Department of Pediatrics and Adolescent Medicine, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.
J Clin Microbiol. 2010 May;48(5):1624-8. doi: 10.1128/JCM.01724-09. Epub 2010 Mar 29.
The purpose of this study was to evaluate the clinical utility of bacterial rRNA-targeted reverse transcription-quantitative PCR (BrRNA RT-qPCR) assays for identifying the bacterial pathogens that cause fever with neutropenia in pediatric cancer patients, by comparing the bacterial detection rate of this technique with that of blood culture. One milliliter of blood was collected from pediatric patients who developed fever with neutropenia following cancer chemotherapy. BrRNA RT-qPCR was performed using 16 primer sets, each designed for a specific type of bacteria. The entire BrRNA RT-qPCR procedure took less than 5 h. Blood culture was performed at the same time, following the standard institutional procedure. Blood from 13 patients was collected during 23 febrile neutropenic episodes. Of these samples, bacteria were identified in 16 by BrRNA RT-qPCR (69.6%) and in 4 by blood culture (17.4%, P<0.001). In all 4 blood culture-positive samples, BrRNA RT-qPCR detected the same type of bacteria as that identified by culture. In 9 samples, more than 4 types of bacteria were identified simultaneously by BrRNA RT-qPCR, most of which were anaerobic bacteria known to be part of the gut flora. We conclude that BrRNA RT-qPCR could be useful in the diagnosis of fever with neutropenia, given its high bacterial detection rate, short turnaround time, and the small blood sample required compared with the standard blood culture techniques. Our findings also indicate that anaerobic intestinal bacteria, which are difficult to detect by standard culture techniques, may be responsible for some cases of febrile neutropenia.
本研究旨在评估细菌 rRNA 靶向逆转录定量 PCR(BrRNA RT-qPCR)检测方法在识别引起化疗后中性粒细胞减少发热的儿科癌症患者的细菌病原体方面的临床效用,方法是将该技术的细菌检测率与血培养进行比较。采集发生化疗后中性粒细胞减少发热的儿科患者 1 毫升血液。使用针对特定细菌类型的 16 个引物组进行 BrRNA RT-qPCR。整个 BrRNA RT-qPCR 过程耗时不到 5 小时。同时按照标准机构程序进行血培养。在 23 次发热性中性粒细胞减少症发作期间从 13 名患者采集血液。在这些样本中,16 个样本通过 BrRNA RT-qPCR(69.6%)和 4 个样本通过血培养(17.4%,P<0.001)鉴定出细菌。在所有 4 个血培养阳性样本中,BrRNA RT-qPCR 检测到与培养鉴定相同类型的细菌。在 9 个样本中,BrRNA RT-qPCR 同时鉴定出超过 4 种细菌,其中大多数是已知属于肠道菌群的厌氧菌。我们得出结论,BrRNA RT-qPCR 可能对发热性中性粒细胞减少症的诊断有用,因为它的细菌检测率高、周转时间短,与标准血培养技术相比,所需的血液样本量小。我们的研究结果还表明,标准培养技术难以检测到的厌氧肠道细菌可能是一些发热性中性粒细胞减少症的原因。