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The lack of homogeneity in field application of Bacillus thuringiensis formulation often results in ingestion of sub-lethal doses of the biopesticide by a fraction of pest population and there by promotes the toxin tolerance and resistance in long term. Gut regeneration seems to be one of the possible mechanism by which this is accomplished. However, the existing information is primarily derived from in vitro studies using mid-gut cell cultures. Present study illustrates cellular and molecular changes in mid-gut epithelium of a Bt-susceptible polyphagous insect pest castor semilooper, Achaea janata in response to a Cry toxin formulation. The present report showed that prolonged exposure to sub-lethal doses of Cry toxin formulation has deleterious effect on larval growth and development. Histological analysis of mid-gut tissue exhibits epithelial cell degeneration, which is due to necrotic form of cell death followed by regeneration through enhanced proliferation of mid-gut stem cells. Cell death is demonstrated by confocal microscopy, flow-cytometry, and DNA fragmentation analysis. Cell proliferation in control vs. toxin-exposed larvae is evaluated by bromodeoxyuridine (BrdU) labeling and toluidine blue staining. Intriguingly, in situ mRNA analysis detected the presence of arylphorin transcripts in larval mid-gut epithelial cells. Quantitative PCR analysis further demonstrates altered expression of arylphorin gene in toxin-exposed larvae when compared with the control. The coincidence of enhanced mid-gut cell proliferation coincides with the elevated arylphorin expression upon Cry intoxication suggests that it might play a role in the regeneration of mid-gut epithelial cells.
Bacillus thuringiensis (Bt) strains synthesize different toxins including crystal (Cry), cytolytic (Cyt), and vegetative insecticidal proteins (Vip). While Cry and Cyt toxins are synthesized during sporulation (Hofte and Whiteley, 1989; Bravo et al., 2007), Vip toxins are produced during the vegetative growth phase (Estruch et al., 1996). Lepidopteran larvae experimentally used to demonstrate the mode of action of Cry toxin, showed sequential event of toxin solubilization, its activation induced by alkaline pH of the gut, proteolytic cleavage, binding of toxin with different receptor molecules, oligomerization, and membrane insertion leading to pore formation and epithelial cell damage (Bravo et al., 2007). Further, in vitro studies suggested that the Cry toxin-induced cell death is primarily of necrotic type (Zhang et al., 2016).
Bt and its insecticidal toxins have been predominantly used for the control of maize and cotton pests (Bravo et al., 2011; Hellmich and Hellmich, 2012). The development of insect resistance to Bt is a major concern for its long-term effectiveness. Extensive studies revealed, alteration in mid-gut binding sites leading to reduced interaction of Bt toxins to their receptor, as a major mechanism for the development of resistance (Pigott and Ellar, 2007). Since many Cry toxins share common binding sites, the probability of cross-resistance was often found to be high (Ferre and Van Rie, 2002; Tabashnik et al., 2013). In agreement with these reports, insects such as diamond black moth, Plutella xylostella; Indian meal moth, Plodia interpunctella, and cabbage looper, Trichoplusia ni have evolved resistance to commercial Bt sprays in the open field and greenhouses (Ferre et al., 1991; Oppert et al., 1997; Janmaat and Myers, 2003). Recently, field-evolved pest resistance to Bt corn (maize stem borer, Busseola fusca; western corn rootworm, Diabrotica virgifera virgifera; and fall armyworm, Spodoptera frugiperda), Bt cotton (cotton bollworm, Helicoverpa armigera, and pink bollworm, Pectinophora gossypiella), and Bt maize (Spodoptera frugiperda) have also been reported (Storer et al., 2010; Dhurua and Gujar, 2011; Kruger et al., 2011; Zhang et al., 2011; Jakka et al., 2015; Pereira et al., 2015).
