Impact of Cell Surface Molecules on Conjugative Transfer of the Integrative and Conjugative Element ICESt3 of Streptococcus thermophilus

ABSTRACT Integrative conjugative elements (ICEs) are chromosomal elements that are widely distributed in bacterial genomes, hence contributing to genome plasticity, adaptation, and evolution of bacteria. Conjugation requires a contact between both the donor and the recipient cells and thus likely depends on the composition of the cell surface envelope. In this work, we investigated the impact of different cell surface molecules, including cell surface proteins, wall teichoic acids, lipoteichoic acids, and exopolysaccharides, on the transfer and acquisition of ICESt3 from Streptococcus thermophilus. The transfer of ICESt3 from wild-type (WT) donor cells to mutated recipient cells increased 5- to 400-fold when recipient cells were affected in lipoproteins, teichoic acids, or exopolysaccharides compared to when the recipient cells were WT. These mutants displayed an increased biofilm-forming ability compared to the WT, suggesting better cell interactions that could contribute to the increase of ICESt3 acquisition. Microscopic observations of S. thermophilus cell surface mutants showed different phenotypes (aggregation in particular) that can also have an impact on conjugation. In contrast, the same mutations did not have the same impact when the donor cells, instead of recipient cells, were mutated. In that case, the transfer frequency of ICESt3 decreased compared to that with the WT. The same observation was made when both donor and recipient cells were mutated. The dominant effect of mutations in donor cells suggests that modifications of the cell envelope could impair the establishment or activity of the conjugation machinery required for DNA transport. IMPORTANCE ICEs contribute to horizontal gene transfer of adaptive traits (for example, virulence, antibiotic resistance, or biofilm formation) and play a considerable role in bacterial genome evolution, thus underlining the need of a better understanding of their conjugative mechanism of transfer. While most studies focus on the different functions encoded by ICEs, little is known about the effect of host factors on their conjugative transfer. Using ICESt3 of S. thermophilus as a model, we demonstrated the impact of lipoproteins, teichoic acids, and exopolysaccharides on ICE transfer and acquisition. This opens up new avenues to control gene transfer mediated by ICEs.

[1]  C. García-Aljaro,et al.  Beyond the canonical strategies of horizontal gene transfer in prokaryotes. , 2017, Current opinion in microbiology.

[2]  P. Azadi,et al.  Characterization of the chemical structures and physical properties of exopolysaccharides produced by various Streptococcus thermophilus strains. , 2017, Journal of dairy science.

[3]  N. Leblond-Bourget,et al.  Diversity of Integrative and Conjugative Elements of Streptococcus salivarius and Their Intra- and Interspecies Transfer , 2017, Applied and Environmental Microbiology.

[4]  J. R. van der Meer,et al.  The hidden life of integrative and conjugative elements , 2017, FEMS microbiology reviews.

[5]  O. Jousson,et al.  Conjugative type IVb pilus recognizes lipopolysaccharide of recipient cells to initiate PAPI-1 pathogenicity island transfer in Pseudomonas aeruginosa , 2017, BMC Microbiology.

[6]  Sara D. Siegel,et al.  Anchoring of LPXTG-Like Proteins to the Gram-Positive Cell Wall Envelope. , 2016, Current topics in microbiology and immunology.

[7]  C. Weidenmaier,et al.  Cell wall glycopolymers of Firmicutes and their role as nonprotein adhesins , 2016, FEBS letters.

[8]  E. Koonin Horizontal gene transfer: essentiality and evolvability in prokaryotes, and roles in evolutionary transitions , 2016, F1000Research.

[9]  Melanie B. Berkmen,et al.  Biology of ICEBs1, an integrative and conjugative element in Bacillus subtilis. , 2016, Plasmid.

[10]  L. Ai,et al.  Bioactive exopolysaccharides from a S. thermophilus strain: Screening, purification and characterization. , 2016, International journal of biological macromolecules.

[11]  A. Grossman,et al.  The Composition of the Cell Envelope Affects Conjugation in Bacillus subtilis , 2016, Journal of bacteriology.

[12]  E. Roux,et al.  Implication of sortase-dependent proteins of Streptococcus thermophilus in adhesion to human intestinal epithelial cell lines and bile salt tolerance , 2016, Applied Microbiology and Biotechnology.

[13]  A. Grossman,et al.  Integrative and Conjugative Elements (ICEs): What They Do and How They Work. , 2015, Annual review of genetics.

[14]  P. Renault,et al.  Genomics of Streptococcus salivarius, a major human commensal. , 2015, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

[15]  P. Renault,et al.  Streptococcus thermophilus Biofilm Formation: A Remnant Trait of Ancestral Commensal Life? , 2015, PloS one.

[16]  B. Rehm,et al.  Bacterial exopolysaccharides: biosynthesis pathways and engineering strategies , 2015, Front. Microbiol..

[17]  N. Buddelmeijer The molecular mechanism of bacterial lipoprotein modification--how, when and why? , 2015, FEMS microbiology reviews.

[18]  A. Grossman,et al.  Identification of host genes that affect acquisition of an integrative and conjugative element in Bacillus subtilis , 2014, Molecular microbiology.

[19]  Nicolas Carraro,et al.  Biology of Three ICE Families: SXT/R391, ICEBs1, and ICESt1/ICESt3. , 2014, Microbiology spectrum.

