Persistent metagenomic signatures of early-life hospitalization and antibiotic treatment in the infant gut microbiota and resistome

被引:180
|
作者
Gasparrini, Andrew J. [1 ]
Wang, Bin [1 ,2 ]
Sun, Xiaoqing [1 ,2 ]
Kennedy, Elizabeth A. [1 ]
Hernandez-Leyva, Ariel [1 ]
Ndao, I. Malick [3 ]
Tarr, Phillip, I [3 ,4 ]
Warner, Barbara B. [3 ]
Dantas, Gautam [1 ,2 ,4 ,5 ]
机构
[1] Washington Univ, Sch Med, Edison Family Ctr Genome Sci & Syst Biol, St Louis, MO 63130 USA
[2] Washington Univ, Dept Pathol & Immunol, Sch Med, St Louis, MO 63130 USA
[3] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
[5] Washington Univ, Dept Biomed Engn, St Louis, MO 63130 USA
基金
美国国家卫生研究院;
关键词
EXTREMELY PRETERM CHILDREN; KLEBSIELLA-PNEUMONIAE; BORN PRETERM; INTESTINAL MICROBIOTA; SYSTEMATIC ANALYSIS; LOW DIVERSITY; YOUNG-ADULTS; BIRTH; RISK; ASSOCIATION;
D O I
10.1038/s41564-019-0550-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hospitalized preterm infants receive frequent and often prolonged exposures to antibiotics because they are vulnerable to infection. It is not known whether the short-term effects of antibiotics on the preterm infant gut microbiota and resistome persist after discharge from neonatal intensive care units. Here, we use complementary metagenomic, culture-based and machine learning techniques to study the gut microbiota and resistome of antibiotic-exposed preterm infants during and after hospitalization, and we compare these readouts to antibiotic-naive healthy infants sampled synchronously. We find a persistently enriched gastrointestinal antibiotic resistome, prolonged carriage of multidrug-resistant Enterobacteriaceae and distinct antibiotic-driven patterns of microbiota and resistome assembly in extremely preterm infants that received early-life antibiotics. The collateral damage of early-life antibiotic treatment and hospitalization in preterm infants is long lasting. We urge the development of strategies to reduce these consequences in highly vulnerable neonatal populations.
引用
收藏
页码:2285 / 2297
页数:13
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