THE PROTEASES AND PATHOGENICITY OF PARASITIC PROTOZOA

被引:345
作者
MCKERROW, JH
SUN, E
ROSENTHAL, PJ
BOUVIER, J
机构
[1] UNIV CALIF SAN FRANCISCO, DEPT PATHOL, SAN FRANCISCO, CA 94143 USA
[2] UNIV CALIF SAN FRANCISCO, DEPT MED, SAN FRANCISCO, CA 94143 USA
[3] UNIV LAUSANNE, INST BIOCHIM, CH-1066 EPALINGES, SWITZERLAND
关键词
PARASITES; PROTEINASE; INHIBITORS; PATHOGENESIS; LIFE CYCLE;
D O I
10.1146/annurev.mi.47.100193.004133
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Protozoan parasites are among the most prevalent pathogens worldwide. Diseases like malaria, leishmaniasis, amebiasis, and trypanosomiasis affect hundreds of millions of people. Recent advances in our understanding of the biochemistry and molecular biology of these organisms has focused attention on specific parasite molecules that are key to the parasite life cycle or the pathogenesis of the diseases they produce. One group of enzymes that plays myriad roles in these processes are the parasite-derived proteases. Different types of proteases are frequently expressed at different stages of the parasite life cycle to support parasite replication and metamorphosis. Intracellular parasites such as those that produce malaria and Chagas' disease express high levels of protease activity to efficiently degrade host proteins like hemoglobin. In other instances, such as infection with Entamoeba histolytica, the causative agent of amebiasis, proteases released by the parasite can damage host cells and tissues, contributing to host tissue damage and parasite invasion. Detailed studies of these enzymes have led to model systems for the study of parasite gene regulation, parasite metabolism, and the host-parasite interplay. In some instances, proteases appear to be promising targets for the development of new antiparasitic chemotherapy.
引用
收藏
页码:821 / 853
页数:33
相关论文
共 259 条
[61]   LEUPEPTIN ALTERS THE PROTEOLYTIC PROCESSING OF P126, THE MAJOR PARASITOPHOROUS VACUOLE ANTIGEN OF PLASMODIUM-FALCIPARUM [J].
DEBRABANT, A ;
DELPLACE, P .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1989, 33 (02) :151-158
[62]   PURIFICATION AND CHARACTERIZATION OF 37-KILODALTON PROTEASES FROM PLASMODIUM-FALCIPARUM AND PLASMODIUM-BERGHEI WHICH CLEAVE ERYTHROCYTE CYTOSKELETAL COMPONENTS [J].
DEGUERCY, A ;
HOMMEL, M ;
SCHREVEL, J .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1990, 38 (02) :233-244
[63]   REQUIREMENT OF MALARIAL PROTEASE IN THE INVASION OF HUMAN RED-CELLS BY MEROZOITES OF PLASMODIUM-FALCIPARUM [J].
DEJKRIENGKRAIKHUL, PN ;
WILAIRAT, P .
ZEITSCHRIFT FUR PARASITENKUNDE-PARASITOLOGY RESEARCH, 1983, 69 (03) :313-317
[64]   PROTEIN-P126 - A PARASITOPHOROUS VACUOLE ANTIGEN ASSOCIATED WITH THE RELEASE OF PLASMODIUM-FALCIPARUM MEROZOITES [J].
DELPLACE, P ;
BHATIA, A ;
CAGNARD, M ;
CAMUS, D ;
COLOMBET, G ;
DEBRABANT, A ;
DUBREMETZ, JF ;
DUBREUIL, N ;
PRENSIER, G ;
FORTIER, B ;
HAQ, A ;
WEBER, J ;
VERNES, A .
BIOLOGY OF THE CELL, 1988, 64 (02) :215-221
[65]   LOCALIZATION, BIOSYNTHESIS, PROCESSING AND ISOLATION OF A MAJOR 126-KDA ANTIGEN OF THE PARASITOPHOROUS VACUOLE OF PLASMODIUM-FALCIPARUM [J].
DELPLACE, P ;
FORTIER, B ;
TRONCHIN, G ;
DUBREMETZ, JF ;
VERNES, A .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1987, 23 (03) :193-201
[66]   PLASMODIUM-FALCIPARUM - PROTEASE INHIBITORS AND INHIBITION OF ERYTHROCYTE INVASION [J].
DLUZEWSKI, AR ;
RANGACHARI, K ;
WILSON, RJM ;
GRATZER, WB .
EXPERIMENTAL PARASITOLOGY, 1986, 62 (03) :416-422
[67]   AMPLIFICATION AND SEQUENCING OF GENOMIC DNA FRAGMENTS ENCODING CYSTEINE PROTEASES FROM PROTOZOAN PARASITES [J].
EAKIN, AE ;
BOUVIER, J ;
SAKANARI, JA ;
CRAIK, CS ;
MCKERROW, JH .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1990, 39 (01) :1-8
[68]  
EAKIN AE, 1992, J BIOL CHEM, V267, P7411
[69]  
EAKIN AE, 1989, NATURE, V342, P132, DOI 10.1038/342132b0
[70]  
EAKIN AE, 1993, IN PRESS J BIOL CHEM