» Articles » PMID: 28754704

Metagenomic Analysis of Dairy Bacteriophages: Extraction Method and Pilot Study on Whey Samples Derived from Using Undefined and Defined Mesophilic Starter Cultures

Abstract

Despite being potentially highly useful for characterizing the biodiversity of phages, metagenomic studies are currently not available for dairy bacteriophages, partly due to the lack of a standard procedure for phage extraction. We optimized an extraction method that allows the removal of the bulk protein from whey and milk samples with losses of less than 50% of spiked phages. The protocol was applied to extract phages from whey in order to test the notion that members of 936 (now ), P335, c2 (now ) and phage groups are the most frequently encountered in the dairy environment. The relative abundance and diversity of phages in eight and four whey mixtures from dairies using undefined mesophilic mixed-strain cultures containing subsp. biovar diacetylactis and species (i.e., DL starter cultures) and defined cultures, respectively, were assessed. Results obtained from transmission electron microscopy and high-throughput sequence analyses revealed the dominance of 936 phages (order , family ) in dairies using undefined DL starter cultures and c2 phages (order , family ) in dairies using defined cultures. The 936 and phages demonstrated limited diversity. Possible coinduction of temperate P335 prophages and satellite phages in one of the whey mixtures was also observed. The method optimized in this study could provide an important basis for understanding the dynamics of the phage community (abundance, development, diversity, evolution, etc.) in dairies with different sizes, locations, and production strategies. It may also enable the discovery of previously unknown phages, which is crucial for the development of rapid molecular biology-based methods for phage burden surveillance systems. The dominance of only a few phage groups in the dairy environment signifies the depth of knowledge gained over the past decades, which served as the basis for designing current phage control strategies. The presence of a correlation between phages and the type of starter cultures being used in dairies might help to improve the selection and/or design of suitable, custom, and cost-efficient phage control strategies.

Citing Articles

Dynamics of the viral community on the surface of a French smear-ripened cheese during maturation and persistence across production years.

Paillet T, Lamy-Besnier Q, Figueroa C, Petit M, Dugat-Bony E mSystems. 2024; 9(7):e0020124.

PMID: 38860825 PMC: 11265279. DOI: 10.1128/msystems.00201-24.


The Application of Metagenomics to Study Microbial Communities and Develop Desirable Traits in Fermented Foods.

Srinivas M, OSullivan O, Cotter P, Van Sinderen D, Kenny J Foods. 2023; 11(20).

PMID: 37431045 PMC: 9601669. DOI: 10.3390/foods11203297.


Longitudinal Study of Phages in a Canadian Cheese Factory.

Jolicoeur A, Lemay M, Beaubien E, Belanger J, Bergeron C, Bourque-Leblanc F Appl Environ Microbiol. 2023; 89(5):e0042123.

PMID: 37074184 PMC: 10231144. DOI: 10.1128/aem.00421-23.


Integrated molecular approaches for fermented food microbiome research.

Walsh A, Leech J, Huttenhower C, Delhomme-Nguyen H, Crispie F, Chervaux C FEMS Microbiol Rev. 2023; 47(2).

PMID: 36725208 PMC: 10002906. DOI: 10.1093/femsre/fuad001.


High Level of Interaction between Phages and Bacteria in an Artisanal Raw Milk Cheese Microbial Community.

Queiroz L, Lacorte G, Isidorio W, Landgraf M, Franco B, Pinto U mSystems. 2022; 8(1):e0056422.

PMID: 36475872 PMC: 9948729. DOI: 10.1128/msystems.00564-22.


References
1.
Sharon I, Battchikova N, Aro E, Giglione C, Meinnel T, Glaser F . Comparative metagenomics of microbial traits within oceanic viral communities. ISME J. 2011; 5(7):1178-90. PMC: 3146289. DOI: 10.1038/ismej.2011.2. View

2.
Smid E, Erkus O, Spus M, Wolkers-Rooijackers J, Alexeeva S, Kleerebezem M . Functional implications of the microbial community structure of undefined mesophilic starter cultures. Microb Cell Fact. 2014; 13 Suppl 1:S2. PMC: 4155819. DOI: 10.1186/1475-2859-13-S1-S2. View

3.
Valyasevi R, Sandine W, Geller B . A membrane protein is required for bacteriophage c2 infection of Lactococcus lactis subsp. lactis C2. J Bacteriol. 1991; 173(19):6095-100. PMC: 208356. DOI: 10.1128/jb.173.19.6095-6100.1991. View

4.
Garneau J, Tremblay D, Moineau S . Characterization of 1706, a virulent phage from Lactococcus lactis with similarities to prophages from other Firmicutes. Virology. 2008; 373(2):298-309. DOI: 10.1016/j.virol.2007.12.002. View

5.
Ali Y, Kot W, Atamer Z, Hinrichs J, Vogensen F, Heller K . Classification of lytic bacteriophages attacking dairy Leuconostoc starter strains. Appl Environ Microbiol. 2013; 79(12):3628-36. PMC: 3675911. DOI: 10.1128/AEM.00076-13. View