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Intratypic characterization of poliovirus type 1 isolates
1Enterovirus Research Centre, Bombay.
The Indian Journal of Medical Research
|July 1, 1991
Summary
Routine oral poliovirus vaccine (OPV) immunization is insufficient to displace wild poliovirus, as evidenced by the isolation of non-vaccine-like strains even in highly vaccinated populations. Antigenic variants were more frequent after outbreaks.
Area of Science:
- Virology
- Epidemiology
- Immunology
Background:
- Poliovirus type 1 circulates globally, posing a significant public health challenge.
- Oral poliovirus vaccine (OPV) is a primary tool for polio eradication.
- Understanding poliovirus strain diversity is crucial for effective vaccination strategies.
Purpose of the Study:
- To serodifferentiate poliovirus type 1 strains isolated from different epidemiological settings.
- To investigate the efficacy of OPV in displacing wild poliovirus strains.
- To characterize antigenic variants of poliovirus.
Main Methods:
- Serodifferentiation of 607 poliovirus type 1 isolates using strain-specific antisera and monoclonal antibodies.
- Analysis of isolates from epidemic, endemic, and vaccinated areas.
- Epitope mapping of detected antigenic variants using monoclonal antibodies.
Main Results:
- Both vaccine-like and non-vaccine-like poliovirus strains were isolated from an epidemic area (Marathwada) with mass OPV vaccination.
- Only non-vaccine-like strains were found in an endemic area (Bombay).
- Despite high OPV coverage (93%) in a previously vaccinated area (Emmaneshwaram), non-vaccine-like strains predominated, indicating OPV insufficiency in displacing wild virus.
- A small number of antigenic variants were detected, with higher frequency following paralytic poliomyelitis outbreaks.
Conclusions:
- Routine OPV immunization alone may not be sufficient to eliminate wild poliovirus.
- The emergence and circulation of non-vaccine-like strains and antigenic variants highlight the need for ongoing surveillance and potentially adapted vaccine strategies.
- Mass vaccination campaigns following outbreaks may increase the frequency of antigenic variants.