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- Vanessa Sperandio
- Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9048; Departments of Microbiology and Immunology and Pediatrics, and Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD 21201; and Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742
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- Alfredo G. Torres
- Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9048; Departments of Microbiology and Immunology and Pediatrics, and Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD 21201; and Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742
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- Bruce Jarvis
- Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9048; Departments of Microbiology and Immunology and Pediatrics, and Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD 21201; and Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742
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- James P. Nataro
- Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9048; Departments of Microbiology and Immunology and Pediatrics, and Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD 21201; and Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742
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- James B. Kaper
- Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9048; Departments of Microbiology and Immunology and Pediatrics, and Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD 21201; and Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742
書誌事項
- 公開日
- 2003-07-07
- DOI
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- 10.1073/pnas.1537100100
- 公開者
- Proceedings of the National Academy of Sciences
この論文をさがす
説明
<jats:p> The interbacterial communication system known as quorum sensing (QS) utilizes hormone-like compounds referred to as autoinducers to regulate bacterial gene expression. Enterohemorrhagic <jats:italic>Escherichia coli</jats:italic> (EHEC) serotype O157:H7 is the agent responsible for outbreaks of bloody diarrhea in several countries. We previously proposed that EHEC uses a QS regulatory system to “sense” that it is within the intestine and activate genes essential for intestinal colonization. The QS system used by EHEC is the LuxS/autoinducer 2 (AI-2) system extensively involved in interspecies communication. The autoinducer AI-2 is a furanosyl borate diester whose synthesis depends on the enzyme LuxS. Here we show that an EHEC <jats:italic>luxS</jats:italic> mutant, unable to produce the bacterial autoinducer, still responds to a eukaryotic cell signal to activate expression of its virulence genes. We have identified this signal as the hormone epinephrine and show that β- and α-adrenergic antagonists can block the bacterial response to this hormone. Furthermore, using purified and <jats:italic>in vitro</jats:italic> synthesized AI-2 we showed that AI-2 is not the autoinducer involved in the bacterial signaling. EHEC produces another, previously undescribed autoinducer (AI-3) whose synthesis depends on the presence of LuxS. These results imply a potential cross-communication between the <jats:italic>luxS</jats:italic> /AI-3 bacterial QS system and the epinephrine host signaling system. Given that eukaryotic cell-to-cell signaling typically occurs through hormones, and that bacterial cell-to-cell signaling occurs through QS, we speculate that QS might be a “language” by which bacteria and host cells communicate. </jats:p>
収録刊行物
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- Proceedings of the National Academy of Sciences
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Proceedings of the National Academy of Sciences 100 (15), 8951-8956, 2003-07-07
Proceedings of the National Academy of Sciences