Dalai Baolige, Zhou Rui, Wan Yun, Kang Mingsong, Li Lu, Li Tingting, Zhang Sihua, Chen Huanchun
Division of Animal Infectious Diseases, State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Shizishan Street 1, Wuhan 430070, China.
Microb Pathog. 2009 Mar;46(3):128-34. doi: 10.1016/j.micpath.2008.11.005. Epub 2008 Dec 6.
Actinobacillus pleuropneumoniae is the causative agent of porcine contagious pleuropneumonia, a very important swine respiratory infectious disease causing great economic losses worldwide. The pathogenesis of this disease is still not completely understood. Biofilm formation contributes to full virulence in many Gram-negative bacterial pathogens. In the present study, two biofilm-producing mutants were identified from the transposon mutagenesis mutant pools of A. pleuropneumoniae strain 4074 of serovar 1 (a non-biofilm forming strain). Inverse PCR and sequencing analysis revealed that the hns gene encoding the histone-like nucleoid structuring protein (H-NS) was inactivated by the mini-Tn10 transposon in both mutant strains. Further analysis revealed that the virulence was attenuated in the mutant strains when their haemolytic activity and 50% lethal doses in mice were compared with the parental strain. Real-time RT-PCR analysis suggested that the down-regulation of the exotoxin genes in the hns mutants may partly contribute to the virulence attenuation. Our data indicate that H-NS plays important roles in regulating biofilm formation and virulence in A. pleuropneumoniae.
胸膜肺炎放线杆菌是猪传染性胸膜肺炎的病原体,猪传染性胸膜肺炎是一种非常重要的猪呼吸道传染病,在全球范围内造成巨大经济损失。该病的发病机制仍未完全明确。生物膜形成在许多革兰氏阴性细菌病原体的完全毒力中起作用。在本研究中,从血清型1的胸膜肺炎放线杆菌菌株4074(非生物膜形成菌株)的转座子诱变突变体库中鉴定出两个产生生物膜的突变体。反向PCR和测序分析表明,在两个突变菌株中,编码类组蛋白核仁结构蛋白(H-NS)的hns基因被mini-Tn10转座子灭活。进一步分析表明,当将突变菌株在小鼠中的溶血活性和50%致死剂量与亲本菌株进行比较时,其毒力减弱。实时RT-PCR分析表明,hns突变体中外毒素基因的下调可能部分导致毒力减弱。我们的数据表明,H-NS在调节胸膜肺炎放线杆菌的生物膜形成和毒力方面发挥重要作用。