Literature DB >> 16349376

Lactococcal bacteriophages require a host cell wall carbohydrate and a plasma membrane protein for adsorption and ejection of DNA.

M R Monteville1, B Ardestani, B L Geller.   

Abstract

The mechanism of the initial steps of bacteriophage infection in Lactococcus lactis subsp. lactis C2 was investigated by using phages c2, ml3, kh, l, h, 5, and 13. All seven phages adsorbed to the same sites on the host cell wall that are composed, in part, of rhamnose. This was suggested by rhamnose inhibition of phage adsorption to cells, competition between phage c2 and the other phages for adsorption to cells, and rhamnose inhibition of lysis of phage-inoculated cultures. The adsorption to the cell wall was found to be reversible upon dilution of the cell wall-adsorbed phage. In a reaction step that apparently follows adsorption to the cell wall, all seven phages adsorbed to a host membrane protein named PIP. This was indicated by the inability of all seven phages to infect a strain selected for resistance to phage c2 and known to have a defective PIP protein. All seven phages were inactivated in vitro by membranes from wild-type cells but not by membranes from the PIP-defective, phage c2-resistant strain. The mechanism of membrane inactivation was an irreversible adsorption of the phage to PIP, as indicated by adsorption of [S] methionine-labeled phage c2 to purified membranes from phage-sensitive cells but not to membranes from the resistant strain, elimination of adsorption by pretreatment of the membranes with proteinase K, and lack of dissociation of S from the membranes upon dilution. Following membrane adsorption, ejection of phage DNA occurred rapidly at 30 degrees C but not at 4 degrees C. These results suggest that many lactococcal phages adsorb initially to the cell wall and subsequently to host cell membrane protein PIP, which leads to ejection of the phage genome.

Entities:  

Year:  1994        PMID: 16349376      PMCID: PMC201790          DOI: 10.1128/aem.60.9.3204-3211.1994

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  34 in total

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Journal:  J Gen Virol       Date:  1971-10       Impact factor: 3.891

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Authors:  T Yokokura
Journal:  Jpn J Microbiol       Date:  1971-09

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Journal:  Proc Natl Acad Sci U S A       Date:  1979-09       Impact factor: 11.205

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Authors:  K Watanabe; S Takesue
Journal:  J Gen Virol       Date:  1972-10       Impact factor: 3.891

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Journal:  Appl Environ Microbiol       Date:  1989-07       Impact factor: 4.792

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Journal:  Appl Microbiol       Date:  1975-06

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Authors:  A Chopin; M C Chopin; A Moillo-Batt; P Langella
Journal:  Plasmid       Date:  1984-05       Impact factor: 3.466

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Authors:  B R Froseth; S K Harlander; L L McKay
Journal:  J Dairy Sci       Date:  1988-02       Impact factor: 4.034

10.  A membrane protein is required for bacteriophage c2 infection of Lactococcus lactis subsp. lactis C2.

Authors:  R Valyasevi; W E Sandine; B L Geller
Journal:  J Bacteriol       Date:  1991-10       Impact factor: 3.490

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  29 in total

1.  Surface expression of the conserved C repeat region of streptococcal M6 protein within the Pip bacteriophage receptor of Lactococcus lactis.

Authors:  B L Geller; N Wade; T D Gilberts; D E Hruby; R Johanson; L Topisirovic
Journal:  Appl Environ Microbiol       Date:  2001-12       Impact factor: 4.792

2.  Surface of lactic acid bacteria: relationships between chemical composition and physicochemical properties.

Authors:  C J Boonaert; P G Rouxhet
Journal:  Appl Environ Microbiol       Date:  2000-06       Impact factor: 4.792

3.  The Lactococcal Plasmid pNP40 Encodes a Third Bacteriophage Resistance Mechanism, One Which Affects Phage DNA Penetration.

Authors:  P Garvey; C Hill; G F Fitzgerald
Journal:  Appl Environ Microbiol       Date:  1996-02       Impact factor: 4.792

4.  Fluorescence correlation spectroscopy to study diffusion and reaction of bacteriophages inside biofilms.

Authors:  R Briandet; P Lacroix-Gueu; M Renault; S Lecart; T Meylheuc; E Bidnenko; K Steenkeste; M-N Bellon-Fontaine; M-P Fontaine-Aupart
Journal:  Appl Environ Microbiol       Date:  2008-02-01       Impact factor: 4.792

5.  Genetic response to bacteriophage infection in Lactococcus lactis reveals a four-strand approach involving induction of membrane stress proteins, D-alanylation of the cell wall, maintenance of proton motive force, and energy conservation.

Authors:  Vincenzo Fallico; R Paul Ross; Gerald F Fitzgerald; Olivia McAuliffe
Journal:  J Virol       Date:  2011-08-31       Impact factor: 5.103

Review 6.  Bacteriophage resistance in Lactococcus.

Authors:  P K Dinsmore; T R Klaenhammer
Journal:  Mol Biotechnol       Date:  1995-12       Impact factor: 2.695

7.  The opening of the SPP1 bacteriophage tail, a prevalent mechanism in Gram-positive-infecting siphophages.

Authors:  Adeline Goulet; Joséphine Lai-Kee-Him; David Veesler; Isabelle Auzat; Gautier Robin; Dale A Shepherd; Alison E Ashcroft; Eric Richard; Julie Lichière; Paulo Tavares; Christian Cambillau; Patrick Bron
Journal:  J Biol Chem       Date:  2011-05-26       Impact factor: 5.157

8.  Cloning of genomic DNA of Lactococcus lactis that restores phage sensitivity to an unusual bacteriophage sk1-resistant mutant.

Authors:  J Kraus; B L Geller
Journal:  Appl Environ Microbiol       Date:  2001-02       Impact factor: 4.792

9.  Visualizing a complete Siphoviridae member by single-particle electron microscopy: the structure of lactococcal phage TP901-1.

Authors:  Cecilia Bebeacua; Livia Lai; Christina Skovgaard Vegge; Lone Brøndsted; Marin van Heel; David Veesler; Christian Cambillau
Journal:  J Virol       Date:  2012-11-07       Impact factor: 5.103

10.  Bacillus subtilis operon encoding a membrane receptor for bacteriophage SPP1.

Authors:  Carlos São-José; Catarina Baptista; Mário A Santos
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

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