Additional physiological responses from larvae alike non-receptor mediated resistance mechanisms could interfere with steps common to all Cry toxins vis-à-vis cross-resistance to a wide range of Bt toxins. One such process is the enhanced mid-gut regeneration response observed in the resistant larvae. Lepidopteran larvae have been shown to recover from exposure to sub-lethal Cry toxin doses (Dulmage and Martinez, 1973) by mid-gut epithelial regeneration (Spies and Spence, 1985). Further few microscopic studies showed enhanced mid-gut healing response to facilitate Cry toxin resistance in the tobacco budworm, Heliothis virescens (Forcada et al., 1999; Martinez-Ramirez et al., 1999). However, there is a dearth of information on the molecular aspects of mid-gut epithelial response to Cry toxin. In addition, most of the information on the regenerative process is derived from in vitro studies using primary mid-gut cell cultures (Loeb et al., 2001; Blackburn et al., 2004; Hakim et al., 2010) mainly due to the lack of mid-gut specific biomarkers to allow quantitative detection of lepidopteran mid-gut cells, their proliferation as well as differentiation. The in vitro data circumvents specific cell/tissue interactions within the insect system. One of the candidate molecules presumed to be involved in the mid-gut response to Bt toxins is arylphorin, which belongs to the hexamerin protein family of insects. Arylphorin was shown to stimulate stem-cell proliferation in vitro as well as upon feeding with diet, where it promoted the growth of gut suggesting its mitogenic effect on gut cells (Blackburn et al., 2004; Hakim et al., 2007).
Foliar spray of Bt formulation often results in the loss of toxicity from degradation by UV light, wash-off by rain, drying, temperature, and soil acidity as well as its chemistry (Pinnock et al., 1975; Leong et al., 1980; Beckwith and Stelzer, 1987; vanFrankenhuyzen and Nystrom, 1989). Under afore mentioned conditions, there is always a possibility of a population of larva to get exposed to sub-lethal doses of toxin which might exhibit a variable effect and escape mortality. In line with these observations the present study is aimed to evaluate the effect of sub-lethal doses of Bt toxin on mid-gut of the larva of Achaea janata, an economically important polyphagous pest prevalent in the Indian subcontinent. In vivo analysis document the necrotic type of cell death associated with regeneration of mid-gut epithelial cells during Cry intoxication. Additionally, the presence of arylphorin transcript in larval mid-gut cells and its differential expression during Cry intoxication is also demonstrated.
For the present study, larvae of A. janata Linn. (Noctuidae: Lepidoptera) were collected from the fields of Indian Institute of Oil Seeds Research, Hyderabad with no prior exposure to any synthetic or Bt pesticides, reared in the laboratory conditions (Budatha et al., 2007). They were maintained for three generations as to obtain homogenous population (in a growth chamber). Larvae were fed with sterile castor leaves and maintained at 27 ± 2°, 14:10 h (light: dark) photoperiod and relative humidity of 60–70% till pupation. Pupae were transferred to moist sand container for adult emergence. Adults were transferred to egg laying chamber and were supplemented with 10% honey containing Vitamin E. Adults laid their eggs on the leaves and the neonate larvae hatched were used for continuous culture as well as experiments.
DOR Bt-1 formulation was obtained from Indian Institute of Oil Seeds Research which exhibited high toxicity against A. janata larvae and various other lepidopteran pests. The PCR analysis of DOR Bt-1 isolate revealed presence of cry1 (cry1Aa, cry1Ab, and cry1Ac) and cry2 (cry2Aa and cry2Ab) genes, which provide broad-spectrum potential against lepidopteran, and dipteran insects (Reddy et al., 2012). The reported LC50 value for the DOR Bt-1 formulation was 247.52 μg/ml for seven-day-old or 3rd instar larvae (Vimala Devi and Sudhakar, 2006). One tenth of LC50 value was used as a sub-lethal dose (i.e., 24.75 μg/ml of water) for the present study. Toxin coated castor leaves were fed to the larvae. Triplicates were maintained, for each treatment 150 larvae were used. They were divided into two sets of experiments, wherein one batch was continuously exposed to sub-lethal dosage of toxin (0.170 μg/cm2) coated castor leaf discs (145 cm2) till 72 h, and a batch of 30 larvae were intermittently transferred to uncoated leaf discs after every 24 h period of toxin exposure for the recovery. Control larvae were maintained on water coated leaf discs. Furthermore, morphological changes occurring during the development and mortality were also recorded in toxin-exposed as well as recovered insects.
Third instar larvae (a batch of 100) exposed to toxin coated leaves were collected at every 12 h interval till 72 h. These were briefly narcotized on ice and dissected in insect Ringer solution (130 mM NaCl, 0.5 mM KCl, and 0.1 mM CaCl2). An incision was made in the abdominal region and extended through the length of the larvae. The gut content was removed and the mid-gut region was specifically isolated. After removal of the gut, the yellowish-white perivisceral fat body was collected. The isolated tissues were used for histology, in-situ hybridization, genomic DNA and total RNA isolation.
