Alhasan Moumen M, Cait Alissa M, Heimesaat Markus M, Blaut Michael, Klopfleisch Robert, Wedel Alexander, Conlon Thomas M, Yildirim Ali Ö, Sodemann Elisa B, Mohn William W, Bereswill Stefan, Conrad Melanie L
Institute of Microbiology, Infectious Diseases and Immunology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Berlin, Germany.
Division of Psychosomatic Medicine, Department of Internal Medicine, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Berlin, Germany.
Allergy. 2020 Aug;75(8):1979-1990. doi: 10.1111/all.14234. Epub 2020 Mar 11.
The use of antibiotics during pregnancy is associated with increased allergic asthma risk in the offspring, and given that approximately 25% of pregnant women are prescribed antibiotics, it is important to understand the mechanisms contributing to this phenomenon. Currently, there are no studies that directly test this association experimentally. Our objective was to develop a mouse model in which antibiotic treatment during pregnancy results in increased offspring asthma susceptibility.
Pregnant mice were treated daily from gestation day 8-17 with an oral solution of the antibiotic vancomycin, and three concentrations were tested. At weaning, offspring were subjected to an adjuvant-free experimental asthma protocol using ovalbumin as an allergen. The composition of the gut microbiome was determined in mothers and offspring with samples collected from five different time points; short-chain fatty acids were also analyzed in allergic offspring.
We found that maternal antibiotic treatment during pregnancy was associated with increased offspring asthma severity in a dose-dependent manner. Furthermore, maternal vancomycin treatment during pregnancy caused marked changes in the gut microbiome composition in both mothers and pups at several different time points. The increased asthma severity and intestinal microbiome changes in pups were also associated with significantly decreased cecal short-chain fatty acid concentrations.
Consistent with the "Developmental Origins Hypothesis," our results confirm that exposure to antibiotics during pregnancy shapes the neonatal intestinal environment and increases offspring allergic lung inflammation.
孕期使用抗生素与后代患过敏性哮喘的风险增加有关,鉴于约25%的孕妇会被开具抗生素处方,了解导致这一现象的机制很重要。目前,尚无研究通过实验直接验证这种关联。我们的目标是建立一种小鼠模型,使孕期抗生素治疗会导致后代哮喘易感性增加。
从妊娠第8天至第17天,每天用抗生素万古霉素口服溶液对怀孕小鼠进行治疗,并测试了三种浓度。断奶时,使用卵清蛋白作为过敏原,让后代接受无佐剂的实验性哮喘方案。从五个不同时间点收集样本,测定母亲和后代肠道微生物群的组成;还对患过敏性疾病的后代进行了短链脂肪酸分析。
我们发现孕期母体抗生素治疗与后代哮喘严重程度增加呈剂量依赖性相关。此外,孕期母体万古霉素治疗在几个不同时间点导致母亲和幼崽的肠道微生物群组成发生显著变化。幼崽哮喘严重程度增加和肠道微生物群变化也与盲肠短链脂肪酸浓度显著降低有关。
与“发育起源假说”一致,我们的结果证实孕期接触抗生素会塑造新生儿肠道环境并增加后代过敏性肺部炎症。