Next Article in Journal
Volume and Distribution of Periprosthetic Bone Cysts in the Distal Tibia and Talus before Early Revision of Total Ankle Arthroplasty
Next Article in Special Issue
Salvia Species as Nutraceuticals: Focus on Antioxidant, Antidiabetic and Anti-Obesity Properties
Previous Article in Journal
Evaluation of Reinforcement and Deep Learning Algorithms in Controlling Unmanned Aerial Vehicles
Previous Article in Special Issue
Transcriptome Analysis of Egg Yolk Sialoglycoprotein on Osteogenic Activity in MC3T3-E1 Cells
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Microbiological Contamination in Different Food Service Units Associated with Food Handling

1
Superior School of Health of Bragança, Polytechnic Institute of Bragança (IPB), 5300-121 Bragança, Portugal
2
Mountain Research Centre (CIMO), Polytechnic Institute of Bragança (IPB), 5300-253 Bragança, Portugal
3
Public Health Laboratory of Bragança, Local Health Unit of the Northeast (ULSNE), 5300-146 Bragança, Portugal
4
LAQV-REQUIMTE, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal
5
EPIUnit—Instituto de Saúde Pública, Universidade do Porto, 4050-600 Porto, Portugal
*
Author to whom correspondence should be addressed.
Appl. Sci. 2021, 11(16), 7241; https://doi.org/10.3390/app11167241
Submission received: 29 June 2021 / Revised: 1 August 2021 / Accepted: 3 August 2021 / Published: 6 August 2021

Abstract

:
Background: A microbiological analysis of samples taken from hands of food handlers and utensils/crockery in food service units was used to assess the risk of food contamination. We aimed to assess indicators of microbiological contamination in different food service units. Methods: We used data for an official inspection proposal (2018–2019) in different food service units serving a district in Northeast Portugal. We showed the proportion of positive samples for each microorganism assessed in samples taken from hands and kitchen utensils/crockery. Results: Out of 471 samples taken from hands of food handlers, 26.8% (n = 126) were classified as “unsatisfactory” due to the presence of at least Escherichia coli, Staphylococcus aureus and/or total and fecal coliforms. Such a proportion varied according to the type of food service unit with a higher proportion being observed in Canteens (40.0%) and in Retirement Home/Day Care Centers (37.8%). More than one third of 649 samples taken from kitchen utensils/crockery were classified as “unsatisfactory” (n = 181; 27.9%) or “bad” (n = 49; 7.6%). There were significant differences in these proportions across food service units, with a higher proportion of “unsatisfactory” samples being observed in Fishmongers and Butcher Shops/Charcuteries (50.0% and 45.1%, respectively), while a higher proportion of “bad” samples was observed in both Pastry/Bakery and Fishmonger establishments (33.3%), followed by Butcher Shops/Charcuteries (14.1%). Conclusions: Our results emphasize the need of awareness of hygiene practices among food handlers of different food service units, particularly in Fishmongers, Pastry/Bakery establishments and Butcher Shops/Charcuteries, highlighting the need of a periodic hygienic evaluation.

