Original Research
Description of non-polio enteroviruses identified in two national surveillance programmes in South Africa
Submitted: 13 March 2020 | Published: 15 December 2020
About the author(s)
Wayne Howard, National Institute for Communicable Diseases, Johannesburg, South Africa; and Faculty of Health, University of Witwatersrand, Johannesburg, South AfricaDana Savulescu, National Institute for Communicable Diseases, Johannesburg, South Africa
Leigh Berrie, Faculty of Health, University of Witwatersrand, Johannesburg, South Africa; and National Priority Programmes, National Health Laboratory Services, Johannesburg, South Africa
Adrian J. Puren, National Institute for Communicable Diseases, Johannesburg, South Africa; and Faculty of Health, University of Witwatersrand, Johannesburg, South Africa
Abstract
Background: Human enteroviruses (EV) consist of 106 serotypes and four species: EV-A, EV-B, EV-C and EV-D. Enteroviruses cause clinical symptoms varying from severe to mild. Knowledge of EV burden in South Africa is limited, and as non-polio EV are important causes of acute flaccid paralysis (AFP) and meningitis, information on the circulating serotypes is vital.
Methods: Between 2010 and 2012, a total of 832 stool and viral isolate specimens were obtained from two national surveillance programmes at the National Institute for Communicable Diseases: the Rotavirus Sentinel Surveillance Programme (RSSP) and the AFP surveillance programme. Real-time polymerase chain reaction and Sanger sequencing were performed to detect and serotype EV.
Results: Non-polio EV were detected in 446 specimens, of which 308 were sequenced. Stool specimens yielded a greater variety of serotypes than viral cultures. EV-B viruses were predominant (58.44%), whilst EV-C viruses were detected in 31% of the specimens tested. South African prevalence for these viruses was higher than other countries, such as France with less than 2%, and Spain and the United States with less than 10%. The most common serotype detected was Enterovirus 99 (EV-C, 8.63%), which has not been reported in other regions.
Conclusion: Direct sequencing from stool specimens yields a broader, more comprehensive description of EV infections compared to sequencing from viral cultures. Disease-associated serotypes were detected, but only in small numbers. This study provides a baseline for EV strain circulation; however, surveillance needs to be expanded to improve EV knowledge in South Africa.
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