Human rhinovirus 87 identified as human enterovirus 68 by VP4-based molecular diagnosis

H Ishiko, R Miura, Y Shimada, A Hayashi, H Nakajima… - Intervirology, 2002 - karger.com
H Ishiko, R Miura, Y Shimada, A Hayashi, H Nakajima, S Yamazaki, N Takeda
Intervirology, 2002karger.com
Human rhinoviruses (HRVs) are the major cause of respiratory infections. We developed a
diagnostic method for HRVs based on the reverse-transcription polymerase chain reaction
(RT-PCR) and VP4-based phylogenetic analysis. A set of primers used in the RT-PCR of
human enteroviruses (EVs) appeared to be capable of amplifying all prototype strains of
HRVs, each of which generated a 530-bp fragment. The single exception was HRV-87,
which generated a 650-bp fragment, as observed in human EVs. The VP4 nucleotide …
Abstract
Human rhinoviruses (HRVs) are the major cause of respiratory infections. We developed a diagnostic method for HRVs based on the reverse-transcription polymerase chain reaction (RT-PCR) and VP4-based phylogenetic analysis. A set of primers used in the RT-PCR of human enteroviruses (EVs) appeared to be capable of amplifying all prototype strains of HRVs, each of which generated a 530-bp fragment. The single exception was HRV-87, which generated a 650-bp fragment, as observed in human EVs. The VP4 nucleotide sequence of HRV-87 showed more than 97% nucleotide identity with human EV-68, and formed a monophyletic cluster along with the prototype strain of EV-68 in the human EV-D cluster. HRV-87 showed the second highest homology (76.8%) with EV-70, another member of the human EV-D, in a sample of 66 human EVs and 12 HRVs. Therefore, HRV-87 should be reclassified into the cluster containing human EV-68.
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