Literature DB >> 8143121

Protease-dependent virus tropism and pathogenicity.

Y Nagai1.   

Abstract

Viral tissue tropism in a susceptible host is often determined by virus-receptor interactions. Nevertheless, closely related viruses utilizing the same receptor molecules can display striking differences in tropism, or a virus can cause a localized infection despite the widespread occurrence of the receptor. These events are now explained by another mechanism of tropism, in which host proteases play a major role by activating viral fusion glycoproteins.

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Year:  1993        PMID: 8143121      PMCID: PMC7133224          DOI: 10.1016/0966-842x(93)90112-5

Source DB:  PubMed          Journal:  Trends Microbiol        ISSN: 0966-842X            Impact factor:   17.079


  63 in total

Review 1.  Mammalian subtilisins: the long-sought dibasic processing endoproteases.

Authors:  P J Barr
Journal:  Cell       Date:  1991-07-12       Impact factor: 41.582

2.  Sequence requirements for cleavage activation of influenza virus hemagglutinin expressed in mammalian cells.

Authors:  Y Kawaoka; R G Webster
Journal:  Proc Natl Acad Sci U S A       Date:  1988-01       Impact factor: 11.205

3.  Functional expression of furin demonstrating its intracellular localization and endoprotease activity for processing of proalbumin and complement pro-C3.

Authors:  Y Misumi; K Oda; T Fujiwara; N Takami; K Tashiro; Y Ikehara
Journal:  J Biol Chem       Date:  1991-09-05       Impact factor: 5.157

4.  The carboxyterminus of the hemagglutinin-neuraminidase of Newcastle disease virus is exposed at the surface of the viral envelope.

Authors:  W Schuy; W Garten; D Linder; H D Klenk
Journal:  Virus Res       Date:  1984       Impact factor: 3.303

5.  Role of Staphylococcus protease in the development of influenza pneumonia.

Authors:  M Tashiro; P Ciborowski; H D Klenk; G Pulverer; R Rott
Journal:  Nature       Date:  1987 Feb 5-11       Impact factor: 49.962

6.  Endoproteolytic cleavage of gp160 is required for the activation of human immunodeficiency virus.

Authors:  J M McCune; L B Rabin; M B Feinberg; M Lieberman; J C Kosek; G R Reyes; I L Weissman
Journal:  Cell       Date:  1988-04-08       Impact factor: 41.582

7.  Is virulence of H5N2 influenza viruses in chickens associated with loss of carbohydrate from the hemagglutinin?

Authors:  Y Kawaoka; C W Naeve; R G Webster
Journal:  Virology       Date:  1984-12       Impact factor: 3.616

8.  Proteolytic cleavage of influenza virus hemagglutinins: primary structure of the connecting peptide between HA1 and HA2 determines proteolytic cleavability and pathogenicity of Avian influenza viruses.

Authors:  F X Bosch; W Garten; H D Klenk; R Rott
Journal:  Virology       Date:  1981-09       Impact factor: 3.616

9.  Expression of factor X and its significance for the determination of paramyxovirus tropism in the chick embryo.

Authors:  T Ogasawara; B Gotoh; H Suzuki; J Asaka; K Shimokata; R Rott; Y Nagai
Journal:  EMBO J       Date:  1992-02       Impact factor: 11.598

10.  Hemagglutinin activation of pathogenic avian influenza viruses of serotype H7 requires the protease recognition motif R-X-K/R-R.

Authors:  M Vey; M Orlich; S Adler; H D Klenk; R Rott; W Garten
Journal:  Virology       Date:  1992-05       Impact factor: 3.616

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  25 in total

1.  Cleavage of the papillomavirus minor capsid protein, L2, at a furin consensus site is necessary for infection.

Authors:  Rebecca M Richards; Douglas R Lowy; John T Schiller; Patricia M Day
Journal:  Proc Natl Acad Sci U S A       Date:  2006-01-23       Impact factor: 11.205

2.  Cleavage of influenza A virus H1 hemagglutinin by swine respiratory bacterial proteases.

Authors:  R J Callan; F A Hartmann; S E West; V S Hinshaw
Journal:  J Virol       Date:  1997-10       Impact factor: 5.103

3.  Transfection of Sendai virus F gene cDNA with mutations at its cleavage site and HN gene cDNA into COS cells induces cell fusion.

Authors:  H Taira; T Sato; H Segawa; M Chiba; T Katsumata; K Iwasaki
Journal:  Arch Virol       Date:  1995       Impact factor: 2.574

4.  Positive and negative host factors for Sendai virus transcription and their organ distribution in rat.

Authors:  T Takagi; M Iwama; K Seta; T Kanda; T Tsukamoto; S Tominaga; K Mizumoto
Journal:  Arch Virol       Date:  1996       Impact factor: 2.574

5.  Deduced amino acid sequences surrounding the fusion glycoprotein cleavage site and of the carboxyl-terminus of haemagglutinin-neuraminidase protein of the avirulent thermostable vaccine strain I-2 of Newcastle disease virus.

Authors:  P N Wambura; J Meers; J A Kattenbelt; A R Gould; P B Spradbrow
Journal:  Vet Res Commun       Date:  2006-12-29       Impact factor: 2.459

6.  Characterization of an alternate form of Newcastle disease virus fusion protein.

Authors:  Homer Pantua; Lori W McGinnes; John Leszyk; Trudy G Morrison
Journal:  J Virol       Date:  2005-09       Impact factor: 5.103

7.  A furin-defective cell line is able to process correctly the gp160 of human immunodeficiency virus type 1.

Authors:  Y Ohnishi; T Shioda; K Nakayama; S Iwata; B Gotoh; M Hamaguchi; Y Nagai
Journal:  J Virol       Date:  1994-06       Impact factor: 5.103

8.  Engineered serine protease inhibitor prevents furin-catalyzed activation of the fusion glycoprotein and production of infectious measles virus.

Authors:  M Watanabe; A Hirano; S Stenglein; J Nelson; G Thomas; T C Wong
Journal:  J Virol       Date:  1995-05       Impact factor: 5.103

9.  Protease-induced infectivity of hepatitis B virus for a human hepatoblastoma cell line.

Authors:  X Lu; T M Block; W H Gerlich
Journal:  J Virol       Date:  1996-04       Impact factor: 5.103

10.  Cleavage of the SARS coronavirus spike glycoprotein by airway proteases enhances virus entry into human bronchial epithelial cells in vitro.

Authors:  Yiu-Wing Kam; Yuushi Okumura; Hiroshi Kido; Lisa F P Ng; Roberto Bruzzone; Ralf Altmeyer
Journal:  PLoS One       Date:  2009-11-17       Impact factor: 3.240

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