Ending all forms of hunger by 2030, as set forward in the UN-Sustainable Development Goal 2 (UN-SDG2), is a daunting but essential task, given the limited timeline ahead and the negative global health and socio-economic impact of hunger. Malnutrition or hidden hunger due to micronutrient deficiencies affects about one third of the world population and severely jeopardizes economic development. Staple crop biofortification through gene stacking, using a rational combination of conventional breeding and metabolic engineering strategies, should enable a leap forward within the coming decade. A number of specific actions and policy interventions are proposed to reach this goal.
Micronutrient malnutrition or hidden hunger, the insufficient intake of vitamins and minerals, has a detrimental impact on human health. Hidden hunger affects more than two billion people worldwide, and has the highest prevalence in the African continent and South Asia. Children and women of reproductive age are most vulnerable to malnutrition, leading to stunted growth, health problems, and several birth related issues. Though seven minerals (iron, zinc, copper, calcium, magnesium, selenium, and iodine1) and several vitamins2 are often lacking in human diets, iron, zinc, vitamin A, and vitamin B9 (folate) deficiencies are amongst the most severe3,4,5. Biofortification, the elevation of the levels of micronutrients in food crops through agricultural technologies, is advocated as a pivotal means to reduce micronutrient malnutrition6.
Impressive progress has been made in biofortification of mainly single micronutrients across an array of primary staple food crops6,7. Biofortified crops have been developed via conventional breeding or genetic engineering, although the latter have yet to receive full approval for release to farmers. Biofortification via genetic engineering can enable high level accumulation of micronutrients and is not constrained by variation in available germplasm. Biofortification strategies can combine conventional breeding with genetic engineering. Genetic engineering enables simultaneous augmentation of multiple micronutrients, along with improving the post-harvest stability of vitamins, whilst also including agronomically important traits, such as enhanced yield and stress resilience.
In the last few years, the cost-effectiveness and feasibility of implementing biofortification using conventional breeding techniques has been established as a key intervention to reduce mineral and vitamin deficiencies in developing countries8. Consequently, a recent World Bank report takes the position that biofortified cereal crops should be the norm rather than the exception9.
HarvestPlus, which is a program under the Consultative Group on International Agricultural Research (CGIAR) Research Program on Agriculture for Nutrition and Health, is an umbrella of institutions working on biofortification in low- and middle-income countries. HarvestPlus collaborating institutions have developed, tested, released, and promoted the uptake by farmers and consumers of the following crops: zinc rice, zinc wheat, zinc maize, provitamin A maize, provitamin A cassava, iron beans, and iron pearl millet7. Approximately 8.5 million farm households across Africa, Asia, and Latin America are growing these biofortified crops (https://www.harvestplus.org). In addition, under the sponsorship of the International Potato Center (CIP), CIP and its partners have led the development, testing, and promotion of orange (high provitamin A) sweet potato10. CIP estimates that nearly seven million farm households, primarily in Africa, are now growing and consuming orange sweet potato (https://www.cipotato.org).
Through their combined efforts, biofortified crops are now released in 40 countries globally.
Additionally, a few other institutions have successfully worked on particular aspects of the development and testing of specific crops to achieve biofortification with minerals and vitamins through conventional breeding. However, these individual efforts are awaiting incorporation into breeding programs or to field applications (for a review, see Garg et al.6).
Despite wide acceptance of the effectiveness of biofortification and demonstrated high return on investment, the increase of only one nutrient per crop (either iron or zinc or provitamin A) remains a limiting factor– for example high zinc wheat, or high provitamin A maize. The breeding and release process for the first wave of biofortified varieties took 8–10 years. In a small number of cases, there is sufficient germplasm variation within the target crop species to add a second nutrient (e.g. high zinc into high provitamin A maize) using conventional breeding techniques, but this is expected to take an additional 8–10 years.
Metabolic engineering through transgenic technology enables introducing multiple biofortification traits, including high iron, high zinc, high provitamin A, or high folate, to most biofortified crop varieties relatively quickly – that is, in significantly <8–10 years. It may also be possible to reduce or stop the decrease of vitamin densities after harvest and during storage, which occurs due to exposure to light, oxygen, and/or high temperature. Furthermore, multi-biofortification can not only create crop products with stable enhanced micronutrients but also take advantage of the most profitable, highest yielding, and locally best-adapted varieties.
Hidden hunger is a huge problem for human health and economies
Hidden hunger is the direct result of insufficient acquisition of minerals and vitamins from the diet. An estimated 2 billion people in the developing world suffer from health effects caused by hidden hunger (mainly related to deficiencies of iron, zinc, vitamin A, and folates (vitamin B9))11. This is primarily the result of poor-quality diets consisting of adequate energy consumption from inexpensive staple crops, but little consumption of expensive vegetable, fruit, pulses, and animal products that are richer in bioavailable minerals and vitamins. Inadequate intakes of essential vitamins and minerals affect disease resistance, cognitive development, physical growth, work productivity, and survival rate. Preschool children and women in their reproductive age are most vulnerable to deficiencies because they require higher micronutrient intakes12. Agricultural systems in developing countries are not providing sufficient minerals and vitamins at affordable prices for optimal nutrition and health. Supplements often do not reach the populations in need13. As impaired micronutrient status aggravates susceptibility to infectious diseases including COVID-1914,15, the current pandemic further underscores the need to improve the nutritional status of poor rural populations and increase their nutritional self-sufficiency through staple crop biofortification.
