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Effect of NaCl-stressed Bacillus thuringiensis (Bt) cotton on the feeding behaviors and nutritional parameters of Helicoverpa armigera

  • Jun-Yu Luo,

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Writing – original draft, Writing – review & editing

    Affiliation State Key Laboratory of Cotton Biology, Chinese Academy of Agricultural Sciences, Anyang, Henan, China

  • Shuai Zhang,

    Roles Formal analysis, Funding acquisition, Project administration

    Affiliation State Key Laboratory of Cotton Biology, Chinese Academy of Agricultural Sciences, Anyang, Henan, China

  • Xiang-Zhen Zhu,

    Roles Investigation

    Affiliation State Key Laboratory of Cotton Biology, Chinese Academy of Agricultural Sciences, Anyang, Henan, China

  • Ji-Chao Ji,

    Roles Investigation

    Affiliation State Key Laboratory of Cotton Biology, Chinese Academy of Agricultural Sciences, Anyang, Henan, China

  • Kai-Xin Zhang,

    Roles Investigation

    Affiliation State Key Laboratory of Cotton Biology, Chinese Academy of Agricultural Sciences, Anyang, Henan, China

  • Chun-Yi Wang,

    Roles Investigation

    Affiliation State Key Laboratory of Cotton Biology, Chinese Academy of Agricultural Sciences, Anyang, Henan, China

  • Li-Juan Zhang,

    Roles Investigation

    Affiliation State Key Laboratory of Cotton Biology, Chinese Academy of Agricultural Sciences, Anyang, Henan, China

  • Li Wang,

    Roles Investigation

    Affiliation State Key Laboratory of Cotton Biology, Chinese Academy of Agricultural Sciences, Anyang, Henan, China

  • Jin-Jie Cui

    Roles Conceptualization, Formal analysis, Methodology

    cuijinjie@126.com

    Affiliation State Key Laboratory of Cotton Biology, Chinese Academy of Agricultural Sciences, Anyang, Henan, China

Abstract

Saline-alkali soil is an arable land resource on which transgenic Bacillus thuringiensis (Bt) cotton has been planted on a large scale in accordance with food security strategies. There are, however, concerns about the insecticidal effects of Bt cotton on target insect pests. In this study, a Bt cotton variety, GK19, and its nontransgenic parent variety, Simian-3, were used as experimental models for investigating the effect of the expression of exogenous insecticidal proteins in Bt cotton under NaCl stress on the feeding behavior and nutritional parameters of Helicoverpa armigera. The results showed that the expression of exogenous insecticidal proteins in GK19 was significantly inhibited under NaCl stress. However, the feeding, crawling, resting and spinning down behavior of the 5th instar H. armigera larvae on GK19 Bt cotton, as well as the amount of food consumed and feces produced by these larvae, did not markedly differ under different NaCl concentrations. In contrast, the mean relative growth rate (MRGR), relative growth rate (RGR), approximate digestibility (AD), efficiency of conversion of ingested food (ECI) and efficiency of conversion of digested food (ECD) of the larvae markedly decreased in response to NaCl stress. Under the same concentration of NaCl, the nutritional parameters of the bollworm larvae on GK19 Bt cotton or Simian-3 nontransgenic cotton were different. However, the interaction between salt stress and cotton variety had no significant effect on the feeding behavior or nutritional parameters of H. armigera larvae. These results may provide a scientific basis for determining the effect of exogenous insecticidal protein expression in Bt cotton under NaCl stress on H. armigera and can therefore be useful for the effective application of Bt cotton in saline-alkali soils to prevent and control H. armigera.

Introduction

Soil salinization is an obstacle that cannot be ignored in the sustainable development of agriculture [12]. In recent years, due to improper irrigation and poor drainage, approximately 300,000 hectares of cultivated land worldwide has experienced secondary salinization [3]. In China, nearly 37 million hectares of saline-alkali soil, accounting for 4.9% of the nation’s arable land, severely hinders crop production [4]. Cotton is an important economic crop and the pioneer crop for saline-alkali lands. The rational development and utilization of saline-alkali land resources are highly important for agricultural production.

