Literature DB >> 31350317

A Specific Sugar Moiety in the Lactococcus lactis Cell Wall Pellicle Is Required for Infection by CHPC971, a Member of the Rare 1706 Phage Species.

Barbara Marcelli1,2, Anne de Jong1, Harma Karsens1, Thomas Janzen3, Jan Kok1,2, Oscar P Kuipers4,2.   

Abstract

Lactococcus lactis is a Gram-positive bacterium widely used as a starter culture for the production of different dairy products, especially a large variety of cheeses. Infection of lactococcal starter cultures by bacteriophages is one of the major causes of fermentation failure and often leads to production halt. Lactococcal bacteriophages belonging to the c2, 936, and P335 species are the most commonly isolated in dairy plants and have been extensively investigated in the past three decades. Information regarding bacteriophages belonging to less commonly isolated species is, on the other hand, less extensive, although these phages can also contribute to starter culture infection. Here, we report the nucleotide sequence of the newly isolated L. lactis phage CHPC971, belonging to the rare 1706 species of lactococcal phages. We investigated the nature of the host receptor recognized by the phage and collected evidence that strongly suggests that it binds to a specific sugar moiety in the cell wall pellicle of its host. An in silico analysis of the genome of phage CHPC971 identified the hypothetical genes involved in receptor binding.IMPORTANCE Gathering information on how lactococcal bacteriophages recognize their host and proliferate in the dairy environment is of vital importance for the establishment of proper starter culture rotation plans and to avoid fermentation failure and consequent great economic losses for dairy industries. We provide strong evidence on the type of receptor recognized by a newly isolated 1706-type lactococcal bacteriophage, increasing knowledge of phage-host interactions relevant to dairying. This information can help to prevent phage infection events that, so far, are hard to predict and avoid.
Copyright © 2019 American Society for Microbiology.

Entities:  

Keywords:  Lactococcus lactiszzm321990; bacteriophage; dairy; phage receptor; phage-host interaction

Year:  2019        PMID: 31350317      PMCID: PMC6752003          DOI: 10.1128/AEM.01224-19

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


  46 in total

1.  Comparative genomics of Streptococcus thermophilus phage species supports a modular evolution theory.

Authors:  S Lucchini; F Desiere; H Brüssow
Journal:  J Virol       Date:  1999-10       Impact factor: 5.103

2.  Analysis of six prophages in Lactococcus lactis IL1403: different genetic structure of temperate and virulent phage populations.

Authors:  A Chopin; A Bolotin; A Sorokin; S D Ehrlich; M Chopin
Journal:  Nucleic Acids Res       Date:  2001-02-01       Impact factor: 16.971

Review 3.  Flavour formation by lactic acid bacteria and biochemical flavour profiling of cheese products.

Authors:  Gerrit Smit; Bart A Smit; Wim J M Engels
Journal:  FEMS Microbiol Rev       Date:  2005-08       Impact factor: 16.408

4.  High-Frequency Transformation, by Electroporation, of Lactococcus lactis subsp. cremoris Grown with Glycine in Osmotically Stabilized Media.

Authors:  H Holo; I F Nes
Journal:  Appl Environ Microbiol       Date:  1989-12       Impact factor: 4.792

5.  A strategy for rotation of different bacteriophage defenses in a lactococcal single-strain starter culture system.

Authors:  W D Sing; T R Klaenhammer
Journal:  Appl Environ Microbiol       Date:  1993-02       Impact factor: 4.792

6.  Identification of four loci isolated from two Streptococcus thermophilus phage genomes responsible for mediating bacteriophage resistance.

Authors:  E Stanley; L Walsh; A van der Zwet; G F Fitzgerald; D van Sinderen
Journal:  FEMS Microbiol Lett       Date:  2000-01-15       Impact factor: 2.742

7.  Complete sequences of four plasmids of Lactococcus lactis subsp. cremoris SK11 reveal extensive adaptation to the dairy environment.

Authors:  Roland J Siezen; Bernadet Renckens; Iris van Swam; Sander Peters; Richard van Kranenburg; Michiel Kleerebezem; Willem M de Vos
Journal:  Appl Environ Microbiol       Date:  2005-12       Impact factor: 4.792

8.  Identification of Lactococcus lactis genes required for bacteriophage adsorption.

Authors:  Kitt Dupont; Thomas Janzen; Finn Kvist Vogensen; Jytte Josephsen; Birgitte Stuer-Lauridsen
Journal:  Appl Environ Microbiol       Date:  2004-10       Impact factor: 4.792

Review 9.  Bacteriophage-resistance systems in dairy starter strains: molecular analysis to application.

Authors:  Aidan Coffey; R Paul Ross
Journal:  Antonie Van Leeuwenhoek       Date:  2002-08       Impact factor: 2.271

10.  Complete genomic sequence of bacteriophage ul36: demonstration of phage heterogeneity within the P335 quasi-species of lactococcal phages.

Authors:  Steve Labrie; Sylvain Moineau
Journal:  Virology       Date:  2002-05-10       Impact factor: 3.616

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  1 in total

1.  Employing lytic phage-mediated horizontal gene transfer in Lactococcus lactis.

Authors:  Barbara Marcelli; Harma Karsens; Mark Nijland; Ruben Oudshoorn; Oscar P Kuipers; Jan Kok
Journal:  PLoS One       Date:  2020-09-14       Impact factor: 3.240

  1 in total

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