Cell death/viability of mid-gut cells was primarily assessed using AnnexinV and Propidium Iodide (PI) staining (Vermes et al., 2000). For this experiment mid-gut was dissected out from both control and toxin exposed (24 h) larvae and maintained in Grace insect cell culture media (Invitrogen Corporation, USA) and incubated with AnnexinV and Propidium Iodide staining solutions (BD Biosciences, UK) and visualized under confocal microscope (LSM 880, Carl Zeiss, Jena). Furthermore, gut cells were strained through 70 μm mesh size MACS® smart strainer (Miltenyi Biotec, Singapore) using phosphate buffer saline (PBS) solution (pH 7.4). The cell reservoir was collected in the funnel and centrifuged at 1,500 rpm for 5 min at 4°C. The cell suspension was collected and immediately processed for FACS (fluorescence-activated cell sorting) analysis. An analysis was carried out using Annexin V-FITC Apoptosis Detection Kit according to the manufacturer's instructions (BD Biosciences, UK). In brief, AnnexinV and Propidium Iodide staining solutions were added to the sieved cell suspension and incubated at room temperature in the dark for 15 min. This was followed by addition of binding buffer and then analyzed using a FACS LSR FortessaTM flow cytometer (BD Biosciences, UK) and BD FACS Diva Software 6.0. For each sample, 10,000 events were acquired. The percentage of live cells vs. cells undergoing death was plotted.
To substantiate that cell death is due to necrosis but not because of apoptosis in larval mid-gut, DNA fragmentation assay was carried out following the protocol of Kasibhatla et al. (2006). Genomic DNA from the mid-gut was isolated using a standard protocol (Lagisz et al., 2010), with minor modifications. The tissue (100 mg) was homogenized using 500 μl of lysis buffer (100 mM Tris-HCl (pH8.0), 50 mM EDTA, 1.5 mM NaCl, 2% CTAB, and 0.1% 2-mercaptoethanol). DNA pellet thus obtained was solubilized in Tris-EDTA buffer (pH 8.0) and analyzed by 0.8% agarose gel electrophoresis.
The isolated mid-guts were fixed overnight in Bouin's fixative (saturated picric acid: formaldehyde: glacial acetic acid; 15:5:1), processed through a series of increasing ethanol concentrations, cleared in xylene and embedded in molten paraplast (Sigma-Aldrich, USA). The tissues were sectioned (~5 μm) using a rotatory microtome (Leica Microsystems, Germany) and stained with haematoxylin-eosin or toluidine blue (Sousa et al., 2010), visualized using Olympus IX-81 microscope (Olympus Corporation, Japan), and photographed.
Streptavidin-biotin based BrdU staining (Invitrogen Corporation, USA) was used for monitoring the cell proliferation in the mid-gut during toxin-induced damage following manufacturer's protocol. Larvae were injected with BrdU labeling reagent (10 μl/g body weight) 4 h prior to isolation of toxin exposed larval mid-gut using a Hamilton syringe. Dissected mid-guts were fixed and processed as mentioned in the previous Section Histological Analysis of Mid-Gut, tissue sections were spread on poly-L-lysine coated slides (Sigma-Aldrich, USA) and incubated overnight at 37°C following which deparaffinization was carried out using xylene and passed through a series of decreasing ethanol concentrations. Peroxidase quenching was performed using 30% H2O2 and absolute methanol (1:9). Denaturation and blocking steps were carried out using the kit based reagent prior to antibody incubation. Biotinylated mouse anti-BrdU was overlaid and the slides were incubated at room temperature (RT). After incubation, streptavidin peroxidase (Invitrogen Corporation, USA) was added to detect the incorporation. Color development was monitored after the addition of secondary antibody mixture provided by the manufacturer. Slides were counterstained and mounted using histomount™ (Invitrogen Corporation, USA) and visualized under Olympus IX-81 microscope.