Bacillus thuringiensis (Bt) cotton is commercially cultivated on a large scale in many countries [57] because it can effectively control specific lepidopteran pests, reduce dependence on chemical insecticides and protect both beneficial arthropod populations and the environment [810]. Although no target pests are beyond the control of extensive Bt cotton use [1112], many reports have indicated that the effects of Bt cotton on lepidopteran pests differ over the cotton growing season [13] and that the Bt insecticidal protein content correlates with cotton variety [1415], cotton growth stage [11,16], and plant parts [1724]. With regard to the response of Bt cotton to abiotic stress, some studies have investigated the effects of salt stress on the insecticidal protein expression in Bt cotton [19, 20,22, 24], but few studies have investigated the effects of salt stress on both the expression of insecticidal proteins in Bt cotton and the nutritional levels of lepidopteran pests.

Under the context that arable land for grain production is diminishing and that cotton must be planted on saline-alkali land, a salt stress test on Bt cotton plants was simulated in the laboratory to study the exogenous insecticidal protein expression in Bt cotton under NaCl stress and the associated interactions with cotton bollworms (Helicoverpa armigera). The results provide a scientific basis for the prevention and control of bollworm populations in Bt cotton fields in saline-alkali soils.

Materials and methods

Plants and insects

The Bt cotton variety GK19 (Cry1Ac) and its non-transgenic parent variety Simian-3 were provided by the Institute of Plant Protection and Soil Science, Hubei Academy of Agricultural Sciences, China. GK19 and Simian-3 seeds were sown in germination boxes. After both cotyledons of the cotton seedlings were opened and spread flat, the cotton roots were washed, and each seedling was transferred to a hydroponic growth box containing nutrient solution. The growth boxes were subsequently placed in a plant culture room (temperature 25±2 °C, humidity 50–60%) until four true leaves grew. Bollworm larvae were provided by the Institute of Cotton Research of the Chinese Academy of Sciences (CAAS). The bollworm larvae were reared with artificial feed [25] in a light incubator under 60±5% relative humidity, 2±1 °C, and a 14:10 (light:darkness) photoperiod. The bollworms were kept on the artificial feed in the room and developed no resistance to the Bt protein.

NaCl stress treatment

The NaCl stress treatments consisted of 3 concentrations, namely, 0 mmol L-1, 75 mmol L-1 and 150 mmol L-1, and each test was repeated 3 times. The cotton nutrient solution and NaCl levels were renewed every 2 days after the initial nutrient and stress application. The nutrient solution was prepared, and the cotton plants were cultivated in accordance with the methods of Jiang et al. [19]; tests were performed for 8 days after the NaCl stress treatment.

Detection of exogenous protein expression

Unfolded leaves were collected from the tops of GK19 Bt cotton plants under different levels of NaCl stress. For each treatment, 5 leaves were collected. The leaves were then mixed evenly, frozen and ground in liquid nitrogen, after which the exogenous insecticidal protein expression was measured using a Cry1Ac/Cry1Ab detection kit (ENVIROLOGIX, USA).

Bollworm behavior on cotton

GK19 Bt cotton and Simian-3 nontransgenic cotton plants under different levels of NaCl stress were collected. Five plants were collected for each treatment, and the cotyledonary nodes and roots were cut and discarded from each plant. The remaining plant portions were placed into a plastic cup containing 1% solidified water agar. A single recently hatched bollworm larva was placed onto each plant. Subsequently, the plastic cup was covered with an inverted plastic cup of equal size, and the cups were sealed together with sealing film. After 10 min, when the bollworm had stabilized, it was observed. This test was repeated 3 times; a total of 15 cotton plants were used. The feeding statuses (feeding, crawling, resting and spinning down) of the bollworm larvae under the different treatments were observed and recorded every 30 min for 6 h.

