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Items: 47

1.

Inhibition of Rho Activity Increases Expression of SaeRS-Dependent Virulence Factor Genes in Staphylococcus aureus, Showing a Link between Transcription Termination, Antibiotic Action, and Virulence.

Nagel A, Michalik S, Debarbouille M, Hertlein T, Gesell Salazar M, Rath H, Msadek T, Ohlsen K, van Dijl JM, Völker U, Mäder U.

MBio. 2018 Sep 18;9(5). pii: e01332-18. doi: 10.1128/mBio.01332-18.

2.

Staphylococcus aureus Transcriptome Architecture: From Laboratory to Infection-Mimicking Conditions.

Mäder U, Nicolas P, Depke M, Pané-Farré J, Debarbouille M, van der Kooi-Pol MM, Guérin C, Dérozier S, Hiron A, Jarmer H, Leduc A, Michalik S, Reilman E, Schaffer M, Schmidt F, Bessières P, Noirot P, Hecker M, Msadek T, Völker U, van Dijl JM.

PLoS Genet. 2016 Apr 1;12(4):e1005962. doi: 10.1371/journal.pgen.1005962. eCollection 2016 Apr.

3.

Staphylococcus aureus FepA and FepB proteins drive heme iron utilization in Escherichia coli.

Turlin E, Débarbouillé M, Augustyniak K, Gilles AM, Wandersman C.

PLoS One. 2013;8(2):e56529. doi: 10.1371/journal.pone.0056529. Epub 2013 Feb 20.

4.

Structural basis for feed-forward transcriptional regulation of membrane lipid homeostasis in Staphylococcus aureus.

Albanesi D, Reh G, Guerin ME, Schaeffer F, Debarbouille M, Buschiazzo A, Schujman GE, de Mendoza D, Alzari PM.

PLoS Pathog. 2013 Jan;9(1):e1003108. doi: 10.1371/journal.ppat.1003108. Epub 2013 Jan 3.

5.

Rga, a RofA-like regulator, is the major transcriptional activator of the PI-2a pilus in Streptococcus agalactiae.

Dramsi S, Dubrac S, Konto-Ghiorghi Y, Da Cunha V, Couvé E, Glaser P, Caliot E, Débarbouillé M, Bellais S, Trieu-Cuot P, Mistou MY.

Microb Drug Resist. 2012 Jun;18(3):286-97. doi: 10.1089/mdr.2012.0005. Epub 2012 Mar 20.

PMID:
22432704
6.

Molecular characterization of a Streptococcus gallolyticus genomic island encoding a pilus involved in endocarditis.

Danne C, Entenza JM, Mallet A, Briandet R, Débarbouillé M, Nato F, Glaser P, Jouvion G, Moreillon P, Trieu-Cuot P, Dramsi S.

J Infect Dis. 2011 Dec 15;204(12):1960-70. doi: 10.1093/infdis/jir666. Epub 2011 Oct 31.

PMID:
22043018
7.

Investigation of the Staphylococcus aureus GraSR regulon reveals novel links to virulence, stress response and cell wall signal transduction pathways.

Falord M, Mäder U, Hiron A, Débarbouillé M, Msadek T.

PLoS One. 2011;6(7):e21323. doi: 10.1371/journal.pone.0021323. Epub 2011 Jul 1.

8.

Bacitracin and nisin resistance in Staphylococcus aureus: a novel pathway involving the BraS/BraR two-component system (SA2417/SA2418) and both the BraD/BraE and VraD/VraE ABC transporters.

Hiron A, Falord M, Valle J, Débarbouillé M, Msadek T.

Mol Microbiol. 2011 Aug;81(3):602-22. doi: 10.1111/j.1365-2958.2011.07735.x. Epub 2011 Jul 4.

9.

Characterization of a serine/threonine kinase involved in virulence of Staphylococcus aureus.

Débarbouillé M, Dramsi S, Dussurget O, Nahori MA, Vaganay E, Jouvion G, Cozzone A, Msadek T, Duclos B.

J Bacteriol. 2009 Jul;191(13):4070-81. doi: 10.1128/JB.01813-08. Epub 2009 Apr 24.

10.

Sigma L is important for cold shock adaptation of Bacillus subtilis.

Wiegeshoff F, Beckering CL, Debarbouille M, Marahiel MA.

J Bacteriol. 2006 Apr;188(8):3130-3.

11.

Staphylococcus aureus develops an alternative, ica-independent biofilm in the absence of the arlRS two-component system.

Toledo-Arana A, Merino N, Vergara-Irigaray M, Débarbouillé M, Penadés JR, Lasa I.

J Bacteriol. 2005 Aug;187(15):5318-29.

12.

New vector for efficient allelic replacement in naturally nontransformable, low-GC-content, gram-positive bacteria.

Arnaud M, Chastanet A, Débarbouillé M.

Appl Environ Microbiol. 2004 Nov;70(11):6887-91.

13.

Essential Bacillus subtilis genes.

