Oxygen therapy is widely used in critically ill patients and usually exposes patients
to hyperoxia, resulting in adverse clinical outcomes [1]. Many studies have explored
the adverse effects of hyperoxia in the lung, heart, and brain. Gut microbiota plays
an important role in human health and disease [2]. However, the impact of hyperoxia
on gut microbiota remains unclear, and studies are limited and have yielded contradictory
results [3, 4]. We attempted to explore the effect of hyperoxia on gut microbiota
by exposing rats to normobaric oxygen for 7 days.
The experimental protocol was approved by the Institutional Animal Care and Use Committee
at Zunyi Medical University. Male Sprague-Dawley rats (8 weeks of age, all the same
strain) were obtained from the Kavans Laboratory Animal Company (Changzhou, China).
All animals had free access to the same chow and water and were maintained in the
same containers. The rats were pooled and randomly divided into the control group
(n = 9) and oxygen group (n = 9). The oxygen group was exposed to 80% normobaric oxygen
for 7 days in a hyperoxia chamber (Changjintech, Changsha, China). The control group
was reared in another chamber with room air for 7 days. Fecal pellets were collected
at days 0 and 7, and DNA was extracted and prepared for 16S ribosomal RNA V3–V4 region
gene sequencing. Sequencing libraries were sequenced on an Illumina MiSeq platform
at Biomarker Technologies Company (Beijing, China). Strain composition analysis and
beta diversity analysis were performed. We used linear discriminant analysis (LDA)
with effect size measurements for the quantitative analysis of biomarkers within different
groups.
Figure 1 shows the relative bacterial abundance at the phylum level and the beta diversity
analysis between the groups. At day 0, a principal coordinates analysis (PCA) plot
showed that the difference between the two groups was not statistically significant,
based on unweighted UniFrac distances (R
2 = 0.086, p = 0.055) (Fig. 1b). At day 7, the PCA plot showed that the scatter points
of the two groups were discrete, and the difference between the groups was statistically
significant, based on unweighted UniFrac distances (R
2 = 0.185, p = 0.001) (Fig. 1d). It was demonstrated that 80% oxygen changed the composition
of the gut microbiome. Further LDA analysis showed the enriched bacteria in the two
groups at day 7 (Fig. 2). Focusing on the pathogenic bacteria, we found that Streptococcus
was enriched in the oxygen group, but Gammaproteobacteria and Proteus were enriched
in the control group.
Fig. 1
Relative bacterial abundance at the phylum level and beta diversity. a Relative bacterial
abundance of the control and the oxygen groups (n = 9) at the phylum level at day
0. b PCA plot of the control and the oxygen groups (n = 9) at day 0 based on unweighted
UniFrac distances (R
2 = 0.086, p = 0.055). c Relative bacterial abundance of the control and the oxygen
groups (n = 9) at the phylum level at day 7. d PCA plot of the control and the oxygen
groups (n = 9) at day 7 based on unweighted UniFrac distances (R
2 = 0.185, p = 0.001**). PCA, principal coordinates analysis. **p < 0.01. The corresponding
phyla of the pathogenic bacteria in this study: Proteobacteria (Gammaproteobacteria
and Proteus) and Firmicutes (Streptococcus)
Fig. 2
LDA along with effect size measurements was applied to the enriched bacteria from
the genus level to the phylum level in the control and oxygen groups at day 7 (n = 9).
LDA, linear discriminant analysis
To date, a great amount of work has been carried out in hyperoxia-related organ damage,
basically and clinically. However, very few studies have explored the impact of hyperoxia
on intestinal microbiota [5]. A previous study has indicated that hyperbaric hyperoxia
alters the composition of the gut microbiota in mice, and one lineage, Anaerostipes,
an obligately anaerobic Firmicute, diminishes after hyperbaric hyperoxia [3]. However,
a recent study has suggested that normobaric hyperoxia cannot change the gut microbiota
in rat pups [4]. However, this study was limited by its small sample size (n = 4).
In our study, we found gut dysbiosis induced by normobaric hyperoxia in an adult rodent
model. Our model consisted of a larger sample size. Compared to hyperbaric oxygen
therapy, normobaric oxygen therapy can expose patients to oxygen for a longer time
and is far more widely used in various settings [6]. It is important to know how normobaric
hyperoxia influences the gut microbiota. In our study, we also found that hyperoxia
influences some pathogenic bacteria, enriching Streptococcus and diminishing Gammaproteobacteria
and Proteus. A possible reason for this different behavior is that hyperoxia has specific
selective effects in different bacteria.
In conclusion, hyperoxia provokes gut dysbiosis in rats, in a complex manner.