Genetically manipulated phages with improved pH resistance for oral administration in veterinary medicine
Genetically manipulated phages with improved pH resistance for oral administration in veterinary medicine
Orally administered phages to control zoonotic pathogens face important challenges, mainly related to the hostile conditions found in the gastrointestinal tract (GIT). These include temperature, salinity and primarily pH, which is exceptionally low in certain compartments. Phage survival under these conditions can be jeopardized and undermine treatment. Strategies like encapsulation have been attempted with relative success, but are typically complex and require several optimization steps. Here we report a simple and efficient alternative, consisting in the genetic engineering of phages to display lipids on their surfaces. Escherichia coli phage T7 was used as a model and the E. coli PhoE signal peptide was genetically fused to its major capsid protein (10 A), enabling phospholipid attachment to the phage capsid. The presence of phospholipids on the mutant phages was confirmed by High Performance Thin Layer Chromatography, Dynamic Light Scattering and phospholipase assays. The stability of phages was analysed in simulated GIT conditions, demonstrating improved stability of the mutant phages with survival rates 102–107 pfu.mL−1 higher than wild-type phages. Our work demonstrates that phage engineering can be a good strategy to improve phage tolerance to GIT conditions, having promising application for oral administration in veterinary medicine.
Luzia De Nobrega, Franklin
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Costa, Ana Rita
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Santos, José F.
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Siliakus, Melvin F.
8f1c7ad2-55fa-49f0-be6e-0b01282243e0
van Lent, Jan W.M.
ca09f648-2778-4318-9c2c-d58c4b7ad650
Kengen, S.W.M.
41a92c4f-01d9-4a49-8d36-238c9c3f52d0
Azeredo, Joana
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Kluskens, Leon
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15 December 2016
Luzia De Nobrega, Franklin
6532795d-88a4-4f05-9b26-6af5b8f21a0d
Costa, Ana Rita
a1d2b803-b767-4418-a21c-516671e9b40d
Santos, José F.
a6f5f2cf-8741-4823-bb2c-eb047b38c301
Siliakus, Melvin F.
8f1c7ad2-55fa-49f0-be6e-0b01282243e0
van Lent, Jan W.M.
ca09f648-2778-4318-9c2c-d58c4b7ad650
Kengen, S.W.M.
41a92c4f-01d9-4a49-8d36-238c9c3f52d0
Azeredo, Joana
0e6aef86-c71c-4b48-a071-0c7cc93fe042
Kluskens, Leon
12623693-d537-4522-8369-3cbe51f59ee3
Luzia De Nobrega, Franklin, Costa, Ana Rita, Santos, José F., Siliakus, Melvin F., van Lent, Jan W.M., Kengen, S.W.M., Azeredo, Joana and Kluskens, Leon
(2016)
Genetically manipulated phages with improved pH resistance for oral administration in veterinary medicine.
Scientific Reports, 6, [39235].
(doi:10.1038/srep39235).
Abstract
Orally administered phages to control zoonotic pathogens face important challenges, mainly related to the hostile conditions found in the gastrointestinal tract (GIT). These include temperature, salinity and primarily pH, which is exceptionally low in certain compartments. Phage survival under these conditions can be jeopardized and undermine treatment. Strategies like encapsulation have been attempted with relative success, but are typically complex and require several optimization steps. Here we report a simple and efficient alternative, consisting in the genetic engineering of phages to display lipids on their surfaces. Escherichia coli phage T7 was used as a model and the E. coli PhoE signal peptide was genetically fused to its major capsid protein (10 A), enabling phospholipid attachment to the phage capsid. The presence of phospholipids on the mutant phages was confirmed by High Performance Thin Layer Chromatography, Dynamic Light Scattering and phospholipase assays. The stability of phages was analysed in simulated GIT conditions, demonstrating improved stability of the mutant phages with survival rates 102–107 pfu.mL−1 higher than wild-type phages. Our work demonstrates that phage engineering can be a good strategy to improve phage tolerance to GIT conditions, having promising application for oral administration in veterinary medicine.
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Accepted/In Press date: 18 November 2016
Published date: 15 December 2016
Identifiers
Local EPrints ID: 443072
URI: http://eprints.soton.ac.uk/id/eprint/443072
ISSN: 2045-2322
PURE UUID: 965aa2f3-5ac0-4e2f-8a57-d498d4d248ea
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Date deposited: 10 Aug 2020 16:30
Last modified: 17 Mar 2024 04:02
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Contributors
Author:
Ana Rita Costa
Author:
José F. Santos
Author:
Melvin F. Siliakus
Author:
Jan W.M. van Lent
Author:
S.W.M. Kengen
Author:
Joana Azeredo
Author:
Leon Kluskens
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