Determination of the nutritional parameters of the bollworms

To determine the nutritional status of the bollworms, 5th instar larvae were used. Leaves were collected from the tops of GK19 Bt cotton and Simian-3 nontransgenic cotton and then placed into clean, sterilized glass test tubes (15 cm×Φ5 cm). Afterward, similarly sized bollworm larvae were placed onto the cotton leaves, and each test tube was plugged with a cotton swab to prevent the bollworms from escaping. One 5th instar bollworm larva was placed in each tube, and larvae were reared for 2 d; 30 larvae were examined per treatment, and every 10 larvae represented one replicate. Before rearing, both the weight of the bollworm larvae and the fresh weight of the cotton leaves were measured; after rearing, the weight of the bollworm larvae and the dry weight of the remaining cotton leaves were measured after drying at 80 °C for 72 h. In addition, the fresh weight of the feces in the test tubes was measured. Ten leaves without bollworms served as blank controls for each treatment. The following nutritional effect parameters were calculated: the mean relative growth rate (MRGR) [26], relative growth rate (RGR), relative metabolic rate (RMR), relative consumption rate (RCR), efficiency of conversion of ingested food (ECI), efficiency of conversion of digested food (ECD) and approximate digestibility (AD) [2728]. The food consumption, amount of feces, larval weight and weight gain of the bollworms were measured.

Data analysis

SPSS 17.0 statistical analysis software for Windows (SPSS, Chicago, IL, USA) was used to analyze significant differences in the sample data. The Bt insecticidal protein expression, nutritional effect parameters and feeding behavior parameters of the bollworms were analyzed via one-way ANOVA with SPSS 17.0. Significant differences between treatments were tested using LSD tests.

Results

Effect of NaCl stress on the expression of exogenous insecticidal protein in Bt cotton leaves

The expression of exogenous proteins in the Bt cotton leaves tended to decrease (Fig 1) with increasing NaCl concentrations. Compared with 0 mmol L-1 NaCl stress, 75 mmol L-1 and 150 mmol L-1 NaCl stress caused 23.16% (p = 0.022) and 59.01% (p = 0.003) lower exogenous protein expression in Bt cotton leaves, respectively. Compared with 75 mmol L-1 NaCl stress, the exogenous protein expression in Bt cotton leaves under 150 mmol L-1 NaCl stress decreased by 46.66% (p<0.001). Together, these results showed that NaCl stress could significantly inhibit the exogenous protein expression in Bt cotton and that the decrease in the exogenous protein expression was related to the degree of salt stress.

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Fig 1. Effect of NaCl stress on exogenous insecticidal protein expression in Bt cotton.

Mean (±SD) exogenous protein contents of cotton bollworms (Helicoverpa armigera) that were fed excised transgenic Bt (Bt) cotton plants grown under NaCl stress. Different lowercase letters indicate significant differences between NaCl stress treatments (LSD test: p<0.05).

https://doi.org/10.1371/journal.pone.0198570.g001

Effect of NaCl-stressed cotton on the feeding behavior of bollworms

The effect of NaCl-stressed Bt cotton on the feeding behavior of bollworm larvae is shown in Fig 2. When GK19 Bt cotton and Simian-3 nontransgenic cotton plants were under NaCl stress, the probability that bollworm larvae would feed on them decreased as the NaCl concentration increased. However, the difference between treatments was not significant. Compared with the feeding probability of bollworm larvae on Simian-3 nontransgenic cotton plants, the feeding probability of bollworm larvae on GK19 Bt cotton plants was overall low. Under 0 mmol L-1 NaCl stress, the feeding probability of bollworm larvae on GK19 was 42.65% (p = 0.037) lower than that on Simian-3. Furthermore, the feeding probability of bollworm larvae did not significantly differ under 75 mmol L-1 and 150 mmol L-1 NaCl stress; even under different levels of NaCl stress, the probabilities of crawling, resting and spinning down behaviors for larvae on Bt cotton were not significantly different from those for larvae on nontransgenic cotton. These results show that NaCl stress did not significantly affect the feeding behavior of bollworm larvae on cotton plants.

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Fig 2. Effect of NaCl-stressed Bt cotton on the feeding behavior of bollworm larvae.

(A) Mean (±SD) feeding, (B) scrawling, (C) resting and (D) spinning-down behaviors of cotton bollworms (Helicoverpa armigera) that were fed excised transgenic Bt (Bt) and nontransgenic (Non) cotton plants grown under NaCl stress. Different lowercase letters indicate significant differences between NaCl stress treatments, and * indicates significant differences between the cotton varieties under the same NaCl stress treatment (LSD test: p<0.05).

https://doi.org/10.1371/journal.pone.0198570.g002

Effect of NaCl-stressed Bt cotton on the nutritional effect parameters in bollworms

Food consumption and the amount of feces.

