Soil-borne fungal pathogens from the genus Fusaria limit the cultivation of more than a hundred plant species including bananas cotton tomato potato and sugar beet. The pathogens causing Fusarium wilt invade and colonize plant roots which leads to rotting. Present methods for the control of soil-born fungi include: breeding for resistance (if feasible) soil fumigation with volatile chemicals and solarization. There is currently no effective method to control Fusarium wilt and the fungus is highly resistant to fungicides.
Biotechnology for climate change adaptation of crops
Breeding for improved performance under environmental stresses involves activities which accumulate favourable alleles (different forms of a gene) which contribute to stress tolerance. Biotechnological contributions to crop adaptation to climate change do not only, or even mainly, concern the placement into the crop of one or more genes from an organism with which the crop could not normally breed (i.e. genetically modified crops). Biotechnological tools focus on providing the ability to directly detect and transfer genes of interest from other plant lines or organisms into the crop of interest without the continuing need to use the appearance or stress response of the plant (its phenotype) as a proxy for the presence of that gene. Phenotyping (measurement of the response of a plant line in a given environment) is still a vital part of the selection process but when a genetic region shown to be conferring an adaptive advantage has been identified, it can be transferred (even across species barriers) much more rapidly and efficiently than has been possible up to now.
Superior genes or alleles can often be found within other lines or races of the same crop and their efficient accumulation can be greatly speeded by molecular breeding where the presence of desirable genes or alleles can be directly and immediately identified, even in seeds or very young plants not exposed to the stress in question. More complex are marker-assisted backcrossing (MAB) and marker-assisted recurrent selection (MARS) techniques, allowing exactly identified pieces of DNA (individual alleles, genes or qualitative trait loci (QTLs) to be included in the desired plant line while minimising the transfer of other, less desirable, genes. Whole genome sequences are now available for soybean, maize, rice, sorghum and recently potato and high throughput ‘next-generation sequencing’ means that this process is rapidly accelerating, allowing the sequencing of large and complex genomes of crops such as wheat and barley. Desirable genetic loci identified in one genome can be quickly searched for in others (more detailed definitation of the terms are given in Figure 1).
Water stress already affects 1.5 to 2.0 billion people. In addition to increasing drought, elevated CO2 and ozone levels, climate change will also bring greater flooding of low-lying lands and increased flooding and runoff from tropical storms resulting in salinity changes and waterlogging. Conventional crop breeding for tolerance to these effects has had considerable success but is slow and largely limited to exploiting the existing genetic variation in crop plants and their very close relatives. Biotechnology and genetic engineering give us the prospect of making more dramatic changes to crop responses to stress than is possible with conventional breeding and making them more rapidly.
Very impressive success in terms of pest control and yield improvements have been seen globally with genetically modified versions of soy, maize and cotton produced for insect pest resistance and/or herbicide tolerance since their first introduction in 1996. More moderate results have been seen with transgenic alfalfa, canola, papaya and squash. To date these commercialised genetic modifications have involved genetically simple (single or double gene) traits. A major reason for the relatively slow progress in conventional breeding responses to the stresses related to climate change arises from the fact that plant adaptation, for example to drought or salinity effects, are not likely to be single gene changes. Whole metabolic pathways or cascades of pathways are likely to be involved. Making such changes is a challenge for biotechnology-supported breeding as much as for conventional breeding and even the most promising biotechnology-supported crop plant products are only now reaching largescale field testing by farming communities. No drought tolerant transgenic crop variety has yet been released. Nevertheless, the underpinning research and development process has considerable scale and momentum, with invaluable techniques moving into more common use and a wide suite of technologies and products are under development which will have exponentially increasing impacts on agricultural strategies in the near future. Of course these technologies are relatively new and are surrounded by considerable concerns as to their potential long-term impacts, safety and the shifts that their adoption may bring to the power of the agro-industrial complex in traditional seed markets.
