In Vitro Genetic Analysis of an Erythrocyte Determinant of Malaria Infection

被引:39
作者
Bei, Amy K. [1 ]
Brugnara, Carlo [2 ]
Duraisingh, Manoj T. [1 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[2] Childrens Hosp, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
RED-BLOOD-CELLS; PLASMODIUM-FALCIPARUM; INVASION; RECEPTOR; GLYCOPHORIN; ANTIBODIES; PARASITES; PATHWAYS;
D O I
10.1086/657157
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Invasion of erythrocytes by Plasmodium falciparum is an obligatory step in the life cycle of the parasite. A major challenge is the unambiguous identification and characterization of host receptors. Because erythrocytes lack nuclei, direct genetic analyses have been limited. In this work, we combined an in vitro erythrocyte culture system, which supports P. falciparum invasion and growth, with lentiviral transduction to knock down gene expression. We genetically demonstrate, in an isogenic background, that glycophorin A is required for efficient strain-specific parasite invasion. We establish the feasibility of in vitro systematic functional analysis of essential erythrocyte determinants of malaria and erythrocyte biology.
引用
收藏
页码:1722 / 1727
页数:6
相关论文
共 15 条
  • [1] Apicomplexan Parasites Co-Opt Host Calpains to Facilitate Their Escape from Infected Cells
    Chandramohanadas, Rajesh
    Davis, Paul H.
    Beiting, Daniel P.
    Harbut, Michael B.
    Darling, Claire
    Velmourougane, Geetha
    Lee, Ming Yeh
    Greer, Peter A.
    Roos, David S.
    Greenbaum, Doron C.
    [J]. SCIENCE, 2009, 324 (5928) : 794 - 797
  • [2] Erythrocyte-binding antigen 175 mediates invasion in Plasmodium falciparum utilizing sialic acid-dependent and -independent pathways
    Duraisingh, MT
    Maier, AG
    Triglia, T
    Cowman, AF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (08) : 4796 - 4801
  • [3] Ex vivo generation of fully mature human red blood cells from hematopoietic stem cells
    Giarratana, MC
    Kobari, L
    Lapillonne, H
    Chalmers, D
    Kiger, L
    Cynober, T
    Marden, MC
    Wajcman, H
    Douay, L
    [J]. NATURE BIOTECHNOLOGY, 2005, 23 (01) : 69 - 74
  • [4] EVIDENCE FOR DIFFERENCES IN ERYTHROCYTE SURFACE RECEPTORS FOR MALARIAL PARASITES, PLASMODIUM-FALCIPARUM AND PLASMODIUM-KNOWLESI
    MILLER, LH
    HAYNES, JD
    MCAULIFFE, FM
    SHIROISHI, T
    DUROCHER, JR
    MCGINNISS, MH
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1977, 146 (01) : 277 - 281
  • [5] Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors
    Miyoshi, H
    Smith, KA
    Mosier, DE
    Verma, IM
    Torbett, BE
    [J]. SCIENCE, 1999, 283 (5402) : 682 - 686
  • [6] Erythrocyte G protein as a novel target for malarial chemotherapy
    Murphy, Sean C.
    Harrison, Travis
    Hamm, Heidi E.
    Lomasney, Jon W.
    Mohandas, Narla
    Haldar, Kasturi
    [J]. PLOS MEDICINE, 2006, 3 (12) : 2403 - 2415
  • [7] PASVOL G, 1989, BLOOD, V74, P1836
  • [8] THE INCREASED SUSCEPTIBILITY OF YOUNG RED-CELLS TO INVASION BY THE MALARIAL PARASITE PLASMODIUM-FALCIPARUM
    PASVOL, G
    WEATHERALL, DJ
    WILSON, RJM
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1980, 45 (02) : 285 - 295
  • [9] PASVOL G, 1982, LANCET, V2, P947
  • [10] Variation in use of erythrocyte invasion pathways by Plasmodium falciparum mediates evasion of human inhibitory antibodies
    Persson, Kristina E. M.
    McCallum, Fiona J.
    Reiling, Linda
    Lister, Nicole A.
    Stubbs, Janine
    Cowman, Alan F.
    Marsh, Kevin
    Beeson, James G.
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (01) : 342 - 351