Mezzomo Bélin Poletto, Miranda-Vilela Ana Luisa, Grisolia Cesar Koppe
Department of Genetics and Morphology, Institute of Biological Sciences, University of Brasilia, Brasilia/DF 70.910-900, Brazil.
Faculty of Medicine, Faciplac, Campus Gama, SIGA Área Especial N° 02 Setor Leste-Gama/DF 72.460-000, Brazil.
Toxins (Basel). 2015 Dec 9;7(12):5348-58. doi: 10.3390/toxins7124881.
In addition to their applicability as biopesticides, Bacillus thuringiensis (Bt) Cry1Ac spore-crystals are being researched in the immunology field for their potential as adjuvants in mucosal and parenteral immunizations. We aimed to investigate the hematotoxicity and genotoxicity of Bt spore-crystals genetically modified to express Cry1Ac individually, administered orally (p.o.) or with a single intraperitoneal (i.p.) injection 24 h before euthanasia, to simulate the routes of mucosal and parenteral immunizations in Swiss mice. Blood samples were used to perform hemogram, and bone marrow was used for the micronucleus test. Cry1Ac presented cytotoxic effects on erythroid lineage in both routes, being more severe in the i.p. route, which also showed genotoxic effects. The greater severity noted in this route, mainly at 6.75 mg/kg, as well as the intermediate effects at 13.5 mg/kg, and the very low hematotoxicity at 27 mg/kg, suggested a possible inverse agonism. The higher immunogenicity for the p.o. route, particularly at 27 mg/kg, suggested that at this dose, Cry 1Ac could potentially be used as a mucosal adjuvant (but not in parenteral immunizations, due to the genotoxic effects observed). This potential should be investigated further, including making an evaluation of the proposed inverse agonism and carrying out cytokine profiling.
除了作为生物杀虫剂的适用性外,苏云金芽孢杆菌(Bt)Cry1Ac芽孢晶体正在免疫学领域进行研究,以探讨其在黏膜和肠胃外免疫中作为佐剂的潜力。我们旨在研究经基因改造以单独表达Cry1Ac的Bt芽孢晶体的血液毒性和遗传毒性,在安乐死24小时前通过口服(p.o.)或单次腹腔内(i.p.)注射给药,以模拟瑞士小鼠的黏膜和肠胃外免疫途径。采集血液样本进行血常规检查,采集骨髓进行微核试验。Cry1Ac在两种途径中均对红细胞谱系产生细胞毒性作用,腹腔内途径更为严重,该途径还表现出遗传毒性作用。该途径中观察到的更高严重程度,主要在6.75mg/kg时,以及在13.5mg/kg时的中等效应,和在27mg/kg时非常低的血液毒性,提示可能存在反向激动作用。口服途径具有更高的免疫原性,特别是在27mg/kg时,表明在该剂量下,Cry1Ac有可能用作黏膜佐剂(但由于观察到的遗传毒性作用,不能用于肠胃外免疫)。这种潜力应进一步研究,包括对所提出的反向激动作用进行评估并进行细胞因子分析。