Kobayashi K, Ehrlich SD, Albertini A, Amati G, Andersen KK, Arnaud M, Asai K, Ashikaga S, Aymerich S, Bessieres P, Boland F, Brignell SC, Bron S, Bunai K, Chapuis J, Christiansen LC, Danchin A, Débarbouille M, Dervyn E, Deuerling E, Devine K, Devine SK, Dreesen O, Errington J, Fillinger S, Foster SJ, Fujita Y, Galizzi A, Gardan R, Eschevins C, Fukushima T, Haga K, Harwood CR, Hecker M, Hosoya D, Hullo MF, Kakeshita H, Karamata D, Kasahara Y, Kawamura F, Koga K, Koski P, Kuwana R, Imamura D, Ishimaru M, Ishikawa S, Ishio I, Le Coq D, Masson A, Mauël C, Meima R, Mellado RP, Moir A, Moriya S, Nagakawa E, Nanamiya H, Nakai S, Nygaard P, Ogura M, Ohanan T, O'Reilly M, O'Rourke M, Pragai Z, Pooley HM, Rapoport G, Rawlins JP, Rivas LA, Rivolta C, Sadaie A, Sadaie Y, Sarvas M, Sato T, Saxild HH, Scanlan E, Schumann W, Seegers JF, Sekiguchi J, Sekowska A, Séror SJ, Simon M, Stragier P, Studer R, Takamatsu H, Tanaka T, Takeuchi M, Thomaides HB, Vagner V, van Dijl JM, Watabe K, Wipat A, Yamamoto H, Yamamoto M, Yamamoto Y, Yamane K, Yata K, Yoshida K, Yoshikawa H, Zuber U, Ogasawara N.

Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4678-83. Epub 2003 Apr 7.

14.

Specificity of the interaction of RocR with the rocG-rocA intergenic region in Bacillus subtilis.

Ali NO, Jeusset J, Larquet E, Le Cam E, Belitsky B, Sonenshein AL, Msadek T, Débarbouillé M.

Microbiology. 2003 Mar;149(Pt 3):739-50.

PMID:
12634342
15.

Regulation of the acetoin catabolic pathway is controlled by sigma L in Bacillus subtilis.

Ali NO, Bignon J, Rapoport G, Debarbouille M.

J Bacteriol. 2001 Apr;183(8):2497-504.

16.

Expression of a new operon from Bacillus subtilis, ykzB-ykoL, under the control of the TnrA and PhoP-phoR global regulators.

Robichon D, Arnaud M, Gardan R, Pragai Z, O'Reilly M, Rapoport G, Débarbouillé M.

J Bacteriol. 2000 Mar;182(5):1226-31.

17.
18.

Characterization of a novel member of the DegS-DegU regulon affected by salt stress in Bacillus subtilis.

Dartois V, Débarbouillé M, Kunst F, Rapoport G.

J Bacteriol. 1998 Apr;180(7):1855-61.

19.

The rpoN (sigma54) gene from Listeria monocytogenes is involved in resistance to mesentericin Y105, an antibacterial peptide from Leuconostoc mesenteroides.

Robichon D, Gouin E, Débarbouillé M, Cossart P, Cenatiempo Y, Héchard Y.

J Bacteriol. 1997 Dec;179(23):7591-4.

20.

Role of the transcriptional activator RocR in the arginine-degradation pathway of Bacillus subtilis.

Gardan R, Rapoport G, Débarbouillé M.

Mol Microbiol. 1997 May;24(4):825-37.

21.

In vitro reconstitution of transcriptional antitermination by the SacT and SacY proteins of Bacillus subtilis.

Arnaud M, Débarbouillé M, Rapoport G, Saier MH Jr, Reizer J.

J Biol Chem. 1996 Aug 2;271(31):18966-72.

22.

Expression of the rocDEF operon involved in arginine catabolism in Bacillus subtilis.

Gardan R, Rapoport G, Débarbouillé M.

J Mol Biol. 1995 Jun 23;249(5):843-56.

PMID:
7540694
23.

Interactions of wild-type and truncated LevR of Bacillus subtilis with the upstream activating sequence of the levanase operon.

Martin-Verstraete I, Débarbouillé M, Klier A, Rapoport G.

J Mol Biol. 1994 Aug 12;241(2):178-92.

PMID:
8057358
24.

RocR, a novel regulatory protein controlling arginine utilization in Bacillus subtilis, belongs to the NtrC/NifA family of transcriptional activators.

Calogero S, Gardan R, Glaser P, Schweizer J, Rapoport G, Debarbouille M.

J Bacteriol. 1994 Mar;176(5):1234-41.

25.

Mutagenesis of the Bacillus subtilis "-12, -24" promoter of the levanase operon and evidence for the existence of an upstream activating sequence.

Martin-Verstraete I, Débarbouillé M, Klier A, Rapoport G.

J Mol Biol. 1992 Jul 5;226(1):85-99.

PMID:
1619665
26.

Regulation of the sacPA operon of Bacillus subtilis: identification of phosphotransferase system components involved in SacT activity.

Arnaud M, Vary P, Zagorec M, Klier A, Debarbouille M, Postma P, Rapoport G.

