J. Fujii et al., NEUROTOXICITY OF INTRATHECAL SHIGA-TOXIN-2 AND PROTECTION BY INTRATHECAL INJECTION OF ANTI-SHIGA-TOXIN-2 ANTISERUM IN RABBITS, Microbial pathogenesis, 25(3), 1998, pp. 139-146
The initial brain lesions in rabbits given intravenous Shiga toxin 2 (
Stx2) were noted at 24 h in an area around the third ventricle (Fujii
et al., Infect Immun 1996, 64: 5053-60). This result implied that Stx2
is present in the cerebrospinal fluid (CSF) despite the fact that the
toxin was administered intravenously. We measured Stx2 activity in CS
F by using a Vero cell cytotoxicity assay at various times after an in
travenous injection of Stx2. Stx2 was detected from 2 h after the inje
ction, and its concentration in CSF remained at a high level for a fur
ther 6 h. Fifty percent lethal doses (LD50) of Stx2 were measured in r
abbits after intravenous and intrathecal Stx2 injections; The LD50 aft
er an intrathecal injection of Stx2 was 0.36 mu g/kg, which was 9.2-fo
ld lower than that of an intravenous injection of Stx2 (3.4 mu g/kg).
Magnetic resonance images obtained after an intrathecal Stx2 injection
(5 mu g/kg) were compared with those obtained after an intravenous St
x2 injection (5 mu g/kg). At 48 h, the cerebellar lesions had spread f
rom the area in contact with the CSF on a T2-weighted image, which sug
gests that the intrathecal Stx2 may invade the cerebellum directly. We
then examined whether anti-Stx2 antiserum injected intrathecally prot
ects rabbits against brain damage. Eighty percent of the rabbits infec
ted with Stx2 at 5 mu g/kg died within 8 days from brain damage. Rabbi
t anti-Stx2 sera (with titres of x 16 and x 64 by the Ouchterlony prec
ipitation method) were administered into the CSF space through the cis
terna magna. All the rabbits (n = 10) survived when they were given an
intrathecal injection of rabbit anti-Stx2 antiserum 2 h before the in
travenous injection of Stx2. Our results suggest that a leakage of Stx
2 into the CSF from the choroid plexus causes brain damage, and that a
n intrathecal injection of anti-Stx2 antiserum could be a therapy for
acute encephalopathy caused by Stx2-producing Escherichia coli. (C) 19
98 Academic Press