How the Technology Contributes to Climate Change Adaptation
Genes that confer a measure of abiotic stress tolerance can be obtained from germbank collections, wild relatives of the crop, or from other organisms known to perform well under water deficit/excess or high salinity or temperatures. Careful use of the molecular breeding tools described above have enabled a three to five-fold increase in rice yields and a five-fold increase in the yields of the best maize lines. These materials are being actively disseminated into breeding lines across Asia and Africa now and, just as importantly, they have been passed to commercial seed companies for the production of superior hybrid lines.
There is a great deal of activity within the major biotechnology life sciences companies and the agricultural research institutes and academic institutions on transgenic research for drought-prone environments (Ortiz et al, 2007 and Varshney et al, 2011). In the developing world, China, Brazil and India are clear leaders. The international donor community is supporting work in this area through the Consultative Group on International Agricultural Research (CGIAR) and in particular through the Generation Challenge Programme in which partners from the CGIAR institutions such as the International Rice Research Centre (IRRI) or the International Maize and Wheat Research Centre (CIMMYT) work with leading ARI and ARS institutes in developing countries. In addition to the plant lines coming out of these collaborations, the Genomics and Integrated Breeding Platform being developed by this programme will provide the technical suite of tools to enable any breeder to utilise these new technologies on-line. In addition, ‘communities of practice’ are under construction to provide the peer support which will be required for their efficient utilisation.
Much of the initial work has been with the plant genetics ‘guinea-pig’ Arabidopsis, however, benefits for field crops are rapidly emerging. For example the HRD gene in transgenic rice has improved water use efficiency and the ratio of biomass produced to the amount of water used, through enhanced photosynthesis and reduced transpiration (Karaba et al, 2007). Correlation of drought tolerance with root architecture (spread, depth and volume) has been examined in cowpea (South Africa, West Africa and India), rice (India) and beans (Central and South America). Other modifications are further from commercialisation (Figure 2).
Advantages of the technology
If biotechnology solutions can be delivered to farmers which mitigate the harmful effects of climate change there is great potential for maintaining food and fibre production in a degrading environment and for expanding the farmable area into currently marginal environments. This is not to imply that environmental remediation is unnecessary but it helps to provide a buffer on its urgency. The major benefit from molecular breeding to date is the speed with which multiple traits can be identified, captured and incorporated into plants and then be tested for stability and efficacy. This has increased exponentially in the last 15 to 20 years. Genetic engineering technologies allow us to utilise capacities outside the range normally available in our crop plants. Because gene insertions can now be targeted and checked in ways that were not previously possible, we can have a higher confidence in the safety of the new plant lines and can be sure that other functional plant genes have not been disrupted by the insertion. Box 4.30 lists some of the existing benefits of genetically modified cotton in India. We can expect similar scale benefits from a whole range of molecular breeding (including genetic engineering) products in the short to medium-term future.
Disadvantages of the technology
Drought and flooding are unpredictable. Ensuring that the developed plants perform well in a wide range of environmental conditions is a challenge that will require even deeper understanding of the molecular basis of responses to stress. As with other areas of modern technology, molecular breeding is becoming more and more complex and inaccessible as a science for those of modest means. The financial investment needed for efficient molecular breeding is high and companies are recouping their investment through higher seed prices and selling their material only as hybrids, effectively preventing replanting any of the seeds produced. On one hand this ensures quality control in seed purity, on the other hand it creates low autonomy on the part of the farmer. Concerns over loss of crop biodiverisity have had a mixed history. India for example now has more than 750 registered Bt cotton varieties, around the same as were available nine years ago when the genetic modified Bt trait was introduced, but there is no doubt that these varieties have a narrower genetic base than formally – Gossypium arboreum previously covered some 40 per cent of the cotton area – and of those areas which were G.hirsutum, 60 per cent was in a range of varieties and only 50 per cent in hybrids. Now over 95 per cent of the country is growing a limited range of G.hirsutum hybrids. This concentration of advanced breeding material seems likely to continue, if only because the manpower and regulatory costs of producing and releasing substantially novel plant lines requires large markets to support the investment marginalising niche market varieties and land races.