Graphical Abstract

1. Introduction

Over the centuries, although they remain underreported and their incidence unknown, foodborne diseases are the ones that most affect the human population. These diseases are due to several microorganisms which are influenced by climate change, changes in food technology, social, economic and demographic habits, as well as the globalization of the food trade [1]. According to the World Health Organization (WHO), foodborne diseases cause 600 million cases and 420,000 deaths annually and the most frequent causes of foodborne illness were diarrheal disease agents [2]. There has been an increasing concern about food quality and safety in order to prevent foodborne diseases. Therefore, the surveillance of products provided by food service units has been an emergent issue in the field of public health.
Microbiological contamination is one of the major challenges when food safety is under discussion. Indeed, the majority of foodborne illnesses has been associated with bacterial contaminants [3,4]. Certain groups, such as elderly, young children, pregnant women or immuno-compromised people, have a high risk of having food-related diseases that can lead to death, by pathogen mechanisms that take advantage of a weak immune system [2,3].
Some foodborne illnesses due to microbiological contamination are associated with poor handling practices during meal processing in food units or food service establishments [5]. Poor hygiene conditions to which food is exposed during processing, storage and distribution contribute to increasing foodborne risk [3]. In addition, cross-contamination is one of the main factors associated with microbiological food contamination before the final preparation step [3,5]. Cross-contamination due to the transfer of microorganisms from objects or surfaces to the food is an important issue. Indeed, a pathogenic microorganism can remain viable in cutting boards and food contact surfaces [6,7,8] demanding the rigorous cleaning and disinfection of kitchen utensils, equipment and surfaces [9,10]. Hands of food handlers have also been considered an important determinant of microbiological contamination of food and washing hands plays a valuable role in preventing the transmission of foodborne illnesses [4,11,12]. Staphylococcus aureus colonizes the nasopharynx of asymptomatic carriers leading to the contamination of the hands of food handlers [13,14]. Antimicrobial resistant strains of S. aureus have been detected in food [12,15,16] and foodborne outbreaks of S. aureus have been related with post-process food contamination by the hands of food handlers [17].
The increasing concern about food safety and food quality demands the compulsory implementation of hygiene procedures to control the microbiological contamination of food in food units and food service establishments. The European Union (EU) has adopted a regulation for improving the quality of food [18]. The training of all those involved in the preparation, processing and distribution of food in order to prevent the incorrect handling and, consequently, the spread of food-borne diseases is fundamental to the application of good food handling practices [5]. However, monitoring the hygienic conditions of food service units is an excellent tool to know if food handlers in food establishments or food units comply with hygiene procedures and to understand which food establishments deserve special attention from public health authorities [18,19,20].
Hygienic conditions are assessed by the index of total and fecal coliforms, belonging to the Enterobacteriaceae family, which are usually found in the intestinal tract of humans and other warm-blooded animals. The presence of fecal coliforms is an indicator of fecal contamination allowing to assess poor hygienic sanitary conditions. Fecal coliforms do not indicate a health risk, but are a premise for the possible existence of other microorganisms considered dangerous for consumer health [21,22,23]. Bacteria belonging to the Enterobacteriaceae family are the main agents of intestinal infection, standing out as the most interesting microorganism in food Escherichia coli. Food associated outbreaks have been particularly associated with verocytotoxin producing E. coli (VTEC), which the strain O157:(H7) has been recognized as a very important cause of food-borne illness [22,23]. This bacterial species is one of the most important indicators of fecal contamination of meat products, vegetables, fruits, juices, milk, drinking water [22,23], as well as fecally contaminated hands of food-handlers [21].
The presence of a large microbial population responsible for food contamination has been assessed by the counts of mesophilic aerobic bacteria (colonies growing at 30 °C). Although there is no distinction between pathogenic microorganisms and microorganisms causing changes in food, the determination of mesophilic aerobic bacteria gives a general indication of the contamination of food or utensils used during storage or processing [8,24]. Therefore, the aerobic mesophilic bacteria, total and fecal coliforms, E. coli and S. aureus have been considered as microbial indicators and have been used for the assessment of a poor hygienic and sanitary food quality [4].
In Portugal, there are public health units working at a local level and they are constituted by the public health doctoral and sanitary staff. These teams are responsible for tasks related with public health surveillance [25]. One of these tasks is the inspection of food units for the assessment of the hygiene status of hands of food handlers and surfaces. By using data collected for official inspection purposes, we aim to evaluate the hygiene level of different food services units serving a district in Northeast Portugal. The main reason for carrying out this type of assessment in food units is to minimize the risk of microbial contamination associated with food unities, leading to an intervention by public health units whenever the results are not satisfactory. This intervention is based on official Portuguese regulations [26] and European laws [27].

2. Materials and Methods

2.1. Study Setting and Data Collection

This is a descriptive study based on data collected between January 2018 and December 2019 for audit proposal in regard to the hygiene and safety in food service units, aiming specifically at the assessment of hygiene status of hands of food handlers and surfaces. Data collection was carried out by Environmental Health Technicians from a Public Health Unity serving a district in Northeast Portugal. Technicians went to different food service units in this geographic area for collecting samples from the hands of the food handlers and from kitchen utensils and crockery used in food handling. Samples were taken by using swabs moistened with tryptone saline solution and placed at 30° angle with the surface from which the sample should be taken.
The microbiological analyses were carried out in Public Health Laboratory (PHL) by microbiological techniques using appropriate culture media for plate counts of coliforms, E. coli, S. aureus and mesophilic microorganisms at 30 °C, in accordance with the sanitary surveillance program at regional level, proposed by the local public health authorities. Out of all samples collected during the time period studied, samples from cheese factory (n = 6) were excluded because there were few to be analyzed according to the type of food service unit. The data analyzed correspond to 1120 samples taken from the surface of the hands of the food handlers (n = 471) and from utensils/crockery used in food handling (n = 649).

2.2. Microbiological Parameters Assessed

In regard to the samples taken from kitchen utensils/crockery, the microbiological parameters of interest were the number of colony forming units (CFU) of mesophilic microorganisms per swab/plate and the presence (positive sample that means 1 CFU or more) of total coliforms, fecal coliforms, E. coli, using an adapted method previously described [26]. In regard to the number of CFUs of mesophilic microorganisms, samples were classified into three groups (<100, 100–999 and ≥1000 CFUs) while the presence of coliform bacteria and E. coli allowed to classify the samples as positive (at least 1 CFU). Briefly, for total coliforms, fecal coliforms and E. coli evaluation, samples were cultured in MacConkey broth and incubated at 37 °C/48 h. Next, bacterial suspensions were inoculated in Brilliant Green Bile medium (2%) at 37 °C and 44 °C/48 h, and Buffered Peptone Water medium at 44 °C/48 h, followed by indole detection.
The microbiological parameters of interest in samples taken from the hands of food handlers were the presence (positive sample that means 1 CFU or more) of total coliforms, fecal coliforms, E. coli and S. aureus according to an adapted procedure described before [26]. For total and fecal bacteria, as well as E. coli, samples were cultured in MacConkey broth and incubated at 37 °C/48 h, followed by incubation in Brilliant Green Bile medium (2%) at 37 °C and 44 °C/48 h, and Buffered Peptone Water medium at 44 °C/48 h and indole detection. For S. aureus determination, the samples were inoculated in Mannitol Salt Agar at 37 °C/48 h and bacteria suspension was tested for coagulase positivity [28,29].
The hygiene status of kitchen utensils/crockery was classified as “satisfactory” if there were less than 100 CFU of mesophilic microorganisms at 30 °C per swab/plate [26] and the detection of coliforms was negative; as “unsatisfactory” if the number of CFU at 30 °C was greater than 100 per swab/plate or if the presence of total coliforms was positive; as “bad” if the detection of fecal coliforms or E. coli was positive [28,29]. The hygiene status of the hands of food handlers was considered “unsatisfactory” if there was sample positivity for at least one type of microorganisms assessed and “satisfactory” otherwise.

