Peptide pheromone-dependent regulation of antimicrobial peptide production in Gram-positive bacteria: a case of multicellular behavior

Quorum sensing enables unicellular organisms to behave in a multicellular way by allowing population-wide synchronized adaptive responses that involve modulation of a wide range of physiological responses in a cell density-, cell proximity- or growth phase-dependent manner. Examples of processes modulated by quorum sensing are the development of genetic competence, conjugative plasmid transfer, sporulation and cell differentiation, biofilm formation, virulence response, production of antibiotics, antimicrobial peptides and toxins, and bioluminescence (for reviews see [38]). The cell-to-cell communication strategies involved in these processes are based on the utilization of small signal molecules produced and released into the environment by the microorganisms. These communication molecules are referred to as pheromones and act as chemical messengers that transmit information across space. The extracellular pheromones accumulate in the environment and trigger a response in the target cells when its concentration reaches a certain threshold value. Elucidation of the chemical nature of the pheromones modulating the processes mentioned above reveals that most of them are unmodified peptides, post-translationally modified peptides, N-acyl homoserine lactones, or butyrolactones. Lactone-based pheromones are the preferred communication signals in Gram-negative bacteria (for review see [47,48]), whereas peptide-based pheromones are the predominant extracellular signals among Gram-positive bacteria (for review see [37,61]). However, lactone-based pheromones are utilized as signals that modulate differentiation and secondary metabolism production in Streptomyces (for review see [20]). This review focuses on the major advances and current views of the peptide-pheromone dependent regulatory circuits involved in production of antimicrobial peptides in Gram-positive bacteria.

[1]  M. Qiao,et al.  Genes responsible for nisin synthesis, regulation and immunity form a regulon of two operons and are induced by nisin in Lactoccocus lactis N8. , 1996, Microbiology.

[2]  Oscar P. Kuipers,et al.  Specific Binding of Nisin to the Peptidoglycan Precursor Lipid II Combines Pore Formation and Inhibition of Cell Wall Biosynthesis for Potent Antibiotic Activity* , 2001, The Journal of Biological Chemistry.

[3]  K. Entian,et al.  Analysis of genes involved in biosynthesis of the lantibiotic subtilin , 1992, Applied and environmental microbiology.

[4]  D. Diep,et al.  Characterization of the locus responsible for the bacteriocin production in Lactobacillus plantarum C11 , 1996, Journal of bacteriology.

[5]  L. Axelsson,et al.  Purification and cloning of sakacin 674, a bacteriocin from Lactobacillus sake Lb674. , 1994, FEMS microbiology letters.

[6]  A. Rincé,et al.  IS1675, a Novel Lactococcal Insertion Element, Forms a Transposon-Like Structure Including the Lacticin 481 Lantibiotic Operon , 2000, Journal of bacteriology.

[7]  G. Dunny,et al.  Cell-cell communication in gram-positive bacteria. , 1997, Annual review of microbiology.

[8]  T. Klaenhammer,et al.  Genetics of Streptococci, Enterococci and Lactococci , 1995 .

[9]  K. Entian,et al.  Genes involved in immunity to the lantibiotic nisin produced by Lactococcus lactis 6F3 , 1995, Applied and environmental microbiology.

[10]  D. Marion,et al.  Divercin V41, a new bacteriocin with two disulphide bonds produced by Carnobacterium divergens V41: primary structure and genomic organization. , 1998, Microbiology.

[11]  S. Stevanović,et al.  Regulation of epidermin biosynthetic genes by EpiQ , 1993, Molecular microbiology.

[12]  R. Siezen,et al.  Influence of charge differences in the C-terminal part of nisin on antimicrobial activity and signaling capacity. , 1997, European journal of biochemistry.

[13]  J. Vederas,et al.  Chemical and genetic characterization of bacteriocins produced by Carnobacterium piscicola LV17B. , 1994, The Journal of biological chemistry.

[14]  W. D. de Vos,et al.  Characterization of the nisin gene cluster nisABTCIPR of Lactococcus lactis. Requirement of expression of the nisA and nisI genes for development of immunity. , 1993, European journal of biochemistry.

[15]  A. Rincé,et al.  Characterization of the lacticin 481 operon: the Lactococcus lactis genes lctF, lctE, and lctG encode a putative ABC transporter involved in bacteriocin immunity , 1997, Applied and environmental microbiology.

[16]  J. Ferretti,et al.  Duplication of the lantibiotic structural gene in M-type 49 group A streptococcus strains producing streptococcin A-M49 , 1994, Applied and environmental microbiology.

