The pir multigene family of Plasmodium: Antigenic variation and beyond

被引:64
作者
Cunningham, Deirdre [1 ]
Lawton, Jennifer [1 ]
Jarra, William [1 ]
Preiser, Peter [2 ]
Langhorne, Jean [1 ]
机构
[1] Natl Inst Med Res, MRC, Div Parasitol, London NW7 1AA, England
[2] Nanyang Technol Univ, Biosci Res Ctr, Singapore, Singapore
基金
英国医学研究理事会;
关键词
Plasmodium; Malaria; Multigene families; pir genes; HUMAN MALARIA PARASITE; VAR GENE-EXPRESSION; FALCIPARUM RIFIN FAMILY; RODENT MALARIA; VARIANT ANTIGENS; MAURERS CLEFTS; LIFE-CYCLE; INFECTED ERYTHROCYTES; PHYLOGENETIC NETWORKS; COMPARATIVE GENOMICS;
D O I
10.1016/j.molbiopara.2009.12.010
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
Multigene families are present on the telomeric and sub-telomeric regions of most chromosomes of the malaria parasite, Plasmodium. The largest gene family identified so far is the Plasmodium interspersed repeat (pir) multigene gene family and is shared by Plasmodium vivax, and simian and rodent malaria species. Most pir genes share a similar structure across the different species; a short first exon, long second exon and a third exon encoding a trans-membrane domain, and some pir genes can be assigned to specific sub-families. Although pir genes can be differentially transcribed in different life cycle stages, suggesting different functions, there is no clear link between sub-family and transcription pattern. Some of the pir genes encode proteins expressed on or near the surface of infected erythrocytes, and therefore could be potential targets of the host's immune response, and involved in antigenic variation and immune evasion. Other functions such as signalling, trafficking and adhesion have been also postulated. The presence of pir in rodent models will allow the investigation of this gene family in vivo and thus their potential as vaccines or in other interventions in human P. vivax infections. Crown Copyright (C) 2009 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:65 / 73
页数:9
相关论文
共 71 条
[1]   Antibodies to Plasmodium falciparum rifin proteins are associated with rapid parasite clearance and asymptomatic infections [J].
Abdel-Latif, MS ;
Dietz, K ;
Issifou, S ;
Kremsner, PG ;
Klinkert, MQ .
INFECTION AND IMMUNITY, 2003, 71 (11) :6229-6233
[2]   Recognition of variant rifin antigens by human antibodies induced during natural Plasmodium falciparum infections [J].
Abdel-Latif, MS ;
Khattab, A ;
Lindenthal, C ;
Kremsner, PG ;
Klinkert, MQ .
INFECTION AND IMMUNITY, 2002, 70 (12) :7013-7021
[3]   Plasmodium chabaudi chabaudi infection in mice induces strong B cell responses and striking but temporary changes in splenic cell distribution [J].
Achtman, AH ;
Khan, M ;
MacLennan, ICM ;
Langhorne, J .
JOURNAL OF IMMUNOLOGY, 2003, 171 (01) :317-324
[4]   Antigenic variation in malaria:: a 3′ genomic alteration associated with the expression of a P-knowlesi variant antigen [J].
Al-Khedery, B ;
Barnwell, JW ;
Galinski, MR .
MOLECULAR CELL, 1999, 3 (02) :131-141
[5]   MAAP: Malarial adhesins and adhesin-like proteins predictor [J].
Ansari, Faraz Alam ;
Kumar, Naveen ;
Subramanyam, Mekapati Bala ;
Gnanamani, Muthiah ;
Ramachandran, Srinivasan .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2008, 70 (03) :659-666
[6]   Lung injury in vivax malaria: Pathophysiological evidence for pulmonary vascular sequestration and posttreatment alveolar-capillary inflammation [J].
Anstey, Nicholas M. ;
Handojo, Tjandra ;
Pain, Michael C. F. ;
Kenangalem, Enny ;
Tjitra, Emiliana ;
Price, Ric N. ;
Maguire, Graeme P. .
JOURNAL OF INFECTIOUS DISEASES, 2007, 195 (04) :589-596
[7]   Absence of Erythrocyte Sequestration and Lack of Multicopy Gene Family Expression in Plasmodium falciparum from a Splenectomized Malaria Patient [J].
Bachmann, Anna ;
Esser, Claudia ;
Petter, Michaela ;
Predehl, Sabine ;
von Kalckreuth, Vera ;
Schmiedel, Stefan ;
Bruchhaus, Iris ;
Tannich, Egbert .
PLOS ONE, 2009, 4 (10)
[8]   Split Decomposition: A New and Useful Approach to Phylogenetic Analysis of Distance Data [J].
Bandelt, Hans-Juergen ;
Dress, Andreas W. M. .
MOLECULAR PHYLOGENETICS AND EVOLUTION, 1992, 1 (03) :242-252
[9]   SPLENIC REQUIREMENT FOR ANTIGENIC VARIATION AND EXPRESSION OF THE VARIANT ANTIGEN ON THE ERYTHROCYTE-MEMBRANE IN CLONED PLASMODIUM-KNOWLESI MALARIA [J].
BARNWELL, JW ;
HOWARD, RJ ;
COON, HG ;
MILLER, LH .
INFECTION AND IMMUNITY, 1983, 40 (03) :985-994
[10]   Plasmodium falciparum STEVOR proteins are highly expressed in patient isolates and located in the surface membranes of infected red blood cells and the apical tips of merozoites [J].
Blythe, Jane E. ;
Yam, Xue Yan ;
Kuss, Claudia ;
Bozdech, Zbynek ;
Holder, Anthony A. ;
Marsh, Kevin ;
Langhorne, Jean ;
Preiser, Peter R. .
INFECTION AND IMMUNITY, 2008, 76 (07) :3329-3336