Genetic Engineer Renounces His GMO Potatoes

Michelle Perro, MD
Published: October 22, 2018
Dr. Caius Rommens developed GMO potatoes that are now in the food supply. He has now renounced his products and written a book warning about the risks. Report: members of the GMOScience advisory board

At-a-glance

  • Dr. Caius Rommens developed GMO potatoes for the biotech firm Simplot but has now renounced his GMO work and written a book about his experiences.
  • Dr. Rommens says his GMO potatoes, which he calls “Pandora’s Potatoes”, pose health risks.
  • Pandora’s Potatoes have been commercialized in the US under names such as Innate, Hibernate, and White Russet.
  • These GMO potatoes are marketed as bruise-resistant and as healthier to eat than regular potatoes because they contain lower than average levels of a natural amino acid that forms carcinogenic acrylamide during cooking.
  • Dr. Rommens says the GMO potatoes are not truly bruise-resistant but bruise-concealing. The concealed bruises can accumulate toxins and pathogens and their lack of discoloration means that processors and consumers cannot identify and remove the problematic damaged tissue.
  • Dr. Rommens says these toxins and pathogens may pose health risks to consumers. He adds that claims that the GMO potatoes are safer than non-GMO potatoes due to reduced acrylamide levels has no solid scientific basis.
  • In addition, mechanisms by which the GM process causes DNA damage can change the plant’s composition in unintended ways, resulting in the production of novel toxins or allergens.
  • As a precaution, consumers should avoid eating these GMO potatoes.

The plant biologist and genetic engineer Dr. Caius Rommens spent many years of his career working for Monsanto and then for the Idaho-based firm J.R. Simplot, where he developed hundreds of thousands of different GM potatoes at a cost of about $50 million. Now he has renounced his GMO work and has written a book warning of the health and agronomic risks that his GMO potatoes pose to consumers and farmers. The book is called Pandora’s Potatoes: The Worst GMOs and is available from Amazon.

Dr Caius Rommens

Dr. Rommens’s GMO potatoes (which he calls in the book “Pandora’s Potatoes”) have been commercialized in the US and Japan, under names such as Innate, Hibernate, and White Russet. They are also approved in Canada but as of October 2018 are not being sold there. They were engineered to be resistant to bruising. They are also claimed to be healthier to eat than regular potatoes because they contain lower than average levels of the natural amino acid asparagine, which forms a carcinogenic substance called acrylamide when the potatoes are cooked at high temperatures, such as in frying.

Caius Rommens’s book, Pandora’s Potatoes

In the case of the Innate potatoes, Dr. Rommens produced these using a genetic engineering procedure known as RNA interference (RNAi). This resulted in the deliberate silencing (shutting down of expression) of two genes: polyphenol oxidase-5 (Ppo5) and asparagine synthetase-1 (Asn1). The Ppo5 enzyme usually causes potatoes to brown or blacken when cut or bruised, but when the Ppo5 gene is silenced in the GMO potato, the enzyme is absent and discoloration does not occur.

The Asn1 enzyme is responsible for synthesizing the amino acid asparagine, but again, when the Asn1 gene is silenced, far lower levels of asparagine are produced.
Stunted, mutated or sterile potatoes
In an interview with Independent Science News, Dr. Rommens said that when he worked at Simplot, “It was my goal to develop GMO potatoes that would be admired by farmers, processors, and consumers.” But the reality was very different. He said, “The almost daily experience I suppressed was that none of my modifications improved potatoes’ vigour or yield potential. In contrast, most GMO varieties were stunted, chlorotic, mutated, or sterile, and many of them died quickly, like prematurely-born babies.”

