Department of Pediatrics, College of Medicine, Jeju National University, Jeju, 23241, Korea.
Department of Pediatrics, Jeju National University Hospital, Jeju, Korea.
Indian J Pediatr. 2023 Jul;90(7):660-664. doi: 10.1007/s12098-022-04121-3. Epub 2022 Mar 14.
To assess the role of 16S ribosomal RNA analysis in microbial identification in febrile infants under six months of age diagnosed with UTI, and compare it with the conventional culture results.
Young infants under 6 mo of age who were suspected UTI from May 2018 to April 2019 had been enrolled. Uropathogens were analyzed by the traditional microbiologic culture system and the 16S rRNA analysis. The 16S rRNA analysis included 16S rRNA amplicon band confirmation and bacterial identification through the sequencing analysis.
A total of 57 infants with the febrile UTI were enrolled, and the median age was 3 mo. Uropathogens were identified in 43 patients (75.4%) in a conventional culture method: Escherichia coli in 38 patients (88.4%), Klebsiella pneumoniae in 3 (7.0%), Enterobacter cloacae in 1 (2.3%), and Pseudomonas aeruginosa in 1 (2.3%). Fifty urine samples (87.8%) had positive 16S rRNA amplicon band on electrophoresis. Among the 16S rRNA-positive urines, 40 samples were available for the sequence analysis of 16S rRNA, and the identification of bacteria were as follows: E. fergusonii in 36, K. pneumoniae in 3, and Shigella flexneri in 1. The sensitivity of 16S rRNA sequencing was 81.4% [95% confidence interval (CI), 67.4-90.3%] and the specificity was 64.3% (95% CI, 38.8-83.7%).
Uropathogen identification using 16S rRNA analysis could be applied to manage the febrile UTI in young infants clinically in combination with the conventional culture.
评估 16S 核糖体 RNA 分析在诊断为尿路感染的 6 个月以下发热婴儿微生物鉴定中的作用,并将其与传统培养结果进行比较。
纳入 2018 年 5 月至 2019 年 4 月期间疑似患有尿路感染的 6 月龄以下婴儿。采用传统微生物培养系统和 16S rRNA 分析方法对尿路病原体进行分析。16S rRNA 分析包括 16S rRNA 扩增子带确认和通过测序分析进行细菌鉴定。
共纳入 57 例发热性尿路感染婴儿,中位年龄为 3 个月。在常规培养方法中,38 例(88.4%)患者确定了病原体:大肠埃希菌 38 例(88.4%)、肺炎克雷伯菌 3 例(7.0%)、阴沟肠杆菌 1 例(2.3%)、铜绿假单胞菌 1 例(2.3%)。50 份尿液样本(87.8%)电泳显示 16S rRNA 扩增子带阳性。在 16S rRNA 阳性尿液中,有 40 份样本可进行 16S rRNA 序列分析,鉴定细菌如下:产酸克雷伯菌 36 株、肺炎克雷伯菌 3 株、福氏志贺菌 1 株。16S rRNA 测序的灵敏度为 81.4%(95%置信区间[CI]:67.4%-90.3%),特异性为 64.3%(95%CI:38.8%-83.7%)。
结合传统培养,16S rRNA 分析可用于临床鉴定 6 个月以下发热婴儿尿路感染的病原体。