A tissue culture system to study respiratory ciliary epithelial adherence of selected swine mycoplasmas

• Published in: Veterinary microbiology 2000-02, Vol.71 (3), p.269-279
• Main Authors: Young, Theresa F., Thacker, Eileen L., Erickson, Barbara Z., Ross, Richard F.
• Format: Article
• Language: English
• Subjects: Animals; Bacterial Adhesion - immunology; Bacteriological methods and techniques used in bacteriology; Bacteriology; Biological and medical sciences; Cell Count; Cilia - microbiology; Cilia - pathology; Cilia - ultrastructure; Ciliated epithelial cells; Culture Techniques - methods; Culture Techniques - veterinary; Epithelial Cells - microbiology; Epithelial Cells - ultrastructure; Fundamental and applied biological sciences. Psychology; Image Processing, Computer-Assisted; Microbiology; Microscopy, Electron - veterinary; Microscopy, Electron, Scanning - veterinary; Mycoplasma - immunology; Mycoplasma - pathogenicity; Mycoplasma flocculare; Mycoplasma hyopneumoniae; Pig-bacteria; Pneumonia of Swine, Mycoplasmal - immunology; Pneumonia of Swine, Mycoplasmal - pathology; Pneumonia of Swine, Mycoplasmal - veterinary; Swine; Swine Diseases - microbiology; Swine Diseases - pathology; Trachea - immunology; Trachea - microbiology
• ISSN: 0378-1135; 1873-2542
• DOI: 10.1016/S0378-1135(99)00176-5

An in vitro culture system for swine tracheal epithelial cells was developed to study the adherence of swine mycoplasmas. Swine tracheal epithelial cells were isolated by enzymatic digestion and cultured on microporous membranes. Growth medium was placed under the membrane support to create air–liquid interface feeding resulting in the cells growing cilia and microvilli on the apical surface. Two strains of Mycoplasma hyopneumoniae (pathogenic strain 91-3 and non-pathogenic type strain J) and two strains of Mycoplasma flocculare (type strain Ms42 and field isolate 7160T) were used in this study. The morphology of the cultured tracheal cells was evaluated by transmission electron microscopy. Adherence of M. hyopneumoniae and M. flocculare and damage to the cilia were demonstrated using scanning electron microscopy. The pathogenic M. hyopneumoniae strain 91-3 adhered to cilia inducing obvious damage. The non-pathogenic M. hyopneumoniae strain J did not adhere to mature cilia. Both M. flocculare strains Ms42 and 7160T adhered to mature and budding cilia. No obvious ciliary damage was observed with strain Ms42. Minimal damage consisting of a slight tangling of the cilia occurred after adherence by strain 7160T. This model will enable us to further study the role of adherence of mycoplasmas on the pathogenesis of swine pneumonia.