2.3. Data Processing

The data obtained were processed using Microsoft Office Excel (Microsoft Office 365 Pro PLUS). We obtained the proportion (%) of “unsatisfactory” samples among the total of samples taken from hands of food handlers and of “unsatisfactory” and “bad” samples among the total of samples taken from kitchen utensils/crockery. Among samples taken from hands, the proportion of positive samples for total coliforms, fecal coliforms, E. coli and S. aureus were computed. The samples taken from kitchen utensils/crockery were classified according to the number of mesophilic microorganisms at 30 °C per swab/plate into less than 100, 100–999 and 1000 CFUs or more and the proportion of samples in each group was obtained. We also computed the proportion of samples taken from kitchen utensils/crockery that were positive for total coliforms, fecal coliforms and E. coli.
All results were stratified according to the type of food service categorized into the following groups: Canteen, School/Kindergarten, Retirement Home/Day Care Center, Pastry/Bakery establishment, Fishmonger, Restaurant/Coffee Shop/Snack Bar, Supermarket/Grocery Store and Butcher Shop/Charcuterie. Differences between the type of food service units in regard to the microbiological parameters were assessed by using the qui-square test (χ2) or the likelihood-ratio chi-square test (LR) when the expected value of the number of sample observations in each group of the variable was less than five. The significance level was set at 0.05.

3. Results

Table 1 shows the distribution of samples taken from hands of food handlers and from crockery/utensils according to the type of food service, as well as, the proportion of samples classified as “unsatisfactory” and “bad”. There were 1120 samples analyzed, the majority of them were obtained from Restaurants/Coffee Shops/Snack Bars (n = 457), followed by Retirement Homes/Day Care Centers (n = 248), Butcher Shops/Charcuteries (n = 141), Schools/Kindergartens (n = 131), Supermarkets/Grocery Stores (n = 53), Pastry/Bakery establishments (n = 41), Fishmongers (n = 26) and Canteens (n = 23).
Out of 471 samples taken from hands of food handlers, 26.8% (n = 126) were classified as “unsatisfactory” due to the presence of at least one type of the microorganisms assessed. Such proportion varied according to the type of food service unit from 11.5% in Supermarket/Grocery Stores to 40.0% in Canteens (χ2 = 15.94; p = 0.026). Instead, more than one third of 649 samples taken from kitchen utensils/crockery were classified as “unsatisfactory” (n = 181; 27.9%) or “bad” (n = 49; 7.6%). There were significant differences in this proportion across food service units (LR = 65.01; p < 0.001), such that the proportion of “unsatisfactory” samples was higher in Fishmongers and Butcher Shops/Charcuteries (50.0% and 45.1%, respectively), while a higher proportion of “bad” samples was observed in both Pastry/Bakery and Fishmonger establishments (33.3%), followed by Butcher Shops/Charcuteries (14.1%) (Table 1).
Of all samples taken from kitchen utensils/crockery, 14.0% (n = 91), 7.4% (n = 48) and 2.9% (n = 19) were positive samples for total coliforms, fecal coliforms and E. coli, respectively. Figure 1 presents the proportion of samples taken from kitchen utensils/crockery, presenting one CFU or more of total coliforms, fecal coliforms or E. coli, according to the type of food service unit (samples could be positive for all microorganisms assessed). There were significant differences in the frequency of positive samples for total coliforms, varying from 7.8% in Canteens to 50% in Fishmonger establishments (LR = 28.29, p < 0.001), for fecal coliforms varying from 2.8% in Restaurants/Coffee Shops/Snack Bars to 33.3% in Pastry/Bakery and Fishmonger establishments (LR = 35.57, p < 0.001) and for E. coli varying from 0.0% in Schools/Kindergartens and Supermarket/Grocery Stores to 25.0% in Fishmonger establishments (LR = 24.90, p < 0.001).
Figure 2 presents the proportion of samples taken from kitchen utensils/crockery, presenting less than 100 CFUs, 100–999 CFUS and 1000 or more CFUs of mesophilic microorganisms at 30 °C per swab/plate according to the food service unit. Concerning this parameter, 17% (n = 109) of samples taken from kitchen utensils/crockery presented between 100 and 999 CFUs and the same proportion of samples presented 1000 or more CFUs. The higher proportion of samples presenting 1000 or more CFUs of mesophilic microorganisms were observed in Fishmonger establishments (75.0%; n = 9), Butcher Shops/Charcuteries (41.0%; n = 29) and Supermarket/Grocery Stores (37.0%; n = 10). Otherwise, the results showed that a higher proportion of samples with the lowest level of mesophilic microorganisms (<100 CFU/utensil) were harvested in Schools/Kindergartens (76.7%), followed by Restaurants/Coffee Shops/Snack Bars (72.7%), Retirement Homes/Day Care Centers (71.4%) and Canteens (69.2%).
In regard to the samples taken from hands of food handlers, there were 21.2% (n = 100), 11.5% (n = 54), 8.9% (n = 42) and 3.6% (n = 17) of positive samples for total coliforms, fecal coliforms, S. aureus and E. coli, respectively. Figure 3 presents the proportion of positive samples taken from hands according to the type of food service unit. There were significant differences in the frequency of positive samples for total coliforms, varying from 7.7% in Supermarket/Grocery Stores to 40% in Canteens (LR = 21.64, p = 0.003) and for fecal coliforms varying from 0.0% in Supermarket/Grocery Stores to 20.0% in Canteens (LR = 20.46, p = 0.005). Positive samples for E. coli were observed in Schools/Kindergartens (n = 2; 3.4%), Retirement Homes/Day Care Centers (n = 7; 6.9%) and Restaurants/Coffee Shops/Snack Bars (n = 8; 4.6%).