To combat vitamin A deficiency, for example, 10 billion vitamin A capsules (at an approximate cost of US dollar 10–15 billion) have been distributed over the past twenty years to preschool children – with the effect of reducing preschool mortality by an estimated 12–24%16. In addition, the Global Burden of Disease Study 2015 estimates that 1.5 billion people suffer from iron (Fe) deficiency anemia, which impairs cognitive function in preschool children17. Nearly 1.2 billion people are also at risk of zinc deficiency, which is associated with weakened immune systems and higher mortality18. Stunting, which likely results from zinc (Zn) deficiency as well, affects one out of four children under the age of five. Stunting is strongly associated with poor brain development and cognitive function19. Moreover, folate deficiency, which causes neural tube defects (NTDs) and megaloblastic anemia, and also aggravates iron deficiency anemia, is a highly underestimated form of hidden hunger. Worldwide, at least 300,000 births are affected by NTDs annually, the majority of which are caused by inadequate maternal folate status20. This number is largely underestimated because of a paucity of data on stillbirths and elective terminations, as well as lacking surveillance systems in low- and middle-income countries.
Progress in achieving the global targets of reducing child stunting by 40% and anemia by 50% by 2025 is still far too slow21. Global losses in economic productivity due to macronutrient and micronutrient deficiencies reach more than 3% of GDP22 at a global cost of US dollar 1.4-2.1 trillion per year3,23. Micronutrient malnutrition poses a great threat to global human health and economic development. Therefore, eliminating or at least restricting its occurrence is of utmost importance, which is in line with the United Nations Sustainable Developmental Goal 2 (UN-SDG2) i.e. achieving zero hunger.
Crop biofortification using conventional breeding techniques
Biofortification aims at increasing the content of one or multiple micronutrients in staple food crops through agricultural technologies. In some cases, conventional breeding can be utilized to achieve this goal, thereby ensuring higher vitamin or mineral intake of the poor populations relying on the specific staple crop. For example, HarvestPlus (https://www.harvestplus.org) seeks to develop and distribute varieties of food crops (rice, wheat, maize, cassava, pearl millet, beans, and sweet potato) that have higher levels of iron, zinc, and provitamin A (one nutrient per crop) through an interdisciplinary global alliance of more than 400 scientific institutions and implementing agencies in developing and developed countries.
To be successful, three requirements must be met for implementation of biofortification. First, high and stable micronutrient density must be combined with high crop yield and productivity at similar costs to be attractive for farmers and consumers. Second, efficacy for human health must be demonstrated – the micronutrient status of human subjects must improve with regular consumption of biofortified varieties. Thus, adequate micronutrient levels must be retained during storage, processing, and cooking, and these nutrients must be sufficiently bioavailable. Third, the biofortified crops must be adopted by farmers and consumed by those suffering from micronutrient malnutrition, which requires incentives, education, and an appropriate delivery strategy.
Through the combined efforts of HarvestPlus and CIP and their collaborating partners, more than 300 varieties of conventionally bred biofortified crops have been approved by varietal release committees in 40 developing countries and are being tested for release in an additional 20 countries (https://www.harvestplus.org and https://www.cipotato.org). Efficacy trials have demonstrated improved zinc, iron, and provitamin A status in malnourished populations, improved cognitive function and work performance, as well as lower morbidity24,25,26. The ultimate vision is for all national agricultural research institutes to make high mineral and vitamin density core, non-negotiable breeding traits.
Biofortified crops offer a rural-based intervention that initially reaches these more remote populations that comprise a majority of the malnourished in many countries. This is then extended to urban populations as production surpluses are marketed. Initial investments in agricultural research at a central location can generate high recurrent benefits as locally adapted biofortified varieties become available in country after country across time at low recurrent costs.
Conventionally bred biofortified crops can provide an extra 20 to ≥100% of the Estimated Average Requirement (EAR; median daily intake value estimated to meet the requirement of half the healthy individuals in a life-stage and gender group) for specific nutrients7,27,28. The average addition to the EAR is ~25% for zinc crops, 35% for iron crops, and >85% for provitamin A crops7,27,28 (https://www.harvestplus.org/content/estimated-average-requirements-provided-biofortification; Table 1).
Increasing multiple minerals using metabolic engineering
When the natural variation in sexually compatible germplasm is insufficient to achieve satisfactory micronutrient levels in a specific crop by conventional breeding, biofortification via metabolic engineering can offer a solution. In rice, this is the case for multiple micronutrients, including iron, provitamin A, and folates.
Increasing Fe and Zn content in rice, which is consumed by ~3.5 billion people, has a remarkable potential to alleviate micronutrient deficiencies. To provide an additional 30% of the EAR in women and children, the iron concentration in polished grain needs to be increased by 11 ppm from the baseline of 2 ppm to reach 13 ppm, assuming of 10% bioavailability; while for zinc, an increase of 12 ppm from 16 ppm will provide an additional 30% of the EAR, assuming of 20% bioavailability7. Micronutrient levels in polished grains are most relevant, as polished grains represent the energy-rich white rice which is consumed by the populations suffering from micronutrient deficiencies. Only a limited variation for iron in polished rice is available in germplasm collections, which limits conventional breeding for this trait. However, there is sufficient natural variation for zinc to reach a concentration of 28 ppm. Several high zinc rice lines, created through conventional breeding, have been released in Bangladesh, and were recently released or are under development for several additional countries (www.harvestplus.org).
In the abovementioned case where conventional breeding is constrained by limited natural variation, genetic engineering can be used to augment micronutrient content in crop plants. Identification of most of the key genes involved in Fe and Zn uptake, translocation, and storage29,30 has facilitated the development of enriched Fe and Zn rice by transgenic approaches31. For the same event, a significant increase in both Fe (up to 15 ppm) and Zn (to 45 ppm) in polished grain was successfully achieved in a high-yielding variety, without increased uptake of unwanted heavy metals (cadmium, arsenic, and lead)32,33. The level of Zn in this transgenic variety is significantly higher than in the released conventionally bred Zn cultivars.
