High pressure processing of shellfish: A review of microbiological and other quality aspects

Many commercially important shellfish are filter feeders and, as a consequence, concentrate microbes from the surrounding waters. Shellfish may be relayed or depurated to reduce the level of microbial contamination, but the efficiency of these purification practices, particularly in relation to viruses and indigenous marine bacteria, is questionable. Therefore additional processing is necessary to ensure the safety of shellfish for human consumption. In recent years high pressure (HP) processing has been investigated as an alternative method for food preservation. HP technology allows inactivation of microorganisms while maintaining sensory and nutritional properties of foods. Currently, HP processing has several commercial food applications, including oysters. As well as enhancing safety and extending shelf-life, HP treatment has the additional advantage of shucking or opening shellfish, making this technology particularly beneficial to the shellfish processing industry and consumers alike.Industrial relevanceHigh pressure (HP) processing is increasingly being used in the commercial processing of oysters, due to its minimal effects on sensory and nutritional quality, the opening or shucking of oysters during treatment, and the reduction of levels of Vibrio vulnificus, a pathogen of concern particularly in the US. However, little is known of the efficacy of HP treatment in reducing other pathogens in shellfish such as human enteric viruses, which are the predominant cause of shellfish-borne disease. This article reviews the inactivation of microorganisms of importance to shellfish, particularly viruses, the commercial HP processing of oysters and the advantages of HP technology as they pertain to the seafood industry.     

High pressure-induced inactivation of Qbeta coliphage and c2 phage in oysters and in culture media

High pressure (HP) treatment inactivates bacteria in shellfish, but its effects on viruses in shellfish have not yet been determined, although viral illness is frequently associated with shellfish consumption. The aim of this study was to investigate the baroresistance of two bacteriophage viruses, Qbeta coliphage and c2 phage, in oysters and in culture media. High numbers (>or=10(7) ml(-1) or g(-1)) of both phages were obtained in culture media and in oysters. Samples were HP treated at 200-800 MPa at 20 degrees C for up to 30 min. Little or no inactivation of either phage was observed in oysters or in culture media after treatment at 相似文献   

Inactivation of hepatitis A virus and a calicivirus by high hydrostatic pressure

Potential application of high hydrostatic pressure processing (HPP) as a method for virus inactivation was evaluated. A 7-log10 PFU/ml hepatitis A virus (HAV) stock, in tissue culture medium, was reduced to nondetectable levels after exposure to more than 450 MPa of pressure for 5 min. Titers of HAV were reduced in a time- and pressure-dependent manner between 300 and 450 MPa. In contrast, poliovirus titer was unaffected by a 5-min treatment at 600 MPa. Dilution of HAV in seawater increased the pressure resistance of HAV, suggesting a protective effect of salts on virus inactivation. RNase protection experiments indicated that viral capsids may remain intact during pressure treatment, suggesting that inactivation was due to subtle alterations of viral capsid proteins. A 7-log10 tissue culture infectious dose for 50% of the cultures per ml of feline calicivirus, a Norwalk virus surrogate, was completely inactivated after 5-min treatments with 275 MPa or more. These data show that HAV and a Norwalk virus surrogate can be inactivated by HPP and suggest that HPP may be capable of rendering potentially contaminated raw shellfish free of infectious viruses.     

Effect of different high pressure treatments on shucking,biochemical, physical and sensory characteristics of oysters to elaborate a traditional Taiwanese oyster omelette

BACKGROUND: Whole oysters (Crassostrea gigas) were processed using high‐pressure (HP) treatment (150–300 MPa) to determine their shucking and biochemical properties. Subsequently, HP‐treated oysters were cooked at 160 °C for 90 s, as when preparing the oyster omelette dish, to evaluate their physical and sensory characteristics as compared to raw oysters. RESULTS: The treatments of 250 and 300 MPa for 2 min and 0 min, respectively, resulted in 100% release. The pH of HP‐treated oysters increased slightly from 6.50 to 6.82, and the moisture contents of the HP‐treated oysters with or without further cooking were all higher than those of the control. The brightness, yellowness and cutting strength of HP‐treated oysters with further cooking changed insignificantly, while the redness decreased compared to the control. Sensory evaluation showed that oysters treated at 250 and 300 MPa oysters after cooking received higher quality scores than the control. CONCLUSIONS: HP processing at 250 and 300 MPa proved to be a good method for oyster shucking. The HP‐treated oysters cooked in the oyster omelette are acceptable to consumers. Overall, the application of HP as a processing method to improve the quality and acceptability of oysters and their related products would be possible. Copyright © 2009 Society of Chemical Industry     