Financial requirements and costs
There have been very different farmer cost experiences with existing bioengineered crops globally depending on the regulatory systems in place. Where private seed companies have been able to monopolise the market they have capitalised it with either famer agreements forbidding seed saving and imposing a technology fee in addition to the increased seed cost (for example, in the USA and Australia). Where this was impractical, such as in India, the seed sector forced a monopoly through the production of only hybrid seeds. Prices began at six to ten times that of non-biotech seed but gradually declined to three to four times because of court requirements and increasing competition. China enforced competition from the beginning and had less seed price inflation. However, even in countries where seed prices were very high, the average balance of financial benefit still rested with the farmer. After a brief period of adaptation around 60 to 80 per cent of the financial benefit of the seed tends to go the farmer and about 10 per cent to the technology developer, with the balance going to the supply chain. Many of the biotechnology responses to climate change are public sector developments intended for free or ‘at cost’ dissemination and are aimed at subsistence farmers with very limited ability to pay for improved inputs, particularly in the marginal environments likely to be first affected by climate change. However, the reality of the global seed distribution system make it likely that the commercial sector will be the most efficient disseminator of seed and the guardian of their purity, provided they are given some proprietary rights. Prices will then be set based on the average advantages to farmers, as in other sectors of the marketplace.
There are rather few publications on the economic impacts of biotechnology products on climate change adaptation. Alpuerto et al (2009) undertook an analysis of salinity and phosphorous tolerance in rice where the cumulative benefit to Bangladeshi farmers using marker assisted breeding rather than conventional breeding are forecast to be US$ 800 million for salinity tolerance and US$ 450 million for Phosphorus deficiency if conventional breeding takes 5 years longer than MAB, which is a conservative estimate. The medium term impact of the work described here and the many other products which are slightly less advanced but are in the pipeline (seeTable 4.16 for examples), is expected to be dramatic.
The knowledge requirements of biotechnology solutions for farmers or extension service providers are relatively low. But like any technology advance, an enabling environment is necessary for benefit maximisation and can sometimes be generated by it. Over-expectation of bioengineered crops has been a problem internationally, for which the seed industry must take some responsibility. Given the seed price implications, it is important the seed industry and extension services give farmers an accurate picture of the extent to which such crops can accommodate adverse environmental conditions and what growth and yield can be expected in local environments.
The limited access of public and developing country breeding programmes to these technologies is being addressed by the Generation Challenge Programme’s molecular breeding platform (GIBS). This is a brave attempt to put these high-tech tools in the hands of small-scale breeders.
Barriers to implementation
The global crop breeding community has found it more difficult than expected to use the outputs of molecular breeding research in its various forms for the rapid development of improved cops for poorer farmers. Even within crop species, genome structure and gene orders have proved to be more variable than expected. The prevalence of polygenic traits with strong genetics/environment interactions have been more marked than was foreseen, making successful expression of the valued trait after intra or inter-specific transfer more elusive than had been hoped. This is slowing (and deepening) research by all organisations (including commercial companies) in this area.
Molecular breeding is not proving to be either faster or cheaper than conventional breeding, though its worth has already been demonstrated for simple traits. The generally polygenic nature of the traits necessary for the amelioration of climate change-induced shifts in the environment, makes this more difficult still. However, unlike conventional breeding, the knowledge gained with molecular breeding is incremental and will enable much more effective, productive, targeted and rapid crop development over time. Trait development is expensive and high quality seed lines are costly to maintain. As with other sections of the seed sector, effective variety/hybrid development and dissemination will depend on the value capture mechanisms available to the players in the seed chain. Properly designed, there is no reason why these mechanisms should delay the delivery of significant benefits to farmers. In the specific area of GMOs we are likely to see continued extremely high costs of regulation, significantly delaying plant provision and significantly increasing costs to farmers and pushing ownerships rights strongly into the hands of larger, often multi-national, companies. It is probably true that this regulatory burden has led to most genetically modified crop dissemination in the developing world starting in the informal sector and products only receiving regulatory approval in retrospect. This is not desirable but seems likely to continue and expand while current regulatory regimes are in place.