Of the GMO potatoes that have been commercialized, Dr. Rommens writes, “As a crop, the potatoes contain genetically unstable traits, two of which appear to have already been lost (or are in the process of being lost), suffer a significant yield drag and reduction in size profile, are designed to conceal bruises and potentially spread diseases, and may be grown and stored in ways that maximize disease and pest pressures. As a processed food, they lost the sensory attributes that make normal potato foods so attractive, and are also likely to contain new toxins.”
Not bruise-resistant but bruise-concealing
Some health risks that Dr. Rommens mentions are linked to the intended bruise-resistance trait produced by RNAi-mediated silencing of the Ppo5 gene. The problem with these GMO potatoes, according to Dr. Rommens, is that they are not really bruise-resistant but bruise-concealing. They bruise just like non-GMO potatoes, but lose the ability to develop the dark pigments that allow processors and shoppers to spot the bruises and remove them.
Dr. Rommens explains in his book that the concealed bruises can accumulate certain toxins that can compromise the food safety and nutritional quality of the potatoes. For example, bruises may accumulate tyramine, an amino acid that builds up in damaged plant tissues.
Some people are sensitive to tyramine, which belongs to a class of substances known as biogenic amines. In humans, biogenic amines play a role in brain activity, physiologic responses such as blood pressure, immune function, and cell growth.
When susceptible individuals eat biogenic amines in foods, they can cause a “hypertensive crisis” – a severe increase in high blood pressure.[1] Thus these individuals have developed the habit of avoiding foods that naturally contain high levels, such as blue cheese and soy sauce. Histamine, a powerful biogenic amine, is the only one for which regulators have set safety limits in the relevant foods – namely fish.[2][3] But, Dr. Rommens writes, “There is no awareness about the potential risk associated with invisibly bruised Pandora’s Potatoes,” so an unsuspecting consumer could unknowingly eat these bruise-concealing GMO potatoes in combination with other other tyramine-rich foods and end up in the emergency room.
Hidden infections
Just as bruises are concealed by the lack of a browning mechanism, so infections can also be concealed, Dr. Rommens says. Farmers and processors will not spot them because of the lack of telltale discoloration. The hidden infections can lead to a buildup of bacterial and fungal pathogens, which can lead to consumers being unknowingly exposed to the toxins, carcinogens, and allergens produced by the pathogens.
Regulators who have approved the GMO potatoes have not considered these aspects, as the standard tests needed to gain regulatory approval do not look for such unintended effects.
Reduced carcinogenicity a mirage?
As we’ve seen, Pandora’s Potatoes contain lower levels of the amino acid asparagine due to RNAi-mediated silencing of the Asn1 gene. Therefore they produce lower levels of the potential carcinogen acrylamide on frying. For this reason it is claimed these GMO potatoes are “safer” than regular non-GMO varieties.
However, even the claimed reduction in the potatoes’ carcinogenicity appears to be misleading. Dr. Rommens writes that acrylamide is present in French fries at levels so low as to be insignificant. It has been found to be carcinogenic only at levels 1,000-10,000 times higher than the levels found in fries.[4] “In other words,” Dr. Rommens says, “lowering the acrylamide levels in French fries is lowering the insignificantly-low levels of a carcinogen to even more insignificantly-low levels.”
Health risks from GMO transformation process
Other health risks from Pandora’s Potatoes arise from the GMO transformation process used to generate them.
The first safety issue stems from the type of RNAi technology used to reduce expression of the Ppo5 and Asn1 genes. The RNAi procedure used is not as precise as is often claimed by its users in agriculture and can interfere with the normal function of a gene or genes other than the one intended. If this were to occur, crop performance or nutritional status could be adversely affected and novel toxins or allergens could be produced in the plants. Scientists have warned that regulators in countries around the world are not taking due account of risks that can arise from off-target effects of RNAi technology.[5] Thus the possible effects on health of eating crops containing gene-silencing constructs have not been studied.
No foreign genes?
