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.

Highlights

  • Microbial monitoring of crewed spacecraft has been an important aspect of infectious disease mitigation since early crewed missions [1,2,3,4,5]

  • Because there is not currently bead beating hardware capable of processing swab tips available for use onboard the International Space Station (ISS), flight-compatible protocols were developed around swab tips that would fit within PCR tubes, utilizing enzymatic and heat-based cell lysis methods

  • The procedure was developed to ensure that immediately following sample collection, the swab tip was transferred to a PCR tube containing the lysis solution while still at the sampling location

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Summary

Introduction

Microbial monitoring of crewed spacecraft has been an important aspect of infectious disease mitigation since early crewed missions [1,2,3,4,5]. On the International Space Station (ISS), all surface materials must be cleanable to a given level of colony forming units (CFU), high-efficiency particulate air (HEPA) filtration is required for the air system, and the Water Processor Assembly (WPA) has mechanisms to reduce microbial contamination, including catalytic oxidation, filtration, and the addition of a biocide [1,2]. Despite these preventative measures, microorganisms cannot, and should not, be completely eliminated from the spaceflight environment. While remediation of areas exceeding the CFU limits can occur within roughly a week of sample collection, remediation due to the presence of organisms that could present a risk to the vehicle or crew takes substantially longer

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