Compositions and methods for regulating bacterial pathogenesis
View Patent ↗The production of a purified extracellular bacterial signal called autoinducer-2 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. Autoinducer-2 stimulates LuxQ luminescence genes, and is believed also to stimulate a variety of pathogenesis related genes in the bacterial species that produce it. A new class of bacterial genes is involved in the biosynthesis of autoinducer-2.
1. A method for identifying a compound that modulates the response of a bacterial strain to a first autoinducer, comprising:
obtaining a bacterial strain that produces a detectable signal in response to the first autoinducer which is not an acyl-homoserine lactone, the first autoinducer being capable of interacting with the Vibrio harveyi LuxQ protein thereby inducing expression of a Vibrio harveyi operon comprising the luxCDABE genes, wherein the bacterial strain has a first genetic alteration in the coding region of the luxS gene that inhibits production of the first autoinducer, wherein the genetic alteration in the luxS gene is an alteration introduced into a nucleotide sequence selected from the group consisting of SEQ ID NOS:1-9;
measuring the responses of the bacterial strain when contacted with the first autoinducer in the presence and absence of a test compound and;
identifying that the test compound modulates the response of the bacterial strain to the first autoinducer.
2. The method of claim 1 , wherein the first genetic alteration has been introduced in the cell by genetic engineering.
3. The method of claim 1 , wherein the first autoinducer is the autoinducer-2 produced by Vibrio harveyi.
4. The method of claim 1 , wherein the first genetic alteration inhibits production of a pentanedione.
5. The method of claim 4 , wherein the pentanedione is 4,5-dihydroxy-2,3-pentanedione.
6. The method of claim 1 , wherein the bacterial strain belongs to a species selected from the group consisting of S. typhimurium and E. coli.
7. The method of claim 1 , wherein the bacterial strain belongs to a species selected from the group consisting of Haemophilus influenzae, Helicobacter pylori, Bacillus subtilis, Borrelia burgdorferi and Vibrio cholerae.
8. The method of claim 1 , wherein the bacterial strain is Vibrio harveyi.
9. The method of claim 1 wherein the bacterial strain is gram negative and has a second genetic alteration that inhibits the ability to detect a second autoinducer, wherein the second autoinducer is an acyl-homoserine lactone.
10. The method of claim 9 , wherein the second autoinducer is N-(3-hydroxyacyl)-L-homoserine lactone and the acyl group comprises 4-12 carbon atoms.
11. The method of claim 10 , wherein the acyl group comprises four carbon atoms.
12. The method of claim 1 , wherein the response of the bacterial strain is bioluminescence.
13. A method for identifying a compound that modulates the response of a bacterial strain to a non-acyl-homoserine lactone autoinducer, comprising:
obtaining an isolated and purified gram negative bacterial strain comprising a first genetic alteration in the coding region of the luxS gene that inhibits production of a first autoinducer that is not an acyl-homoserine lactone, the first autoinducer being capable of interacting with the Vibrio harveyi LuxQ protein thereby inducing expression of a Vibrio harveyi operon comprising the luxCDABE genes, and a second genetic alteration in the coding region of the luxN gene that inhibits the ability to detect a second autoinducer that is an acyl-homoserine lactone, wherein the genetic alteration in the luxS gene is an alteration introduced into a nucleotide sequence selected from the group consisting of SEQ ID NOS:1-9;
contacting the bacterial strain with the first autoinducer in the presence of a test compound and at another time in the absence of the test compound;
measuring the response of the bacterial strain to the first autoinducer in the presence and absence of the test compound and;
selecting the test compound that modulates the response of the bacterial strain to the first autoinducer.
14. The method of claim 13 , wherein the bacterial strain is a strain of Vibrio harveyi.
15. The method of claim 14 , wherein the response is bioluminescence.
16. The method of claim 13 , wherein the first alteration inhibits production of the autoinducer-2 produced by Vibrio harveyi.
17. The method of claim 13 , wherein the bacterial strain belongs to a species other than Vibrio harveyi.
18. The method of claim 17 , wherein the bacterial strain belongs to a species selected from the group consisting of S. typhimurium and E. coli.
19. The method of claim 17 , wherein the bacterial strain belongs to a species selected from the group consisting of Haemophilus influenzae, Helicobacter pylori, Borrelia burgdorferi and Vibrio cholerae.
20. The method of claim 13 , wherein the second autoinducer in N-(3-hydroxyacyl)-L-homoserine lactone and the acyl group comprises 4-12 carbon atoms.
21. The method of claim 14 , wherein the first alteration inhibits production of the autoinducer-2 produced by Vibrio harveyi.
22. The method of claim 13 , wherein the first and second alterations have been introduced into the strain by genetic engineering.
23. The method of claim 13 , wherein the first alteration inhibits production of a pentanedione.
24. The method of claim 13 , wherein the pentanedione is 4,5-dihydroxy-2,3-pentanedione.
25. The method of claim 13 , wherein the second autoinducer is N-(3-hydroxybutanoyl)-L-homoserine lactone.