Functional characterization of PhoPR two component system and its implication in regulating phosphate homeostasis in Bacillus anthracis
Recent report on importance of phosphate starvation (PS) in Bacillus anthracis (BA) pathogenesis warrants further investigation of the underlying regulatory mechanism. Potential role of PhoPR two component system (TCS) in phosphate homeostasis and virulence of several pathogens necessitates the stud...
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Published in | Biochimica et biophysica acta. General subjects Vol. 1861; no. 1; pp. 2956 - 2970 |
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Main Authors | , , , , , , |
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Elsevier B.V
01.01.2017
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Abstract | Recent report on importance of phosphate starvation (PS) in Bacillus anthracis (BA) pathogenesis warrants further investigation of the underlying regulatory mechanism. Potential role of PhoPR two component system (TCS) in phosphate homeostasis and virulence of several pathogens necessitates the study of annotated PhoPR in BA.
Expression of phoP and phoR was analyzed using qRT-PCR. PhoPR was characterized biochemically. DNA-protein interaction was analyzed by EMSA. Docking was done to predict PhoPR interacting residues with further validation by mutational studies. pHCMC05 was used to overexpress PhoP in BA.
In silico analysis revealed Bas4483-4484, as putative PhoR–PhoP. Their expression was decreased with increasing phosphate concentration reflecting some role in PS. Both PhoP (response regulator) and PhoR (histidine kinase) showed characteristic property of TCS i.e., autophosphorylation and phosphotransfer. PhoR showed both kinase and phosphatase activity. PhoP bound with promoter of PS marker genes. In silico and in vitro analysis revealed role of PhoRH370 and PhoPD10, PhoPD53, PhoPM55 in PhoPR interaction. Challenge studies showed decreased survival of mice infected with BApHCMC05-PhoP.
This study affirms that PhoPR forms functional TCS which is upregulated under PS. PhoP binding with promoter of PS marker genes indicates its possible role in regulating PS response. Low survival of mice infected with BApHCMC05-PhoP suggests its role in BA virulence.
Considering the significance of PS in BA infection, possible role of PhoPR in its regulation and exclusive presence of TCS in prokaryotes, PhoP can be proposed as potential drug target against anthrax.
[Display omitted]
•Phosphate starvation (PS) promotes pathogenesis of B. anthracis (BA) within host.•PhoP and PhoR of BA form a functional two component system, regulating PS response.•PhoP is implicated in regulation of PS marker genes.•H370 of PhoR and D10, D53 and M55 of PhoP are involved in PhoPR interaction.•Exclusive in microbes, homology in pathogens, role in virulence & PS make PhoP as a good drug target. |
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AbstractList | Recent report on importance of phosphate starvation (PS) in Bacillus anthracis (BA) pathogenesis warrants further investigation of the underlying regulatory mechanism. Potential role of PhoPR two component system (TCS) in phosphate homeostasis and virulence of several pathogens necessitates the study of annotated PhoPR in BA.
Expression of phoP and phoR was analyzed using qRT-PCR. PhoPR was characterized biochemically. DNA-protein interaction was analyzed by EMSA. Docking was done to predict PhoPR interacting residues with further validation by mutational studies. pHCMC05 was used to overexpress PhoP in BA.
In silico analysis revealed Bas4483-4484, as putative PhoR-PhoP. Their expression was decreased with increasing phosphate concentration reflecting some role in PS. Both PhoP (response regulator) and PhoR (histidine kinase) showed characteristic property of TCS i.e., autophosphorylation and phosphotransfer. PhoR showed both kinase and phosphatase activity. PhoP bound with promoter of PS marker genes. In silico and in vitro analysis revealed role of PhoR
and PhoP
, PhoP
, PhoP
in PhoPR interaction. Challenge studies showed decreased survival of mice infected with BA
.
This study affirms that PhoPR forms functional TCS which is upregulated under PS. PhoP binding with promoter of PS marker genes indicates its possible role in regulating PS response. Low survival of mice infected with BA
suggests its role in BA virulence.
