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Published on: April 27, 2011
Mosaic genome structure of echovirus type 30 that circulated in Taiwan in 2001
1Department of Computer Science and Information Engineering, Chang Gung University, Taoyuan, Taiwan.
Abstract:
An echovirus type 30 (E30) outbreak occurred in Taiwan in 2001. In this study, one 1998 and nineteen 2001 enterovirus isolates from cerebrospinal fluid (CSF) of children with meningitis were genetically analyzed. Although negative results were obtained using the E30-specific monoclocal antibody in an immunofluorescent assay (IFA) test of all 20 isolates, molecular typing by partial VP1 sequences and subsequent neutralization test identified them as E30. Among those, seven of them were misidentified as echovirus type 4 (E4) when E4-specific monoclonal antibody was used. Complete genome sequences of one E30 isolate (TW-2513) that were IFA-positive to E4 and another (TW-3182) that was IFA-negative to both E30 and E4 were determined and analyzed. The overall percentage nucleotide identity in the structural coding region (P1) between these two isolates is 98.4, while those in the nonstructural regions P2 and P3 are only 83.2 and 84.4, respectively, indicating that the two 2001 Taiwanese E30 strains were probably recombinant. Recombination analysis of these two E30 genomes revealed that their genome structures are mosaic, which might have been formed gradually and frequently over time.
Insights
Molecular typing identified echovirus type 30 (E30) during a 2001 Taiwan outbreak, despite initial misidentification. Analysis revealed recombinant E30 strains with mosaic genomes, suggesting frequent recombination events.
Area of Science:
- Virology
- Molecular Biology
- Epidemiology
Background:
- Echovirus type 30 (E30) outbreaks pose public health concerns.
- Accurate identification of viral strains is crucial for outbreak management.
Purpose of the Study:
- To genetically characterize enterovirus isolates from a 2001 Taiwanese meningitis outbreak.
- To investigate discrepancies in viral identification using serological and molecular methods.
Main Methods:
- Genetic analysis of enterovirus isolates from cerebrospinal fluid (CSF).
- Molecular typing using partial VP1 sequences.
- Neutralization tests and immunofluorescent assays (IFA) with specific monoclonal antibodies.
- Complete genome sequencing and recombination analysis.
Main Results:
- Twenty enterovirus isolates were identified as E30 through molecular typing, despite initial negative results with E30-specific antibodies.
- Seven isolates were misidentified as echovirus type 4 (E4) using E4-specific antibodies.
- Complete genome analysis revealed two 2001 Taiwanese E30 strains with mosaic structures, indicating probable recombination.
- Significant nucleotide divergence was observed between structural (P1) and nonstructural (P2, P3) regions, supporting recombinant origins.
Conclusions:
- Molecular methods are essential for accurate identification of E30, especially during outbreaks.
- The 2001 Taiwanese E30 strains exhibit evidence of genetic recombination, suggesting ongoing viral evolution.
- Mosaic genome structures may arise from frequent recombination events in enteroviruses.
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