Opportunities for implementation
These yield stabilising or enhancing technologies are likely to be taken up very quickly by farmers, most particularly where heat/drought/salinity is clearly moving against them over a series of seasons. Seed companies will not be slow to exploit the opportunities offered though it is likely that many of the best parental lines will emerge from public sector programmes.
- Castiglioni, P., et al. (2008) Bacterial RNA chaperones confer abiotic stress resistance in plants and improved grain yield in maize under water limiting conditions. Plant Physiology 147: 446-455
- Karaba, A, S. Dixit, R. Greco, K.R. Trijatmiko, N. Marsch-Martinez, A. Krishnan, K.N. Nataraja, M. Udayakumar, and A. Pereira (2007) Improvement of water use efficiency in rice by expression of HARDY and Arabidopsis drought and salt tolerance gene. Proceedings of the National Academy of Sciences (USA) 104: 15270-15275
- Lightfoot, D.A,, R. Mungur, R. Ameziane, S. Nolte, L. Long, K. Bernhard, A. Colter, K. Jones, M.J. Iqbal, E. Varsa, and B. Young (2007) Improved drought tolerance of transgenic maize Zea mays plants that express the glutamate dehydrogenase gene (gdh4) of E.coli. Euphytica 156: 103-116
- Nelson, D.E. et al (2007) Plant nuclear factor Y (NF-Y) B subunits confer drought tolerance and lead to improved corn yields on water limited acres. Proceedings of the National Academy of Sciences (USA) 104: 16400-16455
- Ortiz, R., M. Iwanaga, M. P. Reynolds, H. Wu, and J. Crouch (2007). Overview on crop genetic engineering for drought prone environments. Journal of Semi-Arid Tropical Agricultural Research.
- Rivero, R.M., M. Kojima, A. Gepstein, A., H. Sakakibara, R. Mittler, S. Gepstein and E. Blumwald (2007). Deayed leaf senescence induces extreme drought tolerance in a flowering plant. Proceedings of the National Academy of Sciences (USA) 104: 19631-19636
- Varshney, R.K., K.C. Bansal, P.K. Aggarwal, S. Datta and P.Q. Craufurd (2011) Agricultural biotechnology for crop improvement in a variable climate: hope or hype? Trends in Plant Science 16(7): 363-371
- Clements, R., J. Haggar, A. Quezada, and J. Torres (2011). Technologies for Climate Change Adaptation – Agriculture Sector. X. Zhu (Ed.). UNEP Risø Centre, Roskilde, 2011.
Biotechnology for climate change adaptation of crops
The life cycle of higher plants consists of two major phases the vegetative phase and the reproductive (flowering) phase. In general plants store matter and energy in the form of carbohydrate reserves during the vegetative phase and then mobilize these reserves in the development of flowers fruit and seeds during the reproductive phase which is often triggered by various light- and circadian-related factors.
Hyperion® is a distinct variety of dogwood tree that it is the result of crossing two varieties (Cornus kousa x Cornus florida hybrid and Cornus kousa). Its large creamy white flowers almost completely cover the tree in an overlapping manner. Attractive strawberry-like fruit are also produced and leaf colors range from a glossy dark green in the summer months to shades of yellow purple and orange during the fall months. Growth is very vigorous with dense branching low to the ground and upright branches.
Iron deficiency afflicts over 3 billion people worldwide and plants are the principal source of iron in most diets. In response to iron deficiency all plants except the grasses induce Fe(III) chelate reductase activity Fe(II) transport activity and proton release into the rhizosphere. Dartmouth researchers have identified an Arabidopsis mutant frd3 that constitutively expresses all three of these iron deficiency responses. Therefore it is tempting to speculate that FRD3 encodes a regulatory factor involved in sensing and/or responding to iron levels in Arabidopsis.