The detection and
enumeration of pathogens in food and on surfaces that come into contact with
food are an important component of any integrated program to ensure the safety
of foods throughout the food supply chain. Both government authorities and food
companies use microbiological analysis to monitor the state of contamination at
all times and analyze its trends so as to detect emerging risks.
Microbiological analysis is also an essential tool for carrying out tests in
accordance with the micro-biological criteria established for each food type,
as well as being essential for evaluating the actions of different management
strategies based on the Hazard Analysis and Critical Control Points (HACCP) system. The implementation
of preventive systems such as the HACCP has greatly improved food
safety, but it will not be fully effective until better methods of analysis are
developed. These new detection methods are the necessary technologies that will
substantially improve our food safety once integrated in the HACCP.
Microbiological
analysis of foods is based on the detection of microorganisms by visual,
biochemical, immunological, or genetic means, either before enrichment
(quantitative or enumerative methods) or
after enrichment (qualitative methods, also known as
presence/absence tests).
In spite of its
importance, the microbiological analysis of food has many limita-tions.
Uncertainty of the analytical result must
be considered when establishing microbiological criteria,
including the variance associated with the sampling plan, method of
analysis, and laboratory performance . The microbiological
analysis of food remains a challenging task for virtually all assays and
technologies, especially for particular pathogenic species.
The problems may be
due to
· The
complexity of food matrices and composition.
· The
heterogeneous distribution of low levels of pathogens.
· The
presence of bacteria from the normal microbiota, especially in raw
foods.
The conventional
methods used to detect foodborne pathogen are time consuming and laborious.
Hence, a variety of methods have been developed for rapid detection of
foodborne pathogens as it is required in many food analyses. Rapid detection
methods can be categorized into nucleic acid-based, biosensor-based and
immunological-based methods. This review emphasizes on the principles and
application of recent rapid methods for the detection of foodborne bacterial
pathogens. Detection methods included are simple polymerase chain reaction (PCR), multiplex PCR, real-time PCR, nucleic acid
sequence-based amplification (NASBA), loop-mediated isothermal amplification
(LAMP) and oligonucleotide DNAmicroarray which classified as
nucleic acid-based methods; optical, electrochemical and mass-based biosensors
which classified as biosensor-based methods; enzyme-linked immunosorbent assay (ELISA) and lateral flow immunoassay which
classified as immunological-based methods. In general, rapid detection methods
are generally time-efficient, sensitive, specific and labor-saving. The
developments of rapid detection methods are vital in prevention and treatment
of foodborne diseases.

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