Transgenes for insect resistance reduce herbivory and enhance fecundity in advanced generations of crop–weed hybrids of rice

Gene flow from transgenic crops allows novel traits to spread to sexually compatible weeds. Traits such as resistance to insects may enhance the fitness of weeds, but few studies have tested for these effects under natural field conditions. We created F2 and F3 crop–weed hybrid lineages of genetically engineered rice (Oryza sativa) using lines with two transgene constructs, cowpea trypsin inhibitor (CpTI) and a Bt transgene linked to CpTI (Bt/CpTI). Experiments conducted in Fuzhou, China, demonstrated that CpTI alone did not significantly affect fecundity, although it reduced herbivory. In contrast, under certain conditions, Bt/CpTI conferred up to 79% less insect damage and 47% greater fecundity relative to nontransgenic controls, and a 44% increase in fecundity relative to the weedy parent. A small fitness cost was detected in F3 progeny with Bt/CpTI when grown under low insect pressure and direct competition with transgene-negative controls. We conclude that Bt/CpTI transgenes may introgress into co-occurring weedy rice populations and contribute to greater seed production when target insects are abundant. However, the net fitness benefits that are associated with Bt/CpTI could be ephemeral if insect pressure is lacking, for example, because of widespread planting of Bt cultivars that suppress target insect populations.


Introduction
The environmental release of transgenic crops has generated considerable debate about the ecological and evolutionary consequences of adopting these crops. A major biosafety concern relates to unwanted effects because of transgene flow from genetically engineered (GE) crops to their wild or weedy relatives (Ellstrand 2003;Snow et al. 2005). For example, the acquisition of traits such as resistance to herbicides, insects, and diseases might allow wild/weedy relatives to become more abundant, perhaps exacerbating weed management problems and displacing non-GE wild genotypes in some situations (Lu and Snow 2005;Andow and Zwahlen 2006).
Crop-to-wild gene flow is well documented in many species (Ellstrand 2003), as is the stable inheritance, expression, and efficacy of transgenes in crop-wild hybrids (Zhu et al. 2004;Ammitzbøll et al. 2005;Xia et al. 2009). Novel transgenic traits that enhance fitness are expected to introgress into recipient populations, whereas traits that are associated with fitness costs may eventually be lost (Jenczewski et al. 2003). However, studies of such fitness consequences under natural biotic and abiotic conditions are uncommon, in part because so few of the currently grown transgenic crops can hybridize with feral, weedy, or wild relatives (exceptions include canola and squash). Nonetheless, the number and diversity of transgenic crops, including the introduction of relatively undomesticated biofuel crops, is expected to increase dramatically in the coming decade (Gressel 2008).
Crop traits such as herbicide resistance are clearly advantageous to weeds that are exposed to these herbicides (Hall et al. 2000). In contrast, possible benefits of transgenes for resistance to diseases or insect herbivores are less obvious and depend on whether wild/weedy populations typically are limited by these biotic factors. Transgenes for virus resistance can be highly advantageous to wild squash in North America (Laughlin et al. 2009;Sasu et al. 2009) and weedy clover populations in Australia (Godfree et al. 2007). In sunflower, field experiments to test for fitness benefits of a Bt transgene showed that transgenic crop-wild hybrids produced significantly more seeds per plant under natural levels of herbivory, with no apparent fitness costs (Snow et al. 2003). In another study of sunflowers, no benefit of a transgene for white mold resistance was found in artificially infected crop-wild hybrids (Burke and Rieseberg 2003).
Here, we investigated the effects of two transgenes for insect resistance in rice, cowpea trypsin inhibitor (CpTI) and a linked Bt/CpTI construct, on the fecundity of hybrids progeny between cultivated and weedy rice. Rice (Oryza sativa L.) is a staple food for nearly half of the global population (FAO 2004). In 2005, Iran became the first country to commercialize Bt transgenic rice (James 2006). China has invested heavily in developing disease-and insect-resistant rice varieties, many of which appear to be close to approval for environmental release. The government of China approved biosafety certificates for Bt rice in 2009 (James 2009), and locally bred rice varieties with Bt transgenes could be widely grown within the next few years. In the USA, hundreds of GE rice lines have been tested in precommercial field trials, but only one type of herbicide-tolerant rice has been deregulated to date and it has yet to be widely grown [Information Systems for Biotechnology, http://www.isb.vt.edu/; (USDA 2006)]. Pharmaceutical-producing GE rice is grown in the USA under a permit system with bioconfinement requirements and small-scale production (National Research Council 2002).
