Advanced Search

CN 34-1304/RISSN 1674-3679

Volume 27 Issue 3
Mar.  2023
Turn off MathJax
Article Contents
DONG Ze-feng, XU Zhi-hui, WANG Di, WU Xue-fei, YA Xue-rong, XIA Yu, SHEN Qiang. Genetic characteristics of coxsackie A4 virus in a cluster of human infections in Suzhou[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2023, 27(3): 363-367. doi: 10.16462/j.cnki.zhjbkz.2023.03.021
Citation: DONG Ze-feng, XU Zhi-hui, WANG Di, WU Xue-fei, YA Xue-rong, XIA Yu, SHEN Qiang. Genetic characteristics of coxsackie A4 virus in a cluster of human infections in Suzhou[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2023, 27(3): 363-367. doi: 10.16462/j.cnki.zhjbkz.2023.03.021

Genetic characteristics of coxsackie A4 virus in a cluster of human infections in Suzhou

doi: 10.16462/j.cnki.zhjbkz.2023.03.021
Funds:

Suzhou Key Technologies for the Prevention and Control of Major and Infectious Diseases GWZX202202

Suzhou Key Technologies for the Prevention and Control of Major and Infectious Diseases GWZX202002

The Key Medical Discipline of Suzhou SZXK202117

"National Tutorial System" Training Project for Young Health Backbone Talents in Suzhou QNGG2022030

Health Talents Training Project GSWS202099

More Information
  • Corresponding author: SHEN Qiang, E-mail: yanhuahuo110@163.com
  • Received Date: 2021-05-12
  • Rev Recd Date: 2021-08-17
  • Available Online: 2023-04-04
  • Publish Date: 2023-03-10
  •   Objective  This study aimed to conduct a preliminary molecular identification of pathogens in throat swab samples from a cluster of of cases with unexplained respiratory infections in Suzhou City.  Methods  Throat swab specimens of the outbreak cases were collected, and Real-time reverse transcription polymerase chain reaction (Real-time RT-PCR) method was employed to detect nucleic acid of common pathogens (influenza A/B viruses, parainfluenza viruses, respiratory syncytial viruses, coronaviruses, rhinoviruses, metapneumoviruses and adenoviruses) for clustered respiratory infections. Concurrently, FilmArray automatic medical PCR analysis system was used for multi-pathogen screening. High-throughput sequencing was performed on the throat swab specimens. And the sequenced results were verified by using specific kit to detect coxsackievirus A4 (CV-A4).  Results  Among the 18 throat swab samples submitted for testing during this outbreak, 4 were positive for CV-A4 by Real-time RT-PCR. CV-A4 specific gene fragments were identified in the throat swab samples via both Real-time RT-PCR and high-throughput sequencing method. Sequence analysis indicated that the complete genome sequence of the virus strain involved in this outbreak in Suzhou City shared the highest similarity (98.11%) to the MN964082 viral nucleic acid in the NCBI database. The VP1 protein amino acid sequence demonstrated a 98.03% similarity to the prototype strain AY421762. Six mutation sites were identified (T23V, A34T, S102A, A200T, I262V, and Y285H) when compared to AY421762.  Conclusions  CV-A4 has the potential to cause clustered respiratory infections. Enhanced health monitoring is necessary for vulnerable groups, particularly school-aged children, to facilitate prompt detection and management of such outbreaks.
  • loading
  • [1]
    Chu PY, Lu PL, Tsai YL, et al. Spatiotemporal phylogenetic analysis and molecular characterization of coxsackievirus A4[J]. Infect Genet Evol, 2011, 11(6): 1426-1435. DOI: 10.1016/j.meegid.2011.05.010.
    [2]
    Hu YF, Yang F, Du J, et al. Complete genome analysis of coxsackievirus A2, A4, A5, and A10 strains isolated from hand, foot, and mouth disease patients in China revealing frequent recombination of human enterovirus A[J]. J Clin Microbiol, 2011, 49(7): 2426-2434. DOI: 10.1128/JCM.00007-11.
    [3]
    Chen P, Wang HY, Tao ZX, et al. Multiple transmission chains of coxsackievirus A4 co-circulating in China and neighboring countries in recent years: phylogenetic and spatiotemporal analyses based on virological surveillance[J]. Mol Phylogenetics Evol, 2018, 118: 23-31. DOI: 10.1016/j.ympev.2017.09.014.
    [4]
    Guo WP, Chen GQ, Xie GC, et al. Mosaic genome of human coxsackievirus A4 associated with herpangina and HFMD in Yancheng, China, 2016 and 2018[J]. Int J Infect Dis, 2020, 96: 538-540. DOI: 10.1016/j.ijid.2020.05.057.
    [5]
    Wang M, Li J, Yao MX, et al. Genome analysis of coxsackievirus A4 isolates from hand, foot, and mouth disease cases in Shandong, China[J]. Front Microbiol, 2019, 10: 1001. DOI: 10.3389/fmicb.2019.01001.
    [6]
    连宪强, 王文祥, 佘玲玲. 一起由柯萨奇病毒A组引起的呼吸道感染疫情病原分子特征分析[J]. 河南预防医学杂志, 2021, 32(2): 100-103. DOI: 10.13515/j.cnki.hnjpm.1006-8414.2021.02.006.

