- Research article
- Open Access
Changes in enterovirus serotype constituent ratios altered the clinical features of infected children in Guangdong Province, China, from 2010 to 2013
BMC Infectious Diseases volume 16, Article number: 399 (2016)
Enterovirus (EV)-related hand, foot, and mouth disease/herpangina (HFMD/HA) has been prevalent in Guangdong Province, China, since 2010.
Clinical data for EV-related HFMD/HA inpatients admitted to the Department of Paediatrics of Zhujiang Hospital from 2010 to 2013 were retrospectively reviewed. The corresponding EV serotypes were also determined by reverse transcription-polymerase chain reaction or BLAST analysis of the sequenced partial lengths of the viral protein1/5′-untranslated region.
A total of 867 eligible inpatients admitted during 2010–2013 were included in the study. Of these, the serotype of the responsible EV was successfully identified in 824 cases. The incidence of enterovirus 71 (EV71) infection amongst pediatric HFMD/HA inpatients decreased dramatically from 55.5 % in 2010 to 8.1 % in 2013, with a similar decrease recorded for coxsackievirus A16 (CVA16). However, the incidence of non-EV71/CVA16 infection increased from 30.0 % in 2010 to 83.8 % in 2013. We noted that the types of infection caused by different EV serotypes varied: EV71 was responsible for 100 % of the paralysis cases (26/26), 84.6 % of the deaths (11/13), and 84.1 % of cases with severe central nervous system involvement (SCNSI) (74/88); echovirus contributed to 16.4 % of the deaths (2/13) and 4.4 % of the SCNSI cases; and coxsackievirus accounted for only 2.2 % of the SCNSI cases (2/90). The clinical features of HFMD/HA cases varied greatly during the time period examined, with drastic changes in the hospitalization rates (45.1, 63.7, 36.4, and 19.1 % for 2010, 2011, 2012, and 21013, respectively), mortality rates (2.3, 0.9, 2.5, and 0.0 %, respectively), paralysis (5.1, 1.2, 5.4, and 0.0 %, respectively), SCNSI (16.8, 7.1, 12.7, and 2.2 %, respectively), and acute respiratory infection (21.1, 22.0, 45.9, and 59.0 %, respectively).
The incidences of infection caused by different EV serotypes, along with the clinical features of HFMD/HA cases, changed drastically in Guangdong Province, China, from 2010 to 2013, with the biggest changes observed in 2013. The changed constituent ratios of the different EV serotypes might therefore be responsible for the differences in the observed clinical features of HFMD/HA during this period.
Many enterovirus (EV) serotypes, including EV71, coxsackievirus A (CVA2, 4, 5, 7, 9, 10, 16), and coxsackievirus B (1, 2, 3, 4, 5), have been reported to cause hand, foot and mouth disease/herpangina (HFMD/HA) in humans. Of these, EV71 and CVA16 have traditionally been the two most common serotypes in mainland China [1–6]. In addition to fever and a rash, respiratory infection, hepatic injury, myocardial injury, meningitis, encephalitis, and acute flaccid paralysis are observed in EV-related HFMD/HA [7–9]. Different serotypes of EV mutually overlap in disease causation, and no serotype is assigned to a particular disease. However, some serotypes are more associated with particular diseases, such as EV71, which is associated with neurogenic pulmonary edema, brainstem encephalitis, and myelitis in young children [10–13]. The constituent ratios of EV serotypes change without cessation on a global basis, and monitoring their associated changes in the constituent ratios of circulating EV serotypes and their associated diseases is essential for public health and efficient allocation of medical resources.
Mainland China is heavily affected by EV-related HFMD/HA, which has caused millions of infections and hundreds of deaths annually since 2009 . Guangdong, a southern province of China, is one of the most severely affected regions [15–17]. Zhujiang Hospital is an officially assigned tertiary hospital for treating HFMD patients in Guangzhou (the provincial capital of Guangdong Province), as well as referral patients from other regions of Guangdong Province. Using a retrospective analysis of clinical information regarding HFMD/HA patients admitted to Zhujiang Hospital with an ascertained EV serotype, the current study aimed to elucidate the serotype constituent evolution of EV, and to explore its effect on HFMD/HA in Guangdong Province, China, between 2010 and 2013.
