@article{mbs:/content/journal/micro/10.1099/mic.0.2006/004812-0, author = "Calvez, Ségolène and Rincé, Alain and Auffray, Yanick and Prévost, Hervé and Drider, Djamel", title = "Identification of new genes associated with intermediate resistance of Enterococcus faecalis to divercin V41, a pediocin-like bacteriocin", journal= "Microbiology", year = "2007", volume = "153", number = "5", pages = "1609-1618", doi = "https://doi.org/10.1099/mic.0.2006/004812-0", url = "https://www.microbiologyresearch.org/content/journal/micro/10.1099/mic.0.2006/004812-0", publisher = "Microbiology Society", issn = "1465-2080", type = "Journal Article", keywords = "ADT, agar diffusion test", keywords = "AU, arbitrary units", keywords = "PDE, phosphodiesterase", keywords = "Ped PA-1/AcH, pediocin PA-1/AcH", keywords = "PTS, phosphotransfersase system", keywords = "DvnRV41, recombinant divercin V41", keywords = "MesY105, mesentericin Y105", keywords = "RAPD, random amplified polymorphic DNA", keywords = "DvnV41, divercin V41", abstract = "It has been suggested that resistance to class IIa bacteriocins occurs at either a low or a high level. In listerial strains, low-level resistance (2–4-fold) to class IIa bacteriocins is attributed to alterations in membrane lipid composition. In Listeria monocytogenes and Enterococcus faecalis, high-level resistance (1000-fold) correlates with inactivation of the mptACD operon, which encodes the EIIMan t mannose permease of the phosphotransferase system (PTS). Previous studies reported that in L. monocytogenes, high-level resistance involved the σ 54 factor and the ManR activator. In this investigation, three genes associated with the resistance of Ent. faecalis JH2-2 to divercin V41, a pediocin-like bacteriocin from Carnobacterium divergens V41, were clearly identified by screening an insertional mutant library of Ent. faecalis JH2-2. These genes correspond to the well-known rpoN gene, which encodes σ 54 factor, and to genes encoding a glycerophosphoryl diester phosphodiesterase (GlpQ) and a protein with a putative phosphodiesterase function (PDE). Resistance of the three mutants defective in the aforementioned genes appeared to be graduated: the rpoN mutant was more resistant than the glpQ mutant, which was more resistant than the pde mutant. Moreover, this resistance was specific to class IIa bacteriocins.", }