL。这些研究结果表明,美国的牛奶供应经巴氏杀菌后是安全的。
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来源期刊
Journal of food protection
Journal of food protection 工程技术-生物工程与应用微生物
CiteScore
4.20
自引率
5.00%
发文量
296
审稿时长
2.5 months
期刊介绍: The Journal of Food Protection® (JFP) is an international, monthly scientific journal in the English language published by the International Association for Food Protection (IAFP). JFP publishes research and review articles on all aspects of food protection and safety. Major emphases of JFP are placed on studies dealing with: Tracking, detecting (including traditional, molecular, and real-time), inactivating, and controlling food-related hazards, including microorganisms (including antibiotic resistance), microbial (mycotoxins, seafood toxins) and non-microbial toxins (heavy metals, pesticides, veterinary drug residues, migrants from food packaging, and processing contaminants), allergens and pests (insects, rodents) in human food, pet food and animal feed throughout the food chain; Microbiological food quality and traditional/novel methods to assay microbiological food quality; Prevention of food-related hazards and food spoilage through food preservatives and thermal/non-thermal processes, including process validation; Food fermentations and food-related probiotics; Safe food handling practices during pre-harvest, harvest, post-harvest, distribution and consumption, including food safety education for retailers, foodservice, and consumers; Risk assessments for food-related hazards; Economic impact of food-related hazards, foodborne illness, food loss, food spoilage, and adulterated foods; Food fraud, food authentication, food defense, and foodborne disease outbreak investigations.
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