Recombination between Polioviruses and Co-Circulating Coxsackie A Viruses: Role in the Emergence of Pathogenic Vaccine-Derived Polioviruses
Open accessAbstract
Ten outbreaks of poliomyelitis caused by pathogenic circulating vaccine-derived polioviruses (cVDPVs) have recently been reported in different regions of the world. Two of these outbreaks occurred in Madagascar. Most cVDPVs were recombinants of mutated poliovaccine strains and other unidentified enteroviruses of species C. We previously reported that a type 2 cVDPV isolated during an outbreak in Madagascar was co-circulating with coxsackieviruses A17 (CA17) and that sequences in the 3' half of the cVDPV and CA17 genomes were related. The goal of this study was to investigate whether these CA17 isolates can act as recombination partners of poliovirus and subsequently to evaluate the major effects of recombination events on the phenotype of the recombinants. We first cloned the infectious cDNA of a Madagascar CA17 isolate. We then generated recombinant constructs combining the genetic material of this CA17 isolate with that of the type 2 vaccine strain and that of the type 2 cVDPV. Our results showed that poliovirus/CA17 recombinants are viable. The recombinant in which the 3' half of the vaccine strain genome had been replaced by that of the CA17 genome yielded larger plaques and was less temperature sensitive than its parental strains. The virus in which the 3' portion of the cVDPV genome was replaced by the 3' half of the CA17 genome was almost as neurovirulent as the cVDPV in transgenic mice expressing the poliovirus cellular receptor gene. The co-circulation in children and genetic recombination of viruses, differing in their pathogenicity for humans and in certain other biological properties such as receptor usage, can lead to the generation of pathogenic recombinants, thus constituting an interesting model of viral evolution and emergence.
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This study showed that a CV-A17 isolate co-circulating with a PV/HEV-C recombinant cVDPV can be a recombination partner for PV.
“This study showed that a CV-A17 isolate co-circulating with a PV/HEV-C recombinant cVDPV can be a recombination partner for PV.”
From Recombination between Poliovirus and Coxsackie A Viruses of Species C: A Model of Viral Genetic Plasticity and Emergence (2011) · cites this paper as [114]
These results also suggested that recombination can, at least in some cases, have a direct effect on the key phenotypic characteristics of recombinants, such as replication level, and may thus favor the emergence of pathogenic cVDPVs.
“These results also suggested that recombination can, at least in some cases, have a direct effect on the key phenotypic characteristics of recombinants, such as replication level, and may thus favor the emergence of pathogenic cVDPVs.”
From Recombination between Poliovirus and Coxsackie A Viruses of Species C: A Model of Viral Genetic Plasticity and Emergence (2011) · cites this paper as [114]
Les études in vitro ont confirmé que les CVA-17 et CVA-13 sont des partenaires de recombinaison compatibles avec le PV.
“Nos études in vitro ont confirmé que ces virus sont des partenaires de recombinaison compatibles [18].”
From Éradication de la poliomyélite et émergence de poliovirus pathogènes dérivés du vaccin: De Madagascar au Cameroun (2013) · cites this paper as [18]
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Delpeyroux, F., Colbère-Garapin, F., Razafindratsimandresy, R., Sadeuh-Mba, S., Joffret, M.-L., Rousset, D., & Blondel, B. (2013) · médecine/sciences · doi:10.1051/medsci/20132911021 · Cited by 11 · see citing works
Self-citationProduction and characterisation of stabilised PV-3 virus-like particles using <i>Pichia pastoris</i>
Sherry, L., Grehan, K., Swanson, J. J., Bahar, M. W., Porta, C., Fry, E. E., Stuart, D. I., Rowlands, D. J., & Stonehouse, N. J. (2022) · doi:10.1101/2022.09.16.508282 · Cited by 18 · see citing works
- Authors
- Jegouic, S., Joffret, M.-L., Blanchard, C., Riquet, F. B., Perret, C., Pelletier, I., Colbere-Garapin, F., Rakoto-Andrianarivelo, M., & Delpeyroux, F.
- Affiliations
- Institut Pasteur (FR)
- Venue
- PLoS Pathogens
- Publisher
- Public Library of Science (PLoS)
- Published
- 2009-05-01
- Volume
- 5
- Issue
- 5
- Pages
- e1000412
- ISSN
- 1553-7366 (ISSN-L)
- 1553-7374
- PMC
- PMC2669712
- OpenAlex
- W2000834719
- Cited by
- 116
- References
- 75
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 6 · 2023: 6 · 2022: 6 · 2021: 5 · 2020: 3 · 2019: 5 · 2018: 7 · 2017: 5 · 2016: 9 · 2015: 4 · 2014: 10 · 2013: 13 · 2012: 11
- FWCI
- 6.69
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS Pathogens (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- HAL (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Centre National de la Recherche Scientifique
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Viral Infections and Immunology Research
- Health Sciences › Medicine › Epidemiology › Virology and Viral Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Keywords
- vaccine-derived poliovirus, poliomyelitis outbreak, temperature sensitivity, neurovirulence, viral evolution
- MeSH terms
- Animals, Cloning, Molecular, Disease Models, Animal, Enterovirus, Female, Humans, Madagascar, Male, Mice, Transgenic, Phylogeny, Viral Plaque Assay, Poliomyelitis, Recombination, Genetic, Temperature, Vaccines, Attenuated, Virulence, Virus Replication, Sequence Alignment, Genome, Viral, Sequence Analysis, DNA, Poliovirus, Poliovirus Vaccines, Cell Line, Tumor, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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