221 related articles for article (PubMed ID: 18310333)
1. Twitching motility is essential for virulence in Dichelobacter nodosus.
Han X; Kennan RM; Davies JK; Reddacliff LA; Dhungyel OP; Whittington RJ; Turnbull L; Whitchurch CB; Rood JI
J Bacteriol; 2008 May; 190(9):3323-35. PubMed ID: 18310333
[TBL] [Abstract][Full Text] [Related]
2. The pathogenesis of ovine footrot.
Kennan RM; Han X; Porter CJ; Rood JI
Vet Microbiol; 2011 Nov; 153(1-2):59-66. PubMed ID: 21596496
[TBL] [Abstract][Full Text] [Related]
3. The type IV fimbrial subunit gene (fimA) of Dichelobacter nodosus is essential for virulence, protease secretion, and natural competence.
Kennan RM; Dhungyel OP; Whittington RJ; Egerton JR; Rood JI
J Bacteriol; 2001 Aug; 183(15):4451-8. PubMed ID: 11443078
[TBL] [Abstract][Full Text] [Related]
4. A two-component regulatory system modulates twitching motility in Dichelobacter nodosus.
Kennan RM; Lovitt CJ; Han X; Parker D; Turnbull L; Whitchurch CB; Rood JI
Vet Microbiol; 2015 Aug; 179(1-2):34-41. PubMed ID: 25891425
[TBL] [Abstract][Full Text] [Related]
5. Type IV fimbrial biogenesis is required for protease secretion and natural transformation in Dichelobacter nodosus.
Han X; Kennan RM; Parker D; Davies JK; Rood JI
J Bacteriol; 2007 Jul; 189(14):5022-33. PubMed ID: 17513472
[TBL] [Abstract][Full Text] [Related]
6. Characterization of a gene, pilU, required for twitching motility but not phage sensitivity in Pseudomonas aeruginosa.
Whitchurch CB; Mattick JS
Mol Microbiol; 1994 Sep; 13(6):1079-91. PubMed ID: 7854122
[TBL] [Abstract][Full Text] [Related]
7. Regulation of type IV fimbrial biogenesis in Dichelobacter nodosus.
Parker D; Kennan RM; Myers GS; Paulsen IT; Songer JG; Rood JI
J Bacteriol; 2006 Jul; 188(13):4801-11. PubMed ID: 16788189
[TBL] [Abstract][Full Text] [Related]
8. Twitching motility contributes to the role of pili in corneal infection caused by Pseudomonas aeruginosa.
Zolfaghar I; Evans DJ; Fleiszig SM
Infect Immun; 2003 Sep; 71(9):5389-93. PubMed ID: 12933890
[TBL] [Abstract][Full Text] [Related]
9. Pseudomonas aeruginosa gene products PilT and PilU are required for cytotoxicity in vitro and virulence in a mouse model of acute pneumonia.
Comolli JC; Hauser AR; Waite L; Whitchurch CB; Mattick JS; Engel JN
Infect Immun; 1999 Jul; 67(7):3625-30. PubMed ID: 10377148
[TBL] [Abstract][Full Text] [Related]
10. Transformation-mediated serogroup conversion of Dichelobacter nodosus.
Kennan RM; Dhungyel OP; Whittington RJ; Egerton JR; Rood JI
Vet Microbiol; 2003 Mar; 92(1-2):169-78. PubMed ID: 12488080
[TBL] [Abstract][Full Text] [Related]
11. Genomic evidence for a globally distributed, bimodal population in the ovine footrot pathogen Dichelobacter nodosus.
Kennan RM; Gilhuus M; Frosth S; Seemann T; Dhungyel OP; Whittington RJ; Boyce JD; Powell DR; Aspán A; Jørgensen HJ; Bulach DM; Rood JI
mBio; 2014 Sep; 5(5):e01821-14. PubMed ID: 25271288
[TBL] [Abstract][Full Text] [Related]
12. [Structural and functional specificity of the Dichelobacter nodosus pili. Synthesis of the protein pilin of D. nodosus in various bacterial recombinant strains].
Zaberezhnyĭ AD; Grabovetskiĭ VV; Panasiuk SD; Alekseeva SV
Mol Gen Mikrobiol Virusol; 2009; (4):3-6. PubMed ID: 20050159
[TBL] [Abstract][Full Text] [Related]
13. Deletion of the C-terminus of polynucleotide phosphorylase increases twitching motility, a virulence characteristic of the anaerobic bacterial pathogen Dichelobacter nodosus.
Palanisamy SK; Fletcher C; Tanjung L; Katz ME; Cheetham BF
FEMS Microbiol Lett; 2010 Jan; 302(1):39-45. PubMed ID: 19895640
[TBL] [Abstract][Full Text] [Related]
14. Functional role of conserved residues in the characteristic secretion NTPase motifs of the Pseudomonas aeruginosa type IV pilus motor proteins PilB, PilT and PilU.
Chiang P; Sampaleanu LM; Ayers M; Pahuta M; Howell PL; Burrows LL
Microbiology (Reading); 2008 Jan; 154(Pt 1):114-126. PubMed ID: 18174131
[TBL] [Abstract][Full Text] [Related]
15. Requirement of novel competence genes pilT and pilU of Pseudomonas stutzeri for natural transformation and suppression of pilT deficiency by a hexahistidine tag on the type IV pilus protein PilAI.
Graupner S; Weger N; Sohni M; Wackernagel W
J Bacteriol; 2001 Aug; 183(16):4694-701. PubMed ID: 11466271
[TBL] [Abstract][Full Text] [Related]
16. Modification of type IV pilus-associated epithelial cell adherence and multicellular behavior by the PilU protein of Neisseria gonorrhoeae.
Park HS; Wolfgang M; Koomey M
Infect Immun; 2002 Jul; 70(7):3891-903. PubMed ID: 12065533
[TBL] [Abstract][Full Text] [Related]
17. Biofilm formation by hyperpiliated mutants of Pseudomonas aeruginosa.
Chiang P; Burrows LL
J Bacteriol; 2003 Apr; 185(7):2374-8. PubMed ID: 12644510
[TBL] [Abstract][Full Text] [Related]
18. Update on ovine footrot in New Zealand: isolation, identification, and characterization of Dichelobacter nodosus strains [corrected].
Cagatay IT; Hickford JG
Vet Microbiol; 2005 Dec; 111(3-4):171-80. PubMed ID: 16280202
[TBL] [Abstract][Full Text] [Related]
19. The type IV pilus protein PilU functions as a PilT-dependent retraction ATPase.
Adams DW; Pereira JM; Stoudmann C; Stutzmann S; Blokesch M
PLoS Genet; 2019 Sep; 15(9):e1008393. PubMed ID: 31525185
[TBL] [Abstract][Full Text] [Related]
20. The subtilisin-like protease AprV2 is required for virulence and uses a novel disulphide-tethered exosite to bind substrates.
Kennan RM; Wong W; Dhungyel OP; Han X; Wong D; Parker D; Rosado CJ; Law RH; McGowan S; Reeve SB; Levina V; Powers GA; Pike RN; Bottomley SP; Smith AI; Marsh I; Whittington RJ; Whisstock JC; Porter CJ; Rood JI
PLoS Pathog; 2010 Nov; 6(11):e1001210. PubMed ID: 21124876
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
