Delayed invasion of the kidney and brain by Borrelia crocidurae in plasminogen-deficient mice

被引:53
作者
Nordstrand, A [1 ]
Shamaei-Tousi, A
Ny, A
Bergström, S
机构
[1] Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden
[2] Umea Univ, Dept Med Biosci, S-90187 Umea, Sweden
关键词
D O I
10.1128/IAI.69.9.5832-5839.2001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Borrelia crocidurae is an etiologic agent of relapsing fever in Africa and is transmitted to humans by the bite of soft ticks of the genus Ornithodoros. The role of the plasminogen (Plg) activation system for the pathogenicity of B. crocidurae was investigated by infection of Plg-deficient (plg(-/-)) and Plg wild-type (plg(+/+)) mice. No differences in spirochetemia were observed between the plg(-/-) and plg(+/+) mice. However, signs indicative of brain invasion, such as neurological symptoms and/or histopathological changes, were more common in plg(+/+) mice. Quantitative immunohistochemical analysis demonstrated infection of spirochetes in kidney interstitium and brain as soon as 2 days postinoculation. Lower numbers of extravascular spirochetes in plg(-/-) mice during the first days of infection suggested a less efficient invasion mechanism in these mice than in the plg(+/+) mice. The invasion of the kidneys in plg(-/-) mice produced no significant inflammation, as seen by quantitative immunohistochemistry of the CD45 common leukocyte marker. However, significant kidney inflammation was observed with infection in the plg(+/+) mice. In brain, inflammation was more severe in plg(+/+) mice than in plg(-/-) mice, and the numbers of CD45(+) cells increased significantly with duration of infection in the plg(+/+) mice. The results show that invasion of brain and kidney occurs as early as 2 days after inoculation. Also, Plg is not required for establishment of spirochetemia by the organism, whereas it is involved in the invasion of organs.
引用
收藏
页码:5832 / 5839
页数:8
相关论文
共 45 条
[1]   A new Borrelia species isolated from patients with relapsing fever in Spain [J].
Anda, P ;
SanchezYebra, W ;
Vitutia, MD ;
Pastrana, EP ;
Rodriguez, I ;
Miller, NS ;
Backenson, PB ;
Benach, JL .
LANCET, 1996, 348 (9021) :162-165
[2]  
Aubry P, 1983, Dakar Med, V28, P413
[3]   BIOLOGY OF BORRELIA SPECIES [J].
BARBOUR, AG ;
HAYES, SF .
MICROBIOLOGICAL REVIEWS, 1986, 50 (04) :381-400
[4]   VARIABLE MAJOR PROTEINS OF BORRELIA-HERMSII - EPITOPE MAPPING AND PARTIAL SEQUENCE-ANALYSIS OF CNBR PEPTIDES [J].
BARSTAD, PA ;
COLIGAN, JE ;
RAUM, MG ;
BARBOUR, AG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 161 (06) :1302-1314
[5]  
BERGERET C., 1948, Bulletin Medical de l'Afrique-Occidentale Francaise, V5, P271
[6]   PLASMINOGEN DEFICIENCY CAUSES SEVERE THROMBOSIS BUT IS COMPATIBLE WITH DEVELOPMENT AND REPRODUCTION [J].
BUGGE, TH ;
FLICK, MJ ;
DAUGHERTY, CC ;
DEGEN, JL .
GENES & DEVELOPMENT, 1995, 9 (07) :794-807
[7]   THE VARIABLE ANTIGENS VMP7 AND VMP21 OF THE RELAPSING FEVER BACTERIUM BORRELIA-HERMSII ARE STRUCTURALLY ANALOGOUS TO THE VSG PROTEINS OF THE AFRICAN TRYPANOSOME [J].
BURMAN, N ;
BERGSTROM, S ;
RESTREPO, BI ;
BARBOUR, AG .
MOLECULAR MICROBIOLOGY, 1990, 4 (10) :1715-1726
[8]   The spirochete Borrelia crocidurae causes erythrocyte resetting during relapsing fever [J].
Burman, N ;
Shamaei-Tousi, A ;
Bergström, S .
INFECTION AND IMMUNITY, 1998, 66 (02) :815-819
[9]   Neuroborreliosis during relapsing Fever: Review of the clinical manifestations, pathology, and treatment of infections in humans and experimental animals [J].
Cadavid, D ;
Barbour, AG .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (01) :151-164
[10]   VARIABILITY OF A BACTERIAL SURFACE PROTEIN AND DISEASE EXPRESSION IN A POSSIBLE MOUSE MODEL OF SYSTEMIC LYME BORRELIOSIS [J].
CADAVID, D ;
THOMAS, DD ;
CRAWLEY, R ;
BARBOUR, AG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (02) :631-642