College of Veterinary Medicine, Huazhong Agricultural UniversityWuhan, China.
Key Lab of Preventive Veterinary Medicine of Hubei Province, Huazhong Agricultural UniversityWuhan, China.
Front Cell Infect Microbiol. 2017 Aug 25;7:382. doi: 10.3389/fcimb.2017.00382. eCollection 2017.
, an avian pathogen, has resulted in enormous economic losses to the duck industry globally. Notwithstanding, little is known regarding the physiological, pathogenic and virulence mechanisms of (RA) infection. However, the role of Ferric uptake regulator (Fur) in the virulence of has not, to date, been demonstrated. Using a genetic approach, unmarked gene deletion system, we evaluated the function of gene in the virulence of . For this purpose, we constructed a suicide vector containing as a counter selectable marker for unmarked deletion of gene to investigate its role in the virulence. After successful transformation of the newly constructed vector, a mutant strain was characterized for genes regulated by iron and Fur using RNA-sequencing and a comparison was made between wild type and mutant strains in both iron restricted and enriched conditions. RNA-seq analysis of the mutant strain in a restricted iron environment showed the downregulation and upregulation of genes which were involved in either important metabolic pathways, transport processes, growth or cell membrane synthesis. Electrophoretic mobility shift assay was performed to identify the putative sequences recognized by Fur. The putative Fur-box sequence was 5'-GATAATGATAATCATTATC-3'. Lastly, the median lethal dose and histopathological investigations of animal tissues also illustrated mild pathological lesions produced by the mutant strain as compared to the wild type RA strain, hence showing declined virulence. Conclusively, an unmarked gene deletion system was successfully developed for RA and the role of the gene in virulence was explored comprehensively.
(RA)是一种禽类病原体,已导致全球养鸭业遭受巨大的经济损失。然而,目前对于 RA 感染的生理、发病和毒力机制知之甚少。但是,铁摄取调节剂(Fur)在 RA 毒力中的作用尚未得到证实。本研究采用遗传方法、无标记基因缺失系统,评估了 基因在 RA 毒力中的功能。为此,我们构建了一个自杀载体,其中包含 作为无标记缺失 基因的反向选择标记,以研究其在毒力中的作用。成功转化新构建的载体后,我们用 RNA 测序对含有 基因的突变株进行了铁调节和 Fur 调控基因的功能表征,并在缺铁和富铁条件下对野生型和突变株进行了比较。在缺铁环境下,对突变株的 RNA-seq 分析显示,参与重要代谢途径、转运过程、生长或细胞膜合成的基因下调和上调。凝胶电泳迁移率变动分析实验用于鉴定 Fur 识别的假定序列。假定的 Fur-box 序列为 5'-GATAATGATAATCATTATC-3'。最后,动物组织的半数致死剂量和组织病理学研究也表明,与野生型 RA 株相比,突变株引起的病理损伤较轻,因此毒力下降。总之,成功开发了用于 RA 的无标记基因缺失系统,并全面探讨了 基因在毒力中的作用。