Page 40 - Read Online
P. 40
Millen et al. Microbiome Res Rep 2023;2:26 https://dx.doi.org/10.20517/mrr.2023.29 Page 13 of 14
Consent for publication
Not applicable.
Copyright
© The Authors 2023.
REFERENCES
1. Mahony J, Murphy J, van Sinderen D. Lactococcal 936-type phages and dairy fermentation problems: from detection to evolution and
prevention. Front Microbiol 2012;3:335. DOI PubMed PMC
2. Oliveira J, Mahony J, Hanemaaijer L, Kouwen TRHM, van Sinderen D. Biodiversity of bacteriophages infecting Lactococcus lactis
starter cultures. J Dairy Sci 2018;101:96-105. DOI PubMed
3. Samson JE, Moineau S. Bacteriophages in food fermentations: new frontiers in a continuous arms race. Annu Rev Food Sci Technol
2013;4:347-68. DOI PubMed
4. Romero DA, Magill D, Millen A, Horvath P, Fremaux C. Dairy lactococcal and streptococcal phage-host interactions: an industrial
perspective in an evolving phage landscape. FEMS Microbiol Rev 2020;44:909-32. DOI PubMed
5. Charneco G, de Waal PP, van Rijswijck IMH, van Peij NNME, van Sinderen D, Mahony J. Bacteriophages in the dairy industry: a
problem solved? Annu Rev Food Sci Technol 2023;14:367-85. DOI PubMed
6. Mahony J, Kot W, Murphy J, et al. Investigation of the relationship between lactococcal host cell wall polysaccharide genotype and
936 phage receptor binding protein phylogeny. Appl Environ Microbiol 2013;79:4385-92. DOI PubMed PMC
7. Ainsworth S, Sadovskaya I, Vinogradov E, et al. Differences in lactococcal cell wall polysaccharide structure are major determining
factors in bacteriophage sensitivity. mBio 2014;5:e00880-14. DOI PubMed PMC
8. Hayes S, Vincentelli R, Mahony J, et al. Functional carbohydrate binding modules identified in evolved dits from siphophages
infecting various gram-positive bacteria. Mol Microbiol 2018;110:777-95. DOI PubMed
9. Sciara G, Bebeacua C, Bron P, et al. Structure of lactococcal phage p2 baseplate and its mechanism of activation. Proc Natl Acad Sci
U S A 2010;107:6852-7. DOI PubMed PMC
10. Mahony J, Oliveira J, Collins B, et al. Genetic and functional characterisation of the lactococcal P335 phage-host interactions. BMC
Genomics 2017;18:146. DOI PubMed PMC
11. Goulet A, Spinelli S, Mahony J, Cambillau C. Conserved and diverse traits of adhesion devices from siphoviridae recognizing
proteinaceous or saccharidic receptors. Viruses 2020;12:512. DOI PubMed PMC
12. Leprince A, Mahillon J. Phage adsorption to gram-positive bacteria. Viruses 2023;15:196. DOI PubMed PMC
13. Broadbent JR, McMahon DJ, Welker DL, Oberg CJ, Moineau S. Biochemistry, genetics, and applications of exopolysaccharide
production in Streptococcus thermophilus: a review. J Dairy Sci 2003;86:407-23. DOI PubMed
14. Forde A, Fitzgerald GF. Analysis of exopolysaccharide (EPS) production mediated by the bacteriophage adsorption blocking plasmid,
pCI658, isolated from Lactococcus lactis ssp. cremoris HO2. Int Dairy J 1999;9:465-72. DOI
15. Looijesteijn PJ, Trapet L, de Vries E, Abee T, Hugenholtz J. Physiological function of exopolysaccharides produced by Lactococcus
lactis. Int J Food Microbiol 2001;64:71-80. DOI PubMed
16. Akçelik M, Şanlibaba P. Characterisation of an exopolysaccharide preventing phage adsorption in Lactococcus lactis subsp. cremoris
MA39. Turkish J Vet Anim Sci 2002;26: 1151-6. Available from: https://journals.tubitak.gov.tr/cgi/viewcontent.cgi?article=3309&
context=veterinary. [Last accessed on 3 Jul 2023].
17. Deveau H, Van Calsteren MR, Moineau S. Effect of exopolysaccharides on phage-host interactions in Lactococcus lactis. Appl
Environ Microbiol 2002;68:4364-9. DOI
18. Millen AM, Romero DA, Horvath P, Magill D, Simdon L. Host-encoded, cell surface-associated exopolysaccharide required for
adsorption and infection by lactococcal P335 phage subtypes. Front Microbiol 2022;13:971166. DOI PubMed PMC
19. Millen AM, Horvath P, Boyaval P, Romero DA. Mobile CRISPR/Cas-mediated bacteriophage resistance in Lactococcus lactis. PLoS
One 2012;7:e51663. DOI PubMed PMC
20. Anderson DG, Mckay LL. Genetic and physical characterization of recombinant plasmids associated with cell aggregation and high-
frequency conjugal transfer in Streptococcus lactis ML3. J Bacteriol 1984;158:954-62. DOI PubMed PMC
21. Duwat P, Cochu A, Ehrlich SD, Gruss A. Characterization of Lactococcus lactis UV-sensitive mutants obtained by ISS1
transposition. J Bacteriol 1997;179:4473-9. DOI PubMed PMC
22. Bebeacua C, Tremblay D, Farenc C, et al. Structure, adsorption to host, and infection mechanism of virulent lactococcal phage p2. J
Virol 2013;87:12302-12. DOI PubMed PMC
23. Coq AM, Cesselin B, Commissaire J, Anba J. Sequence analysis of the lactococcal bacteriophage bIL170: insights into structural
proteins and HNH endonucleases in dairy phages. Microbiology 2002;148:985-1001. DOI PubMed
24. Mahony J, Deveau H, Mc Grath S, et al. Sequence and comparative genomic analysis of lactococcal bacteriophages jj50, 712 and
P008: evolutionary insights into the 936 phage species. FEMS Microbiol Lett 2006;261:253-61. DOI PubMed
25. Maguin E, Prévost H, Ehrlich SD, Gruss A. Efficient insertional mutagenesis in lactococci and other gram-positive bacteria. J
Bacteriol 1996;178:931-5. DOI PubMed PMC

