Department of Paediatrics, University of Otago, Christchurch School of Medicine, Christchurch, New Zealand.
Canterbury Health Laboratories, Christchurch, New Zealand.
Clin Microbiol Rev. 2017 Nov 15;31(1). doi: 10.1128/CMR.00047-17. Print 2018 Jan.
Human parechovirus (HPeV) is increasingly being recognized as a potentially severe viral infection in neonates and young infants. HPeV belongs to the family and is currently divided into 19 genotypes. HPeV-1 is the most prevalent genotype and most commonly causes gastrointestinal and respiratory disease. HPeV-3 is clinically the most important genotype due to its association with severe disease in younger infants, which may partly be explained by its distinct virological properties. In young infants, the typical clinical presentation includes fever, severe irritability, and rash, often leading to descriptions of "hot, red, angry babies." Infants with severe central nervous system (CNS) infections are at an increased risk of long-term sequelae. Considering the importance of HPeV as a cause of severe viral infections in young infants, we recommend that molecular diagnostic techniques for early detection be included in the standard practice for the investigation of sepsis-like illnesses and CNS infections in this age group.
人类肠道病毒(HPeV)越来越被认为是一种潜在的严重新生儿和婴幼儿病毒感染。HPeV 属于 科,目前分为 19 种基因型。HPeV-1 是最常见的基因型,最常引起胃肠道和呼吸道疾病。HPeV-3 由于与婴幼儿严重疾病相关,在临床上是最重要的基因型,这在一定程度上可以用其独特的病毒学特性来解释。在婴幼儿中,典型的临床表现包括发热、严重烦躁不安和皮疹,常被描述为“热、红、怒婴”。患有严重中枢神经系统(CNS)感染的婴儿发生长期后遗症的风险增加。鉴于 HPeV 作为引起婴幼儿严重病毒感染的重要病原体,我们建议在该年龄段疑似败血症样疾病和 CNS 感染的标准检查中纳入用于早期检测的分子诊断技术。