Neuroinvasive Francisella tularensis Infection: Report of 2 Cases and Review of the Literature

Abstract Background Neuroinvasive infection with Francisella tularensis, the causative agent of tularemia, is rare. Establishing clinical suspicion is challenging if risk factors or clinical features classically associated with tularemia are absent. Tularemia is treatable with antibiotics; however,...

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Veröffentlicht in:Clinical infectious diseases 2024-01, Vol.78 (Supplement_1), p.S55-S63
Hauptverfasser: Cash-Goldwasser, Shama, Beeson, Amy, Marzec, Natalie, Ho, Dora Y, Hogan, Catherine A, Budvytiene, Indre, Banaei, Niaz, Born, Donald E, Gephart, Melanie H, Patel, Jatinbhai, Dietrich, Elizabeth A, Nelson, Christina A
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Sprache:eng
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Zusammenfassung:Abstract Background Neuroinvasive infection with Francisella tularensis, the causative agent of tularemia, is rare. Establishing clinical suspicion is challenging if risk factors or clinical features classically associated with tularemia are absent. Tularemia is treatable with antibiotics; however, there are limited data to inform management of potentially fatal neuroinvasive infection. Methods We collected epidemiologic and clinical data on 2 recent US cases of neuroinvasive F. tularensis infection, and performed a literature review of cases of neuroinvasive F. tularensis infection published after 1950. Results One patient presented with focal neurologic deficits and brain lesions; broad-range molecular testing on resected brain tissue detected F. tularensis. The other patient presented with meningeal signs; tularemia was suspected based on animal exposure, and F. tularensis grew in cerebrospinal fluid (CSF) culture. Both patients received combination antibiotic therapy and recovered from infection. Among 16 published cases, tularemia was clinically suspected in 4 cases. CSF often displayed lymphocytic pleocytosis. Among cases with available data, CSF culture was positive in 13 of 16 cases, and F. tularensis antibodies were detected in 11 of 11 cases. Treatment typically included an aminoglycoside combined with either a tetracycline or a fluoroquinolone. Outcomes were generally favorable. Conclusions Clinicians should consider neuroinvasive F. tularensis infection in patients with meningitis and signs suggestive of tularemia or compatible exposures, lymphocyte-predominant CSF, unrevealing standard microbiologic workup, or lack of response to empiric bacterial meningitis treatment. Molecular testing, culture, and serologic testing can reveal the diagnosis. Favorable outcomes can be achieved with directed antibiotic treatment. Francisella tularensis can cause neuroinvasive infection. Clinicians should consider directed, multimodal laboratory testing in patients with central nervous system infection and epidemiologic or clinical features suggestive of tularemia. Combination antibiotic treatment can be curative.
ISSN:1058-4838
1537-6591
DOI:10.1093/cid/ciad719