Phage engineering to overcome bacterial Tmn immunity in Dhillonvirus
Phage engineering to overcome bacterial Tmn immunity in Dhillonvirus
Bacteria possess numerous defense systems against phage infections, which limit phage infectivity and pose challenges for phage therapy. This study aimed to engineer phages capable of evading these defense systems, using the Tmn defense system as a model. We identified an anti-Tmn protein in the ΦSMS22 phage from the Dhillonvirus genus that inhibits Tmn function in Escherichia coli. Introducing this gene into the Tmn-sensitive ΦKSS9 phage enabled it to evade Tmn immunity. Additionally, we found that a single mutation in the nmad5 gene, a DNA modification enzyme in Dhillonvirus, prevented Tmn from sensing phage infection. By mutating the nmad5 gene in the Tmn-sensitive Dhillonvirus, we demonstrated that engineering phages to evade bacterial sensing mechanisms is another viable strategy. These two phage engineering approaches—introducing anti-defense genes and mutating sensing-related genes—present a promising strategy for establishing effective phage therapy by neutralizing bacterial defense systems.
Yamashita, Wakana
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Chihara, Kotaro
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Azam, Aa Haeruman
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Kondo, Kohei
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Ojima, Shinjiro
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Tamura, Azumi
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Imanaka, Matthew
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Nobrega, Franklin L.
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Takahashi, Yoshimasa
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Watashi, Koichi
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Tsuneda, Satoshi
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Kiga, Kotaro
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22 February 2025
Yamashita, Wakana
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Chihara, Kotaro
0d4d93f3-8235-4e78-9eeb-bb8aba42d165
Azam, Aa Haeruman
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Kondo, Kohei
e2fc593a-b1e4-4726-8e93-a4d31b207c2f
Ojima, Shinjiro
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Tamura, Azumi
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Imanaka, Matthew
fe2cb038-6c36-4731-9009-b2ac93e64077
Nobrega, Franklin L.
6532795d-88a4-4f05-9b26-6af5b8f21a0d
Takahashi, Yoshimasa
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Watashi, Koichi
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Tsuneda, Satoshi
91120ea9-3f13-40f2-9c4d-0f0cb4784515
Kiga, Kotaro
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Yamashita, Wakana, Chihara, Kotaro, Azam, Aa Haeruman, Kondo, Kohei, Ojima, Shinjiro, Tamura, Azumi, Imanaka, Matthew, Nobrega, Franklin L., Takahashi, Yoshimasa, Watashi, Koichi, Tsuneda, Satoshi and Kiga, Kotaro
(2025)
Phage engineering to overcome bacterial Tmn immunity in Dhillonvirus.
Communications Biology, 8 (1), [290].
(doi:10.1038/s42003-025-07730-8).
Abstract
Bacteria possess numerous defense systems against phage infections, which limit phage infectivity and pose challenges for phage therapy. This study aimed to engineer phages capable of evading these defense systems, using the Tmn defense system as a model. We identified an anti-Tmn protein in the ΦSMS22 phage from the Dhillonvirus genus that inhibits Tmn function in Escherichia coli. Introducing this gene into the Tmn-sensitive ΦKSS9 phage enabled it to evade Tmn immunity. Additionally, we found that a single mutation in the nmad5 gene, a DNA modification enzyme in Dhillonvirus, prevented Tmn from sensing phage infection. By mutating the nmad5 gene in the Tmn-sensitive Dhillonvirus, we demonstrated that engineering phages to evade bacterial sensing mechanisms is another viable strategy. These two phage engineering approaches—introducing anti-defense genes and mutating sensing-related genes—present a promising strategy for establishing effective phage therapy by neutralizing bacterial defense systems.
Text
s42003-025-07730-8
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Published date: 22 February 2025
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Local EPrints ID: 511528
URI: http://eprints.soton.ac.uk/id/eprint/511528
ISSN: 2399-3642
PURE UUID: fd0eb599-559f-454d-83aa-4f5e6718ec45
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Date deposited: 18 May 2026 17:09
Last modified: 19 May 2026 01:59
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Contributors
Author:
Wakana Yamashita
Author:
Kotaro Chihara
Author:
Aa Haeruman Azam
Author:
Kohei Kondo
Author:
Shinjiro Ojima
Author:
Azumi Tamura
Author:
Matthew Imanaka
Author:
Yoshimasa Takahashi
Author:
Koichi Watashi
Author:
Satoshi Tsuneda
Author:
Kotaro Kiga
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