Synthetic hybrid receptor and genetic circuit in bacteria to detect enteric pathogenic microorganisms
Provided herein are microorganisms engineered with hybrid receptors and genetic circuits. Also provided are hybrid receptors having a CqsS polypeptide and a heterologous histidine kinase domain of a two-component system. Methods for using engineered microorganisms to sense and destroy pathogens (e.g., Vibrio cholerae ) are also provided.
1. An engineered microorganism comprising
a hybrid receptor comprising at least the binding portion of a CqsS polypeptide and a heterologous histidine kinase domain of a two-component system; and
a genetic circuit responsive to the heterologous histidine kinase.
2. The engineered microorganism of claim 1 , wherein the heterologous histidine kinase domain is from NisK or SpaK.
3. The engineered microorganism of claim 2 , wherein the heterologous histidine kinase domain comprises a glutamic acid to glycine mutation at position 225 relative to full length NisK (SEQ ID NO: 5).
4. The engineered microorganism of claim 1 , wherein the hybrid receptor comprises
(i) amino acids 221-447 of NisK (SEQ ID NO: 15),
(ii) amino acids 221-447 of NisK having an E225G mutation (SEQ ID NO: 3),
(iii) the amino acid sequence of SEQ ID NO: 2, or
(iv) the amino acid sequence of SEQ ID NO: 1.
5. The engineered microorganism of claim 1 , wherein the genetic circuit comprises a first promoter that is operably linked to a nucleic acid sequence encoding the hybrid receptor and a second promoter that is responsive to the heterologous histidine kinase domain and is operably linked to a nucleic acid sequence encoding an output molecule.
6. The engineered microorganism of claim 5 , wherein the first promoter is inducible or constitutive, optionally wherein the first promoter is a nisR promoter.
7. The engineered microorganism of claim 1 , wherein the genetic circuit comprises a first promoter that is operably linked to a nucleic acid sequence encoding the hybrid receptor, a second promoter that is operably linked to a nucleic acid sequence encoding a repressor molecule, and a third promoter that is operably linked to a nucleic acid sequence encoding an output molecule;
wherein the second promoter is responsive to the heterologous histidine kinase domain, and
wherein the third promoter is responsive to the repressor molecule, and wherein the repressor molecule binds to the third promoter and represses transcription of the output molecule.
8. The engineered microorganism of claim 7 , wherein the first promoter is inducible or constitutive.
9. The engineered microorganism of claim 7 , wherein the first promoter is a nisR promoter, the second promoter is a nisA promoter, and/or wherein the third promoter is a xyltet2 promoter.
10. The engineered microorganism of claim 5 , wherein the output molecule is an antimicrobial peptide, a, lysing polypeptide, a reporter polypeptide, a peptide that acts on a substrate, or a nucleic acid, optionally wherein the output molecule is mCherry, or β-lactamase.
11. A method of detecting and/or treating a cholera infection, comprising administering to a subject having or at risk of having a cholera infection the engineered microorganism of claim 1 .
12. The method of claim 11 , further comprising administering to the subject an antibiotic agent effective for killing Vibrio cholerae when the engineered microorganism expresses a detectable output molecule.
13. A method of detecting a cholera infection, comprising
(i) obtaining a biological sample from a subject having or at risk of having a cholera infection, and
(ii) contacting the biological sample with the engineered microorganism of claim 1 , thereby creating a reaction mixture.
14. The method of claim 13 , wherein the biological sample is a fecal sample.
15. The method of claim 13 , further comprising (iii) contacting the reaction mixture of (ii) with a substrate, and/or wherein the substrate is a colorimetric substrate, optionally, wherein the substrate is nitrocefin.
16. The method of claim 15 , further comprising (iv), detecting a color change of the reaction mixture of (iii), optionally wherein the detecting comprises spectrophotometry.
17. A method of detecting and treating a cholera infection in a subject, comprising
(a) obtaining a biological sample from a subject having or at risk of having a cholera infection, and
(b) contacting the biological sample with the engineered microorganism of claim 1 , thereby creating a reaction mixture,
(c) determining if the subject has a cholera infection based on (a) and (b), and
(d) administering to the subject the engineered microorganism if it is determined in (c) that the subject has a cholera infection.
18. A hybrid receptor comprising
at least the binding portion of a CqsS polypeptide and a heterologous histidine kinase domain of a two-component system.
19. The hybrid receptor of claim 18 wherein the heterologous histidine kinase domain is from NisK or SpaK, and/or wherein the histidine kinase domain comprises a glutamic acid to glycine mutation at position 225 relative to full length NisK (SEQ ID NO: 5).
20. The hybrid receptor of claim 18 , wherein the hybrid receptor comprises
(i) amino acids 221-447 of NisK (SEQ ID NO: 15),
(ii) amino acids 221-447 of NisK having an E225G mutation (SEQ ID NO: 3),
(iii) the amino acid sequence of SEQ ID NO: 2,
(iv) the amino acid sequence of SEQ ID NO: 1,
(v) an amino acid sequence selected from the group consisting of SEQ ID NOs: 6-13, or
(vi) an amino acid sequence selected from the group consisting of SEQ ID NOs: 16-25.