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Diffusion-weighted MRI Abnormalities in an Outbreak of Streptococcus Agalactiae Serotype III, Multilocus Sequence Type 283 Meningitis

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Date 2016 Jul 30
PMID 27469307
Citations 8
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Abstract

Purpose: In 2015, an outbreak of group B streptococcal (GBS) infection caused by Streptococcus agalactiae Serotype III, multilocus sequence type 283, related to consuming infected raw freshwater fish, affected more than 200 patients in Singapore. We describe the clinical, laboratory, and neuroimaging features of a subgroup of adults with central nervous system (CNS) infections caused by GBS.

Materials And Methods: The database of the Singapore Neurologic Infections Program (SNIP), a national multicenter study for surveillance of infectious neurologic disease, was reviewed to select patients with GBS CNS infection during the outbreak. Cases were diagnosed on the basis of clinical features, cerebrospinal fluid (CSF) findings and identification or isolation of Streptococcus agalactiae in the blood or CSF. Demographic, clinical and neuroradiological information was obtained prospectively and retrospectively abstracted.

Results: Fourteen patients (6 male, 8 female; median age, 58 years) presented with fever, meningism, headache, encephalopathy, focal neurological deficits, and/or seizures. All except two were previously healthy. Diffusion-weighted imaging (DWI) on admission was abnormal in 13 patients, showing tiny hyperintensities in the subarachnoid space (7 patients), ventricles (6 patients) and brain parenchyma (8 patients); 5 patients had cerebellar abnormalities.

Conclusion: Among healthy non-pregnant adults infected with Serotype III, multilocus sequence type 283 GBS meningitis linked to eating infected raw freshwater fish, DWI detected small pus collections and unusual cerebellar involvement. A collaborative national surveillance system that includes MRI can be helpful during unusual food-borne zoonotic infectious disease outbreaks.

Level Of Evidence: 4 J. Magn. Reson. Imaging 2017;45:507-514.

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References
1.
Oyanguren B, Esteban L, Guillan M, de Felipe A, Alonso Canovas A, Navas E . Central nervous system involvement in adult patients with invasive infection caused by Streptococcus agalactiae. Neurologia. 2014; 30(3):158-62. DOI: 10.1016/j.nrl.2013.12.002. View

2.
Ionita C, Siddiqui A, Levy E, Hopkins L, Snyder K, Gibbons K . Acute ischemic stroke and infections. J Stroke Cerebrovasc Dis. 2010; 20(1):1-9. DOI: 10.1016/j.jstrokecerebrovasdis.2009.09.011. View

3.
Umapathi T, Kor A, Venketasubramanian N, Tchoyoson Lim C, Pang B, Yeo T . Large artery ischaemic stroke in severe acute respiratory syndrome (SARS). J Neurol. 2004; 251(10):1227-31. PMC: 7088071. DOI: 10.1007/s00415-004-0519-8. View

4.
Nath A . Neuroinfectious diseases: a crisis in neurology and a call for action. JAMA Neurol. 2014; 72(2):143-4. PMC: 5267936. DOI: 10.1001/jamaneurol.2014.3442. View

5.
Schellinger P, Bryan R, Caplan L, Detre J, Edelman R, Jaigobin C . Evidence-based guideline: The role of diffusion and perfusion MRI for the diagnosis of acute ischemic stroke: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology. 2010; 75(2):177-85. PMC: 2905927. DOI: 10.1212/WNL.0b013e3181e7c9dd. View