Patients and clinical data
A retrospective study was performed using pediatric patients with HFMD/HA admitted to Zhujiang Hospital between January 2010 and December 2013. All cases were from Guangzhou, or were referrals from other regions of Guangdong Province. Pediatric patients fitting the following criteria were included in the study: real-time fluorescence reverse transcription (RT)-polymerase chain reaction (PCR) evidence of positive EV; signs of eruptions or fever; and younger than 16 years of age. To reduce interference from other diseases, inpatients with a medical history of on-going neurological symptoms, congenital heart disease, or obvious bacterial infection were excluded. The clinical records of each inpatient were retrospectively itemized by two researchers, and then confirmed by pediatric clinicians. Patient privacy was maintained as the cases remained anonymous. The study was approved by the Ethics Committee of Zhujiang Hospital (ratification no.: ZJYY-2013-YXJYZX-001).
Stool sample collection and molecular analysis
A stool specimen was collected from each patient as part of standard care, and RNA was extracted from a 140-μL aliquot using a QIAamp Viral RNA Mini Kit (Qiagen, Hilden, Germany) within 1 day of collection. Some of the extracted RNA was used for immediate PCR analysis, while the remaining stool specimen and RNA were stored at −80 °C. Extracted RNA samples were used for real-time fluorescence RT-PCR and/or amplification of partial lengths of the viral protein 1/5′-untranslated region (VP1/5′-UTR). EV71 and CVA16 were jointly identified using EV71 and CVA16 EV kits (Shanghai ZJ Bio-Tech Co., Ltd, Shanghai, China). The serotypes of non-EV71 and non-CVA16 strains were initially determined by amplification of a partial length of VP1, with further amplification of a partial length of the 5′-UTR if necessary for clarification. The VP1/5′-UTR fragments were amplified as described previously [18, 19]. The products were sequenced by the Huada Gene Company (Shenzhen, China), and then analyzed using the BLAST program against sequences available in the GenBank database to identify the serotype.
Central nervous system involvement (CNSI) cases were defined as having two or more of the following: vomiting, irritability, startle reflex, convulsion, changed muscular tension, decreased tendon reflex, headache, neck stiffness, or any sign of altered consciousness. Paralysis and central nervous system lesions (on neuroimaging) were categorized as severe central nervous system involvement (SCNSI). Acute respiratory infection (ARI) was diagnosed by the presence of rhinorrhea and/or cough, and patients with pneumonia or bronchopneumonia were categorized as having a severe ARI. Acute myocardial injury was diagnosed based on laboratory evidence of elevated cardiac troponin I (cTnI), elevated creatine kinase-MB (CK-MB), and anelevated CK-MB/CK ratio. The following values were considered the threshold over which the readings were considered elevated: cTnI >0.04 μg/L, CK-MB/CK >0.25, CK-MB >44 U/L (2–36 month), CK-MB >37 U/L (37–72 month), and CK-MB >31 U/L (>73 month). Patient with an alanine aminotransferase level of >40 U/L was deemed as having acute hepatic injury. Diarrhoea was defined as presenting changed consistency of stool or frequency of defecation ≥3 times/day.
Statistical analysis was performed using SPSS version 13.0 software (SPSS Inc., Chicago, IL, USA). The differences in the categorical variables were analyzed by chi-square test. All tests were two-sided, and p < 0.05 was considered statistically significant.
A total of 2394 EV-related HFMD/HA patients were admitted to the Department of Paediatrics of Zhujiang Hospital during the study period, consisting of 926 inpatients and 1468 outpatients, and 824 inpatients were ascertained infected EV serotype by PCR and/or sequencing. Numbers of inpatients infected with EV71, CVA16 or non-EV71/CVA16 were 390, 127 and 409, respectively; while those of outpatients were 308, 259 and 901, correspondingly. Of the 926 inpatients, 867 were deemed eligible and were included in the current study (2010 (212), 2011 (314), 2012 (201), 2013 (140)), and the numbers of eligible inpatients infected with EV71, CVA16 or non-EV71/CVA16 included to illustrate the clinical features of HFMD/HA were 384, 120 and 363, respectively. The EV serotypes were successfully ascertained from 320/363 inpatients with non-EV71/CVA16 infection, of which the numbers of cases identified by partial VP1 and 5′-UTR sequencing were 295 and 25, respectively. Amongst the 320 identified EV serotypes, CVA6, CVA4, CVA10, echoviruses, and other coxsackieviruses accounted for 209 (65.3 %), 19 (5.9 %), 39 (12.2 %), 17 (5.3 %), and 36 (11.3 %) of the cases, respectively. CVA6 was responsible for more than half of the non-EV71/CVA16 cases each year during the study period as follows: 64.4 % (2010), 58.3 % (2011), 54.5 % (2012), and 83.5 % (2013) (Fig. 1). Of the 17 sporadic cases of echovirus, 14 were admitted in 2012, with the remaining three patients admitted in 2010 and 2011.
