At Arizona State University's Biodesign Institute, Cheryl Nickerson and her team have been investigating the intriguing effects of spaceflight on microbial pathogens.
In a new paper appearing in the current issue of the journal PLOS ONE, the team reports their recent work examining spaceflight-induced responses in and infectious disease potential of the fungal pathogen, Candida albicans. Lead author Aurélie Crabbé joins a multi-institute collaborative research team in this study, which represents the first global gene expression profiling and phenotypic characterization of a fungal pathogen during spaceflight.
The new study reports the differential regulation of 452 genes in spaceflight-cultured C. albicans, compared to fungal cells cultured under otherwise identical ground-based conditions. The expression of a wide variety of functionally diverse gene families was altered, including those regulating cell aggregation and budding, biofilm formation and resistance to pathogenesis-related stresses and antifungal drugs. In agreement with the gene expression data, C. albicans demonstrated enhanced cell aggregation and a differential budding pattern in response to growth under microgravity conditions.
"Our research has important medical implications for spaceflight safety and may also shed light on the as-yet poorly understood mechanisms of pathogen infection and disease trajectory, both in space and on earth," according to Crabbé.
Candida is a type of fungus--a eukaryotic microorganism. It is often found in soils and water and is ubiquitous in man-made environments, including the space shuttle and International Space Station. C. albicans is part of the normal flora of human beings, present on the skin, in the oral cavity, and in the gastrointestinal, urogenital and vaginal tracts.
Although it exists in 80 percent of the human population as an unobtrusive guest, C. albicans is an opportunistic pathogen, turning hostile under particular conditions. This process involves a transition from unicellular, yeast-like cells to a multicellular, filamentous and invasive form, triggered by specific environmental cues.
The pathogen in its transformed state poses a significant infectious disease risk. It is a particularly tenacious foe in immunocompromised individuals, like those undergoing treatment for AIDS, chemotherapy or bone marrow transplantation, and can also cause disease in normal individuals taking antibiotics. The unchecked fungus can cause superficial mucous membrane infections (such as thrush) but also sometimes leads to systemic candidiasis, a potentially lethal condition.
In the current study, fungal cell cultures of C. albicans were flown aboard the space shuttle Atlantis, on NASA Space Shuttle Mission STS-115. C. albicans is a considerable concern during spaceflight missions, as the harsh and rigorous environment encountered by astronauts weakens their immune system, leaving space voyagers especially vulnerable. Indeed, such infections are not uncommon among flight crews and are of grave concern during longer missions.
While the phenotypic changes induced by spaceflight were consistent with features associated with increased virulence, the spaceflight C. albicans cultures did not exhibit heightened virulence when mice were exposed through i.p. injection. Further research is required to conclusively determine if spaceflight alters C. albicans virulence. Of particular importance is to assess whether the compromised immune system of astronauts could influence their susceptibility to C. albicans infecti on. The propensity of C. albicans to cause mucosal and deep tissue infections, coupled with the immunosuppressive condition characteristic of flight crew members, make a more thorough evaluation of virulence potential imperative.
The new research is the first to demonstrate global regulation induced by spaceflight in a eukaryotic pathogen--an essential step in disease-risk assessment. Results from this research will also serve to direct future spaceflight experiments and will allow scientists to further enhance their understanding of the response of microorganisms to the microgravity environment. The potential role of transcriptional regulators like Cap1, as well as other characteristics associated with a virulence phenotype are fertile ground for future study.
"This research serves as a springboard to inform ongoing spaceflight studies of Candida albicans, as well as to put our ground-based studies into context," says co-author Sheila Nielsen-Priess, of the Department of Immunology and Infectious Disease, Montana State University. "The ultimate goal is to achieve a better understanding of how C. albicans causes infection, in space or here on Earth. Studying the yeast in the extreme environment of microgravity provides an additional window through which to view the cellular response and to better understand its behavior."