Combining Fe and Zn traits with other micronutrients and agronomic traits in multiple high-yielding varieties is obviously desirable. With respect to mineral micronutrient enhancement, it should be emphasized that success of biofortification fully depends on both the level and bioavailability of the different minerals in the soil. Where the latter are insufficiently present in the substrate, foliar, or soil fertilization can be applied34. These agronomic strategies are complimentary to metabolic engineering and breeding technologies in poor soils.
Filling in a biosynthetic gap towards provitamin A in rice
An example of how genetic engineering enables introduction of a micronutrient that is essentially absent in a crop species is Golden Rice, which is enriched in provitamin A (β-carotene)35. Rice leaves, and indeed the photosynthetic tissues of all higher plants, produce and accumulate β-carotene. However, non-engineered polished white rice has no detectable provitamin A carotenoids, as the outer layers of the kernel that do contain low amounts of this vitamin are removed during the polishing process. No naturally occurring rice varieties have been reported that accumulate β-carotene in the grain and could be used for conventional breeding, thus genetic engineering provides the only viable approach.
The second-generation Golden Rice (GR2E)36 has been found to accumulate up to 37 ppm dry weight total carotenoids in the polished grains immediately after harvest, although the concentration is dependent on the genetic background and reduces during storage after harvest. To make this trait suitable for cultivation in Asia, the transgenic GR2E rice required breeding into farmer-preferred indica rice varieties, yielding lines containing between 3.5 and 10.9 ppm dry weight total carotenoids in polished grains37. Even with these lower concentrations of provitamin A, it is estimated that 100 g of uncooked GR2E can supply 30−40% of the recommended daily allowance (RDA) of vitamin A for children25, at least 75% of which remains after cooking38.
Golden Rice has provided a number of lessons for future programs to develop and introduce transgenic biofortified crops. The process of moving from proof of concept to a product that can be used by farmers and consumers is difficult, as illustrated by the sequential evaluation of various transgenic GR2 events since 2006. Arguably, a more effective selection earlier in the process would have accelerated the establishment of events qualified for breeding. In addition, the challenges of working with a transgenic regulated product in countries with new or changing regulatory processes cannot be underestimated. These factors, combined with the high public profile of Golden Rice as both a standard bearer for plant biotechnology and a target of activists, have made for an unnecessarily long and arduous journey. However, there is reason for optimism. The December 2019 decision by the Government of the Philippines to authorize the direct use of GR2E in food, feed, and for processing39 is greatly encouraging for its eventual release. Submission of an application for commercial propagation of Golden Rice in the Philippines is anticipated in 2020. In addition to the import approvals already obtained in Australia, Canada, New Zealand, and the US40,41,42, an application for cultivation and food use was submitted in Bangladesh in November 201743, where it remains under review.
The slow progress of Golden Rice in Bangladesh illustrates a fundamental problem for genetically engineered biofortified crops that do not also provide an agronomic benefit. Especially in countries with new and evolving regulatory frameworks, the authorization of a genetically engineered crop requires committed support among all key decision-makers, often at some political risk. New products must not only meet environmental, animal, and human health and safety standards, but must present a compelling value proposition that can garner the support of not only just nutritionists and ministries of health and family welfare, but also ministries of agriculture who wield significant influence in the decision-making process. Also critically important is how the value proposition is framed, and by whom, recognizing that local voices are the most authentic and persuasive.
Reaching the RDA in single food servings
Inadequate intake of B-vitamins is highly prevalent in regions where rice is the main staple food. The natural variation of folates in rice is far too low to reach the necessary increase of at least 100-fold to meet the RDA value for pregnant women with one or two servings of 100 g of white rice44. The first successful example of a genetic engineering approach improving rice for B-vitamins is the 100-fold increase of folates (vitamin B9) in polished rice grains, reaching 1723 µg/100 g fresh weight, which is close to the RDA and more than the EAR in a single serving45.
Genetic engineering of the B-vitamin metabolic pathways has been successful in different staple crops. Increased levels of bioavailable vitamin B6 could be achieved in cassava storage roots46, while folate levels could also be significantly increased in potato tubers47 as well as wheat and maize grains48. Efforts to engineer the vitamin B6 metabolic pathway in rice have revealed limitations in increasing B6 vitamin levels in polished white rice; however, the same strategy was capable of elevating B6 vitamin levels in rice leaves49. Therefore, further research is needed to understand the factors currently impeding the genetic engineering of the B6 and other B-vitamin metabolic pathways in rice endosperm.
Reducing or stopping post-harvest vitamin degradation
A potentially more effective or complementary breeding strategy for high vitamin levels in foods produced from biofortified crops is the reduction or complete prevention of vitamin degradation after harvest. Ensuring post-harvest storage stability of vitamins is of paramount importance, especially considering the longer storage at elevated temperatures, which is a typical practice in populations suffering from vitamin deficiencies50. Provided that sufficient fundamental knowledge on vitamin stabilization is available, engineering these traits in food crops can yield both increased vitamin accumulation as well as elevated stability. The long-term stabilization of vitamin B9 obtained by introduction of genes encoding folate binding proteins or altering folate structure to enable increased (post-harvest) stability are successful and encouraging examples50. Moreover, the combination of this B9 stabilizing strategy with the aforementioned folate biofortification approach has enabled the hyper-accumulation of folate (up to 150-fold of wild-type rice levels) in transgenic polished rice seeds50. Similar approaches might also help to increase vitamin B1 and B6 stability in the polished rice grain.