Transgenes from cultivated rice are expected to spread to weedy rice (O. sativa f. spontanea), also known as red rice, which is a noxious weed that occurs in rice fields in many regions worldwide (Delouche et al. 2007;Londo and Schaal 2007). Weedy rice belongs to the same species as cultivated rice (Harlan and Wet 1971) and possesses variable levels of seed shattering, seed dormancy, chilling tolerance, presence of awns, and a red pericarp (Oard et al. 2000;Gealy et al. 2006). Rice fields are the primary habitat for weedy rice, and the weed can substantially reduce crop yields because it competes for light, space, nutrients, and water and cannot be harvested for food (Delouche et al. 2007). Also, the adventitious presence of dark-colored weedy rice grains can reduce the market value of cultivated rice (Arrieta-Espinoza et al. 2005).
Although cultivated and weedy rice are primarily self-pollinating, gene flow from crop-to-weed and weed-to-crop is well documented (Zhang et al. 2003;Chen et al. 2004;Messeguer et al. 2004;Shivrain et al. 2009). Therefore, it is widely assumed that transgenes introduced into modern rice cultivars will make their way into weedy rice populations (Gealy et al. 2003). Given that gene flow from cultivated rice to co-occurring weedy rice is unavoidable, it is important to understand the consequences of transgene introgression into wild/weedy rice populations. For example, many authors have warned that transgenes for herbicide resistance are likely to spread rapidly to weedy rice unless strong mitigation procedures are in place (Olofsdotter et al. 2000;Kumar et al. 2008;Gressel and Valverde 2009). In Vietnam, Cohen et al. (2008) showed that weedy rice often flowered simultaneously with cultivated rice within the same fields and shared many of the crop's insect pests and pathogens. This suggests that transgenes for insect and disease resistance could introgress into weedy rice and provide protection.
Our previous studies showed that Bt and Bt/CpTI transgenes can substantially enhance crop yields when target insects are abundant, while no beneficial effects on fecundity were seen for CpTI alone (Table 1; Appendix 1). Under very low insect pressure, when net fitness costs might be detected, we observed significant yield reductions because of the Bt/CpTI transgene in cultivated rice in two of the three years (Chen et al. 2006;Xia et al. 2010; Table 1; Appendix 1). However, these costs were seen only when the transgenic plants were grown intermixed with nontransgenic controls, which is likely to amplify small differences in competitive ability. We also found that F 1 hybrids between the GE lines and three weedy rice strains had generally lower seed production per plant, but higher seed germination and survival than their weedy parents (Cao et al. 2009). Thus, the F 1 generation could constitute an effective genetic bridge for transgenes to be transmitted to subsequent generations of weedy rice in this system.
The goals of the present study were to determine the effects of the CpTI and Bt/CpTI transgenes on herbivory and fecundity in the F 2 and F 3 hybrid progeny under two levels of insect pressure (low versus natural). To address these questions, we used segregating transgene-positive and transgene-negative lineages generated from both transgenic constructs under monotypic versus mixed competition treatments. We also compared the fecundity of F 3 hybrid progeny with that of their weedy parents to evaluate the potential for GE weedy rice to become more abundant than its predecessor over time. Information about the relative performance of transgenic weedy rice originating from crop-weed hybridization is essential for determining whether gene flow from current or future GE rice lines could have significant adverse unintended consequences.

