This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lundberg, U.
Right arrow Articles by Baccarini, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lundberg, U.
Right arrow Articles by Baccarini, M.

 Previous Article  |  Next Article 

Journal of Bacteriology, June 1999, p. 3433-3437, Vol. 181, No. 11
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Growth Phase-Regulated Induction of Salmonella-Induced Macrophage Apoptosis Correlates with Transient Expression of SPI-1 Genes

Urban Lundberg,dagger Ursula Vinatzer,Dagger Daniela Berdnik,§ Alexander von Gabain, and Manuela Baccarini*

Institute of Microbiology and Genetics, Vienna Biocenter, University of Vienna, A-1030 Vienna, Austria

Received 16 July 1998/Accepted 30 March 1999

Invasive Salmonella has been reported to induce apoptosis in a fraction of infected macrophages within 2 to 14 h from the time of infection by a mechanism involving the type III secretion machinery encoded by the Salmonella pathogenicity island 1 (SPI-1). Here, we show that bacteria in the transition from logarithmic to stationary phase cause 90% of the macrophages to undergo phagocytosis-independent, caspase-mediated apoptosis within 30 to 60 min of infection. The ability of Salmonella to induce this rapid apoptosis was growth phase regulated and cell type restricted, with epithelial cells being resistant. Apoptosis induction was also abrogated by disruption of the hilA gene (encoding a regulator of SPI-1 genes) and by the expression of a constitutively active PhoPQ. hilA itself and a subset of SPI-1 genes were transiently expressed during aerobic growth in liquid medium. Interestingly, however, hilA was found to be required only for the expression of the prgH gene, while sipB, invA, and invF were expressed in a hilA-independent manner. The expression of SPI-1 genes and the secretion of invasion-associated proteins correlated temporally with the induction of apoptosis and are likely to represent its molecular basis. Thus, growth phase transition regulates the expression and secretion of virulence determinants and represents the most efficient environmental cue for apoptosis induction reported to date.


* Corresponding author. Mailing address: Vienna Biocenter, Department of Cell- and Microbiology, Institute for Microbiology and Genetics, Dr. Bohr Gasse 9, A-1030 Vienna, Austria. Phone: 43 (1) 4277-54607. Fax: 43 (1) 4277-9546. E-mail: manuela{at}gem.univie.ac.at.

dagger Present address: Department of Bacteriology, Baxter Hyland-Immuno, A-2304 Orth/Donau, Austria.

Dagger Present address: Institute for Medical Biology, A-1090 Vienna, Austria.

§ Present address: Institute of Molecular Pathology, A-1030 Vienna, Austria.


