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Initial infections are cleared but chronic infection with mucoid strains ensues in the majority of CF patients and specific interventions to prevent this critical infection transition are lacking. The PA bead model has been widely used to study pulmonary <jats:italic>P.aeruginosa<\/jats:italic> infection but has limitations in animal husbandry and in accurately mimicking human disease. We have developed an adapted agar bead murine model using a clinical mucoid strain that demonstrates the key features of transition from transitory to chronic airways infection. Infected animals show very limited acute morbidity and mortality, but undergo infection-related weight loss and neutrophilic inflammation, development of anti-pseudomonal antibodies, variable bacterial clearance, endobronchial infection and microbial adaptation with PA small colony variants. We anticipate this model will allow research into the host and microbial factors governing this critical period in <jats:italic>Pseudomonas aeruginosa<\/jats:italic> pulmonary pathogenesis when transition to chronicity is occurring.<\/jats:p>","DOI":"10.1038\/srep35838","type":"journal-article","created":{"date-parts":[[2016,11,2]],"date-time":"2016-11-02T10:24:28Z","timestamp":1478082268000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":61,"title":["A murine model of early Pseudomonas aeruginosa lung disease with transition to chronic infection"],"prefix":"10.1038","volume":"6","author":[{"given":"H. 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