Migration of Toxoplasma gondii across biological barriers

被引:134
作者
Barragan, A [1 ]
Sibley, LD
机构
[1] Huddinge Univ Hosp, Karolinska Inst, Dept Med, Ctr Infect Med, SE-14186 Stockholm, Sweden
[2] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
关键词
D O I
10.1016/S0966-842X(03)00205-1
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
The molecular mechanisms underlying migration of pathogens across biological barriers remain poorly characterized. Following oral infection, the apicomplexan parasite Toxoplasma gondii actively crosses non-permissive biological barriers such as the intestine, the bloodbrain barrier and the placenta, thereby gaining access to tissues where it causes severe pathology. Recently, enhanced migration was found to be associated with virulent strains of Toxoplasma, suggesting that this phenotype contributes to pathogenesis. The migratory machinery appears to be morphologically and functionally well conserved within the phylum of apicomplexan parasites, however, the mechanisms for cellular traffic to breach biological barriers remain to be elucidated. As penetration of host tissue is a prerequisite for the establishment of infections by most apicomplexan parasites, understanding parasite migration is crucial for the development of new approaches to combat disease.
引用
收藏
页码:426 / 430
页数:5
相关论文
共 52 条
[11]   Comparative infectivity of Toxoplasma gondii bradyzoites in rats and mice [J].
Dubey, JP .
JOURNAL OF PARASITOLOGY, 1998, 84 (06) :1279-1282
[12]   Bradyzoite-induced murine toxoplasmosis:: Stage conversion, pathogenesis, and tissue cyst formation in mice fed bradyzoites of different strains of Toxoplasma gondii [J].
Dubey, JP .
JOURNAL OF EUKARYOTIC MICROBIOLOGY, 1997, 44 (06) :592-602
[13]   Oocyst-induced murine toxoplasmosis: Life cycle, pathogenicity, and stage conversion in mice fed Toxoplasma gondii oocysts [J].
Dubey, JP ;
Speer, CA ;
Shen, SK ;
Kwok, OCH ;
Blixt, JA .
JOURNAL OF PARASITOLOGY, 1997, 83 (05) :870-882
[14]   Neutrophils emigrate from venules by a transendothelial cell pathway in response to FMLP [J].
Feng, D ;
Nagy, JA ;
Pyne, K ;
Dvorak, HF ;
Dvorak, AM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (06) :903-915
[15]   Some aspects of protozoan infections in immunocompromised patients - A review [J].
Ferreira, MS ;
Borges, AS .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2002, 97 (04) :443-457
[16]   Genotypic characterization of Toxoplasma gondii strains associated with human toxoplasmosis in Spain:: Direct analysis from clinical samples [J].
Fuentes, I ;
Rubio, JM ;
Ramírez, C ;
Alvar, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (04) :1566-1570
[17]   IFN-γ overproduction and high level apoptosis are associated with high but not low virulence Toxoplasma gondii infection [J].
Gavrilescu, LC ;
Denkers, EY .
JOURNAL OF IMMUNOLOGY, 2001, 167 (02) :902-909
[18]   Toxoplasma gondii myosin A and its light chain:: a fast, single-headed, plus-end-directed motor [J].
Herm-Götz, A ;
Weiss, S ;
Stratmann, R ;
Fujita-Becker, S ;
Ruff, C ;
Meyhöfer, E ;
Soldati, T ;
Manstein, DJ ;
Geeves, MA ;
Soldati, D .
EMBO JOURNAL, 2002, 21 (09) :2149-2158
[19]   TOXOPLASMA-GONDII COMPRISES 3 CLONAL LINEAGES - CORRELATION OF PARASITE GENOTYPE WITH HUMAN-DISEASE [J].
HOWE, DK ;
SIBLEY, LD .
JOURNAL OF INFECTIOUS DISEASES, 1995, 172 (06) :1561-1566
[20]   Cellular mechanisms of microbial proteins contributing to invasion of the blood-brain barrier [J].
Huang, SH ;
Jang, AY .
CELLULAR MICROBIOLOGY, 2001, 3 (05) :277-287