Effects of Therapeutic Antibiotic Exposure on the Oropharyngeal and Fecal Microbiota in Infants With Cystic Fibrosis.

IF 2.7 3区 医学 Q1 PEDIATRICS
Hillary S Hayden, Maria T Nelson, Sydney E Ross, Adrian J Verster, Drake C Bouzek, Alex Eng, Adam Waalkes, Kelsi Penewit, Benjamin T Kopp, Christopher Siracusa, Michael J Rock, Stephen J Salipante, Lucas R Hoffman, Don B Sanders
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引用次数: 0

Abstract

Background: Systemic antibiotics can impact all microbes inhabiting patients, regardless of the intended target organism(s). We studied the simultaneous effects on respiratory and fecal microbiomes of β-lactam antibiotics administered for respiratory symptoms in infants with cystic fibrosis (IWCF).

Objective: To compare the magnitude and duration of intended (respiratory) and unintended (fecal) antimicrobial action by analyzing oropharyngeal (OP) and fecal microbiota in IWCF.

Design: Shotgun metagenomic sequencing and qPCR were performed on OP and fecal samples collected longitudinally from 14 IWCF (ages 1-17 months) during ("On Antibiotics") and after ("Off Antibiotics") β-lactam therapy, and from 5 IWCF (3-16 months) never treated with antibiotics.

Results: Total bacterial loads (TBL) for On Antibiotics samples were lower than for both Never (OP and fecal) and Off Antibiotics samples (fecal only). α-diversities (within-sample) for OP On Antibiotics samples were lower than for Never and Off Antibiotics samples but did not differ between fecal sample groups. β-diversity (between-sample) differed between all OP sample groups and between fecal On and Never Antibiotics and Off and Never antibiotics samples; however, fecal On and Off Antibiotics sample β-diversities did not differ. Patterns of change in antibiotic resistance gene abundances reflected shifts in microbial community composition.

Conclusions: β-lactam antibiotic exposure was followed by marked alterations in both OP and fecal microbiota. While microbiota appeared to rebound after treatment in both sample types, our results suggest that fecal microbiota recovered less than OP. The clinical consequences of these findings should be studied in IWCF and other populations frequently treated with antibiotics.

背景:全身性抗生素可影响患者体内的所有微生物,而与目标微生物无关。我们研究了β-内酰胺类抗生素对囊性纤维化婴儿(IWCF)呼吸道症状的影响:通过分析囊性纤维化婴儿口咽(OP)和粪便微生物群,比较预期(呼吸道)和非预期(粪便)抗菌作用的程度和持续时间:设计:对 14 名 IWCF(1-17 个月大)在接受β-内酰胺治疗期间("使用抗生素")和治疗后("停用抗生素")以及 5 名 IWCF(3-16 个月大)从未接受抗生素治疗时采集的口咽和粪便样本进行射枪元基因组测序和 qPCR 分析:结果:"使用抗生素 "样本的细菌总数(TBL)低于 "从未使用抗生素 "样本(OP 和粪便)和 "未使用抗生素 "样本(仅粪便)。使用抗生素的 OP 样本的 α 多样性(样本内)低于从不使用抗生素和不使用抗生素的样本,但粪便样本组之间没有差异。所有 OP 样品组之间、粪便中使用抗生素和从不使用抗生素样本之间以及不使用抗生素和从不使用抗生素样本之间的 β 多样性(样本间)存在差异;但是,粪便中使用抗生素和不使用抗生素样本的 β 多样性没有差异。抗生素耐药基因丰度的变化规律反映了微生物群落组成的变化。虽然两种样本中的微生物群在治疗后都出现了反弹,但我们的结果表明,粪便微生物群的恢复程度低于 OP。这些发现的临床后果应在 IWCF 和其他经常接受抗生素治疗的人群中进行研究。
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来源期刊
Pediatric Pulmonology
Pediatric Pulmonology 医学-呼吸系统
CiteScore
6.00
自引率
12.90%
发文量
468
审稿时长
3-8 weeks
期刊介绍: Pediatric Pulmonology (PPUL) is the foremost global journal studying the respiratory system in disease and in health as it develops from intrauterine life though adolescence to adulthood. Combining explicit and informative analysis of clinical as well as basic scientific research, PPUL provides a look at the many facets of respiratory system disorders in infants and children, ranging from pathological anatomy, developmental issues, and pathophysiology to infectious disease, asthma, cystic fibrosis, and airborne toxins. Focused attention is given to the reporting of diagnostic and therapeutic methods for neonates, preschool children, and adolescents, the enduring effects of childhood respiratory diseases, and newly described infectious diseases. PPUL concentrates on subject matters of crucial interest to specialists preparing for the Pediatric Subspecialty Examinations in the United States and other countries. With its attentive coverage and extensive clinical data, this journal is a principle source for pediatricians in practice and in training and a must have for all pediatric pulmonologists.
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