Like folates, all other vitamins are prone to breakdown during storage, with varying sensitivity depending on the specific vitamin and food matrix. A study of β-carotene corn in Zambia showed that provitamin A levels had dropped by 70% after 6 months51; similar losses were reported for polished Golden Rice38. Nevertheless, amounts remaining after degradation can still provide an additional amount of vitamin A in the diet, ~40% of the EAR, and the rate of degradation asymptotically approaches zero after a certain time point.
Different approaches have been shown to successfully stabilize provitamin A in engineered staple crops. In potato, β-carotene levels can be enhanced and stabilized by introduction of the Orange(Or) gene52. Or induces the formation of chromoplasts, which naturally function as a metabolic sink for carotenoid accumulation. Overexpression of Or together with the two other genes for β-carotene biosynthesis in GR2 enhanced β-carotene levels in polished rice to 26 ppm dry weight, though stability of the provitamin A still needs to be investigated53. Alternatively, engineering towards decreased carotenoid oxidation, an important form of provitamin A degradation, increased provitamin A stability in polished Golden Rice during storage54. Suppressing provitamin A breakdown has also been implemented in wheat to increase β-carotene levels 31-fold55. In another approach, combining engineering towards higher accumulation of tocochromanols, fat-soluble E-vitamins bearing antioxidant properties with the approach used in GR2 has shown that vitamin E can enhance the stability of provitamin A in sorghum grain, more than doubling its metabolic half-life56.
Simultaneously increasing multiple nutrients
Combining, or stacking, multiple nutrient traits into high-yielding varieties is important and preferable over single nutrient enhancement57, similar to the routine stacking of transgenes for insect resistance and herbicide tolerance in cotton and maize58,59. Combining several nutrition-related genes from multiple parents, including genetically engineered crops such as Golden Rice, into a single genotype through conventional backcrossing is possible, but very time-consuming and laborious. Also, care must be taken to avoid undesired alteration of other favorable plant characteristics in the backcrossing process and to prevent segregation of transgenic traits in subsequent generations. Therefore, combining multiple traits through conventional breeding remains a challenge, particularly given that simultaneous selection for multiple traits becomes increasingly difficult as the number of traits increases.
Today’s transgenic technologies substantially reduce the time frame in which a multi-nutrient product can be engineered and identified. For example, a single locus multi-nutrient trait improvement has been recently accomplished by simultaneously increasing iron, zinc, and β-carotene content in polished rice60. This illustrates the relative ease with which multiple micronutrients (iron, zinc, and provitamin A in this case) can be tackled by insertion of a single DNA fragment into the rice genome. This approach is encouraging and opens new perspectives for developing multi-nutrient staple crop varieties in one step. It exemplifies an effective and sustainable way of addressing multiple micronutrient deficiencies that often co-occur in affected populations11,61. Metabolic engineering allows design of strategies to jointly boost an array of different micronutrients (e.g. iron, zinc, vitamin A, and vitamin B9), whilst also taking the aforementioned stability into account. Moreover, with the advent of genome editing technologies, it is now possible to insert a gene cassette at a pre-defined location (safe harbor) in the genome of a crop plant, thereby avoiding adverse effects such as yield losses62. On a cautionary note, researchers need vigilance to recognize unintended metabolic consequences of biofortification. For example, provitamin A biofortification of cassava and sweet potato significantly reduces dry matter content of storage roots63. Since dry matter is a major factor influencing food texture, it is an essential component in product adoption. Enhancing other micronutrients might have a similar negative impact, possibly exacerbated in multi-biofortified crops.
As a health intervention, even single-nutrient biofortification is inherently cost-effective due to very low recurrent costs once varieties have been developed at a central location and widely distributed. Other micronutrient interventions, such as supplementation and industrial fortification of processed foods, involve much higher recurrent costs and are not directed at solving the underlying cause of micronutrient deficiencies, which is that agricultural systems are not producing affordable supplies of required minerals and vitamins7. Multi-nutrient biofortification can realize even more substantial economies of scale. While genetically engineered biofortified crops are associated with substantial development and regulatory costs, they are estimated to be highly cost-effective, often more than conventional or complementary approaches64. Ex-ante evaluation of multi-nutrient rice (provitamin A, folate, zinc, iron) in China, for example, has confirmed the potential, long-term cost-effectiveness65. Aside from synergies through aggregated health impacts and cost savings (from development to dissemination), multi-nutrient biofortification can lead to much higher market coverage, as competition between several single-nutrient biofortified varieties is avoided.
Simultaneous improvement of nutritional and agronomic traits
A multi-nutrient trait locus stacked with genes of interest can be easily transferred to farmer-preferred crops, either by breeding or direct transformation in shorter time period. Genetic cassettes can now combine many more stacked genes and therefore it is conceivable that simultaneous micronutrient improvement of staple crops is no longer limited to three traits. Also, gene stacks for nutritional traits can be combined with important agronomic traits in the same genetic locus, such as pest and disease resistance (e.g., resistance to bacterial blight, army worms, brown plant hoppers, or stem borers in rice) or abiotic stress tolerance (e.g., drought, heat, salinity, cold, flooding tolerance; Fig. 1). This will make it more attractive for farmers to adopt nutritionally improved staple crop varieties and therefore accelerate the percentage of the total supply of rice (or other staple food crops) that is biofortified. Single insert gene cassettes using proven genes can be customized for specific regional needs or consumer preferences, which might also be favorable from a regulatory point of view. In an era of global climate change, the single locus-multiple trait approach combining nutritional traits with stress resilience genes can provide region-specific solutions for sustainable agriculture with benefits both for farmers and consumers. In doing so, genetically engineered biofortified crops might acquire a higher economic value that positively impacts their regulatory review66.