The cotton variety and NaCl stress had marked effects on the amount of food consumed by and the feces produced by bollworm larvae (Fig 3). Under the same NaCl stress condition, the amount of food consumed by and the feces produced by bollworm larvae on GK19 Bt cotton were significantly lower than those on Simian No. 3 nontransgenic cotton (p0 = 0.000, p75 = 0.000, p150 = 0.001). Compared to the 0 mmol L-1 NaCl treatment, the amount of food consumed by and the feces produced by bollworm larvae on the Bt cotton both first increased but then decreased under 75 mmol L-1 and 150 mmol L-1 NaCl stress, and there was no significant difference among the stress treatments. However, the amount of food consumed by and the feces produced by the bollworm larvae on nontransgenic cotton were reduced; under 150 mmol L-1 NaCl stress, food consumption decreased by 25.88% (p = 0.002) and feces production decreased by 23.06% (p = 0.021), respectively. Together, these results showed that the introduction of exogenous genes significantly inhibited the food consumption and the amount of feces produced by bollworm larvae on cotton. However, as the NaCl concentration increased, no significant differences in bollworm food consumption and feces production were observed on either cotton variety.

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Fig 3. Effect of NaCl-stressed Bt cotton on the amount of food consumed and feces produced by bollworm larvae.

(A) Mean amounts of (±SD) food consumption and (B) amount of feces production of cotton bollworms (Helicoverpa armigera) that were fed excised transgenic Bt (Bt) and nontransgenic (Non) cotton plants grown under NaCl stress. Different lowercase letters indicate significant differences between NaCl stress treatments, and * or ** indicates significant differences between cotton varieties under the same NaCl stress treatment (LSD test: p<0.05 and p<0.01, respectively).

https://doi.org/10.1371/journal.pone.0198570.g003

Nutritional effect parameters.

The cotton variety and NaCl stress significantly affected the MRGR, RGR, RCR and RMR of the bollworm larvae (Fig 4). Under the same NaCl stress level, the MRGR, RGR and RCR of bollworm larvae feeding on GK19 Bt cotton were significantly lower than those of bollworm larvae feeding on Simian-3 nontransgenic cotton (p<0.001), but the RMR of the former was significantly higher than that of the latter (p>0.05). Compared to 0 mmol L-1 NaCl stress conditions, the MRGR and RGR of bollworm larvae feeding on both varieties of cotton under 75 mmol L-1 and 150 mmol L-1 NaCl stress decreased. Specifically, the MRGR (p75 = 0.046, p150 = 0.014) and RGR (p75 = 0.027, p150 = 0.050) of bollworm larvae feeding on Bt cotton and nontransgenic cotton under 150 mmol L-1 NaCl stress significantly decreased.

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Fig 4. Effect of NaCl-stressed Bt cotton on the MRGR, RGR, RCR and RMR of bollworm larvae.

(A) Mean (±SD) Mean relative growth rate (MRGR), (B) relative growth rate (RGR), (C) relative consumption rate (RCR), and (D) relative metabolic rate (RMR) of cotton bollworms (Helicoverpa armigera) that were fed excised transgenic Bt (Bt) and nontransgenic (Non) cotton plants grown under NaCl stress. Different lowercase letters indicate significant differences between NaCl stress treatments, and * or ** indicates significant differences between cotton varieties under the same NaCl stress treatment (LSD test: p<0.05 and p<0.01, respectively).

https://doi.org/10.1371/journal.pone.0198570.g004

The RCR and RMR of bollworms feeding on GK19 Bt cotton significantly differed (pRCR = 0.011, pRMR = 0.027) under 75 mmol L-1 NaCl stress. In addition, the RCR of bollworms feeding on Simian No. 3 nontransgenic cotton significantly differed (p = 0.014) under 150 mmol L-1 NaCl stress. Overall, these results showed that both cotton varieties and NaCl stress conditions can significantly affect the MRGR, RGR, RCR and RMR of bollworm larvae.

