Evolutionary Diversity of Coxsackievirus A6 Causing Severe Hand, Foot, and Mouth Disease - China, 2012-2023

被引:4
|
作者
Lu, Huanhuan [1 ,2 ,3 ]
Xiao, Jinbo [1 ,2 ,3 ]
Wang, Wenhui [4 ]
Yan, Dongmei [1 ,2 ,3 ]
Ji, Tianjiao [1 ,2 ,3 ]
Yang, Qian [1 ,2 ,3 ]
Wei, Haiyan [5 ]
Du, Yanhua [6 ]
Zeng, Yunting [7 ]
Guo, Jun [8 ]
Chen, Jianhua [9 ]
Zeng, Hanri [10 ]
Liu, Yingying [11 ]
Zhou, Shuaifeng [12 ]
Ji, Hong [13 ]
Wang, Jianxing [14 ]
Zhou, Xiaofang [15 ]
Zhang, Yong [1 ,2 ,3 ]
机构
[1] Natl Key Lab Intelligent Tracking & Forecasting I, Beijing, Peoples R China
[2] World Hlth Org Polio Reference Lab Western Pacifi, Beijing, Peoples R China
[3] Chinese Ctr Dis Control & Prevent, Natl Inst Viral Dis Control & Prevent, Key Lab Lab Biosafety, Natl Hlth & Key Lab Lab Biosafety Natl Hlth Commi, Beijing, Peoples R China
[4] Linyi Ctr Dis Control & Prevent, Linyi, Shandong, Peoples R China
[5] Henan Prov Ctr Dis Control & Prevent, Zhengzhou, Henan, Peoples R China
[6] Shaanxi Prov Ctr Dis Control & Prevent, Xian, Shaanxi, Peoples R China
[7] Hainan Prov Ctr Dis Control & Prevent, Haikou, Hainan, Peoples R China
[8] Guizhou Prov Ctr Dis Control & Prevent, Guiyang, Guizhou, Peoples R China
[9] Gansu Prov Ctr Dis Control & Prevent, Lanzhou, Gansu, Peoples R China
[10] Guangdong Prov Ctr Dis Control & Prevent, Guangzhou, Guangdong, Peoples R China
[11] Hebei Prov Ctr Dis Control & Prevent, Shijiazhuang, Hebei, Peoples R China
[12] Hunan Prov Ctr Dis Control & Prevent, Changsha, Hunan, Peoples R China
[13] Jiangsu Prov Ctr Dis Control & Prevent, Nanjing, Jiangsu, Peoples R China
[14] Shandong Prov Ctr Dis Control & Prevent, Jinan, Shandong, Peoples R China
[15] Yunnan Prov Ctr Dis Control & Prevent, Kunming, Yunnan, Peoples R China
来源
CHINA CDC WEEKLY | 2024年 / 6卷 / 20期
基金
北京市自然科学基金;
关键词
SEQUENCE; SEROTYPE;
D O I
10.46234/ccdcw2024.086
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Introduction: : Coxsackievirus A6 (CVA6) has emerged as a significant pathogen responsible for severe cases of hand, foot, and mouth disease (HFMD). This study aims to delineate the demographic characteristics and analyze the viral evolution of severe HFMD associated with CVA6, thereby assisting in its surveillance and management. Methods: : In this investigation, 74 strains of CVA6 were isolated from samples collected from severe HFMD cases between 2012 and 2023. The VP1 gene sequences of CVA6 were amplified and analyzed to assess population historical dynamics and evolutionary characteristics using BEAST, DnaSP6, and PopART. Results: : A significant portion (94.4%) % ) of severe CVA6-associated HFMD cases (51 out of 54, with 20 lacking age information) were children under 5 years old. Among the 74 CVA6 strains analyzed, 72 belonged to the D3a sub-genotype, while only two strains were D2 sub-genotype. The average genetic distance between VP1 sequences prior to 2015 was 0.027, which increased to 0.051 when compared to sequences post-2015. Historical population dynamics analysis indicated three significant population expansions of severe CVA6-associated HFMD during 2012-2013, 2013-2014, and 2019-2020, resulting in the formation of 65 distinct haplotypes. Consistent with the MCC tree findings, transitioning between regional haplotypes required multiple base substitutions, showcasing an increase in population diversity during the evolutionary process (from 14 haplotypes in 2013 to 55 haplotypes over the subsequent decade). Conclusions: : CVA6, associated with severe HFMD, is evolving and presents a risk of outbreak occurrence. Thus, enhanced surveillance of severe HFMD is imperative.
引用
收藏
页码:442 / 449
页数:8
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