Application of DNA Barcoding Techniques For Speciation

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Application of DNA Barcoding Techniques For Speciation Bruno J. Giri US Department of Agriculture Office of Public Health Science 1

Objectives Background of catfish speciation Background of DNA barcoding FSIS Verification of catfish barcoding method Future plans and questions extension to other regulatory species? 2

Background of Catfish Regulation In 2001, the FDA changed the definition of catfish to exclude all catfish that are not members of the family Ictaluridae, i.e. North American catfishes only This prohibited all catfishes not of North American origin from labeling their product as such, but also limited the regulatory scope 3

Farm Bill 2008 Prior to 2008: processors subject to announced or unannounced inspections by FDA had the option of a voluntary, fee-for-service grading program from National Marine Fisheries Service (NMFS) The proposed rule amends the1906 s Federal Meat Inspection Act (FMIA) such that catfish are subject to examination and inspection by USDA/FSIS when processed for use as human food in process 4

Definition Blues: Is It a catfish or isn t it? FSIS currently has two proposed definitions of catfish under review: 1. Maintain the narrow definition that includes only members of the North American catfish family (Ictaluridae) OR 2. Broaden the definition to include all true taxonomic catfish or members of the order Siluriformes 5

Channel Catfish Ictalurus punctatus Image source: http://fish.dnr.cornell.edu/nyfish/ictaluridae/channelcatfish.html 6

Protein Methodology (IEF) AOAC Method 980.16: has been in use since the 1980s, currently the gold standard for uncooked fillet (although not extended to cooked) Protocol: Cold water extraction of sarcoplasmic proteins, separation of proteins by isoelectric point by PAGE, staining and visualization of gel with 0.1% acid violet 17 Comparison of banding pattern of authenticated standards with that of unknown samples Process banding patterns with software 7

Example of Unprocessed IEF Gel 8

Example of Processed IEF Gel 9

DNA-based Speciation Technology DNA-based methods: much more recent and quickly becoming the preferred approach Primary reasons for this shift are: (1) Protein degrades more readily than DNA (2) DNA sequences are more robust and less subjective than protein banding patterns (3) DNA sequence-based methodologies are easy to standardize and amenable to the use of a common reference database 10

What is DNA Barcoding? Source: http://www.dnabarcoding.ca/primer/coiprotein.html 11

What is DNA Barcoding? From Handy et al 2011: a process by which species discriminations are achieved through the use of short, standardized gene fragments. (sic) For animals, a target gene region has been selected: a fragment consisting of 648-655 base pairs starting near the 5 end of the COI mitochondrial gene 12

Blue Catfish Ictalurus furcatus Image source: http://www.tpwd.state.tx.us/huntwild/wild/species/blc/ 13

DNA Barcoding Workflow Image source: http://www.springerimages.com/images/rss/1-10.1007_s 10530-010-9709-8-0 14

FSIS Barcoding Method Protocol 1. Extract genomic DNA 2. Amplify cytochrome oxidase I (COI) gene with M13-tailed primers (from Ivanova et al 2007and Baldwin et al 2009) 3. Cleanup with Exo-SAP 4. Sequencing reaction with M13 primers, cleanup with Performa DTR 5. Sequencing by capillary electrophoresis 6. Data analysis using software program 15

FSIS Method Work Flow 1. DNA Extraction Image Source: Qiagen website 2. COI PCR Source: http://bitesizebio.com/articles/the-invention-ofpcr/ 16

FSIS Method Work Flow 3. Exo-sap cleanup Image Source: http://www.affymetrix.com/estore/browse/brand/us b/product.jsp?productid=131310#1_1 4. Seq rxn and Performa DTR cleanup Image source: http://www.edgebio.com/products/performa %C2%AE-spin-columns-13266 17

FSIS Method Work Flow 5. Sequencing by capillary electrophoresis Image source: taken by BG 6. Data analysis with BioNumerics software Image source: screenshot acquired by BG 18

Verification Results I Internal sequence library that now contains barcodes from a total of 31 different fish species including: (a) 2 main commercial domestic catfish species: channel catfish (Ictalurus punctatus) and blue catfish (I. furcatus) (b) 17 species of non-commercial Ictalurids from the genera Noturus (madtoms) and Ameiurus (bullheads) (c) 2 imported commercial species of Asian catfishes from the family Pangasiidae, 1 species of tilapia, and 9 species of commercially important saltwater fishes 19

Verification Results II Method approved by internal quality assurance division for inclusion in FSIS Chemistry Laboratory Guidebook as CLG-FPCR.00 in March 2012 Currently training two analysts in FPCR 20

Iridescent shark - Pangasianodon hypophthalamus Image source: http://www.jjphoto.dk/fish_archive/warm_freshwater/ pangasius_hypophthalmus.htm 21

Future Barcoding Plans Potential extension of the method to single species meat products of various matrices These include: bovine, caprine, equine, ovine, porcine, and poultry food products processed by a variety of approaches Preliminary results have been largely successful and include a total of nine species 22

Acknowledgments USDA /FSIS: Ms. Lynn Cruickshank, Mrs. Maritza Quinn, Drs. Joe Hill, Louis Bluhm, Jeanetta Tankson, Otis Miller, and Emilio Esteban FDA : Drs. Jonathan Deeds and Sara Handy (CFSAN) and Dr. Yuelian Shen (CVM) Florida Department of Agriculture and Consumer Sciences: Drs. Mark French, Yvonne Salfinger, Maria Ishida, and Ms. Amy Bryant Canadian Centre for DNA Barcoding: Drs. Nataly Ivanova, Alex Borisenko, and Paul Hebert Georgia Museum of Natural History: Dr. Byron Freeman Florida Museum of Natural History: Mr. Terry Lott Applied Maths/Bionumerics: Mr. Kyle Kingsley 23

Thanks for your attention Any questions? 24