The cotton variety and NaCl stress significantly affected the AD, ECI and ECD of bollworm larvae (Fig 5). Under the same NaCl stress level, the AD of bollworm larvae feeding on GK19 Bt cotton was higher than that of bollworm larvae feeding on Simian-3 nontransgenic cotton; in addition, the ECD and ECI of the former were lower (p<0.001) than those of the latter only under 75 mmol L-1 and 150 mmol L-1 NaCl stress. Compared with the AD and ECI under 0 mmol L-1 NaCl stress, the AD (p75 = 0.004, p150 = 0.000) and ECI (p75 = 0.000, p150 = 0.000) of bollworm larvae feeding on Bt cotton under 75 mmol L-1 and 150 mmol L-1 NaCl stress significantly decreased, while the ECD decreased (p = 0.049) only under 75 mmol L-1 NaCl stress. The AD, ECI and ECD of bollworm larvae feeding on Simian-3 nontransgenic cotton did not significantly change. Together, these results showed that both the cotton variety and NaCl stress can significantly affect the AD, ECI and ECD of bollworm larvae.

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Fig 5. Effect of NaCl-stressed Bt cotton on the AD, ECI and ECD of bollworm larvae.

(A) Mean (±SD) approximate digestibility (AD), (B) efficiency of conversion of ingested food (ECI), and (C) efficiency of conversion of digested food (ECD) of cotton bollworms (Helicoverpa armigera) that were fed excised transgenic Bt (Bt) and nontransgenic (Non) cotton plants grown under NaCl stress. Different lowercase letters indicate significant differences between NaCl stress treatments, and * or ** indicates significant differences between cotton varieties under the same NaCl stress treatment (LSD test: p<0.05 and p<0.01, respectively).

https://doi.org/10.1371/journal.pone.0198570.g005

Salt stress concentration and cotton variety interaction

Within a certain range, the salt stress concentration, cotton variety, and their interaction have certain effects on the feeding behavior and nutritional parameters of bollworm larvae (Table 1). Both the cotton variety and salt stress significantly affected the nutritional parameters of bollworm larvae after feeding, but their interaction had less of an effect on the nutritional parameters.

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Table 1. Effects of NaCl, cotton variety, and the interaction between NaCl and cotton variety on the feeding behavior and nutritional effect parameters of young cotton bollworm larvae (F-value).

https://doi.org/10.1371/journal.pone.0198570.t001

Discussion

The insecticidal effect of Bt cotton depends on the expression of exogenous insecticidal proteins, which is correlated with plant variety, plant growth stage, plant tissue and abiotic stress [11,14,16,17,18, 19, 20, 22,24]. In this study, the expression of exogenous insecticidal proteins in the leaves of Bt cotton GK19 was measured under NaCl stress. The results showed that NaCl stress could significantly inhibit the expression of exogenous Bt proteins in the Bt cotton plants, which is consistent with the conclusions of Rao [18], Jiang et al. [19], Luo et al. [20] and Iqbal et al. [22]. Based on their salt stress studies, Li et al. [29] and Luo et al. [24] reported similar conclusions under greenhouse and natural field conditions. Together, these results show that salt stress can significantly inhibit the expression of exogenous proteins in Bt cotton and that the degree of inhibition is related to the degree and duration of the salt stress.