The second safety concern arises from mutational (DNA-damaging) effects that are inherent to the GMO transformation process in general. The company that Dr. Rommens worked for when he produced Pandora’s Potatoes, J.R. Simplot, claims on its website that they were generated “with the potato’s own DNA to achieve desirable traits without incorporating any foreign genes”.
However, this is not strictly the case. In its petition to the USDA for deregulated status for Innate GMO potatoes, Simplot states that the RNAi effects on the Ppo5 and Asn1 genes were produced by inserting “fragments of both the asparagine synthetase-1 gene (Asn1) and the polyphenol oxidase-5 gene (Ppo5), arranged as inverted repeats”. The gene cassette (GM gene construct) containing these Ppo5 and Asn1 gene fragments, as well as another cassette containing gene fragments aimed at silencing other genes, are artificial laboratory constructs. By definition, in the field of genetic engineering technology, they constitute “foreign genes”.
Insertional mutagenesis
In addition, the foreign gene fragment cassettes would have inserted randomly into the genome of the potato cells being transformed. This “insertional mutagenesis” would have inevitably resulted in disruption of one or more genes. Furthermore, it is well established that the tissue culture (growing of plant cells in the laboratory) phase of the GMO transformation process, produces hundreds or thousands of random mutations.[6]
These three characteristics of the GMO transformation process used to produce Pandora’s Potatoes – off-target effects of the RNAi technology, insertional mutagenesis of the foreign gene cassettes, and tissue culture-induced mutations – plus the altered biochemistry resulting from the intended gene-silencing effects, can combine to disrupt the GMO plant’s biochemistry. This could lead to adverse crop performance, as well as potentially compromising nutritional value and causing the production of toxins.
These risks are heightened by the fact that potatoes are propagated vegetatively – that is, via tubers and not through setting seed. This means that all the mutations produced during the GMO transformation process (as described above) will be present in the final marketed product, as none will have been bred out through multiple rounds of backcrossing to the non-GMO parent variety.
Contamination risk
The fact that potatoes are propagated vegetatively via tubers means that GMO contamination of non-GMO potatoes will not occur through cross-pollination. However (though Dr. Rommens’s book does not deal with this topic), contamination can occur through “ground keeper” or “volunteer” GMO potatoes that are left in the ground after harvest. They will re-emerge the following year and produce more GMO potatoes. Anyone who has ever grown potatoes will confirm that “volunteers” continue to emerge for years after the last potatoes were intentionally planted in the plot.
It is impossible to tell the difference between GMO and non-GMO potatoes except through molecular analysis by a laboratory, so there is a high risk of GMO contamination from “volunteers” going unnoticed.
Non-organic farmers typically deal with the problem of “volunteers” by spraying them with herbicide when they start growing the following year – adding to the problem of escalating agrochemical use and resulting herbicide residues in food crops.
Claims of enhanced safety not science-based
In conclusion, the implications on the part of the developer company that Pandora’s Potatoes are safer than non-GMO potatoes due to reduced asparagine levels has no solid scientific basis. On the contrary, Pandora’s Potatoes would appear to pose a number of risks to consumers’ health.
Some risks stem from the potatoes’ bruise-concealing trait, which effectively hides the toxins that routinely accumulate in bruised tissues. This means that processors and consumers cannot spot these areas of damage and remove them.
Also, bacterial and fungal pathogens that may be present in bruised parts of the potato can produce known toxins, carcinogens, and allergens. In addition, the multiple mechanisms by which the GM process causes DNA damage can change the plant’s composition in unintended ways, resulting in the production of novel toxins or allergens.
Scientists have expressed concerns that regulators are not adequately considering these risks. Dr. Rommens’s revelations suggest that the developer company also failed to do so.
Thus as a matter of precaution it seems sensible to avoid consuming Pandora’s Potatoes and any processed food products containing them.
References

