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would like to thank Matthew Lera (M.L.), Amy Gresser (A.G.) and Kevin Martin (K.M.) for spaceflight project support"},{"name":"DOI","value":"10.26030/5cd0-qt74"},{"name":"Data Source Accession","value":"GSE138116"},{"name":"Data Source Link","value":"https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE138116"},{"name":"Experiment Platform","value":"FIT (Fly Immunity and Tumors) cassette and changeout platform"},{"name":"Flight Program","value":"International Space Station (ISS)"},{"name":"Funding","value":"NASA\u2019s Space Life and Physical Sciences Research Program (SLPSRA) for the following grants to S.B.: NNX13AN38G and NNX15AB42G"},{"name":"Identifiers","value":""},{"name":"Managing NASA Center","value":"Ames Research Center (ARC)"},{"name":"Mission End","value":"02/11/2015"},{"name":"Mission Link","value":"https://osdr.nasa.gov/bio/repo/data/missions/SpaceX-5"},{"name":"Mission Name","value":"SpaceX-5"},{"name":"Mission Start","value":"01/10/2015"},{"name":"Project 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Additionally, there is growing evidence that suggests that not only is the immune system being altered, but the pathogens that infect the host are significantly influenced by spaceflight and ground-based spaceflight conditions. In this study, we demonstrate that Serratia marcescens (strain Db11) was significantly more lethal to Drosophila melanogaster after growth on the International Space Station than ground-based controls, but that the host immune system is not significantly altered amongst known immune genes. High-throughput sequencing of wild-type (w1118) adult hosts infected with either space or ground-reared S. marcescens revealed few changes in gene expression, with 11 genes significantly differentially expressed (q-values  less than 0.05) and only one gene related to the immune system. This data supports the main findings of the paper, which state that both spaceflight and low-shear modeled microgravity conditions increase the virulence of this pathogen, independent of the host immune system. This data, which shows that there are no significant immune-related changes to the host when infected with space-grown sample compared to ground-grown sample, provides further evidence that there are likely phenotypic changes to the pathogen itself that is causing increased virulence in spaceflight and in low-shear modeled microgravity. RNA was extracted in triplicate from 2 pooled adult (2-3 day old female) Drosophila melanogaster (w1118) per treatment, with 4 total treatment groups (no injection control, sham injection with PBS, ground bacteria-injected, and space bacteria-injected) with poly(A)+ RNA libraries. 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A runsheet was generated with dp_tools (version 1.3.8) and the runsheet and quantification data were imported to R (version 4.4.2) with tximport (version 1.34.0) and normalized with DESeq2 (version 1.46.0) median of ratios method. Normalized gene counts were subject to differential expression analysis. Differential expression analysis was performed in R (version 4.4.2) using DESeq2 (version 1.46.0); all groups were compared pairwise using the Wald test and the likelihood ratio test was used to generate the F statistic p-value. 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