Literature DB >> 8648679

Adenovirus uncoating and nuclear establishment are not affected by weak base amines.

E Rodríguez1, E Everitt.   

Abstract

We have used four established lysosomotropic agents, ammonium chloride, amantadine, chloroquine, and methylamine, to monitor the possible interference with an early low-pH-dependent step during adenovirus replication. Two concentrations of each of the different agents were selected; one was essentially nontoxic to uninfected HeLa cells, and the other resulted in some toxicity as measured by trypan blue staining and by interference with cell monolayer establishment, cell proliferation, and radioisotope labelling. It was separately determined that these concentrations displayed pH-raising effects of the same magnitude as higher concentrations previously used in similar studies. Adenovirus uncoating in vivo, normally reaching its maximum within 1 h after infection, was not affected by any of the agents. The subsequent levels of successful nuclear entry events by the parental genomes were monitored by measuring the extent of transcription of an mRNA species coding for the early 72-kDa DNA-binding protein at 10 to 12 h postinfection. In HeLa, KB, HEp-2, and A549 cells, none of the agents were able to affect the levels of early transcription after administration at the point of infection or at 3 h after infection. The cumulative synthesis of the hexon antigen was assessed late in infection, and inhibitory effects were revealed upon administration of 10, 20, and 40 mM ammonium chloride, 10 mM methylamine, and 0.5 mM amantadine, irrespective of the time point of addition. Ammonium chloride at 5 mM reduced the hexon yield by 20% at the most when added within 50 min after infection. Chloroquine at concentrations of 2.5 and 5 microM specifically reduced the hexon yields by 30 to 40% when administered within the first 50 min of infection. On the basis of the lack of effects of nontoxic concentrations of the four agents on the early virus-cell interactive event of uncoating and the early virus-specified transcription, we conclude that a low-pH-dependent step early in the adenovirus replication cycle is not mandatory for a successful infection.

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Year:  1996        PMID: 8648679      PMCID: PMC190220     

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


  63 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  1978-07       Impact factor: 11.205

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Journal:  Mol Cell Biol       Date:  1984-04       Impact factor: 4.272

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Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

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Authors:  M J Varga; C Weibull; E Everitt
Journal:  J Virol       Date:  1991-11       Impact factor: 5.103

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Journal:  Virology       Date:  1994-01       Impact factor: 3.616

6.  Effect of lysosomotropic agents on the foot-and-mouth disease virus replication.

Authors:  E C Carrillo; C Giachetti; R H Campos
Journal:  Virology       Date:  1984-06       Impact factor: 3.616

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Journal:  J Gen Virol       Date:  1985-03       Impact factor: 3.891

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Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

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Authors:  B Poole; S Ohkuma
Journal:  J Cell Biol       Date:  1981-09       Impact factor: 10.539

10.  Mechanism of entry into the cytosol of poliovirus type 1: requirement for low pH.

Authors:  I H Madshus; S Olsnes; K Sandvig
Journal:  J Cell Biol       Date:  1984-04       Impact factor: 10.539

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  16 in total

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Authors:  Christopher M Wiethoff; Glen R Nemerow
Journal:  Virology       Date:  2015-03-19       Impact factor: 3.616

Review 6.  Role of alpha(v) integrins in adenovirus cell entry and gene delivery.

Authors:  G R Nemerow; P L Stewart
Journal:  Microbiol Mol Biol Rev       Date:  1999-09       Impact factor: 11.056

7.  Internalization of adenovirus by alveolar macrophages initiates early proinflammatory signaling during acute respiratory tract infection.

Authors:  Z Zsengellér; K Otake; S A Hossain; P Y Berclaz; B C Trapnell
Journal:  J Virol       Date:  2000-10       Impact factor: 5.103

8.  Rotavirus capsid protein VP5* permeabilizes membranes.

Authors:  E Denisova; W Dowling; R LaMonica; R Shaw; S Scarlata; F Ruggeri; E R Mackow
Journal:  J Virol       Date:  1999-04       Impact factor: 5.103

9.  The coxsackie B virus and adenovirus receptor resides in a distinct membrane microdomain.

Authors:  Katherine J D Ashbourne Excoffon; Thomas Moninger; Joseph Zabner
Journal:  J Virol       Date:  2003-02       Impact factor: 5.103

10.  Domains required for assembly of adenovirus type 2 fiber trimers.

Authors:  J S Hong; J A Engler
Journal:  J Virol       Date:  1996-10       Impact factor: 5.103

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