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Infection and Immunity, December 1998, p. 5930-5938, Vol. 66, No. 12
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Phosphatidylcholine-Specific Phospholipase C from Listeria
monocytogenes Is an Important Virulence Factor in Murine
Cerebral Listeriosis
Dirk
Schlüter,1,*
Eugen
Domann,2
Christine
Buck,3
Torsten
Hain,2
Herbert
Hof,1
Trinad
Chakraborty,2 and
Martina
Deckert-Schlüter3
Institut für Medizinische Mikrobiologie
und Hygiene, Universitätsklinikum Mannheim, Universität
Heidelberg, Mannheim,1
Institut
für Medizinische Mikrobiologie, Justus-Liebig-Universität
Gießen, Gießen,2 and
Institut
für Neuropathologie, Universitätskliniken Bonn,
Bonn,3 Germany
Received 8 July 1998/Returned for modification 18 August
1998/Accepted 25 September 1998
Meningoencephalitis is a serious and often fatal complication of
Listeria monocytogenes infection. The aim of the present study was to analyze the role of internalin A (InlA) and B, which are
involved in the invasion of L. monocytogenes
into cultivated host tissue cells, and that of
phosphatidylcholine-specific phospholipase C (PlcB), which mainly
promotes the direct cell-to-cell spread of L. monocytogenes, in murine cerebral listeriosis by use of an InlA/B
(
inlAB2)- and a PlcB (
plcB2)-deficient
isogenic deletion mutant strain and the wild-type (WT) L. monocytogenes EGD. Listeria strains were directly
applied to the brain, a technique which has been employed previously to
study the pathogenesis of cerebral listeriosis (D. Schlüter,
S. B. Oprisiu, S. Chahoud, D. Weiner, O. D. Wiestler, H. Hof,
and M. Deckert-Schlüter, Eur. J. Immunol. 25:2384-2391,
1995). We demonstrated that PlcB, but not InlA or InlB, is an
important virulence factor in cerebral listeriosis. Nonimmunized mice
infected intracerebrally with the
plcB2 strain survived
significantly longer and had a reduced intracerebral bacterial load
compared to mice infected with the
inlAB2 strain or WT
bacteria. In addition, immunization with the WT prior to intracerebral
infection significantly increased the survival rate of mice challenged
intracerebrally with the
plcB2 strain compared to that
of mice infected with the WT or
inlAB2 strain.
Histopathology revealed that the major difference between the various
experimental groups was a significantly delayed intracerebral spread of
the
plcB2 mutant strain, indicating that cell-to-cell
spread is an important pathogenic feature of cerebral listeriosis.
Interestingly, irrespective of the Listeria mutant used,
the apoptosis of hippocampal and cerebellar neurons and an internal
hydrocephalus developed in surviving mice, indicating that these
complications are not dependent on the virulence factors InlA/B and
PlcB. In conclusion, this study points to PlcB as a virulence factor
important for the intracerebral pathogenesis of murine L. monocytogenes meningoencephalitis.
*
Corresponding author. Mailing address: Institut
für Medizinische Mikrobiologie und Hygiene,
Universitätsklinikum Mannheim, Universität Heidelberg,
Theodor-Kutzer-Ufer 1-3, D-68167 Mannheim, Germany. Phone: (49)
621/383-2036. Fax: (49) 621/383-3816. E-mail: dirk.schlueter{at}imh.ma.uni-heidelberg.de.
Infection and Immunity, December 1998, p. 5930-5938, Vol. 66, No. 12
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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