Lagging-Strand DNA Replication Origins Are Required for Conjugal Transfer of the Promiscuous Plasmid pMV158

ABSTRACT The promiscuous streptococcal plasmid pMV158 is mobilizable by auxiliary plasmids and replicates by the rolling-circle mechanism in a variety of bacterial hosts. The plasmid has two lagging-strand origins, ssoA and ssoU, involved in the conversion of single-stranded DNA intermediates into double-stranded plasmid DNA during vegetative replication. Transfer of the plasmid also would involve conversion of single-stranded DNA molecules into double-stranded plasmid forms in the recipient cells by conjugative replication. To test whether lagging-strand origins played a role in horizontal transfer, pMV158 derivatives defective in one or in both sso's were constructed and tested for their ability to colonize new hosts by means of intra- and interspecies mobilization. Whereas either sso supported transfer between strains of Streptococcus pneumoniae, only plasmids that had an intact ssoU could be efficiently mobilized from S. pneumoniae to Enterococcus faecalis. Thus, it appears that ssoU is a critical factor for pMV158 promiscuity and that the presence of a functional sso plays an essential role in plasmid transfer.

[1]  T. Santangelo,et al.  Bacteriophage N4 virion RNA polymerase interaction with its promoter DNA hairpin , 2007, Proceedings of the National Academy of Sciences.

[2]  S. Khan Plasmid rolling-circle replication: highlights of two decades of research. , 2005, Plasmid.

[3]  W. J. Brammar,et al.  The activity of a single‐stranded promoter of plasmid ColIb‐P9 depends on its secondary structure , 2004, Molecular microbiology.

[4]  Christopher D Thomas,et al.  Reconstitution of a Staphylococcal Plasmid-Protein Relaxation Complex In Vitro , 2004, Journal of bacteriology.

[5]  Christopher D Thomas,et al.  An Accessory Protein Is Required for Relaxosome Formation by Small Staphylococcal Plasmids , 2004, Journal of bacteriology.

[6]  C. Drainas,et al.  A classification scheme for mobilization regions of bacterial plasmids. , 2004, FEMS microbiology reviews.

[7]  M. E. Farías,et al.  Features of the plasmid pMV158-encoded MobM, a protein involved in its mobilization. , 2004, Journal of molecular biology.

[8]  M. E. Farías,et al.  Conjugal transfer of plasmid pMV158: uncoupling of the pMV158 origin of transfer from the mobilization gene mobM, and modulation of pMV158 transfer in Escherichia coli mediated by IncP plasmids. , 2000, Microbiology.

[9]  S. Khan,et al.  Plasmid rolling‐circle replication: recent developments , 2000, Molecular microbiology.

[10]  W. J. Brammar,et al.  Expression of leading region genes on IncI1 plasmid ColIb-P9: genetic evidence for single-stranded DNA transcription. , 1999, Microbiology.

[11]  S. Khan,et al.  Characterization of a single‐strand origin, ssoU, required for broad host range replication of rolling‐circle plasmids , 1999, Molecular microbiology.

[12]  E. Grohmann,et al.  Expression of the mobM gene of the streptococcal plasmid pMV158 in Lactococcus lactis subsp. lactis. , 1999, FEMS microbiology letters.

[13]  L. Guzmán,et al.  Mobilisation of the streptococcal plasmid pMV158: interactions of MobM protein with its cognate oriT DNA region , 1999, Molecular and General Genetics MGG.

[14]  R. Novick Contrasting lifestyles of rolling-circle phages and plasmids. , 1998, Trends in biochemical sciences.

[15]  T. K. Misra,et al.  Lagging strand replication of rolling-circle plasmids: specific recognition of the ssoA-type origins in different gram-positive bacteria. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[16]  Manuel Espinosa,et al.  Plasmids Replication and Control of Circular Bacterial , 1998 .

[17]  S. Khan,et al.  Lagging-Strand Replication from the ssoA Origin of Plasmid pMV158 in Streptococcus pneumoniae: In Vivo and In Vitro Influences of Mutations in Two ConservedssoA Regions , 1998, Journal of bacteriology.

