Genetic analyses of the fusion protein genes in human parainfluenza virus types 1 and 3 among patients with acute respiratory infections in Eastern Japan from 2011 to 2015

表位 生物 系统发育树 基因 人副流感病毒 病毒学 抗体 否定选择 拉伤 系统发育学 病毒 遗传学 基因组 解剖
作者
Rika Tsutsui,Hiroyuki Tsukagoshi,Koo Nagasawa,Masaki Takahashi,Yuki Matsushima,Akihide Ryo,Makoto Kuroda,Hideki Takami,Hirokazu Kimura
出处
期刊:Journal of Medical Microbiology [Microbiology Society]
卷期号:66 (2): 160-168 被引量:10
标识
DOI:10.1099/jmm.0.000431
摘要

PURPOSE: To genetically explore the fusion protein gene (F) in human parainfluenza virus type 1 (HPIV1) and type 3 (HPIV3) strains, we analysed them in patients with acute respiratory infections in Eastern Japan from 2011 to 2015. METHODOLOGY: We constructed phylogenetic trees based on the HPIV and HPIV3 F gene using the maximum likelihood method and conducted P-distance and selective pressure analyses. We also predicted the linear epitopes of the protein in the prototype strains. Furthermore, we mapped the amino acid substitutions of the proteins. RESULTS: Nineteen strains of HPIV1 and 53 strains of HPIV3 were detected among the clinical acute respiratory infection cases. The phylogenetic trees indicated that the HPIV1 and HPIV3 strains were classified into clusters II and III and cluster C, respectively. The P-distance values of the HPIV1 and HPIV3 F genes were <0.03. Two positive selection sites were inferred in the HPIV1 (aa 8 and aa 10), and one positive selection site was inferred in the HPIV3 (aa 108), but over 10 negative selection sites were inferred. Four epitopes were predicted for the HPIV1 prototype strains, while five epitopes were predicted for the HPIV3 prototype strain. A positive selection site (aa 108) or the HPIV3 F protein was involved in the predicted epitope. Additionally, we found that an amino acid substitution (R73K) in the LC76627 HPIV3 strain presumably may affect the resistance to neutralization by antibodies. CONCLUSION: The F gene of HPIV1 and HPIV3 was relatively well conserved in the eastern part of Japan during the investigation period.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
1秒前
中科路2020完成签到,获得积分10
2秒前
橘子味汽水完成签到 ,获得积分10
2秒前
俊逸的又琴完成签到 ,获得积分10
3秒前
氮源发布了新的文献求助10
5秒前
曾经如冬完成签到,获得积分10
6秒前
伊利丹完成签到,获得积分10
7秒前
8秒前
9秒前
9秒前
9秒前
科研通AI6.4应助zyj采纳,获得10
10秒前
千鸟完成签到,获得积分10
13秒前
14秒前
在学一会完成签到,获得积分10
14秒前
Owen应助彼方250521采纳,获得10
14秒前
伊利丹发布了新的文献求助10
14秒前
氮源完成签到,获得积分10
14秒前
15秒前
空野晨发布了新的文献求助30
15秒前
罗女生发布了新的文献求助10
19秒前
汪小楠吖发布了新的文献求助10
19秒前
汉堡包应助15采纳,获得10
19秒前
song完成签到 ,获得积分10
19秒前
爆米花应助科研通管家采纳,获得10
20秒前
唠叨的背包完成签到,获得积分10
20秒前
20秒前
20秒前
20秒前
xing_xing应助科研通管家采纳,获得20
20秒前
阿木应助科研通管家采纳,获得10
20秒前
情怀应助科研通管家采纳,获得30
20秒前
20秒前
molihuakai应助科研通管家采纳,获得10
21秒前
松2026应助科研通管家采纳,获得30
21秒前
zcl发布了新的文献求助10
21秒前
科研通AI2S应助科研通管家采纳,获得10
21秒前
洛黎应助科研通管家采纳,获得10
21秒前
洛黎应助科研通管家采纳,获得10
21秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 500
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
Management and the Arts 310
Teaching Social and Emotional Learning in Physical Education 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7635791
求助须知:如何正确求助?哪些是违规求助? 9209730
关于积分的说明 19753342
捐赠科研通 7203634
什么是DOI,文献DOI怎么找? 3275259
关于科研通互助平台的介绍 2437151
邀请新用户注册赠送积分活动 2272380