Materials and methods
Cultivar and weedy parents for crosses Two GE rice lines produced by Fujian Academy of Agricultural Sciences, China, were used as pollen donors to create the crop-wild hybrid lineages (Xia et al. 2010). These agrobacterium-transformed lines were bred beyond the seventh generation from an inbred traditional Minghui-86 variety. One line (CpTI) has a CpTI (cowpea trypsin inhibitor) gene, while the other (Bt/CpTI) has the CpTI gene linked to a Bt cryIAc (Bacillus thuringiensis) gene in a double insertion. A selectable marker gene (hy, for hygromycin resistance) is tightly linked to each transgene. Bt, CpTI, and hy genes have constitutive promoters of ubiquitin (derived from maize), ActID (derived from rice), and CaMV35s, respectively. These insect-resistant GE lines were produced to deter lepidopteran pests such as rice stem borers (Scirpophaga incertulas, Chilo suppressalis, and Sesamia inferens) and rice leaf-folder (Cnaphalocrocis medinalis). Because only one transgenic event of each type was available to us, generalizations about other CpTI and Bt/CpTI events should be made with caution.
For brevity, we refer to fitness-related differences between transgene-positive and transgene-negative plants as effects of the transgenes, with the caveat that some of these differences could be influenced by somaclonal variation, pleiotropy, or position effects, such as crop genes that are linked to the insertion sites. Transgenic lines that are being developed for commercial use in China are not expected to have the antibiotic resistance marker used in this study and they are derived from different insertion events. Although our previous studies included a Bt cultivar without the CpTI gene (Chen et al. 2006;Cao et al. 2009), owing to logistical problems, we were not able to obtain hybrid progeny from this line for the present study.
Two weedy rice strains Wa and Wb donated by Dr H. S. Suh of Yeungnam University from South Korea were available and used in this study. Strain Wa is short and has short, narrow leaves, red awns, and medium tillering ability, while strain Wb is taller and has longer, narrow leaves, no awns, and medium tillering ability. Differences between the two strains in fecundity and individual seed mass were negligible (Cao et al. 2009). Given the similar

Crop-weed hybrid lineages
To compare fitness-related traits of hybrid progeny that differed in the presence or absence of transgenes, F 2 and F 3 hybrid progeny were generated by selfing F 1 and F 2 plants, respectively ( Fig. 1). Because weedy rice is a predominantly self-pollinating taxon, F 2 and F 3 generations generated by selfing will be much more common than backcrossed generations. F 1 hybrids were obtained from artificial crosses between the two weedy rice strains each including more than 20 individuals and two insectresistant GE rice lines, resulting in four distinct hybrid lineages (Cao et al. 2009). Weedy rice strains were used as the maternal parents and the GE rice lines as the paternal parents in crosses ( Fig. 1). Both weedy strains were used in the F 2 hybrid progeny, but only Wa (chosen randomly) was used for the F 3 . Hybrid progeny were identified for the presence or absence of transgenes. For identification of F 2 individuals, total genomic DNA was extracted from young leaf samples from each F 2 seedling beyond the 3-leaf stage, prior to transplanting, following the method described by Doyle and Doyle (1987). The identification of transgenepositive and transgene-negative seedlings involved PCR amplification of the target transgenes: the CpTI gene for individuals derived from the CpTI insect-resistant rice line, and the Bt gene for individuals from the Bt/CpTI insect-resistant rice line (Rong et al. 2005). For plants that scored positive for the transgene, we did not attempt to determine whether they were homozygous (++) or hemizygous (+)). In weedy rice, hemizygous and homozygous plants are expected to have similar levels of transgene expression, as shown in wild rice hybrids containing the Bt transgene ), but this was not confirmed in the present study.
For F 3 hybrid progeny, we used the hygromycin-B water solution treatment to identify transgenic individuals (Rong et al. 2005). Groups of about 15 seeds from each transgenic F 2 plant were screened. F 2 individuals from which all the 15 seedlings survived from the hygromycin-B treatment were identified as the transgenic homozygote (++), whereas those from which all the 15 seedlings died from the hygromycin-B treatment were identified as the nontransgenic homozygote ())). F 3 seeds from hemizygous F 2 plants were not included in the F 3 field experiment.

