Performance assessment of three commercial assays for direct detection of Bacillus anthracis spores.
نویسندگان
چکیده
Bacillus anthracis, the cause of anthrax, has been used as a bioterrorism agent. Because the isolation and identification of B. anthracis by culture can take days, first response units (hazardous materials [HAZMAT], firemen, police, and hospital personnel) desire a quick and easy test that can be done in the field to detect possible B. anthracis contamination (1, 4). To our knowledge, there are no peer-reviewed published data on commercially available kits that could guide first responders in their search for such rapid detection methods. We tested three lateral flow immunoassay kits that are designed to test for B. anthracis at 10 to 10 spores per sample: (i) Anthrax BioThreat Alert (BTA) test strips (Tetracore, Gaithersburg, Md.), (ii) BioWarfare Agent Detection Devices (BADD) (Osborne Scientific, Lakeside, Ariz.), and (iii) Anthrax (spore) SMART II (New Horizons Diagnostics, Columbia, Md.). These tests require little technician time and training, and results are available within 15 min. This study was conducted at the Florida Department of Health Laboratory in Tampa, Fla., and employed B. anthracis Pasteur (CDC BC 3132) and Bacillus cereus and Bacillus thuringiensis from our culture collection. Spores were added to the buffer provided by the manufacturer to achieve 10 to 10 (B. anthracis) or 10 (B. cereus and B. thuringiensis) spores per sample. The range of 10 to 10 for B. anthracis spores was chosen in order to include the manufacturer’s claims of sensitivity. We also tested 10 spores in order to achieve a clear, easy-to-read positive result. Because one of the kits did not consistently detect spores at the upper limit (10), we tested 10 spores more than once to see if detection was consistent. All tests were performed according to the manufacturer’s instructions and were allowed to proceed for 15 min, although the positive results were recognized within 5 min. Spore concentrations were verified by viable plate counts on Trypticase soy agar (Remel, Lenexa, Kans.) in duplicate. All of the assay kits were able to detect B. anthracis at 10 spores (Table 1). While BADD and SMART II consistently detected 10 spores, Anthrax BTA detected 10 spores only once in eight attempts (12.5%). BADD yielded a sensitivity of 35.7%, SMART II demonstrated a sensitivity of 41.6%, and Anthrax BTA had a sensitivity of 30.43% (Table 1). Both BADD and Anthrax BTA had a specificity of 100%, while SMART II showed a positive reaction with B. thuringiensis, giving a specificity of 75%. First responders desire a method that accurately detects 100 B. anthracis spores (4). When areas contain numbers of spores lower than the test assay detection limit, the resulting false-negative findings may lead first responders to employ relaxed safety precautions. Although the assays tested are selfcontained and easy to use in the field, their sensitivity fails to meet that of our laboratory experiments (e.g., 10 spores on environmental swab samples) (2). The costs per assay of using the Anthrax BTA, BADD, and SMART II assays are $19.80, $42.50, and $52.10, respectively. These high costs may preclude their being used during times of high sample volume, as was seen during the fall of 2001 when the Laboratory Response Network tested 84,000 samples (3). Only three kits and a limited number of assays were performed due to the unavailability of other products and the cost. Tetracore sells a test strip reader (Guardian Bio Threat Alert Test Strip Reader) that costs approximately $4,000. However, this instrument may only increase the detection level by 1 to 2 logs according to the manufacturer (Guardian Bio-Threat Alert System technical information, Alexeter Technologies, Wheeling, Ill.). When the sensitivity is increased and the costs are reduced, these assay kits may hold promise for field detection by first responders.
منابع مشابه
Gamma irradiation can be used to inactivate Bacillus anthracis spores without compromising the sensitivity of diagnostic assays.
The use of Bacillus anthracis as a biological weapon in 2001 heightened awareness of the need for validated methods for the inactivation of B. anthracis spores. This study determined the gamma irradiation dose for inactivating virulent B. anthracis spores in suspension and its effects on real-time PCR and antigen detection assays. Strains representing eight genetic groups of B. anthracis were e...
متن کاملBacillus spore inactivation methods affect detection assays.
Detection of biological weapons is a primary concern in force protection, treaty verification, and safeguarding civilian populations against domestic terrorism. One great concern is the detection of Bacillus anthracis, the causative agent of anthrax. Assays for detection in the laboratory often employ inactivated preparations of spores or nonpathogenic simulants. This study uses several common ...
متن کاملDevelopment and implementation of a single-chain Fv antibody for specific detection of Bacillus anthracis spores.
A single-chain Fv (scFv) antibody was developed and applied for efficient and specific detection of Bacillus anthracis spores. The antibody was isolated from a phage display library prepared from spleens of mice immunized with a water-soluble extract of the outer membrane of the B. anthracis spore (exosporium). The library (7 x 10(6) PFU) was biopanned against live, native B. anthracis ATCC del...
متن کاملSelection and Characterization of Single Domain Antibodies Specific for Bacillus anthracis Spore Proteins
To obtain thermostable immunoreagents specific for the spore form of Bacillus anthracis two llamas were immunized with a combination of six different recombinant proteins. These proteins BclA, gerQ, SODA1, SOD15, BxpB and the protein p5303 have all been shown as components of the B. anthracis spore and could potentially serve as targets for the detection of spores in multiplexed biosensors. Per...
متن کاملQuantitative immunofluorescence studies of the serology of Bacillus anthracis spores.
A fluorescein-conjugated antibody against formalin-inactivated spores of Bacillus anthracis Vollum reacted only weakly with a variety of Bacillus species in microfluorometric immunofluorescence assays. A conjugated antibody against spores of B. anthracis Sterne showed little affinity for spores of several B. anthracis isolates including B. anthracis Vollum, indicating that more than one anthrax...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Journal of clinical microbiology
دوره 41 7 شماره
صفحات -
تاریخ انتشار 2003