呼吸道合胞病毒非结构蛋白1氨基酸变异及临床特征分析

H Zhai, L Q Gao, L Ren, J Xie, E M Liu
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摘要

目的:探讨呼吸道合胞病毒(RSV)非结构蛋白(NS) 1氨基酸变异与临床特征的关系。方法:回顾性分析病例。2018年12月至2020年1月,重庆医科大学儿童医院呼吸内科RT-PCR或PCR检测为RSV阳性的住院儿童共81例纳入研究。采用PCR扩增RSV A、B亚型NS1基因并测序。分析了氨基酸序列。采用卡方检验和Mann-Whitney秩和检验比较变异组和非变异组中有无NS1变异儿童的临床特征和Ⅰ型干扰素水平。结果:81例患者中,男性58例,女性23例。变异组11例,发病年龄分别为2.0(1.0、11.0)个月,其中A亚型4例(变异位点分别为Lys33Gln 2例,Gly2Asp、Pro67Ser、Leu137Phe 1例),B亚型7例(变异位点分别为Val121Ile 2例,Tyr30Cys、Val65Met、Asn85Ser、Ser118Asn、Asp124Asn 1例)。这些变异位点在NCBI蛋白数据库中出现的频率都很低,为0.08(0.04,0.29)%。无变异组70例,发病年龄为3.5(1.0,7.0)个月。变异组呼吸困难发生率高于非变异组(10/11比47% (33/70),χ2=7.31, p < 0.05。结论:RSV非结构蛋白NS1存在一定的变异位点。儿童可能容易出现NS1变异的呼吸困难。
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[Analysis of respiratory syncytial virus nonstructural protein 1 amino acid variation and clinical characteristics].

Objective: To investigate the relationship between amino acid variations of respiratory syncytial virus (RSV) nonstructural protein (NS) 1 and the clinical characteristics. Method: A retrospective case review was conducted. From December 2018 to January 2020, a total of 81 cases of hospitalized children who were tested only positive for RSV by RT-PCR or PCR at the Department of Respiratory Medicine, Children's Hospital of Chongqing Medical University were included in the study. The NS1 genes of RSV subtype A and subtype B were amplified by PCR and sequenced. The amino acid sequences were analyzed. The Chi-square test and Mann-Whitney rank sum test were used to compare the clinical characteristics and type Ⅰ interferon levels of children with or without NS1 variation in the variation and non-variation groups. Results: Among 81 cases, there were 58 males and 23 females. There were 11 cases in the variation group, the age of onset was 2.0 (1.0, 11.0) months, included 4 cases of subtype A (variant sites were: 2 cases for Lys33Gln, one case for Gly2Asp, Pro67Ser, Leu137Phe, respectively) and 7 cases of subtype B (variant sites were: two cases for Val121Ile, one case for Tyr30Cys, Val65Met, Asn85Ser, Ser118Asn, Asp124Asn, respectively). These variant sites all appeared at a very low frequency 0.08 (0.04, 0.29) % in the NCBI PROTEIN database. There were 70 cases in non-variation group, the onset age was 3.5 (1.0, 7.0) months. The proportion of dyspnea in the variation group was higher than that in the non-variation group (10/11 vs. 47% (33/70), χ2=7.31, P<0.01). Conclusions: There are some variant sites in nonstructural protein NS1 of RSV. Children may be prone to have dyspnea with NS1 variations.

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