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Volume 25, Number 11—November 2019
Molecular and Clinical Comparison of Enterovirus D68 Outbreaks among Hospitalized Children, Ohio, USA, 2014 and 2018
Enterovirus D68 (EV-D68) causes respiratory tract infections and neurologic manifestations. We compared the clinical manifestations from 2 EV-D68 outbreaks in 2014 and 2018 and a low-activity period in 2016 among hospitalized children in central Ohio, USA, and used PCR and sequencing to enable phylogenetic comparisons. During both outbreak periods, infected children had respiratory manifestations that led to an increase in hospital admissions for asthma. The 2018 EV-D68 outbreak appeared to be milder in terms of respiratory illness, as shown by lower rates of pediatric intensive care unit admission. However, the frequency of severe neurologic manifestations was higher in 2018 than in 2014. During the same period in 2016, we noted neither an increase in EV-D68 nor a significant increase in asthma-related admissions. Phylogenetic analyses showed that EV-D68 isolates from 2018 clustered differently within clade B than did isolates from 2014 and are perhaps associated with a different EV-D68 subclade.
Enterovirus D68 (EV-D68) was originally identified in 1962 in children with severe respiratory tract infections in California, USA (1). The virus shares biological features with enteroviruses and rhinoviruses and was reported sporadically after these initial reports (2). However, EV-D68 gained epidemiologic and clinical relevance in 2014 after it was identified as an important pathogen associated with severe lower respiratory tract infections and, in some cases, with central nervous system disease (i.e., acute flaccid myelitis [AFM]) (3–5).
Nationwide Children’s Hospital (NCH) in Columbus, Ohio, USA, experienced a first outbreak of EV-D68 in 2014 that was associated with respiratory distress and disproportionately affected children with asthma; no case of AFM was identified (3). Although EV-D68 reportedly has a biennial seasonality, NCH did not have an EV-D68 outbreak in 2016. EV-D68 emerged again in 2018 and caused respiratory infections and, in some cases, neurologic manifestations.
The objective of this study was to compare differences in clinical characteristics and disease severity among children hospitalized with EV-D68 infection at NCH in 2018 with those identified during the 2014 outbreak and during a low-activity period (2016). We also sought to define the overlap between EV-D68 circulation and hospitalizations for asthma and compare the sequence variation of EV-D68 strains identified during the 2018 outbreak with strains identified in previous years.
Sample Collection and Testing Algorithms
We identified children hospitalized at NCH who had EV-D68 infection during the 2018 outbreak and during a nonoutbreak period (2016) and compared their clinical manifestations and characteristics with those identified during the 2014 outbreak as previously described (3). In brief, during June 1–October 19, 2018, we collected nasopharyngeal samples using flock swabs that went into viral transport media. All samples were obtained in accordance with standard of care for patients <21 years of age who tested positive for rhinovirus/enterovirus (RV/EV) on the FilmArray Respiratory Panel version 1.7 (6) and were stored at −80°C for further testing. We retrospectively identified samples from 2016, collected during the same period, and retrieved them from −80°C storage for testing. After excluding duplicates, we selected samples on the basis of availability, amount of remnant, and integrity for EV-D68 testing using a laboratory-developed real-time reverse transcription PCR (rRT-PCR) targeting the 5′ nontranslated region of the human enterovirus genome as described (3). Because we conducted EV-D68 testing after patient encounters, results were not available to the treating physician.
The sampling selection criteria differed between the 2 outbreak periods (Figure 1). During 2014, we screened a smaller set of samples for EV-D68 and focused on hospitalized patients. In 2018, we screened samples from both outpatients and inpatients. However, for both periods the clinical analyses focused on hospitalized patients only.
We reviewed electronic healthcare records from patients positive for EV-D68 for data collection. Patients in whom EV-D68 was identified but for whom clinical data were not available, those evaluated in the outpatient setting, those >21 years of age, and patients who acquired RV/EV infection during hospitalization were excluded from analyses. We compared differences in clinical characteristics and disease severity parameters among patients from the 2018 EV-D68 outbreak, those identified in 2016, and patients during the 2014 outbreak. The clinical characteristics of patients during the 2014 were previously reported (3). The Institutional Review Board of NCH approved the study.
Admissions for Asthma
We retrieved data related to admissions for asthma during the same time periods in 2014, 2016, and 2018 from the electronic data warehouse. We included patients <21 years of age who were hospitalized with an asthma diagnosis in any NCH inpatient unit. We used the following codes from the International Classification Diseases, Ninth (ICD-9) or Tenth (ICD-10) Revision, for asthma: ICD-9, 493.*; ICD-10, J45.20–J45.998.
EV-D68 rRT-PCR Testing and Sequencing
For EV-D68 detection and quantitation, we used a laboratory-developed rRT-PCR as described previously (3). We selected a subset of EV-D68–positive samples for partial viral protein (VP) 1 gene sequencing of an 805-bp PCR product, as described (7). We performed cycle sequencing with BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, https://www.thermofisher.com) on the automated sequencer 3130xl Genetic Analyzer (Applied Biosystems) bidirectionally. We generated multiple sequence alignments and phylogenetic trees and compared the amino acid sequences (including BE, DC and GH loops) of partial VP1 as described (3,8,9).
We conducted descriptive analyses using frequency distributions or rates and used medians and interquartile ranges to summarize the demographic data and patients’ baseline characteristics. We analyzed associations between categorical variables using the Fisher exact or χ2 test and assessed normality for continuous variables using the Shapiro-Wilk test and 2-tailed Student t tests, Mann-Whitney test, 1-way ANOVA (analysis of variance), or Kruskal-Wallis tests where used as appropriate. Two-tailed p values <0.05 were considered significant. We performed statistical analyses using GraphPad Prism 8 (https://www.graphpad.com).
Sample Selection and Clinical Characteristics of EV-D68–Infected Patients during the 2018 Outbreak
During the 2018 outbreak, of 3,633 samples tested by the FilmArray panel 1,987 (55%) were positive for RV/EV. We further evaluated 1,028 samples, of which 401 (39%) tested positive for EV-D68. This number compares with 213 (46%) EV-D68–positive samples of 459 in the 2014 outbreak (Figure 1).
Of the 401 patient samples that tested positive for EV-D68 in 2018, we excluded 124 (122 because patients were evaluated in the outpatient setting or clinical data were not available and 2 from children with nosocomial EV-D68 infection), leaving a total of 277 patients hospitalized with EV-D68 infection. Of those, 67 (24%) children were previously healthy, 146 (53%) had preexisting asthma or a history of wheezing, and 64 (23%) had another underlying chronic medical condition (Table 1). Children with a history of asthma or wheezing were older (median age 4.1 years) than children who had complex medical conditions (median 2.5 years) or were previously healthy (median 1.4 years; p<0.01); findings did not differ by sex or race. Most children had respiratory symptoms (94%–100%) with or without fever, followed by gastrointestinal manifestations (27%–32%). Eight (2.9%) children had neurologic manifestations, 2 AFM and 1 opsoclonus/myoclonus syndrome (OMS).
Overall, children with asthma required pediatric intensive care unit (PICU) admission more frequently (63%) than did previously healthy children (37%) or children with chronic medical conditions (29%; p<0.0001); however, duration of hospitalization was longer for children with underlying conditions. The EV-D68 semiquantitative viral load (cycle threshold) ranged from an average of 25.1 to 26.1 and did not differ significantly between groups.
Clinical Manifestations during the 2014 and 2018 EV-D68 Outbreaks and the 2016 Low-Activity Period
We compared the demographic and clinical characteristics of children from the 2014 and 2018 EV-D68 outbreaks (Table 2). Overall, children with EV-D68 infection identified in 2018 were significantly younger and more often of white race; we found no differences in sex or presence of asthma or other chronic medical conditions. During the 2018 outbreak, children with EV-D68 infection more commonly had gastrointestinal symptoms than during the 2014 outbreak (28% in 2018 vs. 12% in 2014; p<0.001); symptoms included emesis, abdominal pain, and diarrhea. On the other hand, children with EV-D68 infection identified during the 2014 outbreak had respiratory symptoms and skin rashes more frequently than did children during the 2018 outbreak. The proportion of children who required PICU admission was lower in 2018 (49%) than in 2014 (68%; p<0.0001), and duration of hospitalization was shorter in 2018 (2.5 days) than in 2014 (2.8 days; p = 0.01).
Severe neurologic manifestations occurred more often during the 2018 outbreak. In the 2014 cohort, 4 (2%) patients had febrile seizures, but no other neurologic findings were documented, and no case of AFM was identified. In 2018, however, 8 (2.9%) patients had neurologic manifestations; 2 had AFM and 1 OMS. Two of these 3 children were previously healthy; 1 had underlying asthma. Four additional children sought treatment for complex febrile seizures (3 of these patients had a history of epilepsy), and 1 infant had viral meningitis. In this infant, parechovirus was identified by rRT-PCR in cerebrospinal fluid (Appendix Table 1).
During 2016, of 3,098 samples tested by the FilmArray panel, 1,293 (42%) were positive for RV/EV. Of those, 211 were further tested for EV-D68, and 14 (7%) yielded positive results. Nine of the 14 patients identified with EV-D68 infection were hospitalized; all had respiratory symptoms, and none had neurologic manifestations. Equal proportions of children had asthma or chronic medical conditions or were previously healthy (3 [33%] each).
EV-D68 Seasonality and Asthma
We also compared the proportion of samples in which we detected EV-D68 during June–October 2014, 2016, and 2018 and analyzed the seasonality of EV-D68 in relation to admissions for asthma (Figure 2). The proportion of RV/EV detected from all nasopharyngeal samples analyzed according to the standard of care was 41% in 2014 and 2016 and 55% in 2018; overall EV-D68 detection was 44% in 2014, 7%, in 2016, and 39% in 2018. The proportion of EV-D68 detected among RV/EV-positive samples (Figure 2, panel A) and the number of admissions for asthma (Figure 2, panel B) were calculated weekly during the 3 periods. The duration of the 2014 outbreak was shorter (mid-July through early October, 13 weeks), and peaked the last week of August, coinciding with a disproportionate number of admissions for asthma. In 2018, the first cases of EV-D68 were identified earlier (mid-June) and ended the first week of October (total of 16 weeks), peaking the last week of July/first week of August. In parallel, the number of admissions for asthma increased during July and August but peaked during the last week of August, which was delayed in relation to EV-D68 circulation. Admissions for asthma during the same time period in 2016 were substantially lower, as was EV-D68 detection.
Molecular Characteristics of EV-D68 2018 Strains
We sequenced 130 EV-D68–positive samples from 2018 and aligned them to both NCH strains from prior years and to EV-D68 sequences available at the National Center for Biotechnology Information website. The NCH 2018 strains were >98.5% identical to each other and demonstrated >85% sequence identity to the VP1 regions of the prototype Fermon strain (GenBank accession no. NC_038308). These 2018 strains were also 92%–94% identical to the 2014 and 2011 NCH strains previously reported (3). The most closely related sequences to the NCH 2018 strains were those isolated in 2016 and 2015 from different geographic regions (10,11).
We used 17 NCH strains (10 from 2018, 5 from 2014, and 2 from 2011) for further genetic characterization. Phylogenetic analyses followed by bootstrap analyses indicated that all NCH strains identified during the 2018 outbreak clustered into a new sublineage within major clade B, differently from the 2011 and 2014 NCH strains (Figure 3). Amino acid sequence alignment for the BC, DE, and GH loops (Figure 4) showed that the NCH 2018 strains displayed a unique amino acid signature, and all contained the amino acid residue (218T) that characterizes the EV-D68 clade B3 (10).
The recent emergence of EV-D68 as a cause of severe respiratory disease, coupled with its association with AFM, suggests that a deeper understanding of this virus is needed (12–14). In this study, we examined >1,000 patient specimens from 2 outbreaks and from 1 period with low EV-D68 activity and conducted both molecular and clinical analyses to compare these periods. Although the 2018 EV-D68 outbreak appeared to be milder, as shown by the lower number of hospital admissions for asthma and lower rates of PICU admissions, we observed severe neurologic manifestations only in 2018.
The comparative clinical analyses between outbreaks showed that hospitalized children during 2018 were younger, but the proportion with underling medical conditions, including asthma, was comparable between periods. Symptoms also were similar in the 2 outbreaks, with the notable exceptions of greater gastrointestinal manifestations in 2018, as well as 3 children with severe neurologic manifestations (2 with AFM and 1 with OMS), which we did not observe during 2014 or 2016.
Since 2014, concurrent with the surge of EV-D68 respiratory-associated illness, children with severe neurologic manifestations have been reported in the United States and elsewhere; episodic increases were identified in 2016 and 2018 (5,12,14–21). The cause of AFM has not been established in most cases, despite extensive pathogen-specific or metagenomic sequencing tests. Although a direct link between AFM and EV-D68 has not been established, observational and animal studies suggest a strong association. On the one hand, EV-D68 causes paralytic myelitis in mice; AFM cases have been shown to cluster during periods of EV-D68 circulation, and EV-D68 has been the most common virus detected in respiratory specimens from children with AFM, albeit rarely in cerebrospinal fluid (22–25). Other neurologic conditions associated with EV-D68 have been described, but to our knowledge, no other cases of OMS have been reported in the literature (26,27). Further studies are ongoing, but our findings agree with others and highlight the importance of comprehensive surveillance and research to further characterize the role of EV-D68 in AFM that will enable pursuit of effective therapies and prevention strategies.
Although the EV-D68 rRT-PCR testing in this study was not designed to determine true incidence, it did help to monitor EV-D68 activity and showed a marked increase in EV-D68 circulation during the summers of 2014 and 2018 and little or no activity during the same period in 2016. The increased in EV-D68 activity during 2014 and 2018 mirrored an increase in the number of admissions for asthma during those periods, and although the 2014 outbreak had a sharper increase at the end of August, the duration of the 2018 outbreak was longer. Nonetheless, in both periods admissions for asthma were significantly higher than during 2016. Although reported to have a biennial seasonality (20,24,28–31), the peaks of EV-D68 in 2014 and 2018 were related to an increase in summertime hospitalizations for asthma, which agrees with a recent study conducted in Japan (32). During the same period in 2016, admissions for asthma were low and no peak was observed, nor was there evidence of high EV-D68 circulation based on surveillance testing in our laboratory, which differs from data reported from other states (28,33). The magnitude of the increase in asthma hospitalizations was higher in 2014 than in 2018 (peak of 128 admissions during the peak week in 2014 vs. 61 during 2018). Whether these decreases in EV-D68 activity and severity are continued in subsequent EV-D68 outbreaks in the population studied here needs be determined. Nevertheless, EV-D68 should be suspected when summertime admissions related to asthma increase above baseline.
Phylogenetic analyses showed that EV-D68 isolates from 2014 and 2018 clustered differently within clade B (10,29,34,35). The relationship of these changes in sequence and the pathogenicity of the virus are unclear (36). Nevertheless, at NCH, no AFM cases were identified in 2014, but 2 AFM cases and 1 OMS case occurred in 2018. The pathogenicity and virulence of this new clade needs to be monitored and confirmed by active surveillance, which was implemented at NCH after the 2014 outbreak. Based on our experience, we have made the EV-D68 rRT-PCR test available for respiratory specimens in real time. This test will be used on the basis of clinician orders particularly as it relates to unexplained acute paralysis/muscle weakness.
This study has limitations. We did not test every specimen that was RV/EV-positive for EV-D68; we did however test >40% of all samples that tested positive for RV/EV during these 2 outbreaks and a low-activity period, which provides a good representation of EV-D68 circulation during those periods. The clinical analysis was limited to inpatients, thus possibly biasing the apparent severity of the EV-D68 infections; however, data were comparable between the 3 periods, which was the main study objective. Unfortunately, the samples associated with the 2 AFM cases were not available for sequencing, and thus we cannot make any definitive conclusions about different or more pathogenic viral strains.
In summary, EV-D68 circulation was associated with a significant medical burden. By more consistent and specific testing for EV-D68, a better understanding of the epidemiology of this emerging virus will help inform clinical care (37).
Dr. Wang is an assistant director of clinical microbiology and immunoserology laboratory at NCH. Her primary research interests are molecular microbiology and new test development.
This work was supported by funding within the Department of Pathology at Nationwide Children’s Hospital.
- Schieble JH, Fox VL, Lennette EH. A probable new human picornavirus associated with respiratory diseases. Am J Epidemiol. 1967;85:297–310.
- Oberste MS, Maher K, Schnurr D, Flemister MR, Lovchik JC, Peters H, et al. Enterovirus 68 is associated with respiratory illness and shares biological features with both the enteroviruses and the rhinoviruses. J Gen Virol. 2004;85:2577–84.
- Moyer K, Wang H, Salamon D, Leber A, Mejias A. Enterovirus D68 in hospitalized children: sequence variation, viral loads and clinical outcomes. PLoS One. 2016;11:
- Messacar K, Abzug MJ, Dominguez SR. 2014 outbreak of enterovirus D68 in North America. J Med Virol. 2016;88:739–45.
- Aliabadi N, Messacar K, Pastula DM, Robinson CC, Leshem E, Sejvar JJ, et al. Enterovirus D68 infection in children with acute flaccid myelitis, Colorado, USA, 2014. Emerg Infect Dis. 2016;22:1387–94.
- Leber AL, Everhart K, Daly JA, Hopper A, Harrington A, Schreckenberger P, et al. Multicenter evaluation of BioFire FilmArray Respiratory Panel 2 for detection of viruses and bacteria in nasopharyngeal swab samples. J Clin Microbiol. 2018;56:e01945–17.
- Todd AK, Hall RJ, Wang J, Peacey M, McTavish S, Rand CJ, et al. Detection and whole genome sequence analysis of an enterovirus 68 cluster. Virol J. 2013;10:103.
- Kearse M, Moir R, Wilson A, Stones-Havas S, Cheung M, Sturrock S, et al. Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics. 2012;28:1647–9.
- Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Mol Biol Evol. 2013;30:2725–9.
- Piralla A, Principi N, Ruggiero L, Girello A, Giardina F, De Sando E, et al. Enterovirus-D68 (EV-D68) in pediatric patients with respiratory infection: The circulation of a new B3 clade in Italy. J Clin Virol. 2018;99-100:91–6.
- Pariani E, Pellegrinelli L, Merlone AD, Piralla A, Baldanti F, Binda S. Letter to the editor: need for a European network for enterovirus D68 surveillance after detections of EV-D68 of the new B3 lineage in Sweden and Italy, 2016. Euro Surveill. 2017;22:pii:30440. PMID: 28106530
- Knoester M, Helfferich J, Poelman R, Van Leer-Buter C, Brouwer OF, Niesters HGM; 2016 EV-D68 AFM Working Group. 2016 EV-D68 AFM Working Group. 2016 EV-D68 AFM Working Group. Twenty-nine cases of enterovirus-D68-associated acute flaccid myelitis in Europe 2016: a case series and epidemiologic overview. Pediatr Infect Dis J. 2019;38:16–21.
- Brown DM, Hixon AM, Oldfield LM, Zhang Y, Novotny M, Wang W, et al. Contemporary circulating enterovirus D68 strains have acquired the capacity for viral entry and replication in human neuronal cells. MBio. 2018;9:e01954–18.
- Ruggieri V, Paz MI, Peretti MG, Rugilo C, Bologna R, Freire C, et al. Enterovirus D68 infection in a cluster of children with acute flaccid myelitis, Buenos Aires, Argentina, 2016. Eur J Paediatr Neurol. 2017;21:884–90.
- Ayscue P, Van Haren K, Sheriff H, Waubant E, Waldron P, Yagi S, et al.; Centers for Disease Control and Prevention (CDC). Acute flaccid paralysis with anterior myelitis - California, June 2012-June 2014. MMWR Morb Mortal Wkly Rep. 2014;63:903–6.
- Greninger AL, Naccache SN, Messacar K, Clayton A, Yu G, Somasekar S, et al. A novel outbreak enterovirus D68 strain associated with acute flaccid myelitis cases in the USA (2012-14): a retrospective cohort study. Lancet Infect Dis. 2015;15:671–82.
- Sejvar JJ, Lopez AS, Cortese MM, Leshem E, Pastula DM, Miller L, et al. Acute flaccid myelitis in the United States, August–December 2014: results of nationwide surveillance. Clin Infect Dis. 2016;63:737–45.
- Bjerin O, Martín Muñoz D, Gerald C, Brytting M, Eriksson M. [Acute flaccid myelitis amongst Swedish children with a possible link to an outbreak of enterovirus D68] [in Swedish] [pii:ETDZ.]. Lakartidningen. 2017;114:114.
- Cabrerizo M, García-Iñiguez JP, Munell F, Amado A, Madurga-Revilla P, Rodrigo C, et al. First cases of severe flaccid paralysis associated with enterovirus D68 infection in Spain, 2015–2016. Pediatr Infect Dis J. 2017;36:1214–6.
- Knoester M, Schölvinck EH, Poelman R, Smit S, Vermont CL, Niesters HGM, et al. Upsurge of Enterovirus D68, the Netherlands, 2016. Emerg Infect Dis. 2017;23:140–3.
- Kamau E, Harvala H, Blomqvist S, Nguyen D, Horby P, Pebody R, et al. Increase in enterovirus D68 infections in young children, United Kingdom, 2006–2016. Emerg Infect Dis. 2019;25:1200–3.
- Messacar K, Asturias EJ, Hixon AM, Van Leer-Buter C, Niesters HGM, Tyler KL, et al. Enterovirus D68 and acute flaccid myelitis-evaluating the evidence for causality. Lancet Infect Dis. 2018;18:e239–47.
- Hopkins SE, Elrick MJ, Messacar K. Acute flaccid myelitis—keys to diagnosis, questions about treatment, and future directions. JAMA Pediatr. 2019;173:117–8.
- Messacar K, Pretty K, Reno S, Dominguez SR. Continued biennial circulation of enterovirus D68 in Colorado. J Clin Virol. 2019;113:24–6.
- Hixon AM, Yu G, Leser JS, Yagi S, Clarke P, Chiu CY, et al. A mouse model of paralytic myelitis caused by enterovirus D68. PLoS Pathog. 2017;13:
- Kuban KC, Ephros MA, Freeman RL, Laffell LB, Bresnan MJ. Syndrome of opsoclonus-myoclonus caused by Coxsackie B3 infection. Ann Neurol. 1983;13:69–71.
- Blaes F, Dharmalingam B. Childhood opsoclonus-myoclonus syndrome: diagnosis and treatment. Expert Rev Neurother. 2016;16:641–8.
- Messacar K, Robinson CC, Pretty K, Yuan J, Dominguez SR. Surveillance for enterovirus D68 in colorado children reveals continued circulation. J Clin Virol. 2017;92:39–41.
- Wang G, Zhuge J, Huang W, Nolan SM, Gilrane VL, Yin C, et al. Enterovirus D68 subclade B3 strain circulating and causing an outbreak in the United States in 2016. Sci Rep. 2017;7:1242.
- Dyrdak R, Grabbe M, Hammas B, Ekwall J, Hansson KE, Luthander J, et al. Outbreak of enterovirus D68 of the new B3 lineage in Stockholm, Sweden, August to September 2016. Euro Surveill. 2016;21:30403.
- Kramer R, Sabatier M, Wirth T, Pichon M, Lina B, Schuffenecker I, et al. Molecular diversity and biennial circulation of enterovirus D68: a systematic screening study in Lyon, France, 2010 to 2016. Euro Surveill. 2018;23:23.
- Korematsu S, Nagashima K, Sato Y, Nagao M, Hasegawa S, Nakamura H, et al. “Spike” in acute asthma exacerbations during enterovirus D68 epidemic in Japan: A nation-wide survey. Allergol Int. 2018;67:55–60.
- Srinivasan M, Niesen A, Storch GA. Enterovirus D68 Surveillance, St. Louis, Missouri, USA, 2016. Emerg Infect Dis. 2018;24:2115–7.
- Kaida A, Iritani N, Yamamoto SP, Kanbayashi D, Hirai Y, Togawa M, et al. Distinct genetic clades of enterovirus D68 detected in 2010, 2013, and 2015 in Osaka City, Japan. PLoS One. 2017;12:
- Huang YP, Lin TL, Lin TH, Wu HS. Molecular and epidemiological study of enterovirus D68 in Taiwan. J Microbiol Immunol Infect. 2017;50:411–7.
- Imamura T, Okamoto M, Nakakita S, Suzuki A, Saito M, Tamaki R, et al. Antigenic and receptor binding properties of enterovirus 68. J Virol. 2014;88:2374–84.
- Carrion Martin AI, Pebody RG, Danis K, Ellis J, Niazi S, DE Lusignan S, et al. The emergence of enterovirus D68 in England in autumn 2014 and the necessity for reinforcing enterovirus respiratory screening. Epidemiol Infect. 2017;145:1855–64.
Suggested citation for this article: Wang H, Diaz A, Moyer K, Mele-Casas M, Ara-Montojo MF, Torrus I, et al. Molecular and clinical comparison of enterovirus D68 outbreaks among hospitalized children, Ohio, USA, 2014 and 2018. Emerg Infect Dis. 2019 Nov [date cited]. https://doi.org/10.3201/eid2511.190973
Original Publication Date: 8/27/2019
1Current affiliation: Inova Fairfax Hospital, Falls Church, Virginia, USA.
2Current affiliation: Hospital Sant Joan de Deu, Barcelona, Spain.
3Current affiliation: Hospital Universitario La Paz, Madrid, Spain.