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. 2016 Jul 21;84(8):2198-2208.
doi: 10.1128/IAI.00177-16. Print 2016 Aug.

Bile Acids Function Synergistically To Repress Invasion Gene Expression in Salmonella by Destabilizing the Invasion Regulator HilD (V体育ios版)

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V体育平台登录 - Bile Acids Function Synergistically To Repress Invasion Gene Expression in Salmonella by Destabilizing the Invasion Regulator HilD

Colleen R Eade et al. Infect Immun. .

Abstract

Salmonella spp. are carried by and can acutely infect agricultural animals and humans. After ingestion, salmonellae traverse the upper digestive tract and initiate tissue invasion of the distal ileum, a virulence process carried out by the type III secretion system encoded within Salmonella pathogenicity island 1 (SPI-1). Salmonellae coordinate SPI-1 expression with anatomical location via environmental cues, one of which is bile, a complex digestive fluid that causes potent repression of SPI-1 genes. The individual components of bile responsible for SPI-1 repression have not been previously characterized, nor have the bacterial signaling processes that modulate their effects been determined. Here, we characterize the mechanism by which bile represses SPI-1 expression. Individual bile acids exhibit repressive activity on SPI-1-regulated genes that requires neither passive diffusion nor OmpF-mediated entry. By using genetic methods, the effects of bile and bile acids were shown to require the invasion gene transcriptional activator hilD and to function independently of known upstream signaling pathways. Protein analysis techniques showed that SPI-1 repression by bile acids is mediated by posttranslational destabilization of HilD. Finally, we found that bile acids function synergistically to achieve the overall repressive activity of bile VSports手机版. These studies demonstrate a common mechanism by which diverse environmental cues (e. g. , certain short-chain fatty acids and bile acids) inhibit SPI-1 expression. These data provide information relevant to Salmonella pathogenesis during acute infection in the intestine and during chronic infection of the gallbladder and inform the basis for development of therapeutics to inhibit invasion as a means of repressing Salmonella pathogenicity. .

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Figures

FIG 1
FIG 1
Invasion gene expression is repressed by bile and by individual bile acids. Salmonella Typhimurium was grown with the indicated concentrations of bile or individual bile acids in media buffered with HEPES (pH 8.0; for deoxycholate) or MOPS (pH 6.7; all others). Invasion gene expression was monitored based on sipC::lacZY chromosomal reporter activity. Reporter expression was determined in a β-galactosidase assay. The data are compiled from multiple (n = 3 to 7) repeated experiments. Asterisks indicate a significant difference (P < 0.05) from the untreated condition. Insets depict structures of corresponding bile acids.
FIG 2
FIG 2
Bile and bile acids repress invasion gene induction over time. Salmonella Typhimurium containing a plasmid-borne sopB::luxCDABE reporter was grown with the indicated concentrations of bile or bile acids in media buffered to pH 8.0 (for deoxycholate) or pH 6.7 (all others). Expression of sopB::luxCDABE was determined by luminescent measurement, while culture density was monitored by OD600 readings. Normalized luminescence is the luminescent signal divided by the OD600. Asterisks, shown in the key, indicate treatments for which significant inhibition (compared to vehicle treatment; P < 0.05) of normalized luminescence was observed for any time point. The data are compiled from multiple (n = 4) experimental repeats.
FIG 3
FIG 3
hilD is required for bile to repress invasion gene expression. (A) Map of transposon insertions imparting resistance to repression of sopB::lacZ by bile. Gray arrows represent the open reading frames of the indicated genes, and black arrowheads represent the locations of identified T-POP insertions (arrows indicate the orientation of the outward-facing promoter). Numbers above or below the arrowheads indicate the number of insertions at that location. The relative sizes of the represented genes are shown to scale. (B) A ΔhilD mutant strain carrying a sipC::lacZY reporter was grown with 3% bile or the vehicle. As a control, a ΔhilD ΔinvF double mutant was assayed in vehicle-containing medium for comparison. Reporter expression was determined in a β-galactosidase assay. The data are compiled from multiple (n = 3 to 4) experimental repeats. *, P < 0.05 versus untreated ΔhilD condition.
FIG 4
FIG 4
Bile and cholate affect HilD posttranslational stability and activity. A Salmonella Typhimurium strain containing a tetracycline-inducible HilD-3×FLAG construct and a hilA′-lacZ reporter was grown to log phase in 3% bile, 0.5% cholate, or vehicle. During growth, hilD expression was induced with 1 μg/ml tetracycline, except in the “No Tet” control. For comparison, the same strain with a Δlon mutation was treated in parallel. (A) Transcription and translation were halted by addition of an antibiotic cocktail, and the protein half-life was assessed by Western blotting for HilD-3×FLAG over time. Half-life values are averaged from two independent experiments; blots from one of these experiments are shown. (B) Upon addition of antibiotics, invasion gene expression was assessed via the hilA′-lacZ reporter. Reporter expression was determined in a β-galactosidase assay. The data are compiled from multiple (n = 5 to 18) experimental repeats. Asterisks indicate a significant difference (P < 0.05) from the vehicle treatment.
FIG 5
FIG 5
Bile acids function synergistically to repress invasion gene expression. Salmonella Typhimurium carrying a sipC::lacZY reporter was grown with a mixture of four bile acids that recapitulated the composition of bile (mixed acids). For comparison, separate cultures were grown in an equivalent concentration of bile, or in bile acid combinations at the indicated concentrations, corresponding to the concentration at which they were provided in the mixed acid treatment. All cultures were buffered with MOPS (pH 6.7) (A) or HEPES (pH 8.0) (B). Reporter expression was determined in a β-galactosidase assay. The data are compiled from multiple (n = 3 to 6) experiments repeats. Asterisks indicate a significant difference (P < 0.05) from the untreated condition, except where brackets denote other comparisons.

References

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