Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur.
Department of Social and Preventive Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur.
Clin Infect Dis. 2018 Jul 2;67(2):261-268. doi: 10.1093/cid/ciy063.
Rhinovirus (RV) is one of the main viral etiologic agents of acute respiratory illnesses. Despite the heightened disease burden caused by RV, the viral factors that increase the severity of RV infection, the transmission pattern, and seasonality of RV infections remain unclear.
An observational study was conducted among 3935 patients presenting with acute upper respiratory illnesses in the ambulatory settings between 2012 and 2014.
The VP4/VP2 gene was genotyped from all 976 RV-positive specimens, where the predominance of RV-A (49%) was observed, followed by RV-C (38%) and RV-B (13%). A significant regression in median nasopharyngeal viral load (VL) (P < .001) was observed, from 883 viral copies/µL at 1-2 days after symptom onset to 312 viral copies/µL at 3-4 days and 158 viral copies/µL at 5-7 days, before declining to 35 viral copies/µL at ≥8 days. In comparison with RV-A (median VL, 217 copies/µL) and RV-B (median VL, 275 copies/µL), RV-C-infected subjects produced higher VL (505 copies/µL; P < .001). Importantly, higher RV VL (median, 348 copies/µL) was associated with more severe respiratory symptoms (Total Symptom Severity Score ≥17, P = .017). A total of 83 phylogenetic-based transmission clusters were identified in the population. It was observed that the relative humidity was the strongest environmental predictor of RV seasonality in the tropical climate.
Our findings underline the role of VL in increasing disease severity attributed to RV-C infection, and unravel the factors that fuel the population transmission dynamics of RV.
鼻病毒 (RV) 是引起急性呼吸道疾病的主要病毒病原体之一。尽管 RV 引起的疾病负担加重,但增加 RV 感染严重程度、传播模式和 RV 感染季节性的病毒因素仍不清楚。
在 2012 年至 2014 年期间,对 3935 名在门诊环境中出现急性上呼吸道疾病的患者进行了一项观察性研究。
对所有 976 份 RV 阳性标本的 VP4/VP2 基因进行了基因分型,其中 RV-A(49%)占优势,其次是 RV-C(38%)和 RV-B(13%)。中位鼻咽病毒载量(VL)(P <.001)显著下降,从发病后 1-2 天的 883 拷贝/µL 降至 3-4 天的 312 拷贝/µL 和 5-7 天的 158 拷贝/µL,然后降至≥8 天的 35 拷贝/µL。与 RV-A(中位 VL,217 拷贝/µL)和 RV-B(中位 VL,275 拷贝/µL)相比,RV-C 感染患者产生的 VL 更高(505 拷贝/µL;P <.001)。重要的是,更高的 RV VL(中位数,348 拷贝/µL)与更严重的呼吸道症状相关(总症状严重程度评分≥17,P =.017)。在人群中总共确定了 83 个基于系统发育的传播簇。观察到相对湿度是热带气候中 RV 季节性的最强环境预测因素。
我们的研究结果强调了 VL 在增加由 RV-C 感染引起的疾病严重程度方面的作用,并揭示了促进 RV 人群传播动力学的因素。