Next Article in Journal
Changes of Bioactive Components and Antioxidant Capacity of Pear Ferment in Simulated Gastrointestinal Digestion In Vitro
Previous Article in Journal
Breeding Bread-Making Wheat Varieties for Organic Farming Systems: The Need to Target Productivity, Robustness, Resource Use Efficiency and Grain Quality Traits
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Ultrasound Technology as Inactivation Method for Foodborne Pathogens: A Review

Section of Food Inspection, Department of Veterinary Medicine, School of Specialization in Inspection of Foods of Animal Origin, “G. Tiecco” University of Teramo, 64100 Teramo, Italy
*
Author to whom correspondence should be addressed.
Foods 2023, 12(6), 1212; https://doi.org/10.3390/foods12061212
Submission received: 16 February 2023 / Revised: 2 March 2023 / Accepted: 9 March 2023 / Published: 13 March 2023
(This article belongs to the Section Food Microbiology)

Abstract

:
An efficient microbiological decontamination protocol is required to guarantee safe food products for the final consumer to avoid foodborne illnesses. Ultrasound and non-thermal technology combinations represent innovative methods adopted by the food industry for food preservation and safety. Ultrasound power is commonly used with a frequency between 20 and 100 kHz to obtain an “exploit cavitation effect”. Microbial inactivation via ultrasound derives from cell wall damage, the oxidation of intracellular amino acids and DNA changing material. As an inactivation method, it is evaluated alone and combined with other non-thermal technologies. The evidence shows that ultrasound is an important green technology that has a good decontamination effect and can improve the shelf-life of products. This review aims to describe the applicability of ultrasound in the food industry focusing on microbiological decontamination, reducing bacterial alterations caused by food spoilage strains and relative foodborne intoxication/infection.

1. Introduction

The European Food Safety Authority (EFSA) reported 5175 foodborne outbreaks from 2015 to 2019 [1]; the Centers for Disease Control and Prevention (CDC) publishes yearly reports that highlight interesting data: 48 million people become ill due to foodborne diseases (128,000 are hospitalized, with 3000 deaths [2]). Due to the increase in outbreak numbers, it is necessary to develop efficient food chain surveillance and adequate microbiological decontamination protocols to guarantee safe food products for consumers. To achieve safety and genuineness, food processing technologies represent essential tools for microbiological control and products’ shelf-life enhancement [3,4]. Due to consumers’ growing requests for “minimally processed products”, the food industry applies new technologies to produce safe food matrices that maintain “fresh-like” characteristics [5].
Indeed, in conventional technologies, such as thermal treatments, this concept is not applicable: pasteurization and sterilization, commonly used in food industries, cause color alterations, characteristic flavors and a decrease in nutritional value [6,7,8].
Therefore, the food industry and scientific researchers have evaluated alternative non-thermal technologies (NTTs) that maintain the aroma, nutrient value, texture and color while decreasing bacteria that cause spoilage. Tiwari and coworkers defined NTTs as procedures, performed at efficient sublethal or ambient temperatures, that lead to minimal or no impacts on nutritional and quality food parameters [9] (see Figure 1).
The aim of this review article is to perform an analysis of recent discoveries concerning ultrasound technology application in the food matrix’s shelf-life prolongation (bacterial load decrease) and bacterial foodborne pathogen inactivation, and to demonstrate its applicability as a useful green food technology among physical devices.

2. Ultrasound: Mechanisms of Action Applied in Food Industry

Ultrasound is a form of vibrational energy produced by a transducer converting electrical energy into acoustic energy. It is a wave that exceeds the human hearing threshold [10]. Basing on the frequency, ultrasound can be classified as follows: power ultrasound (20–100 kHz), high-frequency ultrasound (100 kHz–1 MHz), and diagnostic ultrasound (1–500 MHz) [11]. At medium frequencies (200–500 kHz), chemical effects are prevalent, and collapse is less violent. On the other hand, at high frequencies (>1 MHz), chemical and physical effects decrease and cavitation is minimal; in this case, acoustic flow is predominant [11,12]. In the food industry, power ultrasound is commonly used with a frequency between 20 and 100 kHz to obtain an “exploit cavitation effect” [13]. The molecules are compressed and rarefactive when ultrasound is spread through any medium. Alternative pressure changes cause bubble formation in a liquid medium. There are physical and chemical effects correlated with ultrasound: agitation, vibration, pressure, shock waves, shear forces, microjets, compression and rarefaction, acoustic streaming, cavitation, and the formation of free radicals [14].
This phenomenon of the creation of small vapor bubbles (cavities), expansion, and implosive collapse in ultrasonically irradiated liquids is named “acoustic cavitation” [13,15,16]. There are two types of bubbles: transient and stable [17]. Under ultrasound action, bubbles oscillate, grow, and collapse asymmetrically, forming microjets. Outburst produces pressure shocks up to several 1000 atm, strong shock waves with 400 km/h microjets, and the production of hot spots with a 5000 K temperature; the mechanical effects predominate over the chemical ones [18,19]. In the reaction environment, three different phases have been identified: inside the bubble cavity gas environment, the liquid–bubble interface, and the liquid. In the first phase, there are pyrolysis reactions. In the second and third ones, radicals can occur. In the aqueous environment, the most frequently encountered phenomenon is the formation of the hydroxide radical OH-. It is highly reactive and attacks organic substrates or OH- and recombines with another OH- radical, forming H2O2. In the interphase area, the temperature is very high; therefore, the occurring reactions are thermal degradation and solute reactions with OH- radicals. Small bubbles are generated by the diffusion of these radicals due to the cavitation bubble’s disruption. In the interphase zone or in liquid nonvolatile solutes, reactive and volatile solids penetrate the bubble and degrade during collapse [19]. Physical and chemical effects are the basis for ultrasound’s application in the food industry [12].
New technologies, such as as vacuum cooling technology, high-pressure processing, ultrasound, and pulsed electric field technology, could guarantee safe and high-quality products. The aim of these new technologies is to reduce processing times, save energy and solvents, and improve the products’ shelf-life. From a “green” methodological point of view, ultrasound-assisted extraction has huge potential as an emergent and innovative technology. It has a low environmental impact, due to decreasing CO2 emissions, reducing time, and not presenting toxic effects towards human health [20]. There are two types of ultrasound systems applied in the food industry: contact and non-contact [21]. The first one employs liquids as transmission media and generates waves that have chemical and physical effects in food matrices. This technology is employed for different activities: the extraction of bioactive substances [22], the enhancement of drying rates [23] and freezing rates [24], the degassing of liquids [25], fat separation [26], power hydration [27], the intensification of heat and mass transfer [28], emulsification [29], and liquid food pasteurization [30,31]. Nevertheless, when using this technology, erosion could produce effects on the radiating surfaces and cause the consequent contamination of sonicated food [32]. However, new inert materials such as quartz, Pyrex, ceramics, and polyether could limit the use of metal horns, which are instruments used to evaluate ultrasonic irradiation in different materials (see Table 1).
Wang and coworkers [39] underlined that US has a positive effect in decreasing frying times, in the improvement of cooking yields, and improving the sensory evaluation of meat. The major consequences of ultrasound’s irradiation within a liquid are cavitation and agitation. These two factors are useful in improving heat transfer and freezing rates and accelerating freezing processes [54,55]. In the last mentioned process, there are primary and secondary nucleations: the first allows crystal formation in a solution where crystals are not detected. Primary nucleation can take place in two categories: homogenous and heterogeneous. Homogeneous nucleation occurs when the nuclei are formed spontaneously from the random density fluctuation. On the other hand, heterogeneous nucleation occurs due to the presence of solid impurities that form stable surfaces for nuclei formation, and secondary nucleation takes place where pre-existing crystals are present [56]. Ultrasonic application improves drying in all food matrices [56,57].
There are many advantages: water is removed easily, improving water diffusion from the interior to the product surface; intracellular and extracellular cavitation provides new microchannels; US creates air turbulence to remove moisture; it accelerates the process without a temperature increase [57]. This technology can be employed as a pre-treatment: in fact, many authors underlined that US pre-treatment improved the drying period [58]. As previously mentioned, waves involve a rate mass transfer by physically breaking down tissues and the formation of microchannels [20]. Ozuna and coworkers [59] evaluated the improvement in solute distribution during marination, and changes in water retention capability. McDonnel et al. [60] also underlined the possibility of conserving food sensory properties through these methods.
Iguglia et al. [61] investigated how different US frequencies can influence chicken marination times in terms of meat quality, texture, and lipid oxidation.
The applicability of US in seafood products has been evaluated: Pedròs- Garrido et al. [62] investigated US usage (30 kHz for 5 to 45 min) in different fish (salmon, mackerel, cod, hake). They noticed a major reduction in microbiological spoilage in oily fish, due to having higher fat content, which impacted bacterial decontamination. After 45 min of US treatment, there was a reduction in thiobarbituric acid reactive substances; on the other hand, lipids did not show changes.
US has been used for the tenderization of fish: Chang and Wang [53] found that US application for 60 to 90 min in cobia (Rachycentron canadum) improved the time required for tenderizing compared with the traditional aging process and optimized the firmness.
Non-contact technology, known also as the “air-couple technique”, uses a medium to ensure a gap between the transducer and the foodstuff. However, there are some drawbacks, such as the mismatch of the acoustic impedance magnitude between air and matrices [63].

