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Development of a New Method for Detection and Identification of Oenococcus oeni Bacteriophages Based on Endolysin Gene Sequence and Randomly Amplified Polymorphic DNA
Author(s) -
Francesca Doria,
Chiara Napoli,
Antonella Costantini,
Graziella Berta,
JuanCarlos Sáiz,
Emilia García-Moruno
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.01307-13
Subject(s) - oenococcus oeni , biology , malolactic fermentation , lysogenic cycle , rapd , wine , lysin , bacteriophage , microbiology and biotechnology , winemaking , typing , bacteria , genetics , gene , escherichia coli , food science , population , lactic acid , genetic diversity , demography , sociology
Malolactic fermentation (MLF) is a biochemical transformation conducted by lactic acid bacteria (LAB) that occurs in wine at the end of alcoholic fermentation.Oenococcus oeni is the main species responsible for MLF in most wines. As in other fermented foods, where bacteriophages represent a potential risk for the fermentative process,O. oeni bacteriophages have been reported to be a possible cause of unsuccessful MLF in wine. Thus, preparation of commercial starters that take into account the different sensitivities ofO. oeni strains to different phages would be advisable. However, currently, no methods have been described to identify phages infectingO. oeni . In this study, two factors are addressed: detection and typing of bacteriophages. First, a simple PCR method was devised targeting a conserved region of the endolysin (lys ) gene to detect temperateO. oeni bacteriophages. For this purpose, 37O. oeni strains isolated from Italian wines during different phases of the vinification process were analyzed by PCR for the presence of thelys gene, and 25 strains gave a band of the expected size (1,160 bp). This is the first method to be developed that allows identification of lysogenicO. oeni strains without the need for time-consuming phage bacterial-lysis induction methods. Moreover, a phylogenetic analysis was conducted to type bacteriophages. After the treatment of bacteria with UV light, lysis was obtained for 15 strains, and the 15 phage DNAs isolated were subjected to two randomly amplified polymorphic DNA (RAPD)-PCRs. By combining the RAPD profiles andlys sequences, 12 differentO. oeni phages were clearly distinguished.

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