Journal of Bacteriology, June 1999, p. 3433-3437, Vol. 181, No. 11
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Bernal-Bayard, J., Ramos-Morales, F. (2009). Salmonella Type III Secretion Effector SlrP Is an E3 Ubiquitin Ligase for Mammalian Thioredoxin. J. Biol. Chem. 284: 27587-27595 [Abstract] [Full Text]  
  • Nicholson, T. L., Buboltz, A. M., Harvill, E. T., Brockmeier, S. L. (2009). Microarray and Functional Analysis of Growth Phase-Dependent Gene Regulation in Bordetella bronchiseptica. Infect. Immun. 77: 4221-4231 [Abstract] [Full Text]  
  • Gonzalez-Escalona, N., Hammack, T. S., Russell, M., Jacobson, A. P., De Jesus, A. J., Brown, E. W., Lampel, K. A. (2009). Detection of Live Salmonella sp. Cells in Produce by a TaqMan-Based Quantitative Reverse Transcriptase Real-Time PCR Targeting invA mRNA. Appl. Environ. Microbiol. 75: 3714-3720 [Abstract] [Full Text]  
  • Faucher, S. P., Forest, C., Beland, M., Daigle, F. (2009). A novel PhoP-regulated locus encoding the cytolysin ClyA and the secreted invasin TaiA of Salmonella enterica serovar Typhi is involved in virulence. Microbiology 155: 477-488 [Abstract] [Full Text]  
  • Su, J., Gong, H., Lai, J., Main, A., Lu, S. (2009). The Potassium Transporter Trk and External Potassium Modulate Salmonella enterica Protein Secretion and Virulence. Infect. Immun. 77: 667-675 [Abstract] [Full Text]  
  • Jin, D., Ojcius, D. M., Sun, D., Dong, H., Luo, Y., Mao, Y., Yan, J. (2009). Leptospira interrogans Induces Apoptosis in Macrophages via Caspase-8- and Caspase-3-Dependent Pathways. Infect. Immun. 77: 799-809 [Abstract] [Full Text]  
  • Matsui, M., Takaya, A., Yamamoto, T. (2008). {sigma}32-Mediated Negative Regulation of Salmonella Pathogenicity Island 1 Expression. J. Bacteriol. 190: 6636-6645 [Abstract] [Full Text]  
  • Bustamante, V. H., Martinez, L. C., Santana, F. J., Knodler, L. A., Steele-Mortimer, O., Puente, J. L. (2008). HilD-mediated transcriptional cross-talk between SPI-1 and SPI-2. Proc. Natl. Acad. Sci. USA 105: 14591-14596 [Abstract] [Full Text]  
  • Huang, Y., Suyemoto, M., Garner, C. D., Cicconi, K. M., Altier, C. (2008). Formate Acts as a Diffusible Signal To Induce Salmonella Invasion. J. Bacteriol. 190: 4233-4241 [Abstract] [Full Text]  
  • Huang, Y., Leming, C. L., Suyemoto, M., Altier, C. (2007). Genome-Wide Screen of Salmonella Genes Expressed during Infection in Pigs, Using In Vivo Expression Technology. Appl. Environ. Microbiol. 73: 7522-7530 [Abstract] [Full Text]  
  • Choi, J., Shin, D., Ryu, S. (2007). Implication of Quorum Sensing in Salmonella enterica Serovar Typhimurium Virulence: the luxS Gene Is Necessary for Expression of Genes in Pathogenicity Island 1. Infect. Immun. 75: 4885-4890 [Abstract] [Full Text]  
  • Lim, S., Yun, J., Yoon, H., Park, C., Kim, B., Jeon, B., Kim, D., Ryu, S. (2007). Mlc regulation of Salmonella pathogenicity island I gene expression via hilE repression. Nucleic Acids Res 35: 1822-1832 [Abstract] [Full Text]  
  • Dvorak, C. M. T., Hirsch, G. N., Hyland, K. A., Hendrickson, J. A., Thompson, B. S., Rutherford, M. S., Murtaugh, M. P. (2006). Genomic dissection of mucosal immunobiology in the porcine small intestine. Physiol. Genomics 28: 5-14 [Abstract] [Full Text]  
  • Rodrigues, F., Sarkar-Tyson, M., Harding, S. V., Sim, S. H., Chua, H. H., Lin, C. H., Han, X., Karuturi, R. K. M., Sung, K., Yu, K., Chen, W., Atkins, T. P., Titball, R. W., Tan, P. (2006). Global Map of Growth-Regulated Gene Expression in Burkholderia pseudomallei, the Causative Agent of Melioidosis. J. Bacteriol. 188: 8178-8188 [Abstract] [Full Text]  
  • Nakamura, M. M., Liew, S.-Y., Cummings, C. A., Brinig, M. M., Dieterich, C., Relman, D. A. (2006). Growth Phase- and Nutrient Limitation-Associated Transcript Abundance Regulation in Bordetella pertussis.. Infect. Immun. 74: 5537-5548 [Abstract] [Full Text]  
  • Ygberg, S. E., Clements, M. O., Rytkonen, A., Thompson, A., Holden, D. W., Hinton, J. C. D., Rhen, M. (2006). Polynucleotide Phosphorylase Negatively Controls spv Virulence Gene Expression in Salmonella enterica. Infect. Immun. 74: 1243-1254 [Abstract] [Full Text]  
  • Christogianni, A., Douka, E., Koukkou, A. I., Hatziloukas, E., Drainas, C. (2005). Transcriptional Analysis of a Gene Cluster Involved in Glucose Tolerance in Zymomonas mobilis: Evidence for an Osmoregulated Promoter. J. Bacteriol. 187: 5179-5188 [Abstract] [Full Text]  
