SPI-23 of S. Derby: Role in adherence and invasion of porcine tissues

PLoS ONE

Volumn 9, Issue 9, 2014, Pages

  Hayward, Matthew R ^a,b,c   AbuOun, Manal ^b   La Ragione, Roberto M ^a,d   Tchórzewska, Monika A ^e   Cooley, William A ^b   Everest, David J ^b   Petrovska, Liljana ^b   Jansen, Vincent A A ^c   Woodward, Martin J ^f  

^a EUROPEAN MOLECULAR BIOLOGY LABORATORY   (Germany)

^b VETERINARY LABORATORIES AGENCY   (United Kingdom)

^c UNIVERSITY OF LONDON   (United Kingdom)

^d UNIVERSITY OF SURREY   (United Kingdom)

^e UNIVERSITY OF BRISTOL   (United Kingdom)

^f UNIVERSITY OF READING   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

RNA; VIRULENCE FACTOR;

ANIMAL CELL; ANIMAL CELL CULTURE; ANIMAL TISSUE; ARTICLE; BACTERIAL STRAIN; BACTERIUM ADHERENCE; COLON; CONFOCAL MICROSCOPY; CONTROLLED STUDY; IN VITRO STUDY; INTESTINE CELL; IPEC J2 CELL LINE; JEJUNUM; MONOLAYER CULTURE; NONHUMAN; PATHOGENICITY ISLAND; PHENOTYPE; POTR GENE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA EXTRACTION; SALMONELLA DERBY; SALMONELLA ENTERICA; SALMONELLA PATHOGENICITY ISLAND 23; SPECIES INVASION; SWINE; TROPISM; UPREGULATION; ANIMAL; ANIMAL SALMONELLOSIS; BACTERIAL GENE; BACTERIAL GENOME; CELL LINE; CLASSIFICATION; GENE EXPRESSION REGULATION; GENETICS; GENOMIC ISLAND; ISOLATION AND PURIFICATION; MICROBIOLOGY; PATHOGENICITY; PIG; SPECIES DIFFERENCE;

SUS;

ANIMALS; BACTERIAL ADHESION; CELL LINE; COLON; GENE EXPRESSION REGULATION, BACTERIAL; GENES, BACTERIAL; GENOME, BACTERIAL; GENOMIC ISLANDS; JEJUNUM; PHENOTYPE; SALMONELLA ENTERICA; SALMONELLA INFECTIONS, ANIMAL; SPECIES SPECIFICITY; SWINE; UP-REGULATION; VIRULENCE FACTORS;

EID: 84907223059     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0107857     Document Type: Article

References (26)

