[Molecular characteristics of Japanese encephalitis virus carried by Culex tritaeniorhynchus in Dongchuan District, Kunming City, Yunnan Province].

Q3 Medicine
Y Gu, Y He, Y Chen, Z Yang, N Li, S Lü, Y Zhu, F Ruan, J Wang, J Wang
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Baby hamster kidney-21 (BHK-21) cells and <i>Aedes albopictus</i> clone C6/36 cells were used for virus isolation, and positive isolates were identified using flavivirus primers. The positive isolates were amplified using reverse transcription polymerase chain reaction (RT-PCR) assay with 15 pairs of specific primers covering the full length of the genotype I Japanese encephalitis virus, and DNA sequence assembly was performed using the software SeqMan in the DNASTAR package. The obtained sequences were aligned with the complete sequences of 38 Japanese encephalitis virus downloaded from the GenBank with the software MegAlign, and the nucleotide and amino acid homology analyses of the obtained sequences were performed. The difference in amino acid sites was analyzed with the software GeneDoc, and phylogenetic trees were created based on the sequences of the coding region and E protein of the isolated Japanese encephalitis virus with the software Mega X. 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引用次数: 0

Abstract

Objective: To isolate the Japanese encephalitis virus carried by Culex tritaeniorhynchus in Dongchuan District of Yunnan Province and analyze its molecular characteristics, so as to provide insights into the prevention and control of Japanese encephalitis in Yunnan Province.

Methods: Mosquito specimens were collected using mosquito-trapping lamps from pig farms in Batang Village and Xiaoxin Village, Dongchuan District, Kunming City, Yunnan Province in July 2016, and the mosquito species was identified according to the mosquito morphology. Then, 60 to 100 mosquitoes of each species served as a group and were ground. Baby hamster kidney-21 (BHK-21) cells and Aedes albopictus clone C6/36 cells were used for virus isolation, and positive isolates were identified using flavivirus primers. The positive isolates were amplified using reverse transcription polymerase chain reaction (RT-PCR) assay with 15 pairs of specific primers covering the full length of the genotype I Japanese encephalitis virus, and DNA sequence assembly was performed using the software SeqMan in the DNASTAR package. The obtained sequences were aligned with the complete sequences of 38 Japanese encephalitis virus downloaded from the GenBank with the software MegAlign, and the nucleotide and amino acid homology analyses of the obtained sequences were performed. The difference in amino acid sites was analyzed with the software GeneDoc, and phylogenetic trees were created based on the sequences of the coding region and E protein of the isolated Japanese encephalitis virus with the software Mega X. In addition, the secondary and tertiary structures of the E protein of the Japanese encephalitis virus were predicted using the online tool SOPMA and the software Swiss-Model.

Results: A total of 5 820 mosquitoes were collected and 3 843 Cx. tritaeniorhynchus (66.03%) were identified according to the mosquito morphology. A positive virus isolate, termed YNDC55-33, was isolated from Cx. tritaeniorhynchoides following batches of virus isolation from mosquito specimens, and cytopathic effect was observed following inoculation into BHK-21 and C6/36 cells. The YNDC55-33 virus isolate was successfully amplified with the flavivirus primes, and a long sequence containing 300 nucleotides was obtained. Following sequence alignment using the BLAST tool, the sequence of the YNDC55-33 virus isolate had high homology with that of the genotype I Japanese encephalitis virus. A long sequence with 10 845 nucleotides in length, which encoded 3 432 amino acids, was obtained by splicing the full sequence of the YNDC55-33 virus isolate. Phylogenetic analysis based on the whole-genome sequence and E gene sequence of the YNDC55-33 virus isolate showed that the new YNDC55-33 virus isolate was most closely related to the genotype I Guizhou isolate (GenBank accession number: HM366552), with nucleotide homology of 98.5% and amino acid homology of 99.4%, and the YNDC55-33 virus isolate shared 97.96% ± 0.33% nucleotide homology and 99.35% ± 0.08% amino acid homology with other genotype I Japanese encephalitis virus isolates, and < 90% nucleotide homology and < 98% amino acid homology with other genotypes of Japanese encephalitis virus. The YNDC55-33 virus isolate and the live attenuated virus vaccine candidate SA14-14-2 isolate differed at 16 amino acid sites on E gene, and 7 out of 8 key amino acid sites related to neurovirulence. The secondary and tertiary structures of the E protein of the YNDC55-33 virus isolate were predicted to be characterized by random coils.

Conclusions: A genotype I Japanese encephalitis virus was isolated from Cx. tritaeniorhynchus in Dongchuan District, Kunming City. This virus isolate and the live attenuated virus vaccine candidate SA14-14-2 isolate does not differ at antigenic epitopes-related key amino acid sites, and the major protein structure of the virus isolate is random coils. This study adds new data for the epidemiological distribution of Japanese encephalitis virus in Yunnan Province, which may provide insights into the prevention and control of Japanese encephalitis in the province.

