Lactic acid bacteria modulate the CncC pathway to enhance resistance to β-cypermethrin in the oriental fruit fly

Tian Zeng, Qianyan Fu, Fangyi Luo, Jian Dai, Rong Fu, Yixiang Qi, Xiaojuan Deng, Yongyue Lu, Yijuan Xu
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Abstract

The gut microbiota of insects has been shown to regulate host detoxification enzymes. However, the potential regulatory mechanisms involved remain unknown. Here, we report that gut bacteria increase insecticide resistance by activating the cap “n” collar isoform-C (CncC) pathway through enzymatically generated reactive oxygen species (ROS) in Bactrocera dorsalis. We demonstrated that Enterococcus casseliflavus and Lactococcus lactis, two lactic acid (LA)-producing bacteria, increase the resistance of B. dorsalis to β-cypermethrin by regulating cytochrome P450 (P450) enzymes and α-glutathione S-transferase (GST) activities. These gut symbionts also induced the expression of CncC and muscle aponeurosis fibromatosis (Maf). BdCncC knockdown led to a decrease in resistance caused by gut bacteria. Ingestion of the ROS scavenger vitamin C (VC) in resistant strain (RS) affected the expression of BdCncC/BdKeap1/BdMafK, resulting in reduced P450 and GST activity. Furthermore, feeding with E. casseliflavus or L. lactis showed that BdNOX5 increased ROS production, and BdNOX5 knockdown affected the expression of the BdCncC/BdMafK pathway and detoxification genes. Moreover, LA feeding activated the ROS-associated regulation of P450 and GST activity. Collectively, our findings indicate that symbiotic gut bacteria modulate intestinal detoxification pathways by affecting physiological biochemistry, thus providing new insights into the involvement of insect gut microbes in the development of insecticide resistance.
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乳酸菌调节 CncC 通路以增强东方果蝇对 β-氯氰菊酯的抗性
研究表明,昆虫的肠道微生物群能够调节宿主的解毒酶。然而,其中涉及的潜在调控机制仍然未知。在这里,我们报告了肠道细菌通过酶促产生的活性氧(ROS)激活帽 "n "领异构体-C(CncC)通路,从而增强背甲双壳虫对杀虫剂的抗性。我们证实,卡氏肠球菌(Enterococcus casseliflavus)和乳酸球菌(Lactococcus lactis)这两种乳酸(LA)生产菌通过调节细胞色素 P450(P450)酶和α-谷胱甘肽 S-转移酶(GST)的活性,提高了背甲线虫对β-氯氰菊酯的抗性。这些肠道共生菌还能诱导 CncC 和肌肉神经纤维瘤病(Maf)的表达。BdCncC 基因敲除导致肠道细菌引起的抵抗力下降。抗性菌株(RS)摄入 ROS 清除剂维生素 C(VC)会影响 BdCncC/BdKeap1/BdMafK 的表达,导致 P450 和 GST 活性降低。此外,用 E. casseliflavus 或 L. lactis 喂养显示 BdNOX5 增加了 ROS 的产生,而 BdNOX5 的敲除影响了 BdCncC/BdMafK 通路和解毒基因的表达。此外,LA饲喂激活了与ROS相关的P450和GST活性调节。总之,我们的研究结果表明,共生肠道细菌通过影响生理生化调节肠道解毒途径,从而为昆虫肠道微生物参与杀虫剂抗药性的产生提供了新的见解。
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