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Mycobacterium abscessus biofilms have viscoelastic properties which may contribute to their recalcitrance in chronic pulmonary infections

Mycobacterium abscessus biofilms have viscoelastic properties which may contribute to their recalcitrance in chronic pulmonary infections
Mycobacterium abscessus biofilms have viscoelastic properties which may contribute to their recalcitrance in chronic pulmonary infections

Mycobacterium abscessus is emerging as a cause of recalcitrant chronic pulmonary infections, particularly in people with cystic fibrosis (CF). Biofilm formation has been implicated in the pathology of this organism, however the role of biofilm formation in infection is unclear. Two colony-variants of M. abscessus are routinely isolated from CF samples, smooth (Ma Sm) and rough (Ma Rg). These two variants display distinct colony morphologies due to the presence (Ma Sm) or absence (Ma Rg) of cell wall glycopeptidolipids (GPLs). We hypothesized that Ma Sm and Ma Rg variant biofilms might have different mechanical properties. To test this hypothesis, we performed uniaxial mechanical indentation, and shear rheometry on Ma Sm and Ma Rg colony-biofilms. We identified that Ma Rg biofilms were significantly stiffer than Ma Sm under a normal force, while Ma Sm biofilms were more pliant compared to Ma Rg, under both normal and shear forces. Furthermore, using theoretical indices of mucociliary and cough clearance, we identified that M. abscessus biofilms may be more resistant to mechanical forms of clearance from the lung, compared to another common pulmonary pathogen, Pseudomonas aeruginosa. Thus, the mechanical properties of M. abscessus biofilms may contribute to the persistent nature of pulmonary infections caused by this organism.

2045-2322
Gloag, Erin S.
36de1738-c25d-4eb7-acd3-1ad55d9a7cee
Wozniak, Daniel J.
bfa8e8e5-5929-449b-af6a-ec2d86c47eb5
Stoodley, Paul
08614665-92a9-4466-806e-20c6daeb483f
Hall-stoodley, Luanne
9dd7a299-a529-401c-9ae8-63a4807c2807
Gloag, Erin S.
36de1738-c25d-4eb7-acd3-1ad55d9a7cee
Wozniak, Daniel J.
bfa8e8e5-5929-449b-af6a-ec2d86c47eb5
Stoodley, Paul
08614665-92a9-4466-806e-20c6daeb483f
Hall-stoodley, Luanne
9dd7a299-a529-401c-9ae8-63a4807c2807

Gloag, Erin S., Wozniak, Daniel J., Stoodley, Paul and Hall-stoodley, Luanne (2021) Mycobacterium abscessus biofilms have viscoelastic properties which may contribute to their recalcitrance in chronic pulmonary infections. Scientific Reports, 11 (1), [5020]. (doi:10.1038/s41598-021-84525-x).

Record type: Article

Abstract

Mycobacterium abscessus is emerging as a cause of recalcitrant chronic pulmonary infections, particularly in people with cystic fibrosis (CF). Biofilm formation has been implicated in the pathology of this organism, however the role of biofilm formation in infection is unclear. Two colony-variants of M. abscessus are routinely isolated from CF samples, smooth (Ma Sm) and rough (Ma Rg). These two variants display distinct colony morphologies due to the presence (Ma Sm) or absence (Ma Rg) of cell wall glycopeptidolipids (GPLs). We hypothesized that Ma Sm and Ma Rg variant biofilms might have different mechanical properties. To test this hypothesis, we performed uniaxial mechanical indentation, and shear rheometry on Ma Sm and Ma Rg colony-biofilms. We identified that Ma Rg biofilms were significantly stiffer than Ma Sm under a normal force, while Ma Sm biofilms were more pliant compared to Ma Rg, under both normal and shear forces. Furthermore, using theoretical indices of mucociliary and cough clearance, we identified that M. abscessus biofilms may be more resistant to mechanical forms of clearance from the lung, compared to another common pulmonary pathogen, Pseudomonas aeruginosa. Thus, the mechanical properties of M. abscessus biofilms may contribute to the persistent nature of pulmonary infections caused by this organism.

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Published date: 3 March 2021
Additional Information: Funding Information: Funding to LHS was provided by the Ohio State University College of Medicine Office of Research Bridge Funding Program and by the Cystic Fibrosis Foundation (HALLST18I0). ESG was funded by an American Heart Association Career Development Award (19CDA34630005). DJW and PS were funded by the National Institute of Health (R01AI134895 and R01AI143916; DJW) (R01GM124436; PS). Publisher Copyright: © 2021, The Author(s).

Identifiers

Local EPrints ID: 447250
URI: http://eprints.soton.ac.uk/id/eprint/447250
ISSN: 2045-2322
PURE UUID: f152c1fa-87c1-45b0-b8ba-b27e61e14ac4
ORCID for Paul Stoodley: ORCID iD orcid.org/0000-0001-6069-273X

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Date deposited: 05 Mar 2021 17:32
Last modified: 17 Mar 2024 03:18

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Contributors

Author: Erin S. Gloag
Author: Daniel J. Wozniak
Author: Paul Stoodley ORCID iD
Author: Luanne Hall-stoodley

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