[20]  A. Engelman,et al.  Retroviral Integrase Structure and DNA Recombination Mechanism , 2014, Microbiology spectrum.

[21]  J. Scher,et al.  Lactic acid bacteria in dairy food: surface characterization and interactions with food matrix components. , 2014, Advances in colloid and interface science.

[22]  S. Kulakauskas,et al.  Cell wall structure and function in lactic acid bacteria , 2014, Microbial Cell Factories.

[23]  Matthew D. Johnson,et al.  Characterization of mutations in the PAS domain of the EvgS sensor kinase selected by laboratory evolution for acid resistance in Escherichia coli , 2014, Molecular microbiology.

[24]  N. Leblond-Bourget,et al.  Conjugative and mobilizable genomic islands in bacteria: evolution and diversity. , 2014, FEMS microbiology reviews.

[25]  C. Rock,et al.  Bacterial lipids: metabolism and membrane homeostasis. , 2013, Progress in lipid research.

[26]  H. Morita,et al.  Effect of D-Alanine in Teichoic Acid from the Streptococcus thermophilus Cell Wall on the Barrier-Protection of Intestinal Epithelial Cells , 2012, Bioscience, biotechnology, and biochemistry.

[27]  Nicolas Carraro,et al.  Differential regulation of two closely related integrative and conjugative elements from Streptococcus thermophilus , 2011, BMC Microbiology.

[28]  L. Vuyst,et al.  New insights into the exopolysaccharide production of Streptococcus thermophilus , 2011 .

[29]  P. Simpson,et al.  Enzymatic activities and functional interdependencies of Bacillus subtilis lipoteichoic acid synthesis enzymes , 2011, Molecular microbiology.

[30]  B. Rehm Bacterial polymers: biosynthesis, modifications and applications , 2010, Nature Reviews Microbiology.

[31]  R. Briandet,et al.  The biofilm architecture of sixty opportunistic pathogens deciphered using a high throughput CLSM method. , 2010, Journal of microbiological methods.

[32]  A. Gründling,et al.  Two-enzyme systems for glycolipid and polyglycerolphosphate lipoteichoic acid synthesis in Listeria monocytogenes , 2009, Molecular microbiology.

[33]  T. Unoki,et al.  Contribution of Lipoproteins and Lipoprotein Processing to Endocarditis Virulence in Streptococcus sanguinis , 2009, Journal of bacteriology.

[34]  A. Roberts,et al.  Conjugative Transfer of the Integrative Conjugative Elements ICESt1 and ICESt3 from Streptococcus thermophilus , 2009, Journal of bacteriology.

[35]  S. Leppla,et al.  Codon-Optimized Fluorescent Proteins Designed for Expression in Low-GC Gram-Positive Bacteria , 2009, Applied and Environmental Microbiology.

[36]  E. Denham,et al.  Lipoprotein Signal Peptides Are Processed by Lsp and Eep of Streptococcus uberis , 2008, Journal of bacteriology.

[37]  G. Pier,et al.  Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface. , 2008, Microbiology.

[38]  O. Schneewind,et al.  Synthesis of glycerol phosphate lipoteichoic acid in Staphylococcus aureus , 2007, Proceedings of the National Academy of Sciences.

[39]  P. Renault,et al.  Control of EpsE, the Phosphoglycosyltransferase Initiating Exopolysaccharide Synthesis in Streptococcus thermophilus, by EpsD Tyrosine Kinase , 2006, Journal of bacteriology.

[40]  E. Brown,et al.  Wall Teichoic Acid Polymers Are Dispensable for Cell Viability in Bacillus subtilis , 2006, Journal of bacteriology.

[41]  P. Renault,et al.  New insights in the molecular biology and physiology of revealed by comparative genomics , 2005 .

[42]  Laetitia Fontaine,et al.  New insights in the molecular biology and physiology of Streptococcus thermophilus revealed by comparative genomics. , 2005, FEMS microbiology reviews.

[43]  A. Goffeau,et al.  Complete sequence and comparative genome analysis of the dairy bacterium Streptococcus thermophilus , 2004, Nature Biotechnology.

[44]  F. Gomis-Rüth,et al.  Bacterial conjugation: a two‐step mechanism for DNA transport , 2002, Molecular microbiology.

[45]  T. Sekizaki,et al.  Thermosensitive suicide vectors for gene replacement in Streptococcus suis. , 2001, Plasmid.

[46]  B. Ersbøll,et al.  Quantification of biofilm structures by the novel computer program COMSTAT. , 2000, Microbiology.

[47]  P. Francioli,et al.  Expression of Staphylococcus aureusClumping Factor A in Lactococcus lactis subsp.cremoris Using a New Shuttle Vector , 2000, Infection and Immunity.

[48]  S. Ehrlich,et al.  Efficient insertional mutagenesis in lactococci and other gram-positive bacteria , 1996, Journal of bacteriology.

[49]  M. Perego,et al.  Incorporation of D-Alanine into Lipoteichoic Acid and Wall Teichoic Acid in Bacillus subtilis , 1995, The Journal of Biological Chemistry.

[50]  G. Venema,et al.  Construction of a lactococcal expression vector: expression of hen egg white lysozyme in Lactococcus lactis subsp. lactis , 1989, Applied and environmental microbiology.