Pang Maoda, Xie Xing, Dong Yuhao, Du Hechao, Wang Nannan, Lu Chengping, Liu Yongjie
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, China; Key Lab of Food Quality and Safety of Jiangsu Province-State Key Laboratory Breeding Base, Institute of Food Safety, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, China.
Vet Microbiol. 2017 Feb;199:36-46. doi: 10.1016/j.vetmic.2016.12.021. Epub 2016 Dec 20.
Outbreaks of motile Aeromonad septicemia (MAS) in fish caused by sequence type (ST) 251 Aeromonas hydrophila have become a prominent problem for the aquaculture industry. The pathogenesis of A. hydrophila is very complicated, and some virulence factors remain to be identified. In this study, to identify novel virulence-related factors, ST251 A. hydrophila strain NJ-35 was used as the parental strain to construct a mutant library comprising 1030 mutant strains by transposon insertion mutagenesis. Subsequently, 33 virulence-attenuated transposon insertion mutants were identified using Tetrahymena and zebrafish as model hosts in sequence. Thermal asymmetric interlaced (Tail)-PCR and Southern blot analysis identified 21 single transposon insertion sites. Seven of the insertion sites are located in non-coding regions, whereas the other 14 insertion sites are located in genes, including aroA, rmlA, rtxA, chiA and plc. All insertion mutants exhibited attenuated virulence in Tetrahymena and zebrafish. Furthermore, the relationship of two genes, chiA and trkH, to virulence was confirmed by gene inactivation and subsequent restoration assays. This study provides new information about the genetic determinants of A. hydrophila pathogenicity and validates the Aeromonas-Tetrahymena co-culture model for high-throughput screening of A. hydrophila virulence factors.
由序列型(ST)251嗜水气单胞菌引起的鱼类运动性气单胞菌败血症(MAS)暴发已成为水产养殖业的一个突出问题。嗜水气单胞菌的发病机制非常复杂,一些毒力因子仍有待确定。在本研究中,为了鉴定新的毒力相关因子,以ST251嗜水气单胞菌菌株NJ-35为亲本菌株,通过转座子插入诱变构建了一个包含1030个突变菌株的突变文库。随后,依次使用四膜虫和斑马鱼作为模式宿主,鉴定出33个毒力减弱的转座子插入突变体。热不对称交错(Tail)-PCR和Southern杂交分析确定了21个单转座子插入位点。其中7个插入位点位于非编码区,另外14个插入位点位于基因中,包括aroA、rmlA、rtxA、chiA和plc。所有插入突变体在四膜虫和斑马鱼中均表现出毒力减弱。此外,通过基因失活和随后的恢复试验证实了chiA和trkH这两个基因与毒力的关系。本研究提供了关于嗜水气单胞菌致病性遗传决定因素的新信息,并验证了用于高通量筛选嗜水气单胞菌毒力因子的气单胞菌-四膜虫共培养模型。