The Nickerson group has a long and productive track record of examining the effects of microgravity on various pathogenic microorganisms known to cause illness in humans. In previous studies, they sent a variety of pathogens for study aboard several different space shuttle missions to assess alterations in global gene and protein expression, morphology and virulence.
Among the more remarkable findings of this research are that pathogens globally alter their gene expression and disease-related properties during spaceflight culture in ways that cannot be observed during traditional experimental approaches, where the force of gravity can mask key responses.
One of the key factors influencing gene expression and physiological alterations to pathogenic cells in microgravity--both prokaryotic and eukaryotic--is a property known as fluid-shear. This refers to the level of abrasion caused by extracellular fluids flowing over cell surfaces.
Under microgravity conditions, fluid-shear is reduced, triggering changes in gene expression and associated phenotypic alterations. Such changes may in fact mimic conditions microbes encounter on earth, for example, regions in the human body where fluid-shear is similarly reduced, including in the gastrointestinal, urogenital and respiratory tracts.
Previously, the Nickerson team reported the landmark finding that spaceflight increased the virulence of Salmonella typhimurium, which was independently validated on two separate Shuttle missions. Their follow-up studies with NASA collaborators showed altered disease-related responses for Pseudomonas aeruginosa and a methicillin resistant Staphylococcus aureus (MRSA) strain when exposed to either spaceflight or spaceflight-analogue conditions produced on earth.
To simulate microgravity on earth, an apparatus known as a rotating wall vessel (RWV) bioreactor is used. This cylindrical device gently rotates cells, keeping them in suspension in low fluidic conditions relevant to those they encounter in spaceflight and in the human body during infection.
Nickerson and her colleagues demonstrated that a conserved protein known as Hfq serves as a master regulator that controls Salmonella and other bacterial pathogen responses to spaceflight and spaceflight analogue environments. The findings are significant, not only for understanding the mechanisms of bacterial gene regulation but also as a potential target for future therapies against pathogenic infection.
"I am pleased that our team's spaceflight research continues to provide compelling evidence of the value of the unique microgravity platform to unveil novel molecular and cellular responses in a variety of different human pathogens that are relevant to how they cause infection and disease in the body," says Nickerson. The results of this work have downstream implications for the health of both astronauts and the general public on Earth.
The research team consisted of the following participants:
Aurélie Crabbé2,†, Sheila M. Nielsen-Preiss3,†, Christine M. Woolley3, Jennifer Barrila2, Kent Buchanan4,5, James McCracken5,6, Diane O. Inglis7, Stephen C. Searles3, Mayra A. Nelman-Gonzalez8, C. Mark Ott9, James W. Wilson2,5,10, Duane L. Pierson9, Heidemarie M. Stefanyshyn-Piper11, Linda E. Hyman3,12, Cheryl A. Nickerson1,2,5,1 School of Life Sciences, Arizona State University, Tempe, AZ, U.S.A.;2 Center for Infectious Diseases and Vaccinology, The Biodesign Institute, Arizona State University, Tempe, AZ, U.S.A.; 3 Department of Immunology and Infectious Disease, Montana State University, Bozeman, MT, U.S.A.; 4 Department of Biology, Oklahoma City University, Oklahoma City, OK, U.S.A.; 5 Department of Microbiology and Immunology, Program in Molecular Pathogenesis and Immunity, Tulane University Health Sciences Center, New Orleans, LA, U.S.A.; 6 Diabetes and Obesity Center, University of Louisville, Louisville, KY, U.S.A.; 7Department of Genetics, Stanford University Medical School, Stanford, CA, U.S.A.; 8 Wyle Science, Technology and Engineering Group, Houston, TX, U.S.A.; 9 Biomedical Research and Environmental Sciences Division, NASA Johnson Space Center, Houston, TX, U.S.A.; 10Department of Biology, Villanova University, Villanova, PA, U.S.A.; 11 Astronaut Office, NASA Johnson Space Center, Houston, TX, U.S.A.; 12Boston University School of Medicine, Boston, MA, U.S.A
Written by Richard Harth
Science Writer: The Biodesign Institute