Molecular analysis of edible bird's nest and rapid authentication of Aerodramus fuciphagus from its subspecies by PCR-RFLP based on the cytb gene

Edible bird's nest (EBN), for its great nutritional value, is widely used around the world, especially in China and Singapore. EBNs of different origins and types may vary in price and quality. Nowadays, birds' nests are difficult to identify morphologically, except for some whole bird...

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Veröffentlicht in:Analytical methods 2020-06, Vol.12 (21), p.2710-2717
Hauptverfasser: Liu, Kunfeng, Wu, Maoyong, Lin, Xuemei, Lonan, Piyanuch, Chen, Sitai, Wu, Yina, Lai, Xiaoping, Yu, Liangwen, Zhou, Xiaoming, Li, Geng
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container_end_page 2717
container_issue 21
container_start_page 2710
container_title Analytical methods
container_volume 12
creator Liu, Kunfeng
Wu, Maoyong
Lin, Xuemei
Lonan, Piyanuch
Chen, Sitai
Wu, Yina
Lai, Xiaoping
Yu, Liangwen
Zhou, Xiaoming
Li, Geng
description Edible bird's nest (EBN), for its great nutritional value, is widely used around the world, especially in China and Singapore. EBNs of different origins and types may vary in price and quality. Nowadays, birds' nests are difficult to identify morphologically, except for some whole bird's nests of which origins can be roughly identified. In this study, forty-two samples were collected from different regions for sequencing analysis and phylogenetic classification to initially determine their origins. Two stable enzyme digestion sites were found in the analysis of restriction maps of the species. Then, a quick and specific PCR-RFLP method was established to identify the EBN samples' origins. The genetic identification results indicated that the forty-two samples were from five origins. With the Af/g-486bp-F/R primer and restriction enzyme Taq I, Aerodramus fuciphagus (A. fuciphagus) was efficiently differentiated from the other species. Furthermore, the cytb-592bp-F/R primer and the BamH I enzyme were found to be useful in distinguishing Aerodramus fuciphagus (A. fuciphagus) from its subspecies (Aerodramus germani, A. germani). The PCR-RFLP method provides a potential tool for the rapid discrimination of A. fuciphagus at the species and even the subspecies levels to ensure the quality of the EBN products.
doi_str_mv 10.1039/c9ay02548k
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EBNs of different origins and types may vary in price and quality. Nowadays, birds' nests are difficult to identify morphologically, except for some whole bird's nests of which origins can be roughly identified. In this study, forty-two samples were collected from different regions for sequencing analysis and phylogenetic classification to initially determine their origins. Two stable enzyme digestion sites were found in the analysis of restriction maps of the species. Then, a quick and specific PCR-RFLP method was established to identify the EBN samples' origins. The genetic identification results indicated that the forty-two samples were from five origins. With the Af/g-486bp-F/R primer and restriction enzyme Taq I, Aerodramus fuciphagus (A. fuciphagus) was efficiently differentiated from the other species. Furthermore, the cytb-592bp-F/R primer and the BamH I enzyme were found to be useful in distinguishing Aerodramus fuciphagus (A. fuciphagus) from its subspecies (Aerodramus germani, A. germani). 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EBNs of different origins and types may vary in price and quality. Nowadays, birds' nests are difficult to identify morphologically, except for some whole bird's nests of which origins can be roughly identified. In this study, forty-two samples were collected from different regions for sequencing analysis and phylogenetic classification to initially determine their origins. Two stable enzyme digestion sites were found in the analysis of restriction maps of the species. Then, a quick and specific PCR-RFLP method was established to identify the EBN samples' origins. The genetic identification results indicated that the forty-two samples were from five origins. With the Af/g-486bp-F/R primer and restriction enzyme Taq I, Aerodramus fuciphagus (A. fuciphagus) was efficiently differentiated from the other species. Furthermore, the cytb-592bp-F/R primer and the BamH I enzyme were found to be useful in distinguishing Aerodramus fuciphagus (A. fuciphagus) from its subspecies (Aerodramus germani, A. germani). The PCR-RFLP method provides a potential tool for the rapid discrimination of A. fuciphagus at the species and even the subspecies levels to ensure the quality of the EBN products.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>32930302</pmid><doi>10.1039/c9ay02548k</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0724-3649</orcidid><orcidid>https://orcid.org/0000-0002-2441-2427</orcidid><orcidid>https://orcid.org/0000-0003-4269-2108</orcidid><orcidid>https://orcid.org/0000-0001-8828-1617</orcidid></addata></record>
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source MEDLINE; Royal Society Of Chemistry Journals 2008-
subjects Aerodramus fuciphagus
Animals
Birds
Birds - genetics
China
CytB gene
Enzymes
Gene mapping
Nests
Origins
Phylogeny
Polymerase Chain Reaction
Polymorphism, Restriction Fragment Length
Restriction fragment length polymorphism
Sequence analysis
Singapore
Species
title Molecular analysis of edible bird's nest and rapid authentication of Aerodramus fuciphagus from its subspecies by PCR-RFLP based on the cytb gene
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