3. Mechanism of Ultrasound Action against Microorganisms

Thermal treatments are the conventional method to inactivate microorganisms. However, they could lead to reduced sensory quality and nutrient substances [64]. In the last few years, the employment of ultrasound, as a method of decontamination, has been increasing in the food industry to decrease bacterial homeostatic mechanisms. Indeed, if ultrasound is combined with another technology that sensitizes the microorganism structure to the action of ultrasonic waves, microbial disruption, and, consequently, inactivation, will be probably enhanced. On the other hand, ultrasound application will induce the uptake of antimicrobials by disturbing or stressing the membrane, thus reducing the viability of microorganisms. However, its effectiveness depends on the time of exposure, type of treatment, food matrices, and type of microorganism. Indeed, Gram-positive and -negative bacteria have morphological differences: Gram-negative bacteria have a cell wall formed by a multi-layered structure: an outer membrane, lipopolysaccharide bilayer, and peptidoglycans [65]. On the other hand, Gram-positive bacteria have a single layer of peptidoglycan that is 20–80 nm thick [65,66].
Mechanical effects due to cavitation cause different types of physical damage to cell walls: Gram-negative bacteria are more sensible than positive ones. Indeed, microstreams’ action and shockwaves induce mass transfer processes and wall damage; hotspots cause local injury. Locally high temperatures can affect the integrity of layers [67,68]. As previously mentioned, the formation of -OH radicals intracellularly and H2O2 brings about the oxidation of intracellular amino acids (tyrosine, phenylalanine, tryptophan, histidine, methionine, and cysteine) and inhibition corresponding to specific functions [69]. Free radicals also cause chain reactions and consequently lipid oxidation. These reactions influence bacterial membrane fluidity, permeability, and deterioration; finally, when free radicals reach the intracellular space, they damage internal components and consequently the cell collapses [70]. In more detail, H2O2 and -OH attack the polysaccharide layer of the Gram-negative membrane wall, causing the scission of the glycoside backbone and the consequent fragmentation of the biopolymer and alteration of its function [71]. Nucleic acids can also be susceptible to oxidative stress by -OH; in fact, it can break the double helix or modify nitrogen bases [72] (see Figure 2).
Microbial inactivation can be influenced by different parameters, such as the nature of ultrasonic waves, food composition, temperature treatment, volume of food being processed, type of microorganism, and exposure time [73]. For these reasons, it is important to evaluate each individual microorganism with different parameters.

4. Pathogen Escherichia coli

In 2019, 7775 confirmed cases of Shiga toxin-producing E. coli (STEC) infections in humans were reported at the EU level by 27 EU countries [1]. The goal of ultrasound treatment against E. coli is wall damage, indicated as a morphological change during the treatment. Liu and coworkers studied the alterations of membrane permeability using an ultrasonic field [74]. They suggested that the outer membrane was the first target upon ultrasound treatment, and the inner membrane could be destabilized with an increase in time. Che et al. [73] evaluated the responses of bacterial cell membranes to ultrasound exposure with different parameters: 64, 191, 372, and 573 W/cm2, a frequency of 20 kHz, a pulsed mode of 2 sec: 2 sec. The outer membrane of E. coli presents robust and selective permeability [75]. Membrane fluidity, carrier transport, and membrane-bound enzymes are closely correlated with the integrity of the membrane [76]. In these bacteria, it is important to evaluate the absorbance of o-nitrophenol (ONP): ONP is hydrolyzed by β-galactosidase, which is an endoenzyme in E. coli, and progressive outward release from the cytoplasm occurs when the bacterial inner membrane is destroyed [77]. He et al. [78] evaluated morphological modifications through the usage of electron microscopy of E. coli O157:H7 ATCC 35150 after ultrasound treatment with different times and different intensities. They noticed that morphological modification increases with the time of exposure. As illustrated in Table 2, the efficiency of ultrasound treatment in E. coli can be influenced by the treatment time, treatment power, and type of treatment (ultrasound alone or combined). It is very important to evaluate the food matrix. Indeed, every matrix could have a different response: liquid food was found to be more efficient than solid for inactivation treatment in E. coli [79,80].

5. Salmonella spp.

Salmonella spp. is the second most prevalent foodborne pathogen worldwide, as reported by the EFSA [1]. The applicability of ultrasound decontamination for Salmonella spp. has been an object of research since 1992, when Wrigley and Llorca evaluated the killing effect against Salmonella serovar Typhimurium ATCC 14028 by applying 35 and 40 kHz for 15 and 30 min in skim milk and liquid whole eggs [87]. They noticed also that liquid whole eggs protected Salmonella serovar Typhimurium from ultrasonic cavitation. Indeed, the food composition can influence ultrasound’s effects. Techathuvanan and D’Souza evaluated, through scanning electronic microscopy (SEM), the morphological differences between Salmonella spp. untreated and Salmonella spp. treated with high-intensity ultrasound after 5 and 30 min. Their work showed that there is a correlation between the time of exposure and the bacterial reduction after 1 min treatment for a pure culture [88].
The treatment efficiency of ultrasound alone or combined against Salmonella spp. could be variable. It could be influenced by the food matrix: the inactivation response of liquid food such as liquid whole eggs or rice beverages is more efficient than for solid foods as pork meat [85,89]. Extending the time of application leads to increased Salmonella spp. reduction [85,90] (Table 3).

6. Listeria spp.

The genus Listeria is naturally dispersed in soil, water, and manure [96]. The efficiency of ultrasound against Listeria spp. depends on the power, frequency, treatment time, temperature, and geometry reaction, and synergic effects with other technologies (essential oil, cold plasma, nanobubbles, etc.) [96]. Several studies show that the efficiency of the ultrasound inactivation of Listeria spp. is greater in liquid media, such as milk, broth, or juice [97,98,99,100,101]. Pan and coworkers [102] investigated the inactivation of L. monocytogenes by ultrasound and cold plasma; they studied the modification of the membrane fatty acid profile in correlation with different temperatures. They noticed a modification of the fluidity of the membrane and prevalence of fatty acids in relation to the different applications of treatments and temperatures and the presence of radical oxygen. Numerous studies evaluated the efficiency of ultrasound alone and combined with other technologies against Listeria spp. (see Table 4). It is important to observe that the same matrix, such as salmon treated by ultrasound and temperature, presented a different response in terms of microbial inactivation if it was raw or smoked. Ultrasound application showed greater effectiveness in ATCC (ATCC LM 19114, ATCC LM 15313, ATCC LM 19111, ATCC LM 7644, ATCC BAA 679, ATCC BAA 839, ATCC 13932, ATCC 19112) strains than wild ones (food origin) [103,104,105].

7. Staphylococcus spp.

Staphylococcus is normally present on animal and human skin and mucous membranes, and it could be ubiquitous in the environment. For this reason, it could pose an important risk for public health [108]. There is prolific scientific interest in ultrasound’s applicability against Staphilococcus spp., which was used as a study model for Gram-positive microorganisms to understand the modifications after treatment [109,110,111]. The effects of ultrasound technology, alone and combined, on Staphylococcus aureus are summarized in Table 5.
Mansyur et al. [111] analyzed the morphological differences in methicillin-resistant S. aureus (MRSA) applying low-power ultrasonic waves. They noticed that the power of the ultrasonic waves had a significant effect on the death percentage of MRSA (p = 0.0001), while the lethal power as found via regression was 8.432 watts. The death indicators of MRSA affected by ultrasonic waves were changes in shape (p = 0.005) and size (p = 0.70). Liao and coworkers [110] examined intracellular and extracellular changes in S. aureus (ATCC 25923): after ultrasound treatment, they evaluated the fluidity, integrity of the external membrane wall, intracellular and extracellular reactive oxygen species, and DNA damage. They explained that the major resistance of S. aureus against ultrasound could be explained by the thicker, more rigid, and robust properties of Gram-positive microbial cell envelopes [109,112]. The subpopulation of S. aureus lacking cell membrane integrity increased by 20.49% during 12 min of ultrasound treatment. Cell membrane potential is indispensable for normal energy transduction and nutrient uptake in microbial cells and is regarded as an important indicator of physiological activity [109]. The ultrasound treatment interferes with the lipid cell wall and consequently the bacterial growth process. The mechanical ultrasound power determines the separation of the multi-molecular complex and the stretching of the cell wall, limiting the elasticity; thus, the cell is torn, and bacteria die [111]. Few studies have been published on the ultrasound inactivation of S. aureus, an important foodborne pathogen associated with outbreaks worldwide. For this reason, this review article (Table 5) has underlined any substantial scientific criticisms about this important foodborne pathogen, which causes different infectious outbreaks in many geographical areas. This paper seeks to provide directions for further scientific investigations.

8. Campylobacter spp.

Campylobacteriosis is a zoonotic disease and humans could contract this illness via the consumption of raw poultry and water [116]. The ultrasound technology’s effects, alone and combined, on Campylobacter are summarized in Table 6.
Selwet [119] found C. coli in 21 out of 50 water samples. In his study, he evaluated sonication as an important tool for water decontamination. The research demonstrated that ultrasound application with a frequency of 80 kHz reduced the bacterial count from 6.86 log CFU/mL to 3.08 log CFU/mL, whereas a frequency of 37 kHz reduced the bacterial count from 6.75 log CFU/mL to 4.04 log CFU/mL. The study also underlined a temperature increase. Moazzami et al. [118] underlined that Campylobacter spp. reduction through ultrasound associated with steam is a good solution to avoid the risk of disease and preserve the quality of chicken. Manusavian and coworkers [122] valuated ultrasound’s effectiveness against Campylobacter spp. in 648 back, breast, and neck skin samples. The research noticed that there was a different reduction (p < 0.001) dependent on the sampling site (0.8, 1.1, and 0.7 log, respectively); it also evaluated samples after 8 days of refrigeration at 4 °C in control and steam-ultrasound-treated broilers to determine the contamination stability, and the results showed no changes in reductions during refrigeration, indicating that the reduced Campylobacter numbers remained stable in treated broilers.

9. Vibrio spp.

Vibrio species are major causes of fishery foodborne diseases worldwide, due to their presence in marine environments. Indeed, they are found in raw and ready-to-eat food products [123,124]. Thermal treatment is an effective method to reduce Vibrio spp. levels in seafood, but, as reported by Su et al. [125], the major disadvantage is the change in sensory characteristics. Considering the increasing consumer requests for fresh and nutritional food, and the consumption of shellfish such as oysters raw or cooked at a low level, non-thermal technology such as ultrasound could represent an important resource for bacterial inactivation [125]. In the literature consulted, all researchers used ultrasound alone or combined with slightly acidic electrolyzed water, temperature, and ozone (Table 7). As reported by Wang et al. [73], the major results are obtained through combined ultrasound and temperature (47 °C −204 W for 8 min), reducing the bacterial level by 4.01 log CFU/g.
Few studies have been published on the ultrasound inactivation of Vibrio spp., an important foodborne pathogen associated with outbreaks worldwide. For this reason, this review article (Table 7) has underlined any substantial scientific criticisms about this important foodborne pathogen, which causes different infectious outbreaks in many geographical areas. This paper aims to provide directions for further scientific investigations.

