News Release

New rapid tests will detect adulteration of meat products

Peer-Reviewed Publication

Federal Research Centre «Fundamentals of Biotechnology» of the Russian Academy of Science

Scheme of the analysis

image: RPA was performed in the presence of labeled primers using cytochrome b DNA as a template. RPA generated labeled amplicons that were applied to the lateral flow strips. In the presence of the target DNA, an immune complex of a FAM-labeled terminal with an anti-FAM–GNP conjugate was formed as the labeled amplicons passed along the strip. The following streptavidin–biotin reaction occurred in the test zone and caused its colorization via GNP inclusion. view more 

Credit: Ivanov et al. / Molecules, 2021

Meat and sausage products can be found on the shelves of every grocery store. Although sometimes not everything that the manufacturer listed on the package is true. Expensive types of meat, such as beef, are often substituted with cheaper poultry. Existing methods to confirm composition of meat products require testing in specialized laboratories with highly accurate and expensive equipment. As a result, the cost of testing rises while the time of getting the results increases. There is a need to develop alternative, faster, and more affordable highly sensitive methods for detecting adulteration.

“We suggested a simple method of determining ingredients of sausages and other meat-containing products. Our development helps to detect chicken and pork meat in samples fast and without using unnecessary devices,” — says Anatoly Zherdev, the head of the RSF project. Anatoly Zherdev is a Ph.D. in Biology and a leading researcher of the Laboratory of Immunobiochemistry of the Research Center of Biotechnology RAS (Moscow).

Scientists from the Research Center of Biotechnology RAS developed an approach that helps to accurately detect pig and chicken meat in raw and processed products. First, the authors isolated DNA from the samples, added short nucleotide primer chains with tags (biotin and fluorescein), and recombinase polymerase amplification reagents. This process is carried out at a constant temperature, without special instruments for more complex amplifications. As a result, in just 15 minutes, the number of copies of DNA fragment bounded by two primers increases dramatically. In this development, the gene for one of the mitochondrial proteins of a chicken and a pig was used for generate the DNA to be detected. The resulting solution was dripped onto test strips with streptavidin molecules that can selectively bind biotin in the detection zone. As a result, the needed DNA was attached to the strip. After that, scientists added gold nanoparticles with immobilized antibodies to fluorescein — after the binding of the nanoparticles, the color at the test strip appeared. Such a multilayer “sandwich" reduces risks of erroneous results and increases the reliability of the test.

Biochemists tested this system on samples provided by partners from the V.M. Gorbatov Federal Research Center for Food Systems RAS: minced meat with different contents of chicken, pork, and beef, as well as cooked meat products made according to governmental standards. Scientists compared two variants of DNA extraction: standard long-term and rapid. With the reduction of sample preparation time, the brightness of test strip coloration decreased slightly. Nevertheless, three minutes was already enough to reliably detect color changes in the detection area and to make a conclusion about adulteration — if there were a case of adding chicken or pork when it wasn’t supposed to be according to the recipe.

"All stages of our analysis take only 33 minutes. It is the fastest method for detecting chicken and pork additives in meat products. It doesn't require sophisticated equipment or expensive reagents. We hope that our approach will help provide quality products to consumers and protect them from unscrupulous producers," – says Anatoly Zherdev.

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