Flow cytometric assessment of Leishmania spp metacyclic differentiation:: Validation by morphological features and specific markers

被引:40
作者
Saraiva, EM
Pinto-da-Silva, LH
Wanderley, JLM
Bonomo, AC
Barcinski, MA
Moreira, MEC [1 ]
机构
[1] Inst Nacl Canc, Div Expt Med, Direcao Pesquisa, Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Inst Microbiol, BR-21941 Rio De Janeiro, Brazil
[3] Univ Sao Paulo, Inst Ciencias Biomed, BR-05508 Sao Paulo, Brazil
关键词
trypanosomatid parasitic protozoa; metacyclic promastigotes; metacyclogenesis;
D O I
10.1016/j.exppara.2005.01.004
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
Characterization of infective metacyclic promastigotes of Leishmania spp can be an essential step in several experimental protocols. Metacyclic forms of all Leishmania species display a typical morphology with short, narrow cell body, and an elongated flagellum. This feature suggests that metacyclics can be distinguished from procyclic forms by non-fluorimetric flow cytometric parameters thus enabling the follow-up of their appearance and acquisition of specific properties, during metacyclogenesis in in vitro cultures. Here we describe the flow cytometric parameters of stage-specific promastigotes of Leishmania major, Leishmania donovani, Leishmania amazonensis, and Leishmania braziliensis. Our findings were validated by optical microscopy morphology and specific procyclic labeling with FITC-peanut agglutinin. Furthermore, we show that parasite's distribution in the plot during differentiation in culture is not species specific and that the parasites displaying low forward-angle light scatter (FSClow) are three times more infective than the FSChigh ones. The method here described can be applied to the identification of metacyclics of different Leishmania spp within the whole stationary population. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:39 / 47
页数:9
相关论文
共 33 条
[21]  
RYAN JL, 1980, AM J PATHOL, V99, P451
[22]   Molecular aspects of parasite-vector and vector-host interactions in Leishmaniasis [J].
Sacks, D ;
Kamhawi, S .
ANNUAL REVIEW OF MICROBIOLOGY, 2001, 55 :453-483
[23]  
SACKS DL, 1985, J IMMUNOL, V135, P564
[24]   IDENTIFICATION OF AN INFECTIVE STAGE OF LEISHMANIA PROMASTIGOTES [J].
SACKS, DL ;
PERKINS, PV .
SCIENCE, 1984, 223 (4643) :1417-1419
[25]   STAGE-SPECIFIC BINDING OF LEISHMANIA-DONOVANI TO THE SAND FLY VECTOR MIDGUT IS REGULATED BY CONFORMATIONAL-CHANGES IN THE ABUNDANT SURFACE LIPOPHOSPHOGLYCAN [J].
SACKS, DL ;
PIMENTA, PFP ;
MCCONVILLE, MJ ;
SCHNEIDER, P ;
TURCO, SJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (02) :685-697
[26]   METACYCLOGENESIS IN LEISHMANIA PROMASTIGOTES [J].
SACKS, DL .
EXPERIMENTAL PARASITOLOGY, 1989, 69 (01) :100-103
[27]  
SARAIVA EMB, 1986, EUR J CELL BIOL, V40, P219
[28]  
SARAIVA EMB, 1995, PARASITOLOGY, V111, P257
[29]   Leishmania chagasi:: lipophosphoglycan characterization and binding to the midgut of the sand fly vector Lutzomyia longipalpis [J].
Soares, RPP ;
Macedo, ME ;
Ropert, C ;
Gontijo, NF ;
Almeida, IC ;
Gazzinelli, RT ;
Pimenta, PFP ;
Turco, SJ .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2002, 121 (02) :213-224
[30]   A lipophosphoglycan-independent method for isolation of infective Leishmania metacyclic promastigotes by density gradient centrifugation [J].
Späth, GF ;
Beverley, SM .
EXPERIMENTAL PARASITOLOGY, 2001, 99 (02) :97-103