Depuration and Relaying: A Review on Potential Removal of Norovirus from Oysters

Pollution of coastal waters can result in contamination of bivalve shellfish with human enteric viruses, including norovirus (NoV), and oysters are commonly implicated in outbreaks. Depuration is a postharvest treatment involving placement of shellfish in tanks of clean seawater to reduce contaminant levels; this review focuses on the efficacy of depuration in reducing NoV in oysters. There have been many NoV outbreaks from depurated oysters containing around 10³ genome copies/g oyster tissue, far exceeding the median infectious dose (ID50). Half of the published NoV reduction experiments showed no decrease in NoV during depuration, and in the remaining studies it took between 9 and 45.5 d for a 1‐log reduction—significantly longer than commercial depuration time frames. Surrogate viruses are more rapidly depurated than NoV; the mean number of days to reduce NoV by 1 log is 19, and 7.5 d for surrogates. Thus, surrogates do not appear to be suitable for assessing virological safety of depurated oysters; data on reduction of NoV infectivity during depuration would assist evaluations on surrogate viruses and the impact of methods used. The longer persistence of NoV highlights its special relationship with oysters, which involves the binding of NoV to histo‐blood group‐like ligands in various tissues. Given the persistence of NoV and on‐going outbreaks, depuration as currently performed appears ineffective in guaranteeing virologically safe oysters. Conversely, relaying oysters for 4 wk is more successful, with low NoV concentrations and no illnesses associated with products. The ineffectiveness of depuration emphasizes the need for coastal water quality to be improved to ensure oysters are safe to eat.     

Inactivation of foodborne viruses of significance by high pressure and other processes

The overall safety of a food product is an important component in the mix of considerations for processing, distribution, and sale. With constant commercial demand for superior food products to sustain consumer interest, nonthermal processing technologies have drawn considerable attention for their ability to assist development of new products with improved quality attributes for the marketplace. This review focuses primarily on the nonthermal processing technology high-pressure processing (HPP) and examines current status of its use in the control and elimination of pathogenic human viruses in food products. There is particular emphasis on noroviruses and hepatitis A virus with regard to the consumption of raw oysters, because noroviruses and hepatitis A virus are the two predominant types of viruses that cause foodborne illness. Also, application of HPP to whole-shell oysters carries multiple benefits that increase the popularity of HPP usage for these foods. Viruses have demonstrated a wide range of sensitivities in response to high hydrostatic pressure. Viral inactivation by pressure has not always been predictable based on nomenclature and morphology of the virus. Studies have been complicated in part from the inherent difficulties of working with human infectious viruses. Consequently, continued study of viral inactivation by HPP is warranted.     

Coliphage as pressure surrogates for enteric viruses in foods

In this study the potential of using selected bacteriophages as pressure surrogates for hepatitis A virus (HAV) and Aichi virus (AiV) was investigated. The coliphages included, T₄, MS2, Qβ, λ imm 434, λ cI 857 and λ cI 857A. T₄ displayed similar pressure responses as HAV and was chosen for further study. The most pressure-resistant phage, MS2, was selected as a possible surrogate to estimate AiV inactivation by high pressure processing (HPP). HAV, AiV and their selected bacteriophage surrogates were treated at a range of pressures and times in three different media. All four were treated in phosphate-buffered saline (PBS), artificial seawater (ASW) or oyster slurry (OS) at 250, 400 or 500 MPa for 1, 5 or 10 min at 20 °C. While T₄ had similar pressure resistance to HAV under conditions of high (500 MPa) and lower pressure (250 MPa), inactivation trends were very different following treatment at 400 MPa and when the viruses were suspended in OS. MS2 showed similar resistance as AiV but at ambient treatment temperatures only. The highest levels of inactivation of MS2 were achieved at 60 °C and 500 MPa. AiV was eliminated at 60 °C for 5 min at ambient pressure, but > 3 log survived exposure to 60 °C at 500 MPa. This degree of protection by pressure may be important in determining the mechanisms of pressure and heat resistances in other viruses.Industrial relevanceGreater knowledge of the responses of viruses and their surrogates to high pressure will aid in the validation of new high pressure-processed food that may be at risk to contamination from HAV or other enteric viruses.     