  1. Ladero V et al (2010). Toxicological effects of dietary biogenic amines. Current Nutrition & Food Science 6(2):145-156(12).
  2. EU Commission (2005). Commission Regulation (EC) No 2073/2005 of 15 November 2005 on microbiological criteria for foodstuffs (Text with EEA relevance). https://eur-lex.europa.eu/legal-content/en/ALL/?uri=CELEX%3A32005R2073
  3. US FDA (2011). Fish and fishery products hazards and controls guidance. Fourth edition. Appendix 5. https://www.fda.gov/downloads/food/guidanceregulation/ucm251970.pdf
  4. EFSA (2015). Scientific opinion on acrylamide in food. EFSA Journal 13(6):4104. https://efsa.onlinelibrary.wiley.com/doi/epdf/10.2903/j.efsa.2015.4104
  5. Heinemann JA et al (2013). A comparative evaluation of the regulation of GM crops or products containing dsRNA and suggested improvements to risk assessments. Environment International 55 (2013) 43–55.
  6. Latham J et al (2006). The mutational consequences of plant transformation. J Biomed Biotechnol 2006:1–7.

Action Items

Regulatory Oversight

 Enhanced Regulations:

  • The FDA and other regulatory bodies must establish stricter guidelines and permissible limits for toxic metals in infant formula. This action has been already put into our place since our meeting with the FDA prior to the release of our data reported in this blog by Moms Across America.

Regular Testing:

  • Mandatory, routine testing for heavy metals in all infant formula products should be enforced to ensure compliance with safety standards.

Transparent Reporting:

  • Companies should be required to disclose test results publicly, promoting transparency and accountability.

Proactive Measures by Companies

Sourcing and Production Controls:

  • Infant formula manufacturers must implement rigorous controls over their raw materials and production processes to minimize contamination.

Regular Audits:

  • Frequent internal and third-party audits should be conducted to ensure adherence to safety protocols and identify potential sources of contamination.

Research and Development:

  • Investment in research to develop technologies and methods for removing or reducing heavy metal content in infant formulas.

Remediation Solutions

Advanced Filtration Systems:

  • Implementing advanced filtration technologies during production to remove toxic metals.

Ingredient Substitution:

  • Identifying and using alternative, less contaminated sources of raw materials.

Chelating Agents:

  • Exploring the use of safe chelating agents that can bind to metals, making them less bioavailable and reducing their toxic effects.

What the Data Means to Moms

For mothers and caregivers, these findings can be alarming. However, it is essential to understand the implications and take informed steps to ensure the safety of their infants. Breastfeeding remains the best option for infant nutrition, when possible, as it naturally minimizes exposure to contaminants.

Recommendations Based on Data

Prioritize Breastfeeding:

  • Whenever possible, opt for breastfeeding to provide the safest and most natural nutrition for your baby.

Choose Carefully:

  • When breastfeeding is not an option, select infant formulas that have been independently tested and verified for low levels of toxic metals.
  • Maximize moms’ diet utilizing organic regenerative whole foods, including an array of fermented foods, filtered water, and nutritional supplements, such as prenatal vitamins and probiotics.

Stay Informed:

  • Keep abreast of the latest research and reports on infant formula safety to make informed decisions.

Advocate for Change:

  • Support initiatives and petitions calling for stricter regulations and safer infant formula products. (See the end of this article for a petition/call-to-action.)

Sample Considerations

The recommendations based on our findings proved challenging since all formulas tested positive for aluminum and lead. Other difficult considerations were based on the fact that not all metals are equally toxic and it is unclear whether having more metals at lower amounts was more toxic than fewer metals with higher amounts. The literature did not prove helpful in this regard.

Hence, the best attempts were made to offer advice for concerned parents based on this one study of toxic metals without other concomitant toxicants studied. A scorecard was designed, rating the formulas from 1 – 3, with 1 being the best based on 5 toxic metals studied and without consideration of other factors. The formulas were chosen for lowest levels of lead, mercury and cadmium. Lower levels of aluminum were considered since they all tested positive. There were no ideal formulations, and the recommendations were based on the 20 tested. There were differences in the two samples of the same formula which may not be statistically significant.

Overall formula recommendations:1

  1. Similac Sensitive infant formula
  2. Kirkland ProCare Non-GMO infant formula – NOTE: My top choice factoring in other contaminants/pesticides
  3. PurAmino hypoallergenic powder infant formula (For babies with digestive issues requiring predigested formulas)

Formula recommendations:2

  1. Gerber Good Start Gentle Pro
  2. Earth’s Best Organic Sensitivity Formula

Formula recommendations:3

  1. Enfamil Sensitive Infant Formula
  2. Similac Total Comfort Infant Formula
  3. Up & Up Gentle Premium Powder Infant Formula
  4. Up & Up Non-GMO Hypoallergenic Powder Infant Formula
  5. Enfamil Plant-Based Soy Powder Infant Formula

Strategic Recommendations

Targeted Research

Understand Contamination Sources:

  • Conduct further research to understand the sources of metal contamination in infant formulas, including soil contamination with pesticides, water used in manufacturing, and packaging materials.

