FDA & GE Salmon

Michael Scally MD

Doctor of Medicine
10+ Year Member
An overview of Atlantic salmon, its natural history, aquaculture, and genetic engineering
http://www.fda.gov/AdvisoryCommittees/CommitteesMeetingMaterials/VeterinaryMedicineAdvisoryCommittee/ucm222635.htm

Introduction

Aqua Bounty Technologies, Inc., has submitted an application to FDA (the agency, or “we”) for approval of the “AquAdvantage” genetically engineered (GE) salmon. The agency will be holding two public meetings on this topic. The first will address the science-based questions that are the subject of the actual approval; the second will be to obtain comments from the public on how FDA should apply its food labeling framework to foods made from this specific genetically engineered animal.

These two meetings are described in detail at http://www.fda.gov/AdvisoryCommittees/CommitteesMeetingMaterials/VeterinaryMedicineAdvisoryCommittee/ucm201810.htm

This document is intended to provide some basic information on Atlantic salmon, its consumption, and its aquaculture. It also describes the approach that FDA uses to regulate GE animals, including GE fish. The overview is presented in a question and answer format. We have also provided a list of selected salmon web resources, and a bibliography in case readers wish to follow up on any particular topic in more depth.

Note: there is more at the link - http://www.fda.gov/AdvisoryCommittees/CommitteesMeetingMaterials/VeterinaryMedicineAdvisoryCommittee/ucm222635.htm
 
Panel Advises More Aggressive FDA Analysis of Engineered Salmon
Panel Advises More Aggressive FDA Analysis of Engineered Salmon - NYTimes.com

By PAUL VOOSEN
September 21, 2010

ROCKVILLE, Md. -- While a genetically engineered salmon is almost certainly safe to eat, the government should pursue a more rigorous analysis of the fish's possible health effects and environmental impact, members of a federal advisory committee said yesterday.

The independent panel made up largely of veterinary scientists was convened by the Food and Drug Administration (FDA) to discuss the agency's upcoming decision on whether to allow the commercial cultivation of a fast-growing salmon engineered by the biotech firm AquaBounty Technologies. The panel's deliberations, which included no formal vote, are not binding on the agency, but could prompt an internal review of FDA's protocols.

The modified Atlantic salmon would be the first bioengineered fish approved for human consumption; fluorescent aquarium fish carrying a jellyfish gene have been marketed in the United States for nearly a decade. The FDA finalized its oversight of biotech animals last year, and its current deliberation will likely carry heavy precedent in the future.

Because of this precedent, the agency should be more rigorous in its evaluations, said Dicky Dee Griffin, a professor of cattle production at the University of Nebraska, Lincoln.

"It is extremely important how this precedent gets set," he said. "And it's not an economic issue. It may be, but it can't be. Economics is the shovel with which we dig the grave at the very end of these [deliberations]."

The FDA regulates genes spliced into animals somewhat awkwardly as always-on drugs, since Congress has never passed a bill creating new regulations for biotech crops or animals. If the agency moves forward with its approval of the salmon, it would still need to prepare an environmental assessment, subject to public comment. Once approved, the company says, the salmon could be on supermarket shelves in several years. It remains uncertain if the salmon would be labeled when sold, an issue the FDA is discussing in public meetings today.

AquaBounty's salmon, which are effectively sterile, are designed for growth at inland fish farms. Such facilities have proved to be an unprofitable, if environmentally benign, technique in the United States, where much salmon comes from ocean-based fish farms. It is widely agreed that these farms exact, through excess feeding and escaped fish, a heavy toll on surrounding waters and wildlife.

Safety studies conducted by AquaBounty and made public by the FDA earlier this month often relied on small samples, ranging from 60 fish to only a half-dozen or so. Often, the company's research was conducted upon biotech salmon that were fertile, along with the sterile varieties AquaBounty will sell, causing confusing results. And the methods used to cull the salmon prior to study were not described, prompting concern from the panel.

"Given its study design, sample sizes and mixture of fish ... I would have to characterize this body of work as potentially [promising] but preliminary work that would need to be validated and confirmed in other studies," said Jodi Ann Lapidus, a professor of biostatistics at Oregon Health and Science University.

"Because of the issues related to culling and the data that seems to be floating around that's not in our materials leaves a cloud. It's not partly sunny, necessarily," said Jim McKean, a professor of swine veterinary science at Iowa State University. "There are questions that have not been answered by the data."

While the study design may not have been perfect, the sheer biology of AquaBounty's salmon implies that it will be safe to eat, said Kevin Wells, a professor of animal science at the University of Missouri. The biotech salmon carry a growth hormone gene from chinook salmon that is kept continuously active, even in cold conditions, by a DNA switch from the eel-like ocean pout.

"Everything here is something we eat," Wells said.

Rethinking biotech assessments

Lapidus advocated that FDA completely reconsider how it evaluates biotech animals.

Rather than search for how the salmon differs from unaltered varieties, it should mandate studies that seek to prove the animals are equivalent. Such work would define, in consultation with human nutrition experts, a continuum of biologically relevant ingredients found in typical Atlantic salmon. AquaBounty's salmon would then have to be found to sit within these boundaries.

The intensive study of the salmon also underscores uncertainty in some scientific realms. Like most fish, for example, AquaBounty's salmon can cause allergic responses in one subset of the population. When considering the possibility of additional allergenicity, however, there is no sound science describing what allergen levels would have to be present to cause allergies in previously unallergic consumers.

