Infectious cell entry mechanism of influenza virus

Akihiko Yoshimura, K. Kuroda, K. Kawasaki, S. Yamashina, T. Maeda, S. Ohnishi

Research output: Contribution to journalArticle

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Abstract

Interaction between influenza virus WSN strain and MDCK cells was studied by using spin-labeled phospholipids and electron microscopy. Envelope fusion was negligibly small at neutral pH but greatly activated in acidic media in a narrow pH range around 5.0. The half-time was less than 1 min at 37°C at pH 5.0. Virus binding was almost independent of the pH. Endocytosis occurred with a half-time of about 7 min at 37°C at neutral pH, and about 50% of the initially bound virus was internalized after 1 h. Electron micrographs showed binding of virus particles in coated pits in the microvillous surface of plasma membrane and endocytosis into coated vesicles. Chloroquine inhibited virus replication. The inhibition occurred when the drug was added not later than 10 min after inoculation. Chloroquine caused an increase in the lysosomal pH 4.9 to 6.1. The drug did not affect virus binding, endocytosis, or envelope fusion at pH 5.0. Electron micrographs showed many virus particles remaining trapped inside vacuoles even after 30 min at 37°C in the presence of drug, in contrast to only a few particles after 10 min in vacuoles and secondary lysosomes in its absence. Virus replication in an artificial condition, i.e., brief exposure of the inoculum to acidic medium followed by incubation in neural pH in the presence of chloroquine, was also observed. These results are discussed to provide a strong support for the infection mechanism of influenza virus proposed previously: virus uptake by endocytosis, fusion of the endocytosed vesicles with lysosome, and fusion of the virus envelope with the surrounding vesicle membrane in the secondary lysosome because of the low pH. This allows the viral genome to enter the target cell cytoplasm.

Original languageEnglish
Pages (from-to)284-293
Number of pages10
JournalJournal of Virology
Volume43
Issue number1
Publication statusPublished - 1982
Externally publishedYes

Fingerprint

Orthomyxoviridae
Endocytosis
endocytosis
chloroquine
Chloroquine
lysosomes
cells
viruses
Lysosomes
Virus Attachment
Virus Replication
virus replication
Vacuoles
Viruses
virion
drugs
Virion
vacuoles
electrons
Pharmaceutical Preparations

ASJC Scopus subject areas

  • Immunology

Cite this

Yoshimura, A., Kuroda, K., Kawasaki, K., Yamashina, S., Maeda, T., & Ohnishi, S. (1982). Infectious cell entry mechanism of influenza virus. Journal of Virology, 43(1), 284-293.

Infectious cell entry mechanism of influenza virus. / Yoshimura, Akihiko; Kuroda, K.; Kawasaki, K.; Yamashina, S.; Maeda, T.; Ohnishi, S.

In: Journal of Virology, Vol. 43, No. 1, 1982, p. 284-293.

Research output: Contribution to journalArticle

Yoshimura, A, Kuroda, K, Kawasaki, K, Yamashina, S, Maeda, T & Ohnishi, S 1982, 'Infectious cell entry mechanism of influenza virus', Journal of Virology, vol. 43, no. 1, pp. 284-293.
Yoshimura A, Kuroda K, Kawasaki K, Yamashina S, Maeda T, Ohnishi S. Infectious cell entry mechanism of influenza virus. Journal of Virology. 1982;43(1):284-293.
Yoshimura, Akihiko ; Kuroda, K. ; Kawasaki, K. ; Yamashina, S. ; Maeda, T. ; Ohnishi, S. / Infectious cell entry mechanism of influenza virus. In: Journal of Virology. 1982 ; Vol. 43, No. 1. pp. 284-293.
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