Isolation and characterization of HepP: a virulence-related Pseudomonas aeruginosa heparinase
| Autor: | Abdul N. Hamood, John A. Griswold, Nyaradzo Dzvova, Jane A. Colmer-Hamood |
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| Jazyk: | angličtina |
| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
Microbiology (medical) Operon Virulence Factors 030106 microbiology lcsh:QR1-502 Virulence Biology medicine.disease_cause Microbiology Virulence factor lcsh:Microbiology Gene Expression Regulation Enzymologic law.invention 03 medical and health sciences Immunocompromised Host Bacterial Proteins law medicine Escherichia coli Animals Humans C. elegans killing model Pseudomonas Infections Caenorhabditis elegans Whole blood Heparinase Pellicle Pseudomonas aeruginosa Biofilm Gene Expression Profiling biochemical phenomena metabolism and nutrition bacterial infections and mycoses Recombinant Proteins 030104 developmental biology Heparin Lyase Biofilms Mutation Recombinant DNA Burns Research Article |
| Zdroj: | BMC Microbiology BMC Microbiology, Vol 17, Iss 1, Pp 1-16 (2017) |
| ISSN: | 1471-2180 |
| Popis: | Background Pseudomonas aeruginosa is an opportunistic pathogen that causes serious infections in immunocompromised hosts including severely burned patients. In burn patients, P. aeruginosa infection often leads to septic shock and death. Despite numerous studies, the influence of severe thermal injuries on the pathogenesis of P. aeruginosa during systemic infection is not known. Through RNA-seq analysis, we recently showed that the growth of P. aeruginosa strain UCBPP-PA14 (PA14) in whole blood obtained from severely burned patients significantly altered the expression of the PA14 transcriptome when compared with its growth in blood from healthy volunteers. The expression of PA14_23430 and the adjacent gene, PA14_23420, was enhanced by seven- to eightfold under these conditions. Results Quantitative real-time PCR analysis confirmed the enhancement of expression of both PA14_23420 and PA14_23430 by growth of PA14 in blood from severely burned patients. Computer analysis revealed that PA14_23430 (hepP) encodes a potential heparinase while PA14_23420 (zbdP) codes for a putative zinc-binding dehydrogenase. This analysis further suggested that the two genes form an operon with zbdP first. Presence of the operon was confirmed by RT-PCR experiments. We characterized hepP and its protein product HepP. hepP was cloned from PA14 by PCR and overexpressed in E. coli. The recombinant protein (rHepP) was purified using nickel column chromatography. Heparinase assays using commercially available heparinase as a positive control, revealed that rHepP exhibits heparinase activity. Mutation of hepP resulted in delay of pellicle formation at the air-liquid interface by PA14 under static growth conditions. Biofilm formation by PA14ΔhepP was also significantly reduced. In the Caenorhabditis elegans model of slow killing, mutation of hepP resulted in a significantly lower rate of killing than that of the parent strain PA14. Conclusions Changes within the blood of severely burned patients significantly induced expression of hepP in PA14. The heparinase encoded by hepP is a potential virulence factor for PA14 as HepP influences pellicle formation as well as biofilm development by PA14 and the protein is required for full virulence in the C. elegans model of slow killing. Electronic supplementary material The online version of this article (10.1186/s12866-017-1141-0) contains supplementary material, which is available to authorized users. |
| Databáze: | OpenAIRE |
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