[17]  M. Kleerebezem,et al.  Characterization of a locus from Carnobacterium piscicola LV17B involved in bacteriocin production and immunity: evidence for global inducer-mediated transcriptional regulation , 1997, Journal of bacteriology.

[18]  K. Entian,et al.  Biosynthesis of Lantibiotic Nisin , 1996, The Journal of Biological Chemistry.

[19]  D. Diep,et al.  A family of bacteriocin ABC transporters carry out proteolytic processing of their substrates concomitant with export , 1995, Molecular microbiology.

[20]  J. Hansen,et al.  Determination of the sequence of spaE and identification of a promoter in the subtilin (spa) operon in Bacillus subtilis , 1992, Journal of bacteriology.

[21]  S. Banerjee,et al.  Structure, expression, and evolution of a gene encoding the precursor of nisin, a small protein antibiotic. , 1988, The Journal of biological chemistry.

[22]  C. Moran EXPRESSION OF σA AND σH REGULONS DURING STATIONARY PHASE AND ENDOSPORE FORMATION , 1990 .

[23]  M. Kleerebezem,et al.  Improved vectors for nisin-controlled expression in gram-positive bacteria. , 2000, Plasmid.

[24]  K. Entian,et al.  Prepeptide sequence of epidermin, a ribosomally synthesized antibiotic with four sulphide-rings , 1988, Nature.

[25]  W. D. de Vos,et al.  Controlled gene expression systems for Lactococcus lactis with the food-grade inducer nisin , 1996, Applied and environmental microbiology.

[26]  D. Morrison,et al.  Regulation of competence for genetic transformation in Streptococcus pneumoniae by an auto‐induced peptide pheromone and a two‐component regulatory system , 1996, Molecular microbiology.

[27]  L. Axelsson,et al.  Analysis of the sakacin P gene cluster from Lactobacillus sake Lb674 and its expression in sakacin-negative Lb. sake strains. , 1996, Microbiology.

[28]  G. Bierbaum,et al.  Biosynthesis of the Lantibiotic Mersacidin: Organization of a Type B Lantibiotic Gene Cluster , 2000, Applied and Environmental Microbiology.

[29]  R. P. Ross,et al.  Each peptide of the two-component lantibiotic lacticin 3147 requires a separate modification enzyme for activity. , 2000, Microbiology.

[30]  M. Stiles,et al.  Plasmid-associated bacteriocin production by a strain of Carnobacterium piscicola from meat , 1990, Applied and environmental microbiology.

[31]  O. Kuipers,et al.  Molecular and Functional Analyses of themetC Gene of Lactococcus lactis, Encoding Cystathionine β-Lyase , 2000, Applied and Environmental Microbiology.

[32]  H. Sahl,et al.  Cloning, sequencing and production of the lantibiotic mersacidin. , 1995, FEMS microbiology letters.

[33]  J. Tagg,et al.  Cloning of the gene encoding Streptococcin A-FF22, a novel lantibiotic produced by Streptococcus pyogenes, and determination of its nucleotide sequence , 1993, Applied and environmental microbiology.

[34]  C. Hill,et al.  Characterization and Heterologous Expression of the Genes Encoding Enterocin A Production, Immunity, and Regulation inEnterococcus faecium DPC1146 , 1999, Applied and Environmental Microbiology.

[35]  M. Kleerebezem,et al.  Cofactor Engineering: a Novel Approach to Metabolic Engineering in Lactococcus lactis by Controlled Expression of NADH Oxidase , 1998, Journal of bacteriology.

[36]  W. D. de Vos,et al.  Lantibiotics: biosynthesis, mode of action and applications. , 1999, Natural product reports.

[37]  K. Chater,et al.  Genetics of differentiation in Streptomyces. , 1993, Annual review of microbiology.

[38]  M. Kleerebezem,et al.  Adaptation of the Nisin-Controlled Expression System in Lactobacillus plantarum: a Tool To Study In Vivo Biological Effects , 2000, Applied and Environmental Microbiology.

[39]  K. Entian,et al.  Analysis of genes involved in the biosynthesis of lantibiotic epidermin. , 1992, European journal of biochemistry.

[40]  C. Ronson,et al.  Isolation and characterization of the lantibiotic salivaricin A and its structural gene salA from Streptococcus salivarius 20P3 , 1993, Applied and environmental microbiology.

[41]  L. Axelsson,et al.  The synthesis of the bacteriocin sakacin A is a temperature-sensitive process regulated by a pheromone peptide through a three-component regulatory system. , 2000, Microbiology.

[42]  W. D. de Vos,et al.  Identification and characterization of the lantibiotic nisin Z, a natural nisin variant. , 1991, European journal of biochemistry.