10. Pseudomonas spp.

Pseudomonas are found in water, soil, food, humans, plants, and surfaces, due to their versatility [129]. In food matrices, there is no health risk, but the presence of these pathogens causes an off-flavor due to producing volatile and amino acid metabolites and thermotolerant proteolytic enzymes that reduce the quality and shelf-life [130]. Because of the different characteristics of Pseudomonas spp., it is important to obtain an efficient technology for their inactivation. The application of ultrasound is not very efficient; in fact, it causes the insufficient reduction of bacteria as reported by Zhao et al. [131] (Table 8). On the other hand, its application combined with other technologies, such as temperature, is most efficient; in fact, the colony forming units decreased from 3 to 5 log CFU/gr ([132,133,134]) (Table 8). Greater exposure (expressed as time value) enhances the treatment efficiency, as reported by Kordowska-Wiater and Stasiak [82] (Table 8).
Ying and coworkers reported that combined treatment (ultrasound–temperature) against Pseudomonas fluorescens showed high efficacy for biofilm control: applying ultrasound (power > 80 W) and mild heat (up to 50 °C) caused the viable cell count to decrease. Indeed, ultrasound contributed to the release of biofilm bacteria in the environment and at the same time they exposed inner bacteria at the deep layer of the biofilm through shock waves, with acoustic streaming effects [135,136].

11. Conclusions

Ultrasound is an important technology to satisfy consumers’ requests and desire for “fresh-like”, safe, and healthy food. This technology preserves the nutritional, sensory, and compositional properties of food, and it is cheap and green. The environmental sustainability of this kind of physical food processing has attracted more attention among many industries. In more detail, many scientific studies, referring to these possibilities, highlighted a consistent reduction in carbon emissions in the atmosphere. This means a reduced impact on the so-called carbon footprint calculation.
Ultrasound is a noninvasive and cost-effective technique used to improve in terms of time other processes, such as cutting, cooking, freezing, drying, pickling/marinating, tenderization, and shelf-life. Ultrasound should represent a pivotal tool for foodborne pathogens’ (i.e., Listeria monocytogenes, Salmonella spp., Staphylococcus spp., Vibrio spp.) decontamination, with high potential due to its eco-friendly and non-thermal properties: the inactivation performance is variable with different microorganisms (bacteria, viruses, mycotoxins, and fungi) and food matrices. Nonetheless, research results suggest that parameters such as the frequency, intensity, treatment time, and treatment alone or combined with other technologies should be optimized for each food type.
Several studies showed that the applicability of “multiple hurdle technology” is more effective than ultrasound alone; indeed, the combined action of two or more technologies is more efficient than the use of a single one [135,136,137].
Hence, future research must be directed towards the different inactivation mechanisms, microbial inactivation kinesis, and synergetic effects with other technologies.

