Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/24991
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dc.contributor.authorMcDonnell, Brian-
dc.contributor.authorMahony, Jennifer-
dc.contributor.authorHanemaaijer, Laurens-
dc.contributor.authorNeve, Horst-
dc.contributor.authorNOBEN, Jean-Paul-
dc.contributor.authorLugli, Gabriele A.-
dc.contributor.authorVentura, Marco-
dc.contributor.authorKouwen, Thijs R.-
dc.contributor.authorvan Sinderen, Douwe-
dc.date.accessioned2017-10-10T13:59:03Z-
dc.date.available2017-10-10T13:59:03Z-
dc.date.issued2017-
dc.identifier.citationFRONTIERS IN MICROBIOLOGY, 8, p. 1-15 (Art N° 1754)-
dc.identifier.issn1664-302X-
dc.identifier.urihttp://hdl.handle.net/1942/24991-
dc.description.abstractDespite the persistent and costly problem caused by (bacterio) phage predation of Streptococcus thermophilus in dairy plants, DNA sequence information relating to these phages remains limited. Genome sequencing is necessary to better understand the diversity and proliferative strategies of virulent phages. In this report, whole genome sequences of 40 distinct bacteriophages infecting S. thermophilus were analyzed for general characteristics, genomic structure and novel features. The bacteriophage genomes display a high degree of conservation within defined groupings, particularly across the structural modules. Supporting this observation, four novel members of a recently discovered third group of S. thermophilus phages (termed the 5093 group) were found to be conserved relative to both phage 5093 and to each other. Replication modules of S. thermophilus phages generally fall within two main groups, while such phage genomes typically encode one putative transcriptional regulator. Such features are indicative of widespread functional synteny across genetically distinct phage groups. Phage genomes also display nucleotide divergence between groups, and between individual phages of the same group (within replication modules and at the 3' end of the lysis module)-through various insertions and/or deletions. A previously described multiplex PCR phage detection system was updated to reflect current knowledge on S. thermophilus phages. Furthermore, the structural protein complement as well as the antireceptor (responsible for the initial attachment of the phage to the host cell) of a representative of the 5093 group was defined. Our data more than triples the currently available genomic information on S. thermophilus phages, being of significant value to the dairy industry, where genetic knowledge of lytic phages is crucial for phage detection and monitoring purposes. In particular, the updated PCR detection methodology for S. thermophilus phages is highly useful in monitoring particular phage group(s) present in a given whey sample. Studies of this nature therefore not only provide information on the prevalence and associated threat of known S. thermophilus phages, but may also uncover newly emerging and genomically distinct phages infecting this dairy starter bacterium.-
dc.description.sponsorshipThe authors gratefully acknowledge the technical assistance of Erick Royackers in deducing the structural protein complement of phage 0095. We also gratefully acknowledge the technical assistance of Philip Kelleher in performing the panvirome analysis and of Angela Back in performing the electron microscopic analysis. The authors gratefully acknowledge the financial support of DSM Food Specialties. JM is in receipt of a Starting Investigator Research Grant (SIRG) (Ref. No. 15/SIRG/3430) funded by Science Foundation Ireland (SFI). DvS is supported by a Principal Investigator award (Ref. No. 13/IA/1953) through Science Foundation Ireland (SFI).-
dc.language.isoen-
dc.publisherFRONTIERS MEDIA SA-
dc.rightsFrontiers in Microbiology | www.frontiersin.org-
dc.subject.otherpanvirome; methyltransferase; transcriptional regulator; structural proteome; antireceptor-
dc.subject.otherpanvirome; methyltransferase; transcriptional regulator; structural proteome; antireceptor-
dc.titleGlobal Survey and Genome Exploration of Bacteriophages Infecting the Lactic Acid Bacterium Streptococcus thermophilus-
dc.typeJournal Contribution-
dc.identifier.epage15-
dc.identifier.spage1-
dc.identifier.volume8-
local.format.pages15-
local.bibliographicCitation.jcatA1-
dc.description.notes[McDonnell, Brian; Mahony, Jennifer; van Sinderen, Douwe] Univ Coll Cork, Sch Microbiol, Coll Sci Engn & Food Sci, Cork, Ireland. [Mahony, Jennifer; van Sinderen, Douwe] Univ Coll Cork, APC Microbiome Inst, Cork, Ireland. [Hanemaaijer, Laurens; Kouwen, Thijs R.] DSM Biotechnol Ctr, Delft, Netherlands. [Neve, Horst] Max Rubner Inst, Dept Microbiol & Biotechnol, Kiel, Germany. [Noben, Jean-Paul] Hasselt Univ, Biomed Res Inst, Diepenbeek, Belgium. [Lugli, Gabriele A.; Ventura, Marco] Univ Parma, Dept Life Sci, Lab Probiogen, Parma, Italy.-
local.publisher.placeLAUSANNE-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.artnr1754-
local.classdsPublValOverrule/author_version_not_expected-
dc.identifier.doi10.3389/fmicb.2017.01754-
dc.identifier.isi000410272500001-
item.fulltextWith Fulltext-
item.accessRightsOpen Access-
item.fullcitationMcDonnell, Brian; Mahony, Jennifer; Hanemaaijer, Laurens; Neve, Horst; NOBEN, Jean-Paul; Lugli, Gabriele A.; Ventura, Marco; Kouwen, Thijs R. & van Sinderen, Douwe (2017) Global Survey and Genome Exploration of Bacteriophages Infecting the Lactic Acid Bacterium Streptococcus thermophilus. In: FRONTIERS IN MICROBIOLOGY, 8, p. 1-15 (Art N° 1754).-
item.validationecoom 2018-
item.contributorMcDonnell, Brian-
item.contributorMahony, Jennifer-
item.contributorHanemaaijer, Laurens-
item.contributorNeve, Horst-
item.contributorNOBEN, Jean-Paul-
item.contributorLugli, Gabriele A.-
item.contributorVentura, Marco-
item.contributorKouwen, Thijs R.-
item.contributorvan Sinderen, Douwe-
crisitem.journal.eissn1664-302X-
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