Long-Term Health Impacts:

  • Investigate the long-term health impacts of chronic exposure to low levels of these metals in infants.

Consumer Guidance

Interpreting Lab Results:

  • Educate parents on how to interpret lab results and select formulas with the lowest possible contamination levels.

Support Safe Feeding Practices:

  • Provide resources and support for parents to transition to safer feeding practices, whether through breastfeeding support or safer formula alternatives.

Enhanced Testing Protocols

Rigorous Testing:

  • Mandate formula manufacturers to adopt more rigorous testing protocols, including testing for a broader range of contaminants and more frequent testing intervals.

Standardized Procedures:

  • Advocate for standardized testing procedures across the industry to ensure consistency and reliability in reported results.

Supply Chain Transparency

Transparency:

  • Push for greater transparency in the supply chain of infant formula ingredients.
  • This includes sourcing, production processes, and quality control measures.

Traceability:

  • Implement traceability measures to identify and mitigate contamination sources promptly.

Policy and Advocacy

Environmental Contamination:

  • Support policy initiatives aimed at reducing environmental contamination, as many of these metals enter the food chain through polluted air, water, and soil.

International Cooperation:

  • Advocate for international cooperation to address the global nature of food safety, as ingredients are often sourced from multiple countries.

Summary

The presence of toxic metals in infant formula is a critical issue that demands immediate action.

Public education is crucial to raise awareness among parents and caregivers about the potential risks and safety measures. Regulatory action by Congress is necessary to empower the FDA and other agencies to enforce stringent safety standards. Additionally, formula companies must take corrective actions to ensure their products are safe.

To address this issue, we are initiating a petition to urge Congress to remove any barriers preventing the FDA from enforcing these necessary regulations. In the meantime, parents can consider various supplements that may help offset the toxicity, although this should be done in consultation with healthcare professionals.

By working together—regulators, companies, and consumers—we can ensure that infant formula products are safe and healthy for our most vulnerable population, our babies.

Our Petition:

Please cut and paste this letter, add 1-3 sentences at the top to personalize it and increase the chances of it being read, and send it directly to your Senator and Representative today!

Find your Senator and Representatives’ emails and telephone numbers here.

Dear Senator_____ or Representative _______,

I am writing to ask for your support in making baby food and formula safer for our babies. Will you support the Baby Food Safety Act of 2024 and insist that baby formula is included? Please authorize the FDA with the ability to do their job and protect human health. Baby formula is often the ONLY food a baby consumes for the first six months of their lives and must be monitored for heavy metals. Our babies ARE our future and they are the most vulnerable. If swift action is not taken, babies from both sides of the aisle will continue to be severely impacted and their mental, physical, and reproductive health issues will affect the future of America.

GMOScience and The New MDS, Moms Across America, a national educational nonprofit dedicated to empowering mothers and others to create healthy families and communities, today announces the results of testing for five toxic metals in 20 infant formula products. Samples included organic as well as non-organic and plant-based as well as animal product formulas sold by four of the major producers of infant formula in the United States and across the globe. Two samples of each product were tested, for a total of 40 samples.

Concerning findings include:

  • 100% of the 40 samples tested contained aluminum and lead.
  • 57% of the samples tested positive for arsenic, 55% for mercury, and 35% for cadmium.
  • Six of the 20 formulas were positive for all five toxic metals in both samples.
  • At 41,000 ppb, aluminum levels in a goat’s milk baby formula were 4000 – 40,000x higher than other metals in the formulas tested and exceed limits set by the FDA for maximum safety level of aluminum for a preemie.
  • Levels of mercury in four samples measured above the limit allowed by the FDA in drinking water.
  • Levels of cadmium in both samples of one formula were nearly twice the level allowed in drinking water.

