Early detection of vaccine-derived poliovirus outbreaks using nested PCR and nanopore sequencing in the Democratic Republic of Congo, 2021-2022

Author:

Shaw Alexander1,Mampuela Tresor Kabeya2,Lofiko Emmanuel Lokilo2,Pratt Catherine3ORCID,Troman Catherine1,Bujaki Erika4,O'Toole Aine5ORCID,Akello Joyce1ORCID,Aziza Adrienne Amuri2ORCID,Lusamaki Eddy Kinganda2,Cigolo Jean-Claude Makangara2ORCID,Akonga Marceline2,Lay Yvonne2,Nsunda Bibiche2,White Bailey6,Jorgensen David1,Pukuta Elisabeth2,Riziki Yogolelo2,Rankin Kathleen7,Rambaut Andrew8ORCID,Ahuka-Mundeke Steve9,Muyembe Jean-Jacques2,Martin Javier4,Grassly Nicholas1ORCID,Mbala-Kingebeni Placide9

Affiliation:

1. Imperial College London

2. Institut National de Recherche Biomédicale

3. Biosurv International

4. National Institute for Biological Standards and Control

5. Institute of Evolutionary Biology, University of Edinburgh

6. University of Nebraska Medical Center

7. Bill and Melinda Gates Foundation

8. University of Edinburgh

9. National Institute of Biomedical Research

Abstract

Abstract Delayed detection of poliovirus outbreaks is a major threat to polio eradication. Direct molecular Detection and Nanopore Sequencing (DDNS) of stool samples shows promise as a faster method to detect and confirm polio cases compared with cell culture but has not been assessed prospectively during routine surveillance. We report on the implementation of prospective testing of all stool samples received from suspected polio cases and their contacts in the Democratic Republic of Congo between 10th August 2021 to 4th February 2022. DDNS detected polioviruses in 62/2339 (2.7%) of samples whilst the standard algorithm of cell culture, qPCR and Sanger sequencing detected 51/2339 (2.2%). The sensitivity and specificity of DDNS was not significantly different from cell culture. DDNS provided the VP1 sequence required for case confirmation on average 7 days after sample receipt compared with 30 days for the standard algorithm, allowing detection of three new cVPDV2 outbreaks a mean of 23 days earlier (range 6-30 days) and was estimated to cost less per sample tested. The mean sequence similarity between sequences obtained by the two methods was 99.98%. Continued implementation of DDNS in DRC and expansion to other countries will allow further evaluation of this method and inform its potential recommendation by the Global Polio Laboratory Network.

Publisher

Research Square Platform LLC

Reference31 articles.

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2. The role of older children and adults in wild poliovirus transmission;Blake IM;Proceedings of the National Academy of Sciences of the United States of America,2014

3. World Health Organisation, 2021, Polio Eradication Strategy 2022–2026. Available at: https://polioeradication.org/wp-content/uploads/2021/10/9789240031937-eng.pdf. Accsessed 15.06.2022.

4. The Evolutionary Pathway to Virulence of an RNA Virus;Stern A;Cell,2017

5. Evolving epidemiology of poliovirus serotype 2 following withdrawal of the serotype 2 oral poliovirus vaccine;Macklin GR;Science,2020

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