Identification of genes involved in the DNA injection process by lactococcal P335 phages

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dc.check.embargoformatEmbargo not applicable (If you have not submitted an e-thesis or do not want to request an embargo)en
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dc.contributor.advisorvan Sinderen, Douween
dc.contributor.advisorMahony, Jenniferen
dc.contributor.authorErazo Garzon, Andrea
dc.contributor.funderScience Foundation Irelanden
dc.date.accessioned2019-09-17T11:15:37Z
dc.date.available2019-09-17T11:15:37Z
dc.date.issued2019
dc.date.submitted2019
dc.description.abstractBacteriophages (phages) belonging to the P335 lactococcal group are one of the most frequently isolated phages in fermentation processes using Lactococcus lactis strains as the primary starter culture. Despite efforts to prevent phage attack, problems caused due to phage infection during large scale milk fermentations are still regularly reported. Lactococcus lactis subsp. cremoris (L. lactis) 3107 is a dairy starter strain and host for the model lactococcal P335 phage TP901-1. Three derivatives of this strain that are resistant to TP901-1, while remaining sensitive to infection by another P335 phage called LC3 were employed to define molecular players involved in the phage infection pathway. Comparative genomic analysis of L. lactis 3107 and its phageresistant derivatives identified several mutations that may cause the observed resistance. Complementation assays with one specific construct, termed pNZgtfA, restored phage sensitivity and lysogenization frequency in two of the derivative strains. pNZgtfA expresses the L3107_1442 gene (renamed here as gtfA) which encodes a predicted membrane-associated glycosyltransferase (GTF), GtfA. Interestingly, the mutant strains also exhibited reduced sensitivity to the rare lactococcal 949 group phages, 949 and WRP3, while complementation assays fully restored infectivity by these phages, thus suggesting that gtfA is also involved in phage-host interactions of these phages. TP901-1 escape mutants capable of infecting these phage-resistant derivatives possess mutations in the gene encoding the structural and/or lytic domain of the Tail-associated lysin in order to adapt to cells which have acquired phage resistance. Interestingly, the gene gtfA is ubiquitous among Lactococcus genomes, L. lactis subsp. cremoris NZ9000 harbours a 99 % identical homologue of gtfA3107 on its genome, referred to here as gtfANZ9000 (corresponding to locus tag LLNZ_08920). Therefore, a mutation (stop codon) was introduced into the coding sequence of gtfANZ9000 by targeted mutagenesis in order to expose the mutant strain generated to NZ9000-infecting 936 group phages. Results showed that a non-functional GtfA protein has no effect on phages belonging to the lactococcal 936 group. GtfA3107 possess similar characteristics to proteins belonging to the GT-C family of GTFs which are known to be involved in glycosylation of substrates at the out-facing side of the cytoplasmic membrane. Therefore, GtfA is presumed to glycosylate a substrate, most likely a cell envelope-associated glycopolymer, such as a cell wall polysaccharide (CWPS) or teichoic acid (TA). If gtfANZ9000 is involved in the modification of CWP components, the inactivation of this gene may have generated a mutant strain deficient in the glycosylation of PSP or rhamnan. In an attempt to identify the GtfA substrate, the biochemical composition and structure of CWPS components (rhamnan and PSP) of L. lactisstrains 3107 and NZ9000, and a number of derivative strains were analysed. Results showed that derivatives possessing a non-functional gtfA or over-expressing gtfA do not possess any structural modifications in either the rhamnan or PSP components of the CWPS as compared to the 3107 or NZ9000 parent strains. In addition, the biochemical composition and structure of lipoteichoic acids (LTAs) in L. lactis 3107 and a representative phage-resistant derivative was also analysed, results revealed that gtfA is not responsible for terminal galactose substitution of LTA. Currently, further biochemical analysis of TA composition in L. lactis 3107 is being performed in order to identify the GtfA substrate and its relevance to phage infection. Attempts to generate LC3-resistant derivatives of L. lactis 3107 resulted in the isolation of lysogens of this phage that displayed resistance to multiple P335 phages. The LC3-prophage encoded superinfection exclusion (Sie) protein Sie2009/LC3, which is an identical (100 % identity) homologue of the previously identified Sie system Sie2009 was shown to be responsible for the phage resistance observed. Furthermore, superinfection immunity (Sii) against certain phages belonging to the P335 group was also exhibited in the presence of the LC3-prophage encoded repressor protein RepLC3. Overall this study has identified bacterial and phage-encoded protein(s) required for, or interfering with, the infection process of the dairy starter strain L. lactis 3107 by phages belonging to the lactococcal P335 group, as well as 936 and 949 group phages. This study forms the basis for future studies aimed to limit the proliferation of phages in the industrial contexten
dc.description.statusNot peer revieweden
dc.description.versionAccepted Version
dc.format.mimetypeapplication/pdfen
dc.identifier.citationErazo Garzon, A. C. 2019. Identification of genes involved in the DNA injection process by lactococcal P335 phages. PhD Thesis, University College Cork.en
dc.identifier.endpage245en
dc.identifier.urihttps://hdl.handle.net/10468/8537
dc.language.isoenen
dc.publisherUniversity College Corken
dc.rights© 2019, Andrea Erazo Garzon.en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/en
dc.subjectDairyen
dc.subjectP335en
dc.subjectPhageen
dc.subjectLactococcal phagesen
dc.subjectLactococcalen
dc.subjectPhage DNA injectionen
dc.thesis.opt-outfalse
dc.titleIdentification of genes involved in the DNA injection process by lactococcal P335 phagesen
dc.typeDoctoral thesisen
dc.type.qualificationlevelDoctoralen
dc.type.qualificationnamePhDen
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