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Novel P335-like Phage Resistance Arises from Deletion within Putative Autolysin yccB in Lactococcus lactis

Lactococcus lactis and Lactococcus cremoris are broadly utilized as starter cultures for fermented dairy products and are inherently impacted by bacteriophage (phage) attacks in the industrial environment. Consequently, the generation of bacteriophage-insensitive mutants (BIMs) is a standard approac...

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Autores principales: Seiler, Jenny, Millen, Anne, Romero, Dennis A., Magill, Damian, Simdon, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675428/
https://www.ncbi.nlm.nih.gov/pubmed/38005870
http://dx.doi.org/10.3390/v15112193
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author Seiler, Jenny
Millen, Anne
Romero, Dennis A.
Magill, Damian
Simdon, Laura
author_facet Seiler, Jenny
Millen, Anne
Romero, Dennis A.
Magill, Damian
Simdon, Laura
author_sort Seiler, Jenny
collection PubMed
description Lactococcus lactis and Lactococcus cremoris are broadly utilized as starter cultures for fermented dairy products and are inherently impacted by bacteriophage (phage) attacks in the industrial environment. Consequently, the generation of bacteriophage-insensitive mutants (BIMs) is a standard approach for addressing phage susceptibility in dairy starter strains. In this study, we characterized spontaneous BIMs of L. lactis DGCC12699 that gained resistance against homologous P335-like phages. Phage resistance was found to result from mutations in the YjdB domain of yccB, a putative autolysin gene. We further observed that alteration of a fused tail-associated lysin-receptor binding protein (Tal-RBP) in the phage restored infectivity on the yccB BIMs. Additional investigation found yccB homologs to be widespread in L. lactis and L. cremoris and that different yccB homologs are highly correlated with cell wall polysaccharide (CWPS) type/subtype. CWPS are known lactococcal phage receptors, and we found that truncation of a glycosyltransferase in the cwps operon also resulted in resistance to these P335-like phages. However, characterization of the CWPS mutant identified notable differences from the yccB mutants, suggesting the two resistance mechanisms are distinct. As phage resistance correlated with yccB mutation has not been previously described in L. lactis, this study offers insight into a novel gene involved in lactococcal phage sensitivity.
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spelling pubmed-106754282023-10-31 Novel P335-like Phage Resistance Arises from Deletion within Putative Autolysin yccB in Lactococcus lactis Seiler, Jenny Millen, Anne Romero, Dennis A. Magill, Damian Simdon, Laura Viruses Article Lactococcus lactis and Lactococcus cremoris are broadly utilized as starter cultures for fermented dairy products and are inherently impacted by bacteriophage (phage) attacks in the industrial environment. Consequently, the generation of bacteriophage-insensitive mutants (BIMs) is a standard approach for addressing phage susceptibility in dairy starter strains. In this study, we characterized spontaneous BIMs of L. lactis DGCC12699 that gained resistance against homologous P335-like phages. Phage resistance was found to result from mutations in the YjdB domain of yccB, a putative autolysin gene. We further observed that alteration of a fused tail-associated lysin-receptor binding protein (Tal-RBP) in the phage restored infectivity on the yccB BIMs. Additional investigation found yccB homologs to be widespread in L. lactis and L. cremoris and that different yccB homologs are highly correlated with cell wall polysaccharide (CWPS) type/subtype. CWPS are known lactococcal phage receptors, and we found that truncation of a glycosyltransferase in the cwps operon also resulted in resistance to these P335-like phages. However, characterization of the CWPS mutant identified notable differences from the yccB mutants, suggesting the two resistance mechanisms are distinct. As phage resistance correlated with yccB mutation has not been previously described in L. lactis, this study offers insight into a novel gene involved in lactococcal phage sensitivity. MDPI 2023-10-31 /pmc/articles/PMC10675428/ /pubmed/38005870 http://dx.doi.org/10.3390/v15112193 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Seiler, Jenny
Millen, Anne
Romero, Dennis A.
Magill, Damian
Simdon, Laura
Novel P335-like Phage Resistance Arises from Deletion within Putative Autolysin yccB in Lactococcus lactis
title Novel P335-like Phage Resistance Arises from Deletion within Putative Autolysin yccB in Lactococcus lactis
title_full Novel P335-like Phage Resistance Arises from Deletion within Putative Autolysin yccB in Lactococcus lactis
title_fullStr Novel P335-like Phage Resistance Arises from Deletion within Putative Autolysin yccB in Lactococcus lactis
title_full_unstemmed Novel P335-like Phage Resistance Arises from Deletion within Putative Autolysin yccB in Lactococcus lactis
title_short Novel P335-like Phage Resistance Arises from Deletion within Putative Autolysin yccB in Lactococcus lactis
title_sort novel p335-like phage resistance arises from deletion within putative autolysin yccb in lactococcus lactis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675428/
https://www.ncbi.nlm.nih.gov/pubmed/38005870
http://dx.doi.org/10.3390/v15112193
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