Laboratory Diagnostics of Botulism
Лабораторная диагностика ботулизма
2006-04-01
SCID: 54.1/j3sbcbuj
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Clostridium botulinum groups I and IIbotulinum neurotoxin (BoNT)botulismmouse lethality assayneurotoxin gene molecular diagnostics
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Abstract (AI)
Botulism is a potentially lethal paralytic disease caused by botulinum neurotoxin. Human pathogenic neurotoxins of types A, B, E, and F are produced by a diverse group of anaerobic spore-forming bacteria, including Clostridium botulinum groups I and II, Clostridium butyricum, and Clostridium baratii. The routine laboratory diagnostics of botulism is based on the detection of botulinum neurotoxin in the patient. Detection of toxin-producing clostridia in the patient and/or the vehicle confirms the diagnosis. The neurotoxin detection is based on the mouse lethality assay. Sensitive and rapid in vitro assays have been developed, but they have not yet been appropriately validated on clinical and food matrices. Culture methods for C. botulinum are poorly developed, and efficient isolation and identification tools are lacking. Molecular techniques targeted to the neurotoxin genes are ideal for the detection and identification of C. botulinum, but they do not detect biologically active neurotoxin and should not be used alone. Apart from rapid diagnosis, the laboratory diagnostics of botulism should aim at increasing our understanding of the epidemiology and prevention of the disease. Therefore, the toxin-producing organisms should be routinely isolated from the patient and the vehicle. The physiological group and genetic traits of the isolates should be determined.
Key Findings
1
Botulism is caused by botulinum neurotoxins types A, B, E, and F produced by diverse anaerobic spore-forming bacteria (C. botulinum groups I and II, C. butyricum, C. baratii).
2
Culture methods for C. botulinum are poorly developed, and efficient isolation and identification tools are lacking.
3
Laboratory diagnostics should also support epidemiology and prevention by routinely isolating toxin-producing organisms and determining isolates' physiological group and genetic traits.
4
Molecular techniques targeting neurotoxin genes are ideal for detecting and identifying C. botulinum but do not detect biologically active toxin and should not be used alone.
5
Neurotoxin detection is based on the mouse lethality assay; sensitive rapid in vitro assays exist but lack appropriate validation on clinical and food matrices.
6
Routine laboratory diagnosis relies on detection of botulinum neurotoxin in the patient, with detection of toxin-producing clostridia in patient and/or vehicle confirming diagnosis.
Research Object
Laboratory diagnostics of botulism (detection and isolation procedures for botulinum neurotoxin and toxin-producing clostridia)
Research Subject
Methods and performance of detecting biologically active botulinum neurotoxin and identifying/isolation of toxin-producing clostridia (including mouse lethality assay, in vitro assays, culture methods, and molecular detection of neurotoxin genes), and their role in diagnosis, epidemiology, and prevention
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2006-04-01
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