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Longitudinal assessment of antibiotic resistance gene profiles in gut microbiomes of infants at risk of eczema

机译:婴儿肠道微生物肠道抗生素抗性基因谱的纵向评估

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BACKGROUND:While there is increasing knowledge about the gut microbiome, the factors influencing and the significance of the gut resistome are still not well understood. Infant gut commensals risk transferring multidrug-resistant antibiotic resistance genes (ARGs) to pathogenic bacteria. The rapid spread of multidrug-resistant pathogenic bacteria is a worldwide public health concern. Better understanding of the na?ve infant gut resistome may build the evidence base for antimicrobial stewardship in both humans and in the food industry. Given the high carriage rate of extended spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae in Asia, we aimed to evaluate community prevalence, dynamics, and longitudinal changes in antibiotic resistance gene (ARG) profiles and prevalence of ESBL-producing E. coli and K. pneumoniae in the intestinal microbiome of infants participating in the Growing Up in Singapore Towards Healthy Outcomes (GUSTO) study, a longitudinal cohort study of pregnant women and their infants.METHODS:We analysed ARGs in the first year of life among 75 infants at risk of eczema who had stool samples collected at multiple timepoints using metagenomics.RESULTS:The mean number of ARGs per infant increased with age. The most common ARGs identified confer resistance to aminoglycoside, beta-lactam, macrolide and tetracycline antibiotics; all infants harboured these antibiotic resistance genes at some point in the first year of life. Few ARGs persisted throughout the first year of life. Beta-lactam resistant Escherichia coli and Klebsiella pneumoniae were detected in 4 (5.3%) and 32 (42.7%) of subjects respectively.CONCLUSION:In this longitudinal cohort study of infants living in a region with high endemic antibacterial resistance, we demonstrate that majority of the infants harboured several antibiotic resistance genes in their gut and showed that the infant gut resistome is diverse and dynamic over the first year of life.
机译:背景:虽然有关肠道微生物组的了解,但影响肠道耐压的因素仍然不满意。婴儿肠道共生风险转移多药抗生素抗性基因(Args)给病原细菌。多药物抗性细菌的快速传播是全球公共卫生问题。更好地了解Na ve婴儿肠道抑制可以为人类和食品行业的抗菌管道建立抗菌管道的证据基础。鉴于扩展光谱β-内酰胺酶(ESBL)的高乘法率 - 在亚洲进行肠杆菌菌,我们旨在评估抗生素抗性基因(Arg)型抗体抗性基因(Arg)型材的群体流行,动力和纵向变化以及产生ESBL的大肠杆菌的患病率K.肺炎在婴儿的肠道微生物中参与新加坡成长的兴奋剂(Gusto)研究,孕妇及其婴儿的纵向队列研究。方法:我们在75名婴儿的第一年分析了args使用Metagenomics在多个时间点收集肠系的湿疹的风险。结果:每婴儿的args的平均数量随着年龄的增长而增加。最常见的args确定对氨基糖苷,β-内酰胺,大环内酯和四环素抗生素的赋予抵抗力;所有婴儿在生命的第一年的某些时候留下了这些抗生素抗性基因。很少有争论在整个生命的第一年持续存在。在4(5.3%)和32个(42.7%)的受试者中检测到β-内酰胺抗性大肠杆菌和Klebsiella肺炎。结论:在这种纵向队列的婴儿患有高处理抗菌性抗菌性抗菌性的纵向队列中,我们证明了多数婴儿在肠道中留下了几种抗生素抗性基因,并表明婴儿肠道抑制在第一年的生命中是多种多样的。

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