Comparative analysis of LC-MS/MS and real-time PCR assays for efficient detection of potential allergenic silkworm

[Display omitted] •LC-MS/MS and real-time PCR methods were developed for silkworm detection.•The specificity of two methods was validated across 18 different species.•The applicability of the methods was confirmed across various processed foods.•The sensitivity validation was conducted for both meth...

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Veröffentlicht in:Food chemistry 2024-07, Vol.445, p.138761-138761, Article 138761
Hauptverfasser: Suh, Seung-Man, Kim, Kyungdo, Yang, Seung-Min, Lee, Hana, Jun, Minkyung, Byun, Jisun, Lee, Hyeongjoo, Kim, Daseul, Lee, Dain, Cha, Jae-Eun, Kim, Jun-Su, Kim, Eiseul, Park, Zee-Yong, Kim, Hae-Yeong
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Sprache:eng
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Zusammenfassung:[Display omitted] •LC-MS/MS and real-time PCR methods were developed for silkworm detection.•The specificity of two methods was validated across 18 different species.•The applicability of the methods was confirmed across various processed foods.•The sensitivity validation was conducted for both methods using model cookies. The silkworm (Bombyx mori) has long been valued food and feed in East Asia for its abundant nutritional and medicinal attributes, conversely, it can elicit allergic responses in susceptible individuals. Therefore, the development of silkworm detection method is required to avert allergenic incidents. In this study, two methodologies, tandem mass spectrometry (LC-MS/MS) and real-time PCR, were developed to achieve effective silkworm detection. These methods exhibited exceptional sensitivity in identifying silkworm presence in processed foods. Furthermore, model cookies spiked with silkworm were used to validate the sensitivities of LC-MS/MS (0.0005%) and real-time PCR (0.001%). Overall, these techniques were useful for trace silkworm detection in food products; therefore, they may help prevent allergic reactions. To the best of our knowledge, this study represents the first comparison of LC-MS/MS and real-time PCR methods for silkworm detection, marking an important contribution to the field. Data are available from ProteomeXchange under identifier PXD042494.
ISSN:0308-8146
1873-7072
DOI:10.1016/j.foodchem.2024.138761