Gu Hongdan, Tao Enfu, Fan Yijia, Long Gao, Jia Xinyi, Yuan Tianming, Chen Lihua, Shu Xiaoli, Zheng Wei, Jiang Mizu
Pediatric Endoscopy Center and Gastrointestinal Laboratory, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310052, China.
Department of Pediatrics, Wenling Maternal and Child Health Care Hospital, Wenling, Zhejiang, 317500, China.
Ann Clin Microbiol Antimicrob. 2024 Aug 7;23(1):69. doi: 10.1186/s12941-024-00730-2.
β-Lactam antibiotics are a class of antibiotics commonly used to treat bacterial infections. However, the effects of β-lactam antibiotics on term neonatal intestinal flora have not been fully elucidated. Hospitalized full-term newborns receiving β-lactam antibiotics formed the antibiotic group (n = 67), while those without antibiotic treatment comprised the non-antibiotic group (n = 47). A healthy group included healthy full-term newborns (n = 16). Stool samples were collected for 16 S rDNA sequencing to analyze gut microbiota variations. Further investigation was carried out within the β-lactam antibiotic group, exploring the effects of antibiotic use on the newborns' gut microbiota in relation to the duration and type of antibiotic administration, delivery method, and feeding practices. The antibiotic group exhibited significant difference of microbial community composition compared to the other groups. Genera like Klebsiella, Enterococcus, Streptococcus, Alistipes, and Aeromonas were enriched, while Escherichia-Shigella, Clostridium sensu stricto 1, Bifidobacterium, and Parabacteroides were reduced. Klebsiella negatively correlated with Escherichia-Shigella, positively with Enterobacter, while Escherichia-Shigella negatively correlated with Enterococcus and Streptococcus. Regardless of neonatal age, β-lactam antibiotics induced an elevated abundance of Klebsiella and Enterococcus. The impact on gut microbiota varied with the duration and type of antibiotic (cefotaxime or ampicillin/sulbactam). Compared to vaginal delivery, cesarean delivery after β-lactam treatment heightened the abundance of Klebsiella, Enterobacteriaceae_Unclassified, Lactobacillales_Unclassified, and Pectobacterium. Feeding patterns minimally influenced β-lactam-induced alterations. In conclusion, β-lactam antibiotic treatment for neonatal pneumonia and sepsis markedly disrupted intestinal microbiota, favoring Klebsiella, Enterococcus, Streptococcus, Alistipes, and Aeromonas. The impact of β-lactam varied by duration, type, and delivery method, emphasizing heightened disruptions post-cesarean delivery.
β-内酰胺类抗生素是一类常用于治疗细菌感染的抗生素。然而,β-内酰胺类抗生素对足月儿肠道菌群的影响尚未完全阐明。接受β-内酰胺类抗生素治疗的住院足月儿组成抗生素组(n = 67),未接受抗生素治疗的足月儿组成非抗生素组(n = 47)。健康组包括健康足月儿(n = 16)。收集粪便样本进行16S rDNA测序,以分析肠道微生物群的变化。在β-内酰胺类抗生素组内进一步开展研究,探讨抗生素使用对新生儿肠道微生物群的影响,涉及抗生素给药的持续时间和类型、分娩方式及喂养方式。与其他组相比,抗生素组的微生物群落组成存在显著差异。克雷伯菌属、肠球菌属、链球菌属、艾利斯菌属和气单胞菌属等菌属富集,而埃希氏菌-志贺氏菌属、严格梭菌1群、双歧杆菌属和副拟杆菌属减少。克雷伯菌属与埃希氏菌-志贺氏菌属呈负相关,与肠杆菌属呈正相关,而埃希氏菌-志贺氏菌属与肠球菌属和链球菌属呈负相关。无论新生儿年龄如何,β-内酰胺类抗生素都会导致克雷伯菌属和肠球菌属丰度升高。对肠道微生物群的影响因抗生素的持续时间和类型(头孢噻肟或氨苄西林/舒巴坦)而异。与阴道分娩相比,β-内酰胺治疗后的剖宫产分娩增加了克雷伯菌属、肠杆菌科未分类菌属、乳杆菌目未分类菌属和果胶杆菌属的丰度。喂养方式对β-内酰胺类抗生素引起的变化影响极小。总之,用于治疗新生儿肺炎和败血症的β-内酰胺类抗生素治疗显著破坏了肠道微生物群,有利于克雷伯菌属、肠球菌属、链球菌属、艾利斯菌属和气单胞菌属生长。β-内酰胺类抗生素的影响因持续时间、类型和分娩方式而异,强调剖宫产分娩后破坏作用增强。