Detection of biological weapons is a primary concern in force protection, t
reaty verification, and safeguarding civilian populations against domestic
terrorism. One great concern is the detection of Bacillus anthracis, the ca
usative agent of anthrax. Assays for detection in the laboratory often empl
oy inactivated preparations of spores or nonpathogenic simulants. This stud
y uses several common biodetection platforms to detect B. anthracis spores
that have been inactivated by two methods and compares those data to detect
ion of spores that have not been inactivated. The data demonstrate that ina
ctivation methods can affect the sensitivity of nucleic acid- and antibody-
based assays for the detection of B. anthracis spores. These effects should
be taken into consideration when comparing laboratory results to data coll
ected and assayed during field deployment.