Design of field experiments
We evaluated insect damage and fitness-related traits of the F 2 and F 3 hybrid progeny, with or without transgenes, in 2008 and 2009, respectively. The field plots were located at designated Biosafety Assessment Centers in Fuzhou, Fujian Province, China, where the plants were exposed to naturally occurring levels of insect damage (no insecticides). To test for possible fitness costs of the transgenes, we also included a 'low insect pressure' treatment by spraying replicated plots with insecticides that are commonly used in rice fields (Methamidophos, Folimat, Buprofezin, and Monosultap).
The F 2 progeny were evaluated in a randomized, factorial design experiment that included the following factors for each transgene (CpTI or Bt/CpTI): insect pressure (low versus natural), transgene (present [++, +)] versus absent [))]), competition mode (monoculture versus mixture with cultivated rice), and weedy strain (Wa versus Wb), with four replicate plots for each treatment combination. Within each plot, 36 seedlings were transplanted in a 6 · 6 grid with 20 cm-spacing between seedlings, with one seedling in each hill. In the mixed competition plots to simulate the transplanting rice field, half of the plants were individuals of cultivated Minghui-86 (which was not sampled). Therefore, the numbers of experimental plants that were sampled in each plot (replicate) were 36 plants for monocultures, which we refer to as 'pure', and 18 plants for mixed competition plots, which we refer to as 'mixed'. Data from these plants were averaged to provide one measurement for each of the four replicate plots for each treatment combination. The F 3 generation was evaluated in 2009 using similar procedures, with the following exceptions. Only the Wa weedy hybrid lineage was used, and four extra plots were added to include pure plantings of the Wa weedy parent. As noted earlier, all of the transgenic F 3 plants were homozygous for each transgene. In 2009, the mixed competition treatment included 18 transgenic and 18 nontransgenic F 3 plants from the same GE lineage in an alternating pattern, in an attempt to magnify any differences in their growth rates and fecundity (no cultivated Minghui-86 plants were used). In addition, plants in the pure plots were 20 cm apart, while those in the mixed competition plots were only 15 cm apart to intensify competition. Finally, each of the four replicate plots for the F 3 generation included a border row of extra plants (same genotypes) that were not sampled.
Seedlings were started in a small plot at Fudan University, Shanghai, where no target insects were found. F 2 seedlings were transplanted to the field site in Fuzhou 40 days after seed germination and F 3 seedlings were transplanted 28 days after seed germination. There were no significant differences in seedling survival between lineages (unpublished data). Before transplanting, the field site had been treated with herbicide and weeded by hand. Fertilizer was applied at the tillering stage [1 to 1.2 kg nitrogen (urea) per 100 m 2 ], as is common for rice cultivation in the Fuzhou area.

Data collection and analysis
Data collection methods were similar for both years of the study. We measured plant height, number of tillers per plant, the number of blasted tillers (by rice stem borers) and folded leaves (by leaf-folders) at the beginning of flowering time. To avoid seed loss by natural seed shattering, all panicles of an individual were enclosed in a nylon mesh bag 10 days after flowering. Panicles were collected for measurements of number of seeds per plant, seed set (percent of spikelets with filled seeds), and 1000-seed weight. To characterize insect damage, we recorded the percent of blasted tillers and folded leaves. An insect damage index was calculated as the sum of these two percents for each plant.
