Scanga Lori, Chaing Shu, Powell Cynthia, Aylsworth Arthur S, Harrell Lizzie J, Henshaw Nancy G, Civalier Chris J, Thorne Leigh B, Weck Karen, Booker Jessica, Gulley Margaret L
Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, 27599-7525, USA.
J Mol Diagn. 2006 May;8(2):240-5. doi: 10.2353/jmoldx.2006.050075.
Congenital human cytomegalovirus (HCMV) infection affects 1% of children and is the most common infectious cause of sensorineural hearing loss. Due to the difficulty of diagnosing deafness and other neurological disorders in infants, affected individuals may not be recognized until much later when active infection has resolved and culture is no longer informative. To overcome this problem, congenital HCMV infection was diagnosed retrospectively by testing residual blood samples collected from newborns and dried on perinatal cards as part of the North Carolina Newborn Screening Program. We modified the Qiagen method for purifying DNA from dried blood spots to increase the sample size and recovery of the lysate. A multiplex, real-time TaqMan polymerase chain reaction assay on an ABI 7900 instrument measured a highly conserved segment of the HCMV polymerase gene and the APOB human control gene. HCMV DNA was detected in blood dried on perinatal cards from all seven infants with culture-proven congenital infection, and all 24 negative control cases lacked detectable HCMV DNA. Our findings suggest that it is possible to diagnose congenital HCMV infection using dried blood collected up to 20 months earlier. Further studies are warranted on patients with hearing loss or other neurological deficits to determine the percentage that is attributable to congenital HCMV infection.
先天性人类巨细胞病毒(HCMV)感染影响1%的儿童,是感音神经性听力损失最常见的感染原因。由于婴儿期耳聋和其他神经系统疾病的诊断困难,受影响的个体可能直到很久以后才被发现,此时活动性感染已经消退,培养结果也不再有参考价值。为克服这一问题,作为北卡罗来纳州新生儿筛查项目的一部分,通过检测从新生儿采集并干燥在围产期卡片上的残留血样,对先天性HCMV感染进行回顾性诊断。我们改进了Qiagen从干血斑中纯化DNA的方法,以增加样本量和裂解物的回收率。在ABI 7900仪器上进行的多重实时TaqMan聚合酶链反应检测,测量了HCMV聚合酶基因的一个高度保守片段和APOB人类对照基因。在所有7例经培养证实为先天性感染的婴儿的围产期卡片上干燥的血液中检测到HCMV DNA,所有24例阴性对照病例均未检测到可检测的HCMV DNA。我们的研究结果表明,使用早在20个月前采集的干血来诊断先天性HCMV感染是可能的。有必要对听力损失或其他神经功能缺损的患者进行进一步研究,以确定由先天性HCMV感染所致的比例。