[43]  Gary M. Dunny,et al.  Cell-cell signaling in bacteria , 1999 .

[44]  M. Kleerebezem,et al.  Controlled gene expression systems for lactic acid bacteria: transferable nisin-inducible expression cassettes for Lactococcus, Leuconostoc, and Lactobacillus spp , 1997, Applied and environmental microbiology.

[45]  V. Eijsink,et al.  Pheromone‐induced production of antimicrobial peptides in Lactobacillus , 1997, Molecular microbiology.

[46]  W. M. Vos,et al.  Food-grade controlled lysis of Lactococcus lactis for accelerated cheese ripening , 1997, Nature Biotechnology.

[47]  J. Vederas,et al.  Characteristics and genetic determinant of a hydrophobic peptide bacteriocin, carnobacteriocin A, produced by Carnobacterium piscicola LV17A. , 1994, Microbiology.

[48]  K. Entian,et al.  Regulation of nisin biosynthesis and immunity in Lactococcus lactis 6F3 , 1994, Applied and environmental microbiology.

[49]  M. Kleerebezem,et al.  Controlled overproduction of proteins by lactic acid bacteria. , 1997, Trends in biotechnology.

[50]  W. D. de Vos,et al.  Influence of amino acid substitutions in the nisin leader peptide on biosynthesis and secretion of nisin by Lactococcus lactis. , 1994, The Journal of biological chemistry.

[51]  S. Arvidson,et al.  Transcriptional control of the agr‐dependent virulence gene regulator, RNAIII, in Staphylococcus aureus , 1996, Molecular microbiology.

[52]  J. Kok,et al.  Biological and molecular characterization of a two‐peptide lantibiotic produced by Lactococcus lactis IFPL105 , 2000, Journal of applied microbiology.

[53]  V. Eijsink,et al.  Antagonistic Activity of Lactobacillus plantarum C11: Two New Two-Peptide Bacteriocins, Plantaricins EF and JK, and the Induction Factor Plantaricin A , 1998, Applied and Environmental Microbiology.

[54]  Trine Nilsen,et al.  An Exported Inducer Peptide Regulates Bacteriocin Production in Enterococcus faecium CTC492 , 1998, Journal of bacteriology.

[55]  R. Beavis,et al.  Cell density control of staphylococcal virulence mediated by an octapeptide pheromone. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[56]  W. D. de Vos,et al.  Structure, organization, and expression of the lct gene for lacticin 481, a novel lantibiotic produced by Lactococcus lactis. , 1993, The Journal of biological chemistry.

[57]  W. M. Vos,et al.  Maturation pathway of nisin and other lantibiotics: post‐translationally modified antimicrobial peptides exported by Gram‐positive bacteria , 1995, Molecular microbiology.

[58]  J. Hansen,et al.  Identification and Characterization of the Structural and Transporter Genes for, and the Chemical and Biological Properties of, Sublancin 168, a Novel Lantibiotic Produced by Bacillus subtilis 168* , 1998, The Journal of Biological Chemistry.

[59]  V. Eijsink,et al.  Functional analysis of promoters involved in quorum sensing‐based regulation of bacteriocin production in Lactobacillus , 2000, Molecular microbiology.

[60]  W. D. de Vos,et al.  Properties of nisin Z and distribution of its gene, nisZ, in Lactococcus lactis , 1993, Applied and Environmental Microbiology.

[61]  L. Frost,et al.  Transcriptional analysis and regulation of carnobacteriocin production in Carnobacterium piscicola LV17. , 1997, Gene.

[62]  M. Daeschel,et al.  Purification and characterization of plantaricin A, a Lactobacillus plantarum bacteriocin whose activity depends on the action of two peptides. , 1993, Journal of general microbiology.

[63]  T. Klaenhammer,et al.  Genetics of bacteriocins produced by lactic acid bacteria. , 1993, FEMS microbiology reviews.

[64]  J. Vederas,et al.  Characterization of the genetic locus responsible for production and immunity of carnobacteriocin A: the immunity gene confers cross-protection to enterocin B. , 2000, Microbiology.

[65]  M. Kleerebezem,et al.  Use of the Lactococcal nisA Promoter To Regulate Gene Expression in Gram-Positive Bacteria: Comparison of Induction Level and Promoter Strength , 1998, Applied and Environmental Microbiology.

[66]  M. Phansalkar,et al.  Mersacidin, a new antibiotic from Bacillus. Fermentation, isolation, purification and chemical characterization. , 1992, The Journal of antibiotics.

[67]  M. Stiles,et al.  Antibacterial activity of lactic acid bacteria isolated from vacuum-packaged meats. , 1990, The Journal of applied bacteriology.