4. Discussion

This analysis was based on data collected for official inspection proposal in order to assess the hygiene level of food service units based on the detection of microbial indicators. According to our results, there were differences in the hygienic level according to the type of food services. Fishmongers, Butcher Shops/Charcuteries and Pastry/Bakery Shops presented the worst profiles in regard to the microorganisms control in utensils/crockery. Instead, among samples taken from hands of food handlers, a higher proportion of “unsatisfactory” samples were observed in Canteens and Retirement Homes/Day Care Centers.
Since animals slaughtered for human consumption are reservoirs of microorganisms [4,30], presenting a high load in the digestive tract, the evisecretion has been associated with contamination of carcasses and cuts of sheep, cattle and poultry that will be butchered [30,31,32]. In addition, it has been described that Butcher Shop operators often used the same chopping board and knife to split different kinds of meat, increasing the bacterial count during this food preparation process [33]. Thus, the butchering process of contaminated carcasses and cuts of animals is likely to contaminate the utensils used for butchering [6]. Additionally, fish used for human consumption can harbor several pathogenic microorganisms [34]. Therefore, the evisecretion and preparation of fish for sale in Fishmongers can be a strong determinant of microbiological contamination of utensils used in this process. Additionally, Fishmongers require the use of utensils that contact directly with the food, during the scaling and/or evisecretion of the fish [35]. These issues could explain the high proportion of “unsatisfactory” and “bad” samples taken from utensils used in Fishmongers and Butcher Shops/Charcuteries we observed in our setting.
Our results also revealed a worrisome proportion of samples taken from utensils/crockery in Pastry/Bakery establishments classified as “bad” (33%). Because Pastry/Bakery establishments usually serve ready-to-eat foods such as sandwiches, which are not exposed to a high temperature before consumption, our findings posed added concerns in regard to the microbiological quality of these foods. Indeed, foodborne pathogens have been detected in sandwiches pastries and desserts partially explained due to the cross-contamination and mishandling during the food preparation [36].
According to our findings, a higher proportion of positive samples for E. coli, fecal and total coliforms were taken from utensils/crockery in Fishmongers, Pastry/Bakery and Butchery/Charcuterie establishments. The coliform group is part of the family of Enterobacteriaceae which includes microorganisms sensitive to heat treatment [4] and that are usually destroyed by most disinfectant agents used in food production for the cleaning of surfaces and equipment [37]. In this sense, the food units with a high proportion of samples taken from utensils/crockery that were positive for fecal coliforms and/or E. coli reflect poor hygiene conditions.
Our data also revealed that Canteens and Retirement Homes/Day Care Centers had a high proportion of samples taken from hands of food handlers classified as “unsatisfactory”, denoting less adherence to handwashing practices. Indeed, it has been reported that a reduction occurs in counts of Enterobacteriaceae, including E. coli after hand washing, particularly when food handlers use antimicrobial hand soap [11,20]. Additionally, the evaluation of hygienic patterns of the hands of manipulators in different food units also showed that more than 10% of positive samples for S. aureus were found in Fishmongers (14.3%), Schools/Kindergartens (12.1%) and Pastry/Bakery establishments (11.8%). This should be considered worrisome because in Fishmonger and Pastry/Bakery establishments there is a great need for the manipulation of food, exposing it more easily to microbial agents present on the hands [14,35].
Otherwise, our results showed that Schools/Kindergartens, Restaurants/Coffee Shops/Snack Bars, Retirement Homes/Day Care Centers and Canteens presented a low level of mesophilic microorganisms (<100 CFU/utensil). It is possible that these food units are more prone to comply with guidelines to control poor surface hygiene, cross-contamination, insufficient heat treatment and the regulation of the time/temperature of food storage [26]. It is important to highlight that inadequate cooking, cross-contamination and inadequate storage contribute to the foodborne disease burden when foods are contaminated before the final preparation step [5]. Our results also emphasized that Schools/Kindergartens have patterns of good hygiene practices associated with utensils, supported by the absence of E. coli and the highest proportion of samples with mesophilic microorganisms below 100 CFUs. A recent study reported that appropriate food hygiene interventions among child caregivers of weaning infants, focused on safe hand hygiene, safe food preparation and storage, as well as safe feeding, can reduce foodborne exposure to enteric pathogens [38].
The classification of samples taken from utensils/crockery as “unsatisfactory” or “bad” was based on a positivity for the coliforms bacterial group and a high load of mesophilic microorganisms (>100 UFC). According to this classification, Fishmongers, Butcher Shops/Charcuteries and Pastry/Bakery establishments were the food unities with a higher risk of contamination and, therefore, foodborne diseases are more likely to be associated with these food units.
There is a body of research highlighting the association between bacterial counts in utensils and hands during the process of food preparation and the microbiological contamination of food. It has been reported that an increase in bacterial count occurs in meat samples when Butcher Shop operators use the same chopping board and knife to split different kinds of meat [32,33]. In addition, the evisecretion and preparation of fish for sale in Fishmongers can be a strong determinant of microbiological contamination of fish [35]. Moreover, foodborne pathogens detected in sandwiches, pastries and desserts are due to cross-contamination and mishandling during the food preparation [36]. However, to the best of our knowledge, there is no published studies based on the same classification of samples we used, preventing comparisons with previous research.
There is a lack of data about the hygiene practices in food units included in this study, namely the hygiene behavior of the staff and compliance with appropriate cleaning procedures. Data about these issues could give insights about hygiene practices in order to change guidelines and to design training aimed at the hygiene practices among food handlers. Although this limitation, the results here reported provide information on the hygienic status in different food units and, to the best of our knowledge, there is no published studies based on data collected by public health authorities for the assessment of the health status in different types of food units. Based on such information, health authorities can implement strategies to sensitize workers about good hygienic practices in the food sector, in order to prevent possible food outbreaks and to minimize the onset of foodborne diseases [18]. Our results alert the health authorities in regards to some type of food units where it is important to improve training of staff to ensure food safety. In accordance with the legislation, the results were still far from what was desired, although periodic analyses were carried out in samples taken from the hands of food handlers and the utensils used in food preparation [26].

