Experimental chimeras of poliovirus and C-cluster coxsackie A viruses demonstrated viability and neurovirulence, suggesting poliovirus evolved from a C-CAV ancestor that could reemerge by mutation.
Experimental evidence suggests poliovirus may have speciated from C-cluster coxsackie A viruses, implying a theoretical risk of reemergence even after global eradication.
The poliovirus (PV) eradication campaign is conducted on the premise that this virus, because of the lack of a zoonotic reservoir, will not reemerge once eradicated. This report examines the origin of PV using theoretical and experimental approaches. Our rooted phylogenetic analysis suggests a speciation of PV from a C-cluster coxsackie A virus (C-CAV) ancestor through mutation of the capsid that caused a receptor switch from intercellular adhesion molecule-1 to CD155, leading to a change of pathogenicity. This hypothesis is supported experimentally with chimeras generated from three different pairs of PV and C-CAV. Those carrying the PV capsid and the replication proteins of C-CAVs replicated well, whereas their reciprocal counterparts were either debilitated or dead. This phenomenon of asymmetry is observed also in recombinants between PV1 and C-CAV20, selected in tissue culture cells using a previously undescribed protocol. The recombinants are generated at frequencies of 10(-6) typical for PV interserotype recombination. Strikingly, they resemble genetically and phenotypically, including neurovirulence in CD155 transgenic mice, the large majority of circulating vaccine-derived PVs that have caused poliomyelitis outbreaks in different parts of the world. These data provide experimental evidence for C-CAVs being partners to PVs in generating diverse PV progeny by homologous recombination. They support speciation of a novel human pathogen (PV) from a pool of different human pathogens (C-CAVs). In a PV-free world without PV neutralizing antibodies, contemporary C-CAV, like their ancestor(s), could be fertile ground for a PV-like agent to emerge by mutation.
Jiang et al. (Tue,) conducted a other in Poliovirus. Poliovirus and C-cluster coxsackie A virus chimeras was evaluated on Viral replication and neurovirulence in CD155 transgenic mice. Experimental chimeras of poliovirus and C-cluster coxsackie A viruses demonstrated viability and neurovirulence, suggesting poliovirus evolved from a C-CAV ancestor that could reemerge by mutation.