Author Contributions

Conceptualization, L.P. and C.L.; methodology, G.F.; validation, L.P. and A.V.; investigation, C.L.; resources, C.L.; data curation, A.P.; writing—original draft preparation, C.L.; writing—review and editing, L.P.; visualization, G.F.; supervision, A.V. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. European Food Safety Authority European. The European Union One Health 2019 Zoonoses Report. EFSA J. 2021, 19, 6406. [Google Scholar] [CrossRef]
  2. Centers for Disease Control and Prevention, Foodborne Illnesses and Germs. Last modified 18 March 2020. 2021. Available online: https://www.cdc.gov/foodsafety/foodborne-germs.html (accessed on 1 October 2022).
  3. Sango, D.M.; Abela, D.; McElhatton, A.; Valdramidis, V. Assisted ultrasound applications for the production of safe foods. J. Appl. Microbiol. 2014, 116, 1067–1083. [Google Scholar] [CrossRef] [PubMed]
  4. Bevilacqua, A.; Campaniello, D.; Speranza, B.; Altieri, C.; Sinigaglia, M.; Corbo, M.R. Two Nonthermal Technologies for Food Safety and Quality—Ultrasound and High Pressure Homogenization: Effects on Microorganisms, Advances, and Possibilities: A Review. J. Food Prot. 2019, 82, 2049–2064. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Onyeaka, H.; Miri, T.; Hart, A.; Anumudu, C.; Nwabor, O.F. Application of Ultrasound Technology in Food Processing with emphasis on bacterial spores. Food Rev. Int. 2021, 1–26. [Google Scholar] [CrossRef]
  6. Lee, H.S.; Coates, G.A. Effect of thermal pasteurization on Valencia orange juice color and pigments. LWT Food Sci. Technol. 2003, 36, 153–156. [Google Scholar] [CrossRef]
  7. Rattanathanalerk, M.; Chiewchan, N.; Srichumpoung, W. Effect of thermal processing on the quality loss of pineapple juice. J. Food Eng. 2005, 66, 259–265. [Google Scholar] [CrossRef]
  8. Gandy, A.; Schilling, M.; Coggins, P.; White, C.; Yoon, Y.; Kamadia, V. The Effect of Pasteurization Temperature on Consumer Acceptability, Sensory Characteristics, Volatile Compound Composition, and Shelf-Life of Fluid Milk. J. Dairy Sci. 2008, 91, 1769–1777. [Google Scholar] [CrossRef] [Green Version]
  9. Tiwari, B.K.; O’Donnell, C.P.; Cullen, P.J. Effect of nonthermal processing technologies on the anthocyanin content of fruit juices. Trends Food Sci. Technol. 2009, 20, 137–145. [Google Scholar] [CrossRef]
  10. Shung, K.K.; Cannata, J.M.; Zhou, Q.F. Piezoelectric materials for high frequency medical imaging applications: A review. J. Electroceramics 2007, 19, 141–147. [Google Scholar] [CrossRef]
  11. Laborde, J.-L.; Bouyer, C.; Caltagirone, J.-P.; Gérard, A. Acoustic bubble cavitation at low frequencies. Ultrasonics 1998, 36, 589–594. [Google Scholar] [CrossRef]
  12. Feng, H.; Lee, H. Effect of Power Ultrasound on Food Quality. In Ultrasound Tech for Food and Bioprocessing; Springer: New York, NY, USA, 2011; pp. 154–196. [Google Scholar]
  13. Chen, F.; Zhang, M.; Yang, C.-H. Application of ultrasound technology in processing of ready-to-eat fresh food: A review. Ultrason. Sonochem. 2020, 63, 104953. [Google Scholar] [CrossRef]
  14. Ojha, K.S.; Tiwari, B.K.; O’Donnell, C.P. Effect of Ultrasound Technology on Food and Nutritional Quality. Adv. Food Nutr. Res. 2018, 84, 207–240. [Google Scholar] [CrossRef] [PubMed]
  15. Franc, P.; Michel, J.M. Fundamentals of Cavitation; Springer: Dordrecht, The Netherlands, 2004. [Google Scholar] [CrossRef]
  16. Zupanc, M.; Pandur, Ž.; Perdih, T.S.; Stopar, D.; Petkovšek, M.; Dular, M. Effects of cavitation on different microorganisms: The current understanding of the mechanisms taking place behind the phenomenon. A review and proposals for further research. Ultrason. Sonochem. 2019, 57, 147–165. [Google Scholar] [CrossRef] [PubMed]
  17. Feng, H.; Yang, W.; Hielscher, T. Power Ultrasound. Food Sci. Technol. Int. 2008, 14, 433–436. [Google Scholar] [CrossRef]
  18. Pokhrel, P.R.; Bermúdez-Aguirre, D.; Martínez-Flores, H.E.; Garnica-Romo, M.G.; Sablani, S.; Tang, J.; Barbosa-Cánovas, G.V. Combined Effect of Ultrasound and Mild Temperatures on the Inactivation of E. coli in Fresh Carrot Juice and Changes on its Physicochemical Characteristics. J. Food Sci. 2017, 82, 2343–2350. [Google Scholar] [CrossRef]
  19. Chahine, G.L.; Hsiao, C.-T. Modelling cavitation erosion using fluid–material interaction simulations. Interface Focus 2015, 5, 2015–2016. [Google Scholar] [CrossRef]
  20. Chemat, F.; Khan, M.K. Applications of ultrasound in food technology: Processing, preservation and extraction. Ultrason. Sonochem. 2011, 18, 813–835. [Google Scholar] [CrossRef] [PubMed]
  21. Charoux, C.M.G.; Ojha, K.S.; O’Donnell, C.P.; Cardoni, A.; Tiwari, B.K. Applications of airborne ultrasonic technology in the food industry. J. Food Eng. 2017, 208, 28–36. [Google Scholar]
  22. Kumari, B.; Tiwari, B.K.; Hossain, M.B.; Brunton, N.P.; Rai, D.K. Recent advances on application of ultrasound and pulsed electric field technologies in the extraction of bioactives from agro-industrial by-products. Food Bioprocess Tech. 2018, 11, 223–241. [Google Scholar] [CrossRef]
  23. Magalhães, M.L.; Cartaxo, S.J.; Gallão, M.I.; García-Pérez, J.V.; Cárcel, J.A.; Rodrigues, S.; Fernandes, F.A. Drying intensification combining ultrasound pre-treatment and ultrasound-assisted air drying. J. Food Eng. 2017, 215, 72–77. [Google Scholar] [CrossRef]
  24. Islam, M.N.; Zhang, M.; Adhikari, B. Ultrasound-assisted freezing of fruits and vegetables: Design, development, and appli-cations. In Global Food Security and Wellness; Barbosa-Canovas, G., Pastore, G., Candoðan, K., Meza, I.M., Da Silva Lannes, C., Lannes, S., Buckle, K., Yada, R., Rosenthal, A., Eds.; Springer: Berlin/Heidelberg, Germany, 2017; pp. 457–487. [Google Scholar]
  25. Liu, X.; Zhang, C.; Zhang, Z.; Xue, J.; Le, J. The role of ultrasound in hydrogen removal and microstructure refinement by ul-trasonic argon degassing process. Ultrason. Sonochem. 2017, 38, 455–462. [Google Scholar] [CrossRef]
  26. Torkamani, A.E.; Juliano, P.; Fagan, P.; Jimenez-Flores, R.; Ajlouni, S.; Singh, T.K. Effect of ultrasound-enhanced fat separation on whey powder phospholipid composition and stability. J. Dairy Sci. 2016, 99, 4169–4177. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Bhandari, B.; Zisu, B. Effect of ultrasound treatment on the evolution of solubility of milk protein concentrate powder. In Handbook of Ultrasonics and Sonochemistry; Springer: Berlin/Heidelberg, Germany, 2016; pp. 1–19. [Google Scholar]
  28. Gondrexon, N.; Cheze, L.; Jin, Y.; Legay, M.; Tissot, Q.; Hengl, N.; Baup, S.; Boldo, P.; Pignon, F.; Talansier, E. Intensification of heat and mass transfer by ultrasound: Application to heat exchangers and membrane separation processes. Ultrason. Sonochem. 2015, 25, 40–50. [Google Scholar] [CrossRef] [PubMed]
  29. Reboredo-Rodríguez, P.; Rey-Salgueiro, L.; Regueiro, J.; Gonzalez-Barreiro, C.; Cancho- Grande, B.; Simal-Gándara, J. Ultrasound-assisted emulsification– microextraction for the determination of phenolic compounds in olive oils. Food Chem. 2014, 150, 128–136. [Google Scholar] [CrossRef]
  30. Czank, C.; Simmer, K.; Hartmann, P.E. Simultaneous pasteurization and homogenization of human milk by combining heat and ultrasound: Effect on milk quality. J. Dairy Res. 2010, 77, 183–189. [Google Scholar] [CrossRef]
  31. Jambrak, A.R.; Šimunek, M.; Petrovic, M.; Bedic, H.; Herceg, Z.; Juretic, Z. Aromatic profile and sensory characterization of ultrasound treated cranberry juice and nectar. Ultrason. Sonochem. 2017, 38, 783–793. [Google Scholar] [CrossRef]
  32. Kentish, S.; Feng, H. Application of power ultrasound in food processing. Annu. Rev. Food Sci. Technol. 2014, 5, 263–284. [Google Scholar] [CrossRef] [PubMed]
  33. Schneider, Y.; Zahn, S.; Rohm, H. Ultrasonic cutting of foods. In Ultrasound Technologies for Food and Bioprocessing; Feng, H., Barbosa-Canovas, G.V., Weiss, J., Eds.; Springer: New York, NY, USA, 2011. [Google Scholar]
  34. Arnold, G.; Zahn, S.; Legler, A.; Rohm, H. Ultrasonic cutting of foods with inclined moving blades. J. Food Eng. 2011, 103, 394–400. [Google Scholar] [CrossRef]
  35. Arnold, G.; Leiteritz, L.; Zahn, S.; Rohm, H. Ultrasonic cutting of cheese: Composition affects cutting work reduction and energy demand. Int. Dairy J. 2009, 19, 314–320. [Google Scholar] [CrossRef]
  36. Shanmugam, A.; Chandrapala, J.; Ashokkumar, M. The effect of ultrasound on the physical and functional properties of skim milk. Innov. Food Sci. Emerg. Technol. 2012, 16, 251–258. [Google Scholar] [CrossRef]
  37. Flores, D.R.M.; Brasil, C.C.B.; Campagnol, P.C.B.; Jacob-Lopes, E.; Zepka, L.Q.; Wagner, R.; Cichoski, A.J. Application of ultrasound in chicken breast during chilling by immersion promotes a fast and uniform cooling. Food Res. Int. 2018, 109, 59–64. [Google Scholar] [CrossRef]
  38. Al-Hilphy, A.R.; Al-Temimi, A.B.; Al Rubaiy, H.H.M.; Anand, U.; Delgado-Pando, G.; Lakhssassi, N. Ultrasound applications in poultry meat processing: A systematic review. J. Food Sci. 2020, 85, 1386–1396. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. Wang, Y.; Zhang, W.; Zhou, G. Effects of ultrasound-assisted frying on the physiochemical properties and microstructure of fried meatballs. Int. J. Food Sci. Technol. 2019, 54, 2915–2926. [Google Scholar] [CrossRef]
