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Application of a T6SS effector Txe1-based counterselection system for genome editing in Edwardsiella piscicida
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Pengcheng WANG1, Mingming ZHANG1, Chaozheng ZHANG1, Chao LI2, Jianbo CAO1, Xiaojun YAN1, Zhen TAO1
Acta Microbiologica Sinica | 2025, 65(10) : 4565 - 4578
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Acta Microbiologica Sinica | 2025, 65(10): 4565-4578
Research Article
Application of a T6SS effector Txe1-based counterselection system for genome editing in Edwardsiella piscicida
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Pengcheng WANG1, Mingming ZHANG1, Chaozheng ZHANG1, Chao LI2, Jianbo CAO1, Xiaojun YAN1, Zhen TAO1
Affiliations
  • 1College of Fisheries, Zhejiang Ocean University, Zhoushan, Zhejiang, China
  • 2School of Marine Science and Engineering, Qingdao Agricultural University, Qingdao, Shandong, China
Published: 2025-09-04 doi: 10.13343/j.cnki.wsxb.20250220
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Double-crossover homologous recombination using the SacB negative selection system is commonly employed for genome editing in Gram-negative bacteria. However, its negative selection efficiency varies significantly across strains, being frequently compromised by differences in metabolic characteristics or genomic composition. [Objective] To develop a novel counterselection system based on the type VI secretion system (T6SS) effector Txe1 to enhance the efficiency of seamless genome editing. [Methods] We first modified the conventional suicide plasmid pDM4 by introducing a kanamycin resistance gene, generating the derivative plasmid pDM4K. Subsequently, we replaced sacB with an l-arabinose-inducible expression cassette encoding the C-terminal domain of Txe1 (araC-PBAD::txe1CTD ), constructing a novel counterselection plasmid pTL1010. Using the virulence gene tssB of Edwardsiella piscicida FC2 as the target, we systematically evaluated and compared the counterselection efficiency of the Txe1 system with that of the conventional SacB system. [Results] Under induction with l-arabinose, the Txe1-based counterselection system achieved the efficiency of 91.1% (false-positive rate of 8.9%), outperforming the SacB system which had a false-positive rate of 100% (P<0.01). [Conclusion] The newly developed Txe1-based counterselection plasmid pTL1010 significantly enhances the efficiency of seamless genome editing in E. piscicida and provides a highly effective tool for precise genetic manipulation in Gram-negative bacteria.

counterselection marker  /  type VI secretion system  /  Txe1 toxin  /  double-crossover homologous recombination  /  Edwardsiella piscicida
Pengcheng WANG, Mingming ZHANG, Chaozheng ZHANG, Chao LI, Jianbo CAO, Xiaojun YAN, Zhen TAO. Application of a T6SS effector Txe1-based counterselection system for genome editing in Edwardsiella piscicida[J]. Acta Microbiologica Sinica, 2025 , 65 (10) : 4565 -4578 . DOI: 10.13343/j.cnki.wsxb.20250220
  • the National Natural Science Foundation of China(42376108)
Year 2025 volume 65 Issue 10
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Article Info
doi: 10.13343/j.cnki.wsxb.20250220
  • Receive Date:2025-03-19
  • Online Date:2025-11-03
  • Published:2025-09-04
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History
  • Received:2025-03-19
  • Accepted:2025-05-28
Funding
the National Natural Science Foundation of China(42376108)
Affiliations
    1College of Fisheries, Zhejiang Ocean University, Zhoushan, Zhejiang, China
    2School of Marine Science and Engineering, Qingdao Agricultural University, Qingdao, Shandong, China

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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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