  • Parsons, D. A., Heffron, F. (2005). sciS, an icmF Homolog in Salmonella enterica Serovar Typhimurium, Limits Intracellular Replication and Decreases Virulence. Infect. Immun. 73: 4338-4345 [Abstract] [Full Text]  
  • Song, M., Kim, H.-J., Kim, E. Y., Shin, M., Lee, H. C., Hong, Y., Rhee, J. H., Yoon, H., Ryu, S., Lim, S., Choy, H. E. (2004). ppGpp-dependent Stationary Phase Induction of Genes on Salmonella Pathogenicity Island 1. J. Biol. Chem. 279: 34183-34190 [Abstract] [Full Text]  
  • Forsberg, M., Blomgran, R., Lerm, M., Sarndahl, E., Sebti, S. M., Hamilton, A., Stendahl, O., Zheng, L. (2003). Differential effects of invasion by and phagocytosis of Salmonella typhimurium on apoptosis in human macrophages: potential role of Rho-GTPases and Akt. J. Leukoc. Biol. 74: 620-629 [Abstract] [Full Text]  
  • Obregon, C., Dreher, D., Kok, M., Cochand, L., Kiama, G. S., Nicod, L. P. (2003). Human Alveolar Macrophages Infected by Virulent Bacteria Expressing SipB Are a Major Source of Active Interleukin-18. Infect. Immun. 71: 4382-4388 [Abstract] [Full Text]  
  • Thompson, L. J., Merrell, D. S., Neilan, B. A., Mitchell, H., Lee, A., Falkow, S. (2003). Gene Expression Profiling of Helicobacter pylori Reveals a Growth-Phase-Dependent Switch in Virulence Gene Expression. Infect. Immun. 71: 2643-2655 [Abstract] [Full Text]  
  • Dreher, D., Kok, M., Obregon, C., Kiama, S. G., Gehr, P., Nicod, L. P. (2002). Salmonella virulence factor SipB induces activation and release of IL-18 in human dendritic cells. J. Leukoc. Biol. 72: 743-751 [Abstract] [Full Text]  
  • Ruckdeschel, K., Richter, K. (2002). Lipopolysaccharide Desensitization of Macrophages Provides Protection against Yersinia enterocolitica-Induced Apoptosis. Infect. Immun. 70: 5259-5264 [Abstract] [Full Text]  
  • Santos, R. L., Tsolis, R. M., Zhang, S., Ficht, T. A., Baumler, A. J., Adams, L. G. (2001). Salmonella-Induced Cell Death Is Not Required for Enteritis in Calves. Infect. Immun. 69: 4610-4617 [Abstract] [Full Text]  
  • Santos, R. L., Tsolis, R. M., Baumler, A. J., Smith, R. III, Adams, L. G. (2001). Salmonella enterica Serovar Typhimurium Induces Cell Death in Bovine Monocyte-Derived Macrophages by Early sipB-Dependent and Delayed sipB-Independent Mechanisms. Infect. Immun. 69: 2293-2301 [Abstract] [Full Text]  
  • Ruckdeschel, K., Mannel, O., Richter, K., Jacobi, C. A., Trulzsch, K., Rouot, B., Heesemann, J. (2001). Yersinia Outer Protein P of Yersinia enterocolitica Simultaneously Blocks the Nuclear Factor-{{kappa}}B Pathway and Exploits Lipopolysaccharide Signaling to Trigger Apoptosis in Macrophages. J. Immunol. 166: 1823-1831 [Abstract] [Full Text]  
  • Altier, C., Suyemoto, M., Lawhon, S. D. (2000). Regulation of Salmonella enterica Serovar Typhimurium Invasion Genes by csrA. Infect. Immun. 68: 6790-6797 [Abstract] [Full Text]  
  • Jesenberger, V., Procyk, K. J., Yuan, J., Reipert, S., Baccarini, M. (2000). Salmonella-Induced Caspase-2 Activation in Macrophages: A Novel Mechanism in Pathogen-Mediated Apoptosis. JEM 192: 1035-1046 [Abstract] [Full Text]  
  • van der Velden, A. W. M., Lindgren, S. W., Worley, M. J., Heffron, F. (2000). Salmonella Pathogenicity Island 1-Independent Induction of Apoptosis in Infected Macrophages by Salmonella enterica Serotype Typhimurium. Infect. Immun. 68: 5702-5709 [Abstract] [Full Text]  
  • Stanley, T. L., Ellermeier, C. D., Slauch, J. M. (2000). Tissue-Specific Gene Expression Identifies a Gene in the Lysogenic Phage Gifsy-1 That Affects Salmonella enterica Serovar Typhimurium Survival in Peyer's Patches. J. Bacteriol. 182: 4406-4413 [Abstract] [Full Text]  
  • Watson, P. R., Gautier, A. V., Paulin, S. M., Bland, A. P., Jones, P. W., Wallis, T. S. (2000). Salmonella enterica Serovars Typhimurium and Dublin Can Lyse Macrophages by a Mechanism Distinct from Apoptosis. Infect. Immun. 68: 3744-3747 [Abstract] [Full Text]  
  • Procyk, K. J., Rippo, M. R., Testi, R., Hoffmann, F., Parker, P. J., Baccarini, M. (1999). Distinct Mechanisms Target Stress and Extracellular Signal-Activated Kinase 1 and Jun N-Terminal Kinase During Infection of Macrophages with Salmonella. J. Immunol. 163: 4924-4930 [Abstract] [Full Text]  
  • Detweiler, C. S., Cunanan, D. B., Falkow, S. (2001). Host microarray analysis reveals a role for the Salmonella response regulator phoP in human macrophage cell death. Proc. Natl. Acad. Sci. USA 98: 5850-5855 [Abstract] [Full Text]