Discovery of Novel Antigiardiasis Drug Candidates

被引:26
|
作者
Kulakova, Liudmila [1 ]
Galkin, Andrey [1 ]
Chen, Catherine Z. [2 ]
Southall, Noel [2 ]
Marugan, Juan J. [2 ]
Zheng, Wei [2 ]
Herzberg, Osnat [1 ,3 ]
机构
[1] Univ Maryland, Inst Biosci & Biotechnol Res, Rockville, MD 20850 USA
[2] NIH, Div Preclin Innovat, Natl Ctr Adv Translat Sci, Bethesda, MD 20892 USA
[3] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
基金
美国国家卫生研究院;
关键词
GIARDIA-LAMBLIA; METHIONINE AMINOPEPTIDASE; STRUCTURAL BASIS; FUMAGILLIN; METRONIDAZOLE; DUODENALIS; TINIDAZOLE; RESISTANCE; INDUCTION; KINASE;
D O I
10.1128/AAC.03834-14
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Giardiasis is a severe intestinal parasitic disease caused by Giardia lamblia, which inflicts many people in poor regions and is the most common parasitic infection in the United States. Current standard care drugs are associated with undesirable side effects, treatment failures, and an increasing incidence of drug resistance. As follow-up to a high-throughput screening of an approved drug library, which identified compounds lethal to G. lamblia trophozoites, we have determined the minimum lethal concentrations of 28 drugs and advanced 10 of them to in vivo studies in mice. The results were compared to treatment with the standard care drug, metronidazole, in order to identify drugs with equal or better anti-Giardia activities. Three drugs, fumagillin, carbadox, and tioxidazole, were identified. These compounds were also potent against metronidazole-resistant human G. lamblia isolates (assemblages A and B), as determined in in vitro assays. Of these three compounds, fumagillin is currently an orphan drug used within the European Union to treat microsporidiosis in immunocompromised individuals, whereas carbadox and tioxidazole are used in veterinary medicine. A dose-dependent study of fumagillin in a giardiasis mouse model revealed that the effective dose of fumagillin was similar to 100-fold lower than the metronidazole dose. Therefore, fumagillin may be advanced to further studies as an alternative treatment for giardiasis when metronidazole fails.
引用
收藏
页码:7303 / 7311
页数:9
相关论文
共 50 条
  • [31] Literature-based discovery of new candidates for drug repurposing
    Yang, Hsih-Te
    Ju, Jiun-Huang
    Wong, Yue-Ting
    Shmulevich, Ilya
    Chiang, Jung-Hsien
    BRIEFINGS IN BIOINFORMATICS, 2017, 18 (03) : 488 - 497
  • [32] Novel targets for drug discovery
    Wallace, RW
    DRUG DISCOVERY TODAY, 1996, 1 (03) : 91 - 92
  • [33] Novel discovery in drug delivery
    不详
    FUTURE MICROBIOLOGY, 2009, 4 (05) : 500 - 500
  • [34] Novel anticancer drug discovery
    Buolamwini, JK
    CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (04) : 500 - 509
  • [35] Novel proteases for drug discovery
    Moss, M
    DRUG DISCOVERY TODAY, 2001, 6 (15) : 770 - 770
  • [36] NOVEL BIOPOLYMERS FOR DRUG DISCOVERY
    MORAN, EJ
    WILSON, TE
    CHO, CY
    CHERRY, SR
    SCHULTZ, PG
    BIOPOLYMERS, 1995, 37 (03) : 213 - 219
  • [37] New drug candidates and innovation for HAT: from discovery to promising candidates, illustrated by oxaboroles development
    Ribeill, Y.
    TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2011, 16 : 19 - 19
  • [38] Discovery of novel drug candidates for inhibition of soluble epoxide hydrolase of arachidonic acid cascade pathway implicated in atherosclerosis
    Gurung, Arun Bahadur
    Mayengbam, Bishwarjit
    Bhattacharjee, Atanu
    COMPUTATIONAL BIOLOGY AND CHEMISTRY, 2018, 74 : 1 - 11
  • [39] Novel platinum constructs as anticancer drug candidates
    Lippard, Stephen J.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2013, 245
  • [40] Essential Oils as Novel Anthelmintic Drug Candidates
    Panda, Sujogya Kumar
    Daemen, Marijn
    Sahoo, Gunanidhi
    Luyten, Walter
    MOLECULES, 2022, 27 (23):