Abstract

Survivors of sepsis often suffer from prolonged post-critical illness syndrome secondary to the immune system’s reprogramming. It is unclear if this process is static and pervasive due to methodological difficulties studying long-term outcomes of sepsis. The purpose of this study is to evaluate transcriptional profiles longitudinally in Drosophila melanogaster in the aftermath of sepsis to provide preliminary data for targets playing a role in post-sepsis immunostasis. Adult Drosophila melanogaster were infected with E. coli, and survivors were euthanized at 7, 14, and 21 days. Control flies were subjected to sham stress. Gene profiling was done with RNA-seq, and potential miRNA factors were computed. Profiling identified 55 unique genes at seven days, 61 unique genes at 14 days, and 78 genes at 21 days in sepsis survivors vs. sham control. Each post-sepsis timepoint had a distinctive transcriptional pattern with a signature related to oxidative stress at seven days, neuronal signal transduction at 14 days, and metabolism at 21 days. Several potential miRNA patterns were computed as potentially affecting several of the genes expressed in sepsis survivors. Our study demonstrated that post-sepsis changes in the transcriptome profile are dynamic and extend well into the Drosophila melanogaster natural life span.

Highlights

  • Under ideal conditions, sepsis eliminates the offending pathogen without significant collateral damage [1,2]

  • Pervasive increase in mortality is likely secondary to the emergence of alternative states of immunostasis that are distinctive from pre-insult health in victims of sepsis [4,5]

  • The transcriptional profiling indicated that flies at 14 days and 21 days post-sepsis had significant changes to their transcriptomes compared to the sham-treated flies (Figure 2B,C)

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Summary

Introduction

Sepsis eliminates the offending pathogen without significant collateral damage [1,2]. The immune system should refocus on repair and regeneration and eventually de-activate. This intricate process can be derailed, resulting in the host’s demise secondary to excessive, abnormal, persistent, or ineffective immune system activation [3,4,5,6]. Experimental studies suggest a metabolome and immune system being affected in the long term [8,9,10]. Epidemiological studies demonstrate progressive organ damage and altered metabolism in sepsis survivors [3,11,12]. Mechanisms affecting access to DNA information (epigenetic, non-coding RNA, miRNA) were suggested to maintain the post-sepsis reprogramming [1,2,8,9,10,13,14]

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