The engineered salmon would, in the application FDA is currently considering, be approved only for growth at the company's closed spawning facility on Prince Edward Island, Canada, and at a small inland fish farm in the highlands of Panama. However, if successful, the company will seek to sell its eggs to additional farms, each of which would trigger a separate FDA review.

Such a cumulative collection of applications, each separately considered, could see the fish grown at a large scale without ever triggering a broader environmental review. While each farm may have redundant containment systems, future agency assessments would not be available to the public, making it necessary to study the broader effects now, said Anne Kapuscinski, a professor of sustainability science at Dartmouth College.

"The assessment does not adequately address the major questions that should be asked about genetic and ecological risks," she said.

Kapuscinski, who did not serve on the panel, urged the FDA to look beyond the firm's current containment efforts, which she agreed were strong. The agency must complete an environmental impact statement that will fully flesh out the ramifications, however highly unlikely, that fertile biotech salmon could escape to the wild, Kapuscinski said. The company and agency's current assessments stop short of such evaluation, citing redundant containment strategies.

While lauding AquaBounty's containment strategy and saying he would eat the salmon without alarm, Gary Thorgaard, a marine biologist at Washington State University, echoed Kapuscinski's call for a full environmental assessment, to be conducted with other federal agencies.

The accelerated growth provided by the chinook gene would not necessarily cause the fish to enjoy a selective advantage over wild salmon, scientists said. (The fish, while fast-growing, does not grow larger than its domesticated peers.) The engineered salmon's increased food needs could make it more vulnerable to predators. In fact, the salmon could even be preferable to typical domesticated salmon, which often cause havoc on wild salmon populations.

"I'm worried about the transgene getting out much less than [the escape of] domesticated fish," Wells said.
 
Statement from FDA Commissioner Scott Gottlieb, M.D., on continued efforts to advance safe biotechnology innovations, and the deactivation of an import alert on genetically engineered salmon
Statement from FDA Commissioner Scott Gottlieb, M.D., on continued efforts to advance safe biotechnology innovations, and the deactivation of an import alert on genetically engineered salmon

Advancements in the dynamic field of biotechnology are bringing about the development of innovative, new food products. At the U.S. Food and Drug Administration, we’re committed to helping food developers bring biotechnology innovations to market while at the same time providing consumers with confidence that foods available for purchase in the U.S. – whether developed using traditional breeding techniques or biotechnology – meet the FDA’s high safety standards.

Biotechnology is a term used to describe certain methods, including genetic engineering (GE), that scientists use to introduce new, favorable traits or characteristics to an organism. Part of our work implementing the FDA’s vital mission is focused on evaluating the safety of intentional genomic alterations (IGAs) in animals that will ultimately be sold for consumption to American consumers. We recently advanced a comprehensive framework for the efficient development of safe biotechnology products with our new https://www.fda.gov/AnimalVeterinary/NewsEvents/CVMUpdates/ucm624490.htm. In recent years, we’ve taken important steps to help advance novel products, including our 2015 decision to approve an application related to AquAdvantage Salmon, a GE Atlantic salmon that contains the first approved IGA in an animal intended for food use.

Today, we are taking another important step by deactivating a 2016 import alert that prevented GE salmon from entering the U.S. The FDA’s approval of the application related to AquAdvantage Salmon followed a comprehensive analysis of the scientific evidence, which determined that the GE Atlantic salmon met the statutory requirements for safety and effectiveness under the Federal Food, Drug, and Cosmetic Act. However, in 2016, Congress directed the FDA not to allow into commerce any food that contains GE salmon until it issued final labeling guidelines for informing consumers of the GE salmon content in the food. The FDA complied with this requirement by implementing an import alert in 2016 that prevented GE salmon from entering the U.S.


AquaBounty Technologies, Inc. - FDA Lifts Import Alert on AquAdvantage Salmon
AquaBounty Technologies, Inc. - FDA Lifts Import Alert on AquAdvantage Salmon | AquaBounty Technologies, Inc.

MAYNARD, Mass., March 08, 2019 (GLOBE NEWSWIRE) -- AquaBounty Technologies, Inc. (NASDAQ: AQB) (“AquaBounty” or the “Company”), a biotechnology company focused on enhancing productivity in the aquaculture market and a majority-owned subsidiary of Intrexon Corporation (NASDAQ: XON), announces the U.S. Food and Drug Administration (FDA) lifting of the Import Alert, allowing the Company to start farming AquAdvantage Salmon in Indiana.

Sylvia Wulf, Chief Executive Officer of AquaBounty, stated: “We are delighted that FDA has lifted the import alert, which will allow AquaBounty to begin producing and marketing AquAdvantage Salmon in the United States. As FDA notes in this announcement, our salmon was approved by the agency over three years ago based upon a very comprehensive science-based review process, which established that our salmon was safe, nutritious, and environmentally sound and met all other regulatory requirements. We will immediately start the process to import AquAdvantage eggs from our hatchery in Canada to begin grow out at our Indiana facility.”

Approximately 350,000 tons of Atlantic salmon are consumed in the United States with more than 95% of it imported. FDA’s actions will allow for production and sale to begin here in the U.S., bringing opportunity for investment in rural America, creating American jobs, while also reducing dependence on seafood imports.
 
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