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• W48433975 abstract "Classically, microorganisms have been identified by bacteriological means (1). Typically, this would involve plating of the specimen on suitable growth media, incubation at least overnight to allow growth, streak purification of individual suspect colonies followed by another overnight incubation and inoculation of specific biochemical reactions that are useful for differentiation of the organism from other genera or species possibly followed by a third overnight incubation. Thus, the “gold standard” for the identification of bacteria that might be used to identify an organism included in a bioweapon is cultivation followed by differential testing to specifically identify the agent. In the best case, the amount of time needed to identify these organisms could be reduced if specific antiserum was available that could be used after the initial specimen has been plated and incubated to obtain individual bacterial colonies (see Chapter 25). Thus, a presumptive identification using antibody-based methods would be available after approx 24 h. Beside being time consuming, this process produces a large burden in terms of logistics to get the reagents and equipment to the site of testing. The above scenario is for a bacterial agent and the logistical burden is even heavier for viral agents given the specialized reagents and equipment needed for their identification. This is simply not acceptable because therapy for infections caused by these agents generally must begin within the first few hours after exposure if the patient is to survive (2)." @default.
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• W48433975 date "2005-01-01" @default.
• W48433975 modified "2023-09-23" @default.
• W48433975 title "DNA-Based Diagnostic Tests for Detection and Identification of Biological Weapons" @default.
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• W48433975 doi "https://doi.org/10.1385/1-59259-764-5:525" @default.
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