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[2007年北京儿童手足口病与肠道病毒71型/柯萨奇病毒A16型相关性研究]

[Study on the association of hand, foot and mouth disease and enterovirus 71/CA16 among children in Beijing, 2007].

作者信息

Zhu Ru-nan, Qian Yuan, Deng Jie, Xing Jiang-feng, Zhao Lin-qing, Wang Fang, Liao Bin, Ren Xiao-xu, Li Ying, Zhang Qi, Li Jie

机构信息

Laboratory of Virology, Beijing Municipal Laboratory of Infection and Immunity, Capital Institute of Pediatrics, Beijing, China.

出版信息

Zhonghua Liu Xing Bing Xue Za Zhi. 2007 Oct;28(10):1004-8.

PMID:18399150
Abstract

OBJECTIVE

To reveal the etiological agent of hand, foot and mouth disease in children in Beijing.

METHODS

Throat swabs were collected from 6 infants and young children with hand, foot and mouth disease who visited the affiliated Children's Hospital from May to June 2007. Aspirated fluid from tracheal intubatton, serum and cerebral spinal fluid (CSF) were collected from a 9 years old girl (No.4243) having central neural system complication of severe hand, foot and mouth disease and admitted to the hospital from the Emergency Department. Throat swab and aspirated fluid were inoculated into the cell lines Hep-2, MDCK and Vero for virus isolation. RNAs were extracted by Trizol from 6 throat swab specimens and aspirated fluid, serum while CSF was from that severe case (No.4243). The gene fragment from 5' UTR of enterovirus was amplified from throat swabs and aspirated fluid by reverse transcription-polymerase chain reaction (RT-PCR) with the primer pairs located at the untranslated region of all enterovirus. EV71 was identified by RT-PCR with the 2 and half primer pairs located at different parts of VP1 gene of EV71. The PCR products for VP1 encoding gene of EV71 from the specimens were sequenced and sequence analysis was performed by comparing those published VP1 genes of EV71. EV71 and CA16 specific primers were used to identify the isolates by RT-PCR and the sequences were directly determined from PCR products.

RESULTS

Gene fragments with expected molecular weight were amplified from all 6 throat swabs and the aspirate by the primer pairs universal for the 5' UTR of enterovirus, suggesting that these patients with hand, foot and mouth disease were infected by entorovirus. Out of these 7 specimens, 2 throat swabs and the aspirate were also showing positive for the VP1 of the EV71 by different primer sets. Sequence analysis revealed that the sequences for the amplicons from 1 throat swab (No. F4211) and the aspirate shared highest homology with those published EV71, indicating that these specimens were truly positive for EV71. The sequences amplified from these specimens shared 100% and 98.9% homology to each other and were closer to the sequences of EV71 identified from Zhejiang province than those from Taiwan and strain BrCr. Gene fragments for 5' UTR of enterovirus were obtained by RT-PCR after CPE appeared in 6 out of 7 inoculations including that aspirate fluid in Vero cell, indicating that enteroviruses were isolated from these specimens. Virus isolates from one throat swab (No. F4211) and the aspirate (No. 4243) were positive by RT-PCR with the primer pairs for EV71, which was consistent with RT-PCR amplification directly from specimens. Virus isolates from other 4 specimens were CA16 by RT-PCR and sequence analysis.

CONCLUSION

These data suggested that hand, foot and mouth disease recently appeared in children in Beijing was related with EV71 and CA16. EV71 could cause severe clinical manifestations with central nerve system complications even in the child older than 5 years.

摘要

目的

揭示北京地区儿童手足口病的病原体。

方法

收集2007年5月至6月到附属儿童医院就诊的6例手足口病婴幼儿的咽拭子。从一名因重症手足口病合并中枢神经系统并发症于急诊科入院的9岁女孩(4243号)采集气管插管吸出物、血清和脑脊液。将咽拭子和吸出物接种于Hep-2、MDCK和Vero细胞系进行病毒分离。用Trizol从6份咽拭子标本、吸出物、血清以及该重症病例(4243号)的脑脊液中提取RNA。采用位于所有肠道病毒非编码区的引物对,通过逆转录-聚合酶链反应(RT-PCR)从咽拭子和吸出物中扩增肠道病毒5'UTR的基因片段。用位于EV71病毒VP1基因不同部位的2.5对引物通过RT-PCR鉴定EV71。对标本中EV71的VP1编码基因的PCR产物进行测序,并通过与已发表的EV71的VP1基因比较进行序列分析。用EV71和CA16特异性引物通过RT-PCR鉴定分离株,并直接从PCR产物中测定序列。

结果

用肠道病毒5'UTR通用引物对从所有6份咽拭子和吸出物中扩增出预期分子量的基因片段,提示这些手足口病患者感染了肠道病毒。在这7份标本中,2份咽拭子和吸出物用不同引物对检测EV71的VP1也呈阳性。序列分析显示,1份咽拭子(F4211号)和吸出物扩增片段的序列与已发表的EV71序列具有最高同源性,表明这些标本EV71检测为真阳性。从这些标本中扩增的序列彼此间同源性为100%和98.9%,与从浙江省分离的EV71序列比台湾地区和BrCr株的序列更接近。7次接种(包括Vero细胞中的吸出物)中有6次出现细胞病变效应后,通过RT-PCR获得了肠道病毒5'UTR的基因片段,表明从这些标本中分离出了肠道病毒。用EV71引物对通过RT-PCR检测,1份咽拭子(F4211号)和吸出物(4243号)的病毒分离株呈阳性,这与直接从标本进行RT-PCR扩增结果一致。通过RT-PCR和序列分析,其他4份标本的病毒分离株为CA16。

结论

这些数据提示,北京地区近期儿童手足口病与EV71和CA16有关。EV71即使在5岁以上儿童中也可引起伴有中枢神经系统并发症的严重临床表现。

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