Space flight alters bacterial gene expression and virulence and reveals a role for global regulator Hfq

James W. Wilson(Tulane University), C. Mark Ott, Kerstin Höner zu Bentrup(Tulane University), Rajee Ramamurthy(Tulane University), Laura Quick(National Center for Infectious Diseases), Steffen Porwollik(Sidney Kimmel Cancer Center), Pui Cheng(Sidney Kimmel Cancer Center), Michael McClelland(Sidney Kimmel Cancer Center), George Tsaprailis(University of Arizona), Tim Radabaugh(University of Arizona), Andrea Hunt(University of Arizona), D. Fernandez(National Center for Infectious Diseases), Emily Richter(National Center for Infectious Diseases), Miti Shah, Michelle Kilcoyne, Lokesh Joshi, Mayra Nelman‐Gonzalez(Wyle (United States)), Steve Hing(Ames Research Center), Macarena Parra(Ames Research Center), Paula Dumars(Ames Research Center), Kelly L. Norwood(Kennedy Space Center), Ramona Bober(Kennedy Space Center), Jennifer Devich(Kennedy Space Center), Ashleigh Ruggles(Kennedy Space Center), Carla Goulart(University of Colorado Boulder), Mark Rupert(University of Colorado Boulder), Louis Stodieck(University of Colorado Boulder), Phillip Stafford(Center for Innovation), Luke Catella(Kennedy Space Center), Michael J. Schurr(Tulane University), Kent L. Buchanan(Tulane University), Lisa A. Morici(Tulane University), James McCracken(Tulane University), Paul Allen(Tulane University), C. Baker-Coleman(Tulane University), Timothy G. Hammond(Tulane University), Jörg Vogel(Max Planck Institute for Infection Biology), Randy J. Nelson(Arizona State University), D. L. Pierson, Heidemarie M. Stefanyshyn-Piper(National Aeronautics and Space Administration), Cheryl A. Nickerson(Tulane University)
Proceedings of the National Academy of Sciences
September 28, 2007
Cited by 513Open Access
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Abstract

A comprehensive analysis of both the molecular genetic and phenotypic responses of any organism to the space flight environment has never been accomplished because of significant technological and logistical hurdles. Moreover, the effects of space flight on microbial pathogenicity and associated infectious disease risks have not been studied. The bacterial pathogen Salmonella typhimurium was grown aboard Space Shuttle mission STS-115 and compared with identical ground control cultures. Global microarray and proteomic analyses revealed that 167 transcripts and 73 proteins changed expression with the conserved RNA-binding protein Hfq identified as a likely global regulator involved in the response to this environment. Hfq involvement was confirmed with a ground-based microgravity culture model. Space flight samples exhibited enhanced virulence in a murine infection model and extracellular matrix accumulation consistent with a biofilm. Strategies to target Hfq and related regulators could potentially decrease infectious disease risks during space flight missions and provide novel therapeutic options on Earth.


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