From the Department of Neonatology, Gunma Children's Medical Center, Shibukawa.
Department of Pediatrics and Developmental Medicine, Gunma University Graduate School of Medicine.
Pediatr Infect Dis J. 2020 Jun;39(6):546-552. doi: 10.1097/INF.0000000000002623.
Escherichia coli causes neonatal early-onset sepsis (EOS) that is associated with high mortality and increasing antibiotic resistance. Thus, we estimated the prevalence, antibiotic susceptibility and risk factors for colonization of E. coli in premature infants at birth and characterized the pathogenicity of the isolates.
A prospective surveillance study was conducted at three Japanese perinatal centers between August 2014 and February 2017. Infants weighing <2 kg and/or at gestational age <35 weeks at birth were enrolled. We screened the mothers and neonates for E. coli colonization. Pulsed-field gel electrophoresis was used to analyze the relatedness between the maternal and neonatal isolates. Virulence factors for the isolates were determined using polymerase chain reaction.
We enrolled 421 premature infants born to 382 mothers. The rate of colonization in mothers was 47.6%, comprising 5.9% extended-spectrum beta-lactamase-producing E. coli (ESBL-E) and 20.0% ampicillin-resistant strains. Ten (2.4%) infants exhibited colonization; ESBL-E and ampicillin-resistant strains colonized three and four infants, respectively. Three antibiotic-resistant, strain-positive infants developed EOS. Pulsed-field gel electrophoresis revealed vertical transmission of bacteria in four infants. Multivariate logistic regression analysis revealed that ESBL-E-positive mothers [odds ratio (OR), 19.2; 95% confidence interval (CI), 2.5-145.7)] and vaginal delivery (OR, 9.4; 95% CI, 1.7-50.7) were risk factors for neonatal colonization. The infant isolates possessed numerous virulence factors.
Although the prevalence of E. coli-colonized premature infants at birth was low, the rate of antibiotic resistance and the attack rate for EOS were high. Infants with ESBL-E positive mothers should be closely monitored for EOS.
大肠杆菌引起新生儿早发性败血症(EOS),其死亡率高,且抗生素耐药性不断增加。因此,我们评估了出生时早产儿中大肠杆菌定植的流行率、抗生素敏感性和危险因素,并对分离株的致病性进行了特征分析。
2014 年 8 月至 2017 年 2 月,我们在日本三家围产期中心进行了一项前瞻性监测研究。纳入出生时体重<2kg 和/或胎龄<35 周的婴儿。我们对母亲和新生儿进行了大肠杆菌定植筛查。脉冲场凝胶电泳用于分析母亲和新生儿分离株之间的亲缘关系。聚合酶链反应用于确定分离株的毒力因子。
我们纳入了 382 名母亲所生的 421 名早产儿。母亲的定植率为 47.6%,其中 5.9%为产超广谱β-内酰胺酶的大肠杆菌(ESBL-E),20.0%为氨苄西林耐药株。10 名(2.4%)婴儿出现定植,分别有 3 名和 4 名婴儿定植了 ESBL-E 和氨苄西林耐药株。3 名抗生素耐药、分离株阳性的婴儿发生了 EOS。脉冲场凝胶电泳显示 4 名婴儿存在细菌垂直传播。多变量 logistic 回归分析显示,ESBL-E 阳性母亲(比值比 [OR],19.2;95%置信区间 [CI],2.5-145.7)和阴道分娩(OR,9.4;95%CI,1.7-50.7)是新生儿定植的危险因素。婴儿分离株具有多种毒力因子。
虽然出生时大肠杆菌定植的早产儿患病率较低,但抗生素耐药率和 EOS 的发病率较高。应密切监测 ESBL-E 阳性母亲的婴儿是否发生 EOS。