For the preparation of arylphorin cRNA probe, a 160 bp fragment of A. janata arylphorin gene was positioned as forward locked in pGEM-T Easy Vector (Promega Corporation, USA). The vector was linearized with EcoRI and NdeI restriction enzymes (New England Biolabs®, UK). Sp6 promoter was used for the synthesis of antisense probe (positive), while T7 promoter was used for the synthesis of sense probe (negative). Further, RNA probe synthesis was carried out using DIG RNA labeling kit (Roche Diagnostics, Germany). Larval mid-gut and fat body were dissected out and fixed in 4% paraformaldehyde (PFA) (Sigma-Aldrich, USA) in 0.1 M PBS at 4°C overnight. Post-fixation, tissues were embedded in OCT compound medium (Leica Microsystems, Germany). Tissue cross sections were obtained using cryostat microtome (Leica CM1850, Leica Microsystems, Germany) and mounted on poly-L-lysine coated slides. The OCT compound was washed using PBST buffer and the sections were permeabilized using proteinase K (1 μg/ml). Once again 4% PFA was used for further tissue fixation and sections were incubated with 200 μl hybridization buffer (50% formamide, 5X SSC, 5 mM EDTA, 0.1% CHAPS, 1% SDS, 50 μg/ml yeast tRNA, 50 μg/ml heparin) for 1 h at 50°C. The digoxigenin labeled cRNA probe was mixed with 200 μl of hybridization buffer, heat denatured at 80°C for 5 min, draped and covered with parafilm and incubated at 50°C in a sterile incubator overnight. Post-hybridization, the slides were washed four times at 50°C (5 min each) with a wash buffer (SSC, 50% formamide, 0.1% Tween 20) in a series of decreasing SSC concentration. The slides were then processed with solution A (0.5 M NaCl, 5 mM EDTA, 10 mM Tris-HCl, 0.1% Tween 20, pH 8.0) and incubated at RT for 5 min followed by incubation with 20 μg/ml of RNase A for 20 min at RT. Later, the slides were again washed with solution A twice (5 min each) at RT.
For the antibody reaction, the slides were initially washed with maleic acid buffer (100 mM maleic acid, 150 mM NaCl, 0.1% Tween 20, pH 7.5) for 5 min at RT followed by blocking with 10% BSA for 1.5 h at RT. Anti-digoxigenin-ALP (Roche Diagnostics, Germany) was used for the detection of digoxigenin probe (1:2,000) and incubated overnight at 4°C. These slides were then washed with DIG wash buffer (Roche Diagnostics, Germany) for 4 times (15 min each). Incubation with 100 μl BCIP-NBT solution (G-Bioscience, USA) for 10 h at RT was carried out to develop the color. After color development, the slides were overlaid with detection buffer (Roche Diagnostics, Germany), counterstained with nuclear red (Vector Laboratories Inc., USA), and incubated in TE buffer (Ambion, Life Technologies, USA) for 5 min. After washing with PBST buffer, the slides were processed with increasing series of ethanol, mounted using DPX mountant, and visualized under Olympus IX-81 microscope.
Total RNA was isolated from the tissue (100 mg) using TRIzol method® (Ambion, Life Technologies, USA). The quantification of the RNA was carried out using NanoDrop spectrophotometer (ND-2000; NanoDrop Technologies, USA). Quality and integrity of RNA were assessed by formaldehyde denaturing gel electrophoresis. cDNA was synthesized using Revert Aid First Stand cDNA synthesis kit (Thermo Scientific, USA). For quantitative PCR analysis, a custom-made TaqMan gene expression assay was performed (Applied Biosystems, USA). Arylphorin primers of amplicon size 160 bp (Fwd: 5′-GTT AGA GAA GGG CCA GGT GTC TCA TG-3′; Rev: 5′- CTC TGG CTT GGT AGA CTC CTT GGT-3′) were designed from the arylphorin nucleotide sequence (KX462992). Insect rS7 gene (KF984201) was used as an internal control using primers (Fwd: 5′-ACG TGG ACG GTT CAC AAC TCA TCA-3′; Rev: 5′-TTC GCG GCC TGT TAG CTT CTT GTA-3′) which gave rise amplicon of 115 bp, to normalize the transcript expression levels. The real-time expression analysis was performed in triplicates. From the exponential phase of PCR amplification Cycle threshold (Ct) values were obtained. Arylphorin expression was normalized against the expression of rS7 rRNA to generate a ΔCt value (Ct of Arylphorin—Ct of rS7 rRNA). Comparative Ct method was used to calculate the change in the gene expression (Livak and Schmittgen, 2001).
Presented data was calculated using standard error of the mean (SEM) (n = 3) which passed homogeneity and normality tests. Statistical significance was verified using the SigmaPlot v12.3 software (SystatSoftware Inc., USA). Significance between groups was tested using One-Way ANOVA followed by Student-Newman-Keuls (SNK) test for pairwise multiple comparison analysis and the p-value was calculated for each set of experiments.
