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Infection and Immunity, September 2001, p. 5832-5839, Vol. 69, No. 9
Department of Molecular
Biology1 and Medical Biochemistry,
Department of Medical Biosciences,2 Umeå
University, S-90187 Umeå, Sweden
Received 12 March 2001/Returned for modification 12 April
2001/Accepted 29 May 2001
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
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.9.5832-5839.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Delayed Invasion of the Kidney and Brain by
Borrelia crocidurae in Plasminogen-Deficient
Mice

and
/
) 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.
*
Corresponding author. Mailing address: Department of
Molecular Biology, Umeå University, S-90187 Umeå, Sweden. Phone: 46 90 7856735. Fax: 46 90 772630. E-mail:
annika.nordstrand{at}micro.umu.se.
Present address: Karolinska Institute, Microbiology and Tumor Biology
Center, S-17177 Stockholm, Sweden.
Present address: Department of Public Health and Clinical Medicine,
Section for Dermatology and Venereology, Umeå University, S-901 87 Umeå, Sweden.
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