Volume 18, Number 5—May 2012
Coxsackievirus A21, Enterovirus 68, and Acute Respiratory Tract Infection, China
During August 2006–April 2010, in Beijing, China, 2 rare human enterovirus serotypes, coxsackievirus A21 and enterovirus 68, were detected most frequently in human enterovirus–positive adults with acute respiratory tract infections. Thus, during some years, these 2 viruses cause a substantial proportion of enterovirus-associated adult acute respiratory tract infections.
Human enteroviruses (HEVs) are small, nonenveloped RNA viruses belonging to the family Picornaviridae. HEVs are classified into 4 species (HEV-A to -D) according to their molecular and antigenic properties (1). HEVs are associated with diverse clinical syndromes, ranging from mild upper respiratory tract illnesses to severe and potentially fatal conditions, such as aseptic meningitis, encephalitis, myocarditis, acute flaccid paralysis, and hand-foot-and-mouth disease (1).
Although HEV serotypes can cocirculate, spatial and temporal factors determine the predominant serotype. For instance, in France and Spain, echovirus 11 and echovirus 6 are the predominant serotypes in patients with enterovirus respiratory infections (2,3). Clusters of the rare serotype enterovirus 68 (EV68), which causes severe respiratory infections in children, have been recently reported in the Philippines (4) and Japan (5). To help clinicians and public health officials better understand the epidemiologic and clinical profiles of HEV respiratory infections, temporal and geographic patterns of circulation, especially the dynamics of HEV serotype shift, need to be determined. We report that in some years in Beijing, People’s Republic of China, the rarely reported coxsackievirus A21 (CVA21) and EV68 are the predominant serotypes in adults with enterovirus-associated acute respiratory tract infection (ARTI).
From August 2006 through April 2010, throat and nasal swabs were collected from 6,942 (3,158 male and 3,784 female) adult patients (>15 years of age) at the time of admission to the Fever Clinic Department at the Peking Union Medical College Hospital for ARTI. The 6,942 participants were randomly selected by physicians, as described (6). To detect HEV, we amplified 350–400 bp of the viral protein 1 (VP1) gene by reverse transcription PCR (7) and verified the findings by sequence analysis (GenBank accession nos. JN168998–JN169120). According to results of BLAST analysis (www.ncbi.nlm.nih.gov), the HEV detected in a sample was assigned to the serotype with which the amplified sequence shared >75% nt or >88% aa sequence identity (8). All samples were simultaneously screened for influenza viruses (A, B, and C), human parainfluenza viruses (1–4), respiratory syncytial virus, human coronaviruses (229E, NL63, HKU1, and OC43), metapneumovirus, adenovirus, and rhinovirus (6).
HEV was detected in 130 (69 male and 61 female) patients 15–70 years of age (median 27.5 years, mean 29.6 years). We identified 21 HEV serotypes. The most frequently detected serotypes were 2 that are rarely reported: CVA21 and EV68. The only HEV-C serotype detected in this study, CVA21, was found in 34 (26.2%) patients. The only HEV-D serotype detected in this study, EV68, was found in 13 (10%) patients. We also found 7 HEV-A serotypes and 12 HEV-B serotypes (Figure 1, panel A).
We detected 21 cases of CVA21 during August–December 2006 and 8 cases during September–December 2008, which accounted for 41.2% and 26.7% of all cases of HEVs, respectively. A few CVA21-positive cases were also detected in March and during June–August 2007. EV68 was detected in only 11 samples collected during August–October 2006 and in 2 samples in August 2008 (Figure 1, panel B; Table 1). The peaks of CVA21 and EV68 overlapped during August–October 2006. We co-detected other respiratory viruses in only 1 CVA21-positive patient and only 1 EV68-positive patient, indicating that the ARTIs in these patients are primarily associated with CVA21 or EV68 (Table 2).
