National Institute for Biotechnology and Genetic Engineering College, Pakistan Institute of Engineering and Applied Sciences (NIBGE-C, PIEAS), Faisalabad, Pakistan
Brandenburg University of Technology Cottbus-Senftenberg, Senftenberg, Germany.
Appl Environ Microbiol. 2020 Oct 1;86(20). doi: 10.1128/AEM.01068-20.
Avian pathogenic (APEC) is a major bacterial pathogen of commercial poultry contributing to extensive economic losses and contamination of the food chain. One of the initial steps in bacterial infection and successful colonization of the host is adhesion to the host cells. A random transposon mutant library ( = 1,300) of APEC IMT 5155 was screened phenotypically for adhesion to chicken (CHIC-8E11) and human (LoVo) intestinal epithelial cell lines. The detection and quantification of adherent bacteria were performed by a modified APEC-specific antibody staining assay using fluorescence microscopy coupled to automated VideoScan technology. Eleven mutants were found to have significantly altered adhesion to the cell lines examined. Mutated genes in these 11 "adhesion-altered mutants" were identified by arbitrary PCR and DNA sequencing. The genes were amplified from wild-type APEC IMT 5155, cloned, and transformed into the respective adhesion-altered mutants, and complementation was determined in adhesion assays. Here, we report contributions of the , and genes of APEC in adhesion to chicken and human intestinal cell lines. Identification of the roles of these genes in APEC pathogenesis will contribute to prevention and control of APEC infections. Avian pathogenic is not only pathogenic for commercial poultry but can also cause foodborne infections in humans utilizing the same attachment and virulence mechanisms. Our aim was to identify genes of avian pathogenic involved in adhesion to chicken and human cells in order to understand the colonization and pathogenesis of these bacteria. In contrast to the recent studies based on genotypic and bioinformatics data, we have used a combination of phenotypic and genotypic approaches for identification of novel genes contributing to adhesion in chicken and human cell lines. Identification of adhesion factors remains important, as antibodies elicited against such factors have shown potential to block colonization and ultimately prevent disease as prophylactic vaccines. Therefore, the data will augment the understanding of disease pathogenesis and ultimately in designing strategies against the infections.
禽致病性大肠杆菌(APEC)是一种主要的商业家禽细菌病原体,导致广泛的经济损失和食物链污染。细菌感染和成功定植宿主的初始步骤之一是与宿主细胞粘附。APEC IMT 5155 的随机转座子突变体库(=1300)在表型上筛选对鸡(CHIC-8E11)和人(LoVo)肠上皮细胞系的粘附。通过使用荧光显微镜结合自动 VideoScan 技术偶联的改良 APEC 特异性抗体染色测定法检测和定量粘附细菌。发现 11 个突变体对所检查的细胞系的粘附有明显改变。通过任意 PCR 和 DNA 测序鉴定这些 11 个“粘附改变突变体”中的突变基因。将这些基因从野生型 APEC IMT 5155 中扩增,克隆,并转化为各自的粘附改变突变体,并在粘附测定中确定互补性。在这里,我们报告了 APEC 的 、 和 基因在粘附鸡和人肠细胞系中的作用。鉴定这些基因在 APEC 发病机制中的作用将有助于预防和控制 APEC 感染。禽致病性大肠杆菌不仅对商业家禽具有致病性,而且还可以利用相同的附着和毒力机制引起食源性感染。我们的目的是鉴定参与粘附鸡和人细胞的禽致病性大肠杆菌基因,以了解这些细菌的定植和发病机制。与基于基因型和生物信息学数据的最近研究不同,我们使用表型和基因型方法的组合鉴定了参与鸡和人细胞系粘附的新基因。鉴定粘附因子仍然很重要,因为针对这些因子产生的抗体已显示出有潜力作为预防性疫苗阻断定植并最终预防疾病。因此,这些数据将增加对疾病发病机制的理解,并最终设计针对感染的策略。