Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais 31270-901, Brazil.
Departamento de Análises Clínicas e Toxicológicas, Faculdade de Farmácia, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais 31270-901, Brazil.
J Appl Microbiol. 2024 Mar 1;135(3). doi: 10.1093/jambio/lxae044.
The aim of the study was to evaluate the efficiency of mimivirus as a potential therapeutic and prophylactic tool against Acanthamoeba castellanii, the etiological agent of Acanthamoeba keratitis, a progressive corneal infection, that is commonly associated with the use of contact lenses and can lead to blindness if not properly treated.
Mimivirus particles were tested in different multiplicity of infection, along with commercial multipurpose contact lenses' solutions, aiming to assess their ability to prevent encystment and excystment of A. castellanii. Solutions were evaluated for their amoebicidal potential and cytotoxicity in MDCK cells, as well as their effectiveness in preventing A. castellanii damage in Madin-Darby canine kidney (MDCK) cells. Results indicated that mimivirus was able to inhibit the formation of A. castellanii cysts, even in the presence of Neff encystment solution. Mimivirus also showed greater effectiveness in controlling A. castellanii excystment compared to commercial solutions. Additionally, mimivirus solution was more effective in preventing damage caused by A. castellanii, presented greater amoebicidal activity, and were less cytotoxic to MDCK cells than commercial MPS.
Mimivirus demonstrates a greater ability to inhibit A. castellanii encystment and excystment compared to commercial multipurpose contact lens solutions. Additionally, mimivirus is less toxic to MDCK cells than those commercial solutions. New studies utilizing in vivo models will be crucial for confirming safety and efficacy parameters.
本研究旨在评估 mimivirus 作为一种潜在的治疗和预防工具对抗棘阿米巴角膜炎(Acanthamoeba keratitis)的疗效,棘阿米巴角膜炎是一种进行性角膜感染,通常与隐形眼镜的使用有关,如果不及时治疗,可能导致失明。
研究人员测试了不同感染复数的 mimivirus 颗粒,以及市售多功能隐形眼镜护理液,旨在评估它们预防棘阿米巴原虫包囊形成和囊内体释放的能力。评估了这些溶液对 MDCK 细胞的杀阿米巴活性和细胞毒性,以及它们在预防 Madin-Darby 犬肾(MDCK)细胞中棘阿米巴原虫损伤方面的效果。结果表明,即使在 Neff 包囊形成溶液存在的情况下,mimivirus 也能够抑制棘阿米巴原虫的形成。与市售溶液相比,mimivirus 还显示出在控制棘阿米巴原虫释放方面更高的效果。此外,mimivirus 溶液在预防棘阿米巴原虫引起的损伤方面更有效,表现出更强的杀阿米巴活性,对 MDCK 细胞的细胞毒性低于市售 MPS。
与市售多功能隐形眼镜护理液相比,mimivirus 显示出更强的抑制棘阿米巴原虫包囊形成和释放的能力。此外,mimivirus 对 MDCK 细胞的毒性低于这些商业溶液。利用体内模型进行新的研究对于确认安全性和疗效参数至关重要。