  40. Dehghannya, J.; Abedpour, L. Influence of a three stage hybrid ultrasound-osmotic-frying process on production of low-fat fried potato strips. J. Sci. Food Agric. 2018, 98, 1485–1491. [Google Scholar] [CrossRef]
  41. Cadòn-Abant, S.; Arroyo, C.; Álvarez, I.; Brunton, N.; Whyte, P.; Lyng, J.G. An assessment of the application of ultrasound in the processing of ready-to-eat whole brown crab (Cancer pagurus). Ultrason. Sonochem. 2018, 40, 497–504. [Google Scholar] [CrossRef] [Green Version]
  42. Qui, L.; Zhang, M.; Chitrakar, B.; Bhandari, B. Application of power ultrasound in freezing and thawing Processes: Effect on process efficiency and product quality. Ultrason. Sonochem. 2020, 68, 105230. [Google Scholar] [CrossRef]
  43. Sun, Q.; Sun, F.; Xia, X.; Xu, H.; Kong, B. The comparison of ultrasound-assisted immersion freezing, air freezing and immersion freezing on the muscle quality and physicochemical properties of common carp (Cyprinus carpio) during freezing storage. Ultrason. Sonochem. 2019, 51, 281–291. [Google Scholar] [CrossRef] [PubMed]
  44. Fan, K.; Zhang, M.; Mujumdar, A.S. Application of airborne ultrasound in the convective drying of fruits and vegetables: A review. Ultrason. Sonochem. 2017, 39, 47–57. [Google Scholar] [CrossRef] [PubMed]
  45. Başlar, M.; Kılıçlı, M.; Toker, O.S.; Sağdıç, O.; Arici, M. Ultrasonic vacuum drying technique as a novel process for shortening the drying period for beef and chicken meats. Innov. Food Sci. Emerg. Technol. 2014, 26, 182–190. [Google Scholar] [CrossRef]
  46. Başlar, M.; Kılıçlı, M.; Yalinkilic, B. Dehydration kinetics of salmon and trout fillets using ultrasonic vacuum drying as a novel technique. Ultrason. Sonochem. 2015, 27, 495–502. [Google Scholar] [CrossRef]
  47. Huang, D.; Men, K.; Li, D.; Wen, T.; Gong, Z.; Sunden, B.; Wu, Z. Application of ultrasound technology in the drying of food products. Ultrason. Sonochem. 2019, 63, 104950. [Google Scholar] [CrossRef]
  48. Shi, H.; Zhang, X.; Chen, X.; Fang, R.; Zou, Y.; Wang, D.; Xu, W. How ultrasound combined with potassium alginate marination tenderizes old chicken breast meat: Possible mechanisms from tissue to protein. Food Chem. 2020, 328, 127144. [Google Scholar] [CrossRef]
  49. Yilmaz, B.; Cakmak, H.; Tavman, S. Ultrasonic pretreatment of carrot slices: Effects of sonication source on drying kinetics and product quality. An. Da Acad. Bras. De Ciências 2019, 91, e20180447. [Google Scholar] [CrossRef] [Green Version]
  50. Sánchez, E.S.; Simal, S.; Femenia, A.; Rosselló, C. Effect of acoustic brining on the transport of sodium chloride and water in Mahon cheese. Eur. Food Res. Technol. 2000, 212, 39–43. [Google Scholar] [CrossRef]
  51. Turhan, S.; Saricaogliu, T.; Oz, F. The Effect of Ultrasonic Marinating on the Transport of Acetic Acid and Salt in Anchovy Marinades. Food Sci. Technol. Res. 2013, 19, 849–853. [Google Scholar] [CrossRef] [Green Version]
  52. Alarcon-Rojo, A.; Carrillo-Lopez, L.M.; Reyes-Villagrana, R.; Huerta-Jimenez, M.; Garcia-Galicia, G. Ultrasound, and meat quality: A review. Ultrason. Sonochem. 2019, 55, 369–382. [Google Scholar] [CrossRef]
  53. Chang, H.-C.; Wong, R.-X. Textural and biochemical properties of cobia (Rachycentron canadum) sashimi tenderized with the ultrasonic water bath. Food Chem. 2012, 132, 1340–1345. [Google Scholar] [CrossRef] [PubMed]
  54. Wang, W.; Chen, W.; Zou, M.; Lv, R.; Wang, D.; Hou, F.; Feng, H.; Ma, X.; Zhong, J.; Ding, T.; et al. Applications of power ultrasound in oriented modification and degradation of pectin: A review. J. Food Eng. 2018, 234, 98–107. [Google Scholar] [CrossRef]
  55. Kiani, H.; Sun, D.-W.; Delgado, A.; Zhang, Z. Investigation of the effect of power ultrasound on the nucleation of water during freezing of agar gel samples in tubing vials. Ultrason. Sonochem. 2012, 19, 576–581. [Google Scholar] [CrossRef]
  56. Musielak, G.; Mierzwa, D.; Kroehnke, J. Food drying enhancement by ultrasound—A review. Trends Food Sci. Technol. 2016, 56, 126–141. [Google Scholar] [CrossRef]
  57. Bhargava, N.; Mor, R.S.; Kumar, K.; Sharanagat, V.S. Advances in application of ultrasound in food processing: A review. Ultrason. Sonochem. 2021, 70, 105293. [Google Scholar] [CrossRef]
  58. Wiktor, A.; Dadan, M.; Nowacka, M.; Rybak, K.; Witrowa-Rajchert, D. The impact of combination of pulsed electric field and ultrasound treatment on air drying kinetics and quality of carrot tissue. LWT Food Sci. Technol. 2019, 110, 71–79. [Google Scholar] [CrossRef]
  59. Ozuna, C.; Puig, A.; García-Pérez, J.V.; Mulet, A.; Cárcel, J.A. Influence of high intensity ultrasound application on mass transport, microstructure and textural properties of pork meat (Longissimus dorsi) brined at different NaCl concentrations. J. Food Eng. 2013, 119, 84–93. [Google Scholar] [CrossRef]
  60. McDonnell, C.K.; Lyng, J.G.; Arimi, J.M.; Allen, P. The acceleration of pork curing by power ultrasound: A pilot-scale pro-duction. Innov. Food Sci. Emerg. Technol. 2014, 26, 191–198. [Google Scholar] [CrossRef]
  61. Inguglia, E.S.; Burgess, C.M.; Kerry, J.P.; Tiwari, B.K. Ultrasound-Assisted Marination: Role of Frequencies and Treatment Time on the Quality of Sodium-Reduced Poultry Meat. Foods 2019, 8, 473. [Google Scholar] [CrossRef] [Green Version]
  62. Pedros-Garrido, S.; Condon-Abanto, S.; Beltran, J.; Lyng, J.; Brunton, N.; Bolton, D.; Whyte, P. Assessment of high intensity ultrasound for surface decontamination of salmon (S. salar), mackerel (S. scombrus), cod (G. morhua) and hake (M. mer- luc-cius) fillets, and its impact on fish quality. Innov. Food Sci. Emerg. Technol. 2017, 41, 64–70. [Google Scholar] [CrossRef]
  63. Khairi, M.T.M.; Ibrahim, S.; Yunus, M.A.M.; Faramarzi, M. Contact and non-contact ultrasonic measurement in the food industry: A review. Meas. Sci. Technol. 2015, 27, 12001. [Google Scholar] [CrossRef]
  64. Manas, P.; Pagan, R. Microbial inactivation by new technologies of food preservation. J. Appl. Microbiol. 2005, 98, 1387–1399. [Google Scholar] [CrossRef]
  65. Madigan, M.T.; Bender, K.S.; Buckley, D.H.; Sattley, W.M.; Stahl, D.A. Brock Biology of Microorganisms, 13th ed.; Pearson: Boston, MA, USA, 2012. [Google Scholar]
  66. Vadillo-Rodríguez, V.; Dutcher, J.R. Viscoelasticity of the bacterial cell envelope. Soft Matter 2011, 7, 4101–4110. [Google Scholar] [CrossRef]
  67. Wigginton, K.R.; Pecson, B.M.; Sigstam, T.; Bosshard, F.; Kohn, T. Virus inactivation mechanisms: Impact of disinfectants on virus function and structural integrity. Environ. Sci. Tech. 2012, 46, 12069–12078. [Google Scholar] [CrossRef] [PubMed]
  68. Yusof, N.S.M.; Babgi, B.; Alghamdi, Y.; Aksu, M.; Madhavan, J.; Ashokkumar, M. Physical and chemical effects of acoustic cavitation in selected ultrasonic cleaning applications. Ultrason. Sonochem. 2016, 29, 568–576. [Google Scholar] [CrossRef]
  69. Labas, M.D.; Zalazar, C.S.; Brandi, R.J.; Cassano, A.E. Reaction kinetics of bacteria disinfection employing hydrogen peroxide. Biochem. Eng. J. 2008, 38, 78–87. [Google Scholar] [CrossRef]
  70. Rahman, M.; Ninomiya, K.; Ogino, C.; Shimizu, N. Ultrasound-induced membrane lipid peroxidation and cell damage of Escherichia coli in the presence of non- woven TiO2 fabrics. Ultrason. Sonochem. 2010, 17, 738–743. [Google Scholar] [CrossRef] [PubMed]
  71. Duan, J.; Kasper, D.L. Oxidative depolymerization of polysaccharides by reactive oxygen/nitrogen species. Glycobiology 2011, 21, 401–409. [Google Scholar] [CrossRef] [PubMed]
  72. Mayer, B.K.; Yang, Y.; Gerrity, D.W.; Abbaszadegan, M. The Impact of Capsid Proteins on Virus Removal and Inactivation during Water Treatment Processes. Microbiol. Insights 2015, 8, MBI-S31441. [Google Scholar] [CrossRef] [Green Version]
  73. Chen, Z. Microbial Inactivation in Foods by Ultrasound. J. Food: Microbiol. Saf. Hyg. 2017, 2, E102. [Google Scholar] [CrossRef]
  74. Liu, J.; Li, L.; Zhou, L.; Li, B.; Xu, Z. Effect of ultrasonic field on the enzyme activities and ion balance of potential pathogen Saccharomyces cerevisiae. Microb. Pathog. 2018, 119, 216–220. [Google Scholar] [CrossRef]
  75. Sarkinas, A.; Sakalauskiene, K.; Raisutis, R.; Zeime, J.; Salaseviciene, A.; Puidaite, E.; Mockus, E.; Cernauskas, D. Inactivation of some pathogenic bacteria and phytoviruses by ultrasonic treatment. Microb. Pathog. 2018, 123, 144–148. [Google Scholar] [CrossRef] [PubMed]
  76. Cleach, J.; Watier, D.; Fur, B.L.; Brauge, T.; Duflos, G.; Grard, T.; Lencel, P. Use of ratiometric probes with a spectrofluorometer for bacterial viability measurement. J. Microbiol. Biotech. 2018, 28, 1782–1790. [Google Scholar] [CrossRef] [Green Version]
  77. Li, J.; Ma, L.; Liao, X.; Liu, D.; Lu, X.; Chen, S.; Ye, X.; Ding, T. Ultrasound-Induced Escherichia coli O157:H7 Cell Death Exhibits Physical Disruption and Biochemical Apoptosis. Front. Microbiol. 2018, 9, 2486. [Google Scholar] [CrossRef] [Green Version]
  78. He, Q.; Liu, D.; Ashokkumar, M.; Ye, X.; Jin, T.Z.; Guo, M. Antibacterial mechanism of ultrasound against Escherichia coli: Alterations in membrane microstructures and properties. Ultrason. Sonochem. 2021, 73, 105509. [Google Scholar] [CrossRef]
  79. Park, S.Y.; Ha, S.-D. Reduction of Escherichia coli and Vibrio parahaemolyticus Counts on Freshly Sliced Shad (Konosirus punctatus) by Combined Treatment of Slightly Acidic Electrolyzed Water and Ultrasound Using Response Surface Methodology. Food Bioprocess Technol. 2015, 8, 1762–1770. [Google Scholar] [CrossRef]
