2012
DOI: 10.1128/iai.00180-12
|View full text |Cite
|
Sign up to set email alerts
|

A Novel Phage Element of Salmonella enterica Serovar Enteritidis P125109 Contributes to Accelerated Type III Secretion System 2-Dependent Early Inflammation Kinetics in a Mouse Colitis Model

Abstract: ABSTRACTSalmonella entericasubsp. I serovar Enteritidis exhibits type III secretion system 2 (TTSS2)-dependent early colonization and inflammation kinetics faster than those of closely relatedS. entericaserovar Typhi… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
24
0
1

Year Published

2012
2012
2021
2021

Publication Types

Select...
7
2

Relationship

4
5

Authors

Journals

citations
Cited by 25 publications
(25 citation statements)
references
References 47 publications
0
24
0
1
Order By: Relevance
“…The monolayer cells were seeded on 24 well tissue culture plates (Nest Biotech, China) and the confluent cells were washed thrice with PBS. S. Enteritidis was grown overnight and subcultured for 4 h in LB medium [36]. Bacterial cells were washed and resuspended in DMEM and infected to HCT-116 cell lines at a multiplicity of infection (MOI) of 100:1.…”
Section: Methodsmentioning
confidence: 99%
“…The monolayer cells were seeded on 24 well tissue culture plates (Nest Biotech, China) and the confluent cells were washed thrice with PBS. S. Enteritidis was grown overnight and subcultured for 4 h in LB medium [36]. Bacterial cells were washed and resuspended in DMEM and infected to HCT-116 cell lines at a multiplicity of infection (MOI) of 100:1.…”
Section: Methodsmentioning
confidence: 99%
“…The pM2155 vector system was used for the complementation of flgD and yciG in their respective mutants (11). The genes were amplified with nPFU special DNA polymerase (Enzynomics, South Korea) using primers containing BamHI and HindIII restriction sites at the 5= and 3= ends, respectively.…”
mentioning
confidence: 99%
“…For identifying the promoter, a sequence 1000 bp upstream of tomB was retrieved and analysed by BPROM software maintained by Softberry (http://www.softberry.com/berry.phtml?topic=bprom&group=programs&subgroup=gfindb)37. Predicted promoters were cloned into a promoterless GFP plasmid pM96838 between XbaI and BamHI restriction sites to create the constructs pMp201, pMp622 and pMp922.…”
Section: Methodsmentioning
confidence: 99%