Inactivation of hepatitis A virus,poliovirus and a norovirus surrogate by high pressure processing

Hepatitis A virus (HAV), feline calicivirus (FCV, a surrogate for non-culturable norovirus), and poliovirus (PV), suspended in buffered cell culture media, were treated with pressures ranging from 200 to 600 MPa at ambient temperature for between 30 and 600 s. HAV was inactivated by > 1-log₁₀ tissue culture infectious dose 50% mL^− 1 (TCID₅₀ mL^− 1) and > 2-log₁₀ TCID₅₀ mL^− 1 after 600 s treatment with 300 and 400 MPa, respectively, and was undetectable (> 3.5-log₁₀ TCID₅₀ mL^− 1 reduction) within 300 s treatment with 500 MPa. FCV was inactivated by 3.6-log₁₀ TCID₅₀ mL^− 1 after 120 s treatment with 300 MPa, and was undetectable after 180 s treatment with 300 MPa. PV was the most resistant with little or no substantial reduction in titre after 300 s treatment with 600 MPa. The studies were designed to determine the efficacy of using high pressure to inactivate enteric viruses and generate inactivation data to assist in determining appropriate process criteria for safe shellfish production.Industrial relevanceThe high pressure treatment of raw oysters has proved commercially successful, due in part to a marked increase in the product’s shelf life, yet little alteration of its organoleptic properties. Illnesses from human enteric viruses such as hepatitis A virus and norovirus have traditionally been associated with shellfish consumption, and for this reason, studies have examined the stability of enteric viruses under high pressure. However, kinetic data on enteric virus stability under pressure is needed by processors to better understand the response of viruses throughout the entire treatment time. The kinetic data obtained in this study may be useful for processors wishing to alter high pressure processing conditions to ensure a high quality product in terms of organoleptic and microbiological properties.     

Effect of high hydrostatic pressure processing on freely suspended and bivalve-associated T7 bacteriophage

The effectiveness of hydrostatic pressure processing (HPP) for inactivating viruses has been evaluated in only a limited number of studies, and most of the work has been performed with viruses freely suspended in distilled water. In this work, HPP inactivation of freely suspended and shellfish-associated bacteriophage T7 was studied. T7 was selected in hopes that it could serve as a model for animal virus behavior. Clams (Mercenaria mercenaria) and oysters (Crassostrea virginica) were homogeneously blended separately and inoculated with bacteriophage T7. The inoculated bivalve meat and the freely suspended virus samples were subjected to HPP under the following conditions: 2, 4, and 6 min at 241.3, 275.8, and 344.7 MPa pressure and temperatures of 29.4 to 35, 37.8 to 43.3, and 46.1 to 51.7 degrees C. Reductions of 7.8 log PFU (100% inactivation) were achieved for freely suspended T7 at 344.7 MPa for 2 min at 37.8 to 43.3 degrees C. At 46.1 to 51.7 degrees C, T7 associated with either clams or oysters was inactivated at nearly 100% (>4 log PFU) at all pressure levels and durations tested. These results indicate that T7 is readily inactivated by HPP under the proper conditions, may be made more susceptible to HPP by mixing with shellfish meat, and may serve as a viable model for the response of several animal viruses to HPP.     

Viral Inactivation in Foods: A Review of Traditional and Novel Food‐Processing Technologies

ABSTRACT: Over one‐half of foodborne illnesses are believed to be viral in origin. The ability of viruses to persist in the environment and foods, coupled with low infectious doses, allows even a small amount of contamination to cause serious problems. An increased incidence of foodborne illnesses and consumer demand for fresh, convenient, and safe foods have prompted research into alternative food‐processing technologies. This review focuses on viral inactivation by both traditional processing technologies such as use of antimicrobial agents and the application of heat, and also novel processing technologies including high‐pressure processing, ultraviolet‐ and gamma‐irradiation, and pulsed electric fields. These industrially applicable control measures will be discussed in relation to the 2 most common causes of foodborne viral illnesses, hepatitis A virus and human noroviruses. Other enteric viruses, including adenoviruses, rotaviruses, aichi virus, and laboratory and industrial viral surrogates such as feline caliciviruses, murine noroviruses, bacteriophage MS2 and ΦX174, and virus‐like particles are also discussed. The basis of each technology, inactivation efficacy, proposed mechanisms of viral inactivation, factors affecting viral inactivation, and applicability to the food industry with a focus on ready‐to‐eat foods, produce, and shellfish, are all featured in this review.     