Significant changes occurred in the constituent ratios of EV serotypes in Guangdong Province between 2010 and 2013
The constituent ratios of inpatients infected with EV71, CVA16, and non-EV71/CVA16 changed greatly between 2010 and 2013 (Fig. 2). The incidence of EV71-infected inpatients decreased from 55.5 % in 2010 to 8.1 % in 2013, with the incidence of CVA16 infection dropping from 14.5 % in 2010 to 8.1 % in 2013. In contrast, the incidence of non-EV71/CVA16 infection increased from 30.0 % in 2010 to 83.8 % in 2013. Figure 2 shows similar changes in the constituent ratios of outpatients infected with EV71, CVA16, and non-EV71/CVA16. Statistially significant differences were observed in the constituent ratios of EV serotypes in outpatients amongst these years (2011 vs 2012 (p = 0.029), others (p < 0.01)), and statistially significant differences also observed in inpatients amongst these years (p < 0.05), except for 2010 vs 2011 (p =0.966).
Clinical features of HFMD/HA infection changed during the study period
The clinical features of children with HFMD/HA varied greatly over the study period. The hospitalization rate for HFMD/HA cases decreased from 63.7 % in 2010 to 19.1 % in 2013, while the rates of mortality, paralysis, SCNSI, and CNSI fluctuated drastically between 2010 and 2013 (Fig. 3). Additionally, ARI gradually replaced CNSI as the leading complication of HFMD/HA (Fig. 3). The risk of HFMD/HA sharply declined in 2013, with decreasing incidences of CNSI and SCNSI and no occurrences of paralysis or death.
The risks of severe complications of HFMD/HA varied depending on EV serotype
Of the 824 cases with an ascertained EV serotype (EV71 (n = 384, 46.6 %), coxsackievirus (n = 423, 51.3 %), and echovirus (n = 17, 2.1 %)), the mortality rates and neurological complications were disproportionately high in infections caused by EV71 and echoviruses, while severe complications were relatively low in cases caused by coxsackievirus. EV71 was responsible for 100 % of the paralysis cases (26/26), 84.6 % of the deaths (11/13), and 82.2 % of the cases of SCNSI (74/90), echovirus was responsible for 16.4 % of the deaths (2/13) and 4.4 % of the cases of SCNSI, while coxsackievirus was responsible for only 2.2 % of the cases of SCNSI (2/90), without causing death or paralysis.
This retrospective study demonstrated that the constituent ratios of EV serotypes in Guangdong Province, China, changed significantly between 2010 and 2013. EV71 was the predominant serotype at the beginning of the study period, but was less prevalent by 2013, with the reverse trend observed for CVA6. By 2013, EV71 infections accounted for less than 10 % of cases, whereas non-EV71/CVA16 serotypes caused more than 80 % of infections (Fig. 2). The overwhelming majority of non-EV71/CVA16 infections were caused by CVA6, indicating that CVA6 was the predominant serotype in Guangdong Province in 2013. Two previous studies also confirmed that CVA6 had become the dominant serotype in Guangdong during late 2012 and 2013 [17, 20], with similar reports from other regions of China in 2013 [21, 22]. CVA6 also replaced EV71 as the dominant serotype in other areas of the Asia-Pacific region, such as Taiwan, Thailand and Janpan in recent years [23–25]. The underlying mechanisms driving the shift of EV serotype constituent in an area maybe caused by the declining number of susceptible population caused by previous dominated serotype circulation and genetic mutation of certain EV serotype gaining edges on circulation.
