Marine Research Station, Institute of Cellular and Organismic Biology, Academia Sinica, 23-10 Dahuen Road, Jiaushi, Ilan, 262, Taiwan.
Department of Obstetrics and Gynecology, Taipei Veterans General Hospital, Taipei, Taiwan; Department of Obstetrics and Gynecology, National Yang-Ming University School of Medicine, Taipei, Taiwan.
Peptides. 2019 Feb;112:139-148. doi: 10.1016/j.peptides.2018.12.004. Epub 2018 Dec 12.
Trichomoniasis is caused by infection with the protozoan parasite Trichomonas vaginalis, and prolonged persistence may lead to serious ill effects in patients. Thus, the development of new therapeutic strategies to combat drug-resistant T. vaginalis would be clinically beneficial. Antimicrobial peptides (AMPs) comprise an emerging class of molecules that may serve as effective alternatives to antibiotics. In this report, we demonstrate that the synthetic fish AMP, Epinecidin-1 (Epi-1), acts against T. vaginalis both in vitro and in vivo. Under in vitro conditions, Epi-1 disrupted the membrane of metronidazole-resistant T. vaginalis and completely killed the pathogen. To mimic human infection in vivo, estradiol-stimulated mice with vaginal Lactobacillus acidophilus colonization were infected with T. vaginalis, followed by treatment with Epi-1, Vigill, metronidazole or furazolidone. After seven days, the T. vaginalis content was effectively decreased in Epi-1 treated mice, as measured by acridine orange staining of wet smears and tissue biopsies, as well as qPCR of vaginal discharge DNA. Taken together, our results demonstrate that Epi-1 is a strong candidate for development as an alternative therapeutic for T. vaginalis infection.
滴虫病是由原生动物寄生虫阴道毛滴虫感染引起的,如果持续时间较长,可能会对患者造成严重的不良影响。因此,开发新的治疗策略来对抗耐药性阴道毛滴虫将具有临床意义。抗菌肽 (AMPs) 是一类新兴的分子,可能成为抗生素的有效替代品。在本报告中,我们证明了合成的鱼类 AMP,Epinecidin-1 (Epi-1),在体外和体内都能对抗阴道毛滴虫。在体外条件下,Epi-1 破坏了耐甲硝唑的阴道毛滴虫的膜,并完全杀死了病原体。为了在体内模拟人类感染,用雌二醇刺激并使阴道乳杆菌定殖的小鼠感染阴道毛滴虫,然后用 Epi-1、 Vigill、甲硝唑或呋喃唑酮进行治疗。七天后,通过吖啶橙染色湿涂片和组织活检以及阴道分泌物 DNA 的 qPCR 测量,Epi-1 处理的小鼠中的阴道毛滴虫含量有效降低。综上所述,我们的结果表明 Epi-1 是开发治疗阴道毛滴虫感染替代疗法的有力候选药物。