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Building a Teleost Fish Traceability Program Based on Genetic Data from Pacific Panama Fish Markets

Edgardo Diaz-Ferguson, Magaly Chial, Maribel Gonzalez,Edgardo Munoz,Olga Chen,Ovidio Duran,Angel Javier Vega, Carlos Ramos Delgado

ANIMALS(2023)

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Abstract
Simple Summary Molecular identification of fish tissue samples from 203 individuals was conducted based on cytochrome oxidase I gene segment sequencing. A total of 34 species from 14 families (Ariidae, Caranjidae, Centropomidae, Gerreidae, Haemulidae, Lobotidae, Lutjanidae, Malacanthidae, Mugilidae, Serranidae, Scianidae, Scombridae, Sphyraenidae, Stromateidae) were identified at the species level from 164 obtained sequences. Three Caribbean species were also molecularly identified among the analyzed samples (Mycteroperca xenarcha, Paralonchurus brasilensis and Lobotes surinamensis). Species diversity was slightly higher in the Gulf of Panama than in the Gulf of Chiriqui. Genetic diversity and connectivity between Gulf areas was compared using values of haplotypic diversity and nucleotide diversity for genetic diversity and genetic distances and genetic differentiation (Fst) for connectivity. A high level of connectivity was observed between the Gulf of Chiriqui and the Gulf of Montijo, showing the existence of a single stock in that area for the following species: Scomberomorus sierra, Caranx caninus and Lutjanus guttatus. The demographic history of the most common species was examined, and population expansion was evidenced for two snapper species, L. peru and L. argentiventris (significant and negative values of Tajimas D). Another important contribution from this research was the design of primers and dual-labeled probes for environmental DNA and qPCR detection for three of the most abundant species. Fish tissue samples from 203 adult individuals were collected in the main ports and markets of the Pacific coast of Panama. Molecular identification based on a cytochrome oxidase I gene segment of all species was verified by GENBANK reference sequences. A total of 34 species from 14 families (Ariidae, Caranjidae, Centropomidae, Gerreidae, Haemulidae, Lobotidae, Lutjanidae, Malacanthidae, Mugilidae, Scianidae, Scombridae, Serranidae, Sphyraenidae, Stromateidae) were identified at the species level from 164 sequences. Additionally, three Caribbean species were molecularly identified among the analyzed samples (Mycteroperca xenarcha, Paralonchurus brasilensis and Lobotes surinamensis). Species diversity was slightly higher in the Gulf of Panama than in the Gulf of Chiriqui. For species with five or more individual sequences, genetic diversity and genetic connectivity parameters such as total number of haplotypes (H), haplotype diversity (Hd), and nucleotide diversity (& pi;) were calculated. Overall, pelagic-migratory species showed higher values of genetic diversity than coastal and estuarine species with some exceptions. Connectivity between Gulf areas was compared using values of genetic distances and genetic differentiation (Fst). The high level of connectivity observed between the Gulf of Chiriqui and the Gulf of Montijo indicates the existence of a single stock in that area for the following species: Scomberomorus sierra, Caranx caninus and Lutjanus guttatus. The demographic history of the most common species was examined using Tajima's D values, suggesting population expansion for two snapper species, L. peru and L. argentiventris, having significant and higher values. Another important contribution from this research was the production of primers and dual-labeled probes for environmental DNA detection using qPCR for the five most abundant species (spotted rose snapper, yellow snapper, green jack, Pacific crevalle jack and the Pacific sierra fish). These markers represent a new set of tools for environmental DNA (eDNA) detection and molecular traceability of three commercially important fish species along the supply chain including landing sites and markets of the main fishery areas.
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Key words
COI,nucleotide diversity,haplotypic diversity,qPCR,demographic history,environmental DNA
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