The four-way ANOVA analysis was carried out by the GLM multivariate procedure for the CpTI and Bt/CpTI hybrid lineages separately in F 2 hybrid progeny. Because the factor of weedy strains (Wa versus Wb) did not show significant effect on fecundity (the number of good seeds), the main variable of interest, this factor was removed from the ANOVA analysis. Thus, for the F 2 generation, we used a three-way ANOVA to test the effects of insect pressure (low versus natural), transgenic genotype (positive versus negative), and competition (pure versus mixed) on insect damage and number of seeds per plant. All the model factors were considered as fixed under the GLM multivariate procedure. To further examine transgene effects on insect damage and fecundity, independent t-tests (for F 2 and pure plots in F 3 ) and paired t-tests (for mixed plots in F 3 ) were used to test for significant differences between means for transgene-positive and transgene-negative plants in each lineage and treatment combination. In addition, for fecundity and other fitness-related traits, we used Duncan's multiple range test followed by the more conservative Bonferroni correction to test for significant differences among means of four groups [CpTI (+)versus CpTI ()) versus Bt/CpTI (+) versus Bt/CpTI ())] in the F 2 generation, and five groups [CpTI (+) versus CpTI ()) versus Bt/CpTI (+) versus Bt/CpTI ())versus Wa] in the F 3 generation (pure competition only). Independent t-test (for F 2 and pure plots in F 3 ) and paired t-test (for mixed plots in F 3 ) were used to test for significant differences between means for transgene-positive and transgene-negative plants in each lineage and treatment combination. All statistical analyses were performed using the software package SPSS ver. 15.0 for Windows (SPSS Inc., Chicago, IL, USA, 2006).

Insect pressure and competition
Natural levels of insect damage on nontransgenic plants were relatively high in both years of the experiment (28 and 22%; Table 1; Figs 2 and 3). Insecticide applications substantially reduced insect damage (to 8% in both years). These differences caused by insecticides allowed us to test for net fitness benefits of the transgenes when plants were exposed to target herbivores, as well as net fitness costs of the transgenes when insect pressure was reduced (note that fitness costs can be offset by benefits and vice versa, resulting in no net fitness effects; e.g. Chen et al. 2006). Seed production was lower in the mixed competition plots than with pure competition in both generations. This treatment involved competition with the cultivar in 2008, and closer spacing between plants than with pure competition in 2009. Major effects of the transgenes on plant performance are presented in more detail below and in Tables 2 and 3. The transgenes had no effect on seedling survival (data not shown), which will not be considered further.

Performance of F 2 hybrid progeny
Both transgenes were associated with reduced insect damage, but this effect was much weaker in the CpTI treatment and was not strong enough to enhance seed production under natural levels of insect pressure ( Fig. 2; Appendix 2). However, Bt/CpTI clearly affected fecundity, and the interaction between insect pressure and transgene presence/absence was significant ( Fig. 2; Appendix 2). The effects of each transgene on weedy types Wa and Wb were generally similar, so these data are pooled in Fig. 2 and Table 2 for ease of presentation. Bt/CpTI was associated with much lower insect damage and a substantial increase in seed production under both competition treatments ( Fig. 2; Appendices 3 and 4). In general, the  Figure 3 Effects of transgenic genotype (positive versus negative), insect pressure (low versus natural), and competition (pure versus mixed) on insect damage and number of seeds per plant in crop-weed hybrids from two transgenic crop lines, cowpea trypsin inhibitor (CpTI) or Bt/CpTI, in the F 3 generation. Means and SE are shown. The comparison was made between transgene-positive and transgene-negative plots based on independent t-tests (for pure plots) and paired t-tests (mixed plot). Levels of significance: *P < 0.05, **P < 0.01, ***P < 0.001; P < 0.10. increase in fecundity in plants with the Bt/CpTI transgene was associated with greater panicle production and percent seed set (Table 2; Appendices 3 and 4).
The insecticide treatment substantially reduced insect damage but did not completely prevent it ( Fig. 2; Appendices 3 and 4). Under low insect pressure, 5 to 10% of the leaves and tillers on nontransgenic plants sustained damage. For the Bt/CpTI plants, transgene-positive plants had somewhat less insect damage than transgene-negative plants, especially under mixed competition ( Fig. 2;  Appendices 3 and 4). However, the numbers of seeds per plant were similar in comparisons between transgenepositive versus transgene-negative plants across treatments with low insect pressure. Different letters after the means and standard error (±) in the same row indicate significant differences according to Duncan's multiple range tests followed by Bonferroni correction in the same treatment. N = 4 plots. Table 2. Effects of the two transgenic events (cowpea trypsin inhibitor (CpTI) and Bt/CpTI) on fitness-related traits in F 2 progeny of crop-weed hybridization under low versus natural insect pressure and pure versus mixed cultivation.
