Abstract

Background: The neonatal period is a critical period for the establishment of the intestinal microbial community. Antibiotics can change the composition of gut microbiota.Methods: Fecal samples were collected from 14 patients with pneumonia and 14 patients with meningitis before and after antibiotic treatment, and fecal samples from five healthy neonates at the 14th and 21st days after birth were collected as well. DNA of fecal samples was extracted, and PCR amplification was performed targeting the V3–V4 variable region of 16S rDNA. After detection by high-throughput sequencing, OTU (operational taxonomic unit) clustering, species annotation, and α diversity analysis were calculated and analyzed statistically.Results: In the healthy control group, the abundance of Bifidobacterium increased significantly from 16.75 to 40.42%, becoming the most dominant bacteria. The results of α diversity analysis suggested that the Sobs indexes of the gut microbiota in the pneumonia and meningitis groups were significantly lower than that in the healthy control group (p < 0.05). PCoA analysis showed that the gut microbiota of pneumonia and meningitis groups clustered distinctly with the control group (Adonis p = 0.001, R2 = 0.565), and there was no significant change in the diversity of gut microbiota before and after the use of antibiotics.Conclusions: The gut microbiota of neonates with infectious diseases were mainly related to the disease conditions. The initial state of neonatal gut microbiome determines its state after 1-week antibiotic treatment. Antibiotic application with 7 days had little effect on the community richness and some effect on the composition of gut microbiota of neonates with pneumonia or meningitis.

Highlights

  • Human gut microbiota refers to the general term of microorganisms inhabiting the human digestive tract system, including bacteria, archaea, viruses, fungi, and protozoa

  • The patients with pneumonia or meningitis were diagnosed according to the diagnosis criteria mentioned above

  • 14 patients with pneumonia, 14 patients with meningitis, and 5 healthy neonates as control were involved according to our inclusion criteria and exclusion criteria (Figure 1)

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Summary

Introduction

Human gut microbiota refers to the general term of microorganisms inhabiting the human digestive tract system, including bacteria, archaea, viruses, fungi, and protozoa. There are direct or indirect interactions between gut microbiota and the host to form a complex interaction network. This network constitutes a dynamic balance of the micro-ecosystem, which is closely related to human health and disease [1, 2]. Current studies show that gut microbiota is closely associated with the occurrence and development of various chronic diseases, including diabetes, hypertension, cardiovascular diseases, brain diseases, and tumors [3]. The early formation and development of this system is mainly regulated by human genetics and immunity, and the composition of microbial community is related to the habitat. Antibiotics can change the composition of gut microbiota

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