  80. Lin, L.; Wang, X.; Li, C.; Cui, H. Inactivation mechanism of E. coli O157:H7 under ultrasonic sterilization. Ultrason. Sonochem. 2019, 59, 104751. [Google Scholar] [CrossRef]
  81. Fitriyanti, M.; Narsimhan, G. Synergistic effect of low power ultrasonication on antimicrobial activity of cecropin P1 against E. coli in food systems. LWT Food Sci. Technol. 2018, 96, 175–181. [Google Scholar] [CrossRef]
  82. Wang, W.; Li, M.; Li, Y. Modeling the Thermoultrasound Inactivation of Vibrio parahaemolyticus in Raw Peeled Shrimps. J. Food Prot. 2013, 76, 1712–1718. [Google Scholar] [CrossRef]
  83. Cruz-Cansino, N.; Reyes-Hernández, I.; Delgado-Olivares, L.; Jaramillo-Bustos, D.P.; Ortega, J.A.A.; Ramírez-Moreno, E. Effect of ultrasound on survival and growth of Escherichia coli in cactus pear juice during storage. Braz. J. Microbiol. 2016, 47, 431–437. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  84. Kang, D.; Jiang, Y.; Xing, L.; Zhou, G.; Zhang, W. Inactivation of Escherichia coli O157:H7 and Bacillus cereus by power ultrasound during the curing processing in brining liquid and beef. Food Res. Int. 2017, 102, 717–727. [Google Scholar] [CrossRef]
  85. Bonah, E.; Huang, X.; Hongying, Y.; Aheto, J.H.; Yi, R.; Yu, S.; Tu, H. Nondestructive monitoring, kinetics and antimicrobial properties of ultrasound technology applied for surface decontamina-tion of bacterial foodborne pathogen in pork. Ultrason. Sonochem. 2021, 70, 105344. [Google Scholar] [CrossRef]
  86. Zhao, Y.-M.; Oliveira, M.; Burgess, C.M.; Cropotova, J.; Rustad, T.; Sun, D.-W.; Tiwari, B.K. Combined effects of ultrasound, plasma-activated water, and peracetic acid on decontamination of mackerel fillets. LWT 2021, 150, 111957. [Google Scholar] [CrossRef]
  87. Wrigley, D.; Llorca, N.G. Decrease of Salmonella typhlmurium in Skim Milk and Egg by Heat and Ultrasonic Wave Treatment. J. Food Prot. 1992, 55, 678–680. [Google Scholar] [CrossRef] [PubMed]
  88. Techathuvanan, C.; D’Souza, D.H. High Intensity Ultrasound forSalmonellaEnteritidis Inactivation in Culture and Liquid Whole Eggs. J. Food Sci. 2018, 83, 1733–1739. [Google Scholar] [CrossRef]
  89. Bi, X.; Wang, X.; Chen, Y.; Chen, L.; Xing, Y.; Che, Z. Effects of combination treatments of lysozyme and high power ultrasound on the Salmonella typhimurium inactivation and quality of liquid whole egg. Ultrason. Sonochem. 2020, 60, 104763. [Google Scholar] [CrossRef]
  90. Kordowska-Wiater, M.; Stasiak, D.M. Effect of ultrasound on survival of gram-negative bacteria on chicken skin surface. Bull. Vet. Inst. Pulawy 2011, 55, 207–210. [Google Scholar]
  91. Campaniello, D.; Bevilacqua, A.; Speranza, B.; Sinigaglia, M.; Corbo, M.R. Inactivation of Salmonella enterica in a Rice Beverage by Ultrasound: Study of the Parameters Affecting the Antibacterial Effect. Food Bioprocess Technol. 2018, 11, 1139–1148. [Google Scholar] [CrossRef]
  92. Morbiato, G.; Zambon, A.; Toffoletto, M.; Poloniato, G.; Dall’Acqua, S.; de Bernard, M.; Spilimbergo, S. Supercritical carbon dioxide combined with high power ultrasound as innovate drying process for chicken breast. J. Supercrit. Fluids 2019, 147, 24–32. [Google Scholar] [CrossRef]
  93. Seo, M.; Jeong, H.; Han, S.; Kang, I.; Ha, S. Impact of ethanol and ultrasound treatment on mesophilic aerobic bacteria, coliforms, and Salmonella Typhimurium on chicken skin. Poult. Sci. 2019, 98, 6954–6963. [Google Scholar] [CrossRef]
  94. Joo, H.; Mizan, F.R.; Hossain, I.; Lee, D.; Ha, S. Enhanced elimination of Salmonella Typhimurium and Campylobacter jejuni on chicken skin by sequential exposure to ultrasound and peroxyacetic acid. J. Food Saf. 2020, 40, e12803. [Google Scholar] [CrossRef]
  95. Mortazavi, N.; Aliakbarlu, J. Antibacterial Effects of Ultrasound, Cinnamon Essential Oil, and Their Combination Against Listeria monocytogenes and Salmonella Typhimurium in Milk. J. Food Sci. 2019, 84, 3700–3706. [Google Scholar] [CrossRef] [PubMed]
  96. Jeyaletchumi, P.; Tunung, R.; Selina, P.M.; Chai, L.C.; Radu, S.; Farinazleen, M.G.; Cheah, Y.K.; Mitsuaki, N.; Yoshitsugu, N.; Kumar, M.P. Assessment of Listeria monocytogenes in salad vegetables through kitchen simulation study. J. Trop. Agric. Food Sci. 2012, 40, 55–62. [Google Scholar]
  97. Gabriel, A.A. Inactivation of Listeria monocytogenes in milk by multifrequency power ultrasound. J. Food Process. Preserv. 2015, 39, 846–853. [Google Scholar] [CrossRef]
  98. Gabriel, A.A. Inactivation behaviors of foodborne microorganisms in multi-frequency power ultrasound-treated orange juice. Food Control 2014, 46, 189–196. [Google Scholar] [CrossRef]
  99. Franco-Vega, A.; Ramirez-Corona, N.; Lopez-Malo, A.; Palou, E. Estimation of Listeria monocytogenes survival during thermoultrasonic treatments in non-iso- thermal conditions: Effect of ultrasound on temperature and survival profiles. Food Microbiol. 2015, 52, 124–130. [Google Scholar] [CrossRef]
  100. Dolan, H.L.; Bastarrachea, L.J.; Tikekar, R.V. Inactivation of Listeria innocua by a combined treatment of low-frequency ul-trasound and zinc oxide. Lebensm. Wiss. Technol. 2018, 88, 146–151. [Google Scholar] [CrossRef]
  101. Bahrami, A.; Baboli, Z.M.; Schimmel, K.; Jafari, S.M.; Williams, L. Efficiency of novel processing technologies for the control of Listeria monocytogenes in food products. Trends Food Sci. Technol. 2020, 96, 61–78. [Google Scholar] [CrossRef]
  102. Pan, Y.; Zhang, Y.; Cheng, J.-H.; Sun, D.-W. Inactivation of Listeria Monocytogenes at various growth temperatures by ultrasound pretreatment and cold plasma. LWT 2020, 118, 108635. [Google Scholar] [CrossRef]
  103. Miks-Krajnik, M.; James Feng, L.X.; Bang, W.S.; Yuk, H.-G. Inactivation of Listeria monocytogenes and natural microbiota on raw salmon fillets using acidic electrolyzed water, ultraviolet light or/and ultrasounds. Food Control 2017, 74, 54–60. [Google Scholar] [CrossRef]
  104. Pennisi, L.; Di Clerico, D.; Costantini, L.; Festino, A.R.; Vergara, A. Ultrasonic decontamination in smoked salmon experimentally contaminated with Listeria monocytogenes: Preliminary results. Ital. J. Food Saf. 2020, 9, 8398. [Google Scholar] [CrossRef] [Green Version]
  105. Baumann, A.R.; Martin, S.E.; Feng, H. Power ultrasound treatment of Listeria monocytogenes in apple cider. J. Food Prot. 2005, 68, 2333–2340. [Google Scholar] [CrossRef] [PubMed]
  106. Zhang, H.; Tsai, S.; Tikekar, R.V. Inactivation of Listeria innocua on blueberries by novel ultrasound washing processes and their impact on quality during storage. Food Control. 2021, 121, 107580. [Google Scholar] [CrossRef]
  107. Rafeeq, S.; Ovissipour, R. The Effect Ultrasound and Surfactants on Nanobubbles Efficacy against Listeria innocua and Escherichia coli O157:H7, in Cell Suspension and on Fresh Produce Surfaces. Foods 2021, 10, 2154. [Google Scholar] [CrossRef]
  108. Grace, D.; Fetsch, A. Chapter 1—Staphylococcus aureus—A Foodborne Pathogen: Epidemiology, Detection, Characterization, Prevention, and Control: An Overview. In Staphylococcus aureus; Fetsch, A., Ed.; Academic Press: Cambridge, MA, USA, 2018; pp. 3–10. [Google Scholar] [CrossRef]
  109. Huang, G.; Chen, S.; Dai, C.; Sun, L.; Sun, W.; Tang, Y.; Xiong, F.; He, R.; Ma, H. Effects of ultrasound on microbial growth and enzyme activity. Ultrason. Sonochem. 2017, 37, 144–149. [Google Scholar] [CrossRef]
  110. Liao, X.; Li, J.; Suo, Y.; Chen, S.; Ye, X.; Liu, D.; Ding, T. Multiple action sites of ultrasound on Escherichia coli and Staphylococcus aureus. Food Sci. Hum. Wellness 2018, 7, 102–109. [Google Scholar] [CrossRef]
  111. Mansyur, M.; Yudaningtyas, E.; Prawiro, S.; Widjajanto, E. The Effect of Low Power Ultrasonic Wave Exposure to Suppress Methicillin-Resistant Staphylococcus aureus (MRSA) In Vitro. J. Trop. Life Sci. 2018, 8, 144–150. [Google Scholar] [CrossRef]
  112. Ahmed, F.; Russell, C. Synergism between ultrasonic waves and hydrogen peroxide in the killing of microorganisms. J. Appl. Bacteriol. 1975, 39, 31–40. [Google Scholar] [CrossRef] [PubMed]
  113. Sesal, N.C.; Kekeç, Ö. Inactivation of Escherichia coli and Staphylococcus aureus by Ultrasound. J. Ultrasound Med. 2014, 33, 1663–1668. [Google Scholar] [CrossRef]
  114. Piñon, M.; Alarcon-Rojo, A.; Renteria, A.; Carrillo-López, L.M. Microbiological properties of poultry breast meat treated with high-intensity ultrasound. Ultrasonics 2020, 102, 105680. [Google Scholar] [CrossRef]
  115. Herceg, Z.; Rezek Jambrak, A.; Lelas, V.; Mededovic Thagard, S. The effect of high intensity ultrasound treatment on the amount of Staphylococcus aureus and Escherichia coli in milk. Food Technol. Biotechnol. 2012, 50, 46–52. [Google Scholar]
  116. Kaakoush, N.O.; Castaño-Rodríguez, N.; Mitchell, H.M.; Man, S.M. Global Epidemiology of Campylobacter Infection. Clin. Microbiol. Rev. 2015, 28, 687–720. [Google Scholar] [CrossRef] [Green Version]
  117. Vetchapitak, T.; Shinki, T.; Sasaki, S.; Taniguchi, T.; Luangtongkum, T.; Misawa, N. Evaluation of chemical treatment combined with vacuum and ultrasonication with a water resonance system for reducing Campylobacter on naturally contaminated chicken carcasses. Food Control. 2020, 112, 107087. [Google Scholar] [CrossRef]
