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A Specific Sugar Moiety in the Lactococcus lactis Cell Wall Pellicle Is Required for Infection by CHPC971, a Member of the Rare 1706 Phage Species

Marcelli, B., de Jong, A., Karsens, H. A., Janzen, T., Kok, J., & Kuipers, O. P. (2019) · Applied and Environmental Microbiology · doi:10.1128/aem.01224-19 · Cited by 10

Use of M17 and a milk-based medium enables isolation of two distinct and diverse populations of Lactococcus lactis strains from undefined mesophilic starter cultures

Frantzen, C. A., Kleppen, H. P., & Holo, H. (2015) · International Dairy Journal · doi:10.1016/j.idairyj.2015.09.005 · Cited by 10

Cell Surface Polysaccharides Represent a Common Strategy for Adsorption among Phages Infecting Lactic Acid Bacteria: Lessons from Dairy Lactococci and Streptococci

Mahony, J. (2021) · mSystems · doi:10.1128/msystems.00641-21 · Cited by 9

Host genetic requirements for DNA release of lactococcal phage TP901 ‐1

Ruiz‐Cruz, S., Garzon, A. E., Kelleher, P., Bottacini, F., Breum, S. Ø., Neve, H., Heller, K. J., Vogensen, F. K., Palussière, S., Courtin, P., et al. (2022) · Microbial Biotechnology · doi:10.1111/1751-7915.14156 · Cited by 9

Reduced synthesis of phospho-polysaccharide in Lactococcus as a strategy to evade phage infection

Giesbers, C. A. P., Fagan, J., Parlindungan, E., Palussière, S., Courtin, P., Lugli, G. A., Ventura, M., Kulakauskas, S., Chapot, M.-P., Mahony, J., et al. (2023) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2023.110415 · Cited by 8

A multifaceted investigation of lactococcal strain diversity in undefined mesophilic starter cultures

White, K., Eraclio, G., McDonnell, B., Bottacini, F., Lugli, G. A., Ventura, M., Volontè, F., Bello, F. D., Mahony, J., & van Sinderen, D. (2024) · Applied and Environmental Microbiology · doi:10.1128/aem.02152-23 · Cited by 8

Lactococcus lactis phages from the perspective of their diversity, thermal and biocidal resistance

Sadiq, F. A., He, G., Sakandar, H. A., Li, Y., & Ou, K. (2018) · International Dairy Journal · doi:10.1016/j.idairyj.2018.11.001 · Cited by 8

An extraordinary dairy phage and its properties: Occurrence, growth, inactivation, survival

Atamer, Z. (2022) · International Dairy Journal · doi:10.1016/j.idairyj.2022.105336 · Cited by 8

Novel cell wall polysaccharide genotypes and structures of lactococcal strains isolated from milk and fermented foods

Parlindungan, E., Sadovskaya, I., VINOGRADOV, E. V., Lugli, G. A., Ventura, M., van Sinderen, D., & Mahony, J. (2024) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2024.110840 · Cited by 7

A Lactococcal Phage Protein Promotes Viral Propagation and Alters the Host Proteomic Response During Infection

Lemay, M.-L., Maaß, S., Otto, A., Hamel, J., Plante, P.-L., Rousseau, G. M., Tremblay, D. M., Shi, R., Corbeil, J., Gagné, S. M., et al. (2020) · Viruses · doi:10.3390/v12080797 · Cited by 7

Viral Proteins Involved in the Adsorption Process of Deep-Purple, a Siphovirus Infecting Members of the Bacillus cereus Group

Leprince, A., Nuytten, M., & Mahillon, J. (2022) · Applied and Environmental Microbiology · doi:10.1128/aem.02478-21 · Cited by 5

Does the high biodiversity of lactococcal bacteriophages allow predictions about their different UV-C susceptibilities?

