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Engineering Bacteriophages as Versatile Biologics
Viruses of bacteria (bacteriophages or phages) are highly evolved nanomachines that recognize bacterial cell walls, deliver genetic information, and kill or transform their targets with unparalleled specificity. For a long time, the use of genetically modified phages was limited to phage display app...
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Published in: | Trends in microbiology (Regular ed.) 2019-04, Vol.27 (4), p.355-367 |
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creator | Kilcher, Samuel Loessner, Martin J. |
description | Viruses of bacteria (bacteriophages or phages) are highly evolved nanomachines that recognize bacterial cell walls, deliver genetic information, and kill or transform their targets with unparalleled specificity. For a long time, the use of genetically modified phages was limited to phage display approaches and fundamental research. This is mostly because phage engineering has been a complex and time-consuming task, applicable for only a few well characterized model phages. Recent advances in sequencing technology and molecular biology gave rise to rapid and precise tools that enable modification of less-well-characterized phages. These methods will pave the way for the development of modular designer-phages as versatile biologics that efficiently control multidrug-resistant bacteria and provide novel tools for pathogen detection, drug development, and beyond.
The increasing prevalence of antibiotic-resistant pathogenic bacteria has sparked renewed interest in bacteriophage therapy.
Synthetic biology methods allow design, straightforward construction, and testing of engineered bacteriophages that target both Gram-positive and Gram-negative bacteria.
Phages with small genomes are easier to engineer using synthetic methods, while recombination-based approaches are currently the method of choice for larger phages.
The efficiency, safety, and therapeutic suitability of phage-based antimicrobials can be specifically tailored through targeted phage engineering.
In contrast to non-modified viruses, engineered phages offer intellectual property protection opportunities that may fuel the commercial implementation of phage therapy in many countries. |
doi_str_mv | 10.1016/j.tim.2018.09.006 |
format | article |
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The increasing prevalence of antibiotic-resistant pathogenic bacteria has sparked renewed interest in bacteriophage therapy.
Synthetic biology methods allow design, straightforward construction, and testing of engineered bacteriophages that target both Gram-positive and Gram-negative bacteria.
Phages with small genomes are easier to engineer using synthetic methods, while recombination-based approaches are currently the method of choice for larger phages.
The efficiency, safety, and therapeutic suitability of phage-based antimicrobials can be specifically tailored through targeted phage engineering.
In contrast to non-modified viruses, engineered phages offer intellectual property protection opportunities that may fuel the commercial implementation of phage therapy in many countries.</description><identifier>ISSN: 0966-842X</identifier><identifier>EISSN: 1878-4380</identifier><identifier>DOI: 10.1016/j.tim.2018.09.006</identifier><identifier>PMID: 30322741</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Bacteria ; bacteriophage ; Biological evolution ; Biopharmaceuticals ; Cell walls ; Drug development ; Engineering ; Genetic modification ; genome engineering ; Modular design ; Molecular biology ; Multidrug resistance ; Phage display ; phage therapy ; Phages ; synthetic biology ; Viruses</subject><ispartof>Trends in microbiology (Regular ed.), 2019-04, Vol.27 (4), p.355-367</ispartof><rights>2018 Elsevier Ltd</rights><rights>Copyright © 2018 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Apr 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-ba0a1db20ac3398a5396ebd25142326c0e9820e3ce3ab3efa455451e854d76483</citedby><cites>FETCH-LOGICAL-c447t-ba0a1db20ac3398a5396ebd25142326c0e9820e3ce3ab3efa455451e854d76483</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30322741$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kilcher, Samuel</creatorcontrib><creatorcontrib>Loessner, Martin J.</creatorcontrib><title>Engineering Bacteriophages as Versatile Biologics</title><title>Trends in microbiology (Regular ed.)</title><addtitle>Trends Microbiol</addtitle><description>Viruses of bacteria (bacteriophages or phages) are highly evolved nanomachines that recognize bacterial cell walls, deliver genetic information, and kill or transform their targets with unparalleled specificity. For a long time, the use of genetically modified phages was limited to phage display approaches and fundamental research. This is mostly because phage engineering has been a complex and time-consuming task, applicable for only a few well characterized model phages. Recent advances in sequencing technology and molecular biology gave rise to rapid and precise tools that enable modification of less-well-characterized phages. These methods will pave the way for the development of modular designer-phages as versatile biologics that efficiently control multidrug-resistant bacteria and provide novel tools for pathogen detection, drug development, and beyond.
The increasing prevalence of antibiotic-resistant pathogenic bacteria has sparked renewed interest in bacteriophage therapy.
Synthetic biology methods allow design, straightforward construction, and testing of engineered bacteriophages that target both Gram-positive and Gram-negative bacteria.
