scholarly journals Could food or food contact surfaces be the favourable hideouts for Listeria monocytogenes in Perak, Malaysia?

Food Research ◽  
2021 ◽  
Vol 5 (3) ◽  
pp. 174-182
Author(s):  
S.N. Chen ◽  
M.L. Yap ◽  
C.H. Kuan ◽  
Son Radu ◽  
S.H. Saw

Listeria monocytogenes is a causative agent of foodborne listeriosis which causes a high rate of hospitalisation (>90%) and death (20-30%) worldwide. Due to its ubiquitous nature and high resistance to a stressful environment, L. monocytogenes is able to multiply to a threatening level during food processing, distribution and storage, which then causes an immense case of foodborne disease outbreak. Hence, the control of L. monocytogenes is required at all stages in the food chain to prevent its occurrence in the final product. The present study aimed to determine the prevalence of L. monocytogenes in food as well as food contact surfaces from food processing plants and food service premises located in Perak, Malaysia. A total number of 170 food samples, including raw, minimally processed, processed and ready-to-eat food, as well as 152 samples from surfaces, including food-contact and non-food-contact, were collected and isolated on culture, and confirmation was done using polymerase chain reaction (PCR). A total of 26 food samples (15.29%) were positive for L. monocytogenes, with the highest prevalence found in processed and minimally processed food at 33.33% and 31.25%, respectively; following by raw and ready-to-eat food at 26.32% and 4.26% respectively. On the other hand, a higher prevalence of L. monocytogenes was detected from food-contact surfaces at 11.83% compared to non-food contact surfaces at 6.78%. These findings demonstrated the potential risk of contamination by L. monocytogenes in food and it might be due to the exposure of the bacteria on food processing surfaces. Thus, regular surveillance and strict assessment should be conducted by the local authorities to ensure the safety of the food consumption for residents in Perak.

Food Control ◽  
2018 ◽  
Vol 92 ◽  
pp. 240-248 ◽  
Author(s):  
C. Ripolles-Avila ◽  
A.S. Hascoët ◽  
A.E. Guerrero-Navarro ◽  
J.J. Rodríguez-Jerez

2018 ◽  
Vol 81 (4) ◽  
pp. 582-592 ◽  
Author(s):  
HYE RI JEON ◽  
MI JIN KWON ◽  
KI SUN YOON

ABSTRACT Biofilm formation on food contact surfaces is a potential hazard leading to cross-contamination during food processing. We investigated Listeria innocua biofilm formation on various food contact surfaces and compared the washing effect of slightly acidic electrolyzed water (SAEW) at 30, 50, 70, and 120 ppm with that of 200 ppm of sodium hypochlorite (NaClO) on biofilm cells. The risk of L. innocua biofilm transfer and growth on food at retail markets was also investigated. The viability of biofilms that formed on food contact surfaces and then transferred cells to duck meat was confirmed by fluorescence microscopy. L. innocua biofilm formation was greatest on rubber, followed by polypropylene, glass, and stainless steel. Regardless of sanitizer type, washing removed biofilms from polypropylene and stainless steel better than from rubber and glass. Among the various SAEW concentrations, washing with 70 ppm of SAEW for 5 min significantly reduced L. innocua biofilms on food contact surfaces during food processing. Efficiency of transfer of L. innocua biofilm cells was the highest on polypropylene and lowest on stainless steel. The transferred biofilm cells grew to the maximum population density, and the lag time of transferred biofilm cells was longer than that of planktonic cells. The biofilm cells that transferred to duck meat coexisted with live, injured, and dead cells, which indicates that effective washing is essential to remove biofilm on food contact surfaces during food processing to reduce the risk of foodborne disease outbreaks.


2002 ◽  
Vol 65 (6) ◽  
pp. 999-1004 ◽  
Author(s):  
ANIL TAKU ◽  
BALDEV R. GULATI ◽  
PAUL B. ALLWOOD ◽  
KERRIN PALAZZI ◽  
CRAIG W. HEDBERG ◽  
...  

Outbreaks of human Norwalk virus (NV) and Norwalk-like viruses often originate in food service establishments. No reliable method is available for the detection of these human caliciviruses on food contact surfaces. We describe a simple method for the detection of NV from stainless steel work surfaces using cultivable feline calicivirus (FCV) as a model. Stainless steel surfaces were artificially contaminated with known amounts of FCV, followed by its elution in a buffer solution. Three methods of virus elution were compared. In the first method, moistened cotton swabs or pieces of nylon filter (1MDS) were used to elute the contaminating virus. The second method consisted of flooding the contaminated surface with eluting buffer, allowing it to stay in contact for 15 min, followed by aspiration of the buffer (aspiration method) after a contact period of 15 min. The third method, the scraping-aspiration method, was similar to the aspiration method, except that the surfaces were scraped with a cell scraper before buffer aspiration. Maximum virus recovery (32 to 71%) was obtained with the scraping-aspiration method using 0.05 M glycine buffer at pH 6.5. Two methods (organic flocculation and filter adsorption elution) were compared to reduce the volume of the eluate recovered from larger surfaces. The organic flocculation method gave an average overall recovery of 55% compared to the filter-adsorption-elution method, which yielded an average recovery of only 8%. The newly developed method was validated for the detection of NV by artificial contamination of 929-cm2 stainless steel sheets with NV-positive stool samples and for the detection of the recovered virus by reverse transcription–polymerase chain reaction.


2017 ◽  
Vol 81 (1) ◽  
pp. 37-42 ◽  
Author(s):  
Woo-Ju Kim ◽  
Ki-Ok Jeong ◽  
Dong-Hyun Kang

ABSTRACT Following sanitation interventions in food processing facilities, sublethally injured bacterial cells can remain on food contact surfaces. We investigated whether injured Salmonella Typhimurium cells can attach onto abiotic surfaces, which is the initial stage for further biofilm development. We utilized heat, UV, hydrogen peroxide, and lactic acid treatments, which are widely utilized by the food industry. Our results showed that heat, UV, and hydrogen peroxide did not effectively change populations of attached Salmonella Typhimurium. Cells treated with hydrogen peroxide had a slightly higher tendency to adhere to abiotic surfaces, although there was no significant difference between the populations of control and hydrogen peroxide–treated cells. However, lactic acid effectively reduced the number of Salmonella Typhimurium cells attached to stainless steel. We also compared physicochemical changes of Salmonella Typhimurium after application of lactic acid and used hydrogen peroxide as a positive control because only lactic acid showed a decreased tendency for attachment and hydrogen peroxide induced slightly higher numbers of attached bacteria cells. Extracellular polymeric substance produced by Salmonella Typhimurium was not detected in any treatment. Significant differences in hydrophobicity were not observed. Surface charges of cell membranes did not show relevant correlation with numbers of attached cells, whereas autoaggregation showed a positive correlation with attachment to stainless steel. Our results highlight that when lactic acid is applied in a food processing facility, it can effectively interfere with adhesion of injured Salmonella Typhimurium cells onto food contact surfaces.


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