Department of Parasitology and Tropical Medicine, Institute of Health Science, Gyeongsang National University College of Medicine, Jinju 52727, Korea.
Department of Convergence Medical Science, Gyeongsang National University, Jinju 52727, Korea.
Parasites Hosts Dis. 2024 May;62(2):169-179. doi: 10.3347/PHD.23103. Epub 2024 May 27.
Naegleria fowleri invades the brain and causes a fatal primary amoebic meningoencephalitis (PAM). Despite its high mortality rate of approximately 97%, an effective therapeutic drug for PAM has not been developed. Approaches with miltefosine, amphotericin B, and other antimicrobials have been clinically attempted to treat PAM, but their therapeutic efficacy remains unclear. The development of an effective and safe therapeutic drug for PAM is urgently needed. In this study, we investigated the anti-amoebic activity of Pinus densiflora leaf extract (PLE) against N. fowleri. PLE induced significant morphological changes in N. fowleri trophozoites, resulting in the death of the amoeba. The IC50 of PLE on N. fowleri was 62.3±0.95 μg/ml. Alternatively, PLE did not significantly affect the viability of the rat glial cell line C6. Transcriptome analysis revealed differentially expressed genes (DEGs) between PLE-treated and non-treated amoebae. A total of 5,846 DEGs were identified, of which 2,189 were upregulated, and 3,657 were downregulated in the PLE-treated amoebae. The DEGs were categorized into biological process (1,742 genes), cellular component (1,237 genes), and molecular function (846 genes) based on the gene ontology analysis, indicating that PLE may have dramatically altered the biological and cellular functions of the amoeba and contributed to their death. These results suggest that PLE has anti-N. fowleri activity and may be considered as a potential candidate for the development of therapeutic drugs for PAM. It may also be used as a supplement compound to enhance the therapeutic efficacy of drugs currently used to treat PAM.
福氏耐格里阿米巴原虫侵袭大脑,引起致命的原发性阿米巴脑膜脑炎(PAM)。尽管其死亡率约为 97%,但尚未开发出有效的治疗 PAM 的药物。米替福新、两性霉素 B 和其他抗菌药物的方法已在临床上尝试用于治疗 PAM,但它们的治疗效果仍不清楚。迫切需要开发一种有效的、安全的 PAM 治疗药物。在这项研究中,我们研究了松叶提取物(PLE)对福氏耐格里阿米巴原虫的抗阿米巴活性。PLE 诱导福氏耐格里阿米巴原虫滋养体发生显著的形态变化,导致阿米巴死亡。PLE 对福氏耐格里阿米巴原虫的 IC50 为 62.3±0.95 μg/ml。此外,PLE 对大鼠神经胶质细胞系 C6 的活力没有显著影响。转录组分析显示,PLE 处理和未处理的阿米巴之间存在差异表达基因(DEGs)。共鉴定出 5846 个 DEGs,其中 PLE 处理的阿米巴中 2189 个上调,3657 个下调。根据基因本体分析,这些 DEGs 被归类为生物过程(1742 个基因)、细胞成分(1237 个基因)和分子功能(846 个基因),表明 PLE 可能显著改变了阿米巴的生物学和细胞功能,并导致其死亡。这些结果表明,PLE 具有抗福氏耐格里阿米巴原虫的活性,可能被视为开发治疗 PAM 的药物的潜在候选药物。它也可以用作补充化合物,以增强目前用于治疗 PAM 的药物的治疗效果。