5. Conclusions

Based on data collected for an official inspection proposal of food service units between 2018 and 2019 in different food service units serving a district in Northeast Portugal, we found that a high rate of contamination of utensils/crockery was observed in Fishmongers, Pastry/Bakery establishments and Butcher Shops/Charcuteries, while a high rate of “unsatisfactory” samples taken from hands of food handlers were observed in Canteens and Retirement Homes/Day Care Centers. Samples taken from utensils/crockery were positive for total coliforms, fecal coliforms, E. coli and colonies of mesophilic microorganisms.
The analysis of the data presented in this study emphasizes the need of awareness of hygiene practices among food handlers of different food service units, particularly in Fishmongers, Pastry/Bakery establishments and Butcher Shops/Charcuteries. The design of training for staff adapted to each type of food unit seems be an important issue in improving food safety. These interventions should sensitize workers and inform them about the mandatory hygiene procedures such as frequent hand washing, the use of gloves or correct storage of kitchen utensils, to improve the hygiene status of these food units. In this sense, it would be important to carry out studies, particularly in food units where the results were worse, in order to verify if the implemented actions by the local public health entities were effective.

Author Contributions

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

Funding

This study received no external research funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by Ethics Committe of the Unidade Local de Saúde do Nordeste (number 27/2020, at 24-09-2020).

Informed Consent Statement

The patient’s consent was waived because data was collected during official inspection of food service units. Researchers received anonymized data, there is no way of identifying these food service units.

Data Availability Statement

Data isn’t publicly available. Data is available only for research purpose restricting access to authorized researchers.

