Microgravity validation of a novel system for RNA isolation and multiplex quantitative real time PCR analysis of gene expression on the International Space Station

The International Space Station (ISS) National Laboratory is dedicated to studying the effects of space on life and physical systems, and to developing new science and technologies for space exploration. A key aspect of achieving these goals is to operate the ISS National Lab more like an Earth-based laboratory, conducting complex end-to-end experimentation, not limited to simple microgravity exposure. Towards that end NASA developed a novel suite of molecular biology laboratory tools, reagents, and methods, named WetLab-2, uniquely designed to operate in microgravity, and to process biological samples for real-time gene expression analysis on-orbit. This includes a novel fluidic RNA Sample Preparation Module and fluid transfer devices, all-in-one lyophilized PCR assays, centrifuge, and a real-time PCR thermal cycler. Here we describe the results from the WetLab-2 validation experiments conducted in microgravity during ISS increment 47/SPX-8. Specifically, quantitative PCR was performed on a concentration series of DNA calibration standards, and Reverse Transcriptase-quantitative PCR was conducted on RNA extracted and purified on-orbit from frozen Escherichia coli and mouse liver tissue. Cycle threshold (Ct) values and PCR efficiencies obtained on-orbit from DNA standards were similar to Earth (1 g) controls. Also, on-orbit multiplex analysis of gene expression from bacterial cells and mammalian tissue RNA samples was successfully conducted in about 3 h, with data transmitted within 2 h of experiment completion. Thermal cycling in microgravity resulted in the trapping of gas bubbles inside septa cap assay tubes, causing small but measurable increases in Ct curve noise and variability. Bubble formation was successfully suppressed in a rapid follow-up on-orbit experiment using standard caps to pressurize PCR tubes and reduce gas release during heating cycles. The WetLab-2 facility now provides a novel operational on-orbit research capability for molecular biology and demonstrates the feasibility of more complex wet bench experiments in the ISS National Lab environment.

[1]  E. Blaber,et al.  Mechanical unloading of bone in microgravity reduces mesenchymal and hematopoietic stem cell-mediated tissue regeneration. , 2014, Stem cell research.

[2]  M Lebert,et al.  The influence of microgravity on Euglena gracilis as studied on Shenzhou 8. , 2014, Plant biology.

[3]  Klaus Slenzka,et al.  Fundamentals of space biology : research on cells, animals, and plants in space , 2006 .

[4]  Piero Pianetta,et al.  Microgravity Induces Pelvic Bone Loss through Osteoclastic Activity, Osteocytic Osteolysis, and Osteoblastic Cell Cycle Inhibition by CDKN1a/p21 , 2013, PloS one.

[5]  T. Sugita,et al.  Comprehensive analysis of the skin fungal microbiota of astronauts during a half-year stay at the International Space Station. , 2016, Medical mycology.

[6]  L. Stodieck,et al.  Microarray analysis of spaceflown murine thymus tissue reveals changes in gene expression regulating stress and glucocorticoid receptors , 2010, Journal of cellular biochemistry.

[7]  Hanns-Christian Gunga,et al.  Gene Expression Profiling in Slow-Type Calf Soleus Muscle of 30 Days Space-Flown Mice , 2017, PloS one.

[8]  G. Gerard,et al.  Reverse Transcriptase , 1997, Molecular biotechnology.

[9]  Yuzuru Takamura,et al.  Circumventing air bubbles in microfluidic systems and quantitative continuous-flow PCR applications , 2006, Analytical and bioanalytical chemistry.

[10]  S. Wyatt,et al.  Transcriptome and proteome responses in RNAlater preserved tissue of Arabidopsis thaliana , 2017, PloS one.

[11]  Millie Hughes-Fulford,et al.  Spaceflight alters expression of microRNA during T‐cell activation , 2011, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[12]  R. Abramson,et al.  Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[13]  Roland Zengerle,et al.  Digital droplet PCR on disk. , 2016, Lab on a chip.

[14]  Douglas J. Botkin,et al.  Nanopore DNA Sequencing and Genome Assembly on the International Space Station , 2016, bioRxiv.

[15]  Ruth K. Globus,et al.  Microgravity Reduces the Differentiation and Regenerative Potential of Embryonic Stem Cells , 2015, Stem cells and development.

[16]  Santiago Pindado,et al.  Surface tension and microgravity , 2014 .

[17]  R. Borrow,et al.  Contamination and Sensitivity Issues with a Real-Time Universal 16S rRNA PCR , 2000, Journal of Clinical Microbiology.

[18]  H. Hogrefe,et al.  Novel mutations in Moloney Murine Leukemia Virus reverse transcriptase increase thermostability through tighter binding to template-primer , 2008, Nucleic acids research.

[19]  Alan Feiveson,et al.  Cellular responses and gene expression profile changes due to bleomycin-induced DNA damage in human fibroblasts in space , 2017, PloS one.

[20]  Comparing protocols for preparation of DNA-free total yeast RNA suitable for RT-PCR , 2005, BMC Molecular Biology.

[21]  H. Ochman,et al.  The Nature and Dynamics of Bacterial Genomes , 2006, Science.

[22]  M. Saito,et al.  An optimal design method for preventing air bubbles in high-temperature microfluidic devices , 2010, Analytical and bioanalytical chemistry.

[23]  Bernhards Ogutu,et al.  Sample-ready multiplex qPCR assay for detection of malaria , 2014, Malaria Journal.

[24]  M. Bizzarri,et al.  How Microgravity Affects the Biology of Living Systems , 2015, BioMed research international.

[25]  Ali Nadim,et al.  Mechanical Disruption of Lysis-Resistant Bacterial Cells by Use of a Miniature, Low-Power, Disposable Device , 2011, Journal of Clinical Microbiology.

[26]  Michael W Pfaffl,et al.  RNA integrity and the effect on the real-time qRT-PCR performance. , 2006, Molecular aspects of medicine.

[27]  Angela M Yu,et al.  Nanopore sequencing in microgravity , 2015, npj Microgravity.