Shaw Alexander G, Sim Kathleen, Randell Paul, Cox Michael J, McClure Zoë E, Li Ming-Shi, Donaldson Hugo, Langford Paul R, Cookson William O C M, Moffatt Miriam F, Kroll J Simon
Department of Medicine, Section of Paediatrics, Imperial College London, London, United Kingdom.
Department of Molecular Genetics and Genomics, National Heart and Lung Institute, Imperial College London, London, United Kingdom.
PLoS One. 2015 Jul 13;10(7):e0132923. doi: 10.1371/journal.pone.0132923. eCollection 2015.
Late-onset bloodstream infection (LO-BSI) is a common complication of prematurity, and lack of timely diagnosis and treatment can have life-threatening consequences. We sought to identify clinical characteristics and microbial signatures in the gastrointestinal microbiota preceding diagnosis of LO-BSI in premature infants.
Daily faecal samples and clinical data were collected over two years from 369 premature neonates (<32 weeks gestation). We analysed samples from 22 neonates who developed LO-BSI and 44 matched control infants. Next-generation sequencing of 16S rRNA gene regions amplified by PCR from total faecal DNA was used to characterise the microbiota of faecal samples preceding diagnosis from infants with LO-BSI and controls. Culture of selected samples was undertaken, and bacterial isolates identified using MALDI-TOF. Antibiograms from bloodstream and faecal isolates were compared to explore strain similarity.
From the week prior to diagnosis, infants with LO-BSI had higher proportions of faecal aerobes/facultative anaerobes compared to controls. Risk factors for LO-BSI were identified by multivariate analysis. Enterobacteriaceal sepsis was associated with antecedent multiple lines, low birth weight and a faecal microbiota with prominent Enterobacteriaceae. Staphylococcal sepsis was associated with Staphylococcus OTU faecal over-abundance, and the number of days prior to diagnosis of mechanical ventilation and of the presence of centrally-placed lines. In 12 cases, the antibiogram of the bloodstream isolate matched that of a component of the faecal microbiota in the sample collected closest to diagnosis.
The gastrointestinal tract is an important reservoir for LO-BSI organisms, pathogens translocating across the epithelial barrier. LO-BSI is associated with an aberrant microbiota, with abundant staphylococci and Enterobacteriaceae and a failure to mature towards predominance of obligate anaerobes.
迟发性血流感染(LO-BSI)是早产常见的并发症,缺乏及时诊断和治疗可能会产生危及生命的后果。我们试图确定早产儿在诊断LO-BSI之前胃肠道微生物群的临床特征和微生物特征。
在两年时间里,从369例孕周<32周的早产新生儿中每日收集粪便样本和临床数据。我们分析了22例发生LO-BSI的新生儿和44例匹配的对照婴儿的样本。使用PCR从总粪便DNA中扩增16S rRNA基因区域进行下一代测序,以表征LO-BSI婴儿和对照婴儿在诊断前粪便样本的微生物群。对选定样本进行培养,并使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF)鉴定细菌分离株。比较血流和粪便分离株的抗菌谱,以探索菌株相似性。
在诊断前一周,与对照组相比,LO-BSI婴儿粪便需氧菌/兼性厌氧菌的比例更高。通过多变量分析确定了LO-BSI的危险因素。肠杆菌科败血症与先前的多条静脉通路、低出生体重以及粪便微生物群中肠杆菌科突出有关。葡萄球菌败血症与粪便中葡萄球菌OTU的过度丰富、诊断前机械通气的天数以及中心静脉置管的存在有关。在12例病例中,血流分离株的抗菌谱与最接近诊断时采集的样本中粪便微生物群的一个成分相匹配。
胃肠道是LO-BSI病原体的重要储存库,病原体可穿过上皮屏障。LO-BSI与微生物群异常有关,葡萄球菌和肠杆菌科丰富,且未能向专性厌氧菌占优势的方向成熟。