Dong Zefeng, Xia Yu, Ya Xuerong, Chen Liling, Liu Cheng, Wang Ruyan, Shen Qiang
Suzhou Center for Disease Prevention and Control, Suzhou, 215004, China.
Suzhou Municipal Hospital, Suzhou, 215004, China.
Virus Genes. 2018 Apr;54(2):182-189. doi: 10.1007/s11262-018-1534-7. Epub 2018 Feb 5.
Human infections with H7N9 viruses can cause severe pneumonia and even death. To characterize the epidemiology and genetics of the H7N9 viruses circulating during from October 2016 to April 2017 in Suzhou, China, all pharyngeal swab samples were collected from severe acute respiratory infections (SARI) cases during this fifth wave of infection, and we amplified the H7N9 H7 and N9 genes using a real-time polymerase chain reaction (PCR). Positive samples were subjected to virus isolation and gene sequencing to analyze the evolution and variation of the H7N9 strains. The epidemiological features of H7N9 patients have not changed and there were no significant mutations in the key sites of the hemagglutinin (HA) gene sequence, but we identified the K526R and E627 K substitutions in the PB2 protein. In the neuraminidase (NA) protein, drug-resistant mutations (R294 K and H276Y) occurred in a few strains. Most of the H7N9 viruses isolated from Suzhou had no drug resistance mutations, but it is necessary to closely monitor and analyze the probable emergence of mutations and the spread of resistant strains. The reduction of the N-glycosylation site at position 42 of NA was observed in some strains.
人感染H7N9病毒可导致严重肺炎甚至死亡。为了阐明2016年10月至2017年4月在中国苏州流行的H7N9病毒的流行病学特征和遗传学特征,我们收集了第五波感染期间所有严重急性呼吸道感染(SARI)病例的咽拭子样本,并使用实时聚合酶链反应(PCR)扩增H7N9的H7和N9基因。对阳性样本进行病毒分离和基因测序,以分析H7N9毒株的进化和变异情况。H7N9患者的流行病学特征没有变化,血凝素(HA)基因序列的关键位点没有明显突变,但我们在PB2蛋白中鉴定出了K526R和E627K替换。在神经氨酸酶(NA)蛋白中,少数毒株出现了耐药性突变(R294K和H276Y)。从苏州分离出的大多数H7N9病毒没有耐药性突变,但有必要密切监测和分析可能出现突变以及耐药毒株传播的情况。在一些毒株中观察到NA第42位的N-糖基化位点减少。