J Bacteriol. 1992 May;174(10):3161-70.

27.

The Bacillus subtilis sigL gene encodes an equivalent of sigma 54 from gram-negative bacteria.

Débarbouillé M, Martin-Verstraete I, Kunst F, Rapoport G.

Proc Natl Acad Sci U S A. 1991 Oct 15;88(20):9092-6.

28.

Positive and negative regulation controlling expression of the sac genes in Bacillus subtilis.

Débarbouillé M, Martin-Verstraete I, Arnaud M, Klier A, Rapoport G.

Res Microbiol. 1991 Sep-Oct;142(7-8):757-64. Review. No abstract available.

PMID:
1784813
29.

The transcriptional regulator LevR of Bacillus subtilis has domains homologous to both sigma 54- and phosphotransferase system-dependent regulators.

Débarbouillé M, Martin-Verstraete I, Klier A, Rapoport G.

Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2212-6.

30.

A gene encoding a tyrosine tRNA synthetase is located near sacS in Bacillus subtilis.

Glaser P, Kunst F, Débarbouillé M, Vertès A, Danchin A, Dedonder R.

DNA Seq. 1991;1(4):251-61.

PMID:
1806041
31.

Levanase operon of Bacillus subtilis includes a fructose-specific phosphotransferase system regulating the expression of the operon.

Martin-Verstraete I, Débarbouillé M, Klier A, Rapoport G.

J Mol Biol. 1990 Aug 5;214(3):657-71.

PMID:
2117666
32.

The sacT gene regulating the sacPA operon in Bacillus subtilis shares strong homology with transcriptional antiterminators.

Debarbouille M, Arnaud M, Fouet A, Klier A, Rapoport G.

J Bacteriol. 1990 Jul;172(7):3966-73.

33.

Induction and metabolite regulation of levanase synthesis in Bacillus subtilis.

Martin I, Debarbouille M, Klier A, Rapoport G.

J Bacteriol. 1989 Apr;171(4):1885-92.

34.

Deduced polypeptides encoded by the Bacillus subtilis sacU locus share homology with two-component sensor-regulator systems.

Kunst F, Debarbouille M, Msadek T, Young M, Mauel C, Karamata D, Klier A, Rapoport G, Dedonder R.

J Bacteriol. 1988 Nov;170(11):5093-101.

35.

Distinct control sites located upstream from the levansucrase gene of Bacillus subtilis.

Klier A, Fouet A, Débarbouillé M, Kunst F, Rapoport G.

Mol Microbiol. 1987 Sep;1(2):233-41.

PMID:
2835582
36.

Characterization of the levanase gene of Bacillus subtilis which shows homology to yeast invertase.

Martin I, Débarbouillé M, Ferrari E, Klier A, Rapoport G.

Mol Gen Genet. 1987 Jun;208(1-2):177-84.

PMID:
3112519
37.

Mutations affecting antigenic determinants of an outer membrane protein of Escherichia coli.

Desaymard C, Débarbouillé M, Jolit M, Schwartz M.

EMBO J. 1986 Jun;5(6):1383-8.

38.

In situ enzyme immunodetection of surface or intracellular bacterial antigens using nitrocellulose sheets.

Guesdon JL, Bouges Bocquet B, Débarbouillé M, Hofnung M.

J Immunol Methods. 1985 Nov 28;84(1-2):53-63.

PMID:
2999249
39.
40.

Use of deletions created in vitro to map transcriptional regulatory signals in the malA region of Escherichia coli.

Raibaud O, Débarbouillé M, Schwartz M.

J Mol Biol. 1983 Jan 25;163(3):395-408.

PMID:
6339728
41.

A role for mRNA secondary structure in the control of translation initiation.

Hall MN, Gabay J, Débarbouillé M, Schwartz M.

Nature. 1982 Feb 18;295(5850):616-8. No abstract available.

PMID:
6799842
43.

A DNA sequence containing the control sites for gene malT and for the malPQ operon.

Debarbouille M, Cossart P, Raibaud O.

Mol Gen Genet. 1982;185(1):88-92.

PMID:
6283313
44.

Mutations that affect lamB gene expression at a posttranscriptional level.

Schwartz M, Roa M, Débarbouillé M.

Proc Natl Acad Sci U S A. 1981 May;78(5):2937-41.

45.

Mutants which make more malT product, the activator of the maltose regulon in Escherichia coli.

Débarbouillé M, Schwartz M.

Mol Gen Genet. 1980;178(3):589-95.

PMID:
6993855
46.

The use of gene fusions to study the expression of malT the positive regulator gene of the maltose regulon.

Debarbouille M, Schwartz M.

J Mol Biol. 1979 Aug 15;132(3):521-34. No abstract available.

PMID:
118263
47.

Dominant constitutive mutations in malT, the positive regulator gene of the maltose regulon in Escherichia coli.

Débarbouillé M, Shuman HA, Silhavy TJ, Schwartz M.

J Mol Biol. 1978 Sep 15;124(2):359-71. No abstract available.

PMID:
101676

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