Exploration of pathogenic microorganism within the small intestine of necrotizing enterocolitis

• Published in: World journal of pediatrics : WJP Vol. 20; no. 2; pp. 165 - 172
• Main Authors: Wang, Yan, Jiang, Kun, Xia, Qiao, Kang, Xia, Wang, Shan, Yu, Ji-Hong, Ni, Wen-Feng, Qi, Xiao-Qin, Zhang, Ying-Na, Han, Jin-Bao, Liu, Gang, Hou, Lei, Feng, Zhi-Chun, Huang, Liu-Ming
• Format: Journal Article
• Language: English
• Published: Singapore Springer Nature Singapore 01.02.2024
• Subjects: Critical Care Medicine; Enterocolitis, Necrotizing; Female; Fetal Diseases; Humans; Imaging; Infant; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Intensive; Intestine, Small; Intestines - microbiology; Maternal and Child Health; Medicine; Medicine & Public Health; Original Article; Pediatric Surgery; Pediatrics; Radiology; RNA, Ribosomal, 16S - genetics; Surgery; Necrotizing enterocolitis; Microbiota; 16S rDNA; Small intestine
• ISSN: 1708-8569; 1867-0687
• DOI: 10.1007/s12519-023-00756-0

Background Necrotizing enterocolitis (NEC) is the most common severe gastrointestinal emergency in neonates. We designed this study to identify the pathogenic microorganisms of NEC in the microbiota of the small intestine of neonates. Methods Using the 16S ribosomal DNA (rDNA) sequencing method, we compared and analyzed the structure and diversity of microbiotas in the intestinal feces of different groups of neonates: patients undergoing jejunostomy to treat NEC (NP group), neonates undergoing jejunostomy to treat other conditions (NN group), and neonates with NEC undergoing conservative treatment (NC group). We took intestinal feces and saliva samples from patients at different time points. Results The beta diversities of the NP, NN, and NC groups were all similar. When comparing the beta diversities between different time points in the NP group, we found similar beta diversities at time points E1 to E3 but significant differences between the E2–E3 and E4 time points: the abundances of Klebsiella and Enterococcus (Proteobacteria) were higher at the E1–E3 time points; the abundance of Escherichia - Shigella (Proteobacteria) increased at the E2 time point, and the abundance of Klebsiella decreased significantly, whereas that of Streptococcus increased significantly at the E4 time point. Conclusions Our results suggest that the pathological changes of intestinal necrosis in the small intestine of infants with NEC are not directly caused by excessive proliferation of pathogenic bacteria in the small intestine. The sources of microbiota in the small intestine of neonates, especially in premature infants, may be affected by multiple factors.