Optimized production of a biologically active Clostridium perfringens glycosyl hydrolase phage endolysin PlyCP41 in plants using virus-based systemic expression

Abstract Background Clostridium perfringens, a gram-positive, anaerobic, rod-shaped bacterium, is the third leading cause of human foodborne bacterial disease and a cause of necrotic enteritis in poultry. It is controlled using antibiotics, widespread use of which may lead to development of drug-res...

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Main Authors: Rosemarie W. Hammond, Steven M. Swift, Juli A. Foster-Frey, Natalia Y. Kovalskaya, David M. Donovan
Format: Article
Language:English
Published: BMC 2019-12-01
Series:BMC Biotechnology
Subjects:
Online Access:https://doi.org/10.1186/s12896-019-0594-7
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spelling doaj-cdadf63053314b40b58356495d0173392020-12-20T12:20:55ZengBMCBMC Biotechnology1472-67502019-12-0119111010.1186/s12896-019-0594-7Optimized production of a biologically active Clostridium perfringens glycosyl hydrolase phage endolysin PlyCP41 in plants using virus-based systemic expressionRosemarie W. Hammond0Steven M. Swift1Juli A. Foster-Frey2Natalia Y. Kovalskaya3David M. Donovan4USDA ARS NEA BARC Molecular Plant Pathology LaboratoryUSDA ARS NEA BARC Animal Biosciences and Biotechnology LaboratoryUSDA ARS NEA BARC Animal Biosciences and Biotechnology LaboratoryUSDA ARS NEA BARC Molecular Plant Pathology LaboratoryUSDA ARS NEA BARC Animal Biosciences and Biotechnology LaboratoryAbstract Background Clostridium perfringens, a gram-positive, anaerobic, rod-shaped bacterium, is the third leading cause of human foodborne bacterial disease and a cause of necrotic enteritis in poultry. It is controlled using antibiotics, widespread use of which may lead to development of drug-resistant bacteria. Bacteriophage-encoded endolysins that degrade peptidoglycans in the bacterial cell wall are potential replacements for antibiotics. Phage endolysins have been identified that exhibit antibacterial activities against several Clostridium strains. Results An Escherichia coli codon-optimized gene encoding the glycosyl hydrolase endolysin (PlyCP41) containing a polyhistidine tag was expressed in E. coli. In addition, The E. coli optimized endolysin gene was engineered for expression in plants (PlyCP41p) and a plant codon-optimized gene (PlyCP41pc), both containing a polyhistidine tag, were expressed in Nicotiana benthamiana plants using a potato virus X (PVX)-based transient expression vector. PlyCP41p accumulated to ~ 1% total soluble protein (100μg/gm f. wt. leaf tissue) without any obvious toxic effects on plant cells, and both the purified protein and plant sap containing the protein lysed C. perfringens strain Cp39 in a plate lysis assay. Optimal systemic expression of PlyCP41p was achieved at 2 weeks-post-infection. PlyCP41pc did not accumulate to higher levels than PlyCP41p in infected tissue. Conclusion We demonstrated that functionally active bacteriophage PlyCP41 endolysin can be produced in systemically infected plant tissue with potential for use of crude plant sap as an effective antimicrobial agent against C. perfringens.https://doi.org/10.1186/s12896-019-0594-7Alternative antimicrobialBacteriophageEndolysinNicotiana benthamianaPlant production of recombinant proteinsPlant virus-based gene expression
collection DOAJ
language English
format Article
sources DOAJ
author Rosemarie W. Hammond
Steven M. Swift
Juli A. Foster-Frey
Natalia Y. Kovalskaya
David M. Donovan
spellingShingle Rosemarie W. Hammond
Steven M. Swift
Juli A. Foster-Frey
Natalia Y. Kovalskaya
David M. Donovan
Optimized production of a biologically active Clostridium perfringens glycosyl hydrolase phage endolysin PlyCP41 in plants using virus-based systemic expression
BMC Biotechnology
Alternative antimicrobial
Bacteriophage
Endolysin
Nicotiana benthamiana
Plant production of recombinant proteins
Plant virus-based gene expression
author_facet Rosemarie W. Hammond
Steven M. Swift
Juli A. Foster-Frey
Natalia Y. Kovalskaya
David M. Donovan
author_sort Rosemarie W. Hammond
title Optimized production of a biologically active Clostridium perfringens glycosyl hydrolase phage endolysin PlyCP41 in plants using virus-based systemic expression
title_short Optimized production of a biologically active Clostridium perfringens glycosyl hydrolase phage endolysin PlyCP41 in plants using virus-based systemic expression
title_full Optimized production of a biologically active Clostridium perfringens glycosyl hydrolase phage endolysin PlyCP41 in plants using virus-based systemic expression
title_fullStr Optimized production of a biologically active Clostridium perfringens glycosyl hydrolase phage endolysin PlyCP41 in plants using virus-based systemic expression
title_full_unstemmed Optimized production of a biologically active Clostridium perfringens glycosyl hydrolase phage endolysin PlyCP41 in plants using virus-based systemic expression
title_sort optimized production of a biologically active clostridium perfringens glycosyl hydrolase phage endolysin plycp41 in plants using virus-based systemic expression
publisher BMC
series BMC Biotechnology
issn 1472-6750
publishDate 2019-12-01
description Abstract Background Clostridium perfringens, a gram-positive, anaerobic, rod-shaped bacterium, is the third leading cause of human foodborne bacterial disease and a cause of necrotic enteritis in poultry. It is controlled using antibiotics, widespread use of which may lead to development of drug-resistant bacteria. Bacteriophage-encoded endolysins that degrade peptidoglycans in the bacterial cell wall are potential replacements for antibiotics. Phage endolysins have been identified that exhibit antibacterial activities against several Clostridium strains. Results An Escherichia coli codon-optimized gene encoding the glycosyl hydrolase endolysin (PlyCP41) containing a polyhistidine tag was expressed in E. coli. In addition, The E. coli optimized endolysin gene was engineered for expression in plants (PlyCP41p) and a plant codon-optimized gene (PlyCP41pc), both containing a polyhistidine tag, were expressed in Nicotiana benthamiana plants using a potato virus X (PVX)-based transient expression vector. PlyCP41p accumulated to ~ 1% total soluble protein (100μg/gm f. wt. leaf tissue) without any obvious toxic effects on plant cells, and both the purified protein and plant sap containing the protein lysed C. perfringens strain Cp39 in a plate lysis assay. Optimal systemic expression of PlyCP41p was achieved at 2 weeks-post-infection. PlyCP41pc did not accumulate to higher levels than PlyCP41p in infected tissue. Conclusion We demonstrated that functionally active bacteriophage PlyCP41 endolysin can be produced in systemically infected plant tissue with potential for use of crude plant sap as an effective antimicrobial agent against C. perfringens.
topic Alternative antimicrobial
Bacteriophage
Endolysin
Nicotiana benthamiana
Plant production of recombinant proteins
Plant virus-based gene expression
url https://doi.org/10.1186/s12896-019-0594-7
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