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利用纳米孔测序技术在国际空间站上实时进行非培养微生物分析。

Real-Time Culture-Independent Microbial Profiling Onboard the International Space Station Using Nanopore Sequencing.

机构信息

JES Tech, Houston, TX 77058, USA.

UCSC Genomics Institute, University of California, Santa Cruz, CA 95064, USA.

出版信息

Genes (Basel). 2021 Jan 16;12(1):106. doi: 10.3390/genes12010106.

Abstract

For the past two decades, microbial monitoring of the International Space Station (ISS) has relied on culture-dependent methods that require return to Earth for analysis. This has a number of limitations, with the most significant being bias towards the detection of culturable organisms and the inherent delay between sample collection and ground-based analysis. In recent years, portable and easy-to-use molecular-based tools, such as Oxford Nanopore Technologies' MinION™ sequencer and miniPCR bio's miniPCR™ thermal cycler, have been validated onboard the ISS. Here, we report on the development, validation, and implementation of a swab-to-sequencer method that provides a culture-independent solution to real-time microbial profiling onboard the ISS. Method development focused on analysis of swabs collected in a low-biomass environment with limited facility resources and stringent controls on allowed processes and reagents. ISS-optimized procedures included enzymatic DNA extraction from a swab tip, bead-based purifications, altered buffers, and the use of miniPCR and the MinION. Validation was conducted through extensive ground-based assessments comparing current standard culture-dependent and newly developed culture-independent methods. Similar microbial distributions were observed between the two methods; however, as expected, the culture-independent data revealed microbial profiles with greater diversity. Protocol optimization and verification was established during NASA Extreme Environment Mission Operations (NEEMO) analog missions 21 and 22, respectively. Unique microbial profiles obtained from analog testing validated the swab-to-sequencer method in an extreme environment. Finally, four independent swab-to-sequencer experiments were conducted onboard the ISS by two crewmembers. Microorganisms identified from ISS swabs were consistent with historical culture-based data, and primarily consisted of commonly observed human-associated microbes. This simplified method has been streamlined for high ease-of-use for a non-trained crew to complete in an extreme environment, thereby enabling environmental and human health diagnostics in real-time as future missions take us beyond low-Earth orbit.

摘要

在过去的二十年中,国际空间站(ISS)的微生物监测一直依赖于需要返回地球进行分析的依赖于培养的方法。这存在许多局限性,其中最显著的是偏向于可培养生物的检测以及从样本采集到地面分析之间固有的延迟。近年来,便携式且易于使用的基于分子的工具,例如牛津纳米孔技术的 MinION™测序仪和 miniPCR bio 的 miniPCR™热循环仪,已经在国际空间站上得到验证。在这里,我们报告了一种拭子到测序仪方法的开发、验证和实施,该方法为国际空间站上实时微生物分析提供了一种非培养的解决方案。方法开发侧重于在具有有限设施资源和严格控制允许过程和试剂的低生物量环境中分析拭子。针对国际空间站进行了优化的程序包括从拭子尖端进行酶促 DNA 提取、基于珠子的纯化、改变缓冲液以及使用 miniPCR 和 MinION。通过与当前标准的依赖于培养的方法和新开发的非依赖于培养的方法进行广泛的地面评估来进行验证。两种方法观察到相似的微生物分布;但是,正如预期的那样,非依赖于培养的方法揭示了更多样化的微生物分布。分别在 NASA 极端环境任务操作(NEEMO)模拟任务 21 和 22 中进行了协议优化和验证。通过模拟测试获得的独特微生物分布验证了拭子到测序仪方法在极端环境中的适用性。最后,两名机组人员在国际空间站上进行了四次独立的拭子到测序仪实验。从国际空间站拭子中鉴定出的微生物与历史上基于培养的微生物数据一致,主要由常见的与人相关的微生物组成。这种简化的方法已经针对非训练机组人员在极端环境中的高易用性进行了优化,从而能够实时进行环境和人类健康诊断,因为未来的任务将把我们带离近地轨道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50cf/7830261/282f324ac150/genes-12-00106-g001.jpg

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