Comparative analysis of viral pathogens and potential indicators in shellfish

Shellfish can be responsible of outbreaks of infectious diseases and current health measures do not guarantee the absence of viral pathogens in this product. Here we examine the presence of pathogenic viruses and potential indicators in shellfish in a comparative analysis.Sixty shellfish samples collected in three areas with different levels of faecal contamination were analysed for Escherichia coli, total coliforms, Clostridium perfringens, somatic coliphages, F-specific phages of RNA (F-RNA), bacteriophages infecting Bacteroides fragilis RYC2056, human adenovirus, enterovirus and hepatitis A virus (HAV). Viruses were eluted in a glycine buffer at pH 10.The overall percentage of viral pathogens detected was 47% for human adenoviruses, 19% for enteroviruses and 24% for HAV. Since all the samples positive for enterovirus and HAV were also positives for human adenovirus, the latter may be considered useful as a molecular index of viral contamination in shellfish. No significant differences in the bioaccumulation of bacteria and bacteriophages for oysters or mussels were observed. It was found that the probability of detection of any of the pathogenic virus decreases as the temperature of shellfish growing waters increases. However, the probability of detecting viruses increases when phages of B. fragilis are found. Although more data are needed in order to fulfil the need of viral indicators for controlling the presence of human viruses in shellfish, the obtained results indicate that phages infecting B. fragilis RYC2056 could be a suitable group of bacteriophages to be used as an indicator of the presence of viruses in shellfish.     

Effects of high-pressure treatment on the microflora of oysters (Crassostrea gigas) during chilled storage

The microbiological quality of oysters high-pressure (HP)-treated in-shell at 260 MPa for 3 min, or 500 or 800 MPa for 5 min and then stored at 2 °C, were investigated. Microbial counts after HP treatment showed that the bacterial load was reduced after treatment at all pressures to levels below the detection limit. Randomly-selected isolates from the total aerobic viable counts of untreated and HP-treated oysters after 14 days of storage were identified by the API identification system. Bacteria isolated from oysters HP-treated at 260 MPa were Shewanella putrifaciens and Pseudomonas fluorescens. For oysters HP-treated at 500 or 800 MPa, the main bacteria isolated were Pseudomonas spp. Vibrio spp. comprised 44% of the microflora in untreated oysters after storage for 14 days at 2 °C, but no Vibrio were detected in HP-treated oysters. This study confirmed that HP processing can inactivate microorganisms and delay microbial growth in chilled stored oysters.

Industrial relevance

High-pressure (HP) treatment is being increasingly employed for commercial processing of oysters but no studies of the microflora of HP-treated in-shell oysters have been reported. HP treatment significantly changed the microflora of oysters and apparently has good potential for inactivation of Vibrio spp as HP treatment, in combination with adequate chilled storage, can improve the microbiological shelf-life and safety of oysters.     

桑沟湾养殖牡蛎中贝类毒素监测及预警

利用高效液相色谱-串联质谱(high performance liquid chromatography-tandem mass spectrometry,HPLCMS/MS)方法监测养殖牡蛎中5种腹泻性贝类毒素与6种麻痹性贝类毒素含量变化及分布特征,分别利用HP20大孔型吸附树脂与SP700吸附树脂作为富集树脂,富集养殖海域海水中5种腹泻性贝类毒素与6种麻痹性贝类毒素,利用HPLC-MS/MS检测方法分析其中毒素含量,同步监测了养殖海域内牡蛎与海水中毒素含量,探究了两者之间的关系,建立了牡蛎内贝类毒素含量随海水内贝类毒素含量之间的变化规律。结果显示:在该海域内一共监测到OA、DTX-1、GYM、PTX-2 4种腹泻性贝类毒素与STX、dc STX两种麻痹性贝类毒素;在整个监控期内,海水中所监测贝类毒素随时间变化呈现先增长,达到峰值后逐渐降低趋势。牡蛎中毒素含量与海水中毒素含量呈正相关关系,即牡蛎内毒素的增长随海水内毒素的增长而增长,但牡蛎内毒素含量的峰值出现时间在海水中毒素含量出现峰值之后,延后时间为14 d。根据固相吸附毒素跟踪技术原理,可以提前14 d预警牡蛎内毒素含量。     

