Gene mutation of coxsackievirus A4 VP1 from Shenzhen, China, 2014
YAO Xiang-jie1, HE Ya-qing1, CAI Chun-lin2, ZHUO Fei2, YANG Gui-qing2
1.Laboratory of Infectious Diseases and Surveillance,Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, China; 2.Luohu Center for Disease Control and Prevention, Shenzhen 518020, China
Abstract:We identified the pathogen causing an outbreak of herpangina in Shenzhen in 2014. Phylogenic analysis was carried out on VP1 genetic region of coxsackievirus A4 isolated from this outbreak. Eight throat swab specimens were collected from patients during the outbreak. The RNA was extracted from the virus and real-time RT-PCR method was used to test virus such as human enterovirus71, coxsackievirus Al6, coxsackievirus A4, coxsackievirus A6, and coxsackievirus A10. Complete VP1 gene of CVA4 identified in the outbreak was amplified by RT-PCR technique. Phylogenetic trees based on entire and partial VP1 sequences were constructed among CVA4 gene and others published in GenBank. It showed that CVA4 with GIB type was the pathogen in this outbreak. Data from homological comparisons indicated 4 CVA4 strains amplified in this outbreak had the highest nucleotide acid identity with the isolates from Yunnan in 2004 (AB268278), Shenzhen in 2009 (HQ728260), and Taiwan in 2008 (AB571570). The homologies of nucleotide sequences among them were 94.1%- 94.8%, which has the lowest identity (84.3%) with the prototype strain (HIGHPOINT strain). However, the 4 CVA4 strains amplified in this outbreak had the highest amino acid identity (99.3%) with the isolates from Taiwan in 2006 (AB571563), Jilin in 2009 (JQ715709), and the lowest amino acid identity (97.1%) with the isolates from Shandong in 2006 (GQ253375). Comparing with the CVA4 isolate from Shenzhen in 2009, 6 amino mutation were found in the four CVA4 strain (N22S,T34A, N63S, A165D, T200A and V126A ). Result of the analysis on phylogenetic tree showed that the 4 CVA4 stains were still belong to GIB subtype, however, it is obviously different with other stains in GIB group gained in other place in different time. In conclusion, the four CVA4 stains identified in Shenzhen, 2014 belongs to GIB subtype, which were found to have great difference on VP1 region.
姚相杰, 何雅青, 蔡春林, 卓菲, 杨贵清. 深圳地区2014年柯萨奇病毒A组4型VP1区基因特征分析[J]. 中国人兽共患病学报, 2015, 31(6): 565-568.
YAO Xiang-jie, HE Ya-qing, CAI Chun-lin, ZHUO Fei, YANG Gui-qing. Gene mutation of coxsackievirus A4 VP1 from Shenzhen, China, 2014. Chinese Journal of Zoonoses, 2015, 31(6): 565-568.
[1] Ji YL, Wang YQ, Identification and sequence analysis of the 5'UTR-VP4-VP2 region of coxsakievirus A4 isolated from patients with hand foot and mouth disease[J]. Chin Prev Med, 2012, 13(9): 675-678. (in Chinese) 吉彦莉,王永全.手足口病患儿柯萨奇病毒A4的鉴定及其5'UTR-VP4-VP2区序列分析[J].中国预防医学杂志,2012,13(9):675-678. [2] Yang F, Zhang T,Hu Y, et al. Survey of enterovirus infections from hand, foot and mouth disease outbreak in China, 2009[J]. Viral J,2011,8(508): 1-4. [3] Wu Y,Yeo A, Phoon MC,et al. The largest outbreak of hand,foot and mouth disease in Singapore in 2008:the role of enterovirus71 and coxsackievirus A strains[J].Int J Infect Dis,2010,14(12):e1076-1081. [4] Liu JF, Zhang Y, Li H, et al. Genetic characterization of VP4-VP2 of two Coxsackievirus A4 isolated from patient with hand, foot and mouth disease[J].Chin J Vaccine Immunizat, 2009, 15(4): 345-349. (in Chinese) 刘建锋,张勇,李慧,等.从手足口病病例分离的两株柯萨奇病毒A组4型毒株的VP4~VP2区基因特征分析[J].中国疫苗和免疫,2009,15(4):345-349. [5] Oberste MS, Penaranda S,Maher K,et al.Complete genome sequences of all members of the species Human enterovirus A[J].J Gen Virol,2004,85(Pt 6): 1597-1607. [6] 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. [7] Zhen RN,Zhang Y,Xie HP,et al.Sequence analysis of coxsackievirus A4 and coxsackievirus A10 in Guangzhou city, 2010-2012[J]. Chin J Prev Med,2014,48(6):445-450.(in Chinese) 甄若楠,张颖,谢华萍,等.2010-2012年广州市柯萨奇病毒A4、A10型VPl基因特征分析[J].中华预防医学杂志,2014,48(6):445-450.