Direct Evaluation of Pseudomonas aeruginosa Biofilm Mediators in a Chronic Infection Model

Author:

Byrd Matthew S.1,Pang Bing1,Hong Wenzhou1,Waligora Elizabeth A.1,Juneau Richard A.1,Armbruster Chelsie E.1,Weimer Kristen E. D.1,Murrah Kyle1,Mann Ethan E.23,Lu Haiping1,Sprinkle April14,Parsek Matthew R.5,Kock Nancy D.67,Wozniak Daniel J.238,Swords W. Edward1

Affiliation:

1. Department of Microbiology and Immunology, Wake Forest University Health Sciences, Medical Center Blvd., Winston-Salem, North Carolina 27157

2. Center for Microbial Interface Biology, The Ohio State University, Columbus, Ohio 43210

3. Infectious Disease, The Ohio State University, Columbus, Ohio 43210

4. Present address: Department of Neurosurgery, Wake Forest University Health Sciences, Medical Center Blvd., Winston-Salem, NC 27157.

5. Department of Microbiology, University of Washington, Seattle, Washington 98195

6. Department of Pathology, Wake Forest University Health Sciences, Medical Center Blvd., Winston-Salem, North Carolina 27157

7. Department of Pathology/Comparative Medicine, Wake Forest University Health Sciences, Medical Center Blvd., Winston-Salem, North Carolina 27157

8. Microbiology, The Ohio State University, Columbus, Ohio 43210

Abstract

ABSTRACT Biofilms contribute to Pseudomonas aeruginosa persistence in a variety of diseases, including cystic fibrosis, burn wounds, and chronic suppurative otitis media. However, few studies have directly addressed P. aeruginosa biofilms in vivo . We used a chinchilla model of otitis media, which has previously been used to study persistent Streptococcus pneumoniae and Haemophilus influenzae infections, to show that structures formed in vivo are biofilms of bacterial and host origin within a matrix that includes Psl, a P. aeruginosa biofilm polysaccharide. We evaluated three biofilm and/or virulence mediators of P. aeruginosa known to affect biofilm formation in vitro and pathogenesis in vivo —bis-(3′,5′)-cyclic dimeric GMP (c-di-GMP), flagella, and quorum sensing—in a chinchilla model. We show that c-di-GMP overproduction has a positive impact on bacterial persistence, while quorum sensing increases virulence. We found no difference in persistence attributed to flagella. We conclude from these studies that a chinchilla otitis media model provides a means to evaluate pathogenic mediators of P. aeruginosa and that in vitro phenotypes should be examined in multiple infection systems to fully understand their role in disease.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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