Acknowledgments

The Public Health Laboratory in Northeast Portugal (PHLNP) is thanked for having provided the data collected for the study.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Viegas, S. Alterações do Estado de Saúde Associadas à Alimentação—Contaminação Microbiológica dos Alimentos. 2010. Available online: http://hdl.handle.net/10400.18/143 (accessed on 18 June 2021).
  2. WHO. WHO Estimates of the Global Burden of Foodborne Diseases: Executive Summary. WHO Executive Summary, 257. 2015. Available online: http://www.who.int/foodsafety/publications/foodborne_disease/fergreport/en/ (accessed on 18 June 2021).
  3. Fung, F.; Wang, H.-S.; Menon, S. Food safety in the 21st century. Biomed. J. 2018, 41, 88–95. [Google Scholar] [CrossRef] [PubMed]
  4. Valero, A.; Rodríguez, M.-Y.; Posada-Izquierdo, G.D.; Pérez-Rodríguez, F.; Carrasco, E.; García-Gimeno, R.M. Risk Factors Influencing Microbial Contamination in Food Service Centers. In Significance, Prevention and Control of Food Related Diseases; IntechOpen Limited: London, UK, 2016; Available online: https://dx.doi.org/10.5772/63029 (accessed on 18 June 2021).
  5. Augustin, J.-C.; Kooh, P.; Bayeux, T.; Guillier, L.; Meyer, T.; Silva, N.J.-D.; Villena, I.; Sanaa, M.; Cerf, O.; on Behalf of the Anses Working Group on Consumer Information on Foodborne Biological Risks. Contribution of Foods and Poor Food-Handling Practices to the Burden of Foodborne Infectious Diseases in France. Foods 2020, 9, 1644. [Google Scholar] [CrossRef] [PubMed]
  6. Dantas, S.T.A.; Rossi, B.F.; Bonsaglia, E.C.R.; Castilho, I.G.; Hernandes, R.T.; Fernandes, A.; Rall, V.L.M.; Júnior, A.F. Cross-Contamination and Biofilm Formation by Salmonella enterica Serovar Enteritidis on Various Cutting Boards. Foodborne Pathog. Dis. 2018, 15, 81–85. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Tang, J.Y.H.; Nishibuchi, M.; Nakaguchi, Y.; Ghazali, F.M.; Saleha, A.A.; Son, R. Transfer of Campylobacter jejuni from raw to cooked chicken via wood and plastic cutting boards. Lett. Appl. Microbiol. 2011, 52, 581–588. [Google Scholar] [CrossRef] [PubMed]
  8. Garayoa, R.; Abundancia, C.; Díez-Leturia, M.; Vitas, A.I. Essential tools for food safety surveillance in catering services: On-site inspections and control of high risk cross-contamination surfaces. Food Control 2017, 75, 48–54. [Google Scholar] [CrossRef]
  9. Byrd-Bredbenner, C.; Berning, J.; Martin-Biggers, J.; Quick, V. Food Safety in Home Kitchens: A Synthesis of the Literature. Int. J. Environ. Res. Public Health 2013, 10, 4060–4085. [Google Scholar] [CrossRef] [Green Version]
  10. Cardoso, M.J.; Ferreira, V.; Truninger, M.; Maia, R.; Teixeira, P. Cross-contamination events of Campylobacter spp. in domestic kitchens associated with consumer handling practices of raw poultry. Int. J. Food Microbiol. 2021, 338, 108984. [Google Scholar] [CrossRef]
  11. Adhikari, U.; Esfahanian, E.; Mitchell, J.; Charbonneau, D.; Song, X.; Lu, Y. Quantitation of Risk Reduction of E. coli Transmission after Using Antimicrobial Hand Soap. Pathogens 2020, 9, 778. [Google Scholar] [CrossRef]
  12. Yap, M.; Chau, M.L.; Hartantyo, S.H.P.; Oh, J.Q.; Aung, K.T.; Gutiérrez, R.A.; Ng, L.C. Microbial Quality and Safety of Sushi Prepared with Gloved or Bare Hands: Food Handlers’ Impact on Retail Food Hygiene and Safety. J. Food Prot. 2019, 82, 615–622. [Google Scholar] [CrossRef]
  13. Ho, J.; Boost, M.; O’Donoghue, M. Sustainable reduction of nasal colonization and hand contamination with Staphylococcus aureus in food handlers, 2002–2011. Epidemiol. Infect. 2015, 143, 1751–1760. [Google Scholar] [CrossRef]
  14. Castro, A.; Santos, C.; Meireles, H.; Silva, J.; Teixeira, P. Food handlers as potential sources of dissemination of virulent strains of Staphylococcus aureus in the community. J. Infect. Public Health 2016, 9, 153–160. [Google Scholar] [CrossRef] [Green Version]
  15. Mahros, M.A.; Abd-Elghany, S.M.; Sallam, K.I. Multidrug-, methicillin-, and vancomycin-resistant Staphylococcus aureus isolated from ready-to-eat meat sandwiches: An ongoing food and public health concern. Int. J. Food Microbiol. 2021, 346, 109165. [Google Scholar] [CrossRef]
  16. Kroning, I.S.; Iglesias, M.A.; Sehn, C.P.; Valente Gandra, T.K.; Mata, M.M.; da Silva, W.P. Staphylococcus aureus isolated from handmade sweets: Biofilm formation, enterotoxigenicity and antimicrobial resistance. Food Microbiol. 2016, 58, 105–111. [Google Scholar] [CrossRef] [PubMed]
