Screening of the 'Open Scaffolds' collection from Compounds Australia identifies a new chemical entity with anthelmintic activities against different developmental stages of the barber's pole worm and other parasitic nematodes

被引:29
|
作者
Preston, Sarah [1 ,2 ]
Jiao, Yaqing [1 ]
Baell, Jonathan B. [3 ]
Keiser, Jennifer [4 ,5 ]
Crawford, Simon [6 ]
Koehler, Anson V. [1 ]
Wang, Tao [1 ]
Simpson, Moana M. [7 ]
Kaplan, Ray M. [8 ]
Cowley, Karla J. [9 ]
Simpson, Kaylene J. [9 ,10 ]
Hofmann, Andreas [1 ,7 ]
Jabbar, Abdul [1 ]
Gasser, Robin B. [1 ]
机构
[1] Univ Melbourne, Fac Vet & Agr Sci, Parkville, Vic, Australia
[2] Federat Univ, Fac Sci & Technol, Ballarat, Vic 3350, Australia
[3] Monash Univ, Inst Pharmaceut Sci MIPS, Parkville, Vic, Australia
[4] Swiss Trop & Publ Hlth Inst, Basel, Switzerland
[5] Univ Basel, Basel, Switzerland
[6] Univ Melbourne, Sch Biosci, Parkville, Vic, Australia
[7] Griffith Univ, Griffith Inst Drug Discovery, Don Young Rd, Nathan, Qld, Australia
[8] Univ Georgia, Coll Vet Med, Dept Infect Dis, Athens, GA USA
[9] Peter MacCallum Canc Ctr, Victorian Ctr Funct Genom, Parkville, Vic, Australia
[10] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会; 英国惠康基金;
关键词
'Open Scaffolds' compound collection; Whole organism screening; Haemonchus; Nematodes; Anthelmintic; HAEMONCHUS-CONTORTUS; DRUG DISCOVERY; MONEPANTEL; RESISTANCE; EFFICACY; ASSAY; MOTILITY; HISTORY; SHEEP; PAINS;
D O I
10.1016/j.ijpddr.2017.05.004
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The discovery and development of novel anthelmintic classes is essential to sustain the control of socioeconomically important parasitic worms of humans and animals. With the aim of offering novel, lead-like scaffolds for drug discovery, Compounds Australia released the 'Open Scaffolds' collection containing 33,999 compounds, with extensive information available on the physicochemical properties of these chemicals. In the present study, we screened 14,464 prioritised compounds from the 'Open Scaffolds' collection against the exsheathed third-stage larvae (xL3s) of Haemonchus contortus using recently developed whole-organism screening assays. We identified a hit compound, called SN00797439, which was shown to reproducibly reduce xL3 motility by >= 70%; this compound induced a characteristic, "coiled" xL3 phenotype (IC50 = 3.46-5.93 mu M), inhibited motility of fourth-stage larvae (L4s; IC50 = 0.31 -12.5 mM) and caused considerable cuticular damage to L4s in vitro. When tested on other parasitic nematodes in vitro, SN00797439 was shown to inhibit (IC50 = 3-50 mu M) adults of Ancylostoma ceylanicum (hookworm) and first-stage larvae of Trichuris muris (whipworm) and eventually kill (>90%) these stages. Furthermore, this compound completely inhibited the motility of female and male adults of Brugia malayi (50-100 mu M) as well as microfilariae of both B. malayi and Dirofilaria immitis (heartworm). Overall, these results show that SN00797439 acts against genetically (evolutionarily) distant parasitic nematodes i.e. H. contortus and A. ceylanicum [strongyloids] vs. B. malayi and D. immitis [filarioids] vs. T. muris [enoplid], and, thus, might offer a novel, lead-like scaffold for the development of a relatively broad-spectrum anthelmintic. Our future work will focus on assessing the activity of SN00797439 against other pathogens that cause neglected tropical diseases, optimising analogs with improved biological activities and characterising their targets. (C) 2017 The Authors. Published by Elsevier Ltd on behalf of Australian Society for Parasitology.
引用
收藏
页码:286 / 294
页数:9
相关论文
empty
未找到相关数据