Phages with small genomes are easier to engineer using synthetic methods, while recombination-based approaches are currently the method of choice for larger phages.
The efficiency, safety, and therapeutic suitability of phage-based antimicrobials can be specifically tailored through targeted phage engineering.
In contrast to non-modified viruses, engineered phages offer intellectual property protection opportunities that may fuel the commercial implementation of phage therapy in many countries.</description><subject>Bacteria</subject><subject>bacteriophage</subject><subject>Biological evolution</subject><subject>Biopharmaceuticals</subject><subject>Cell walls</subject><subject>Drug development</subject><subject>Engineering</subject><subject>Genetic modification</subject><subject>genome engineering</subject><subject>Modular design</subject><subject>Molecular biology</subject><subject>Multidrug resistance</subject><subject>Phage display</subject><subject>phage therapy</subject><subject>Phages</subject><subject>synthetic biology</subject><subject>Viruses</subject><issn>0966-842X</issn><issn>1878-4380</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kDtPwzAUhS0EoqXwA1hQJRaWhOtX4oiJVuUhVWIBxGY5zm1xlSbFTpD497hqYWBgumf4ztHVR8g5hZQCza5XaefWKQOqUihSgOyADKnKVSK4gkMyhCLLEiXY24CchLACACmZPCYDDpyxXNAhobNm6RpE75rleGJsF1O7eTdLDGMTxq_og-lcjeOJa-t26Ww4JUcLUwc8298RebmbPU8fkvnT_eP0dp5YIfIuKQ0YWpUMjOW8UEbyIsOyYpIKxllmAQvFALlFbkqOCyOkFJKikqLKM6H4iFztdje-_egxdHrtgsW6Ng22fdCMMsilLCSL6OUfdNX2vonfacagkAokQKTojrK-DcHjQm-8Wxv_pSnorU-90tGn3vrUUOjoM3Yu9st9ucbqt_EjMAI3OwCjik-HXgfrsLFYOY-201Xr_pn_BqaSg6c</recordid><startdate>201904</startdate><enddate>201904</enddate><creator>Kilcher, Samuel</creator><creator>Loessner, Martin J.</creator><general>Elsevier Ltd</general><general>Elsevier Science Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201904</creationdate><title>Engineering Bacteriophages as Versatile Biologics</title><author>Kilcher, Samuel ; Loessner, Martin J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-ba0a1db20ac3398a5396ebd25142326c0e9820e3ce3ab3efa455451e854d76483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Bacteria</topic><topic>bacteriophage</topic><topic>Biological evolution</topic><topic>Biopharmaceuticals</topic><topic>Cell walls</topic><topic>Drug development</topic><topic>Engineering</topic><topic>Genetic modification</topic><topic>genome engineering</topic><topic>Modular design</topic><topic>Molecular biology</topic><topic>Multidrug resistance</topic><topic>Phage display</topic><topic>phage therapy</topic><topic>Phages</topic><topic>synthetic biology</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kilcher, Samuel</creatorcontrib><creatorcontrib>Loessner, Martin J.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Trends in microbiology (Regular ed.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kilcher, Samuel</au><au>Loessner, Martin J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Engineering Bacteriophages as Versatile Biologics</atitle><jtitle>Trends in microbiology (Regular ed.)</jtitle><addtitle>Trends Microbiol</addtitle><date>2019-04</date><risdate>2019</risdate><volume>27</volume><issue>4</issue><spage>355</spage><epage>367</epage><pages>355-367</pages><issn>0966-842X</issn><eissn>1878-4380</eissn><abstract>Viruses of bacteria (bacteriophages or phages) are highly evolved nanomachines that recognize bacterial cell walls, deliver genetic information, and kill or transform their targets with unparalleled specificity. 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The increasing prevalence of antibiotic-resistant pathogenic bacteria has sparked renewed interest in bacteriophage therapy.
Synthetic biology methods allow design, straightforward construction, and testing of engineered bacteriophages that target both Gram-positive and Gram-negative bacteria.
Phages with small genomes are easier to engineer using synthetic methods, while recombination-based approaches are currently the method of choice for larger phages.
The efficiency, safety, and therapeutic suitability of phage-based antimicrobials can be specifically tailored through targeted phage engineering.
In contrast to non-modified viruses, engineered phages offer intellectual property protection opportunities that may fuel the commercial implementation of phage therapy in many countries.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>30322741</pmid><doi>10.1016/j.tim.2018.09.006</doi><tpages>13</tpages></addata></record> |
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subjects | Bacteria bacteriophage Biological evolution Biopharmaceuticals Cell walls Drug development Engineering Genetic modification genome engineering Modular design Molecular biology Multidrug resistance Phage display phage therapy Phages synthetic biology Viruses |
title | Engineering Bacteriophages as Versatile Biologics |
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