[68]  H. Sahl,et al.  Identification of Genes Encoding Two-Component Lantibiotic Production in Staphylococcus aureus C55 and Other Phage Group II S. aureus Strains and Demonstration of an Association with the Exfoliative Toxin B Gene , 1999, Infection and Immunity.

[69]  H. Sahl,et al.  The Lantibiotic Mersacidin Inhibits Peptidoglycan Synthesis by Targeting Lipid II , 1998, Antimicrobial Agents and Chemotherapy.

[70]  J. Kornblum,et al.  Synthesis of staphylococcal virulence factors is controlled by a regulatory RNA molecule. , 1993, The EMBO journal.

[71]  J. S. Parkinson,et al.  Communication modules in bacterial signaling proteins. , 1992, Annual review of genetics.

[72]  D. Diep,et al.  Identification of the DNA-binding sites for two response regulators involved in control of bacteriocin synthesis in Lactobacillus plantarum C11 , 1998, Molecular and General Genetics MGG.

[73]  M. Kleerebezem,et al.  A two-component signal-transduction cascade in Carnobacterium piscicola LV17B: two signaling peptides and one sensor-transmitter , 2001, Peptides.

[74]  V. Eijsink,et al.  Induction of bacteriocin production in Lactobacillus sake by a secreted peptide , 1996, Journal of bacteriology.

[75]  G. Heijne Membrane protein structure prediction. Hydrophobicity analysis and the positive-inside rule. , 1992, Journal of molecular biology.

[76]  K. Entian,et al.  Biosynthesis of the lantibiotic subtilin is regulated by a histidine kinase/response regulator system , 1993, Applied and environmental microbiology.

[77]  E. Campbell,et al.  A competence regulon in Streptococcus pneumoniae revealed by genomic analysis , 1998, Molecular microbiology.

[78]  E. Greenberg,et al.  Census and consensus in bacterial ecosystems: the LuxR-LuxI family of quorum-sensing transcriptional regulators. , 1996, Annual review of microbiology.

[79]  I. Nes,et al.  Identification of the streptococcal competence‐pheromone receptor , 1996, Molecular microbiology.

[80]  W. D. de Vos,et al.  Functional analysis of promoters in the nisin gene cluster of Lactococcus lactis , 1996, Journal of bacteriology.

[81]  K. Entian,et al.  Nisin, a peptide antibiotic: cloning and sequencing of the nisA gene and posttranslational processing of its peptide product , 1989, Journal of bacteriology.

[82]  E. Greenberg,et al.  Self perception in bacteria: quorum sensing with acylated homoserine lactones. , 1998, Current opinion in microbiology.

[83]  N. Russell,et al.  A comparison of thermal adaptation of membrane lipids in psychrophilic and thermophilic bacteria , 1990 .

[84]  A. Ninfa,et al.  Protein phosphorylation and regulation of adaptive responses in bacteria. , 1989, Microbiological reviews.

[85]  J. Tagg,et al.  Genetic Basis of Streptococcin A-FF22 Production , 1976, Antimicrobial Agents and Chemotherapy.

[86]  A. Driessen,et al.  Plantaricin A is an amphiphilic alpha-helical bacteriocin-like pheromone which exerts antimicrobial and pheromone activities through different mechanisms. , 1998, Biochemistry.

[87]  A. Grossman,et al.  Biochemical and genetic characterization of a competence pheromone from B. subtilis , 1994, Cell.

[88]  G. Seibert,et al.  Mersacidin, a new antibiotic from Bacillus. In vitro and in vivo antibacterial activity. , 1992, The Journal of antibiotics.

[89]  H. Sahl,et al.  The lantibiotic mersacidin inhibits peptidoglycan biosynthesis at the level of transglycosylation. , 1997, European journal of biochemistry.

[90]  W. D. de Vos,et al.  Effects of gene disruptions in the nisin gene cluster of Lactococcus lactis on nisin production and producer immunity. , 1999, Microbiology.

[91]  J. Vederas,et al.  Effect of Amino Acid Substitutions on the Activity of Carnobacteriocin B2 , 1997, The Journal of Biological Chemistry.

[92]  J. Ferretti,et al.  Nucleotide sequence of the streptococcin A-FF22 lantibiotic regulon: model for production of the lantibiotic SA-FF22 by strains of Streptococcus pyogenes. , 1999, FEMS microbiology letters.

[93]  K. Entian,et al.  Growth phase-dependent regulation and membrane localization of SpaB, a protein involved in biosynthesis of the lantibiotic subtilin , 1994, Applied and environmental microbiology.