Our data also showed that the drastically changed constituent ratios of the EV serotypes fundamentally altered the clinical features associated with HFMD/HA in Guangdong Province during the same time period. Overall, the hospitalization rate declined substantially, from 45.1 % in 2010 to 19.1 % in 2013, with the rates of SCNSI, paralysis, and death also declining, apart from a rebound in 2012. The incidence of ARI increased over the 4-year period, and became the most common complication of HFMD/HA in 2012 and 2013 (Fig. 3). The risk of severe complications of HFMD/HA significantly deceased in 2013, with only three inpatients developing SCNSI, and no cases of paralysis or death. This decline was predominantly caused by the decreased constituent ratio of EV71 infections and the increased prevalence of coxsackievirus infection, which causes less severe clinical features in HFMD/HA patients. In agreement with our results, EV71 was repeatedly reported to be responsible for most of the cases resulting in death, encephalitis, or paralysis in HFMD epidemics in the Asia-Pacific region [10–13], whereas the two most common coxsackievirus serotypes, i.e., CVA6 and CVA16, were generally mild with low incidences of SCNSI and death in children [1, 25–27]. Low incidence of diarrhea in HFMD/HA inpatients was observed in each year, which is somehow akin to previous studies [28, 29].
Echovirus was shown to match the capacity of EV71 for causing death and SCNSI (the 17 echovirus infections contributed to 16.4 % of deaths and 4.4 % of the cases of SCNSI), although its relatively low constituent ratio (2.1 %) reduced its influence on the clinical features of HFMD/HA in Guangdong Province over the study period. The two deaths were infected with Echo 2 and Echo 3, respectively; while the four SCNSI cases infected by Echo 2 (2 cases), Echo 3 (1 case) and Echo 1 (1 case) (data not shown). However, a cluster of echovirus infections contributed to the increase in mortality rates and SCNSI in 2012. Therefore, we concluded that the reduced prevalence of EV71 and the increase in coxsackievirus infections were responsible for the changes in clinical features associated with HFMD/HA between 2010 and 2013. In accordance with our results, other countries or regions that experienced a declined threat of HFMD/HA also documented a decrease in EV71 infections and an increase in coxsackievirus infections.
Because this study constitutes a retrospective analysis of patients admitted to an officially designated HFMD hospital that treats patients from the provincial capital and referrals from other regions of Guangdong Province, there is an inherent bias in the study results. Additionally, bias might be generated by uneven patient distribution from the different districts, which might affect the degree to which the clinical features and serotype constituent ratios for EV-related HFMD/HA in Guangdong Province between 2010 and 2013 are represented.
Our study demonstrated that EV71 was the predominant serotype in Guangdong Province at the beginning of the study period, but had declined in prevalence by 2013. In comparison, the incidence of CVA6 infections significantly increased over the same period, with CVA6 becoming the dominant serotype in 2013. Additionally, our data suggested that the changed constituent ratios of the EV serotypes might have influenced the clinical features of HFMD/HA infection in Guangdong Province, China, from 2010 to 2013.
ALT, alanine amino transferase; ARI, acute respiratory infection; CA, coxsackievirus A; CK, creatine kinase; CK-MB, creatine kinase-MB; CNSI, central nervous system involvement; cTnI, cardiac troponin I; EV, enterovirus; HFMD/HA, hand-foot-mouth disease/herpangina; non-EV71/CVA16, non-enterovirus 71 and non-coxsackievirus A16; RT-PCR, reverse transcription-polymerase chain reaction; SCNSI, severe central nervous system involvement; UTR, untranslated region; VP1, viral protein 1
Mao Q, Wang Y, Yao X, Bian L, Wu X, Xu M, Liang Z. Coxsackievirus A16: epidemiology, diagnosis, and vaccine. Hum Vaccin Immunother. 2014;10(2):360–7.
Li W, Yi L, Su J, Lu J, Ke C, Zeng H, Guan D, Ma C, Zhang W, Xiao H, et al. Seroprevalence of human enterovirus 71 and coxsackievirus A16 in Guangdong, China, in pre- and post-2010 HFMD epidemic period. PLoS One. 2013;8(12):e80515.
Yang F, Zhang T, Hu Y, Wang X, Du J, Li Y, Sun S, Sun X, Li Z, Jin Q. Survey of enterovirus infections from hand, foot and mouth disease outbreak in China, 2009. Virol J. 2011;8:508.
Chang ZR, Zhang J, Sun JL, Zhang WD, Wang ZJ. Epidemiological features of hand, foot and mouth disease in China, 2008–2009. Zhonghua Liu Xing Bing Xue Za Zhi. 2011;32(7):676–80.