Small-scale farmers and low-income rural communities in Africa and Asia are the ones suffering most from micronutrient deficiencies and are likely also the ones that will be hit hardest by climate change and related weather extremes. Genetic engineering technologies alone are not a magic bullet that will solve these problems, but they can help considerably in making small-farm systems more productive, resilient, and nutrition-sensitive. In the past, with conventional breeding approaches, breeding for higher yields was sometimes associated with lower crop robustness and lower nutritional value. Such tradeoffs can now be avoided. Another important advantage of genetic engineering is the much greater speed of breeding, especially against the background of climatic changes leading to new weather and pest infestation conditions that are not always predictable. Studies suggest that harnessing new breeding technologies for combining nutritional and agronomic traits can lead to large economic and social benefits in developing countries and represent an important step towards sustainable food security67,68.
Proposed actions and policy interventions
UN-SDG2 of ending all forms of hunger and malnutrition by 2030 needs much swifter actions than those that are currently deployed. Implementation of biofortified crops, either obtained by conventional breeding, genetic engineering, or their combination can substantially contribute to reach this goal. Fortunately, the speed at which novel crops can be developed is more rapid than ever due to advances in gene cloning and genome editing technologies69,70. Together, these technologies provide the means of minimizing trait loss due to instable genomic context and optimization of gene expression levels.
Reaching health-relevant nutritional targets is often not possible by conventional breeding. Presently, the combination of genetic engineering and conventional breeding is the most powerful approach when aiming at multi-nutrient crops. There are currently no examples of sufficient nutrient enhancement via genome editing approaches. Genome editing technologies alone are indeed not solving the problem until we have a better understanding of the tissue-specific activity of relevant gene promoters or unless mutations can be identified that boost the reaction rate of required enzymes. Genetic engineering should go hand in hand with conventional breeding and could be assisted by novel breeding technologies for site-specific (safe harbor) insertion.
Conventionally bred biofortified crops have been extensively tested for efficacy, even showing improved functional outcomes such as lower morbidity, improved cognitive performance, and work capacity. These trials have taken into account nutrient losses due to processing and cooking, and during storage. The presumption is that higher nutrient levels, as consumed, in transgenic foods will show even better nutrition and functional outcomes, although trials are needed to confirm this. Modern breeding technologies including genetic engineering should be applied to elite germplasm for combining nutritional and agronomic traits to produce high quality-high yield crops.
In this context, therefore, the following specific actions and policy interventions are recommended (Fig. 2):
There is a need to expand germplasm collections as well as screen existing germplasm to better characterize natural diversity of micronutrients as the benefit could be two-fold: availability of genotypes for conventional breeding approaches and genetic material to better understand vitamin biosynthesis and micronutrient accumulation in planta.
Key to making biofortified crops successful is their accessibility in a way that vulnerable population groups and smallholder/subsistence farmers can affordably receive these biofortified crops. Release of the biofortified crop products needs to be preceded by ethically approved and well-designed dietary studies supporting their effect. Humanitarian licenses will be needed from institutions that own intellectual property rights on these crops as well as genome editing technologies and genetic elements used in biofortification approaches. This enforces independence from seed companies, which will allow for a better public perception of genetic engineering technology, especially if clear health (consumer-related) and economic (farmer-related) benefits are demonstrated.
Single locus, multi-nutrient trait strategies facilitate qualitative product improvement without altering plant health and creating environmental issues. The safety of genetically engineered crops for consumers and the environment was endorsed by Science Academies worldwide (http://nas-sites.org/ge-crops/category/report/) and by over 100 Nobel laureates71. However, there is still a need to provide independent and science-based information to the public on safety of genetically modified crops.
Regulatory frameworks for genetically engineered foods and crops need to be established, or updated and modernized in different countries, to acknowledge three decades of experience and evidence of their safety. Regulations should be proportionate to the level of risk, considering both familiarity and history of safe use. The May 2020 announcement by the U.S. Department of Agriculture’s Animal and Plant Health Inspection Service (APHIS) to exempt certain categories of gene edited plants from its regulatory oversight signals an important shift from process-based regulation to an approach that focuses on the new traits themselves. Many countries (e.g. in Africa) either do not have a regulatory framework or very restrictive for the release of transgenic crops. The establishment of local non-profit organizations (e.g. Cornell Alliance for Science) aiding the public, media and policymakers in understanding the implications of introduction of multi-biofortified crops, both from a health and a socio-economic perspective, should ease the process towards cultivation of biofortified crops by small-scale farmers and release of the products to low-income rural communities. Publicly funded bodies, preferably with additional financial backing of charitable organizations, coordinated by governments in concert with local academics could ensure a non-profit route towards population groups in need.
Capacity needs to be built in developing countries to increase impact by implementation of technologies in farmer- and consumer-preferred crop varieties. Empowering research and product development capacities in regions where metabolically engineered biofortified crops are needed is the key to facilitate technology adoption72,73. Regional research centers and universities, for instance, can focus on the development of genetic transformation and genome editing tools in local recalcitrant genotypes. Likewise, local agricultural institutions, particularly in regulatory-benign countries, can be involved in the development phase of the work under the form of field trials. This is particularly important for crops requiring extensive breeding programs due to a long life-cycle, asynchronous flowering, and high heterozygosity.
