Identification of a piroplasm protein of Theileria orientalis that binds to bovine erythrocyte band 3

被引:10
作者
Kim, JY
Yokoyama, N
Kumar, S
Inoue, N
Inaba, M
Fujisaki, K
Sugimoto, C
机构
[1] Obihiro Univ Agr & Vet Med, Natl Res Ctr Protozoan Dis, Obihiro, Hokkaido 0808555, Japan
[2] Hokkaido Univ, Grad Sch Vet Med, Sapporo, Hokkaido 0600818, Japan
基金
日本学术振兴会;
关键词
Theileria orientalis; piroplasm; microneme-rhoptry protein; band 3-binding protein; escape;
D O I
10.1016/j.molbiopara.2004.05.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Theileria orientalis infects cattle and causes various disease symptoms, including anaemia and icterus. The erythrocytic stages are responsible for these symptoms but the molecular events involved in these stages have not yet been fully elucidated. In this study, we identified a T orientalis cDNA that encodes a polypeptide related to identity to the microneme-rhoptry protein of Theileria parva. Analysis of its recombinant product (ToMRP) by indirect fluorescent-antibody test revealed that it is specifically expressed at the early erythrocytic stage after invasion. This expression disappears during the intermediate stages of intra-erythrocytic development. Its expression then reappears at the late stages after the parasite has divided by binary fission into diad or tetrad forms and before these forms are released from the host erythrocyte. In vitro erythrocyte binding assays showed that ToMRP associates with the Triton X-insoluble fraction of erythrocytes membrane but not with intact erythrocytes. Cosedimentation and Western blot analyses revealed that ToMRP binds to band 3, a membrane component of bovine erythrocytes. These observations suggest that ToMRP may be involved in the parasite's egress from and/or invasion into the host erythrocytes by interacting with a protein in the membrane skeleton of the erythrocyte and thereby modifying the structure and function of the cell. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:193 / 200
页数:8
相关论文
共 57 条
[1]   EVALUATION OF STRUCTURAL INTERDEPENDENCE OF MEMBRANE-SPANNING AND CYTOPLASMIC DOMAINS OF BAND-3 [J].
APPELL, KC ;
LOW, PS .
BIOCHEMISTRY, 1982, 21 (09) :2151-2157
[2]  
BAEK B K, 1992, Korean Journal of Parasitology, V30, P133, DOI 10.3347/kjp.1992.30.2.133
[3]  
Baek Byeong Kirl, 1994, Korean Journal of Parasitology, V32, P111, DOI 10.3347/kjp.1994.32.2.111
[4]  
Baek Byeong Kirl, 1992, Korean Journal of Parasitology, V30, P201, DOI 10.3347/kjp.1992.30.3.201
[5]   Apical organelles of Apicomplexa: biology and isolation by subcellular fractionation [J].
Blackman, MJ ;
Bannister, LH .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2001, 117 (01) :11-25
[6]  
BOULTER N, 2000, ADV PARASITOLOGY, V44
[7]  
Brown JS, 1999, EVOL ECOL RES, V1, P49
[8]   Identification of a critical ankyrin-binding loop on the cytoplasmic domain of erythrocyte membrane band 3 by crystal structure analysis and site-directed mutagenesis [J].
Chang, SH ;
Low, PS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (09) :6879-6884
[9]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[10]   MECHANISM OF REGULATION OF MALARIAL INVASION BY EXTRAERYTHROCYTIC LIGANDS [J].
CLOUGH, B ;
PAULITSCHKE, M ;
NASH, GB ;
BAYLEY, PM ;
ANSTEE, DJ ;
WILSON, RJM ;
PASVOL, G ;
GRATZER, WB .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1995, 69 (01) :19-27