The tal gene of lactococcal bacteriophage TP901-1 is involved in DNA release following host adsorption.

Autor:	Ruiz-Cruz S; School of Microbiology & APC Microbiome Ireland, University College Cork, Cork, Ireland., Erazo Garzon A; School of Microbiology & APC Microbiome Ireland, University College Cork, Cork, Ireland., Cambillau C; School of Microbiology & APC Microbiome Ireland, University College Cork, Cork, Ireland.; Laboratoire d'Ingénierie des Systèmes Macromoléculaires (LISM), Institut de Microbiologie, Bioénergies et Biotechnologie (IMM), Aix-Marseille Université-CNRS, Marseille, France., Ortiz Charneco G; School of Microbiology & APC Microbiome Ireland, University College Cork, Cork, Ireland., Lugli GA; Department of Chemistry, Life Sciences, and Environmental Sustainability, Laboratory of Probiogenomics, University of Parma, Parma, Italy., Ventura M; Department of Chemistry, Life Sciences, and Environmental Sustainability, Laboratory of Probiogenomics, University of Parma, Parma, Italy., Mahony J; School of Microbiology & APC Microbiome Ireland, University College Cork, Cork, Ireland., van Sinderen D; School of Microbiology & APC Microbiome Ireland, University College Cork, Cork, Ireland.
Jazyk:	angličtina
Zdroj:	Applied and environmental microbiology [Appl Environ Microbiol] 2024 Sep 18; Vol. 90 (9), pp. e0069424. Date of Electronic Publication: 2024 Aug 12.
DOI:	10.1128/aem.00694-24
Abstrakt:	Temperate P335 phage TP901-1 represents one of the best-characterized Gram-positive phages regarding its structure and host interactions. Following its reversible adsorption to the polysaccharidic side-chain of the cell wall polysaccharide of its host Lactococcus cremoris 3107, TP901-1 requires a glucosylated cell envelope moiety to trigger its genome delivery into the host cytoplasm. Here, we demonstrate that three distinct single amino acid substitutions in the Tal protein of TP901-1 baseplate are sufficient to overcome the TP901-1 resistance of three L. cremoris 3107 derivatives, whose resistance is due to impaired DNA release of the phage. All of these Tal alterations are located in the N-terminally located gp27-like domain of the protein, conserved in many tailed phages. AlphaFold2 predictions of the Tal mutant proteins suggest that these mutations favor conformational changes necessary to reposition the Tal fiber and thus facilitate release of the tape measure protein from the tail tube and subsequent DNA ejection in the absence of the trigger otherwise required for phage genome release. Importance: Understanding the molecular mechanisms involved in phage-host interactions is essential to develop phage-based applications in the food and probiotic industries, yet also to reduce the risk of phage infections in fermentations. Lactococcus , extensively used in dairy fermentations, has been widely employed to unravel such interactions. Phage infection commences with the recognition of a suitable host followed by the release of its DNA into the bacterial cytoplasm. Details on this latter, irreversible step are still very scarce in lactococci and other Gram-positive bacteria. We demonstrate that a component of the baseplate of the lactococcal phage TP901-1, the tail-associated lysin (Tal), is involved in the DNA delivery into its host, L. cremoris 3107. Specifically, we have found that three amino acid changes in Tal appear to facilitate structural rearrangements in the baseplate necessary for the DNA release process, even in the absence of an otherwise required host trigger. Competing Interests: The authors declare no conflict of interest.
Databáze:	MEDLINE
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