Decontamination effect of hot-air drying against bacterial pathogen and surrogate strains on basil leaves, from laboratory to pilot scale settings
Introduction
Dried herbs are frequently used as ingredients and added into minimally processed or ready-to-eat foods to enhance their sensorial and healthy attributes (Székács et al., 2018). As with many other agricultural products, herbs are exposed to microbial contamination during pre- and post-harvest (Gurtler, Doyle, & Kornacki, 2014). Prevalence results showed that around 1.5% (2/132) and 1.1% (31/2833) of dried herbs tested positive for Salmonella in production and retail samples, respectively (Sagoo et al., 2009). Between 1973 and 2012, 28 outbreaks implicating herbs and spices have been documented, which caused a total of 2228 reported cases, 134 hospitalization and 2 deaths (FAO, 2014). There have been increasing concerns regarding the microbial safety of dried herbs in recent years (Székács et al., 2018; Szűcs, Szabó, Lakner, & Székács, 2018). Processing measures that reduce the contamination level on dried herbs could provide added value for food safety, especially for products that undergo no additional heating steps (Little, Omotoye, & Mitchell, 2003).
Drying processes are frequently used in the production of herbs (Lewicki, 2006). It is assumed that hot-air drying with its thermal effect could reduce the presence of foodborne pathogens. However, the processing conditions are often designed out of technological nature to achieve desired product quality and accomplish long-term ambient stability. The decontamination effect against foodborne pathogens is rarely investigated (Bourdoux, Li, Rajkovic, Devlieghere, & Uyttendaele, 2016). Moreover, heat resistance of foodborne pathogens, such as Salmonella, is known to increase at reduced water activity (aw) (Podolak, Lucore, & Harris, 2017). Considering that the moisture content of food products decreases with the progress of drying, it is important to identify the critical inactivation parameters in order to understand the fate of pathogens on herbs during dynamic drying. Besides, the process lethality of any given technology needs to be validated at an industrial level where the introduction of pathogenic strains is not allowed due to biological hazard concerns. Hence, the use of surrogate strains, which utilizes non-pathogenic proxies that response to a treatment in an equivalent or more resistant manner than the pathogen of concern, is of increasing interests (Busta et al., 2003; Hu & Gurtler, 2017; NACMCF, 2010). However, the proper selection of surrogate strains depends highly on the type of process, product and targeted pathogens. Evaluation of surrogate strains and paired comparison between surrogate and pathogenic strains on herbs during hot-air drying need to be established.
Using basil leaves (Ocimum basilicum) as a case study, the present study firstly compares the thermal resistance of various bacterial strains on fresh and semi-dried herbs. Inactivation kinetics of selected strains on basil leaves during hot-air drying were further evaluated in a laboratory oven. Finally, the process lethality of hot-air drying against bacterial surrogates was evaluated in a pilot scale dryer to validate the microbial reductions simulating an industrial drying process. These experiments fill in the missing information of the decontamination efficiency of hot-air drying process, providing insights on critical processing parameters and conditions needed to reach sufficient microbial reductions on dried herbs.
Section snippets
Bacterial strains and inoculum preparation
Five foodborne pathogens were used in the present study. Salmonella Senftenberg 775W (ATCC 43845) and Salmonella Enteritidis PT 30 (ATCC BAA-1045) were selected for their significant thermal resistance (Rachon, Peñaloza, & Gibbs, 2016). Salmonella Thompson RM1987 was isolated from a cilantro outbreak, kindly provided by Dr. Maria Brandl (ARS USDA). Listeria monocytogenes 4b (LMG 23194) was obtained from the LMG culture collection (Laboratory of Microbiology, Department of Biochemistry and
Thermal resistance of bacterial strains on basil leaves at constant water activity
The thermal resistance of S. Thompson, S. Senftenberg, S. Enteritidis PT 30, L. monocytogenes, E.coli O157:H7 and three surrogates E.coli P1, L. innocua, E. faecium on fresh basil leaves (aw 0.99) were compared at 60 °C in a warm water bath (Fig. 2). Product reached a temperature of 60 °C within 2 min of the treatments. S. Thompson and L. monocytogenes were the most sensitive pathogenic strains tested. After a 5 min treatment at 60 °C, more than 4-log average reductions were reached for both
Discussion
With increasing concerns on the microbial safety of dried herbs, this study represents an attempt to investigate the decontamination of common foodborne pathogens and their surrogates on basil during hot-air drying by characterizing the thermal resistance of strains in aw-adjusted herbs and collecting inactivation data generated under various drying processes. Considering that no specific safe processing harbors have been established for the decontamination of most plant-based products (Peng et
Conclusion
In summary, the decontamination efficiency of hot-air drying against bacterial strains on herbs is reported for the first time in a comprehensive way in the present study. With critical processing temperature and product moisture content defined, hot-air drying at > 60 °C was shown to sufficiently (>4-log reduction) inactivate Salmonella on basil leaves and the inactivation was most significant at the beginning of drying. Compared to the commonly used E. faecium, E. coli P1 showed to be a more
CRediT authorship contribution statement
Zijin Zhou: Methodology, Investigation, Visualization, Writing - original draft. Sophie Zuber: Conceptualization, Writing - review & editing, Project administration. Matteo Campagnoli: Conceptualization, Resources. Mireille Moser: Visualization, Software. Frank Devlieghere: Conceptualization, Supervision. Mieke Uyttendaele: Conceptualization, Writing - review & editing, Supervision.
Acknowledgement
We thank Nicolas Meneses and the Buhler Group for providing the pilot scale dryer and their help during this project. We also express our gratitude to Thierry Putallaz, Severien Malfait and Alana Antierens for helping with the microbial analysis.
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