Smielewska Anna, Pearson Callum, Popay Ashley, Roddick Iain, Reacher Mark, Emmott Edward, He Jenny, Thaxter Rachel, Chenery Carol, Goodfellow Ian, Burke Amos, Jalal Hamid
Division of Virology, Department of Pathology, University of Cambridge Addenbrooke's Hospital Cambridge, Cambridge, Cambridgeshire, CB2 0QQ, UK.
Public Health Laboratory, Cambridge University Hospitals NHS Foundation Trust, Public Health England, Cambridge, Cambridgeshire, CB2 0QQ, UK.
Wellcome Open Res. 2018 Sep 19;3:119. doi: 10.12688/wellcomeopenres.14732.1. eCollection 2018.
Human parainfluenza viruses (HPIVs) are significant causes of both upper and lower respiratory tract infections with type 3 (HPIV3) causing the most severe disease in the immunocompromised cohorts. The objective of this study was to analyse the epidemiological nature of a cluster of cases of HPIV3 in a pediatric oncology unit of a major teaching hospital. In order to determine whether the activity observed represented a deviation from the norm, seasonal trends of HPIV3 in the surrounding geographical area as well as on the ward in question were analysed. The genetic link between cases was established by the phylogenetic analysis of the non-coding hypervariable region between the M (Matrix) and F (fusion) genes of HPIV3. The 15 cases involved and 15 unrelated cases were sequenced. Transmission routes were subsequently inferred and visualized using Konstanz Information Miner (KNIME) 3.3.2. Of the 15 cases identified, 14 were attributed to a point source outbreak. Two out of 14 outbreak cases were found to differ by a single mutation A182C. The outbreak strain was also seen in 1 out of 15 unrelated cases, indicating that it was introduced from the community. Transmission modeling was not able to link all the cases and establish a conclusive chain of transmission. No staff were tested during the outbreak period. No deaths occurred as a result of the outbreak. A point source outbreak of HPIV3 was recognized on an oncology pediatric unit in a major teaching hospital. This raised concern about the possibility of a future more serious outbreak. Weaknesses in existing systems were identified and a new dedicated respiratory virus monitoring system introduced. Pediatric oncology units require sophisticated systems for early identification of potentially life-threatening viral outbreaks.
人副流感病毒(HPIVs)是上呼吸道和下呼吸道感染的重要病因,其中3型(HPIV3)在免疫功能低下人群中引发的疾病最为严重。本研究的目的是分析一家大型教学医院儿科肿瘤科一组HPIV3病例的流行病学特征。为了确定观察到的活动是否偏离正常情况,分析了周围地理区域以及相关病房中HPIV3的季节性趋势。通过对HPIV3的M(基质)基因和F(融合)基因之间的非编码高变区进行系统发育分析,确定了病例之间的遗传联系。对15例相关病例和15例无关病例进行了测序。随后使用康斯坦茨信息挖掘器(KNIME)3.3.2推断并可视化传播途径。在确定的15例病例中,14例归因于点源暴发。14例暴发病例中有2例被发现存在单个突变A182C。在15例无关病例中的1例中也发现了暴发菌株,表明它是从社区引入的。传播模型无法将所有病例联系起来并建立确凿的传播链。暴发期间未对工作人员进行检测。此次暴发未导致死亡。一家大型教学医院的儿科肿瘤科确认了一次HPIV3点源暴发。这引发了对未来可能发生更严重暴发的担忧。确定了现有系统的薄弱环节,并引入了新的专用呼吸道病毒监测系统。儿科肿瘤科需要精密系统来早期识别可能危及生命的病毒暴发。