Major symptoms associated with HEV infection included pharyngeal congestion, headache, myalgia, chills, and sore throat but not increased respiratory rate or difficulty breathing. According to the Guidelines for Surveillance on Severe Acute Respiratory Infections at Sentinel Hospitals (2011) issued by the Chinese Ministry of Health (www.moh.gov.cn/publicfiles/business/htmlfiles/mohjbyfkzj/s3577/201102/50590.htm), ARTI patients >5 years of age who had increased respiratory rate (>25 breaths/min) or difficulty breathing were considered to have a severe ARTI. Our data showed that all CVA21- or EV68-positive patients identified in this study had mild ARTIs.
The VP1 nucleotide sequences of the CVA21 and EV68 strains identified showed high sequence identity and were located in the same cluster in their phylogenetic trees, HEV-C and HEV-D, respectively (Figure 2). Nucleotide identity among the CVA21 strains identified was 95.6%–100% and that among EV68 strains was 92.3%–99.7%. However, the CVA21 and EV68 strains had low nucleotide identity compared with their prototype strains (CVA21, GenBank accession no. AF546702, 87%–89.2%; EV68, GenBank accession no. AY426531, 76.6%–78.9%). Alignment of the putative VP1 amino acid sequences of HEV strains with their respective prototype strains revealed a limited divergence; only 2 substitutions were found in CVA21, and 9 substitutions and 1 deletion was found in EV68 (data not shown). These findings suggest that the CVA21 or EV68 strains were similar but are changing and diverging from their prototype strains.
The frequency of detecting CVA21 and EV68 among HEV-positive adults with ARTIs in Beijing, China, was high. The difference in the HEV serotypes we detected compared with serotypes detected by others (2,3) suggests that the spectrum of HEV serotypes associated with ARTIs differs among geographic regions.
Since isolation of these viruses, infections with CVA21 and EV68 have been rarely reported (9,10). In the United States, only 42 detections of CVA21 and 26 detections of EV68 have been reported during 36 years of HEV surveillance (11). However, EV68 was recently associated with ARTIs in France, the Netherlands, the United States, the Philippines, and Japan (4,5,12–15), indicating epidemics of EV68 are increasing in number and severity.
The reason for the high frequency of CVA21 and EV68 infections in Beijing is unclear. The EV68 strains identified in this study are probably novel strains or genetic variants to which the population is immune. Moreover, the deduced amino acid identity of the EV68 strains with strains detected in children in Japan (GenBank accession nos. AB601872–AB601885) (5) was 89.4%–93.8%, indicating the possible co-existence of 2 distinct phylogenetic lineages of EV68 strains (13). The emergence of new genetic lineages might be the reason for increasing activity of EV68 (5,13). Because the median age of CVA21-positive patients was significantly lower than that of other HEV-positive patients (Table 2), we suspect that years of CVA21quiescence probably resulted in increased susceptibility of the younger population (11). Outbreaks of classical HEVs tend to occur in several-year cycles (11). We noted that CVA21 infections were concentrated in 2006 and 2008. However, because patients were not enrolled in our study after April 2010, our data on HEV circulation might be incomplete. Longer surveillance would be useful for determining the cycle of CVA21 and EV68 infections. Another limitation of this study is that samples were collected from outpatients but not hospitalized patients, which could bias the classification of illness toward being mild. However, this study presents evidence that CVA21 and EV68 cause mild disease and fills a void left by other studies that included only hospitalized patients.
In conclusion, we provide evidence that during some years in adults in Beijing, China, the rarely reported HEV serotypes CVA21 and EV68 are responsible for a substantial proportion of enterovirus-associated ARTIs. Our findings provide further insight into the pathogenesis of HEVs and increase our awareness of their clinical role. To predict possible outbreaks, global surveillance and investigation of HEV serotypes in patients with ARTIs should be strengthened.
Dr Xiang is an associate professor at the Christophe Mérieux Laboratory (Institute of Pathogen Biology, Chinese Academy of Medical Science–Fondation Mérieux) and the MOH Key Laboratory of Systems Biology of Pathogens (Institute of Pathogen Biology, Chinese Academy of Medical Sciences). Her research is focused on the etiology of respiratory infections and pathogenesis of respiratory viruses.
We thank Lan Chen, Jing Zhang, Wei Wang, and Qingqing Yang for their excellent technical assistance and the clinicians from Peking Union Medical College Hospital for their help with sample collection.
