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Journal article

In vivo study of experimental pneumococcal meningitis using magnetic resonance imaging

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National Center for Antimicrobials and Infection Control, Statens Serum Institut, Copenhagen, Denmark. ctb@ssi.dk1

Magnetic Resonance Imaging (MRI) methods were evaluated as a tool for the study of experimental meningitis. The identification and characterisation of pathophysiological parameters that vary during the course of the disease could be used as markers for future studies of new treatment strategies. Rats infected intracisternally with S. pneumoniae (n = 29) or saline (n = 13) were randomized for imaging at 6, 12, 24, 30, 36, 42 or 48 hours after infection.

T1W, T2W, quantitative diffusion, and post contrast T1W images were acquired at 4.7 T. Dynamic MRI (dMRI) was used to evaluate blood-brain-barrier (BBB) permeability and to obtain a measure of cerebral and muscle perfusion. Clinical- and motor scores, bacterial counts in CSF and blood, and WBC counts in CSF were measured.

MR images and dMRI revealed the development of a highly significant increase in BBB permeability (P < 0.002) and ventricle size (P < 0.0001) among infected rats. Clinical disease severity was closely related to ventricle expansion (P = 0.024). Changes in brain water distribution, assessed by ADC, and categorization of brain 'perfusion' by cortex DeltaSI(bolus) were subject to increased inter-rat variation as the disease progressed, but without overall differences compared to uninfected rats (P > 0.05).

Areas of well-'perfused' muscle decreased with the progression of infection indicative of septicaemia (P = 0.05). The evolution of bacterial meningitis was successfully followed in-vivo with MRI. Increasing BBB-breakdown and ventricle size was observed in rats with meningitis whereas changes in brain water distribution were heterogeneous.

MRI will be a valuable technique for future studies aiming at evaluating or optimizing adjunctive treatments.

Language: English
Publisher: BioMed Central
Year: 2008
Pages: 1
ISSN: 14712342
Types: Journal article
DOI: 10.1186/1471-2342-8-1
ORCIDs: Lundgren, Jens D and 0000-0002-3381-4380

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