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热固定可使病毒和细菌病原体失活,并与下游基质辅助激光解吸电离质谱组织成像兼容。

Heat fixation inactivates viral and bacterial pathogens and is compatible with downstream MALDI mass spectrometry tissue imaging.

作者信息

Cazares Lisa H, Van Tongeren Sean A, Costantino Julie, Kenny Tara, Garza Nicole L, Donnelly Ginger, Lane Douglas, Panchal Rekha G, Bavari Sina

机构信息

Henry M. Jackson Foundation, Maryland, USA.

DoD Biotechnology High Performance Computing Software Applications Institute (BHSAI/TATRC), Frederick, Maryland, USA.

出版信息

BMC Microbiol. 2015 May 13;15:101. doi: 10.1186/s12866-015-0431-7.

Abstract

BACKGROUND

Tissue samples should be fixed and permanently stabilized as soon as possible ex-vivo to avoid variations in proteomic content. Tissues collected from studies involving infectious microorganisms, must face the additional challenge of pathogen inactivation before downstream proteomic analysis can be safely performed. Heat fixation using the Denator Stabilizor System (Gothenburg, Sweden) utilizes conductive heating, under a mild vacuum, to rapidly eliminate enzymatic degradation in tissue samples. Although many studies have reported on the ability of this method to stop proteolytic degradation and other sample changes immediately and permanently, pathogen inactivation has not been studied.

RESULTS

We examined the ability of the heat fixation workflow to inactivate bacterial and viral pathogens and the suitability of this tissue for Matrix Assisted Laser Desorption Ionization mass spectrometry imaging (MALDI-MSI). Mice were infected with viral or bacterial pathogens representing two strains of Venezuelan Equine Encephalitis virus (VEEV) and two strains of Burkholderia. Additionally, a tissue mimetic model was employed using Escherichia, Klebsiella and Acinetobacter isolates. Infected tissue samples harvested from each animal or mimetic model were sectioned in half. One half was heat fixed and the other remained untreated. Lysates from each sample were checked for organism viability by performing plaque (infectivity) assays or plating on nutrient agar for colony forming unit (CFU) calculation. Untreated infected control tissue demonstrated the presence of each viable pathogen by positive plaque or colony formation, whereas heat fixation resulted in complete inactivation of both the viral and bacterial pathogens. MALDI-MSI images produced from heat fixed tissue were reflective of molecular distributions within brain, spleen and lung tissue structures.

CONCLUSIONS

We conclude that heat fixation inactivates viral and bacterial pathogens and is compatible with proteomic analysis by MALDI-MSI. This treatment will enable the use of infected tissue from studies performed in bio-safety level 3 laboratories with VEEV and Burkholderia to be safely used for proteomic, small molecule drug detection, and imaging mass spectrometry analysis.

摘要

背景

组织样本离体后应尽快固定并永久稳定,以避免蛋白质组含量发生变化。从涉及传染性微生物的研究中收集的组织,在能够安全地进行下游蛋白质组分析之前,必须面对病原体灭活这一额外挑战。使用Denator Stabilizor系统(瑞典哥德堡)进行热固定,利用传导加热,在轻度真空下快速消除组织样本中的酶促降解。尽管许多研究报告了该方法立即且永久停止蛋白水解降解和其他样本变化的能力,但尚未对病原体灭活进行研究。

结果

我们研究了热固定流程灭活细菌和病毒病原体的能力,以及这种组织用于基质辅助激光解吸电离质谱成像(MALDI-MSI)的适用性。用代表两株委内瑞拉马脑炎病毒(VEEV)和两株伯克霍尔德菌的病毒或细菌病原体感染小鼠。此外,使用大肠杆菌、克雷伯菌和不动杆菌分离株建立了组织模拟模型。从每只动物或模拟模型中采集的感染组织样本切成两半。一半进行热固定,另一半不做处理。通过进行噬斑(感染性)测定或在营养琼脂平板上培养以计算菌落形成单位(CFU),检查每个样本的裂解物中生物体的活力。未经处理的感染对照组织通过阳性噬斑或菌落形成证明存在每种活病原体,而热固定导致病毒和细菌病原体完全失活。从热固定组织生成的MALDI-MSI图像反映了脑、脾和肺组织结构内的分子分布。

结论

我们得出结论,热固定可灭活病毒和细菌病原体,并且与MALDI-MSI蛋白质组分析兼容。这种处理将使来自生物安全3级实验室使用VEEV和伯克霍尔德菌进行的研究中的感染组织能够安全地用于蛋白质组学、小分子药物检测和成像质谱分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d71/4429342/626ab28f746e/12866_2015_431_Fig1_HTML.jpg

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