The larvae that fed on toxin-coated leaves exhibited reduced growth in a time-dependent manner (24–72 h; Figure Figure1A).1A). The 24 h toxin-exposed larvae could recover and grow when transferred to normal leaves (Figure (Figure1B),1B), whereas the 48 and 72 h toxin-fed groups often showed slow and poor recovery. Further, the body weight of the toxin exposed larvae was fairly low and were only 50% of that of the age matched control groups after 72 h of recovery, when the larvae were exposed to toxin for 48 and 72 h (Figure (Figure1B1B).
Confocal analysis revealed the presence of PI positive cells in toxin exposed larvae but not in controls (Figure (Figure2A).2A). Mid-gut cell suspension prepared from toxin exposed insects showed a distinct shift into the upper left quadrant (Q1) representing necrotic type of cell death (Figure (Figure2B).2B). Further, the cells undergoing necrosis have increased gradually from 12 to 36 h upon toxin-exposure. However, it was noteworthy that the number of necrotic cells reduced drastically in 48 and 72 h toxin-exposed samples (Figure (Figure2B2B).
The result from DNA fragmentation assay revealed that the DNA integrity was preserved in both control and toxin-exposed mid-gut samples and the absence of DNA fragmentation in all the samples rules out the possibility of apoptotic form of cell death (Figure (Figure2C).2C). Microscopic, FACS and DNA fragmentation analyses indicated that necrosis was the most likely reason for cell death upon Cry intoxication.
The results presented in Figure Figure33 show few pockets of BrdU-positive cells (brown stained nuclei) were identified in the mid-gut collected from toxin exposed larvae (Figure (Figure3A).3A). The dividing cells which were mostly observed in the basal region of the gut epithelium could be ascribed as mid-gut stem cells (Figure (Figure3B,3B, inset).
Figure Figure44 shows the histological changes seen in toxin exposed larval mid-gut from 12 to 72 h. The mid-gut cells showed degeneration with a condensed nucleus and fairly low cytoplasmic content. In addition, a large number of vacuoles were seen in them. Maximum cell death was observed between 24 and 36 h (Figures 4C,D). However, it was interesting to note that active cell proliferation as depicted by toluidine blue was seen extensively in 36 h Cry toxin exposed larvae (Figures 4C,D). BrdU labeling, histological and toluidine blue staining studies in parallel confirmed that not only cell death but also regeneration occurred in larval mid-gut upon Cry intoxication in A. janata.
Detectable but low expression of arylphorin in the mid-gut as compared to the fat body was observed using qRT-PCR analysis (Figure (Figure5A).5A). In accordance to this, in situ hybridization results revealed the localization of arylphorin transcript in the gut epithelium primarily in the basal cells (Figure (Figure5B5B).
In control insects, arylphorin transcript level was fairly low throughout the time points monitored, but a steep incline was observed at 72 h (Figure (Figure6).6). On the other hand, arylphorin expression gradually increased from 6 h and reached maximum at 36 h in Cry intoxicated larvae, thereafter the mRNA levels declined significantly in 48 h and remained low till 72 h.
In the present study, the effects of a sub-lethal dose of Bt toxin was analyzed through the mid-gut responses in A. janata larvae. As observed in this pest and other reported lepidopteran models, Bt exposed larvae usually have fairly low digestive activity concomitant with their reduced body weight associated with altered growth and development (Hernández-Martinez et al., 2010). DOR Bt-1 toxin administration triggered significant changes in the gut epithelium including nuclear condensation, vacuolization, low cytoplasmic content, and loosening of cell followed by necrosis. These observations corroborated well with an earlier study (Budatha et al., 2007) and suggested that even in A. janata, the binding of Cry to mid-gut cell receptors promote cell death. However, there is increasing evidence that Cry toxin induced cell death is a fairly complex cellular response. Zhang et al. (2006) using cabbage looper ovarian cell culture demonstrated that Cry1Ab toxin manifests its effect through Mg2+dependent adenylyl cyclase/protein kinase A signaling pathway. Present microscopic and FACS analyses in A. janata showed Cry toxin induced necrotic type of cell death in larval mid-gut under in-vivo condition without DNA fragmentation (a hallmark of apoptosis). Recently, using toxin-host interaction system in Caenorhabditis elegans, Cry6Aa was shown to promote cell death through necrotic signaling pathway (Zhang et al., 2016). In addition, many bacterial toxins such as β-toxin from Clostridium perfringens, delta-toxin from Clostridium septicum, and VacA from Helicobacter pylori were shown to cause cell necrosis (Knapp et al., 2010; Radin et al., 2011; Sridharan and Upton, 2014; Seike et al., 2016). Taken together, the results obtained in the present study confirm that exposure to sub-lethal doses of Cry toxin triggers cell death in larval mid-gut of A. janata through necrosis.
