Sung Dayoung, Choi Garam, Ahn Minji, Byun Hokyung, Kim Tae Young, Lee Hojun, Lee Zee-Won, Park Ji Yong, Jung Young Hyun, Han Ho Jae, Choi Sang Ho
National Research Laboratory of Molecular Microbiology and Toxicology, Department of Agricultural Biotechnology, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea.
Department of Veterinary Physiology, College of Veterinary Medicine and Research Institute for Veterinary Science, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea.
Nucleic Acids Res. 2025 Jan 24;53(3). doi: 10.1093/nar/gkae1238.
For successful infection, the life-threatening pathogen Vibrio vulnificus elaborately regulates the expression of survival and virulence genes using various transcription factors (TFs). In this study, a library of the V. vulnificus mutants carrying specific signature tags in 285 TF genes was constructed and subjected to 16 phenotypic analyses. Consequently, 89 TFs affecting more than one phenotype of V. vulnificus were identified. Of these, 59 TFs affected the in vitro survival including growth, stress resistance, biofilm formation and motility, and 64 TFs affected the virulence of V. vulnificus. Particularly, 27 of the 64 TFs enhanced the in vitro hemolytic or cytotoxic activities, and 8 of the 27 TFs also increased the in vivo brine shrimp or murine infectivities of V. vulnificus. Among the eight TFs, HlyU, IscR, NagC, MetJ and Tet2 did not affect the growth of V. vulnificus but still regulated the expression of major exotoxin genes, including rtxA, vvhA and plpA, thereby emerging as potential drug targets for anti-virulence therapies with low selective pressure for developing resistance. Altogether, this study characterized the functions of TFs at a genome-wide scale and identified novel targets to control the virulence of V. vulnificus.
为了成功感染,危及生命的病原菌创伤弧菌利用多种转录因子(TFs)精细地调控生存和毒力基因的表达。在本研究中,构建了一个在285个TF基因中携带特定特征标签的创伤弧菌突变体文库,并进行了16种表型分析。结果,鉴定出89个影响创伤弧菌一种以上表型的转录因子。其中,59个转录因子影响体外生存,包括生长、抗逆性、生物膜形成和运动性,64个转录因子影响创伤弧菌的毒力。特别地,64个转录因子中的27个增强了体外溶血或细胞毒性活性,27个转录因子中的8个也增加了创伤弧菌在体内对卤虫或小鼠的感染性。在这8个转录因子中,HlyU、IscR、NagC、MetJ和Tet2不影响创伤弧菌的生长,但仍调控包括rtxA、vvhA和plpA在内的主要外毒素基因的表达,从而成为抗毒力治疗的潜在药物靶点,产生耐药性的选择压力较低。总之,本研究在全基因组范围内表征了转录因子的功能,并确定了控制创伤弧菌毒力的新靶点。