  118. Moazzami, M.N.M.; Bergenkvist, E.; Fernström, L.-L.; Rydén, J.; Hansson, I. Reducing Campylobacter jejuni,Enterobacteriaceae, Escherichia coli, and Total Aerobic Bacteria on Broiler Carcasses Using Combined Ultrasound and Steam. J. Food Prot. 2021, 84, 572–578. [Google Scholar] [CrossRef]
  119. Selwet, M. Use of Ultrasounds to Reduce the Count of Campylobacter coli in Water. Pol. J. Microbiol. 2021, 70, 339–343. [Google Scholar] [CrossRef] [PubMed]
  120. Kassem, A.; Meade, J.; McGill, K.; Walsh, C.; Gibbons, J.; Lyng, J.; Whyte, P. An investigation of high intensity ultrasonication and chemical immersion treatments on Campylobacter jejuni and spoilage bacteria in chicken. Innov. Food Sci. Emerg. Technol. 2018, 45, 298–305. [Google Scholar] [CrossRef]
  121. Musavian, H.S.; Krebs, N.H.; Nonboe, U.; Corry, J.E.; Purnell, G. Combined steam and ultrasound treatment of broilers at slaughter: A promising intervention to significantly reduce numbers of naturally occurring campylobacters on carcasses. Int. J. Food Microbiol. 2014, 176, 23–28. [Google Scholar] [CrossRef] [PubMed]
  122. Musavian, H.S.; Butt, T.M.; Ormond, A.; Keeble, D.; Krebs, N.H. Evaluation of Steam-Ultrasound Decontamination on Naturally Contaminated Broilers through the Analysis of Campylobacter, Total Viable Count, and Enterobacteriaceae. J. Food Prot. 2022, 85, 196–202. [Google Scholar] [CrossRef] [PubMed]
  123. Yang, Z.; Jiao, X.; Zhou, X.; Cao, G.; Fang, W.; Gu, R. Isolation and molecular characterization of Vibrio parahaemolyticus from fresh, low temperature preserved, dried, and salted seafood products in two coastal areas of eastern China. Int. J. Food Microbiol. 2008, 125, 279–285. [Google Scholar] [CrossRef]
  124. Iwahori, J.; Yamamoto, A. Quantitative risk assessment of Vibrio parahaemolyticus in finfish: A model of raw horse mackerel consumption in Japan. Risk Anal. 2010, 30, 1817–1832. [Google Scholar] [CrossRef] [PubMed]
  125. Su, Y.C.; Liu, C.C. Vibrio parahaemolyticus: A concern of seafood safety. Food Microbiol. 2007, 24, 549–558. [Google Scholar] [CrossRef] [PubMed]
  126. Park, S.Y.; Mizan, M.D.F.R.; Ha, S. Inactivation of Cronobacter sakazakii in head lettuce by using a combination of ultrasound and sodium hypochlorite. Food Control 2016, 60, 582–587. [Google Scholar] [CrossRef]
  127. Borazjani, A.; Andrews, L.S.; Veal, C.D. Novel nonthermal methods to reduce vibrio vulnificus in raw oysters. J. Food Saf. 2003, 23, 179–187. [Google Scholar] [CrossRef]
  128. Burleson, G.R.B.; Murray, T.M.; Polland, M. Inactivation of Viruses and Bacteria by Ozone, With and Without Sonication. Am. Soc. Microbiol. Appl. Microbiol. 1975, 29, 340–344. [Google Scholar] [CrossRef] [PubMed]
  129. Quintieri, L.; Fanelli, F.; Caputo, L. Antibiotic Resistant Pseudomonas Spp. Spoilers in Fresh Dairy Products: An Underestimated Risk and the Control Strategies. Foods 2019, 8, 372. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  130. Decimo, M.; Cabeza, M.C.; Ordóñez, J.A.; De Noni, I.; Brasca, M. Volatile organic compounds associated with milk spoilage by psychrotrophic bacteria. Int. J. Dairy Technol. 2018, 71, 593–600. [Google Scholar] [CrossRef]
  131. Villamiel, M.; de Jong, P. Inactivation of Pseudomonas fluorescens and Streptococcus thermophilus in Trypticase® Soy Broth and total bacteria in milk by continuous-flow ultrasonic treatment and conventional heating. J. Food Eng. 2000, 45, 171–179. [Google Scholar] [CrossRef]
  132. Shin, J.K.; Jung, K.J.; Pyun, Y.R.; Chung, M.S. Application of pulsed electric fields with square wave pulse to milk inoculated with E. coli, P. fluorescens, and B. stearothermophilus. Food Sci. Biotechnol. 2007, 16, 1082–1084. [Google Scholar]
  133. Mansur, A.R.; Oh, D.-H. Combined Effect of Thermosonication and Slightly Acidic Electrolyzed Water to Reduce Foodborne Pathogens and Spoilage Microorganisms on Fresh-cut Kale. J. Food Sci. 2015, 80, M1277–M1284. [Google Scholar] [CrossRef]
  134. Su, Y.; Jiang, L.; Chen, D.; Yu, H.; Yang, F.; Guo, Y.; Xie, Y.; Yao, W. In vitro and in silico approaches to investigate antimicrobial and biofilm removal efficacies of combined ultrasonic and mild thermal treatment against Pseudomonas fluorescens. Ultrason. Sonochem. 2022, 83, 105930. [Google Scholar] [CrossRef]
  135. Bevilacqua, A.; Speranza, B.; Iorio, M.C.; Loi, M.; Sinigaglia, M.; Corbo, M.R. US-Inactivation of foodborne bacteria: Screening in distilled water and combination with citrus extract in skim milk. LWT 2016, 70, 135–141. [Google Scholar] [CrossRef]
  136. Alakomi, H.L.; Skyttä, E.; Helander, I.; Ahvenainen, R. The hurdle concept. In Minimal Processing Technologies in the Food Industries; Woodhead Publishing: Cambridge, UK, 2002; pp. 174–195. [Google Scholar]
  137. Leistner, L.; Gould, G.W. Hurdle Technologies: Combination Treatments for Food Stability, Safety and Quality; Springer Science & Business Media: Berlin, Germany, 2012. [Google Scholar]
Figure 1. Overview of non-thermal technologies (created with Biorender.com).
Figure 1. Overview of non-thermal technologies (created with Biorender.com).
Foods 12 01212 g001
Figure 2. Mechanism of action of ultrasound against bacteria (created with Biorender.com).
Figure 2. Mechanism of action of ultrasound against bacteria (created with Biorender.com).
Foods 12 01212 g002
Table 1. Use of ultrasound in food industry: mechanisms, advantages, products.
Table 1. Use of ultrasound in food industry: mechanisms, advantages, products.
ApplicationConventional MethodAdvantagesUltrasound PrincipleProductsReference
CuttingKnifeSmall deformation
Less cracks and crumbling
Cavitation phenomenonFragile and frozen foods
Viscoelastic products
Heterogenous products
[33]
[34,35]
[36]
CookingStove
Fried
Water
Homogeneous cooking
Less time
Uniform heat
transfer
Poultry
Beef
Vegetables
Fruit
Crustaceans
[37,38]
[39]
[40]
[39]
[41]
FreezingIceLess freezing time
Homogeneous cooking
Less damage to cells
Cavitation
Fragmentation of large ice crystals
Triggering secondary ice nucleation
Vegetables
Meat
Fish
[42]
[39]
[43]
DryingHot gas streaming
Pulverization
Less time
Improved heat transfer
Uniform heat transferVegetables
Meat
Fish
Fruit
[44]
[45]
[46]
[47]
Pickling/marinatingBrineImproved organoleptic quality
Less time
Uniform heat
transfer
Microchannel
Meat
Vegetables
Cheese
Fish
[48]
[49]
[50]
[51]
TenderizationTimeImproved meat
tenderization
Acoustic cavitationMeat
Fish
[52]
[53]
Table 2. Ultrasound effects as single or combined non-thermal technology: Escherichia coli.
Table 2. Ultrasound effects as single or combined non-thermal technology: Escherichia coli.
OrganismMatrixTreatmentParameterUltrasound EffectsReference
Escherichia coli O157:H7Fresh
vegetables
Ultrasound at low frequencyP: 100 W, T: 7.0 min, and I: 50 w/cm2Inactivation treatment (P: 100 W, T: 4 min, I: 10 w/cm2)[80]
Escherichia coli O157:H7Milk
Orange juice
Ultrasound at low frequency
Ultrasound + antimicrobial peptides
P: 40 W, 160 W, T 30 min, T60 min
P: 40 W, 160 W, T 30, T60
Inactivation of inoculated E. coli
Synergic effects
[81]
Escherichia coli O157:H7Bacterial cell suspensionUltrasound at low frequencyP: 0.667 and 6.67 W/mL, I: 25.5 and 255 W/cm2, T: 0, 5, 15, 25 minDifferent time for low and high intensity[77]
Escherichia coli O157:H7Bacterial cell suspensionUltrasound
Ultrasound + nisin
P 20 W, 40 W, 60 W, and 80% by 20 kHz (total P: 950 W) 242.04 W, 484.08 W, 726.12 W, and 968.16 W/cm2; T: 15 minInactivation by ultrasound and with nisin[82]
Escherichia coliCactus pear juiceUltrasound at high frequencyP: 1500 W 20, 40, 60, and 80% by 20 kHz, t 2 sec 5 minInactivation 60%, 80% for 5 min[83]
Escherichia coli (ATCC 11755)Fresh carrot juiceUltrasound + temperature24 kHz, 120 μm, and 400 W with temperatures of 50, 54, and 58 °C and T: 0 to 10 min5 log CFU/mL reduction after 2 min at 54 °C and 58 °C
3.5 log CFU/mL reduction after 10 min at 50 °C
[18]
Escherichia coli O157:H7BeefUltrasound at low frequency2.39, 6.23, 11.32, and 20.96 Wcm−2
30, 60, 90, and 120 min
20.96 W cm−2 for 120 min was the optimal treatment for bacterial reductions[84]
Escherichia coli
K12 TEAG 1133
Pork meatUltrasound + NaClP: 95 W, T: 1 hTreatment could assist current sodium reduction strategies, improving processing time and decontamination of brining tanks, increasing the shelf-life[85]
Escherichia coliSliced shad (Konosirus punctatus)Ultrasound
Slightly acidic electrolyzed water + ultrasound
Ultrasound 37 kHz, 380 W 0, 50, and 100 min
pH range 5.0–6.5, oxidation–reduction potential 650– 1000 mV, available chlorine concentration 10–80 mg/L containing 0, 15, and 30 ppm chlorine and ultrasound 37 kHz, 380 W for 0, 50, and 100 min
Treatment not sufficient
1.04–1.86 log CFU/g
Reduction in T
[79]
Escherichia coli K12Mackerel
fillets
Ultrasound
Ultrasound + plasma
Ultrasound + peracetic acid
Ultrasound + plasma-activated water + peracetic acid
25 kHz, 550 W, 10 min
25 kHz, 550 W, 10 min + 11 L/min
25 kHz, 550 W, 10 min + 200 ppm
25 kHz, 550 W, 10 min + 11 L/min, 10 min + 200 ppm
Inactivation of 0.38 CFU/g
Inactivation of 0.2 CFU/g
Inactivation of 0.59 CFU/g
Inactivation of 0.59 CFU/g
[86]
Table 3. Ultrasound effects as individual or combined non-thermal technology: Salmonella spp.
Table 3. Ultrasound effects as individual or combined non-thermal technology: Salmonella spp.
