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新生儿感染在小鼠模型中会引发肠道微生物群的长期失调。

Neonatal infection induces long-lasting dysbiosis of the gut microbiota in a mouse model.

作者信息

Li Yuanyuan, Xu Ximing, Guo Ziyao, Li Qinyuan, Wang Yiying, Jian Ding, Zhang Guangli, Tian Xiaoyin, Chen Shiyi, Luo Zhengxiu

机构信息

Department of Respiratory Medicine of Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, China.

Chongqing Key Laboratory of Pediatrics, Chongqing Key Laboratory of Child Infection and Immunity, Chongqing, China.

出版信息

Front Microbiol. 2022 Aug 18;13:961684. doi: 10.3389/fmicb.2022.961684. eCollection 2022.

Abstract

Early life is a "critical window" for gut microbiota development, antibiotic use during this period exerts a profound effect on gut microbial dysbiosis and asthma. In clinical practice, antibiotics are usually used in patients with bacterial infections, we previously showed that neonatal pneumonia promoted adult-onset asthma in mice model, while it remains unclear whether neonatal infection have long-term effects on gut microbiota. Neonatal BALB/c mice were inoculated with 5*10 CFU D39 to establish non-lethal pneumonia model. At 2, 3, 8 weeks of age, feces in the cecum were prepared for 16S rRNA sequencing, lungs were collected for histopathologic and lung function analysis. -infected neonatal mice exhibited histopathologic lesions in their lungs and increased airway hyperresponsiveness, obvious alterations in alpha and beta diversities in the entire gut microbiota, and changes of the community structure during the breastfeeding period, infancy, and adulthood. Furthermore, gut microbial composition was modified after neonatal infection, with a decreased relative abundance of Lactobacillus in the breastfeeding period and infancy; in adulthood, the relative abundance of Allobaculum diminished while that of Proteobacteria was augmented. Neonatal infection induced a long-term alteration in microbial community composition.

摘要

早期生活是肠道微生物群发育的“关键窗口”,在此期间使用抗生素会对肠道微生物失调和哮喘产生深远影响。在临床实践中,抗生素通常用于细菌感染患者,我们之前表明新生儿肺炎会在小鼠模型中引发成年后患哮喘,而新生儿感染是否对肠道微生物群有长期影响仍不清楚。将5×10 CFU的D39接种到新生BALB/c小鼠体内以建立非致死性肺炎模型。在2、3、8周龄时,取盲肠粪便进行16S rRNA测序,收集肺组织进行组织病理学和肺功能分析。感染的新生小鼠肺部出现组织病理学病变,气道高反应性增加,整个肠道微生物群的α和β多样性明显改变,并且在哺乳期、婴儿期和成年期群落结构发生变化。此外,新生儿感染后肠道微生物组成发生改变,哺乳期和婴儿期乳酸杆菌相对丰度降低;成年期,别氏菌属相对丰度减少而变形菌门相对丰度增加。新生儿感染引起微生物群落组成的长期改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51ab/9433971/63dc0f6cbe31/fmicb-13-961684-g001.jpg

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