Metabolic engineering, combined with conventional breeding, can catalyze a much more rapid approach to the realization of zero hunger and to reducing malnutrition by crop biofortification along the successful path paved by HarvestPlus and other public institutions. Based on decades of experience with the widespread and safe production of transgenic maize and soybean as food crops, the consensus among Academies of Science globally is that transgenic crops introduced thus far are not harmful to the environment and are safe for human consumption. Considering the fact that many crop species, including sweet potato, yams, and banana, are naturally transformed by T-DNA from Agrobacterium74, common sense should prevail when governments decide on legal frameworks for the release of transgenic crops. Such decisions should be solely driven by the determination to improve human welfare and sustainability. However, scientists have an important role to play beyond the walls of their labs, notably in transferring of knowledge and making sure that regulatory decisions are based on ratio. Academies of Science over the globe can, together with the publicly funded bodies advocated above, function as a motor in the process of knowledge transfer towards policymakers.
Biofortification, in combination with dietary diversification and nutrition education, holds great potential to eradicate micronutrient malnutrition and increase global human health (Fig. 3). The next gene revolution should focus on sustainable solutions for malnutrition, as part of a humanitarian intervention, concerted with educational efforts as a cornerstone to halt population growth, improve living standards, and bring about global peace.
Source Data are provided with this paper.
White, P. J. & Broadley, M. R. Biofortification of crops with seven mineral elements often lacking in human diets - iron, zinc, copper, calcium, magnesium, selenium and iodine. New Phytol. 182, 49–84 (2009).
Fitzpatrick, T. B. et al. Vitamin deficiencies in humans: can plant science help? Plant Cell 24, 395–414 (2012).
FAO. FAOSTAT. Food and Agriculture Organization of the United Nations (2017).
Ruel-Bergeron J. C. et al. Global update and trends of hidden hunger, 1995-2011: the hidden hunger index. PLoS ONE 10, e0143497 (2015).
Beall T., Massiot E., Arsenault J. E., Smith M. R., Hijmans R. J. Global trends in dietary micronutrient supplies and estimated prevalence of inadequate intakes. PLoS ONE 12, e0175554 (2017).
Garg, M. et al. Biofortified crops generated by breeding, agronomy and transgenic approaches are improving lives of millions of people around the world. Front. Nutr. 5, 12 (2018).
Bouis, H. E. & Saltzman, A. Improving nutrition through biofortification: a review of evidence from HarvestPlus, 2003 through 2016. Glob. Food Sec. 12, 49–58 (2017). This is the primary article reviewing HarvestPlus accomplishments.
CDC. Micronutrient facts. https://www.cdc.gov/nutrition/micronutrient-malnutrition/micronutrients/index.html (National Center for Chronic Disease Prevention and Health Promotion, 2019).
WorldBank. An overview of links between obesity and food systems. http://documents.worldbank.org/curated/en/222101499437276873/pdf/117200-REVISED-WP-Obesity-Overview-Web-PUBLIC-002.pdf (Worldbank, 2017).
Low, J. W., Mwanga, R. O., Andrade, M., Carey, E. & Ball, A.-M. Tackling vitamin A deficiency with biofortified sweetpotato in sub-Saharan Africa. Glob. Food Sec. 14, 23–30 (2017). This is the primary article reviewing CIP accomplishments.
Bailey, R. L., West, K. P. & Black, R. E. The epidemiology of global micronutrient deficiencies. Ann. Nutr. Metab. 66, 22–33 (2015).
UNICEF. The State of the world’s children 2019. Children, food and nutrition: growing well in a changing world. https://www.unicef.org/reports/state-of-worlds-children-2019 (UNICEF, New York, 2019).
Mostafa, I. et al. Factors affecting low coverage of the vitamin A supplementation program among young children admitted in an urban diarrheal treatment facility in Bangladesh. Glob. Health Action 12, 1588513 (2019).
Akhtar, S. et al. Nutritional perspectives for the prevention and mitigation of COVID-19. Nutr. Rev. https://doi.org/10.1093/nutrit/nuaa063 (2020).
Huizar, M. I., Arena, R., Laddu, D. R. The global food syndemic: the impact of food insecurity, malnutrition and obesity on the healthspan amid the COVID-19 pandemic. Prog. Cardiovasc. Dis. https://doi.org/10.1016/j.pcad.2020.07.002 (2020).
Imdad, A., Mayo-Wilson, E., Herzer, K., Bhutta, Z. A. Vitamin A supplementation for preventing morbidity and mortality in children from six months to five years of age. Cochrane Database Syst. Rev. 3, CD008524 (2017).
Vos, T. et al. Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990-2015: a systematic analysis for the global burden of disease study 2015. Lancet 388, 1545–1602 (2016).
Black, R. E. et al. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet 382, 427–451 (2013).
Alderman, H. & Fernald, L. The nexus between nutrition and early childhood development. Annu. Rev. Nutr. 37, 447–476 (2017).
Flores, A. L., Vellozzi, C., Valencia, D. & Sniezek, J. Global burden of neural tube defects, risk factors, and prevention. Indian J. Community Health 26, 3–5 (2014).
Development Initiatives. 2018 Global Nutrition Report: Shining a light to spur action on nutrition. Bristol (UK) (Development Initiatives, 2018).
WorldBank. The World Bank Annual Report 2006. Washington, DC. © World Bank, https://openknowledge.worldbank.org/handle/10986/7526 License: CC BY 3.0 IGO. (2006).
Von Grebmer, K. et al. Global hunger index: the challenge of hidden hunger, 2014 (International Food Policy Research Institute, and Concern Worldwide, Bonn, Washington, DC, and Dublin. Washington, DC, USA and Dublin, 2015).
De Moura, F. F. et al. Are biofortified staple food crops improving vitamin A and iron status in women and children? New evidence from efficacy trials. Adv. Nutr. 5, 568–570 (2014).
