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Neurologic melioidosis
Martin Deuble1, Chloe Aquilina, Robert Norton
1Townsville Hospital, Townsville, Queensland, Australia. mjdeuble@gmail.com
Abstract:
Melioidosis is an important cause of morbidity and mortality in northern Australia and Southeast Asia. Diagnosis is best made by isolation of Burkholderia pseudomallei from clinical specimens. A variety of clinical presentations are described, including neurologic disease. The aim of this study was to review admissions with confirmed neurologic melioidosis to a regional hospital in a region to which melioidosis is endemic during 1995-2011. There were 12 culture-confirmed cases of neurologic melioidosis, of which two were detected by analysis of cerebrospinal fluid. Four of these cases were in children. Significant clinical features were fever, headache, and ataxia. Common changes on magnetic resonance imaging T2-weighted scans included ring-enhancing lesions and leptomeningeal enhancement. There were four deaths and an additional four patients had significant long-term neurologic sequelae. When considering the etiology of undifferentiated neurologic disease, an awareness of the possibility of neurologic melioidosis is important in disease-endemic regions.
Insights
Neurologic melioidosis, caused by Burkholderia pseudomallei, presents with fever, headache, and ataxia in endemic areas. Early diagnosis and awareness are crucial, as it can lead to significant mortality and long-term neurologic sequelae.
Area of Science:
- Infectious Diseases
- Neurology
- Tropical Medicine
Background:
- Melioidosis is a significant cause of illness and death in Southeast Asia and northern Australia.
- Burkholderia pseudomallei is the causative agent, diagnosed via clinical specimen culture.
- Neurologic manifestations of melioidosis can vary widely.
Purpose of the Study:
- To review cases of confirmed neurologic melioidosis admitted to a regional hospital between 1995 and 2011.
- To identify clinical features, diagnostic findings, and outcomes of neurologic melioidosis.
- To emphasize the importance of considering melioidosis in neurologic disease diagnosis in endemic regions.
Main Methods:
- Retrospective review of hospital admissions for culture-confirmed neurologic melioidosis.
- Analysis of patient demographics, clinical presentations, diagnostic methods (including cerebrospinal fluid analysis), and neuroimaging findings (MRI T2-weighted scans).
- Assessment of treatment outcomes, mortality, and long-term neurologic sequelae.
Main Results:
- Twelve culture-confirmed cases of neurologic melioidosis were identified.
- Two cases were diagnosed via cerebrospinal fluid analysis.
- Common symptoms included fever, headache, and ataxia; MRI showed ring-enhancing lesions and leptomeningeal enhancement.
- Four patients died, and four experienced significant long-term neurologic deficits.
Conclusions:
- Neurologic melioidosis is a serious condition with high mortality and morbidity in endemic areas.
- Clinical features like fever, headache, and ataxia, along with specific MRI findings, are characteristic.
- Increased awareness of neurologic melioidosis is vital for diagnosing undifferentiated neurologic diseases in affected regions.
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