Role of the C-terminal region of vervet monkey polyomavirus 1 VP1 in virion formation

Hiroki Yamaguchi, Shintaro Kobayashi, Junki Maruyama, Michihito Sasaki, Ayato Takada, Takashi Kimura, Hirofumi Sawa, Yasuko Orba

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Recently, we detected novel vervet monkey polyomavirus 1 (VmPyV) in a vervet monkey. Among amino acid sequences of major capsid protein VP1s of other polyomaviruses, VmPyV VP1 is the longest with additional amino acid residues in the C-terminal region. To examine the role of VmPyV VP1 in virion formation, we generated virus-like particles (VLPs) of VmPyV VP1, because VLP is a useful tool for the investigation of the morphological characters of polyomavirus virions. After the full-length VmPyV VP1 was subcloned into a mammalian expression plasmid, the plasmid was transfected into human embryonic kidney 293T (HEK293T) cells. Thereafter, VmPyV VLPs were purified from the cell lysates of the transfected cells via sucrose gradient sedimentation. Electron microscopic analyses revealed that VmPyV VP1 forms VLPs with a diameter of approximately 50 nm that are exclusively localized in cell nuclei. Furthermore, we generated VLPs consisting of the deletion mutant VmPyV VP1 (ΔC VP1) lacking the C-terminal 116 amino acid residues and compared its VLP formation efficiency and morphology to those of VLPs from wild-type VmPyV VP1 (WT VP1). WT and ΔC VP1 VLPs were similar in size, but the number of ΔC VP1 VLPs was much lower than that of WT VP1 VLPs in VP1-expressing HEK293T cells. These results suggest that the length of VP1 is unrelated to virion morphology; however, the C-terminal region of VmPyV VP1 affects the efficiency of its VLP formation.

Original languageEnglish (US)
Pages (from-to)637-644
Number of pages8
JournalJournal of Veterinary Medical Science
Volume76
Issue number5
DOIs
StatePublished - Jan 1 2014
Externally publishedYes

Fingerprint

Polyomavirus
Cercopithecus aethiops
virus-like particles
virion
Virion
kidney cells
Polyomaviridae
HEK293 Cells
plasmids
Plasmids
amino acids
cell nucleus
Kidney
Amino Acids
coat proteins
Capsid Proteins
Cell Nucleus
amino acid sequences

Keywords

  • Electron microscopy
  • Polyomavirus
  • Vervet monkey
  • Virus-like particles (VLPs)

ASJC Scopus subject areas

  • veterinary(all)

Cite this

Role of the C-terminal region of vervet monkey polyomavirus 1 VP1 in virion formation. / Yamaguchi, Hiroki; Kobayashi, Shintaro; Maruyama, Junki; Sasaki, Michihito; Takada, Ayato; Kimura, Takashi; Sawa, Hirofumi; Orba, Yasuko.

In: Journal of Veterinary Medical Science, Vol. 76, No. 5, 01.01.2014, p. 637-644.

Research output: Contribution to journalArticle

Yamaguchi, H, Kobayashi, S, Maruyama, J, Sasaki, M, Takada, A, Kimura, T, Sawa, H & Orba, Y 2014, 'Role of the C-terminal region of vervet monkey polyomavirus 1 VP1 in virion formation', Journal of Veterinary Medical Science, vol. 76, no. 5, pp. 637-644. https://doi.org/10.1292/jvms.13-0568
Yamaguchi, Hiroki ; Kobayashi, Shintaro ; Maruyama, Junki ; Sasaki, Michihito ; Takada, Ayato ; Kimura, Takashi ; Sawa, Hirofumi ; Orba, Yasuko. / Role of the C-terminal region of vervet monkey polyomavirus 1 VP1 in virion formation. In: Journal of Veterinary Medical Science. 2014 ; Vol. 76, No. 5. pp. 637-644.
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