Abstract

Following the 2014 outbreak, active surveillance of the EV-D68 has been implemented in many countries worldwide. Despite subsequent EV-D68 outbreaks (2014 and 2016) reported in many areas, EV-D68 circulation remains largely unexplored in Africa except in Senegal, where low levels of EV-D68 circulation were first noted during the 2014 outbreak. Here we investigate subsequent epidemiology of EV-D68 in Senegal from June to September 2016 by screening respiratory specimens from ILI and stool from AFP surveillance. EV-D68 was detected in 7.4% (44/596) of patients; 40 with ILI and 4 with AFP. EV-D68 detection was significantly more common in children under 5 years (56.8%, p = 0.016). All EV-D68 strains detected belonged to the newly defined subclade B3. This study provides the first evidence of EV-D68 B3 subclade circulation in Africa from patients with ILI and AFP during a 2016 outbreak in Senegal. Enhanced surveillance of EV-D68 is needed to better understand the epidemiology of EV-D68 in Africa.

Highlights

  • After the 2014 outbreak, active surveillance of the EV-D68 was implemented in many countries in Asia, Europe and America

  • From June to September 2016, 537 nasopharyngeal swabs from patients with ILI and 59 fecal specimens from acute flaccid paralysis (AFP) patients were screened for EV-D68 (Table 1)

  • EV-D68 was detected in 7.4% (44/596) of patients: 7.5% (40/537) of ILI cases and 6.8% (4/59) of AFP cases

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Summary

Introduction

After the 2014 outbreak, active surveillance of the EV-D68 was implemented in many countries in Asia, Europe and America. This surveillance has demonstrated continued circulation of the EV-D68 and associated AFM detected outbreaks in the United States[9,10], France[11], Spain[12], Netherlands[13], Denmark[14], Sweden[15], Taiwan[16] and Italy[17]. EV-D68 has not been previously reported in association with AFP or AFM cases in Africa, despite previous studies conducted in Gambia, Senegal[19], Kenya[20,21] and South Africa[22,23].

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