Hutchinson R A, Costeloe K L, Wade W G, Millar M R, Ansbro K, Stacey F, Fleming P F
Queen Mary University of London, London, UK.
Homerton University Hospital NHS Foundation Trust, London, UK.
Gut Pathog. 2023 Apr 21;15(1):18. doi: 10.1186/s13099-023-00544-1.
BACKGROUND: Intestinal dysbiosis is implicated in the origins of necrotising enterocolitis and late-onset sepsis in preterm babies. However, the effect of modulators of bacterial growth (e.g. antibiotics) upon the developing microbiome is not well-characterised. In this prospectively-recruited, retrospectively-classified, case-control study, high-throughput 16S rRNA gene sequencing was combined with contemporaneous clinical data collection, to assess the within-subject relationship between antibiotic administration and microbiome development, in comparison to preterm infants with minimal antibiotic exposure. RESULTS: During courses of antibiotics, diversity progression fell in comparison to that seen outside periods of antibiotic use (-0.71units/week vs. + 0.63units/week, p < 0.01); Enterobacteriaceae relative abundance progression conversely rose (+ 10.6%/week vs. -8.9%/week, p < 0.01). After antibiotic cessation, diversity progression remained suppressed (+ 0.2units/week, p = 0.02). CONCLUSIONS: Antibiotic use has an acute and longer-lasting impact on the developing preterm intestinal microbiome. This has clinical implications with regard to the contribution of antibiotic use to evolving dysbiosis, and affects the interpretation of existing microbiome studies where this effect modulator is rarely accounted for.
背景:肠道菌群失调与早产儿坏死性小肠结肠炎及晚发性败血症的发病有关。然而,细菌生长调节剂(如抗生素)对发育中的微生物群的影响尚未得到充分表征。在这项前瞻性招募、回顾性分类的病例对照研究中,高通量16S rRNA基因测序与同期临床数据收集相结合,以评估与抗生素暴露极少的早产儿相比,抗生素使用与微生物群发育之间的个体内关系。 结果:在抗生素治疗过程中,与未使用抗生素期间相比,多样性进展下降(-0.71单位/周对+0.63单位/周,p<0.01);相反,肠杆菌科相对丰度进展上升(+10.6%/周对-8.9%/周,p<0.01)。抗生素停用后,多样性进展仍然受到抑制(+0.2单位/周,p=0.02)。 结论:抗生素使用对发育中的早产肠道微生物群有急性和持久的影响。这对于抗生素使用对不断发展的菌群失调的影响具有临床意义,并影响现有微生物群研究的解释,在这些研究中这种影响调节因素很少被考虑。
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