Anthelmintic metabolism in parasitic helminths: proteomic insights

被引:21
作者
Brophy, Peter M. [1 ]
Mackintosh, Neil [1 ]
Morphew, Russell M. [1 ]
机构
[1] Aberystwyth Univ, Inst Biol Environm & Rural Sci, Parasitol Grp, Aberystwyth SY23 3FG, Ceredigion, Wales
基金
英国生物技术与生命科学研究理事会;
关键词
Proteomics; helminth; anthelmintic; anthelmintic resistance; xenobiotic; EXCRETORY-SECRETORY PRODUCTS; SCHISTOSOMA-MANSONI; FASCIOLA-HEPATICA; GLUTATHIONE TRANSFERASE; IN-VITRO; CAENORHABDITIS-ELEGANS; HAEMONCHUS-CONTORTUS; IMMUNOPROTEOMIC ANALYSIS; DRUG-RESISTANCE; EX-VIVO;
D O I
10.1017/S003118201200087X
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程]; 100103 [病原生物学];
摘要
Anthelmintics are the cornerstone of parasitic helminth control. Surprisingly, understanding of the biochemical pathways used by parasitic helminths to detoxify anthelmintics is fragmented, despite the increasing global threat of anthelmintic resistance within the ruminant and equine industries. Reductionist biochemistry has likely over-estimated the enzymatic role of glutathione transferases in anthelmintic metabolism and neglected the potential role of the cytochrome P-450 superfamily (CYPs). Proteomic technologies offers the opportunity to support genomics, reverse genetics and pharmacokinetics, and provide an integrated insight into both the cellular mechanisms underpinning response to anthelmintics and also the identification of biomarker panels for monitoring the development of anthelmintic resistance. To date, there have been limited attempts to include proteomics in anthelmintic metabolism studies. Optimisations of membrane, post-translational modification and interaction proteomic technologies in helminths are needed to especially study Phase I CYPs and Phase III ABC transporter pumps for anthelmintics and their metabolites.
引用
收藏
页码:1205 / 1217
页数:13
相关论文
共 84 条
[1]
HelmCoP: An Online Resource for Helminth Functional Genomics and Drug and Vaccine Targets Prioritization [J].
Abubucker, Sahar ;
Martin, John ;
Taylor, Christina M. ;
Mitreva, Makedonka .
PLOS ONE, 2011, 6 (07)
[2]
Cysteine conjugate β-lyase activity in three species of parasitic helminth [J].
Adcock, HJ ;
Brophy, PM ;
Teesdale-Spittle, PH ;
Buckberry, LD .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1999, 29 (04) :543-548
[3]
Alvarez Ana I., 2006, Current Drug Delivery, V3, P199, DOI 10.2174/156720106776359195
[4]
Altered drug influx/efflux and enhanced metabolic activity in triclabendazole-resistant liver flukes [J].
Alvarez, LI ;
Solana, HD ;
Mottier, ML ;
Virkel, GL ;
Fairweather, I ;
Lanusse, CE .
PARASITOLOGY, 2005, 131 :501-510
[5]
Parasite proteomics [J].
Barrett, J ;
Jefferies, JR ;
Brophy, PM .
PARASITOLOGY TODAY, 2000, 16 (09) :400-403
[6]
Cytochrome P450 in parasitic protozoa and helminths [J].
Barrett, J .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-PHARMACOLOGY TOXICOLOGY & ENDOCRINOLOGY, 1998, 121 (1-3) :181-183
[7]
Helminth detoxification mechanisms [J].
Barrett, J .
JOURNAL OF HELMINTHOLOGY, 1997, 71 (02) :85-89
[8]
Characterisation and properties of an intracellular lipid-binding protein from the tapeworm Moniezia expansa [J].
Barrett, J ;
Saghir, N ;
Timanova, A ;
Clarke, K ;
Brophy, PM .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 250 (02) :269-275
[9]
Brugia malayi Excreted/Secreted Proteins at the Host/Parasite Interface: Stage- and Gender-Specific Proteomic Profiling [J].
Bennuru, Sasisekhar ;
Semnani, Roshanak ;
Meng, Zhaojing ;
Ribeiro, Jose M. C. ;
Veenstra, Timothy D. ;
Nutman, Thomas B. .
PLOS NEGLECTED TROPICAL DISEASES, 2009, 3 (04)
[10]
Identification of proteins in excretory/secretory extracts of Echinostoma friedi (Trematoda) from chronic and acute infections [J].
Bernal, D ;
Carpena, I ;
Espert, AM ;
De la Rubia, JE ;
Esteban, JG ;
Toledo, R ;
Marcilla, A .
PROTEOMICS, 2006, 6 (09) :2835-2843