Trichomonas vaginalis virulence against epithelial cells and morphological variability:: the comparison between a well-established strain and a fresh isolate

被引:34
作者
Jesus, JB
Vannier-Santos, MA
Britto, C
Godefroy, P
Silva, FC
Pinheiro, AAS
Rocha-Azevedo, B
Lopes, AHCS
Meyer-Fernandes, JR [1 ]
机构
[1] Univ Fed Rio de Janeiro, Dept Bioquim Med, ICB, BR-21941590 Rio de Janeiro, Brazil
[2] Inst Oswaldo Cruz, Dept Bioquim & Biol Mol, BR-20001 Rio De Janeiro, Brazil
[3] Fundacao Oswaldo Cruz, Ctr Pesquisas Goncalo Moniz, Salvador, BA, Brazil
[4] Fac Med Valenca, Disciplina Parasitol, Valencia, RJ, Brazil
[5] Univ Fed Rio de Janeiro, Inst Microbiol Prof Paulo De Goes, Rio de Janeiro, Brazil
[6] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, Rio de Janeiro, Brazil
关键词
D O I
10.1007/s00436-004-1134-4
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
The FMVI strain of Trichomonas vaginalis was freshly isolated from an asymptomatic patient, and its morphological properties and virulence in vitro compared with the well-established JT strain. The morphological variability of the parasites was assessed by differential interference microscopy and both scanning and transmission electron microscopy. The FMV1 strain presented nearly 20% amoeboid cells whereas the JT strain presented high percentages of ellipsoid but no amoeboid cells. The FMV1 morphotype population was unaltered after at least 1 year of subculturing. Electron microscopy revealed that this strain produced numerous pseudopod structures which mediated intimate contact and interdigitation among trophozoites. Dead FMV1 parasites were often phagocytosed by conspecific cells. We also compared the cytolytic capacity of these two populations against epithelial MDCK cells and its contact dependence. The FMV1 strain rapidly adhered to plastic or glass surfaces and to MDCK monolayers. This strain destroyed about 93% of the epithelial cells in 90 min whereas the cytolytic activity of the JT parasites was very much lower (about 41%). Parasite supernatants displayed no cytolytic activity, indicating contact-mediated lysis. The protozoan virulence in vitro did not correlate well with the clinical observations. The implications of these results are discussed.
引用
收藏
页码:369 / 377
页数:9
相关论文
共 48 条
[1]   IDENTIFICATION AND PROPERTIES OF TRICHOMONAS-VAGINALIS PROTEINS INVOLVED IN CYTADHERENCE [J].
ALDERETE, JF ;
GARZA, GE .
INFECTION AND IMMUNITY, 1988, 56 (01) :28-33
[2]   SPECIFIC NATURE OF TRICHOMONAS-VAGINALIS PARASITISM OF HOST-CELL SURFACES [J].
ALDERETE, JF ;
GARZA, GE .
INFECTION AND IMMUNITY, 1985, 50 (03) :701-708
[3]  
ALDERETE JF, 1984, BRIT J VENER DIS, V60, P99
[4]   THE MECHANISMS AND MOLECULES INVOLVED IN CYTOADHERENCE AND PATHOGENESIS OF TRICHOMONAS-VAGINALIS [J].
ALDERETE, JF ;
LEHKER, MW ;
ARROYO, R .
PARASITOLOGY TODAY, 1995, 11 (02) :70-74
[5]   An ecto-protein tyrosine phosphatase of Entamoeba histolytica induces cellular detachment by disruption of actin filaments in HeLa cells [J].
Anaya-Ruiz, M ;
Pérez-Santos, JLM ;
Talamás-Rohana, P .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2003, 33 (07) :663-670
[6]   MOLECULAR-BASIS OF HOST EPITHELIAL-CELL RECOGNITION BY TRICHOMONAS-VAGINALIS [J].
ARROYO, R ;
ENGBRING, J ;
ALDERETE, JF .
MOLECULAR MICROBIOLOGY, 1992, 6 (07) :853-862
[7]   TRICHOMONAS-VAGINALIS SURFACE PROTEINASE ACTIVITY IS NECESSARY FOR PARASITE ADHERENCE TO EPITHELIAL-CELLS [J].
ARROYO, R ;
ALDERETE, JF .
INFECTION AND IMMUNITY, 1989, 57 (10) :2991-2997
[8]   SIGNALING OF TRICHOMONAS-VAGINALIS FOR AMEBOID TRANSFORMATION AND ADHESIN SYNTHESIS FOLLOWS CYTOADHERENCE [J].
ARROYO, R ;
GONZALEZROBLES, A ;
MARTINEZPALOMO, A ;
ALDERETE, JF .
MOLECULAR MICROBIOLOGY, 1993, 7 (02) :299-309
[9]   Characterization cloning and immunolocalization of a coronin homologue in Trichomonas vaginalis [J].
Bricheux, G ;
Coffe, G ;
Bayle, D ;
Brugerolle, G .
EUROPEAN JOURNAL OF CELL BIOLOGY, 2000, 79 (06) :413-422
[10]   Evidence for an uncommon α-actinin protein in Trichomonas vaginalis [J].
Bricheux, G ;
Coffe, G ;
Pradel, N ;
Brugerolle, G .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1998, 95 (02) :241-249