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首页> 外文期刊>Pediatric allergy and immunology: official publication of the European Society of Pediatric Allergy and Immunology >Prenatal administration of Lactobacillus rhamnosus has no effect on the diversity of the early infant gut microbiota.
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Prenatal administration of Lactobacillus rhamnosus has no effect on the diversity of the early infant gut microbiota.

机译:产前鼠李糖乳杆菌对早期婴儿肠道菌群的多样性没有影响。

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摘要

We have recently shown that maternal administration of Lactobacillus rhamnosus GG (LGG) during late pregnancy can have beneficial effects on the early development of infant gut microbiota, promoting a bifidobacteria profile similar to that of a healthy breastfed infant. It is uncertain, however, whether such probiotic supplementation could influence the diversity of infant gut microbiota. We investigated the effect of pre-natal LGG on gut microbial diversity in the early post-natal period. Day-7 faecal samples were collected from 98 infants at high risk of allergic disease, whose mothers participated in a pre-natal probiotic eczema prevention study. Faecal microbial diversity was assessed by terminal restriction fragment length polymorphism using restriction enzymes Sau96I and AluI. A greater number of peaks represent greater diversity of bacterial communities. Administration of LGG to mothers during late pregnancy had no effects on the mean number of peaks in faecal samples from 1-wk-old infants as compared to placebo (AluI 14.4 vs. 15.5, p?=?0.17, 95% CI -0.4, 2.5; Sau96I 17.3 vs. 15.8, p?=?0.15, 95% CI -3.5, 0.5). Prenatal LGG failed to modulate diversity of early infant gut microbiota despite promoting a beneficial bifidobacteria profile.
机译:我们最近显示,孕妇在妊娠晚期使用鼠李糖乳杆菌GG(LGG)可以对婴儿肠道菌群的早期发育产生有益的影响,从而促进双歧杆菌的分布,类似于健康母乳喂养的婴儿。但是,尚不确定这种益生菌补充剂是否会影响婴儿肠道菌群的多样性。我们调查了产后早期LGG对肠道微生物多样性的影响。第7天的粪便样本是从98名高变态反应疾病高危婴儿中收集的,他们的母亲参加了产前益生菌湿疹预防研究。通过使用限制酶Sau96I和AluI的末端限制片段长度多态性评估粪便微生物多样性。更大数量的峰代表更大的细菌群落多样性。与安慰剂相比,在妊娠后期向母亲服用LGG对1周龄婴儿的粪便样本中平均峰数没有影响(AluI 14.4 vs. 15.5,p?=?0.17,95%CI -0.4, 2.5; Sau96I 17.3对15.8,p =α0.15,95%CI -3.5,0.5)。尽管产前LGG促进了有益的双歧杆菌特征,但未能调节早期婴儿肠道菌群的多样性。

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