Enhanced fecundity in transgenic weedy rice Yang et al.

Performance of F 3 hybrid progeny and the weedy parent
Similar effects of the Bt/CpTI transgenes were seen in the F 3 hybrid generation (Table 3; Fig. 3; Appendix 5), which was obtained by selfing F 2 hybrid progeny from weedy strain Wa. Under natural insect pressure, CpTI had no effect on herbivory or fecundity, while plants in the pure competition treatment with the Bt/CpTI transgene had 79% less insect damage and produced 47% more seeds than their nontransgenic counterparts. An unexpected result in 2009 is the low level of protection from the Bt/ CpTI transgene and relatively lower damage on nontransgenic plants in the mixed competition treatment with natural insect pressure. This resulted in similar levels of seed production in comparisons between transgene-positive and transgene-negative plants, in contrast to what we observed in 2008 with F 2 plants. The mixed competition treatment is not directly comparable between years because the competitors were different and the plants were closer together in 2009 (see Table 1). Under low insect pressure, Bt/CpTI was associated with a fitness cost of 19% lower fecundity relative to nontransgenic control plants in mixed competition (P < 0.05; Table 1; Fig. 3; Appendix 5); no cost effect was detected in pure cultivation. Plants with the Bt/CpTI transgene had less insect damage than nontransgenic controls, but only under pure competition. Plants with CpTI alone had greater insect damage under mixed competition, counter to expectations. Neither of these differences in insect damage affected fecundity.
We also compared the original weedy parent genotypes directly with their F 3 crop-weed hybrid offspring in the pure competition treatment (Table 3). Weedy and hybrid genotypes produced similar numbers of seeds per plant under both natural and low insect treatments, with the exception of the Bt/CpTI F 3 plants, which had 79% less insect damage (P < 0.001) and produced 44% (P < 0.01) more seeds than their weedy parents under the natural insect treatment. Thus, fecundity of the F 3 hybrid generation was similar to the weedy parent, and we observed a strong benefit of having the Bt/CpTI transgene under natural insect pressure.

Discussion
This study confirms that insect-resistance transgenes from cultivated rice are effective when transferred to weedy rice and can increase fecundity of weedy rice when target insects are present. Results from the F 2 and F 3 hybrid generations were generally consistent, demonstrating that the Bt/CpTI transgene can result in lower insect damage and greater seed production under natural field conditions, with no effects on survival. The CpTI transgene was also associated with reduced insect damage, but to a much smaller extent than Bt/CpTI, and it was not linked to increased fecundity or survival. Therefore, the benefits of CpTI alone were small relative to those of the Bt transgene. We also found that Bt/CpTI-positive F 3 hybrid progeny produced 44% more seeds than their weedy parents in the pure competition treatment. Because fecundity is a key component of fitness, our results suggest that Bt/ CpTI transgenes could increase in frequency in weedy rice populations when target insects are sufficiently common, perhaps contributing to larger seed banks and more pervasive weedy rice problems, at least in the short term.
Populations of target insects fluctuate from year to year (e.g. Xia et al. 2010; this study), so the fitness benefit of a Bt/CpTI transgene is expected to vary accordingly. In cultivated rice, lepidopteran herbivores occur in about half of the area of rice cultivation in China (e.g., Sheng et al. 2003), but the extent of lepidopteran damage on weedy rice has not been quantified to our knowledge. However, Cohen et al. (2008) reported similar occurrences of lepidopteran damage on weedy and cultivated rice in the Mekong Delta of Vietnam, suggesting that pests of the crop also attack weedy rice.
