Whole-genome analyses reveal gene content differences between nontypeable Haemophilus influenzae isolates from chronic obstructive pulmonary disease compared to other clinical phenotypes

Author:

KC Rajendra1ORCID,Leong Kelvin W.C.2ORCID,Harkness Nicholas M.3,Lachowicz Julia3,Gautam Sanjay S.1ORCID,Cooley Louise A.4ORCID,McEwan Belinda4,Petrovski Steve5ORCID,Karupiah Gunasegaran1ORCID,O'Toole Ronan F.2ORCID

Affiliation:

1. Tasmanian School of Medicine, College of Health and Medicine, University of Tasmania, Tasmania, Australia

2. Department of Pharmacy and Biomedical Sciences, School of Molecular Sciences, College of Science, Health and Engineering, La Trobe University, Victoria, Australia

3. Department of Respiratory and Sleep Medicine, Royal Hobart Hospital, Tasmania, Australia

4. Department of Microbiology and Infectious Diseases, Royal Hobart Hospital, Tasmania, Australia

5. Department of Physiology, Anatomy and Microbiology, School of Life Sciences, La Trobe University, Victoria, Australia

Abstract

Nontypeable Haemophilus influenzae (NTHi) colonizes human upper respiratory airways and plays a key role in the course and pathogenesis of acute exacerbations of chronic obstructive pulmonary disease (COPD). Currently, it is not possible to distinguish COPD isolates of NTHi from other clinical isolates of NTHi using conventional genotyping methods. Here, we analysed the core and accessory genome of 568 NTHi isolates, including 40 newly sequenced isolates, to look for genetic distinctions between NTHi isolates from COPD with respect to other illnesses, including otitis media, meningitis and pneumonia. Phylogenies based on polymorphic sites in the core-genome did not show discrimination between NTHi strains collected from different clinical phenotypes. However, pan-genome-wide association studies identified 79 unique NTHi accessory genes that were significantly associated with COPD. Furthermore, many of the COPD-related NTHi genes have known or predicted roles in virulence, transmembrane transport of metal ions and nutrients, cellular respiration and maintenance of redox homeostasis. This indicates that specific genes may be required by NTHi for its survival or virulence in the COPD lung. These results advance our understanding of the pathogenesis of NTHi infection in COPD lungs.

Funder

La Trobe University

Publisher

Microbiology Society

Subject

General Medicine

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