[18]  S. Khan,et al.  Plasmid rolling circle replication: identification of the RNA polymerase‐directed primer RNA and requirement for DNA polymerase I for lagging strand synthesis , 1997, The EMBO journal.

[19]  K. Arai,et al.  F rpo : A Novel Single-Stranded DNA Promoter for Transcription and for Primer RNA Synthesis of DNA Replication , 1997, Cell.

[20]  L. Guzmán,et al.  The mobilization protein, MobM, of the streptococcal plasmid pMV158 specifically cleaves supercoiled DNA at the plasmid oriT. , 1997, Journal of molecular biology.

[21]  J. Alonso,et al.  Broad‐host‐range plasmid replication: an open question , 1996, Molecular microbiology.

[22]  G. del Solar,et al.  Lagging-strand origins of the promiscuous plasmid pMV158: physical and functional characterization. , 1995, Microbiology.

[23]  D. J. Leblanc,et al.  Identification and characterization of a mobilization gene in the streptococcal plasmid, pVA380-1. , 1993, Plasmid.

[24]  D. J. Leblanc,et al.  Molecular, genetic, and functional analysis of the basic replicon of pVA380-1, a plasmid of oral streptococcal origin. , 1992, Plasmid.

[25]  L. Rothman-Denes,et al.  Specific sequences and a hairpin structure in the template strand are required for N4 virion RNA polymerase promoter recognition , 1992, Cell.

[26]  S. Bron,et al.  Conjugal mobilization of streptococcal plasmid pMV158 between strains of Lactococcus lactis subsp. lactis , 1990, Journal of bacteriology.

[27]  S. Lacks,et al.  Region of the streptococcal plasmid pMV158 required for conjugative mobilization , 1989, Journal of bacteriology.

[28]  R. Novick,et al.  Comparative analysis of five related Staphylococcal plasmids. , 1988, Plasmid.

[29]  G. del Solar,et al.  Initiation signals for the conversion of single stranded to double stranded DNA forms in the streptococcal plasmid pLS1. , 1987, Nucleic acids research.

[30]  R. Novick,et al.  Functional analysis of a palindromic sequence required for normal replication of several staphylococcal plasmids. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[31]  M. Espinosa,et al.  Replication of the streptococcal plasmid pMV158 and derivatives in cell-free extracts of Escherichia coli , 1987, Molecular and General Genetics MGG.

[32]  S. Lacks,et al.  Identification and analysis of genes for tetracycline resistance and replication functions in the broad-host-range plasmid pLS1. , 1986, Journal of molecular biology.

[33]  S. Ehrlich,et al.  Are single‐stranded circles intermediates in plasmid DNA replication? , 1986, The EMBO journal.

[34]  R. Koepsel,et al.  The replication initiator protein of plasmid pT181 has sequence-specific endonuclease and topoisomerase-like activities. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[35]  L. Rothman-Denes,et al.  N4 virion RNA polymerase sites of transcription initiation , 1985, Cell.

[36]  S. Lacks,et al.  Facilitation of Plasmid Transfer in Streptococcus pneumoniae by Chromosomal Homology , 1982, Journal of bacteriology.

[37]  S. Lacks,et al.  Cloning of chromosomal genes in Streptococcus pneumoniae. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[38]  V. Burdett,et al.  Identification of tetracycline-resistant R-plasmids in Streptococcus agalactiae (group B) , 1980, Antimicrobial Agents and Chemotherapy.

[39]  M. Espinosa,et al.  Large-scale filter mating assay for intra- and inter-specific conjugal transfer of the promiscuous plasmid pMV158 in Gram-positive bacteria. , 2009, Plasmid.

[40]  S. Lacks,et al.  Interspecific plasmid transfer between Streptococcus pneumoniae and Bacillus subtilis , 2004, Molecular and General Genetics MGG.

[41]  G. del Solar,et al.  A functional lagging strand origin does not stabilize plasmid pMV158 inheritance in Escherichia coli. , 2000, Plasmid.

[42]  E. Lanka,et al.  DNA processing reactions in bacterial conjugation. , 1995, Annual review of biochemistry.