Microarray chip development using infrared imaging for the identification of catfish species.

Appl Spectrosc

Office of Regulatory Science, Center for Food Safety and Applied Nutrition, US Food and Drug Administration, 5100 Paint Branch Parkway, College Park, MD 20740 USA.

Published: July 2015

AI Article Synopsis

  • Several families of catfish are farmed globally, but only Ictaluridae catfish are recognized as "catfish" in the U.S.; others are misbranded.
  • Increased misbranding has prompted interest in DNA-based methods, like DNA barcoding and microarrays, to accurately identify fish species.
  • This study successfully used DNA microarrays and mid-infrared imaging to identify seven catfish species by targeting specific regions of the cytochrome c oxidase 1 gene, marking a novel approach in species identification.

Article Abstract

Several families of catfish species are extensively aquacultured around the world; however, only those from the family Ictaluridae can be labeled as catfish in the United States. Non-Ictalurid catfish species that are marketed as "catfish" in the USA are considered misbranded. Misbranding in general has led to an increased interest in developing deoxyribonucleic acid (DNA)-based methods such as DNA barcoding, polymerase chain reaction restriction fragment length polymorphism, and DNA microarrays with fluorescence detection for the identification of fish species. In this proof-of-concept study, DNA microarrays coupled with a newly developed mid-infrared imaging detection method were applied to the identification of seven species of catfish for the first time. Species-specific DNA probes targeting three regions per species of the cytochrome c oxidase 1 (barcoding) gene were developed and printed as microarrays on glass slides. Deoxyribonucleic acid targets labeled with biotin were hybridized to their complementary probes using a strategy that allowed the selective formation of a silver layer on hybridized spots needed for detection. Using this three-probe format, the seven species were all identified correctly, even when a limited number of false positive spots were observed. Raman spectroscopy was employed to further characterize the arrays.

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Source
http://dx.doi.org/10.1366/14-07505DOI Listing

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