Department of Medicine, Faculty of Medicine, University of Malaya, 50603, Kuala Lumpur, Malaysia.
School of Healthcare and Medical Sciences, Sunway University, 47500, Kuala Lumpur, Selangor, Malaysia.
Virol J. 2018 May 23;15(1):91. doi: 10.1186/s12985-018-1005-8.
Human metapneumovirus (HMPV) is established as one of the causative agents of respiratory tract infections. To date, there are limited reports that describe the effect of HMPV genotypes and/or viral load on disease pathogenesis in adults. This study aims to determine the role of HMPV genetic diversity and nasopharyngeal viral load on symptom severity in outpatient adults with acute respiratory tract infections.
Severity of common cold symptoms of patients from a teaching hospital was assessed by a four-category scale and summed to obtain the total symptom severity score (TSSS). Association between the fusion and glycoprotein genes diversity, viral load (quantified using an improved RT-qPCR assay), and symptom severity were analyzed using bivariate and linear regression analyses.
Among 81/3706 HMPV-positive patients, there were no significant differences in terms of demographics, number of days elapsed between symptom onset and clinic visit, respiratory symptoms manifestation and severity between different HMPV genotypes/sub-lineages. Surprisingly, elderly patients (≥65 years old) had lower severity of symptoms (indicated by TSSS) than young and middle age adults (p = 0.008). Nasopharyngeal viral load did not correlate with nor predict symptom severity of HMPV infection. Interestingly, at 3-5 days after symptom onset, genotype A-infected patients had higher viral load compared to genotype B (4.4 vs. 3.3 log RNA copies/μl) (p = 0.003).
Overall, HMPV genetic diversity and viral load did not impact symptom severity in adults with acute respiratory tract infections. Differences in viral load dynamics over time between genotypes may have important implications on viral transmission.
人偏肺病毒(HMPV)已被确定为呼吸道感染的病原体之一。迄今为止,关于 HMPV 基因型和/或病毒载量对成人疾病发病机制的影响的报道有限。本研究旨在确定 HMPV 遗传多样性和鼻咽病毒载量对急性呼吸道感染门诊成人症状严重程度的作用。
通过四级量表评估教学医院患者普通感冒症状的严重程度,并将其相加得到总症状严重程度评分(TSSS)。使用双变量和线性回归分析来分析融合和糖蛋白基因多样性、病毒载量(使用改良的 RT-qPCR 测定法定量)与症状严重程度之间的关系。
在 3706 例 HMPV 阳性患者中的 81 例中,不同 HMPV 基因型/亚系之间,在人口统计学特征、症状出现和就诊之间的天数、呼吸道症状表现和严重程度方面,没有显著差异。令人惊讶的是,老年患者(≥65 岁)的症状严重程度(由 TSSS 表示)低于年轻和中年成年人(p=0.008)。鼻咽病毒载量与 HMPV 感染的症状严重程度无关,也不能预测其严重程度。有趣的是,在症状出现后 3-5 天,基因型 A 感染患者的病毒载量高于基因型 B(4.4 对 3.3 log RNA 拷贝/μl)(p=0.003)。
总体而言,HMPV 遗传多样性和病毒载量对急性呼吸道感染的成人症状严重程度没有影响。不同基因型之间病毒载量随时间的动态变化可能对病毒传播有重要影响。