Investigation of Mass Catering Establishments in Shopping Centers of Istanbul Regarding the Food Safety and Critical Hygienic Criteria

Research Article

Austin J Nutri Food Sci. 12(2): 1181.

Investigation of Mass Catering Establishments in Shopping Centers of Istanbul Regarding the Food Safety and Critical Hygienic Criteria

Sinan Taskir¹; Esra Kurt Klont²*; Özer Ergün³

1BakirkÖy Province Directorate of Food, Agriculture and Livestock, Istanbul, Turkey

2Istanbul University, Faculty of Veterinary Medicine, Department of Food Hygiene and Technology, Istanbul, Turkey

3Istanbul Health and Technology University, Faculty of Health Sciences, Department of Nutrition and Dietetics, Istanbul, Turkey

*Corresponding author: Esra Kurt Klont, Istanbul University, Faculty of Veterinary Medicine, Department of Food Hygiene and Technology, Istanbul, Turkey. Email: esrakurt@hotmail.com

Received: October 25, 2024; Accepted: November 11, 2024 Published: November 18, 2024

Abstract

This study, conducted in 100 mass catering establishments in 10 shopping centers in Istanbul in terms of food safety and preservation of public health by using a control form, 200 audits were performed. Establishments were evaluated by the control form over 100 points in 5 categories as A (VERY GOOD), B (GOOD), C (MEDIUM), D (BAD), E (VERY BAD). 29% of the enterprises were evaluated as “A”, 52% as “B”, 18% as “C”, 1% as “D”. According to the results of establishments, shopping centers were evaluated as B (GOOD). Total polar compounds (%) of frying oil of 326 samples used in the establishments were measured and 95% found appropriate. In total 2,220 hygiene samples which are 1,000 from food contact surfaces (countertop, cutting board, chopping knife, knife and plate), 800 from the staff, 400 from air and 20 from water have been taken and analyzed. TMAB, coliform, E. coli were searched on surfaces, Staphylococcus aureus (S. Auerus), coliform, Escherichia coli (E. coli) in hands of the staff, enterococcus, coliform, E. coli in water and mold-yeast in air. 61% of the food contact surfaces, 44% of the staff, 87% of air samples, 100% of water samples were approved. Bacterial load was mostly found in chopping boards and knives-chopping knives. It has been detected that 72.8% of the staff who are working in the business have been trained in hygiene; however, it has been determined that the management systems of food security are not applied, records are not kept well, traceability is not provided properly and the controls of heat and moisture are not being made sufficiently.

Keywords: Shopping centers; Food security; Food control; Food companies; Hygiene

Introduction

Currently, more than half of the population of the developed counties, and one tenth of the population of our country eats at least one meal in places that supplies mass consumption s [13]. That is why food safety is composed of all measures taken to eliminate the physical, chemical, biological and any other damage that may arise from food, public health problems and food poisoning are increasingly gaining significance in all countries. One of the most important criteria for healthy nutrition is the production of foodstuffs under hygienic conditions and ensuring the consumption without deterioration in the hygiene chain [16]. Even a small negligence during the preparation, cooking, storing and service of food can negatively affect consumers' health which may lead to food poisoning and even deaths [33].

In this case study, samples were taken from the kitchen countertops, tools and equipment contacting with food, hands of personnel, air and water of the mass catering enterprises located in shopping malls in Istanbul province, with the purpose of determining the occupational hygiene and food safety. In Addition, the frying oils used in the operating kitchen are examined by the polar material measuring device and the risks that exist in the enterprises are determined clearly to protect consumer and public health.

Materials and Methods

Selection and Collection of Samples

In each enterprise samples were taken from 4 personnel, 5 food contact surfaces and 2 ambient air. The number of total samples received is 2,220 units formed of 800 units (4X100X2) from personnel, 1,000 units (5X100X2) from food contact surfaces, 400 units (2X100X2) from air and 20 units (1X10X2) from water. In Addition, a total of 326 pieces of frying oil samples used in the enterprises were analyzed. All samples received were delivered to the laboratory within 2 hours under cold chain conditions at 4 °C and analyzed on the same day.

Microbiological Analyses of Personnel Hand and Food Contact Surfaces Samples

Samples taken from personnel, surface and equipment (countertop surface, cutting board, chopper-knife, and ready-toserve plate) were collected in compliance with double swap (wet-dry swap) technique and ISO 18593:2004 standards [2,26,31]. Different dilutes were prepared from the test tubes which were delivered to the laboratory and kept in swap. Double-parallel inoculations were conducted in v feeding places and colonies were evaluated at the end of the incubation period for the determination of TAMB, coliform, E. coli and S. aureus [2]. Plate Count Agar was used for TMAB analysis (PCA; Oxoid CM0463) and inoculation was made with the pour plate inoculation technique. The colonies were evaluated 48 hours after media in incubated at 37°C [26,28]. For the purpose of counting S. aureus egg yolks and potassium tellurite has been added and Baird Parker Agar (BPA; Oxoid CM1127) spread plate technique method was used. Typical and atypical colonies were evaluated as staphylococcus after the Petri dishes were incubated 48 hours at 37°C. Catalase and coagulase testing were conducted for verification of suspected colonies [Brain Heart infusion Broth (BHIB-Oxoid CM225)] [24,26]. Violet Red Bile Lactose Agar (VRB; Oxoid CM0968) was inoculated to media by spreading plate method and left for 24- hour incubation at 37 °C for coliform analysis. In order to confirm the suspected colonies, it was transferred to Brilliant Green Bile Lactose (BGLB, Merk 1.05454) tubes and those generating gas after incubation at 37°C were considered positive [26,27. For the detection of E. coli, inoculation was conducted to Tryptone Bile X-glucuronide Medium (TBX, Oxoid CM0945) with spreading plate method. The Petri dishes were released to incubation firstly at 30°C for 4 hours and then 18 hours at 44°C. The bluish/green colonies formed after incubation were evaluated as E. coli [25,26].