Genetic and phylogenetic analysis of enteroviruses showed that in the
5'NCR enteroviruses formed three clusters: polioviruses (PVs), coxsack
ievirus A type 21 (CAV21), CAV24 and enterovirus type 70 (ENV70) forme
d one cluster; coxsackievirus B isolates (CBVs), CAV9, CAV16, ENV71, e
chovirus type 11 (EV11), EV12 and all partially sequenced echoviruses
and swine vesicular disease virus (SVDV) belonged to another cluster a
nd bovine enteroviruses (BEVs) formed the third cluster, In the capsid
coding region five clusters were seen: PVs, CAV21 and CAV24 formed on
e cluster (PV-like); ENV70 formed a cluster of its own; all CBVs, CAV9
, EV11, EV12 and SVDV formed the third cluster (CBV-like); CAV16, CAV2
and ENV71 belonged to the fourth cluster (CAV16-like) and BEVs formed
their own cluster (BEV-like), In the 3'NCR the same clusters were see
n as in the coding region suggesting a close association of the 3'NCR
with viral proteins while the cellular environment may be more importa
nt in the evolution of the 5'NCR, Secondary structures were predicted
in the 3'NCR, which showed two different patterns among the five clust
ers, A potential pseudoknot region common in all five clusters was ide
ntified, Although the BEV-like viruses formed a separate cluster in al
l genomic regions, in the coding region they seem to be phylogenetical
ly related to the CAV16-like viruses.