Compositions and methods for regulating bacterial pathogenesis
AssigneesPrinceton University, University Technologies International Inc.
InventorsBonnie L. Bassler, Michael G. Surette
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Abstract
This invention provides a purified extracellular bacterial autoinducer-2 signaling molecule, the production of which is regulated by changes in environmental conditions associated with a shift from a free-living existence to a colonizing or pathogenic existence in a host organism. The signaling molecule stimulates LuxQ luminescence genes, and is believed also to stimulate a variety of pathogenesis related genes in the bacterial species that produce it. This invention also provides is a new class of bacterial genes involved in the biosynthesis of the signaling molecule.
Claims6
An isolated nucleic acid that comprises the sequence of SEQ ID NO:1, wherein the sequence encodes a polypeptide that catalyzes conversion of S-ribosylhomocysteine to homocysteine, wherein the sequence is operably linked to a heterologous regulatory sequence, and wherein the heterologous regulatory sequence directs expression of the polypeptide encoded by SEQ ID NO:1.
An isolated nucleic acid that encodes a polypeptide that catalyses the conversion of S-ribosylhomocysteine to homocysteine, that is operably linked to a heterologous regulatory sequence that directs expression of the polypeptide, and that hybridizes to the sequence of SEQ ID NO:
- 1 under high stringency hybridization conditions, the high stringency hybridization conditions being 5×SSC, 5× Denhardt's reagent, 1.0% SDS, 100 g/ml denatured, fragmented salmon sperm DNA, 0.05% sodium pyrophosphate and up to 50% formamide at 37-42° C. for at least six hours, followed by washing for 5 minutes at room temperature in 2×SSC and 1% SDS, for 15 minutes at room temperature in 2×SSC and 0.1% SDS, for 30 minutes-1 hour at 37° C. in 1×SSC and 1% SDS, and for 2 hours at 42-65° C. in 1×SSC and 1% SDS.
Dependencies are inferred from the claim text.