Literature DB >> 7097857

Demonstration of hemolytic and fusion activities of influenza C virus.

M Ohuchi, R Ohuchi, K Mifune.   

Abstract

Influenza C virus showed a marked hemolytic activity when incubated with murine erythrocytes at 37 degrees C in acidic medium. The virus-specific hemolysis was most efficient at pH 5.0. Extensive cell fusion also occurred when the erythrocytes were treated with the virus at acidic pH. When propagated in MDCK cells, the virus had an extremely low infectivity and did not display hemolytic activity in any pH range. When the inactive virus was subjected to mild trypsin treatment, hemolytic activity was drastically manifested, accompanying a drastic increase in infectivity. The glycoprotein in the inactive virus was cleaved into smaller components by trypsin treatments. These results indicated that the envelope of influenza C virus can fuse with the cellular membrane under acidic conditions and that the activation of influenza C virus by cleavage was due to the appearance of this envelope fusion activity.

Entities:  

Mesh:

Substances:

Year:  1982        PMID: 7097857      PMCID: PMC256943          DOI: 10.1128/JVI.42.3.1076-1079.1982

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  16 in total

1.  Enhancement of the infectivity of influenza A and B viruses by proteolytic cleavage of the hemagglutinin polypeptide.

Authors:  S G Lazarowitz; P W Choppin
Journal:  Virology       Date:  1975-12       Impact factor: 3.616

2.  Activation of influenza A viruses by trypsin treatment.

Authors:  H D Klenk; R Rott; M Orlich; J Blödorn
Journal:  Virology       Date:  1975-12       Impact factor: 3.616

3.  Properties of the erythrocyte receptors for influenza C virus.

Authors:  M Ohuchi; M Homma; M Muramatsu; S Ohyama
Journal:  Microbiol Immunol       Date:  1978       Impact factor: 1.955

4.  Glycoprotein staining following electrophoresis on acrylamide gels.

Authors:  R M Zacharius; T E Zell; J H Morrison; J J Woodlock
Journal:  Anal Biochem       Date:  1969-07       Impact factor: 3.365

5.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

6.  A comparison of "influenza C" with prototype myxoviruses: receptor-destroycing activity (neuraminidase) and structural polypeptides.

Authors:  A P Kendal
Journal:  Virology       Date:  1975-05       Impact factor: 3.616

7.  A precursor glycoprotein in influenza C virus.

Authors:  G Herrler; R W Compans; H Meier-Ewert
Journal:  Virology       Date:  1979-11       Impact factor: 3.616

8.  Absence of neuraminidase from influenza C virus.

Authors:  K Nerome; M Ishida; M Nakayama
Journal:  Arch Virol       Date:  1976       Impact factor: 2.574

9.  The multiplication of an influenza C virus in an established line of canine kidney (MDCK) cells.

Authors:  K Nerome; M Ishida
Journal:  J Gen Virol       Date:  1978-04       Impact factor: 3.891

10.  On the entry of Semliki forest virus into BHK-21 cells.

Authors:  A Helenius; J Kartenbeck; K Simons; E Fries
Journal:  J Cell Biol       Date:  1980-02       Impact factor: 10.539

View more
  21 in total

1.  Cell surface expression of biologically active influenza C virus HEF glycoprotein expressed from cDNA.

Authors:  A Pekosz; R A Lamb
Journal:  J Virol       Date:  1999-10       Impact factor: 5.103

2.  The E3 protein of bovine coronavirus is a receptor-destroying enzyme with acetylesterase activity.

Authors:  R Vlasak; W Luytjes; J Leider; W Spaan; P Palese
Journal:  J Virol       Date:  1988-12       Impact factor: 5.103

3.  Influenza C virus hemagglutinin: comparison with influenza A and B virus hemagglutinins.

Authors:  S Nakada; R S Creager; M Krystal; R P Aaronson; P Palese
Journal:  J Virol       Date:  1984-04       Impact factor: 5.103

4.  9-O-acetylated sialic acids have widespread but selective expression: analysis using a chimeric dual-function probe derived from influenza C hemagglutinin-esterase.

Authors:  A Klein; M Krishna; N M Varki; A Varki
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-02       Impact factor: 11.205

5.  Serine 71 of the glycoprotein HEF is located at the active site of the acetylesterase of influenza C virus.

Authors:  G Herrler; G Multhaup; K Beyreuther; H D Klenk
Journal:  Arch Virol       Date:  1988       Impact factor: 2.574

6.  Evidence that the matrix protein of influenza C virus is coded for by a spliced mRNA.

Authors:  M Yamashita; M Krystal; P Palese
Journal:  J Virol       Date:  1988-09       Impact factor: 5.103

7.  Rescue of influenza C virus from recombinant DNA.

Authors:  Bernadette Crescenzo-Chaigne; Sylvie van der Werf
Journal:  J Virol       Date:  2007-08-08       Impact factor: 5.103

8.  Activity of influenza C virus O-acetylesterase with O-acetyl-containing compounds.

Authors:  A Garcia-Sastre; E Villar; J C Manuguerra; C Hannoun; J A Cabezas
Journal:  Biochem J       Date:  1991-01-15       Impact factor: 3.857

9.  Cell surface expression of fusogenic vesicular stomatitis virus G protein from cloned cDNA.

Authors:  H Riedel; C Kondor-Koch; H Garoff
Journal:  EMBO J       Date:  1984-07       Impact factor: 11.598

10.  An efficient method for introducing defined lipids into the plasma membrane of mammalian cells.

Authors:  G van Meer; K Simons
Journal:  J Cell Biol       Date:  1983-11       Impact factor: 10.539

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.