Schubert, C., Biere, N., Brinks, E., Samtlebe, M., Neve, H., Franz, C. M. A. P., Hinrichs, J., & Atamer, Z. (2023) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2023.110274 · Cited by 5

Evolved distal tail protein of skunaviruses facilitates adsorption to exopolysaccharide-encoding lactococci

Millen, A. M., Magill, D., Romero, D. A., & Simdon, L. (2023) · Microbiome Research Reports · doi:10.20517/mrr.2023.29 · Cited by 5

Engineering laboratory/factory-specific phage-resistant strains of Escherichia coli by mutagenesis and screening

Shen, Q., Zhou, X., Guo, Q., Xue, Y., & Zheng, Y. (2022) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-022-03239-y · Cited by 5

Genome Sequences of Eight Prophages Isolated from Lactococcus lactis Dairy Strains

Oliveira, J., Mahony, J., Lugli, G. A., Hanemaaijer, L., Kouwen, T. R. H. M., Ventura, M., & van Sinderen, D. (2016) · Genome Announcements · doi:10.1128/genomea.00906-16 · Cited by 4

Mixed culture engineering for steering starter functionality

Spus, M. (2016) · doi:10.18174/383695 · Cited by 4

“Expanding the Lactococcal Cell Wall Polysaccharide Paradigm: Novel Structures and Metabolic Pathways in the Emerging Dairy Species Pseudolactococcus laudensis and Pseudolactococcus raffinolactis ”

Soto‐Serrano, A., Sadovskaya, I., VINOGRADOV, E. V., Li, W., Yu, J., White, K., van Sinderen, D., Krych, Ł., Deptula, P., & Mahony, J. (2025) · MicrobiologyOpen · doi:10.1002/mbo3.70133 · Cited by 3

Lactococcal phage–host profiling through binding studies between cell wall polysaccharide types and Skunavirus receptor-binding proteins

White, K., Eraclio, G., McDonnell, B., Lugli, G. A., Crowley, T., Ventura, M., Volontè, F., Cambillau, C., Bello, F. D., Mahony, J., et al. (2025) · Microbial Genomics · doi:10.1099/mgen.0.001395 · Cited by 3

Distinct shifts in bacteriophage diversity and abundance during various stages of Gouda-type cheese production

Yu, J., Lugli, G. A., Ventura, M., van der Vaart, R., Nauta, A., Mahony, J., & van Sinderen, D. (2025) · Applied and Environmental Microbiology · doi:10.1128/aem.00651-25 · Cited by 3

Bacteriophage genotyping using BOXA repetitive-PCR

Damnjanović, D., Vázquez-Campos, X., Winter, D. L., Harvey, M. L., & Bridge, W. J. (2020) · BMC Microbiology · doi:10.1186/s12866-020-01770-2 · Cited by 3

Recognition of Protein-coding Genes Based on Z-curve Algorithms

Guo, F., Lin, Y., & Chen, L.-L. (2014) · Current Genomics · doi:10.2174/1389202915999140328162724 · Cited by 3

Analysis of the cell wall binding domain in bacteriocin-like lysin LysL from Lactococcus lactis LAC460

Mokhtari, S., Li, Y., Saris, P. E. J., & Takala, T. M. (2024) · Archives of Microbiology · doi:10.1007/s00203-024-04066-5 · Cited by 2

Alternative phage-host interaction in Lactococcus lactis : the carrier state drives rapid evolution of phagesPreprint

Marcelli, B., de Jong, A., Janzen, T., Kok, J., & Kuipers, O. P. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.27.063958 · Cited by 2

Differences in Lactococcal Cell Wall Polysaccharide Structure Are Major Determining Factors in Bacteriophage Sensitivity

Ainsworth, S., Sadovskaya, I., Vinogradov, E., Courtin, P., Guérardel, Y., Mahony, J., Grard, T., Cambillau, C., Chapot, M.-P., & van Sinderen, D. (2014) · mBio · doi:10.1128/mbio.00880-14 · Cited by 112

Lactococcal 949 Group Phages Recognize a Carbohydrate Receptor on the Host Cell Surface

Mahony, J., Randazzo, W., Neve, H., Settanni, L., & van Sinderen, D. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.00143-15 · Cited by 39

Molecular, physiological and phylogenetic traits of Lactococcus 936-type phages from distinct dairy environments

Chmielewska-Jeznach, M., Bardowski, J. K., & Szczepankowska, A. K. (2018) · Scientific Reports · doi:10.1038/s41598-018-30371-3 · Cited by 25

Molecular Insights on the Recognition of a Lactococcus lactis Cell Wall Pellicle by the Phage 1358 Receptor Binding Protein

Farenc, C., Spinelli, S., VINOGRADOV, E. V., Tremblay, D. M., Blangy, S., Sadovskaya, I., Moineau, S., & Cambillau, C. (2014) · Journal of Virology · doi:10.1128/jvi.00739-14 · Cited by 70

Biodiversity of lactococcal bacteriophages and associated phage-host interactions

Oliveira, J. (2017) · Cork Open Research Archive (University College Cork, Ireland)