Palmer, A. C. et al. Provitamin A carotenoid-biofortified maize consumption increases pupillary responsiveness among Zambian children in a randomized controlled trial. J. Nutr. 146, 2551–2558 (2016).
Sazawal, S. et al. Efficacy of high zinc biofortified wheat in improvement of micronutrient status, and prevention of morbidity among preschool children and women - a double masked, randomized, controlled trial. Nutr. J. 17, 86 (2018).
Andersson, M. S., Saltzman, A., Virk, P. & Pfeiffer, W. Progress update: crop development of biofortified staple food crops under HarvestPlus. Afr. J. Food Agric. Nutr. Dev. 17, 11905–11935 (2017).
FAO, HarvestPlus. Biofortification: a food-systems solution to help end hidden hunger. http://www.fao.org/publications/card/en/c/CA8711EN/ (HarvestPlus, 2019).
Bashir, K., Ishimaru, Y. & Nishizawa, N. K. Iron uptake and loading into rice grains. Rice 3, 122–130 (2010).
Ishimaru, Y., Bashir, K. & Nishizawa, N. K. Zn uptake and translocation in rice plants. Rice 4, 21–27 (2011).
Wirth, J. et al. Rice endosperm iron biofortification by targeted and synergistic action of nicotianamine synthase and ferritin. Plant Biotechnol. J. 7, 718–718 (2009).
Trijatmiko, K. R. et al. Biofortified indica rice attains iron and zinc nutrition dietary targets in the field. Sci. Rep. 6, 19792 (2016).
Wu, T. Y., Gruissem, W. & Bhullar, N. K. Targeting intracellular transport combined with efficient uptake and storage significantly increases grain iron and zinc levels in rice. Plant Biotechnol. J. 17, 9–20 (2019).
Zou, C. et al. Effects of foliar spraying of selenium fertilizer on yield, selenium content and heavy metals content in waxy maize. Southwest China J. Agric. Sci. 32, 854–859 (2019).
Ye, X. D. et al. Engineering the provitamin A (beta-carotene) biosynthetic pathway into (carotenoid-free) rice endosperm. Science 287, 303–305 (2000).
Paine, J. A. et al. Improving the nutritional value of Golden Rice through increased pro-vitamin A content. Nat. Biotechnol. 23, 482–487 (2005).
Swamy, B. P. M. et al. Compositional analysis of genetically engineered GR2E “Golden Rice” in comparison to that of conventional rice. J. Agric. Food Chem. 67, 7986–7994 (2019).
Bollinedi, H. et al. Kinetics of beta-carotene degradation under different storage conditions in transgenic Golden Rice (R) lines. Food Chem. 278, 773–779 (2019).
BPI. Biosafety permit for direct use as food, feed, or for processing Number 19-060FFP. Department of Agriculture, Bureau for Plant Industry. December 10, 2019. http://biotech.da.gov.ph/upload/BiosafetyPermit_GR2E.pdf (Department of Agriculture, Republic of the Philippines, 2019).
FDA. FDA (2018). Biotechnology notification file no. 000158. GR2E rice with altered composition (provitamin A carotenoids (mainly beta-carotene)). https://www.fda.gov/media/113374/download (US Food and Drug Administration, 2018).
FSANZ. Approval Report – Application A1138: Food derived from provitamin A rice line GR2E. https://www.foodstandards.gov.au/code/applications/Documents/A1138%20Approval%20report.pdf (Food Standards Australia New Zealand, 2017).
HC. Novel Food Information: Provitamin A biofortified rice event GR2E (Golden Rice). https://www.canada.ca/en/health-canada/services/food-nutrition/genetically-modified-foods-other-novel-foods/approved-products/novel-food-information-golden-rice-gr2e.html (Health Canada, 2018).
Kader F. et al. Updates of Golden Rice Research in Bangladesh. In Proc. 6th Annual South Asia Biosafety Conference. September 15–17, 2018. Dhaka, Bangladesh (Agriculture & Food Systems Institute, 2018).
Strobbe, S. & Van Der Straeten, D. Folate biofortification in food crops. Curr. Opin. Biotechnol. 44, 202–211 (2017).
Storozhenko, S. et al. Folate fortification of rice by metabolic engineering. Nat. Biotechnol. 25, 1277–1279 (2007).
Li, K. T. et al. Increased bioavailable vitamin B-6 in field-grown transgenic cassava for dietary sufficiency. Nat. Biotechnol. 33, 1029–1032 (2015).
De Lepeleire, J. et al. Folate biofortification of potato by tuber-specific expression of four folate biosynthesis genes. Mol. Plant 11, 175–188 (2018).
Liang, Q. et al. Improved folate accumulation in genetically modified maize and wheat. J. Exp. Bot. 70, 1539–1551 (2019).
Mangel, N. et al. Enhancement of vitamin B-6 levels in rice expressing Arabidopsis vitamin B-6 biosynthesis de novo genes. Plant J. 99, 1047–1065 (2019).
Blancquaert, D. et al. Improving folate (vitamin B-9) stability in biofortified rice through metabolic engineering. Nat. Biotechnol. 33, 1076–1078 (2015). This paper demonstrates that introducing a folate binding protein can stabilize the accumulating folates in biofortified rice, ensuring adequate storage stability.
Mugode, L. et al. Carotenoid retention of biofortified provitamin A maize (Zea mays L.) after Zambian traditional methods of milling, cooking and storage. J. Agric. Food Chem. 62, 6317–6325 (2014).
Li, L. et al. The Or gene enhances carotenoid accumulation and stability during post-harvest storage of potato tubers. Mol. Plant 5, 339–352 (2012).
