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通过校准的高光谱反射显微镜区分活的可存活细菌芽孢与死的细菌芽孢。

Differentiation of live-viable versus dead bacterial endospores by calibrated hyperspectral reflectance microscopy.

作者信息

Anderson J, Reynolds C, Ringelberg D, Edwards J, Foley K

机构信息

US Army Engineer Research and Development Center, Alexandria, Virginia, USA.

出版信息

J Microsc. 2008 Oct;232(1):130-6. doi: 10.1111/j.1365-2818.2008.02074.x.

Abstract

This paper describes the use of hyperspectral imaging microscopy (HIM) for the characterization and differentiation of live viable versus dead/non-viable bacterial endospores for two species of Bacillus. To accomplish this, endospore-forming Bacillus were cultured and differentiated into endospores. Non-viable endospores were produced using sporicidal methods representing standard decontamination procedures incorporating chlorine and peroxide. Finally, endospore samples were lyophilized to prepare them for spectral analysis. Prior to HIM, baseline spectral reflectance characterizing the endospores was measured using an ASD (400-900 nm) reflectance spectrometer. These data were used to calibrate the resulting spectral image data. HIM data comprising 32 images ranging from 400 to 720 nm (visible to near infrared) were recorded using a C-mounted VariSpec hyperspectral camera attached to an epifluorescent microscope. The images produced by the system record the reflectance and absorption features of endospores based on the structure of the outer coat. Analysis of the HIM data was performed using accepted image and spectral processing routines. Where peroxide was the sporicide, changes in the outer endospore coat contributed to structurally significant visible and near infrared signature differences between live-viable versus dead, non-viable endospores. A statistical test for divergence, a method for scoring spectral structural diversity, also showed the difference between viable and non-viable peroxide killed endospores to be statistically significant. These findings may lead to an improved optical procedure to rapidly identify viable and non-viable endospores in situations of decontamination.

摘要

本文描述了利用高光谱成像显微镜(HIM)对两种芽孢杆菌的活的、有活力的与死的/无活力的细菌芽孢进行表征和区分。为实现这一目标,将形成芽孢的芽孢杆菌进行培养并分化为芽孢。使用代表包含氯和过氧化物的标准去污程序的杀孢子方法产生无活力的芽孢。最后,将芽孢样品冻干以准备进行光谱分析。在进行高光谱成像显微镜分析之前,使用ASD(400 - 900纳米)反射光谱仪测量表征芽孢的基线光谱反射率。这些数据用于校准所得的光谱图像数据。使用连接到落射荧光显微镜的C型安装的VariSpec高光谱相机记录了包含32张范围从400至720纳米(可见光至近红外光)图像的高光谱成像显微镜数据。该系统产生的图像基于芽孢外壳的结构记录芽孢的反射和吸收特征。使用公认的图像和光谱处理程序对高光谱成像显微镜数据进行分析。当过氧化物作为杀孢子剂时,芽孢外膜的变化导致有活力的与死的、无活力的芽孢之间在结构上有显著的可见光和近红外特征差异。一种用于评估光谱结构多样性的统计发散检验也表明,有活力的和经过氧化物处理杀死的无活力芽孢之间的差异具有统计学意义。这些发现可能会带来一种改进的光学程序,用于在去污情况下快速识别有活力和无活力的芽孢。

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