Different pests exhibit different behavioral responses to transgenic crops. Furthermore, for even the same pest, larvae at different instars respond differently to the same transgenic crop, and the same pest can exhibit different avoidance behaviors to different toxins or genetically modified crop species [3033]. This study investigated the feeding behavior of newly hatched bollworm larvae on GK19 Bt cotton and its nontransgenic parent Simian-3 under NaCl stress. The results showed that the feeding probability of bollworm larvae on GK19 Bt cotton and Simian-3 nontransgenic cotton under NaCl stress decreased as the NaCl concentration increased; however, there were no significant differences among salt treatments. When compared to the probability of bollworm larvae feeding on Simian-3 nontransgenic cotton, that on GK19 Bt cotton was lower overall and decreased significantly only under no salt stress (0 mmol L-1); these results are similar to those under normal planting conditions [31]. However, under salt stress conditions, there was no significant difference in the feeding rate of the newly hatched bollworm larvae on the two varieties of cotton, most likely due to the decrease in bollworm avoidance behavior resulting from the reduced expression of exogenous insecticidal proteins in Bt cotton under NaCl stress [3436]. The probability that bollworm larvae would exhibit crawling, resting and spinning down behaviors on GK19 Bt cotton was not significantly different from those on Simian-3 nontransgenic cotton, and these probabilities did not significantly differ among the NaCl stress treatments. These findings show that NaCl stress had no significant effect on the feeding behavior of bollworm larvae on cotton, as shown by the results of previous experiments investigating the selection of hosts for oviposition in rice brown planthoppers (Nilaparvata lugens) [37].

When grass-feeding insects feed on transgenic insect-resistant plants, food consumption and use may be affected [38]. Whittaker et al. [39] studied the effects of elevated CO2 concentrations on plant-herbivore interactions, and their results showed that Bt cotton and elevated CO2 concentrations could slow the development of bollworms and consequently reduce larval weight gain, RGR and MRGR. The present study investigated the effects of GK19 Bt cotton and its nontransgenic parent Simian-3 under NaCl stress on the nutritional parameters of 5th instar bollworm larvae. The results showed that under the same NaCl stress level, the amount of food consumed and the amount of feces produced by bollworm larvae were significantly lower on GK19 Bt cotton than on Simian-3 nontransgenic cotton; these results are consistent with the conclusions of Shobana et al. [40] and Roy et al. [38]. However, there were no significant differences among the stress treatments involving different NaCl concentrations. NaCl stress resulted in significant decreases in the MRGR, RGR, AD, ECI and ECD of the 5th instar bollworm larvae, which was essentially consistent with the results of both Whittaker et al. [39] and Chen et al. [41], who investigated the effects of abiotic stress-induced CO2 elevation on the nutritional parameters of bollworms feeding on Bt cotton. While Somashekara et al. [42] reported that the AD of bollworms decreased after feeding on Bt cotton, in this study, the AD of 5th instar bollworm larvae feeding on GK19 Bt cotton was much higher than that of 5th instar larvae feeding on non-transgenic cotton. Our results are consistent with those of Chen et al. [43], who reported the nutritional parameters of different generations of beet armyworms that fed on transgenic cotton. In addition, the results of the present study suggest that the nutritional parameters of bollworms that feed on transgenic and non-transgenic cotton plants differ under NaCl stress. The variations between these studies and insects may be due to either the response of phytophagous insects to different hosts, which correlates with the growth status of the host plants [4445,40], or to the food compensatory effects of the insects [44]. Additional short-term and long-term experiments are needed to study this question.

The analysis of the interactive effects revealed that Bt cotton could inhibit the feeding behavior of bollworm larvae; however, salt stress did not affect the probability that larvae would feed on cotton. Although both salt stress and cotton variety significantly affected the nutritional parameters of bollworm larvae after feeding, they had no significant interactive effects on the feeding behavior or nutritional parameters of bollworm larvae. Furthermore, both salt stress and increases in CO2 concentration are abiotic stressors, and the effects on cotton and insects may be similar [41].

Under the context of planting Bt cotton on saline-alkali land, this study investigated the complexity of the response of bollworm larvae to Bt cotton grown under NaCl stress. The results showed that NaCl stress could not induce taxis or reduce the feeding behavior of bollworm larvae on cotton but could affect the growth, development, and nutritional parameters of bollworm larvae. The food utilization rates of phytophagous insects of different species and generations substantially differ, and further research is needed 1) to clarify the effect of reductions in the expression of exogenous proteins on the feeding behavior of bollworms on Bt cotton plants under salt-alkali stress, and 2) to quantify the nutritional indicators of herbivores on transgenic insect-resistant plants to determine the impact of these plants on target or nontarget organisms. These findings provide a basis for the control of pests on Bt cotton plants on saline-alkali lands.

Supporting information

Acknowledgments

We are grateful for the financial support from the National Natural Science Foundation of China (31501253).

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