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Genetic and phenotypic stability of poliovirus shed from infants who received novel type 2 or Sabin type 2 oral poliovirus vaccines in Panama: an analysis of two clinical trials

Authors :
Rahnuma Wahid
Laina D Mercer
Tirza De Leon
Rodrigo DeAntonio
Xavier Sáez-Llorens
Andrew Macadam
Konstantin Chumakov
Jeroen Strating
Björn Koel
Jennifer L Konopka-Anstadt
M Steven Oberste
Cara C Burns
Raul Andino
Erman Tritama
Ananda S Bandyopadhyay
Gabriela Aguirre
Ricardo Rüttimann
Chris Gast
John O Konz
Source :
The Lancet Microbe. 3:e912-e921
Publication Year :
2022
Publisher :
Elsevier BV, 2022.

Abstract

Sabin strains used in oral poliovirus vaccines (OPV) can revert to virulence and, in rare instances, cause disease or generate vaccine-derived strains leading to outbreaks in areas of low immunisation coverage. A novel OPV2 (nOPV2) was designed to stabilise the viral genome against reversion and reduce recombination events that might lead to virulent strains. In this study, we evaluated the genetic and phenotypic stability of shed poliovirus following administration of one dose of monovalent OPV2 (mOPV2) or nOPV2 to infants aged 18-22 weeks.In two similarly designed clinical trials (NCT02521974 and NCT03554798) conducted in Panama, infants aged 18-22-weeks, after immunisation with three doses of bivalent OPV (types 1 and 3) and one dose of inactivated poliovirus vaccine, were administered one or two doses of mOPV2 or nOPV2. In this analysis of two clinical trials, faecally shed polioviruses following one dose of mOPV2 or nOPV2 were isolated from stools meeting predetermined criteria related to sample timing and viral presence and quantity and assessed for nucleotide polymorphisms using next-generation sequencing. A transgenic mouse neurovirulence test was adapted to assess the effect of the possible phenotypic reversion of shed mOPV2 and nOPV2 with a logistic regression model.Of the 91 eligible samples, 86 were able to be sequenced, with 72 evaluated in the transgenic mouse assay. Sabin-2 poliovirus reverts rapidly at nucleotide 481, the primary attenuation site in domain V of the 5' untranslated region of the genome. There was no evidence of neurovirulence-increasing polymorphisms in domain V of shed nOPV2. Reversion of shed Sabin-2 virus corresponded with unadjusted paralysis rates of 47·6% at the 4 logThe data indicate increased genetic stability of domain V of nOPV2 relative to mOPV2, with significantly lower neurovirulence of shed nOPV2 virus compared with shed mOPV2. While this vaccine is currently being deployed under an emergency use listing, the data on the genetic stability of nOPV2 will support further regulatory and policy decision-making regarding use of nOPV2 in outbreak responses.BillMelinda Gates Foundation.

Details

ISSN :
26665247
Volume :
3
Database :
OpenAIRE
Journal :
The Lancet Microbe
Accession number :
edsair.doi.dedup.....ec72ee600f674eaae8f36254bc736d02
Full Text :
https://doi.org/10.1016/s2666-5247(22)00254-3