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在猪感染模型中使用签名标签诱变技术鉴定胸膜肺炎放线杆菌毒力基因。

Identification of Actinobacillus pleuropneumoniae virulence genes using signature-tagged mutagenesis in a swine infection model.

作者信息

Fuller T E, Martin S, Teel J F, Alaniz G R, Kennedy M J, Lowery D E

机构信息

Animal Health Discovery Research, Pharmacia & Upjohn, Kalamazoo, MI 49001, USA.

出版信息

Microb Pathog. 2000 Jul;29(1):39-51. doi: 10.1006/mpat.2000.0364.

Abstract

Actinobacillus pleuropneumoniae is a significant respiratory pathogen of swine causing a severe and often fatal fibrinous hemorrhagic bronchopneumonia with significant economic losses resulting from chronic as well as acute infections. This study describes the application of a signature-tagged mutagenesis (STM) system to identify in vivo critical genes of A. pleuropneumoniae. Twenty pools representing over 800 A. pleuropneumoniae mutants were screened in a natural-host porcine infection model and presumptive attenuated mutants were selected. The identity of the disrupted gene in each mutant was determined using an inverse PCR approach to amplify DNA sequences adjacent to the transposon insertion, followed by sequencing of the PCR product and comparison to bacterial databases. In vitro and in vivo competitive indices were determined for each unique mutant, and a total of 20 unique, attenuating gene disruptions were identified including insertions into homologues of genes involved in biosynthesis, virulence determinants, regulation, translation and unknown functions. Three of the genes required for virulence of A. pleuropneumoniae in this study were also identified in a previous STM study of Pasteurella multocida. Seven of the STM-derived mutants were also evaluated for their potential as live vaccine strains and provided good protection against homologous challenge.

摘要

胸膜肺炎放线杆菌是猪的一种重要呼吸道病原体,可引发严重且通常致命的纤维蛋白性出血性支气管肺炎,急性和慢性感染都会造成重大经济损失。本研究描述了应用一种签标签诱变(STM)系统来鉴定胸膜肺炎放线杆菌的体内关键基因。在天然宿主猪感染模型中筛选了代表800多个胸膜肺炎放线杆菌突变体的20个库,并选择了推定的减毒突变体。使用反向PCR方法扩增转座子插入位点附近的DNA序列,然后对PCR产物进行测序并与细菌数据库进行比较,以确定每个突变体中被破坏基因的身份。测定了每个独特突变体的体外和体内竞争指数,共鉴定出20个独特的减毒基因破坏,包括插入参与生物合成、毒力决定因素、调控、翻译和未知功能的基因同源物。在先前多杀性巴氏杆菌的STM研究中也鉴定出了本研究中胸膜肺炎放线杆菌毒力所需的三个基因。还评估了7个STM衍生突变体作为活疫苗株的潜力,它们对同源攻击提供了良好的保护。

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