Yan XF, Gao S, Xia JF, Ye R, Yu H, Long JE. Epidemic characteristics of hand, foot, and mouth disease in Shanghai from 2009 to 2010: Enterovirus 71 subgenotype C4 as the primary causative agent and a high incidence of mixed infections with coxsackievirus A16. Scand J Infect Dis. 2012;44(4):297–305.
Xing W, Liao Q, Viboud C, Zhang J, Sun J, Wu JT, Chang Z, Liu F, Fang VJ, Zheng Y, et al. Hand, foot, and mouth disease in China, 2008–12: an epidemiological study. Lancet Infect Dis. 2014;14(4):308–18.
Tapparel C, Siegrist F, Petty TJ, Kaiser L. Picornavirus and enterovirus diversity with associated human diseases. Infect Genet Evol. 2013;14:282–93.
Rhoades RE, Tabor-Godwin JM, Tsueng G, Feuer R. Enterovirus infections of the central nervous system. Virology. 2011;411(2):288–305.
Stalkup JR, Chilukuri S. Enterovirus infections: a review of clinical presentation, diagnosis, and treatment. Dermatol Clin. 2002;20(2):217–23.
Solomon T, Lewthwaite P, Perera D, Cardosa MJ, McMinn P, Ooi MH. Virology, epidemiology, pathogenesis, and control of enterovirus 71. Lancet Infect Dis. 2010;10(11):778–90.
Lee TC, Guo HR, Su HJ, Yang YC, Chang HL, Chen KT. Diseases caused by enterovirus 71 infection. Pediatr Infect Dis J. 2009;28(10):904–10.
Weng KF, Chen LL, Huang PN, Shih SR. Neural pathogenesis of enterovirus 71 infection. Microbes Infect. 2010;12(7):505–10.
Wang SM, Liu CC, Tseng HW, Wang JR, Huang CC, Chen YJ, Yang YJ, Lin SJ, Yeh TF. Clinical spectrum of enterovirus 71 infection in children in southern Taiwan, with an emphasis on neurological complications. Clin Infect Dis. 1999;29(1):184–90.
National statutory report of incidence and death statistics of infectious disease. http://www.chinacdc.cn/tjsj_6693/fdcrbbg/. Accessed 7 Aug 2016.
Wang YR, Sun LL, Xiao WL, Chen LY, Wang XF, Pan DM. Epidemiology and clinical characteristics of hand foot, and mouth disease in a Shenzhen sentinel hospital from 2009 to 2011. BMC Infect Dis. 2013;13:539.
Deng T, Huang Y, Yu S, Gu J, Huang C, Xiao G, Hao Y. Spatial-temporal clusters and risk factors of hand, foot, and mouth disease at the district level in Guangdong Province, China. PLoS One. 2013;8(2):e56943.
Lu J, Zeng H, Zheng H, Yi L, Guo X, Liu L, Sun L, Tan X, Li H, Ke C, et al. Hand, foot and mouth disease in Guangdong, China, in 2013: new trends in the continuing epidemic. Clin Microbiol Infect. 2014;20(7):O442–5.
Nix WA, Oberste MS, Pallansch MA. Sensitive, seminested PCR amplification of VP1 sequences for direct identification of all enterovirus serotypes from original clinical specimens. J Clin Microbiol. 2006;44(8):2698–704.
Ge S, Yan Q, He S, Zhuang S, Niu J, Xia N. Specific primer amplification of the VP1 region directed by 5′ UTR sequence analysis: enterovirus testing and identification in clinical samples from hand-foot-and-mouth disease patients. J Virol Methods. 2013;193(2):463–9.
Li JL, Yuan J, Yang F, Wu ZQ, Hu YF, Xue Y, Zhou BP, Jin Q. Epidemic characteristics of hand, foot, and mouth disease in southern China, 2013: coxsackievirus A6 has emerged as the predominant causative agent. J Infect. 2014;69(3):299–303.
Han JF, Xu S, Zhang Y, Zhu SY, Wu DL, Yang XD, Liu H, Sun BX, Wu XY, Qin CF. Hand, foot, and mouth disease outbreak caused by coxsackievirus A6, China, 2013. J Infect. 2014;69(3):303–5.
Hongyan G, Chengjie M, Qiaozhi Y, Wenhao H, Juan L, Lin P, Yanli X, Hongshan W, Xingwang L. Hand, foot and mouth disease caused by coxsackievirus A6, Beijing, 2013. Pediatr Infect Dis J. 2014;33(12):1302–3.
