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Food safety, satisfaction and quality have always been an important concern of consumers. Several pathogens such as E. coli (Shiga toxin and verocytotoxin-producers), S. aureus, etc are recognized as important human pathogens of animal origin that are responsible for mastitis, bloody diarrhea, haemorrhagic colitis and haemolytic uraemic syndrome in humans and constitute the most important causes of food-borne disease and therefore is a major health concern and is the most economically important disease of dairy industries around the world. To detect these harmful pathogens, microbiological culture methods are used which are time consuming and species identification require more than 48 hours. Therefore many rapid methods to detect, differentiate, and identify pathogens in food have been developed which are safe, reliable, standardized, and above all achieve rapid results for safe food production within hours. Such methods include, PCR, microcalorimetry, impedance, turbidimetry, fluorimetry, reflectometry, and radiometry.
This essay will focus on two rapid microbiological methods namely PCR and impedance methods used in food safety and quality analysis, to monitor the microorganisms present in the food which are important for food industry.
PCR rapid method
Infectious diseases such as mastitis in cattle are caused by pathogen Staphylococcus aureus (S.aureus) which produces toxins. Due to the rise of this concern dairy products are diagnosed for prevention of pathogens in food. The commonly used standard methods for
detection of microorganism in food is biological culture method which has many disadvantages, one of the main one is it is time consuming and may take up to days to produce results and may not give accurate result of bacterial count yield and is unable to detect pathogens in presence of other residues (such as antibiotics, milk preservatives, etc). Therefore, PCR has been successfully used to identify various pathogens. PCR is a rapid method for detecting pathogens even in the presence of other residues and preservatives and are believed to overcome problems associated with selective cultivation and isolation of microorganisms from natural samples and are generally characterized by their simplicity, speed, cost-effectiveness , reliability, high species output, accurate results within hours rather than days. In many performed experiments it has been shown that PCR is more sensitive and specific for pathogen and better than standard biological culture method (Ghorbanpoor, et al, 2007; Ahmadi et al, 2010 ).
Samples of milk were collected from cows in industrial dairy and transported to laboratory for detection of pathogen in milk by PCR method. First the DNA extracted from sample was centrifuged for 3-4 minutes and the supernatant was discarded and the pallet was re-suspended and washes with PCR buffer couple of times (Tris-EDTA buffer) until a clear solution was obtained. Lysozyme and proteinase K were added to the sample and the sample was then incubated at room temperature. The final DNA pallet was dissolved in 100ml of distilled water for using in PCR. PCR amplification was the next step carried out were specific primers (e.g. prfA- derived primers, PRFA1 and PRFA2, were applied for identification of Listeria monocytogenes, or S. aureus primers as shown in table 1) were used to detect the genes and proteins in bacteria that are responsible for causing the infection (Holko et al, 2002). One major concern when applying PCR for the detection of pathogens in foods is the false negative results i.e. the failure to detect a pathogen when present. This can occur as a result of interference with target-cell lysis during nucleic acid extraction, nucleic acid degradation, or direct inhibition of the PCR. Therefore a set of control primers are used to provide correct interpretation of PCR results. The PCR mixture comprising of DNA polymerase, MdNTPs, PCR buffer, extracted DNA, MGCL2 and sterile water were mixed in a 0.2 PCR microtube and the reaction was carried out in a PCR thermo cycler. Amplification was performed. The PCR products were electrophoreses in agarose gel and visualized by ultraviolet light transillumination (Ahmadi et al, 2010; Ghorbanpoor et al, 2007; Liming et al, 2004; Murphy et al 2007)).
Sequence (5 - 3 )
PCR product size (bp)
Table.1. Sequence of positive set of primers for identification of S. aureus (Ghorbanpoor et al, 2007).
Impedance rapid method
Impedance is a rapid physiochemical methods used to detect food pathogens within 24 hours. It is based on the measurement of changes in electrical impedance of a medium or a reaction solution resulting from the bacterial growth (electrolyte impedance and interface impedance). Milk and dairy products Dairy can be contaminated with salmonella and other pathogens and so samples collected with dairy farms are tested for the presence of these food borne pathogens (Yang et al, 2003).
IN one of the experiment impedance measurements were performed using an IM-6 impedance analyzer. A water-jacketed glass vial (15 ml) containing 4.5 ml of SC/T/M broth was used as an incubator for Salmonella growth. One pole of the IME was connected to both the test and sense probes, and another pole was connected to both the reference and counter electrodes of the IM-6 impedance analyzer. The temperature of the broth was controlled by circulating water in the water-jacket with a thermostatic water bath. After the broth temperature reached 37 °C and remained at 37±0.5 °C, the broth was inoculated with 0.5 ml Salmonella culture at a desired bacterial concentration. Impedance measurement started immediately after the inoculation. Bacteria cells attached to the electrode surface caused an increase in resistance, which compensated for the decrease in medium resistance. The effects of electrode materials and configurations on the impedance measurement suggested a significant role of electrode impedance in response to the bacterial growth .These research results indicate that electrode impedance is an important component in the total impedance. One can expect that electrode (including its size, shape, materials, etc.) could be a considerable factor for the performance of impedance measurement in the detection of bacterial growth. Impedance have received great attention in the area of electroanalytical chemistry in recent years. Impedance showed higher sensitivities than conventional electrodes in electrochemical measurement of neurotransmitter (Kleiss et al , 1995)
PCR method used identified and detected multiple microorganisms present in milk and dairy products in a single reaction and showed to have high sensitivity. Several specific primer sets are combined into a single PCR assay. Hence, PCR is undoubtedly useful to rapidly identify several isolates and it enables the selection of various species and represents the fastest culture-independent approach for strain-specific detection in complex matrices. It has been applied successfully in many fields of microbiology for faster identification, direct detection and differentiation of microorganisms with or without previous isolation and cultivation. However, there remains a lack of standardisation and internationally accepted PCR-based methods, although some progress has been made in producing general principals and best practice guidelines for the analysis of food.
Since the impedance sensor was based on the detection of an electrical signal, it offers the advantage over optical detection for food samples, usually murky solutions. As compared to other methods it detects the pathogen bacteria without any need of pre treatment of food samples.