    Lian XQ, Wang WX, She LL. Pathogen-Associated molecular characteristics of a respiratory infection outbreak caused by CVA4[J]. Henan J Prev Med, 2021, 32(2): 100-103. DOI: 10.13515/j.cnki.hnjpm.1006-8414.2021.02.006.
    [7]
    Mine I, Taguchi M, Sakurai Y, et al. Bilateral idiopathic retinal vasculitis following coxsackievirus A4 infection: a case report[J]. BMC Ophthalmol, 2017, 17(1): 128. DOI: 10.1186/s12886-017-0523-2.
    [8]
    Akuzawa N, Harada N, Hatori T, et al. Myocarditis, hepatitis, and pancreatitis in a patient with coxsackievirus A4 infection: a case report[J]. Virol J, 2014, 11: 3. DOI: 10.1186/1743-422X-11-3.
    [9]
    Lee CJ, Huang YC, Yang S, et al. Clinical features of coxsackievirus A4, B3 and B4 infections in children[J]. PLoS One, 2014, 9(2): e87391. DOI: 10.1371/journal.pone.0087391.
    [10]
    Li JS, Dong XG, Qin M, et al. Outbreak of febrile illness caused by coxsackievirus A4 in a nursery school in Beijing, China[J]. Virol J, 2015, 12: 92. DOI: 10.1186/s12985-015-0325-1.
    [11]
    Timmermans A, Melendrez MC, Se Y, et al. Human sentinel surveillance of influenza and other respiratory viral pathogens in border areas of western Cambodia[J]. PLoS One, 2016, 11(3): e0152529. DOI: 10.1371/journal.pone.0152529.
    [12]
    Ji TJ, Guo Y, Lv L, et al. Emerging recombination of the C2 sub-genotype of HFMD-associated CV-A4 is persistently and extensively circulating in China[J]. Sci Rep, 2019, 9(1): 13668. DOI: 10.1038/s41598-019-49859-7.
    [13]
    姚学君, 姜仁杰, 管书慧, 等. 中国大陆地区柯萨奇病毒A组4型VP1区基因特征分析[J]. 中国人兽共患病学报, 2018, 34(11): 1021-1025. DOI: 10.3969/j.issn.1002-2694.2018.00.185.

    Yao XJ, Jiang RJ, Guan SH, et al. Genetic characteristics of the VP1 region of coxsackievirus A4 in mainland China[J]. Chinese Journal of Zoonoses, 2018, 34(11): 1021-1025. DOI: 10.3969/j.issn.1002-2694.2018.00.185.
    [14]
    Lau SKP, Zhao PSH, Sridhar S, et al. Molecular epidemiology of coxsackievirus A6 circulating in Hong Kong reveals common neurological manifestations and emergence of novel recombinant groups[J]. J Clin Virol, 2018, 108: 43-49. DOI: 10.1016/j.jcv.2018.09.002.
    [15]
    Yu F, Zhu R, Jia L, et al. Sub-genotype change and recombination of coxsackievirus A6s may be the cause of it being the predominant pathogen for HFMD in children in Beijing, as revealed by analysis of complete genome sequences[J]. Int J Infect Dis, 2020, 99: 156-162. DOI: 10.1016/j.ijid.2020.07.010.
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Figures(2)  / Tables(1)

    Article Metrics

    Article views (431) PDF downloads(35) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return