Literature DB >> 10214692

Proteinases and associated genes of parasitic helminths.

J Tort1, P J Brindley, D Knox, K H Wolfe, J P Dalton.   

Abstract

Many parasites have deployed proteinases to accomplish some of the tasks imposed by a parasitic life style, including tissue penetration, digestion of host tissue for nutrition and evasion of host immune responses. Information on proteinases from trematodes, cestodes and nematode parasites is reviewed, concentrating on those worms of major medical and economical importance. Their biochemical characterization is discussed, along with their putative biological roles and, where available, their associated genes. For example, proteinases expressed by the various stages of the schistosome life-cycle, in particular the well-characterized cercarial elastase which is involved in the penetration of the host skin and the variety of proteinases, such as cathepsin B (Sm31), cathepsin L1, cathepsin L2, cathepsin D, cathepsin C and legumain (Sm32), which are believed to be involved in the catabolism of host haemoglobin. The various endo- and exoproteinases of Fasciola hepatica, the causative agent of liver fluke disease, are reviewed, and recent reports of how these enzymes have been successfully employed in cocktail vaccines are discussed. The various proteinases of cestodes and of the diverse superfamilies of parasitic nematodes are detailed, with special attention being given to those parasites for which most is known, including species of Taenia, Echinococcus, Spirometra, Necator, Acylostoma and Haemonchus. By far the largest number of papers in the literature and entries to the sequence data bases dealing with proteinases of parasitic helminths report on enzymes belonging to the papain superfamily of cysteine proteinases. Accordingly, the final section of the review is devoted to a phylogenetic analysis of this superfamily using over 150 published sequences. This analysis shows that the papain superfamily can be divided into two major branches. Branch A contains the cathepin Bs, the cathepsin Cs and a novel family termed cathepsin Xs, while Branch B contains the cruzipains, cathepsin Ls, papain-like and aleurain/cathepsin H-like proteinases. The relationships of the helminth proteinases, and similar proteinases from protozoan parasites and other organisms, within these groups are discussed.

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Year:  1999        PMID: 10214692     DOI: 10.1016/s0065-308x(08)60243-2

Source DB:  PubMed          Journal:  Adv Parasitol        ISSN: 0065-308X            Impact factor:   3.870


  75 in total

1.  Structural and immunological characteristics of a 28-kilodalton cruzipain-like cysteine protease of Paragonimus westermani expressed in the definitive host stage.

Authors:  D H Yun; J Y Chung; Y B Chung; Y Y Bahk; S Y Kang; Y Kong; S Y Cho
Journal:  Clin Diagn Lab Immunol       Date:  2000-11

2.  Characterization of the humoral immune response against Gnathostoma binucleatum in patients clinically diagnosed with gnathostomiasis.

Authors:  José Francisco Zambrano-Zaragoza; Ma de Jesús Durán-Avelar; Maud Messina-Robles; Norberto Vibanco-Pérez
Journal:  Am J Trop Med Hyg       Date:  2012-06       Impact factor: 2.345

3.  Schistosome asparaginyl endopeptidase (legumain) is not essential for cathepsin B1 activation in vivo.

Authors:  Greice Krautz-Peterson; Patrick J Skelly
Journal:  Mol Biochem Parasitol       Date:  2008-01-04       Impact factor: 1.759

4.  Molecular cloning and analysis of stage and tissue-specific expression of Cathepsin L-like protease from Clonorchis sinensis.

Authors:  Yanwen Li; Xuchu Hu; Xiaoquan Liu; Jing Xu; Fengyu Hu; Changling Ma; Xinbing Yu
Journal:  Parasitol Res       Date:  2009-03-24       Impact factor: 2.289

5.  Partial characterization of a 29 kDa cysteine protease purified from Taenia solium metacestodes.

Authors:  Ji Young Kim; Hyun Jong Yang; Kwang Sig Kim; Young Bae Chung
Journal:  Korean J Parasitol       Date:  2005-12       Impact factor: 1.341

6.  Ov-APR-1, an aspartic protease from the carcinogenic liver fluke, Opisthorchis viverrini: functional expression, immunolocalization and subsite specificity.

Authors:  Sutas Suttiprapa; Jason Mulvenna; Ngo Thi Huong; Mark S Pearson; Paul J Brindley; Thewarach Laha; Sopit Wongkham; Sasithorn Kaewkes; Banchob Sripa; Alex Loukas
Journal:  Int J Biochem Cell Biol       Date:  2008-10-19       Impact factor: 5.085

7.  Screening of different classes of proteases in microfilarial and adult stages of Setaria cervi.

Authors:  Daya Ram Pokharel; Elesela Srikanth; Sushma Rathaur
Journal:  Parasitol Res       Date:  2009-01-29       Impact factor: 2.289

8.  In vivo imaging of schistosomes to assess disease burden using positron emission tomography (PET).

Authors:  Nicolas Salem; Jason D Balkman; Jing Wang; David L Wilson; Zhenghong Lee; Christopher L King; James P Basilion
Journal:  PLoS Negl Trop Dis       Date:  2010-09-21

9.  SmCL3, a gastrodermal cysteine protease of the human blood fluke Schistosoma mansoni.

Authors:  Jan Dvorák; Susan T Mashiyama; Mohammed Sajid; Simon Braschi; Melaine Delcroix; Eric L Schneider; Wilson H McKerrow; Mahmoud Bahgat; Elizabeth Hansell; Patricia C Babbitt; Charles S Craik; James H McKerrow; Conor R Caffrey
Journal:  PLoS Negl Trop Dis       Date:  2009-06-02

10.  Analysis of regulatory protease sequences identified through bioinformatic data mining of the Schistosoma mansoni genome.

Authors:  David H Bos; Chris Mayfield; Dennis J Minchella
Journal:  BMC Genomics       Date:  2009-10-21       Impact factor: 3.969

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