Considering the significance of PS in BA infection, possible role of PhoPR in its regulation and exclusive presence of TCS in prokaryotes, PhoP can be proposed as potential drug target against anthrax. Recent report on importance of phosphate starvation (PS) in Bacillus anthracis (BA) pathogenesis warrants further investigation of the underlying regulatory mechanism. Potential role of PhoPR two component system (TCS) in phosphate homeostasis and virulence of several pathogens necessitates the study of annotated PhoPR in BA.BACKGROUNDRecent report on importance of phosphate starvation (PS) in Bacillus anthracis (BA) pathogenesis warrants further investigation of the underlying regulatory mechanism. Potential role of PhoPR two component system (TCS) in phosphate homeostasis and virulence of several pathogens necessitates the study of annotated PhoPR in BA.Expression of phoP and phoR was analyzed using qRT-PCR. PhoPR was characterized biochemically. DNA-protein interaction was analyzed by EMSA. Docking was done to predict PhoPR interacting residues with further validation by mutational studies. pHCMC05 was used to overexpress PhoP in BA.METHODSExpression of phoP and phoR was analyzed using qRT-PCR. PhoPR was characterized biochemically. DNA-protein interaction was analyzed by EMSA. Docking was done to predict PhoPR interacting residues with further validation by mutational studies. pHCMC05 was used to overexpress PhoP in BA.In silico analysis revealed Bas4483-4484, as putative PhoR-PhoP. Their expression was decreased with increasing phosphate concentration reflecting some role in PS. Both PhoP (response regulator) and PhoR (histidine kinase) showed characteristic property of TCS i.e., autophosphorylation and phosphotransfer. PhoR showed both kinase and phosphatase activity. PhoP bound with promoter of PS marker genes. In silico and in vitro analysis revealed role of PhoRH370 and PhoPD10, PhoPD53, PhoPM55 in PhoPR interaction. Challenge studies showed decreased survival of mice infected with BApHCMC05-PhoP.RESULTSIn silico analysis revealed Bas4483-4484, as putative PhoR-PhoP. Their expression was decreased with increasing phosphate concentration reflecting some role in PS. Both PhoP (response regulator) and PhoR (histidine kinase) showed characteristic property of TCS i.e., autophosphorylation and phosphotransfer. PhoR showed both kinase and phosphatase activity. PhoP bound with promoter of PS marker genes. In silico and in vitro analysis revealed role of PhoRH370 and PhoPD10, PhoPD53, PhoPM55 in PhoPR interaction. Challenge studies showed decreased survival of mice infected with BApHCMC05-PhoP.This study affirms that PhoPR forms functional TCS which is upregulated under PS. PhoP binding with promoter of PS marker genes indicates its possible role in regulating PS response. Low survival of mice infected with BApHCMC05-PhoP suggests its role in BA virulence.CONCLUSIONThis study affirms that PhoPR forms functional TCS which is upregulated under PS. PhoP binding with promoter of PS marker genes indicates its possible role in regulating PS response. Low survival of mice infected with BApHCMC05-PhoP suggests its role in BA virulence.Considering the significance of PS in BA infection, possible role of PhoPR in its regulation and exclusive presence of TCS in prokaryotes, PhoP can be proposed as potential drug target against anthrax.GENERAL SIGNIFICANCEConsidering the significance of PS in BA infection, possible role of PhoPR in its regulation and exclusive presence of TCS in prokaryotes, PhoP can be proposed as potential drug target against anthrax. Recent report on importance of phosphate starvation (PS) in Bacillus anthracis (BA) pathogenesis warrants further investigation of the underlying regulatory mechanism. Potential role of PhoPR two component system (TCS) in phosphate homeostasis and virulence of several pathogens necessitates the study of annotated PhoPR in BA.Expression of phoP and phoR was analyzed using qRT-PCR. PhoPR was characterized biochemically. DNA-protein interaction was analyzed by EMSA. Docking was done to predict PhoPR interacting residues with further validation by mutational studies. pHCMC05 was used to overexpress PhoP in BA.In silico analysis revealed Bas4483-4484, as putative PhoR–PhoP. Their expression was decreased with increasing phosphate concentration reflecting some role in PS. Both PhoP (response regulator) and PhoR (histidine kinase) showed characteristic property of TCS i.e., autophosphorylation and phosphotransfer. PhoR showed both kinase and phosphatase activity. PhoP bound with promoter of PS marker genes. In silico and in vitro analysis revealed role of PhoRH370 and PhoPD10, PhoPD53, PhoPM55 in PhoPR interaction. Challenge studies showed decreased survival of mice infected with BApHCMC05-PhoP.This study affirms that PhoPR forms functional TCS which is upregulated under PS. PhoP binding with promoter of PS marker genes indicates its possible role in regulating PS response. Low survival of mice infected with BApHCMC05-PhoP suggests its role in BA virulence.Considering the significance of PS in BA infection, possible role of PhoPR in its regulation and exclusive presence of TCS in prokaryotes, PhoP can be proposed as potential drug target against anthrax. Recent report on importance of phosphate starvation (PS) in Bacillus anthracis (BA) pathogenesis warrants