Bai, C. et al. Bottlenecks in carotenoid biosynthesis and accumulation in rice endosperm are influenced by the precursor-product balance. Plant Biotechnol. J. 14, 195–205 (2016).
Gayen, D., Ali, N., Sarkar, S. N., Datta, S. K. & Datta, K. Down-regulation of lipoxygenase gene reduces degradation of carotenoids of golden rice during storage. Planta 242, 353–363 (2015).
Zeng, J. et al. Metabolic engineering of wheat provitamin A by simultaneously overexpressing CrtB and silencing carotenoid hydroxylase (TaHYD). J. Agric. Food Chem. 63, 9083–9092 (2015).
Che, P. et al. Elevated vitamin E content improves all-trans beta-carotene accumulation and stability in biofortified sorghum. Proc. Natl Acad. Sci. USA 113, 11040–11045 (2016).
Joshi, R. K. & Nayak, S. Gene pyramiding-A broad spectrum technique for developing durable stress resistance in crops. Biotechnol. Mol. Biol. Rev. 5, 51–60 (2010).
de Cerqueira, D. T. R., Schafer, A. C., Fast, B. J. & Herman, R. A. Agronomic performance of insect-protected and herbicide-tolerant MON 89034 x TC1507 x NK603 x DAS-40278-9 corn is equivalent to that of conventional corn. GM Crops Food 8, 149–155 (2017).
ISAAA G. Approval database. http://www.isaaa.org/gmapprovaldatabase/default.asp (The International Service for the Acquisition of Agri-biotech Applications, 2019).
Singh, S. P., Gruissem, W. & Bhullar, N. K. Single genetic locus improvement of iron, zinc and beta-carotene content in rice grains. Sci. Rep. 7, 1–11 (2017). This paper demonstrates simultaneous enhancement iron, zinc, and provitamin A in rice seeds, confirming the potential of genetic engineering to increase multiple micronutrients using a single DNA insertion.
Gernand, A. D., Schulze, K. J., Stewart, C. P., West, K. P. & Christian, P. Micronutrient deficiencies in pregnancy worldwide: health effects and prevention. Nat. Rev. Endocrinol. 12, 274–289 (2016).
Dong, O. X. et al. Marker-free carotenoid-enriched rice generated through targeted gene insertion using CRISPR-Cas9. Nat. Commun. 11, 1–10 (2020). Here, a cassette containing genes for provitamin A accumulation is successfully introduced in a safe-harbor in the rice genome, which allows creation of provitamin A-rich rice lines without usage of a selectable marker.
Beyene, G. et al. Provitamin A biofortification of cassava enhances shelf life but reduces dry matter content of storage roots due to altered carbon partitioning into starch. Plant Biotechnol. J. 16, 1186–1200 (2018).
De Steur, H., Demont, M., Gellynck, X. & Stein, A. J. The social and economic impact of biofortification through genetic modification. Curr. Opin. Biotechnol. 44, 161–168 (2017).
De Steur, H. et al. Potential impact and cost-effectiveness of multi-biofortified rice in China. New Biotechnol. 29, 432–442 (2012).
Napier, J. A., Haslam, R. P., Tsalavouta, M. & Sayanova, O. The challenges of delivering genetically modified crops with nutritional enhancement traits. Nat. Plants 5, 563–567 (2019). This paper reviews the present state of nutritionally enhanced crops obtained by genetic engineering and discusses the hurdles occurring in the path towards their deployment.
Qaim, M. Role of new plant breeding technologies for food security and sustainable agricultural development. Appl. Econ. Perspect. Policy 42, 129–150 (2020). This article discusses the current and potential impact of crops obtained via genetic engineering and gene-editing technologies, and covers regulatory issues associated with their implementation.
Zaidi, S. S. E. A. et al. New plant breeding technologies for food security. Science 363, 1390–1391 (2019).
Sarrion-Perdigones, A. et al. GoldenBraid 2.0: a comprehensive DNA assembly framework for plant synthetic biology. Plant Physiol. 162, 1618–1631 (2013).
Lee, K. et al. CRISPR/Cas9-mediated targeted T-DNA integration in rice. Plant Mol. Biol. 99, 317–328 (2019).
Roberts, R. J. The Nobel laureates’ campaign supporting GMOs. J. Innov. Knowl. 3, 61–65 (2018).
Vanderschuren, H. Strengthening African R&D through effective transfer of tropical crop biotech to African institutions. Nat. Biotechnol. 30, 1170–1172 (2012). This paper advocates a roadmap to build a self-sustainable scientific workforce in Africa, including training, development of top education and research institutions, as well as the creation of local technology platforms.
Lee H. Capacity building for agricultural biotechnology in developing countries. Open Agric. J. 12, 36–45 (2018).
Matveeva, T. V. & Otten, L. Widespread occurrence of natural genetic transformation of plants by Agrobacterium. Plant Mol. Biol. 101, 415–437 (2019).
D.V.D.S. is grateful to Ghent University for financial support (BOF Special Research Fund, GOA project 01G00409). S.S. acknowledges the Ghent University Special Research Fund for a Post-Doctoral fellowship (BOF.P-DO.2019.0008.01). H.B. was director of HarvestPlus during 2003-2016 and interim CEO of HarvestPlus during 2018-2019. HarvestPlus has been supported by multiple donors (https://www.harvestplus.org/).
The authors declare no competing interests.
Peer review information Nature Communications thanks Leena Tripathi, Philip White and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
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Van Der Straeten, D., Bhullar, N.K., De Steur, H. et al. Multiplying the efficiency and impact of biofortification through metabolic engineering. Nat Commun 11, 5203 (2020). https://doi.org/10.1038/s41467-020-19020-4