Changes in the Gut Microbiome Community of nonhuman primate following radiation injury

Abstract

<jats:title>Abstract</jats:title> <jats:p>Background Composition and maintenance of the microbiome is vital to gut homeostasis. However, there is limited knowledge regarding the impact of high doses of radiation, which can occur as a result of cancer radiation therapy, nuclear accidents or intentional release of a nuclear or radioactive weapon, on the composition of the gut microbiome. Therefore, we sought to analyze alterations to the gut microbiome of nonhuman primates (NHPs) exposed to high doses of radiation. Methods Fecal samples were collected from 19 NHPs (Chinese rhesus macaques, <jats:italic>Macaca mulatta</jats:italic>) one day prior and one and four days after exposure to 7.4 Gy cobalt-60 gamma-radiation (LD<jats:sub>70 − 80/60</jats:sub>). The 16S V4 rRNA sequences were extracted from each sample, followed by bioinformatics analysis using the QIIME platform. Results Alpha Diversity (Shannon Diversity Index), revealed no major difference between pre- and post-irradiation, whereas Beta diversity analysis showed significant differences in the microbiome after irradiation (day + 4) compared to baseline (pre-irradiation). The Firmicutes/Bacteriodetes ratio, a factor known to be associated with disruption of metabolic homeostasis, decreased from 1.2 to less than 1 post-radiation exposure. <jats:italic>Actinobacillus, Bacteroides, Prevotella (Paraprevotellaceae family) and Veillonella</jats:italic> genera were significantly increased by more than 2-fold and <jats:italic>Acinetobacter</jats:italic> and <jats:italic>Aerococcus</jats:italic> genus were decreased by more than 10-fold post-irradiation. Fifty-two percent (10/19) of animals exposed to radiation demonstrated diarrhea at day 4 post-irradiation. Comparison of microbiome composition of feces from animals with and without diarrhea at day 4 post-irradiation revealed an increase in <jats:italic>Lactobacillus reuteri</jats:italic> associated with diarrhea and a decrease of <jats:italic>Lentisphaerae</jats:italic> and <jats:italic>Verrucomicrobioa</jats:italic> phyla and <jats:italic>Bacteroides</jats:italic> in animals exhibiting diarrhea. Conclusion Our findings demonstrate that substantial alterations in the microbiome composition of NHPs occur following radiation injury and provide insight into early changes with high-dose, whole-body radiation exposure. Future studies will help identify microbiome biomarkers of radiation exposure and develop effective therapeutic intervention to mitigate the radiation injury.</jats:p>