Wei SH, Huang YP, Liu MC, Tsou TP, Lin HC, Lin TL, Tsai CY, Chao YN, Chang LY, Hsu CM. An outbreak of coxsackievirus A6 hand, foot, and mouth disease associated with onychomadesis in Taiwan, 2010. BMC Infect Dis. 2011;11:346.
Fujimoto T, Iizuka S, Enomoto M, Abe K, Yamashita K, Hanaoka N, Okabe N, Yoshida H, Yasui Y, Kobayashi M, et al. Hand, foot, and mouth disease caused by coxsackievirus A6, Japan, 2011. Emerg Infect Dis. 2012;18(2):337–9.
Puenpa J, Chieochansin T, Linsuwanon P, Korkong S, Thongkomplew S, Vichaiwattana P, Theamboonlers A, Poovorawan Y. Hand, foot, and mouth disease caused by coxsackievirus A6, Thailand, 2012. Emerg Infect Dis. 2013;19(4):641–3.
Di B, Zhang Y, Xie H, Li X, Chen C, Ding P, He P, Wang D, Geng J, Luo L, et al. Circulation of Coxsackievirus A6 in hand-foot-mouth disease in Guangzhou, 2010–2012. Virol J. 2014;11:157.
Yang F, Yuan J, Wang X, Li J, Du J, Su H, Zhou B, Jin Q. Severe hand, foot, and mouth disease and coxsackievirus A6-Shenzhen, China. Clin Infect Dis. 2014;59(10):1504–5.
Rao DC, Reddy H, Sudheendra K, Raghavendra A, Varadharaj V, Edula S, Goparaju R, Ratnakar B, Srinivasa Rao AS, Maiya PP, et al. Non-polio enterovirus association with persistent diarrhea in children as revealed by a follow-up study of an Indian cohort during the first two years of life. J Clin Virol. 2014;61(1):125–31.
Rao DC, Ananda Babu M, Raghavendra A, Dhananjaya D, Kumar S, Maiya PP. Non-polio enteroviruses and their association with acute diarrhea in children in India. Infect Genet Evol. 2013;17:153–61.
We thank Fu Ning (Department of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China) for her considerable advice and for revising the manuscript, all the doctors in the Department of Paediatrics at Zhujiang Hospital, China, for providing the inpatient medical records, and Xia N (National Institute of Diagnostics and Vaccine Development in Infectious Disease, Xiamen University, Xiamen, China) for providing the primers for amplifying the enteroviral 5′-UTR. This work was supported by National Projects of Major Infectious. Disease Control and Prevention of China (grant number 2012ZX10004213), and by the National High Technology Research and Development Programme of China (863 Programme) (grant number 2011AA02A116). The funders played no role in study design, in the collection, analysis, or interpretation of data, in the writing of the manuscript, or in the decision to submit the manuscript for publication.
The work was supported by National Projects of Major Infectious Disease Control and Prevention of China (grant number 2012ZX10004213), and by the National High Technology Research and Development Programme of China (863 Programme) (grant number 2011AA02A116).
Availability of data and materials
H-TZ collected data for the clinical investigation, performed the serotype identification analysis, and drafted the original manuscript. Y-HG participated in the serotype identification analysis and carried out the RT-PCR analysis. BW confirmed the clinical features of the cases. M-JC collected the clinical specimens. Y-XP performed the virus isolation. LX participated in collecting and analyzing the data. S-HT jointly confirmed the clinical features of the cases. NY performed the RT-PCR analysis and revised the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Verbal consent of participating the project was obtained from their legal guardian, father or mother, and we guaranteed the privacy of each case was not violated by processing data anonmously. No individual persons data is involved in this manuscript, therefore, consent of patient to participate the project is not necessary.
Ethics approval and consent to participate
The study was approved by the Ethics Committee of Zhujiang Hospital (ratification no.: ZJYY-2013-YXJYZX-001).
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Zhou, HT., Guo, YH., Chen, MJ. et al. Changes in enterovirus serotype constituent ratios altered the clinical features of infected children in Guangdong Province, China, from 2010 to 2013. BMC Infect Dis 16, 399 (2016). https://0-doi-org.brum.beds.ac.uk/10.1186/s12879-016-1690-0
- Foot and mouth disease
- Clinical features