further investigation of the underlying regulatory mechanism. Potential role of PhoPR two component system (TCS) in phosphate homeostasis and virulence of several pathogens necessitates the study of annotated PhoPR in BA. Expression of phoP and phoR was analyzed using qRT-PCR. PhoPR was characterized biochemically. DNA-protein interaction was analyzed by EMSA. Docking was done to predict PhoPR interacting residues with further validation by mutational studies. pHCMC05 was used to overexpress PhoP in BA. In silico analysis revealed Bas4483-4484, as putative PhoR–PhoP. Their expression was decreased with increasing phosphate concentration reflecting some role in PS. Both PhoP (response regulator) and PhoR (histidine kinase) showed characteristic property of TCS i.e., autophosphorylation and phosphotransfer. PhoR showed both kinase and phosphatase activity. PhoP bound with promoter of PS marker genes. In silico and in vitro analysis revealed role of PhoRH370 and PhoPD10, PhoPD53, PhoPM55 in PhoPR interaction. Challenge studies showed decreased survival of mice infected with BApHCMC05-PhoP. This study affirms that PhoPR forms functional TCS which is upregulated under PS. PhoP binding with promoter of PS marker genes indicates its possible role in regulating PS response. Low survival of mice infected with BApHCMC05-PhoP suggests its role in BA virulence. Considering the significance of PS in BA infection, possible role of PhoPR in its regulation and exclusive presence of TCS in prokaryotes, PhoP can be proposed as potential drug target against anthrax. [Display omitted] •Phosphate starvation (PS) promotes pathogenesis of B. anthracis (BA) within host.•PhoP and PhoR of BA form a functional two component system, regulating PS response.•PhoP is implicated in regulation of PS marker genes.•H370 of PhoR and D10, D53 and M55 of PhoP are involved in PhoPR interaction.•Exclusive in microbes, homology in pathogens, role in virulence & PS make PhoP as a good drug target. |
Author | Somani, Vikas Kumar Aggarwal, Somya Bhatnagar, Rakesh Singh, Damini Kaur, Jaspreet Grover, Abhinav Gupta, Vatika |
Author_xml | – sequence: 1 givenname: Somya surname: Aggarwal fullname: Aggarwal, Somya organization: Molecular Biology and Genetic Engineering Laboratory, School of Biotechnology, Jawaharlal Nehru University, New Delhi, India – sequence: 2 givenname: Vikas Kumar surname: Somani fullname: Somani, Vikas Kumar organization: Molecular Biology and Genetic Engineering Laboratory, School of Biotechnology, Jawaharlal Nehru University, New Delhi, India – sequence: 3 givenname: Vatika surname: Gupta fullname: Gupta, Vatika organization: Molecular Biology and Genetic Engineering Laboratory, School of Biotechnology, Jawaharlal Nehru University, New Delhi, India – sequence: 4 givenname: Jaspreet surname: Kaur fullname: Kaur, Jaspreet organization: School of Biotechnology, Jawaharlal Nehru University, New Delhi, India – sequence: 5 givenname: Damini surname: Singh fullname: Singh, Damini organization: Molecular Biology and Genetic Engineering Laboratory, School of Biotechnology, Jawaharlal Nehru University, New Delhi, India – sequence: 6 givenname: Abhinav surname: Grover fullname: Grover, Abhinav organization: School of Biotechnology, Jawaharlal Nehru University, New Delhi, India – sequence: 7 givenname: Rakesh surname: Bhatnagar fullname: Bhatnagar, Rakesh email: rakeshbhatnagar@jnu.ac.in organization: Molecular Biology and Genetic Engineering Laboratory, School of Biotechnology, Jawaharlal Nehru University, New Delhi, India |
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Keywords | RR Bacillus anthracis PhoPR HK PS TCS HRP Response regulator AcP AP Histidine kinase EMSA Phosphate starvation Two component system MBP MSA ELISA |
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Snippet | Recent report on importance of phosphate starvation (PS) in Bacillus anthracis (BA) pathogenesis warrants further investigation of the underlying regulatory... |
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SubjectTerms | Amino Acid Sequence Amino Acids - metabolism Animals anthrax Bacillus anthracis Bacillus anthracis - drug effects Bacillus anthracis - genetics Bacillus anthracis - metabolism Bacillus anthracis - pathogenicity Bacterial Proteins - chemistry Bacterial Proteins - metabolism Base Sequence Computer Simulation DNA, Bacterial - metabolism drugs Gene Expression Regulation, Bacterial - drug effects genetic markers Histidine kinase homeostasis Homeostasis - drug effects Mice Molecular Dynamics Simulation Operon - genetics pathogenesis pathogens PhoPR Phosphate starvation phosphates Phosphates - metabolism Phosphates - pharmacology Phosphorylation - drug effects prokaryotic cells Promoter Regions, Genetic Protein Binding - drug effects protein phosphorylation quantitative polymerase chain reaction Real-Time Polymerase Chain Reaction Reproducibility of Results Response regulator reverse transcriptase polymerase chain reaction Sequence Homology, Amino Acid Signal Transduction - drug effects starvation Survival Analysis Two component system Up-Regulation - drug effects virulence Virulence - drug effects Virulence - genetics |
Title | Functional characterization of PhoPR two component system and its implication in regulating phosphate homeostasis in Bacillus anthracis |
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