[云南省昆明市东川区三带喙库蚊携带日本脑炎病毒的分子特征]。
目的分离云南省东川区三带喙库蚊携带的日本脑炎病毒,分析其分子特征,为云南省日本脑炎的防控提供参考:2016年7月在云南省昆明市东川区八塘村和小新村的养猪场用诱蚊灯采集蚊子标本,根据蚊子形态鉴定蚊子种类。然后,以每种蚊子 60 至 100 只为一组,进行研磨。用小仓鼠肾-21(BHK-21)细胞和白纹伊蚊克隆C6/36细胞进行病毒分离,并用黄病毒引物鉴定阳性分离株。用 15 对特异性引物(覆盖基因型 I 日本脑炎病毒的全长)进行反转录聚合酶链反应(RT-PCR),扩增阳性分离物,并用 DNASTAR 软件包中的 SeqMan 软件进行 DNA 序列组装。用 MegAlign 软件将获得的序列与从 GenBank 下载的 38 个日本脑炎病毒的完整序列进行比对,并对获得的序列进行核苷酸和氨基酸同源性分析。此外,还利用在线工具 SOPMA 和软件 Swiss-Model 预测了日本脑炎病毒 E 蛋白的二级和三级结构:结果:共收集了 5 820 只蚊子,根据蚊子的形态鉴定出 3 843 只三线蓟马(66.03%)。在从蚊子标本中分批分离病毒后,从三带喙蚊中分离出了一个阳性病毒分离物,称为 YNDC55-33,接种到 BHK-21 和 C6/36 细胞后观察到细胞病理效应。YNDC55-33 病毒分离物经黄病毒原核扩增成功,获得了包含 300 个核苷酸的长序列。使用 BLAST 工具进行序列比对后,YNDC55-33 病毒分离物的序列与基因型 I 日本脑炎病毒的序列具有高度同源性。通过拼接 YNDC55-33 病毒分离株的全序列,得到了一个长度为 10 845 个核苷酸的长序列,该序列编码 3 432 个氨基酸。基于 YNDC55-33 病毒分离株全基因组序列和 E 基因序列的系统进化分析表明,新的 YNDC55-33 病毒分离株与基因 I 型贵州分离株(GenBank 编号:HM366552)的亲缘关系最密切,核苷酸同源性为 98.5%,氨基酸同源性为 99.4%,YNDC55-33病毒分离株与其他基因型I日本脑炎病毒分离株的核苷酸同源性为97.96%±0.33%,氨基酸同源性为99.35%±0.08%,与其他基因型日本脑炎病毒的核苷酸同源性<90%,氨基酸同源性<98%。YNDC55-33病毒分离株与候选减毒活疫苗SA14-14-2分离株在E基因上有16个氨基酸位点不同,在与神经毒性相关的8个关键氨基酸位点中有7个不同。据预测,YNDC55-33 病毒分离株 E 蛋白的二级和三级结构以随机线圈为特征:结论:从昆明市东川区三带喙蝮蛇中分离到了一种基因I型日本脑炎病毒。该病毒分离株与减毒活疫苗候选株SA14-14-2在抗原表位相关的关键氨基酸位点上无差异,病毒分离株的主要蛋白结构为随机线圈。这项研究为日本脑炎病毒在云南省的流行病学分布增添了新的数据,可为云南省日本脑炎的防控提供启示。
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来源期刊
中国血吸虫病防治杂志
中国血吸虫病防治杂志 Medicine-Medicine (all)
CiteScore
1.30
自引率
0.00%
发文量
7021
期刊介绍: Chinese Journal of Schistosomiasis Control (ISSN: 1005-6661, CN: 32-1374/R), founded in 1989, is a technical and scientific journal under the supervision of Jiangsu Provincial Health Commission and organised by Jiangsu Institute of Schistosomiasis Control. It is a scientific and technical journal under the supervision of Jiangsu Provincial Health Commission and sponsored by Jiangsu Institute of Schistosomiasis Prevention and Control. The journal carries out the policy of prevention-oriented, control-oriented, nationwide and grassroots, adheres to the tenet of scientific research service for the prevention and treatment of schistosomiasis and other parasitic diseases, and mainly publishes academic papers reflecting the latest achievements and dynamics of prevention and treatment of schistosomiasis and other parasitic diseases, scientific research and management, etc. The main columns are Guest Contributions, Experts‘ Commentary, Experts’ Perspectives, Experts' Forums, Theses, Prevention and Treatment Research, Experimental Research, The main columns include Guest Contributions, Expert Commentaries, Expert Perspectives, Expert Forums, Treatises, Prevention and Control Studies, Experimental Studies, Clinical Studies, Prevention and Control Experiences, Prevention and Control Management, Reviews, Case Reports, and Information, etc. The journal is a useful reference material for the professional and technical personnel of schistosomiasis and parasitic disease prevention and control research, management workers, and teachers and students of medical schools.    The journal is now included in important domestic databases, such as Chinese Core List (8th edition), China Science Citation Database (Core Edition), China Science and Technology Core Journals (Statistical Source Journals), and is also included in MEDLINE/PubMed, Scopus, EBSCO, Chemical Abstract, Embase, Zoological Record, JSTChina, Ulrichsweb, Western Pacific Region Index Medicus, CABI and other international authoritative databases.
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