Generation of Leishmania donovani axenic amastigotes:: their growth and biological characteristics

被引:182
作者
Debrabant, A
Joshi, MB
Pimenta, PFP
Dwyer, DM
机构
[1] NIAID, Cell Biol Sect, Parasit Dis Lab, Div Intramural Res,NIH, Bethesda, MD 20892 USA
[2] US FDA, Ctr Biol Evaluat & Res, Div Emerging & Transfus Transmitted Dis, Bethesda, MD USA
[3] Fdn Oswaldo Cruz, Ctr Pesquisas Rene Rachou, Lab Med Entomol, Belo Horizonte, MG, Brazil
基金
美国国家卫生研究院;
关键词
trypanosomatid; leishmaniasis; parasite; culture system; infectivity; virulence;
D O I
10.1016/j.ijpara.2003.10.011
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
In this report, we describe an in vitro culture system for the generation and propagation of axenic amastigotes from the well characterised 1S-CL2D line of Leishmania donovani. Fine structure analyses of these in vitro-grown amastigotes demonstrated that they possessed morphological features characteristic of L. donovani tissue-derived amastigotes. Further, these axenic amastigotes (LdAxAm) were shown to synthesise and release a secretory acid phosphatase isoform similar to that produced by intracellular amastigotes. Such LdAxAm also expressed surface membrane 3'-nucleotidase enzyme activity similar to that of tissue-derived amastigotes. Moreover, LdAxAm, in contrast to promastigotes, expressed significant levels of the amastigote-specific A2 proteins. In addition, LdAxAm, derived from long term cultures of Ld 1S-CL2D promastigotes, had significant infectivity for both human macrophages in vitro and for hamsters in vivo. Thus, the in vitro culture system described herein provides a useful tool for the generation of large quantities of uniform populations of axenic amastigotes of the L. donovani 1S-CL2D line. The availability of such material should greatly facilitate studies concerning the cell and molecular biology of this parasite developmental stage. (C) 2003 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:205 / 217
页数:13
相关论文
共 44 条
[1]   Functional analysis of an inosine-guanosine transporter from Leishmania donovani -: The role of conserved residues, aspartate 389 and arginine 393 [J].
Arastu-Kapur, S ;
Ford, E ;
Ullman, B ;
Carter, NS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (35) :33327-33333
[2]   BIOSYNTHESIS AND SECRETION OF ACID-PHOSPHATASE BY LEISHMANIA-DONOVANI PROMASTIGOTES [J].
BATES, PA ;
DWYER, DM .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1987, 26 (03) :289-296
[3]   LEISHMANIA-DONOVANI - GENERATION OF MONOSPECIFIC ANTIBODY REAGENTS TO SOLUBLE ACID-PHOSPHATASE [J].
BATES, PA ;
KURTZ, MK ;
GOTTLIEB, M ;
DWYER, DM .
EXPERIMENTAL PARASITOLOGY, 1987, 64 (02) :157-164
[4]   CHARACTERIZATION OF DEVELOPMENTALLY-REGULATED NUCLEASES IN PROMASTIGOTES AND AMASTIGOTES OF LEISHMANIA-MEXICANA [J].
BATES, PA .
FEMS MICROBIOLOGY LETTERS, 1993, 107 (01) :53-58
[5]   LEISHMANIA-DONOVANI - IDENTIFICATION OF GLYCOPROTEINS RELEASED BY PROMASTIGOTES DURING GROWTH-INVITRO [J].
BATES, PA ;
GOTTLIEB, M ;
DWYER, DM .
EXPERIMENTAL PARASITOLOGY, 1988, 67 (02) :199-209
[6]   Identification of genes mediating lipophosphoglycan biosynthesis by functional complementation of Leishmania donovani mutants [J].
Beverley, SM ;
Turco, SJ .
ANNALS OF TROPICAL MEDICINE AND PARASITOLOGY, 1995, 89 :11-17
[7]   Antileishmanial activities of several classes of aromatic dications [J].
Brendle, JJ ;
Outlaw, A ;
Kumar, A ;
Boykin, DW ;
Patrick, DA ;
Tidwell, RR ;
Werbovetz, KA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (03) :797-807
[8]   DEVELOPMENTAL GENE-EXPRESSION IN LEISHMANIA-DONOVANI - DIFFERENTIAL CLONING AND ANALYSIS OF AN AMASTIGOTE-STAGE-SPECIFIC GENE [J].
CHAREST, H ;
MATLASHEWSKI, G .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (05) :2975-2984
[9]   ISOLATION AND CHARACTERIZATION OF THE GENE ENCODING THE SURFACE-MEMBRANE 3'-NUCLEOTIDASE NUCLEASE OF LEISHMANIA-DONOVANI [J].
DEBRABANT, A ;
GOTTLIEB, M ;
DWYER, DM .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1995, 71 (01) :51-63
[10]   Dissection of the functional domains of the Leishmania surface membrane 3′-nucleotidase/nuclease, a unique member of the class I nuclease family [J].
Debrabant, A ;
Ghedin, E ;
Dwyer, DM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (21) :16366-16372