As noted previously, the major lepidopteran pests of rice are rice stem borers (S. incertulas, C. suppressalis, and S. inferens) and rice leaf-folder (C. medinalis). These insects also have other host plants; for example, C. suppressalis can feed on Zizania latifolia, maize, sugarcane, and sorghum (Harris 1990;Hou et al. 2009). If non-Bt host crops occur near cultivated rice, this may help delay the evolution of resistant insects by sustaining susceptible genotypes in the area (Carriere et al. 2010). In regions where Bt or Bt/CpTI rice cultivars are planted very widely, and where resistance does not evolve in the target insects, these insect populations may decline dramatically, as documented in Bt cotton (Wu et al. 2008). This could reduce or even eliminate the fecundity advantage of transgenepositive plants. Another ecological factor that could diminish the benefits of Bt/CpTI transgenes is the emergence of secondary insect pests such as hemipterans if they are released from competition with lepidopteran pests. Although complex ecological and evolutionary interactions among rice taxa and their insect herbivores make it challenging to predict long-term fitness consequences of Bt cultivars, our results point to a strong fitness benefit for crop-weed hybrids with Bt/CpTI in the short term when target insect pests are abundant.
A fitness cost was detected in F 3 progeny containing Bt/CpTI under conditions where competition between transgene-positive and transgene-negative was introduced. In previous studies with cultivated rice, we observed reduced fecundity of Bt/CpTI in mixed competition plots where GE and non-GE plants competed with each other, but not in monotypic plots, in two of three years with very low insect pressure (Table 1; Appendix 1). Likewise, in the present study, significantly lower fecundity of transgene-positive Bt/CpTI, F 3 plants was observed in mixed competition plots with low insect pressure (P < 0.01), and no net gain in fecundity was observed in this treatment combination under natural insect pressure (Table 3; Fig. 3; Appendix 5). This is because of relatively low insect pressure in the mixed-cultivation plots caused by the presence of transgene-positive plants. Therefore, it seems possible that benefits of Bt/CpTI transgenes could be countered by small or moderate fitness costs in years when the target insect populations are very low, but further research involving larger sample sizes is needed to test this hypothesis. The apparent absence of fitness costs associated with transgenes introgressing into wild/weedy populations has also been reported in Brassica rapa and Helianthus annuus (Snow et al. 1999;Burke and Rieseberg 2003;Snow et al. 2003), while an inducible trypsin proteinase inhibitor was associated with a strong fitness cost in Nicotiana attenuata (Zavala et al. 2004).
To our knowledge, this is one of the first studies to document fecundity benefits of transgenes for insect resistance in weedy relatives of a transgenic crop. Similar benefits were seen in wild sunflowers in the USA , but Bt sunflowers have not been proposed for deregulation (Dalton 2002). In contrast, deployment of Bt rice is already taking place in Iran and China. Although we cannot be sure that our results pertain to other Bt constructs, other weedy rice populations, and other regions, our findings are consistent with the hypothesis that seed production of weedy rice is limited by lepidopteran insect pests, and the introgression of transgenes that confer resistance to these pests can enhance the fitness of recipient populations. Because weedy rice is largely selfpollinating and has high levels of seedling recruitment (Langevin et al. 1990), a small number of crop-wild hybrids with beneficial transgenes could quickly generate transgenic progeny that could then disperse broadly as seeds, while also becoming established in long-lived seed banks. However, we also expect that the widespread cultivation of Bt rice could lead to dramatic declines in local populations of target insects, which may or may not evolve resistance to the Bt toxins in rice. Further studies of annual and regional variation in target insect abundances are needed to gain a deeper understanding of the anticipated prevalence of fitness benefits for Bt or Bt/CpTI weedy rice. To minimize unwanted side effects of growing Bt rice, agricultural practices that reduce weedy rice populations and delay the introgression of crop genes into weedy rice populations, such as hand-weeding prior to seed shattering, could be encouraged in regions where Bt rice is adopted. The factors include insect pressure (low versus natural), transgenic genotype (positive versus negative), and competition (pure versus mixed) on insect damage and number of seeds per plant of F 2 hybrid progeny for two transgenic events (CpTI or Bt/CpTI) separately. The DF N (numerator degrees of freedom), DF D (denominator degrees of freedom), F value and P value were shown.
Enhanced fecundity in transgenic weedy rice Yang et al.