[94]  D. Dubnau,et al.  Genetic competence in Bacillus subtilis. , 1991, Microbiological reviews.

[95]  S. Banerjee,et al.  Structure and expression of a gene encoding the precursor of subtilin, a small protein antibiotic. , 1988, The Journal of biological chemistry.

[96]  W. D. de Vos,et al.  Autoregulation of Nisin Biosynthesis in Lactococcus lactis by Signal Transduction (*) , 1995, The Journal of Biological Chemistry.

[97]  A. Rincé,et al.  Cloning, expression, and nucleotide sequence of genes involved in production of lactococcin DR, a bacteriocin from lactococcus lactis subsp. lactis , 1994, Applied and environmental microbiology.

[98]  B. de Kruijff,et al.  The lantibiotic nisin, a special case or not? , 1999, Biochimica et biophysica acta.

[99]  A. Poon,et al.  Induction of bacteriocin in Carnobacterium piscicola LV17 , 1995 .

[100]  W. Hammes,et al.  Cloning and sequencing of sakP encoding sakacin P, the bacteriocin produced by Lactobacillus sake LTH 673. , 1994, Microbiology.

[101]  R. Siezen,et al.  Cloning, Characterization, Controlled Overexpression, and Inactivation of the Major Tributyrin Esterase Gene of Lactococcus lactis , 2000, Applied and Environmental Microbiology.

[102]  H. Sahl,et al.  Two-Component Anti-Staphylococcus aureusLantibiotic Activity Produced by Staphylococcus aureusC55 , 1998, Applied and Environmental Microbiology.

[103]  M. Stiles,et al.  Mobilization and expression of bacteriocin plasmids from Carnobacterium piscicola isolated from meat , 1992 .

[104]  D. Diep,et al.  A bacteriocin‐like peptide induces bacteriocin synthesis in Lactobacillus plantarum C11 , 1995, Molecular microbiology.

[105]  Michiel Kleerebezem,et al.  Quorum sensing by peptide pheromones and two‐component signal‐transduction systems in Gram‐positive bacteria , 1997, Molecular microbiology.

[106]  D. Morrison,et al.  An unmodified heptadecapeptide pheromone induces competence for genetic transformation in Streptococcus pneumoniae. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[107]  M. Gasson,et al.  Molecular analysis of the regulation of nisin immunity. , 1996, Microbiology.

[108]  L. Axelsson,et al.  Cloning and nucleotide sequence of a gene from Lactobacillus sake Lb706 necessary for sakacin A production and immunity , 1993, Applied and environmental microbiology.

[109]  I. Nes,et al.  Biochemical and genetic characterization of enterocin A from Enterococcus faecium, a new antilisterial bacteriocin in the pediocin family of bacteriocins , 1996, Applied and environmental microbiology.

[110]  Trine Nilsen,et al.  Enterocin B, a new bacteriocin from Enterococcus faecium T136 which can act synergistically with enterocin A. , 1997, Microbiology.

[111]  R. Siezen,et al.  Homology modelling of the Lactococcus lactis leader peptidase NisP and its interaction with the precursor of the lantibiotic nisin. , 1995, Protein engineering.

[112]  K. Entian,et al.  Biosynthesis of the lantibiotic nisin: genomic organization and membrane localization of the NisB protein , 1992, Applied and Environmental Microbiology.

[113]  L. Axelsson,et al.  Purification and amino acid sequence of sakacin A, a bacteriocin from Lactobacillus sake Lb706. , 1992, Journal of general microbiology.

[114]  W. D. de Vos,et al.  University of Groningen Characterization of the Lactococcus lactis Nisin A Operon Genes nisP , Encoding a Subtilisin-Like Serine Protease Involved in Precursor Processing , and nisR , Encoding a Regulatory Protein Involved in Nisin Biosynthesis , 2019 .

[115]  O. Kuipers,et al.  Use of the cell wall precursor lipid II by a pore-forming peptide antibiotic. , 1999, Science.

[116]  A. Mattick,et al.  A Powerful Inhibitory Substance Produced by Group N Streptococci , 1944, Nature.

[117]  Lixin Zhou,et al.  Competence for genetic transformation in Streptococcus pneumoniae: organization of a regulatory locus with homology to two lactococcin A secretion genes. , 1995, Gene.

[118]  L. Axelsson,et al.  The genes involved in production of and immunity to sakacin A, a bacteriocin from Lactobacillus sake Lb706 , 1995, Journal of bacteriology.

[119]  D. Diep,et al.  The gene encoding plantaricin A, a bacteriocin from Lactobacillus plantarum C11, is located on the same transcription unit as an agr-like regulatory system , 1994, Applied and environmental microbiology.