Chauhan Vinod K, Dhania Narender K, Chaitanya R K, Senthilkumaran Balasubramanian, Dutta-Gupta Aparna
Department of Animal Biology, School of Life Sciences, University of HyderabadHyderabad, India.
Centre for Animal Sciences, School of Basic and Applied Sciences, Central University of PunjabBathinda, India.
Front Physiol. 2017 Sep 5;8:662. doi: 10.3389/fphys.2017.00662. eCollection 2017.
The lack of homogeneity in field application of 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 studies using mid-gut cell cultures. Present study illustrates cellular and molecular changes in mid-gut epithelium of a -susceptible polyphagous insect pest castor semilooper, 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, 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.
制剂在田间应用缺乏均一性,常常导致一部分害虫种群摄入亚致死剂量的生物农药,从而长期促进了毒素耐受性和抗性。肠道再生似乎是实现这一过程的可能机制之一。然而,现有信息主要来自于使用中肠细胞培养的研究。本研究阐述了一种易感多食性害虫蓖麻夜蛾中肠上皮细胞和分子的变化,以响应一种Cry毒素制剂。本报告表明,长期暴露于亚致死剂量的Cry毒素制剂对幼虫生长发育具有有害影响。中肠组织的组织学分析显示上皮细胞变性,这是由于坏死形式的细胞死亡,随后通过中肠干细胞的增殖增强而再生。通过共聚焦显微镜、流式细胞术和DNA片段化分析证实了细胞死亡。通过溴脱氧尿苷(BrdU)标记和甲苯胺蓝染色评估对照幼虫与毒素处理幼虫中的细胞增殖。有趣的是,mRNA分析在幼虫中肠上皮细胞中检测到芳基脂蛋白转录本的存在。定量PCR分析进一步表明,与对照相比,毒素处理幼虫中芳基脂蛋白基因的表达发生了改变。Cry毒素中毒后中肠细胞增殖增强与芳基脂蛋白表达升高同时出现,这表明它可能在中肠上皮细胞的再生中发挥作用。