OrganismMatrixTreatmentParameterUltrasound EffectsReference
Salmonella TyphimuriumLiquid whole eggHigh-power
ultrasound +
lysozyme
35–45 °C and 605–968 W/cm2 for 5–35 minUltrasound and
ultrasound + Lys caused a reduction of 3.31 and 4.26 log10 cycles
[89]
Salmonella
Enteritidis
Liquid whole eggHigh-power
ultrasound
20 kHz HIU for 0, 1, 5, 10, and 30 minSignificant reduction in cells up to 3.6 log CFU/mL[88]
Salmonella
Enterica
ATCC 35664
Rice beverageLow-power
ultrasound
20 kHz 130 W T 2, 6, 10 min P 40%, 60%, 100%Confirmation of the strong effect of both power and time, although the correlation with the antibacterial action was not strictly linear[91]
Salmonella spp.Raw chicken meatHigh-power
ultrasound + carbon dioxide
40 kHz/30 min/40 °CInactivation of inoculated Salmonella[92]
Salmonella TyphimuriumChicken skinUltrasound + ethanolEthanol 70% +
ultrasound (37 kHz, 380 W)
Inactivation of inoculated Salmonella, change in Hunter color and skin texture[93]
Salmonella Typhimurium CICC2295Pork meatUltrasound20 kHzf T: 10, 20, 30 min1–4.3 and 1–4.6 log CFU/g reduction[85]
Salmonella TyphimuriumChicken skinUltrasound
Ultrasound + peroxyacetic acid
37 kHz, 380 W 5 min
37 kHz, 380 W 5 min +
50–200 ppm
Treatment not sufficient
Reductions of 2.21 and 2.08 log CFU/g
[94]
Salmonella Typhimurium
ATCC 14028
Low-fat and high-fat milkUltrasound
Ultrasound +
cinnamon
essential oil
24 kHz and 400 W power at 124 μm (100%) wave amplitude 15 min
24 kHz and 400 W power at 124 μm (100%) wave amplitude 15 min + cinnamon
Reduction of 1.6 log cycle
Reduction of 2.7 log CFU/mL in low-fat milk and 3.8 log CFU/mL in high-fat milk
[95]
Salmonella
Enterica
Anatum
Chicken skinUltrasound
Ultrasound +
lactic acid
aqueous
solution
40 kHz, 2.5 W/cm2 for 3 or 6 min
40 kHz, 2.5 W/cm2 for 3 or 6 min
0.6 log CFU/cm2
1 log CFU/cm2
1.6 log CFU/cm2
2.7 log CFU/cm2
[90]
Table 4. Ultrasound effects as single or combined non-thermal technology: Listeria spp.
Table 4. Ultrasound effects as single or combined non-thermal technology: Listeria spp.
OrganismMatrixTreatmentParameterUltrasound EffectsReference
Listeria innocuaBlueberryUltrasound +
carvacrol + carbonated water
20 kHz 500 W, 1/3.3 MHz 10 W + solution of carvacrolAfter 10 min of treatment with 2 mM carvacrol (CR), carbonated water (CW), 20 kHz ultrasound (20 kHz), or 1 MHz ultrasound (1 MHz) alone, there was a 2.4–2.6 log CFU/g reduction (P < 0.05) in bacteria from blueberry surface from the initial load of 5.2 log CFU/g[106]
Listeria
monocytogenes
LM ATCC 19114, LM ATCC 15313, LM ATCC 19111, LM ATCC 7644
Smoked salmonUltrasound + temperature20 kHz, 100% amplitude, 20 °C, 25 °C, 30 °C, 40 °C, 50 °C, T: 5, 10, 15 minInactivation was 2.02, 2.12, and 2.44 log CFU/g at 30 °C for 15 min, at 40 °C for 15 min, and at 50 °C for 5 min[104]
L. monocytogenes ATCC19115Bacterial cell
suspension
Ultrasound + cold plasma + temperature500 W and 40 kHz T 0, 2, 5, 10 min + plasma treatment 2 minInactivation by ultrasound and cold plasma, increasing
temperature
[102]
Listeria innocuaMackerel filletsUltrasound
Ultrasound + plasma
Ultrasound + peracetic acid
Ultrasound + plasma-activated water + peracetic acid
25 kHz, 550 W, 10 min
25 kHz, 550 W, 10 min + 11 L/min
25 kHz, 550 W, 10 min + 200 ppm
25 kHz, 550 W, 10 min + 11 L/min, 10 min + 200 ppm
Inactivation of 0.33 CFU/g
Inactivation of 0.20 CFU/g
Inactivation of 0.72 CFU/g
Inactivation of 0.65 CFU/g
[86]
Listeria
monocytogenes ATCC 19115
Low-fat and high-fat milkUltrasound
Ultrasound +
cinnamon essential oil
24 kHz and 400 W power at 124 μm (100%) wave amplitude 15 min
24 kHz and 400 W power at 124 μm (100%) wave amplitude 15 min +
cinnamon
Reduction of 2.5 and 3 log cycles
Reduction of 4.3 and 4.5 log cycles
[95]
Listeria innocuaSpinach leavesUltrasound
Ultrasound +
nanobubble
Did not significantly reduce bacteria
More than 6 log CFU/mL reduction after 15 min
[107]
Listeria
monocytogenes
Salmon
filets
Ultrasound200 W, 45 kHzReduction of 0.6 log CFU/mL[103]
Table 5. Ultrasound effects as single or combined non-thermal technology: Staphylococcus aureus.
Table 5. Ultrasound effects as single or combined non-thermal technology: Staphylococcus aureus.
OrganismMatrixTreatmentParameterUltrasound EffectsReference
Staphylococcus aureus
ATCC 25923
Broth
colony
Ultrasound30 kHz 100 W from 5 to 3° minNot sufficient[112]
Methicillin-resistant
Staphylococcus aureus
Broth
colony
Ultrasound20 kHz 2, 3, 4, 5, or 6 watts for 2 minLethal power = 8.432 watts[113]
Staphylococcus aureus
ATCC 25923
Broth
colony
Ultrasound198 W, 252 W/cm2, 20 kHzBacterial damage[110]
Staphylococcus aureusChicken breastUltrasoundUltrasonic bath 9.6 W/cm2 /40 kHz/0, 30, and 50 min/5 °CS. aureus increased[114]
Staphylococcus aureusMilkUltrasound +
temperature
20 kHz, 600 W, 120 lm, 12 min + 60 C0.94 log
CFU ml1
[115]
Table 6. Ultrasound effects as single or combined non-thermal technology: Campylobacter spp.
Table 6. Ultrasound effects as single or combined non-thermal technology: Campylobacter spp.
OrganismMatrixTreatmentParameterUltrasound EffectsReference
Campylobacter jejuniChicken carcassesUltrasound + vacuum1200 W/130 Hz/15 min + 0.1% cetylpyridinium chloride or 0.01% sodium hypochlorite and a vacuum of −0.02 MPaFrom 0.94 to 1.19 log10 MPN (most probable number)/10 gr[117]
Campylobacter jejuniChicken carcassesUltrasound + steam30 to 40 kHz and steam at 84 to 85 °C0.5–0.8 log CFU/g[118]
Campylobacter jejuniChicken skinUltrasound
Ultrasound +
peroxyacetic acid
37 kHz, 380 W 5 min
37 kHz, 380 W 5 min + 50–200 ppm
Not sufficient at 0.25 log CFU/g
Reduction of 2.08 log CFU/g
[94]
Campylobacter coli
ATCC 33559
WaterUltrasound37 kHz and 80 kH + 5 minFrequency of 80 kHz reduction from 6.86 log
CFU/mL to 3.08 log CFU/mL, 37 kHz reduction 6.75 log CFU/mL to 4.04 log CFU/mL
[119]
Campylobacter jejuniRaw chickenUltrasound +
temperature
4, 25, and 54 °C, 40 kHz, ultrasound power of 120 W, 1, 2 or 3 minReduction[120]
Campylobacter jejuniChicken carcassUltrasound +
temperature
90–94 °C and +
t 30–40 kHz
Reduction of
0.7 log10 CFU
[121]
Table 7. Ultrasound effects as single or combined non-thermal technology: Vibrio spp.
Table 7. Ultrasound effects as single or combined non-thermal technology: Vibrio spp.
OrganismMatrixTreatmentParameterUltrasound EffectsReference
Vibrio
paraemoliticus
KCTC 2471
Sliced shad
(Konosirus punctatus)
Ultrasound
Slightly acidic electrolyzed water + ultrasound
Ultrasound 37 kHz, 380 W 0, 50, and 100 min
pH range 5.0–6.5, oxidation–reduction potential 650– 1000 mV, available chlorine concentration 10–80 mg/L containing 0, 15, and 30 ppm chlorine and ultrasound 0.37 kHz, 380 W, 0, 50, and 100 min
Treatment not sufficient
1.02–1.42 log CFU/g reduction
[126]
Vibrio
paraemoliticus
ATCC 33847
Raw peeled shrimpUltrasound
Ultrasound + temperature
0, 96, 150, and 204 W
0, 96, 150, and 204 W, 47, 50, and 53 °C
Limited reduction of 0.59, 0.60, and 0.68 log CFU/g
47 °C reductions of 1.76, 2.63, and 4.01 log CFU/g 96, 150, and 204 W, respectively, for 8 min
[82]
Vibrio
vulnificus
Oysters (Crossostrea virginica)Ultrasound100 W, 500 W/cm for 30 minTreatment not sufficient[127]
Vibrio choleraeBroth
solution
Ultrasound
Ultrasound + ozone
40 kHz, 150 W 10 minTreatment not sufficient
Treatment not sufficient
[128]
Table 8. Ultrasound effects as single or combined non-thermal technology: Pseudomonas spp.
Table 8. Ultrasound effects as single or combined non-thermal technology: Pseudomonas spp.
OrganismMatrixTreatmentParameterUltrasound EffectsReference
Pseudomonas
fluorescens
Mackerel filletsUltrasound
Ultrasound + plasma
Ultrasound + peracetic acid
Ultrasound + plasma-activated water + peracetic acid
25 kHz, 550 W, 10 min
25 kHz, 550 W, 10 min + 11 L/min
25 kHz, 550 W, 10 min + 200 ppm
25 kHz, 550 W, 10 min + 11 L/min, 10 min + 200 ppm
Inactivation of 0.50 CFU/g
Inactivation of 0.13 CFU/g
Inactivation of 0.46 CFU/g
Inactivation of 0.30 CFU/g
[86]
Pseudomonas
fluorescens
Chicken skinUltrasound
Ultrasound + lactic acid aqueous
solution
40 kHz, 2.5 W/cm2 for 3 or 6 min
40 kHz, 2.5 W/cm2 for 3 or 6 min
0.5 log CFU/cm2
1 log CFU/cm2
3 log CFU/cm2
4.1 log CFU/cm2
[94]
Pseudomonas
fluorescens
MilkUltrasound + temperature20 kHz, 150 W + 62 °C3.1 CFU/mL[131]
Pseudomonas
fluorescens
Raw milkUltrasound + temperature60 kV/cm, 200 μs, 40 °C (Tin)5 CFU/mL[132]
Pseudomonas
putida
MilkUltrasound20 kHz, 100 WBacteriostatic effect[133]
Pseudomonas fluorescensFresh-cut kaleUltrasound + temperature100 W/L at 25, 40, or 50 °CReduced by 3 log CFU/mL[134]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Lauteri, C.; Ferri, G.; Piccinini, A.; Pennisi, L.; Vergara, A. Ultrasound Technology as Inactivation Method for Foodborne Pathogens: A Review. Foods 2023, 12, 1212. https://doi.org/10.3390/foods12061212

AMA Style

Lauteri C, Ferri G, Piccinini A, Pennisi L, Vergara A. Ultrasound Technology as Inactivation Method for Foodborne Pathogens: A Review. Foods. 2023; 12(6):1212. https://doi.org/10.3390/foods12061212

Chicago/Turabian Style

Lauteri, Carlotta, Gianluigi Ferri, Andrea Piccinini, Luca Pennisi, and Alberto Vergara. 2023. "Ultrasound Technology as Inactivation Method for Foodborne Pathogens: A Review" Foods 12, no. 6: 1212. https://doi.org/10.3390/foods12061212

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop