Enterovirus 68 causes
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: João André Alves Silva, M.D. [2]
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Overview
Taxonomy
Viruses; ssRNA viruses; ssRNA positive-strand viruses, no DNA stage; Picornavirales; Picornaviridae; Enterovirus; Enterovirus D[1]
Biology
Genome
Structure
Tropism
Natural Reservoir
Origin and Serotypes
Based on their pathogenesis in humans and experimental animals, enteroviruses were originally divided into four species: poliovirus, coxsackie A virus, coxsackie B virus, and echovirus. However, further studies reported that some coxsackie and echoviruses have overlapping antigenic properties with respect to the diseases they caused in mice. As a result, they were all later described as enterovirus and numbered sequentially, beginning with EV68. Current classifications systems are based on molecular, antigenic as well as biological properties of these viruses. The enterovirus family is currently subgrouped into 5 categories: poliovirus, human enterovirus A (HEV-A), HEV-B, HEV-C and HEV-D. EV68 is one of the 3 serotypes of the HEV-D subgroup.[2]
Human rhinovirus 87 was isolated at the same time as EV68. Corn is a prototype of HRV87 and is very unique in its receptor quality. Cross neutralization and partial capsid sequence studies revealed that HRV-87 Corn belongs to the same group as EV68.[3] A study on 1962 isolates of EV68 reported the genome sequences of the 5′-non-translated (NTR) and 3D polymerase coding regions and complete VP1 capsid protein coding region sequence. These are closely related with the genome sequence of human rhinovirus 87 (HRV 87) and are consistent with the fact that the two viruses are closely related.
Identification of Isolates
Serotype specific rabbit antisera are used for typing of EV68 isolates. Partial sequencing of VP1 capsid gene, using primer 292 (5'-MIGCIGYIGARACNGG-3') and 222 (5'-CICCIGGIGGIAYRWACAT-3') is another method used for sequencing. The serotype is determined by comparing partial sequence of isolates with a database containing partial sequences of all known enterovirus serotypes.[4]
Two commercially available FDA approved multipathogen detection systems, Luminex xTAG RVP and Idaho Technologies Film Array Respiratory Panel are currently being used in the United States. Both techniques use broadly reactive primers that can pick both enterovirus as well as human rhinovirus.[5]
References
- ↑ "Enterovirus D68".
- ↑ "ICTV Virus Taxonomy". Retrieved 28 February 2014.
- ↑ Ishiko, H.; Miura, R.; Shimada, Y.; Hayashi, A.; Nakajima, H.; Yamazaki, S.; Takeda, N. (2002). "Human rhinovirus 87 identified as human enterovirus 68 by VP4-based molecular diagnosis". Intervirology. 45 (3): 136–41. doi:65866 Check
|doi=value (help). PMID 12403917. - ↑ Oberste, MS.; Maher, K.; Schnurr, D.; Flemister, MR.; Lovchik, JC.; Peters, H.; Sessions, W.; Kirk, C.; Chatterjee, N. (2004). "Enterovirus 68 is associated with respiratory illness and shares biological features with both the enteroviruses and the rhinoviruses". J Gen Virol. 85 (Pt 9): 2577–84. doi:10.1099/vir.0.79925-0. PMID 15302951. Unknown parameter
|month=ignored (help) - ↑ "Clusters of acute respiratory illness associated with human enterovirus 68--Asia, Europe, and United States, 2008-2010". MMWR Morb Mortal Wkly Rep. 60 (38): 1301–4. 2011. PMID 21956405. Unknown parameter
|month=ignored (help)