Using Caenorhabditis elegans for antimicrobial drug discovery

被引:31
作者
Desalermos, Athanasios [1 ]
Muhammed, Maged [1 ]
Glavis-Bloom, Justin [1 ]
Mylonakis, Eleftherios [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Infect Dis, Boston, MA 02114 USA
关键词
Caenorhabditis elegans; Candida albicans; drug discovery; high throughput; model host; THROUGHPUT SCREENING ASSAYS; HOST-PATHOGEN INTERACTIONS; ANIMAL INFECTION MODEL; CRYPTOCOCCUS-NEOFORMANS; C-ELEGANS; CANDIDA-ALBICANS; INNATE IMMUNITY; ACINETOBACTER-BAUMANNII; ANTIFUNGAL COMPOUNDS; ALZHEIMERS-DISEASE;
D O I
10.1517/17460441.2011.573781
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The number of microorganism strains with resistance to known antimicrobials is increasing. Therefore, there is a high demand for new, nontoxic and efficient antimicrobial agents. Research with the microscopic nematode Caenorhabditis elegans can address this high demand for the discovery of new antimicrobial compounds. In particular, C. elegans can be used as a model host for in vivo drug discovery through high-throughput screens of chemical libraries. Areas covered: This review introduces the use of substitute model hosts and especially C. elegans in the study of microbial pathogenesis. The authors also highlight recently published literature on the role of C. elegans in drug discovery and outline its use as a promising host with unique advantages in the discovery of new antimicrobial drugs. Expert opinion: Caenorhabditis elegans can be used, as a model host, to research many diseases, including fungal infections and Alzheimer's disease. In addition, high-throughput techniques for screening chemical libraries can also be facilitated. Nevertheless, C. elegans and mammals have significant differences that both limit the use of the nematode in research and the degree by which results can be interpreted. That being said, the use of C. elegans in drug discovery still holds promise and the field continues to grow, with attempts to improve the methodology already underway.
引用
收藏
页码:645 / 652
页数:8
相关论文
共 93 条
[21]   Characterization of Plant-Derived Saponin Natural Products against Candida albicans [J].
Coleman, Jeffrey J. ;
Okoli, Ikechukwu ;
Tegos, George P. ;
Holson, Edward B. ;
Wagner, Florence F. ;
Hamblin, Michael R. ;
Mylonakis, Eleftherios .
ACS CHEMICAL BIOLOGY, 2010, 5 (03) :321-332
[22]   The Tangled Web of Signaling in Innate Immunity [J].
Coleman, Jeffrey J. ;
Mylonakis, Eleftherios .
CELL HOST & MICROBE, 2009, 5 (04) :313-315
[23]   Extracellular phospholipase activity is a virulence factor for Cryptococcus neoformans [J].
Cox, GM ;
McDade, HC ;
Chen, SCA ;
Tucker, SC ;
Gottfredsson, M ;
Wright, LC ;
Sorrell, TC ;
Leidich, SD ;
Casadevall, A ;
Ghannoum, MA ;
Perfect, JR .
MOLECULAR MICROBIOLOGY, 2001, 39 (01) :166-175
[24]   CUTICLE OF CAENORHABDITIS ELEGANS - ITS ISOLATION AND PARTIAL CHARACTERIZATION [J].
COX, GN ;
KUSCH, M ;
EDGAR, RS .
JOURNAL OF CELL BIOLOGY, 1981, 90 (01) :7-17
[25]   Caenorhabditis elegans ABL-1 antagonizes p53-mediated germline apoptosis after ionizing irradiation [J].
Deng, XZ ;
Hofmann, ER ;
Villanueva, A ;
Hobert, O ;
Capodieci, P ;
Veach, DR ;
Yin, XL ;
Campodonico, L ;
Glekas, A ;
Cordon-Cardo, C ;
Clarkson, B ;
Bornmann, WG ;
Fuks, Z ;
Hengartner, MO ;
Kolesnick, R .
NATURE GENETICS, 2004, 36 (08) :906-912
[26]   Nosocomial bloodstream infections in United States hospitals: A three-year analysis [J].
Edmond, MB ;
Wallace, SE ;
McClish, DK ;
Pfaller, MA ;
Jones, RN ;
Wenzel, RP .
CLINICAL INFECTIOUS DISEASES, 1999, 29 (02) :239-244
[27]  
Elbein A D, 1974, Adv Carbohydr Chem Biochem, V30, P227, DOI 10.1016/S0065-2318(08)60266-8
[28]  
Enwuru CA, 2008, AFR HEALTH SCI, V8, P142
[29]   Using non-mammalian hosts to study fungal virulence and host defense [J].
Fuchs, Beth Burgwyn ;
Mylonakis, Eleftherios .
CURRENT OPINION IN MICROBIOLOGY, 2006, 9 (04) :346-351
[30]   Phospholipase B activity enhances adhesion of Cryptococcus neoformans to a human lung epithelial cell line [J].
Ganendren, Ranjini ;
Carter, Elizabeth ;
Sorrell, Tania ;
Widmer, Fred ;
Wright, Lesley .
MICROBES AND INFECTION, 2006, 8 (04) :1006-1015