Antagonistic Pleiotropy in the Bifunctional Surface Protein FadL (OmpP1) during Adaptation of Haemophilus influenzae to Chronic Lung Infection Associated with Chronic Obstructive Pulmonary Disease

Author:

Moleres Javier1,Fernández-Calvet Ariadna1,Ehrlich Rachel L.2345,Martí Sara67,Pérez-Regidor Lucía8,Euba Begoña16,Rodríguez-Arce Irene1,Balashov Sergey2,Cuevas Ester9,Liñares Josefina67,Ardanuy Carmen67,Martín-Santamaría Sonsoles8,Ehrlich Garth D.234510,Mell Joshua Chang2345,Garmendia Junkal16

Affiliation:

1. Instituto de Agrobiotecnología, CSIC-Universidad Pública Navarra-Gobierno Navarra, Mutilva, Spain

2. Department of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA

3. Center for Genomic Sciences, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA

4. Center for Advanced Microbial Processing, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA

5. Center for Surgical Infections and Biofilms, Institute for Molecular Medicine and Infectious Disease, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA

6. Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), Madrid, Spain

7. Microbiology Department, Hospital Universitari Bellvitge, University of Barcelona, IDIBELL, Barcelona, Spain

8. Department of Structural and Chemical Biology, Centro de Investigaciones Biológicas, CIB-CSIC, Madrid, Spain

9. Pneumology Department, Hospital Universitari Bellvitge, University of Barcelona, IDIBELL, Barcelona, Spain

10. Department of Otolaryngology, Head and Neck Surgery, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA

Abstract

Nontypeable Haemophilus influenzae is an important pathogen in patients with chronic obstructive pulmonary disease (COPD). To elucidate the bacterial pathways undergoing in vivo evolutionary adaptation, we compared bacterial genomes collected over time from 13 COPD patients and identified recurrent genetic changes arising in independent bacterial lineages colonizing different patients. Besides finding changes in phase-variable genes, we found recurrent loss-of-function mutations in the ompP1 ( fadL ) gene. We show that loss of OmpP1/FadL function reduces this bacterium’s ability to infect cells via the hCEACAM1 epithelial receptor but also increases its resistance to bactericidal fatty acids enriched within the COPD lung, suggesting a case of antagonistic pleiotropy that restricts Δ fadL strains’ niche. These results show how H. influenzae adapts to host-generated inflammatory mediators in the COPD airways.

Funder

Sociedad Española de Neumología y Cirugía Torácica

U.S. National Institutes of Health

Ministerio de Economía y Competitividad

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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