278 related articles for article (PubMed ID: 19767427)
1. The dlt operon of Bacillus cereus is required for resistance to cationic antimicrobial peptides and for virulence in insects.
Abi Khattar Z; Rejasse A; Destoumieux-Garzón D; Escoubas JM; Sanchis V; Lereclus D; Givaudan A; Kallassy M; Nielsen-Leroux C; Gaudriault S
J Bacteriol; 2009 Nov; 191(22):7063-73. PubMed ID: 19767427
[TBL] [Abstract][Full Text] [Related]
2. The dlt operon confers resistance to cationic antimicrobial peptides in Clostridium difficile.
McBride SM; Sonenshein AL
Microbiology (Reading); 2011 May; 157(Pt 5):1457-1465. PubMed ID: 21330441
[TBL] [Abstract][Full Text] [Related]
3. The insect Galleria mellonella as a powerful infection model to investigate bacterial pathogenesis.
Ramarao N; Nielsen-Leroux C; Lereclus D
J Vis Exp; 2012 Dec; (70):e4392. PubMed ID: 23271509
[TBL] [Abstract][Full Text] [Related]
4. Inactivation of the dlt operon in Staphylococcus aureus confers sensitivity to defensins, protegrins, and other antimicrobial peptides.
Peschel A; Otto M; Jack RW; Kalbacher H; Jung G; Götz F
J Biol Chem; 1999 Mar; 274(13):8405-10. PubMed ID: 10085071
[TBL] [Abstract][Full Text] [Related]
5. A functional dlt operon, encoding proteins required for incorporation of d-alanine in teichoic acids in gram-positive bacteria, confers resistance to cationic antimicrobial peptides in Streptococcus pneumoniae.
Kovács M; Halfmann A; Fedtke I; Heintz M; Peschel A; Vollmer W; Hakenbeck R; Brückner R
J Bacteriol; 2006 Aug; 188(16):5797-805. PubMed ID: 16885447
[TBL] [Abstract][Full Text] [Related]
6. The pbgPE operon in Photorhabdus luminescens is required for pathogenicity and symbiosis.
Bennett HP; Clarke DJ
J Bacteriol; 2005 Jan; 187(1):77-84. PubMed ID: 15601690
[TBL] [Abstract][Full Text] [Related]
7. A ferric dicitrate uptake system is required for the full virulence of Bacillus cereus.
Harvie DR; Ellar DJ
Curr Microbiol; 2005 May; 50(5):246-50. PubMed ID: 15886918
[TBL] [Abstract][Full Text] [Related]
8. An antimicrobial peptide-resistant minor subpopulation of Photorhabdus luminescens is responsible for virulence.
Mouammine A; Pages S; Lanois A; Gaudriault S; Jubelin G; Bonabaud M; Cruveiller S; Dubois E; Roche D; Legrand L; Brillard J; Givaudan A
Sci Rep; 2017 Mar; 7():43670. PubMed ID: 28252016
[TBL] [Abstract][Full Text] [Related]
9. CodY orchestrates the expression of virulence determinants in emetic Bacillus cereus by impacting key regulatory circuits.
Frenzel E; Doll V; Pauthner M; Lücking G; Scherer S; Ehling-Schulz M
Mol Microbiol; 2012 Jul; 85(1):67-88. PubMed ID: 22571587
[TBL] [Abstract][Full Text] [Related]
10. A protein important for antimicrobial peptide resistance, YdeI/OmdA, is in the periplasm and interacts with OmpD/NmpC.
Pilonieta MC; Erickson KD; Ernst RK; Detweiler CS
J Bacteriol; 2009 Dec; 191(23):7243-52. PubMed ID: 19767429
[TBL] [Abstract][Full Text] [Related]
11. Two sporulated Bacillus enhance immunity in Galleria mellonella protecting against Candida albicans.
Barros PP; Rossoni RD; Ribeiro FC; Silva MP; Souza CM; Jorge AOC; Junqueira JC
Microb Pathog; 2019 Jul; 132():335-342. PubMed ID: 31100407
[TBL] [Abstract][Full Text] [Related]
12. The plcR regulon is involved in the opportunistic properties of Bacillus thuringiensis and Bacillus cereus in mice and insects.
Salamitou S; Ramisse F; Brehélin M; Bourguet D; Gilois N; Gominet M; Hernandez E; Lereclus D
Microbiology (Reading); 2000 Nov; 146 ( Pt 11)():2825-2832. PubMed ID: 11065361
[TBL] [Abstract][Full Text] [Related]
13. Formation of D-alanyl-lipoteichoic acid is required for adhesion and virulence of Listeria monocytogenes.
Abachin E; Poyart C; Pellegrini E; Milohanic E; Fiedler F; Berche P; Trieu-Cuot P
Mol Microbiol; 2002 Jan; 43(1):1-14. PubMed ID: 11849532
[TBL] [Abstract][Full Text] [Related]
14. The Clostridium difficile Dlt Pathway Is Controlled by the Extracytoplasmic Function Sigma Factor σV in Response to Lysozyme.
Woods EC; Nawrocki KL; Suárez JM; McBride SM
Infect Immun; 2016 Jun; 84(6):1902-1916. PubMed ID: 27068095
[TBL] [Abstract][Full Text] [Related]
15. Cationic antimicrobial peptides activate a two-component regulatory system, PmrA-PmrB, that regulates resistance to polymyxin B and cationic antimicrobial peptides in Pseudomonas aeruginosa.
McPhee JB; Lewenza S; Hancock RE
Mol Microbiol; 2003 Oct; 50(1):205-17. PubMed ID: 14507375
[TBL] [Abstract][Full Text] [Related]
16. Imd pathway is involved in the interaction of Drosophila melanogaster with the entomopathogenic bacteria, Xenorhabdus nematophila and Photorhabdus luminescens.
Aymeric JL; Givaudan A; Duvic B
Mol Immunol; 2010 Aug; 47(14):2342-8. PubMed ID: 20627393
[TBL] [Abstract][Full Text] [Related]
17. Using an insect model to assess correlation between temperature and virulence in Bacillus weihenstephanensis and Bacillus cereus.
Stenfors Arnesen L; Granum PE; Buisson C; Bohlin J; Nielsen-LeRoux C
FEMS Microbiol Lett; 2011 Apr; 317(2):196-202. PubMed ID: 21276046
[TBL] [Abstract][Full Text] [Related]
18. Identification of Bacillus cereus internalin and other candidate virulence genes specifically induced during oral infection in insects.
Fedhila S; Daou N; Lereclus D; Nielsen-LeRoux C
Mol Microbiol; 2006 Oct; 62(2):339-55. PubMed ID: 16978259
[TBL] [Abstract][Full Text] [Related]
19. Antimicrobial Peptide Resistance Genes in the Plant Pathogen Dickeya dadantii.
Pandin C; Caroff M; Condemine G
Appl Environ Microbiol; 2016 Nov; 82(21):6423-6430. PubMed ID: 27565623
[TBL] [Abstract][Full Text] [Related]
20. The PmrA-PmrB two-component system responding to acidic pH and iron controls virulence in the plant pathogen Erwinia carotovora ssp. carotovora.
Hyytiäinen H; Sjöblom S; Palomäki T; Tuikkala A; Tapio Palva E
Mol Microbiol; 2003 Nov; 50(3):795-807. PubMed ID: 14617142
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
