Development of a real-time PCR target for the detection of Hermetia illucens in feed.
- Marien, A. , Debode, F. , Aerts, C. , Ancion, C. , Francis, F. & Berben, G. (2017). Development of a real-time PCR target for the detection of Hermetia illucens in feed. Jana Pulkrabová, Monika Tomaniová, Michel Nielen and Jana Hajšlová. Proceedings in: 8th International Symposium on Recent Advances in Food Analysis, Prague, Czech Republic, November 7–10, 2017, 342.
Type | Conference Proceedings |
Year of conference | 2017 |
Title | Development of a real-time PCR target for the detection of Hermetia illucens in feed. |
Editor | Jana Pulkrabová, Monika Tomaniová, Michel Nielen and Jana Hajšlová |
Conference name | 8th International Symposium on Recent Advances in Food Analysis |
Conference location | Prague, Czech Republic |
Volume | book of abstracts |
Pages | 342 |
Label | U16-conf-Marien-2017-01 |
conference Date | November 7–10, 2017 |
Endnote Keywords | insect, Hermetia illucens, black soldier fly, detection, real-time PCR |
Abstract | Insects are rich in proteins and could be an alternative source of macronutrients to feed animals and humans. Numerous companies have started the production of insects for feed purposes. In Europe, the processed animal proteins obtained from seven insect species are authorized since 1 st July 2017 for aquaculture by EU regulation 2017/893. Methods of authentication are required to check the conformity of the products. In this study, we propose a real-time PCR method for the specific detection of the black soldier fly (Hermetia illucens L), one of the most widely used insects for feed production. The developed PCR assays amplify a fragment of 67 bp based on the mitochondrial COX3 gene coding for the subunit 3 of the cytochrome C oxidase. The qualitative method was tested according to several performance criteria. The specificity was tested against 50 insect species. The specificity was also checked against plant species and other animal species as crustacean, mammals and birds. The sensitivity, efficiency and robustness of the PCR test were successfully tested. The applicability of the test was proved through the analysis of real-life processed samples (industrial meals) of H. illucens. |
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Authors | Marien, A., Debode, F., Aerts, C., Ancion, C., Francis, F., Berben, G. |