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Microbial Monitoring of Common Opportunistic Pathogens by Comparing Multiple Real-Time PCR Platforms for Potential Space Applications

机译:通过比较潜在空间应用的多个实时PCR平台对常见机会病原菌进行微生物监测

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摘要

Because the International Space Station is a closed environment with rotations of astronauts and equipment that each introduce their own microbial flora, it is necessary to monitor the air, surfaces, and water for microbial contamination. Current microbial monitoring includes labor- and time-intensive methods to enumerate total bacterial and fungal cells, with limited characterization, during in-flight testing. Although this culture-based method is sufficient for monitoring the International Space Station, on future long-duration missions more detailed characterization will need to be performed during flight, as sample return and ground characterization may not be available. At a workshop held in 2011 at NASA's Johnson Space Center to discuss alternative methodologies and technologies suitable for microbial monitoring for these long-term exploration missions, molecular-based methodologies such as polymerase chain reaction (PCR) were recommended. In response, a multi-center (Marshall Space Flight Center, Johnson Space Center, Jet Propulsion Laboratory, and Kennedy Space Center) collaborative research effort was initiated to explore novel commercial-off-the-shelf hardware options for space flight environmental monitoring. The goal was to evaluate quantitative or semi-quantitative PCR approaches for low-cost in-flight rapid identification of microorganisms that could affect crew safety. The initial phase of this project identified commercially available platforms that could be minimally modified to perform nominally in microgravity. This phase was followed by proof-of-concept testing of the highest qualifying candidates with a universally available challenge organism, Salmonella enterica. The analysis identified two technologies that were able to perform sample-to-answer testing with initial cell sample concentrations between 50 and 400 cells. In addition, the commercial systems were evaluated for initial flight safety and readiness.
机译:由于国际空间站是一个封闭的环境,宇航员和设备轮流旋转,每一个都会引入自己的微生物菌群,因此有必要监测空气,表面和水中的微生物污染情况。当前的微生物监测包括费力和时间密集的方法,以在飞行测试中以有限的特征枚举总细菌和真菌细胞。尽管这种基于文化的方法足以监视国际空间站,但在未来的长期任务中,由于可能无法获得样本返回和地面特征,因此在飞行过程中将需要进行更详细的特征描述。在2011年于美国国家航空航天局(NASA)的约翰逊太空中心(Johnson Space Center)举行的研讨会上,讨论了适用于这些长期探索任务的微生物监测的替代方法和技术,建议采用基于分子的方法,例如聚合酶链反应(PCR)。作为响应,发起了一个多中心(马歇尔太空飞行中心,约翰逊太空中心,喷气推进实验室和肯尼迪太空中心)的合作研究工作,以探索用于太空飞行环境监测的新型商用现货硬件选项。目的是评估定量或半定量PCR方法,以低成本在飞行中快速识别可能影响机组人员安全的微生物。该项目的初始阶段确定了可商购的平台,可以对其进行最小程度的修改以在名义上实现微重力。在此阶段之后,使用普遍可用的挑战性生物沙门氏菌对最高合格的候选人进行概念验证测试。分析确定了两种技术,这些技术能够对初始细胞样品浓度在50到400个细胞之间进行样品到答案的测试。此外,还对商用系统的初始飞行安全性和准备情况进行了评估。

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