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Classification of Lytic Bacteriophages Attacking Dairy Leuconostoc Starter Strains
Author(s) -
Yahya Ali,
Witold Kot,
Zeynep Atamer,
Jï¿ ⁄ rg Hinrichs,
Finn K. Vogensen,
Knut J. Heller,
Horst Neve
Publication year - 2013
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.00076-13
Subject(s) - siphoviridae , biology , lytic cycle , microbiology and biotechnology , bacteriophage , genetics , gene , escherichia coli , virus
A set of 83 lytic dairy bacteriophages (phages) infecting flavor-producing mesophilic starter strains of theLeuconostoc genus was characterized, and the first in-depth taxonomic scheme was established for this phage group. Phages were obtained from different sources, i.e., from dairy samples originating from 11 German dairies (50Leuconostoc pseudomesenteroides [Ln. pseudomesenteroides ] phages, 4Ln. mesenteroides phages) and from 3 external phage collections (17Ln. pseudomesenteroides phages, 12Ln. mesenteroides phages). All phages belonged to theSiphoviridae family of phages with isometric heads (diameter, 55 nm) and noncontractile tails (length, 140 nm). With the exception of one phage (i.e., phage ΦLN25), allLn. mesenteroides phages lysed the same host strains and revealed characteristic globular baseplate appendages. Phage ΦLN25, with different Y-shaped appendages, had a unique host range. Apart from two phages (i.e., phages P792 and P793), allLn. pseudomesenteroides phages shared the same host range and had plain baseplates without distinguishable appendages. They were further characterized by the presence or absence of a collar below the phage head or by unique tails with straight striations. Phages P792 and P793 with characteristic fluffy baseplate appendages could propagate only on other specific hosts. AllLn. mesenteroides and allLn. pseudomesenteroides phages were members of two (host species-specific) distinct genotypes but shared a limited conserved DNA region specifying their structural genes. A PCR detection system was established and was shown to be reliable for the detection of allLeuconostoc phage types.

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