  17. Bennett, S.D.; Walsh, K.A.; Gould, L.H. Foodborne disease outbreaks caused by Bacillus cereus, Clostridium perfringens, and Staphylococcus aureus—United States, 1998–2008. Clin. Infect. Dis. Off. Publ. Infect. Dis. Soc. Am. 2013, 57, 425–433. [Google Scholar] [CrossRef]
  18. European Parliament and Council. Regulation (EC) No 852/2004 of the European Parliament and of the Council of 29 April 2004. On the Hygiene of Foodstuffs. Available online: https://eur-lex.europa.eu/eli/reg/2004/852/oj (accessed on 20 July 2021).
  19. Osimani, A.; Aquilanti, L.; Tavoletti, S.; Clementi, F. Evaluation of the HACCP System in a University Canteen: Microbiological Monitoring and Internal Auditing as Verification Tools. Int. J. Environ. Res. Public Health 2013, 10, 1572–1585. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Duthoo, E.; Krings, S.; Daube, G.; Leroy, F.; Taminiau, B.; Heyndrickx, M.; De Reu, K. Monitoring of Hygiene in Institutional Kitchens in Belgium. J. Food Prot. 2020, 83, 305–314. [Google Scholar] [CrossRef]
  21. Atnafie, B.; Paulos, D.; Abera, M.; Tefera, G.; Hailu, D.; Kasaye, S.; Amenu, K. Occurrence of Escherichia coli O157:H7 in cattle feces and contamination of carcass and various contact surfaces in abattoir and butcher shops of Hawassa, Ethiopia. BMC Microbiol. 2017, 17, 24. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Newell, D.G.; Koopmans, M.; Verhoef, L.; Duizer, E.; Aidara-Kane, A.; Sprong, H.; Opsteegh, M.; Langelaar, M.; Threfall, J.; Scheutz, F.; et al. Food-borne diseases—The challenges of 20years ago still persist while new ones continue to emerge. Int. J. Food Microbiol. 2010, 139, S3–S15. [Google Scholar] [CrossRef]
  23. Wilson, D.; Dolan, G.; Aird, H.; Sorrell, S.; Dallman, T.J.; Jenkins, C.; Robertson, L.; Gorton, R. Farm-to-fork investigation of an outbreak of Shiga toxin-producing Escherichia coli O157. Microb. Genom. 2018, 4, e000160. [Google Scholar] [CrossRef]
  24. Gil, A.I.; Lanata, C.F.; Hartinger, S.M.; Mäusezahl, D.; Padilla, B.; Ochoa, T.J.; Lozada, M.; Pineda, I.; Verastegui, H. Fecal contamination of food, water, hands, and kitchen utensils at the household level in rural areas of Peru. J. Environ. Health 2014, 76, 102. [Google Scholar]
  25. Simões, J.A.; Augusto, G.F.; Fronteira, I.; Hernández-Quevedo, C. Portugal: Health system review. Health Syst. Transit. 2017, 19, 1–184. Available online: https://www.euro.who.int/__data/assets/pdf_file/0007/337471/HiT-Portugal.pdf (accessed on 30 July 2021).
  26. INSA. Interpretação de Resultados de Ensaios Microbiológicos em Alimentos Prontos Para Consumo e em Superfícies do Ambiente de Preparação e Distribuição Alimentar: Valores Guia; INSA: Lisboa, Portugal, 2019. [Google Scholar]
  27. European Parliament and Council. Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002. Laying down the General Principles and Requirements of Food Law, Establishing the European Food Safety Authority and Laying down Procedures in Matters of Food Safety. Available online: https://eur-lex.europa.eu/eli/reg/2002/178/oj (accessed on 20 July 2021).
  28. INSA. Monitorização do Estado Higiénico de Louças e Talheres em Contacto com Alimentos; INSA: Porto, Portugal, 2001. [Google Scholar]
  29. INSA. Monitorização do Estado Higiénico de Mãos e Mãos com Luvas; INSA: Porto, Portugal, 2001. [Google Scholar]
  30. Rouger, A.; Tresse, O.; Zagorec, M. Bacterial Contaminants of Poultry Meat: Sources, Species, and Dynamics. Microorganisms 2017, 5, 50. [Google Scholar] [CrossRef] [PubMed]
  31. Salmela, S.P.; Fredriksson-Ahomaa, M.; Hatakka, M.; Nevas, M. Microbiological contamination of sheep carcases in Finland by excision and swabbing sampling. Food Control 2013, 31, 372–378. [Google Scholar] [CrossRef]
  32. Bakhtiary, F.; Sayevand, H.R.; Remely, M.; Hippe, B.; Hosseini, H.; Haslberger, A.G. Evaluation of Bacterial Contamination Sources in Meat Production Line. J. Food Qual. 2016, 39, 750–756. [Google Scholar] [CrossRef]
  33. Wang, S.; Fu, L.; Chen, G.; Xiao, H.; Pan, D.; Shi, R.; Yang, L.; Sun, G. Multisite survey of bacterial contamination in ready-to-eat meat products throughout the cooking and selling processes in urban supermarket, Nanjing, China. Food Sci. Nutr. 2020, 8, 2427–2435. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Novoslavskij, A.; Terentjeva, M.; Eizenberga, I.; Valciņa, O.; Bartkevičs, V.; Bērziņš, A. Major foodborne pathogens in fish and fish products: A review. Ann. Microbiol. 2016, 66, 1–15. [Google Scholar] [CrossRef]
