王瑞, 肖勇, 鲍静, 管红霞, 周琪, 於淳安, 张志明, 马广源. 2016-2018年江苏省无锡市儿童呼吸道合胞病毒流行病学特征及G基因变异分析[J]. 疾病监测, 2024, 39(3): 324-330. DOI: 10.3784/jbjc.202302280074
引用本文: 王瑞, 肖勇, 鲍静, 管红霞, 周琪, 於淳安, 张志明, 马广源. 2016-2018年江苏省无锡市儿童呼吸道合胞病毒流行病学特征及G基因变异分析[J]. 疾病监测, 2024, 39(3): 324-330. DOI: 10.3784/jbjc.202302280074
Wang Rui, Xiao Yong, Bao Jing, Guan Hongxia, Zhou Qi, Yu Chunan, Zhang Zhiming, Ma Guangyuan. Epidemiological characteristics and G gene variation analysis of respiratory syncytial virus in children in Wuxi city, Jiangsu province, 2016−2018[J]. Disease Surveillance, 2024, 39(3): 324-330. DOI: 10.3784/jbjc.202302280074
Citation: Wang Rui, Xiao Yong, Bao Jing, Guan Hongxia, Zhou Qi, Yu Chunan, Zhang Zhiming, Ma Guangyuan. Epidemiological characteristics and G gene variation analysis of respiratory syncytial virus in children in Wuxi city, Jiangsu province, 2016−2018[J]. Disease Surveillance, 2024, 39(3): 324-330. DOI: 10.3784/jbjc.202302280074

2016-2018年江苏省无锡市儿童呼吸道合胞病毒流行病学特征及G基因变异分析

Epidemiological characteristics and G gene variation analysis of respiratory syncytial virus in children in Wuxi city, Jiangsu province, 2016−2018

  • 摘要:
    目的 分析2016年1月至2018年12月江苏省无锡市儿童中呼吸道合胞病毒(RSV)感染的流行特征及RSV-G基因变异情况,为江苏省无锡市RSV预防控制提供科学数据。
    方法 采集2016 — 2018年江苏省无锡市儿童医院的急性上呼吸道感染样本,使用实时荧光定量聚合酶链式反应技术对采集的样本进行RSV检测,使用双重荧光聚合酶链式反应方法明确A/B亚型,选取部分阳性样本进行G基因测序,比对测序结果与已知的RSV基因序列,确定基因型别和分析G基因的变异情况。
    结果  2016 — 2018年RSV总体检出率为9.01%(281/3120),RSV A亚型为4.07%(127/3120),RSV B亚型为4.87%(152/3120),A、B亚型混合感染仅2例。 婴幼儿检出率最高为10.77%(196/1820)。 每年11月至次年2月占比(69.97%,191/281)远高于其他月份。 2016年1月至2017年4月以B亚型为主,2017年9月至2018年12月以A亚型为主。 RSV A亚型 有1种基因型:ON1,RSV B亚型有1种基因型:BA10。 RSV A亚型核苷酸同源性为95.70%~99.00%,RSV B亚型核苷酸同源性97.10%~99.50%。 A亚型易发生E262K、L274P突变,B亚型均发生T270I和V271A突变。 ON1型N-糖基化位点只有237位点与ON1原型株一致,BA10型N-糖基化位点与BA原型株一致。
    结论 婴幼儿是江苏省无锡市RSV感染的主要人群,每年11月至次年2月为RSV感染高峰期,呈现A亚型和B亚型交替流行的特点。 ON1基因型和BA10基因型分别是RSV A、B亚型的唯一基因型。 RSV-G基因同源性差异较小,均有ON1、BA10基因型的典型氨基酸位点突变,ON1型N-糖基化位点比BA10型较易发生变异。

     

    Abstract:
    Objective To analyse the epidemiological characteristics of respiratory syncytial virus (RSV) infection and RSV- G gene variation among children in Wuxi city, Jiangsu province from January 2016 to December 2018, and to provide scientific data for the prevention and control of RSV in Wuxi city, Jiangsu province.
    Methods To collect specimens of acute upper respiratory tract infections from Wuxi Children's Hospital from 2016 to 2018, use real-time fluorescence quantitative polymerase chain reaction to detect RSV in the collected specimens, use double fluorescence polymerase chain reaction method to clarify A/B subtypes, select some positive specimens to perform G-gene sequencing, and compare the sequencing results with the known RSV gene sequences, to determine genotypes and to analyse the variability of the G-gene.
    Results The overall RSV detection rate in 2016−2018 was 9.01% (281/3120), 4.07% (127/3120) for RSV subtype A, 4.87% (152/3120) for RSV subtype B, and only 2 cases of mixed subtypes A and B infections. The highest detection rate was 10.77% (196/1820) in infants and young children. The proportion from November to February each year (69.97%, 191/281) was much higher than other months. Subtype B predominated from January 2016 to April 2017, and subtype A predominated from September 2017 to December 2018. There was one genotype for RSV subtype A: ON1, and one genotype for RSV subtype B: BA10. The nucleotide homology of RSV subtype A was 95.70%–99.00% and the nucleotide homology of RSV subtype B was 97.10%–99.50%. Subtype A is prone to E262K and L274P mutations, and subtype B has T270I and V271A mutations. only 237 N-glycosylation sites in ON1 are identical to those in the prototype ON1 strain, and the N-glycosylation sites in BA10 are identical to those in the prototype BA strain.
    Conclusion Infants are the main population infected with RSV in Wuxi city, Jiangsu province, and the peak period of RSV infection is from November to February every year, showing the characteristics of alternating epidemics of subtypes A and B. The ON1 and BA10 genotypes are the only genotypes of subtypes A and B of RSV, respectively. The homozygosity of the RSV-G gene is relatively small, and both of them have the typical amino acid site mutations of the ON1 and BA10 genotypes, and the N-glycosylation site of the ON1 type is more prone to mutation than that of the BA10 type. N-glycosylation sites were more likely to be mutated in the ON1 type than in the BA10 type.

     

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