贝类开壳技术与装备研究现状及发展趋势

开壳是贝类加工中必不可少的一项重要工序,其效果直接影响着后续加工产品的品质。为了解目前国内外 贝类开壳技术及装备的现状和存在的问题,本文对人工开壳、热力开壳、超高压开壳和微波开壳等贝类开壳技术与 装备的研究进展和应用现状进行分析,对不同开壳方法的优缺点进行对比,对存在的主要问题进行归纳总结,并提 出了解决方案,同时对贝类开壳技术与装备的发展趋势进行了展望,以期丰富贝类开壳加工理论基础,为贝类开壳 技术创新和设备研发提供一定的参考和借鉴。     

超高压处理在毛蚶脱壳和减菌化中的作用研究

目的明确超高压处理对毛蚶脱壳效果、感官品质以及细菌总数的影响,建立超高压技术在毛蚶加工中的工艺参数。方法以鲜活毛蚶为对照,在250~500 MPa的压力范围内设置6个超高压处理组,根据闭壳肌是否脱离以及壳的完整情况记录毛蚶脱壳效果,通过感官评定、电子鼻气味分析,以及p H、TVB-N、细菌总数等指标的测定评价不同压力处理对毛蚶品质和微生物的影响。结果 300 MPa及以下的处理压力对毛蚶闭壳肌作用小,脱壳效果较差,而450 MPa及以上的压力处理会造成毛蚶壳的破损。毛蚶经超高压处理后,感官评分略有下降,其中350 MPa及以下压力的处理组与对照组之间无显著性差异(P0.05),而400 MPa及以上压力处理组由于气味的变化,对应的感官评分显著降低(P0.05)。超高压处理对毛蚶TVB-N无显著影响(P0.05),300 MPa及以上压力处理组的p H显著升高(P0.05)。毛蚶细菌总数随处理压力的增大显著下降。结论综合考虑脱壳效果、感官品质以及减菌化效果,350~400 MPa的区间范围比较适宜作为毛蚶的超高压处理工艺。     

Conditions for a 5-log reduction of Vibrio vulnificus in oysters through high hydrostatic pressure treatment

Vibrio vulnificus is frequently associated with oysters, and since oysters are typically consumed raw on a half shell, they can pose a threat to public health due to ingestion of this pathogenic marine microorganism. Oysters should be processed to reduce the number of this pathogen. High pressure processing is gaining more and more acceptance among oyster processors due to its ability to shuck oysters while keeping the fresh-like characteristics of oysters. Nine strains of V. vulnificus were tested for their sensitivities to high pressure. The most pressure-resistant strain of V. vulnificus, MLT 403, was selected and used in the subsequent experiments to represent a worst case scenario for evaluation of the processing parameters for inactivation of V. vulnificus in oysters. To evaluate the effect of temperature on pressure inactivation of V. vulnificus, oyster meats were inoculated with V. vulnificus MLT 403 and incubated at room temperature for 24 h. Oyster meats were then blended and treated at 150 MPa for 4 min, and 200 MPa for 1 min. Pressure treatments were carried out at -2, 1, 5, 10, 20, 30, 40, and 45 degrees C. Cold temperatures (<20 degrees C) and slightly elevated temperatures (>30 degrees C) substantially increased pressure inactivation of V. vulnificus. For example, a 4-min treatment of 150 MPa at -2 and 40 degrees C reduced the counts of V. vulnificus by 4.7 and 2.8 log, respectively, while at 20 degrees C the same treatment only reduced counts by 0.5 log. Temperatures of -2 and 1 degrees C were used to determine the effect of pressure level, temperature, and treatment time on the inactivation of V. vulnificus infected to live oysters through feeding. To achieve a >5-log reduction in the counts of V. vulnificus in a relatively short treatment time (or=250 MPa at -2 or 1 degrees C.     