  35. Kalimuddin, S.; Chen, S.; Lim, C.T.K.; Koh, T.H.; Tan, T.Y.; Kam, M.; Wong, C.W.; Mehershahi, K.S.; Chau, M.L.; Ng, L.C.; et al. 2015 Epidemic of Severe Streptococcus agalactiae Sequence Type 283 Infections in Singapore Associated with the Consumption of Raw Freshwater Fish: A Detailed Analysis of Clinical, Epidemiological, and Bacterial Sequencing Data. Clin. Infect. Dis. 2017, 64, S145–S152. [Google Scholar] [CrossRef] [Green Version]
  36. Kotzekidou, P. Microbiological examination of ready-to-eat foods and ready-to-bake frozen pastries from university canteens. Food Microbiol. 2013, 34, 337–343. [Google Scholar] [CrossRef]
  37. Sato, Y.; Ishihara, M.; Nakamura, S.; Fukuda, K.; Kuwabara, M.; Takayama, T.; Hiruma, S.; Murakami, K.; Fujita, M.; Yokoe, H. Comparison of Various Disinfectants on Bactericidal Activity Under Organic Matter Contaminated Environments. Biocontrol Sci. 2019, 24, 103–108. [Google Scholar] [CrossRef] [Green Version]
  38. Mumma, J.; Simiyu, S.; Aseyo, E.; Anderson, J.; Czerniewska, A.; Allen, E.; Dreibelbis, R.; Baker, K.K.; Cumming, O. The Safe Start trial to assess the effect of an infant hygiene intervention on enteric infections and diarrhoea in low-income informal neighbourhoods of Kisumu, Kenya: A study protocol for a cluster randomized controlled trial. BMC Infect. Dis. 2019, 19, 1066. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Proportion of positive samples for each group of microorganisms assessed in samples taken from kitchen utensils/crockery.
Figure 1. Proportion of positive samples for each group of microorganisms assessed in samples taken from kitchen utensils/crockery.
Applsci 11 07241 g001
Figure 2. Proportion of samples taken from kitchen utensils/crockery according to the number of CFUs of mesophilic microorganisms at 30 °C per swab/plate.
Figure 2. Proportion of samples taken from kitchen utensils/crockery according to the number of CFUs of mesophilic microorganisms at 30 °C per swab/plate.
Applsci 11 07241 g002
Figure 3. Proportion of positive samples for each group of microorganisms assessed in samples taken from hands of food handlers.
Figure 3. Proportion of positive samples for each group of microorganisms assessed in samples taken from hands of food handlers.
Applsci 11 07241 g003
Table 1. Distribution of samples taken from hands of food handlers and from crockery/utensils according to the type of food service.
Table 1. Distribution of samples taken from hands of food handlers and from crockery/utensils according to the type of food service.
Samples Taken from Kitchen Utensils/Crockery n = 649Samples Taken from Hands of Food Handlers n = 471
Type of Food ServiceTotal UnsatisfactoryBadp-ValueTotalUnsatisfactoryp-Value
n n (%)n (%) n n (%)
Canteen133 (23.1)1 (7.7)<0.001 *104 (40.0)0.026 ǂ
School/Kindergarten7317 (23.3)3 (4.1)5814 (24.1)
Retirement Home/Day Care Center14731 (21.1)13 (8.8)10138 (37.6)
Pastry/Bakery246 (25.0)8 (33.3)175 (29.4)
Fishmonger124 (50.0)6 (33.3)144 (28.6)
Restaurant/Coffee Shop/Snack Bar28275 (26.6)8 (2.8)17548 (27.4)
Supermarket/Grocery2711 (40.7)2 (7.4)263 (11.5)
Butcher Shop/Charcuterie7132 (45.1)10 (14.1)7010 (14.3)
* likelihood-ratio chi-square test; ǂ chi-square test.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Alves, A.; Viveiros, C.; Lopes, J.; Nogueira, A.; Pires, B.; Afonso, A.F.; Teixeira, C. Microbiological Contamination in Different Food Service Units Associated with Food Handling. Appl. Sci. 2021, 11, 7241. https://doi.org/10.3390/app11167241

AMA Style

Alves A, Viveiros C, Lopes J, Nogueira A, Pires B, Afonso AF, Teixeira C. Microbiological Contamination in Different Food Service Units Associated with Food Handling. Applied Sciences. 2021; 11(16):7241. https://doi.org/10.3390/app11167241

Chicago/Turabian Style

Alves, Ana, Cristina Viveiros, Jéssica Lopes, António Nogueira, Bruno Pires, Andrea F. Afonso, and Cristina Teixeira. 2021. "Microbiological Contamination in Different Food Service Units Associated with Food Handling" Applied Sciences 11, no. 16: 7241. https://doi.org/10.3390/app11167241

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