Zhang Si-Ming, Buddenborg Sarah K, Adema Coen M, Sullivan John T, Loker Eric S
Center for Evolutionary and Theoretical Immunology, Department of Biology, The University of New Mexico, Albuquerque, New Mexico, United States of America.
Department of Biology, University of San Francisco, San Francisco, California, United States of America.
PLoS Negl Trop Dis. 2015 Oct 9;9(10):e0004131. doi: 10.1371/journal.pntd.0004131. eCollection 2015.
In view of the call by the World Health Organization (WHO) for elimination of schistosomiasis as a public health problem by 2025, use of molluscicides in snail control to supplement chemotherapy-based control efforts is likely to increase in the coming years. The mechanisms of action of niclosamide, the active ingredient in the most widely used molluscicides, remain largely unknown. A better understanding of its toxicology at the molecular level will both improve our knowledge of snail biology and may offer valuable insights into the development of better chemical control methods for snails. We used a recently developed Biomphalaria glabrata oligonucleotide microarray (31K features) to investigate the effect of sublethal exposure to niclosamide on the transcriptional responses of the snail B. glabrata relative to untreated snails. Most of the genes highly upregulated following exposure of snails to niclosamide are involved in biotransformation of xenobiotics, including genes encoding cytochrome P450s (CYP), glutathione S-transferases (GST), and drug transporters, notably multi-drug resistance protein (efflux transporter) and solute linked carrier (influx transporter). Niclosamide also induced stress responses. Specifically, six heat shock protein (HSP) genes from three super-families (HSP20, HSP40 and HSP70) were upregulated. Genes encoding ADP-ribosylation factor (ARF), cAMP response element-binding protein (CREB) and coatomer, all of which are involved in vesicle trafficking in the Golgi of mammalian cells, were also upregulated. Lastly, a hemoglobin gene was downregulated, suggesting niclosamide may affect oxygen transport. Our results show that snails mount substantial responses to sublethal concentrations of niclosamide, at least some of which appear to be protective. The topic of how niclosamide's lethality at higher concentrations is determined requires further study. Given that niclosamide has also been used as an anthelmintic drug for decades and has been found to have activity against several types of cancer, our findings may be of relevance in understanding how both parasites and neoplastic cells respond to this compound.
鉴于世界卫生组织(WHO)呼吁到2025年消除血吸虫病这一公共卫生问题,在未来几年,使用杀螺剂控制钉螺以补充基于化疗的控制措施的情况可能会增加。最广泛使用的杀螺剂中的活性成分氯硝柳胺的作用机制在很大程度上仍不为人知。在分子水平上更好地了解其毒理学,既能增进我们对钉螺生物学的认识,也可能为开发更好的钉螺化学控制方法提供有价值的见解。我们使用最近开发的光滑双脐螺寡核苷酸微阵列(31K特征),研究亚致死剂量氯硝柳胺暴露对光滑双脐螺相对于未处理螺的转录反应的影响。在螺暴露于氯硝柳胺后高度上调的大多数基因都参与了异生素的生物转化,包括编码细胞色素P450(CYP)、谷胱甘肽S-转移酶(GST)的基因以及药物转运蛋白,特别是多药耐药蛋白(外排转运蛋白)和溶质连接载体(内流转运蛋白)。氯硝柳胺还诱导了应激反应。具体而言,来自三个超家族(HSP20、HSP40和HSP70)的六个热休克蛋白(HSP)基因被上调。编码ADP-核糖基化因子(ARF)、cAMP反应元件结合蛋白(CREB)和衣被蛋白复合物的基因也被上调,所有这些基因都参与哺乳动物细胞高尔基体中的囊泡运输。最后,一个血红蛋白基因被下调,表明氯硝柳胺可能影响氧气运输。我们的结果表明,螺对亚致死浓度的氯硝柳胺会产生大量反应,其中至少一些反应似乎具有保护作用。氯硝柳胺在较高浓度下的致死性如何确定这一话题需要进一步研究。鉴于氯硝柳胺作为驱虫药也已使用了数十年,并且已发现其对几种类型的癌症有活性,我们的发现可能与理解寄生虫和肿瘤细胞如何对这种化合物作出反应有关。