Microbiome and Metagenome Analyses of a Closed Habitat during Human Occupation

Ganesh Babu Malli Mohan; Ceth W Parker; Camilla Urbaniak; Nitin K Singh; Anthony Hood; Jeremiah J Minich; Rob Knight; Michelle Rucker; Kasthuri Venkateswaran

doi:10.1128/mSystems.00367-20

Microbiome and Metagenome Analyses of a Closed Habitat during Human Occupation

mSystems. 2020 Jul 28;5(4):e00367-20. doi: 10.1128/mSystems.00367-20.

Authors

Affiliations

¹ Biotechnology and Planetary Protection Group, Jet Propulsion Laboratory, California Institute of Technology, Pasadena, California, USA.
² Exploration Integration and Science Directorate, NASA Johnson Space Center, Houston, Texas, USA.
³ Marine Biology Research Division, Scripps Institute of Oceanography, University of California San Diego, La Jolla, California, USA.
⁴ Departments of Pediatrics, Bioengineering, and Computer Science & Engineering, and Center for Microbiome Innovation, University of California San Diego, La Jolla, California, USA.
⁵ Biotechnology and Planetary Protection Group, Jet Propulsion Laboratory, California Institute of Technology, Pasadena, California, USA kjvenkat@jpl.nasa.gov.

^# Contributed equally.

Abstract

Microbial contamination during long-term confinements of space exploration presents potential risks for both crew members and spacecraft life support systems. A novel swab kit was used to sample various surfaces from a submerged, closed, analog habitat to characterize the microbial populations. Samples were collected from various locations across the habitat which were constructed from various surface materials (linoleum, dry wall, particle board, glass, and metal), and microbial populations were examined by culture, quantitative PCR (qPCR), microbiome 16S rRNA gene sequencing, and shotgun metagenomics. Propidium monoazide (PMA)-treated samples identified the viable/intact microbial population of the habitat. The cultivable microbial population ranged from below the detection limit to 10⁶ CFU/sample, and their identity was characterized using Sanger sequencing. Both 16S rRNA amplicon and shotgun sequencing were used to characterize the microbial dynamics, community profiles, and functional attributes (metabolism, virulence, and antimicrobial resistance). The 16S rRNA amplicon sequencing revealed abundance of viable (after PMA treatment) Actinobacteria (Brevibacterium, Nesternkonia, Mycobacterium, Pseudonocardia, and Corynebacterium), Firmicutes (Virgibacillus, Staphylococcus, and Oceanobacillus), and Proteobacteria (especially Acinetobacter) on linoleum, dry wall, and particle board (LDP) surfaces, while members of Firmicutes (Leuconostocaceae) and Proteobacteria (Enterobacteriaceae) were high on the glass/metal surfaces. Nonmetric multidimensional scaling determined from both 16S rRNA and metagenomic analyses revealed differential microbial species on LDP surfaces and glass/metal surfaces. The shotgun metagenomic sequencing of samples after PMA treatment showed bacterial predominance of viable Brevibacterium (53.6%), Brachybacterium (7.8%), Pseudonocardia (9.9%), Mycobacterium (3.7%), and Staphylococcus (2.1%), while fungal analyses revealed Aspergillus and Penicillium dominance.IMPORTANCE This study provides the first assessment of monitoring cultivable and viable microorganisms on surfaces within a submerged, closed, analog habitat. The results of the analyses presented herein suggest that the surface material plays a role in microbial community structure, as the microbial populations differed between LDP and metal/glass surfaces. The metal/glass surfaces had less-complex community, lower bioburden, and more closely resembled the controls. These results indicated that material choice is crucial when building closed habitats, even if they are simply analogs. Finally, while a few species were associated with previously cultivated isolates from the International Space Station and MIR spacecraft, the majority of the microbial ecology of the submerged analog habitat differs greatly from that of previously studied analog habitats.

Keywords: Analog habitat; closed habitat; extravehicular activity; functional metagenomics; metagenomics; microbial diversity; microbiome; spacecraft microbiome.