National validation study of a swab protocol for the recovery of Bacillus anthracis spores from surfaces

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• 作者：Lisa R. Hodges ; Laura J. Rose ; Heather O'Connell ; Matthew J. Arduino
• 关键词：Bacillus anthracis spores ; Swabs ; Surface sampling
• 刊名：Journal of Microbiological Methods
• 出版年：2010
• 出版时间：May 2010
• 年：2010
• 卷：81
• 期：2
• 页码：141-146
• 全文大小：252 K

文摘

Twelve Laboratory Response Network (LRN) affiliated laboratories participated in a validation study of a macrofoam swab protocol for the recovery, detection, and quantification of viable B. anthracis (BA) Sterne spores from steel surfaces. CDC personnel inoculated steel coupons (26 cm²) with 1–4 log₁₀ BA spores and recovered them by sampling with pre-moistened macrofoam swabs. Phase 1 (P1) of the study evaluated swabs containing BA only, while dust and background organisms were added to swabs in Phase 2 (P2) to mimic environmental conditions. Laboratories processed swabs and enumerated spores by culturing eluted swab suspensions and counting colonies with morphology consistent with BA. Processed swabs were placed in enrichment broth, incubated 24 h, and cultured by streaking for isolation. Real-time PCR was performed on selected colonies from P2 samples to confirm the identity of BA. Mean percent recovery ( % R) of spores from the surface ranged from 15.8 to 31.0 % (P1) and from 27.9 to 55.0 % (P2). The highest mean percent recovery was 31.0 % (sd 10.9 % ) for P1 (4 log₁₀ inoculum) and 55.0 % (sd 27.6 % ) for P2 (1 log₁₀ inoculum). The overall % R was higher for P2 (44.6 % ) than P1 (24.1 % ), but the overall reproducibility (between-lab variability) was lower in P2 than in P1 (25.0 vs 16.5 % CV, respectively). The overall precision (within-lab variability) was close to identical for P1 and P2 (44.0 and 44.1, respectively), but varied greatly between inoculum levels. The protocol demonstrated linearity in % R over the three inoculum levels and is able to detect between 26 and 5 × 10⁶ spores/26 cm². Sensitivity as determined by culture was > 98.3 % for both phases and all inocula, suggesting that the culture method maintains sensitivity in the presence of contaminants. The enrichment broth method alone was less sensitive for sampled swabs (66.4 % ) during P2, suggesting that the presence of background organisms inhibited growth or isolation of BA from the broth. The addition of real-time PCR testing to the assay increased specificity from > 85.4 % to > 95.0 % in P2. Although the precision was low at the 1 log₁₀ inoculum level in both phases (59.0 and 50.2 % ), this swab processing protocol, was sensitive, specific, precise, and reproducible at 2–4 log₁₀/26 cm² spore concentrations.