Conditions for high pressure inactivation of Vibrio parahaemolyticus in oysters

The objective of this study was to identify the high pressure processing conditions (pressure level, time, and temperature) needed to achieve a 5-log reduction of Vibrio parahaemolyticus in live oysters (Crassostrea virginica). Ten strains of V. parahaemolyticus were separately tested for their resistances to high pressure. The two most pressure-resistant strains were then used as a cocktail to represent baro-tolerant environmental strains. To evaluate the effect of temperature on pressure inactivation of V. parahaemolyticus, Vibrio-free oyster meats were inoculated with the cocktail of V. parahaemolyticus and incubated at room temperature (approximately 21 degrees C) for 24 h. Oyster meats were then blended and treated at 250 MPa for 5 min, 300 MPa for 2 min, and 350 MPa for 1 min. Pressure treatments were carried out at -2, 1, 5, 10, 20, 30, 40, and 45 degrees C. Temperatures >/=30 degrees C enhanced pressure inactivation of V. parahaemolyticus. To achieve a 5-log reduction of V. parahaemolyticus in live oysters, pressure treatment needed to be >/=350 MPa for 2 min at temperatures between 1 and 35 degrees C and >/=300 MPa for 2 min at 40 degrees C.     

Inactivation of internalized and surface contaminated enteric viruses in green onions

With increasing outbreaks of gastroenteritis associated with produce, it is important to assess interventions to reduce the risk of illness. UV, ozone and high pressure are non-thermal processing technologies that have potential to inactivate human pathogens on produce and allow the retention of fresh-like organoleptic properties. The objective of this study was to determine if UV, ozone, and high pressure are effective technologies compared to traditional chlorine spray on green onions to reduce enteric viral pathogens and to determine the effect of location of the virus (surface or internalized) on the efficacy of these processes. Mature green onion plants were inoculated with murine norovirus (MNV), hepatitis A virus (HAV) and human adenovirus type 41 (Ad41) either on the surface through spot inoculation or through inoculating contaminated hydroponic solution allowing for uptake of the virus into the internal tissues. Inoculated green onions were treated with UV (240 mJ s/cm²), ozone (6.25 ppm for 10 min), pressure (500 MPa, for 5 min at 20 °C), or sprayed with calcium hypochlorite (150 ppm, 4 °C). Viral inactivation was determined by comparing treated and untreated inoculated plants using cell culture infectivity assays. Processing treatments were observed to greatly affect viral inactivation. Viral inactivation for all three viruses was greatest after pressure treatment and the lowest inactivation was observed after chlorine and UV treatment. Both surface inoculated viruses and viruses internalized in green onions were inactivated to some extent by these post-harvest processing treatments. These results suggest that ozone and high pressure processes aimed to reduce the level of microbial contamination of produce have the ability to inactivate viruses if they become localized in the interior portions of produce.     

A combined treatment of UV-assisted TiO2 photocatalysis and high hydrostatic pressure to inactivate internalized murine norovirus

Human norovirus (HuNoV) is a major cause of foodborne illness associated with shellfish consumption. A solidified agar matrix (SAM) was experimentally prepared using agar solution for inactivation of murine norovirus (MNV-1) as a surrogate for HuNoV in a simulation model approach. MNV-1 was injected inside the SAM for virus internalization, and the effects of single and combined UV-assisted TiO₂ photocatalysis (UVTP) and high hydrostatic pressure (HHP) treatments were determined. The internalized MNV-1 were reduced by 2.9-log₁₀ and 3.5-log₁₀, respectively, after single treatments of UVTP (4.5 mW/cm², 10 min) and HHP (500 MPa, 5 min, ambient temperature). However, the internalized MNV-1 was reduced by 5.5-log₁₀ (below the detection limit) when UVTP was followed by HHP, indicating a synergistic inactivation effect. Analysis of viral morphology, proteins, and genomic RNA allowed elucidation of mechanisms involved in the synergistic antiviral activity of combined treatments, which appeared to disrupt the MNV-1 structure and damage both the capsid protein and genomic RNA.Industrial relevanceHHP treatment of raw oysters has proved commercially successful, but there is a less evidence available regarding the potential of HHP for inactivation of localized viruses present inside foods. A sequential combination of UV-assisted TiO₂ photocatalysis (UVTP) and high hydrostatic pressure (HHP) achieved significantly higher inactivation of localized virus compared to individual treatments due to a synergistic mechanism. An experimentally prepared model food system was found useful to simulate foods with morphological variations and unpredictable viral internalization patterns. This UVTP-HHP combined treatment for inactivation of localized MNV-1 can be useful for disinfection of raw oysters and other similar foods.