The FDA concluded many years ago that babies and young children are particularly vulnerable to the harmful effects of food contaminants because of their small bodies and rapid cellular growth. In 1962, the FDA launched the Total Diet Study, recently published in July, 2002, analyzing 910 foods, including only four infant formulas. Two of the four formulas contained toxic metals, including uranium. In April 2021, the FDA announced its “Closer to Zero” plan, wherein it committed to proposing allowable levels of lead in various baby foods by April 2022, levels of inorganic arsenic by April 2024, and cadmium and mercury sometime after 2024. None of those deadlines, however, have been met, and all of them have been removed from the Closer to Zero website.

To date, the only actionable limits the agency has set are for one toxic metal only (inorganic arsenic) in one type of baby food product (infant rice cereal).

Citing findings of nearly 400 childhood lead poisoning cases in fall 2023 linked to recalled cinnamon applesauce pouches. A coalition of 20 Attorneys General led by New York’s Attorney General Letitia James issued a letter to the FDA on February 15 of this year to call on the federal agency to protect babies and young children in the United States from lead and other toxic metals in baby food. That letter followed an October 2021 petition and subsequent June 2022 petition, asking the FDA to issue specific guidance to the baby food industry to require testing of all finished food products for lead and other toxic metals.

It has been over two years! Action must be taken now!

Moms Across America, GlyphosateFacts, and GMOScience presented the new baby formula test results and science from Stephanie Seneff and others in meetings with congressional representatives and the FDA in Washington, DC from April 29 to May 2. They were informed by Jim Jones, Deputy Commissioner for Human Foods at the FDA, that the agency is waiting for Congress to pass legislation that would mandate testing for lead and other harmful chemicals in food. On May 9, US lawmakers introduced the Baby Food Safety Act of 2024, which, with Congressional approval, would allow the FDA to regulate and enforce limits on levels of heavy metals found in baby food and potentially formula.

Please support the Baby Food Safety Act of 2024 and insist that baby formula is added to the bill so that the FDA may regulate and monitor levels of heavy metals in both baby food and baby formula.

Thank you.

Signed with Gratitude,

Your constituent __________________

References:

  1. https://www.fda.gov/food/resources-you-food/infant-formula#oversee
  2. https://www.fda.gov/food/resources-you-food/infant-formula
  3. https://www.fda.gov/food/buy-store-serve-safe-food/handling-infant-formula-safely-what-you-need-know
  4. https://www.fda.gov/food/consumers/agricultural-biotechnology
  5. https://www.fda.gov/food/people-risk-foodborne-illness/food-safety-infants-toddlers
  6. https://www.fda.gov/food/infant-formula-guidance-documents-regulatory-information/enforcement-discretion-manufacturers-increase-infant-formula-supplies#regular
  7. https://www.fda.gov/media/71695/download?attachment
  8. https://www.scirp.org/journal/paperinformation?paperid=53106
  9. https://www.researchgate.net/profile/David-Kennedy-40/publication/333582853_Environmental_toxicants_and_infant_mortality_in_America_Peertechz_Journal_of_Biological_Research_and_Development_11_36-61/links/5d111f6592851cf440492ee1/Environmental-toxicants-and-infant-mortality-in-America-Peertechz-Journal-of-Biological-Research-and-Development-11-36-61.pdf
  10. unsafe at any level
  11. https://reneedufault.com/
  12. https://gmoscience.org/
  13. https://www.momsacrossamerica.com/
  14. https://www.ewg.org/research/ewgs-guide-infant-formula-and-baby-bottles
  15. https://www.inonaround.org/baby-formula/
  16. https://projecttendr.thearc.org/
  17. https://hbbf.org/
  18. https://www.hbbf.org/solutions/healthy-baby-foods
  19. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415012/: Developmental pesticide exposure reproduces features of attention deficit hyperactivity disorder
  20. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871549/:Prenatal Mercury Exposure and Neurodevelopment up to the Age of 5 Years: A Systematic Review
  21. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461492/:Fetal and postnatal metal dysregulation in autism
  22. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1764574/:Lead and mercury exposures: interpretation and action

https://www.nass.usda.gov/Surveys/Guide_to_NASS_Surveys/Chemical_Use/WheatPostharvestChemicalUseFactSheet.pdf

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