Inspite of mid-gut cell death, larva did survive the exposure to sub-lethal doses of Bt toxin. Replenishment of injured cells is facilitated by normal feeding leading to recovery and metamorphosis (Spies and Spence, 1985; Loeb et al., 2001), while high doses of Bt toxin are known to kill insect pests (Tabashnik et al., 2013). Like many other tissues, renewal of epithelium is carried out by regenerative cells localized in the basal crypts, termed as mid-gut stem cells. These are the only cell present in gut capable of division and thus represent the sole source of new cells during tissue repair and growth. Continuous replacement of damaged cells by regenerative cells under toxin environment is likely to cause an alteration in cellular properties, leading to the development of resistance in insects against Cry formulations (Martinez-Ramirez et al., 1999; Castagnola and Jurat-Fuentes, 2016). Majority of cases of resistance against Cry toxins, reported reduction in binding of Bt toxins to their specific mid-gut receptors, i.e., cadherins, aminopeptidases, and alkaline phosphatases, which resulted in cross-resistance to Cry toxins sharing common altered receptor site (Morin et al., 2003; Pigott and Ellar, 2007; Zhang et al., 2009). However, Cry toxin resistance involving alterations in toxin processing by mid-gut secretion was also reported (Oppert et al., 1997; Caccia et al., 2012).
A number of growth factors promoting mid-gut cell culture regeneration have been reported, which include fetal bovine serum, ecdysteroids (Loeb, 2010), mammalian growth-promoting factor (Nishino and Mitsuhashi, 1995), alpha-arylphorin, MDFs (Blackburn et al., 2004; Hakim et al., 2010), and AlbuMAX II (Castagnola et al., 2011). The proliferation and differentiation of mid-gut epithelial cell seen upon Cry intoxication in A. janata might have been triggered and modulated by similar factors. Hexamerin proteins, particularly exogenous arylphorin (fat body synthesized arylphorin) were shown to promote proliferation of mid-gut cells in culture (Hakim et al., 2007). Mid-gut transcriptome profile showed up-regulation of arylphorin transcripts in the Xentari™ resistant Spodoptera exigua larvae (Hernández-Martinez et al., 2010). The transcriptome analysis with A. janata larval mid-gut also revealed up-regulation of arylphorin upon Cry intoxication (Unpublished data). In addition, in the present study in situ hybridization provided direct evidence for the localization of arylphorin transcripts in the actively dividing cells of mid-gut, which were primarily confined in the basal region of the epithelium. Expression analysis using Cry intoxicated larva mid-gut further showed time dependent increase in endogenous arylphorin gene expression during active cell proliferation, which was not only seen upon Cry intoxication but also during molting in control larvae where regeneration has been well-documented (Webb and Riddiford, 1988; Kawaguchi et al., 1993).
The present study, not only demonstrated cell death and damage of mid-gut epithelium upon Cry intoxication but also proliferation of stem/regenerative cells that allow the larvae to repair its gut epithelium and generate differentiated cells to facilitate their survival. This is further substantiated by the presence of a large number of BrdU positive cells in the basal crypts of the gut epithelium, while toludine blue staining reveals a sizable increase in the number of proliferative cell upon Cry intoxication in time dependent manner. Given the versatility of arylphorin, its presence and altered expression in the mid-gut during Cry toxin exposure, it is possible that a low concentration of arylphorin produced endogenously in mid-gut is critical and probably inculcates mitogenic effect during the Cry intoxication. Further characterization of the gut regenerative process in the future will help in obtaining a better understanding of the resistance mechanism.
Conceived and designed the experiments: AD, VC, and ND; Performance of the experiments: VC and ND; Analysis of the data: AD, VC, ND, and RC; Suggestion and help for in-situ analysis: BS; Manuscript writing: VC and ND; Manuscript editing: AD, BS, and RC.
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The present study was financially supported by DST-SERB (Grant No. SB/SO/AS-047/2013) and UPE-II. The authors especially thank Dr. P. S. Vimala Devi, Indian Institute of Oil Seeds Research, Hyderabad for providing Achaea janata insect culture and DOR Bt-1 formulation. VC thanks, Department of Biotechnology, Govt. of India and ND thanks University Grants Commission, India for providing research fellowships. BS is the recipient of DBT-TATA Innovation Fellowship. Authors acknowledge DST-FIST, DBT- CREBB, and DST-PURSE for the instrumentation facilities of the department and school.