TY - JOUR
T1 - Alterations in the virulence potential of enteric pathogens and bacterial-host cell interactions under simulated microgravity conditions
AU - Chopra, V.
AU - Fadl, A. A.
AU - Sha, J.
AU - Chopra, S.
AU - Galindo, C. L.
AU - Chopra, A. K.
N1 - Funding Information:
Salmonella typhimurium cultures were grown at 37°C in HARVs (NG versus SMG environment) to an optical density (OD600nm) of 0.6 and RNA was isolated using RiboPure-Bacterial RNA isolation kit (Ambion, Austin, TX), according to manufacturer’s instructions. After processing, the resulting labeled cDNA was applied to S. typhimurium LT2 genome microarrays, developed by the Institute for Genomic Research (TIGR, Rockville, MD) and provided by the Pathogen Functional Genome Resource Center (PFGRC) of the National Institutes of Health. The genome microarrays consisted of polymerase chain reaction (PCR) products representing segments of 5405 open reading frames from strain LT2. Preparation of fluorescence probes, hybridization, initial data processing, and normalization were performed by the Genomic Core facility (UTMB, Galveston, TX). To generate reproducible and statistically significant data, three microarray slides were used for each experiment, and three independent experiments were performed. The microarray data were analyzed as previously described (Galindo et al., 2003).
Funding Information:
This work was supported by a grant from the Advanced Technology Program of Texas Higher Education Coordinating Board. Cristi L. Galindo, a predoctoral fellow, obtained funding from the National Science Foundation. A. A. Fadl received support from the McLaughlin Postdoctoral Fellowship. Dr. T. Wood, from the department of Human Biological Chemistry and Genetics (HBC&G) at UTMB, provided the facility of his core laboratory for microarray studies. Dr. A. Kurosky, from the Department of HBC&G at UTMB, provided the facility of his core laboratory for proteomics studies. Dr. V. Popov, from the Department of Pathology at UTMB, provided the facility of his core laboratory for electron microscopy studies. We appreciate the help rendered by summer undergraduate students J. Wolfe, A. Randall, and K. Hansen, high school teacher D. Baker, and former graduate student D. Ribardo in performing some of the experiments. Excellent technical assistance provided by K. Kuhl and graphics expertise provided by Microsoft professional Celso Gutierrez, Jr., are also acknowledged.
PY - 2006
Y1 - 2006
N2 - Host immune mechanisms were proposed to decline under microgravity conditions during spaceflights, which might result in severe infections in astronauts. Therefore, it was important to investigate the effects of microgravity on infecting organisms and their interaction with host cells. Data showed that simulated microgravity (SMG) conditions markedly increased production of the enterotoxigenic Escherichia coli (ETEC) heat-labile enterotoxin, which induced fluid secretory responses in a mouse model. SMG also enhanced production of tumor necrosis factor-α in murine macrophages infected with enteropathogenic E. coli (EPEC). In a similar fashion, simulated microgravity conditions augmented the invasive potential of Salmonella enterica serovar typhimurium and enhanced production of tumor necrosis-factor α in S. typhimurium -infected epithelial cells. Furthermore, coculturing of macrophages and S. typhimurium in a simulated microgravity environment resulted in activation of stress-associated mitogen-activated protein kinase kinase 4. Using the antiorthostatic tail suspension mouse model, which simulates some aspects of microgravity, oral inoculation of S. typhimurium markedly reduced the 50% lethal dose compared to mice infected under normal gravitational conditions. Microarray analysis revealed simulated microgravity-induced alterations in the expression of 22 genes in S. typhimurium , and protein expression profiles were altered in both EPEC and S. typhimurium , based on two-dimensional gel electrophoresis. These studies indicated alterations in the virulence potential of bacteria and in host responses to these pathogens under simulated microgravity conditions, which may represent an important environmental signal. Such studies are essential for better understanding bacterial-host cell interactions, particularly in the context of spaceflights and space habitations of long duration. Copyright
AB - Host immune mechanisms were proposed to decline under microgravity conditions during spaceflights, which might result in severe infections in astronauts. Therefore, it was important to investigate the effects of microgravity on infecting organisms and their interaction with host cells. Data showed that simulated microgravity (SMG) conditions markedly increased production of the enterotoxigenic Escherichia coli (ETEC) heat-labile enterotoxin, which induced fluid secretory responses in a mouse model. SMG also enhanced production of tumor necrosis factor-α in murine macrophages infected with enteropathogenic E. coli (EPEC). In a similar fashion, simulated microgravity conditions augmented the invasive potential of Salmonella enterica serovar typhimurium and enhanced production of tumor necrosis-factor α in S. typhimurium -infected epithelial cells. Furthermore, coculturing of macrophages and S. typhimurium in a simulated microgravity environment resulted in activation of stress-associated mitogen-activated protein kinase kinase 4. Using the antiorthostatic tail suspension mouse model, which simulates some aspects of microgravity, oral inoculation of S. typhimurium markedly reduced the 50% lethal dose compared to mice infected under normal gravitational conditions. Microarray analysis revealed simulated microgravity-induced alterations in the expression of 22 genes in S. typhimurium , and protein expression profiles were altered in both EPEC and S. typhimurium , based on two-dimensional gel electrophoresis. These studies indicated alterations in the virulence potential of bacteria and in host responses to these pathogens under simulated microgravity conditions, which may represent an important environmental signal. Such studies are essential for better understanding bacterial-host cell interactions, particularly in the context of spaceflights and space habitations of long duration. Copyright
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U2 - 10.1080/15287390500361792
DO - 10.1080/15287390500361792
M3 - Article
C2 - 16760141
AN - SCOPUS:33746748794
VL - 69
SP - 1345
EP - 1370
JO - Journal of Toxicology and Environmental Health - Part A: Current Issues
JF - Journal of Toxicology and Environmental Health - Part A: Current Issues
SN - 1528-7394
IS - 14
ER -