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Published on: July 28, 2016
Recombinant Myeloperoxidase as a New Class of Antimicrobial Agents
1Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, University of Alabama School of Medicine, Birmingham, Alabama, USA.
Abstract:
Heme-containing peroxidases are widely distributed in the animal and plant kingdoms and play an important role in host defense by generating potent oxidants. Myeloperoxidase (MPO), the prototype of heme-containing peroxidases, exists in neutrophils and monocytes. MPO has a broad spectrum of microbial killing. The difficulty of producing MPO at a large scale hinders its study and utilization. This study aimed to overexpress recombinant human MPO and characterize its microbicidal activities in vitro and in vivo. A human HEK293 cell line stably expressing recombinant MPO (rMPO) was established as a component of this study. rMPO was overexpressed and purified for studies on its biochemical and enzymatic properties, as well as its microbicidal activities. In this study, rMPO was secreted into culture medium as a monomer. rMPO revealed enzymatic activity similar to that of native MPO. rMPO, like native MPO, was capable of killing a broad spectrum of microorganisms, including Gram-negative and -positive bacteria and fungi, at low nM levels. Interestingly, rMPO could kill antibiotic-resistant bacteria, making it very useful for treatment of nosocomial infections and mixed infections. The administration of rMPO significantly reduced the morbidity and mortality of murine lung infections induced by Pseudomonas aeruginosa or methicillin-resistant Staphylococcus aureus. In animal safety tests, the administration of 100 nM rMPO via tail vein did not result in any sign of toxic effects. Taken together, the data suggest that rMPO purified from a stably expressing human cell line is a new class of antimicrobial agents with the ability to kill a broad spectrum of pathogens, including bacteria and fungi with or without drug resistance. IMPORTANCE Over the past 2 decades, more than 20 new infectious diseases have emerged. Unfortunately, novel antimicrobial therapeutics are discovered at much lower rates. Infections caused by resistant microorganisms often fail to respond to conventional treatment, resulting in prolonged illness, greater risk of death, and high health care costs. Currently, this is best seen with the lack of a cure for coronavirus disease 2019 (COVID-19). To combat such untreatable microorganisms, there is an urgent need to discover new classes of antimicrobial agents. Myeloperoxidase (MPO) plays an important role in host defense. The difficulty of producing MPO on a large scale hinders its study and utilization. We have produced recombinant MPO at a large scale and have characterized its antimicrobial activities. Most importantly, recombinant MPO significantly reduced the morbidity and mortality of murine pneumonia induced by Pseudomonas aeruginosa or methicillin-resistant Staphylococcus aureus. Our data suggest that recombinant MPO from human cells is a new class of antimicrobials with a broad spectrum of activity.
Insights
Recombinant human myeloperoxidase (MPO) effectively kills a broad range of pathogens, including antibiotic-resistant bacteria. This new antimicrobial agent shows promise in treating infections and reducing disease severity in animal models with no observed toxicity.
Area of Science:
- Biochemistry and Microbiology
- Host Defense Mechanisms
- Antimicrobial Therapeutics
Background:
- Heme-containing peroxidases, like myeloperoxidase (MPO), are crucial for host defense, generating potent oxidants.
- MPO, found in neutrophils and monocytes, exhibits broad-spectrum antimicrobial activity but faces production challenges.
- The emergence of infectious diseases and antimicrobial resistance necessitates novel therapeutic agents.
Purpose of the Study:
- To overexpress recombinant human MPO (rMPO) for large-scale production and characterization.
- To evaluate the biochemical properties and microbicidal activities of rMPO in vitro and in vivo.
- To assess the potential of rMPO as a novel antimicrobial agent.
Main Methods:
- Established a human HEK293 cell line for stable expression of recombinant MPO (rMPO).
- Overexpressed and purified rMPO, analyzing its enzymatic activity and biochemical properties.
- Tested rMPO's microbicidal efficacy against various microorganisms and evaluated its therapeutic effect in murine infection models.
Main Results:
- Secreted rMPO demonstrated enzymatic activity comparable to native MPO.
- rMPO exhibited potent microbicidal activity against Gram-negative bacteria, Gram-positive bacteria, and fungi at low nanomolar concentrations.
- rMPO effectively reduced morbidity and mortality in murine models of Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus infections.
- Safety tests showed no toxic effects upon administration of rMPO.
Conclusions:
- Recombinant human MPO is a potent antimicrobial agent with broad-spectrum activity against diverse pathogens, including drug-resistant strains.
- rMPO demonstrates significant therapeutic potential for treating bacterial and fungal infections, including nosocomial and mixed infections.
- Large-scale production of rMPO from a human cell line offers a viable strategy for developing new antimicrobial therapies.
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