| Literature DB >> 32747599 |
Haiyan Wang1, Zhenzhen Zhang1, Xing Xie1, Beibei Liu1, Yanna Wei1, Yuan Gan1, Ting Yuan1, Bo Ni1, Jia Wang1, Lei Zhang1, Qiyan Xiong1, Guoqing Shao1, Zhixin Feng2.
Abstract
Mycoplasma hyopneumoniae is an important respiratory pathogen of pigs that causes persistent and secondary infections. However, the mechanisms by which this occurs are unclear. In this study, we established air-liquid interface culture systems for pig bronchial epithelial cells (ALI-PBECs) that were comparable to the conditions in the native bronchus in vivo We used this ALI-PBECs model to study the infection and migration characteristics of M. hyopneumoniae in vitro Based on the results, we confirmed that M. hyopneumoniae was able to adhere to ALI-PBECs and disrupt mucociliary function. Importantly, M. hyopneumoniae could migrate to the basolateral chamber through the paracellular route but not the transcellular pathway, and this was achieved by reversibly disrupting tight junctions (TJs) and increasing the permeability and damaging the integrity of the epithelial barrier. We examined the migration ability of M. hyopneumoniae using an ALI-PBECs model for the first time. The disruption of the epithelial barrier allowed M. hyopneumoniae to migrate to the basolateral chamber through the paracellular route, which may be related to immune evasion, extrapulmonary dissemination, and persistent infection of M. hyopneumoniae.Entities:
Keywords: Mycoplasma hyopneumoniaezzm321990; air-liquid interface; barrier function; migration; pig bronchial epithelial cells
Mesh:
Year: 2020 PMID: 32747599 PMCID: PMC7504950 DOI: 10.1128/IAI.00470-20
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441