Related Experiment Video
Updated: Oct 9, 2026

EPA Method 1615. Measurement of Enterovirus and Norovirus Occurrence in Water by Culture and RT-qPCR. Part III. Virus Detection by RT-qPCR
Published on: January 16, 2016
Molecular identification of new picornaviruses and characterization of a proposed enterovirus 73 serotype
M Steven Oberste1, David Schnurr2, Kaija Maher1
1Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road NE, Mailstop G-17, Atlanta, GA 30333, USA1.
Abstract:
Enteroviruses (EV) have traditionally been identified by using serotype-specific antisera in a virus-neutralization test. Three EV strains isolated in California, USA, in 1955, 1964 and 1978, and a 1995 Oman isolate, were found to be antigenically related to one another; however, the strains were not neutralized by standard EV typing antisera, suggesting that they may represent a new EV serotype. The isolates were characterized genetically by RT-PCR coupled with amplicon sequencing and comparison to a database of enterovirus nucleotide sequences. The strains were 75.3 to 87.2% identical to one another in complete VP1 nucleotide sequence, but no more than 68% identical in sequence to the prototype strain of any EV serotype. Their complete capsid sequences were closely related to one another, but only distantly related to those of any EV prototype strain. The California and Oman isolates were most closely related to members of EV cluster B, suggesting that they are unclassified members (i.e. a new serotype) of cluster B. The complete genome sequence was determined for one isolate, CA55-1988, and the predicted polyprotein sequence was 86.5 to 89.2% identical to those of other cluster B EV and 56.7 to 61.9% identical to the polyprotein sequences of EV belonging to other clusters. Isolation of this new EV serotype from samples obtained on two continents and over a period of 40 years suggests continued circulation over a wide geographical area. In keeping with standard picornavirus nomenclature, we propose that this new serotype be named 'enterovirus 73' (EV73).
Insights
Researchers identified a new enterovirus serotype, enterovirus 73 (EV73), through genetic analysis of strains from California and Oman. This discovery suggests EV73 has circulated globally for decades.
Area of Science:
- Virology
- Molecular Biology
- Infectious Diseases
Background:
- Enteroviruses (EV) traditionally identified using virus-neutralization tests with serotype-specific antisera.
- Newly isolated EV strains from California and Oman showed antigenic relatedness but were not neutralized by standard EV typing antisera.
Purpose of the Study:
- To genetically characterize novel EV strains that were unidentifiable by standard serotyping methods.
- To determine if these strains represent a new EV serotype and its phylogenetic placement.
Main Methods:
- Reverse transcription-polymerase chain reaction (RT-PCR) coupled with amplicon sequencing.
- Comparative nucleotide sequence analysis of VP1, complete capsid, and complete genome sequences.
- Phylogenetic analysis using a comprehensive enterovirus sequence database.
Main Results:
- EV strains exhibited 75.3–87.2% nucleotide sequence identity to each other in VP1, but ≤68% identity to known EV serotypes.
- Sequencing revealed close relatedness among isolates and distant relation to known EV prototype strains.
- Phylogenetic analysis placed the isolates within EV cluster B, suggesting they are unclassified members.
Conclusions:
- The genetic data strongly support the classification of these isolates as a new enterovirus serotype.
- The proposed name for this new serotype is enterovirus 73 (EV73).
- The isolation of EV73 from samples spanning 40 years and two continents indicates its sustained circulation and wide geographical distribution.
Related Concept Videos
Poliomyelitis
Rapid Identification of Pathogens