This study was supported by the National Major S & T Project for the Control and Prevention of Major Infectious Diseases in China (2009ZX10004-206) and Fondation Mérieux.
- Pallansch M, Roos R. Enteroviruses: polioviruses, coxsackieviruses, echoviruses, and newer enteroviruses. In: Knipe DM, Howley PM, editors. Fields virology, 5th ed. Philadelphia: Lippincott Williams & Wilkins; 2007.
- Jacques J, Moret H, Minette D, Lévêque N, Jovenin N, Deslée G, Epidemiological, molecular, and clinical features of enterovirus respiratory infections in French children between 1999 and 2005. J Clin Microbiol. 2008;46:206–13.
- Trallero G, Avellon A, Otero A, De Miguel T, Pérez C, Rabella N, Enteroviruses in Spain over the decade 1998–2007: virological and epidemiological studies. J Clin Virol. 2010;47:170–6.
- Imamura T, Fuji N, Suzuki A, Tamaki R, Saito M, Aniceto R, Enterovirus 68 among children with severe acute respiratory infection, the Philippines. Emerg Infect Dis. 2011;17:1430–5.
- Kaida A, Kubo H, Sekiguchi J, Kohdera U, Togawa M, Shiomi M, Enterovirus 68 in children with acute respiratory tract infections, Osaka, Japan. Emerg Infect Dis. 2011;17:1494–7.
- Ren L, Gonzalez R, Wang Z, Xiang Z, Wang Y, Zhou H, Prevalence of human respiratory viruses in adults with acute respiratory tract infections in Beijing, 2005–2007. Clin Microbiol Infect. 2009;15:1146–53.
- 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;44:2698–704.
- Oberste MS, Maher K, Kilpatrick DR, Pallansch MA. Molecular evolution of the human enteroviruses: correlation of serotype with VP1 sequence and application to picornavirus classification. J Virol. 1999;73:1941–8.
- Lennette EH, Fox VL, Schmidt NJ, Culver JO. The Coe virus: an apparently new virus recovered from patients with mild respiratory disease. Am J Hyg. 1958;68:272–87.
- Schieble JH, Fox VL, Lennette EH. A probable new human picornavirus associated with respiratory diseases. Am J Epidemiol. 1967;85:297–310.
- Khetsuriani N, Lamonte–Fowlkes A, Oberst S, Pallansch MA. Enterovirus surveillance—United States, 1970–2005. MMWR Surveill Summ. 2006;55:1–20.
- Petitjean–Lecherbonnier J, Dina J, Nguyen E, Gouarin S, Lebigot E, Vabret A. Molecular diagnosis of respiratory enterovirus infections: use of PCR and molecular identification for a best approach of the main circulating strains during 2008. Pathol Biol (Paris). 2011;59:113–21.
- Rahamat–Langendoen J, Riezebos–Brilman A, Borger R, van der Heide R, Brandenburg A, Schölvinck E, Upsurge of human enterovirus 68 infections in patients with severe respiratory tract infections. J Clin Virol. 2011;52:103–6.
- Centers for Disease Control and Prevention. Clusters of acute respiratory illness associated with human enterovirus 68—Asia, Europe, and United States, 2008–2010. MMWR Morb Mortal Wkly Rep. 2011;60:1301–4.
- Hasegawa S, Hirano R, Okamoto-Nakagawa R, Ichiyama T, Shirabe K. Enterovirus 68 infection in children with asthma attacks: virus-induced asthma in Japanese children. Allergy. 2011;66:1618–20.
Suggested citation for this article: Xiang Z, Gonzalez R, Wang Z, Ren L, Xiao Y, Li J, et al. Coxsackievirus A21, enterovirus 68, and acute respiratory tract infection, China. Emerg Infect Dis [serial on the Internet]. 2012 May [date cited]. http://dx.doi.org/10.3201/eid1805.111376
Comments to the Authors
Comments to the EID Editors
Please contact the EID Editors via our Contact Form.
- Page created: April 12, 2012
- Page last updated: April 12, 2012
- Page last reviewed: April 12, 2012
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)