Glaesserella parasuis serotype 4 exploits fibronectin via RlpA for tracheal colonization following porcine circovirus type 2 infection

• Published in: PLoS pathogens Vol. 20; no. 9; p. e1012513
• Main Authors: Guo, Mengru, Li, Yuhui, Tang, Jinsheng, Wang, Qing, Wang, Qiancheng, Zhou, Hong, Lin, Huixing, Ma, Zhe, Fan, Hongjie
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 12.09.2024
• Subjects: Animals; Bacterial Adhesion; Biology and life sciences; Circovirus - metabolism; Circovirus - pathogenicity; Coinfection - microbiology; Coinfection - virology; Diseases; DNA viruses; Fibronectins; Fibronectins - metabolism; Gram-negative bacteria; Haemophilus Infections - metabolism; Haemophilus Infections - microbiology; Haemophilus Infections - virology; Haemophilus parasuis - metabolism; Health aspects; Lipoprotein A; Medicine and Health Sciences; Pasteurellaceae Infections - metabolism; Pasteurellaceae Infections - microbiology; Pasteurellaceae Infections - veterinary; Pasteurellaceae Infections - virology; Physiological aspects; Serogroup; Swine; Swine Diseases - metabolism; Swine Diseases - microbiology; Swine Diseases - virology; Trachea; Trachea - metabolism; Trachea - microbiology; Trachea - virology; Viral proteins; China
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1012513

Porcine circovirus type 2 (PCV2) often causes disease through coinfection with other bacterial pathogens, including Glaesserella parasuis (G. parasuis), which causes high morbidity and mortality, but the role played by PCV2 and bacterial and host factors contributing to this process have not been defined. Bacterial attachment is assumed to occur via specific receptor-ligand interactions between adhesins on the bacterial cell and host proteins adsorbed to the implant surface. Mass spectrometry (MS) analysis of PCV2-infected swine tracheal epithelial cells (STEC) revealed that the expression of Extracellular matrix protein (ECM) Fibronectin (Fn) increased significantly on the infected cells surface. Importantly, efficient G. parasuis serotype 4 (GPS4) adherence to STECs was imparted by interactions with Fn. Furthermore, abrogation of adherence was gained by genetic knockout of Fn, Fn and Integrin β1 antibody blocking. Fn is frequently exploited as a receptor for bacterial pathogens. To explore the GPS4 adhesin that interacts with Fn, recombinant Fn N-terminal type I and type II domains were incubated with GPS4, and the interacting proteins were pulled down for MS analysis. Here, we show that rare lipoprotein A (RlpA) directly interacts with host Fibronectin mediating GPS4 adhesion. Finally, we found that PCV2-induced Fibronectin expression and adherence of GPS4 were prevented significantly by TGF-β signaling pathway inhibitor SB431542. Our data suggest the RlpA-Fn interaction to be a potentially promising novel therapeutic target to combat PCV2 and GPS4 coinfection.