1. Suar M, Jantsch J, Hapfelmeier S, Kremer M, Stallmach T, et al. (2006) Virulence of Broad- and Narrow-Host-Range Salmonella enterica Serovars in the Streptomycin-Pretreated Mouse Model. Infect. Immun. 74: 632-644.
2. Suar M, Jantsch J, Hapfelmeier S (2006) Virulence of broad-and narrow-hostrange Salmonella enterica serovars in the streptomycin-pretreated mouse model. Infect. Immun. 74: 632-644.
3. Baumler AJ, Tsolis RMRM, Ficht TA, Adams LG, Tsolis EM, et al. (1998) Evolution of Host Adaptation in Salmonella enterica. Infect. Immun. 66: 4579-4587.
4. Kingsley R, Bäumler J (2000) Host adaptation and the emergence of infectious disease: The Salmonella paradigm. J. Mol Biol. 36: 1006-1014.
5. AHVLA DEFRA (2011) Salmonella in livestock production, annual report. Weybridge, UK.
6. CDC PHLIS (2010) Salmonella annual survey 2009. Volume 2010. Atlanta, USA.
7. CDC (2011) National Enteric Disease Surveillance: Salmonella Surveillance Overview. Atlanta USA.
8. Hayward MR, Jansen VA, Woodward MJ (2013) Comparative genomics of Salmonella enterica serovars Derby and Mbandaka, two prevalent serovars associated with different livestock species in the UK. BMC Genomics 14:365.
9. Samudrala R, Heffron F, McDermott JE (2009) Accurate prediction of secreted substrates and identification of a conserved putative secretion signal for type III secretion systems. PLoS pathog. 5:e1000375.
10. Hapfelmeier S, Ehrbar K, Barthel M, Kremer M, Hardt W (2004) Role of the Salmonella Pathogenicity Island 1 Effector Proteins SipA, SopB, SopE, and SopE2 in Salmonella enterica Subspecies 1 Serovar Typhimurium Colitis in Streptomycin-Pretreated Mice. Infect. Immun. 72:795-809.
11. Waterman SR, Holden DW (2003) Functions and effectors of the Salmonella pathogenicity island 2 type III secretion system. Cell. Microbiol. 5:501-511.
12. Collins JW, Coldham NG, Salguero FJ, Cooley WA, Newell WR, et al. (2010) Response of porcine intestinal in vitro organ culture tissues following exposure to Lactobacillus plantarum JC1 and Salmonella enterica serovar Typhimurium SL1344. Appl. Environ. Microbiol. 76:6645-57.
13. Schierack P, Nordhoff M, Pollmann M, Weyrauch KD, Amasheh S, et al. (2006) Characterization of a porcine intestinal epithelial cell line for in vitro studies of microbial pathogenesis in swine. Histochem. Cell. Biol. 125:293-305.
14. Green BT, Brown DR (2006) Differential effects of clathrin and actin inhibitors on internalization of Escherichia coli and Salmonella Choleraesuis in porcine jejunal Peyer's patches. Vet. Microbiol. 113:117-22.
15. Watson PR, Paulin SM, Jones PW, Wallis TS (2000) Interaction of Salmonella serotypes with porcine macrophagesin vitro does not correlate with virulence. Microbiol. 146: 1639-1649.
16. Paulin SM, Watson PR, Benmore AR, Stevens MP, Jones PW, et al. (2002) Analysis of Salmonella enterica serotype-host specificity in calves: avirulence of S. enterica serotype gallinarum correlates with bacterial dissemination from mesenteric lymph nodes and persistence in vivo. Infect. Immun. 70: 6788-6797.
17. Schmidt LD, Kohrt LJ, Brown DR (2008) Comparison of growth phase on Salmonella enterica serovar Typhimurium invasion in an epithelial cell line (IPEC J2) and mucosal explants from porcine small intestine. Comp. Immunol. Microbiol. Infect. Dis. 31:63-69.
18. Wood RL, Pospischil A, Rose R (1989) Distribution of persistent Salmonella typhimurium infection in internal organs of swine. Am. J. Vet. Res. 50:1015-21.
19. Santos RL, Raffatellu M, Bevins CL, Adams LG, Tükel C, et al. (2009) Life in the inflamed intestine, Salmonella style. Trends. Microbiol. 17:498-506.
20. Tam CKP, Morris C, Hackett J (2006) The Salmonella enterica serovar Typhi type IVB self-association pili are detached from the bacterial cell by the PilV minor pilus proteins. Infect. Immun. 74:5414-8.
21. Morris C, Yip CMC, Tsui ISMI, Wong DK, Hackett J, et al. (2003) The Shufflon of Salmonella enterica Serovar Typhi Regulates Type IVB Pilus- Mediated Bacterial Self-Association. Infect. Immun. 71:1141-1146.
22. Seth-Smith HMB (2008) SPI-7: Salmonella's Vi-Encoding Pathogenicity Island. J. Infect. Dev. Ctries. 2:267-271.
23. White AP, Gibson DL, Grassl GA, Kay WW, Finlay BB, et al. (2008) Aggregation via the red, dry, and rough morphotype is not a virulence adaptation in Salmonella enterica serovar Typhimurium. Infect. Immun. 76:1048-58.
24. Searle LEJ, Best A, Nunez A, Salguero FJ, Johnson L, et al. (2009) A mixture containing galactooligosaccharide, produced by the enzymic activity of Bifidobacterium bifidum, reduces Salmonella enterica serovar Typhimurium infection in mice. J. Med. Microbiol. 58:37-48.
25. Hoben DA, Ashton DH, Peterson AC (1973) Some observations on the incorporation of novobiocin into Hektoen enteric agar for improved Salmonella isolation. Appl. Microbiol. 26:126-7.
26. López-Garrido J, Casadesús J (2010) Regulation of Salmonella enterica pathogenicity island 1 by DNA adenine methylation. Genetics 184:637-49