Busting biofilms: free-living amoebae disrupt preformed methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium bovis biofilms
Biofilm-associated infections are difficult to eradicate because of their ability to tolerate antibiotics and evade host immune responses. Amoebae and/or their secreted products may provide alternative strategies to inhibit and disperse biofilms on biotic and abiotic surfaces. We evaluated the poten...
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Published in | Microbiology (Society for General Microbiology) Vol. 166; no. 8; pp. 695 - 706 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
Microbiology Society
01.08.2020
|
Subjects | |
Online Access | Get full text |
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Summary: | Biofilm-associated infections are difficult to eradicate because of their ability to tolerate antibiotics and evade host immune responses. Amoebae and/or their secreted products may provide alternative strategies to inhibit and disperse biofilms on biotic and abiotic surfaces. We evaluated the potential of five predatory amoebae -
,
,
,
and
- and their cell-free secretions to disrupt biofilms formed by methicillin-resistant
(MRSA) and
. The biofilm biomass produced by MRSA and
was significantly reduced when co-incubated with
,
and
, and their corresponding cell-free supernatants (CFS).
spp. generally produced CFS that mediated biofilm dispersal rather than directly killing the bacteria; however,
CFS demonstrated active killing of MRSA planktonic cells when the bacteria were present at low concentrations. The active component(s) of the
CFS is resistant to freezing, but can be inactivated to differing degrees by mechanical disruption and exposure to heat.
and its CFS also reduced preformed
biofilms, whereas
only decreased
biofilm biomass when amoebae were added. These results highlight the potential of using select amoebae species or their CFS to disrupt preformed bacterial biofilms. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1350-0872 1465-2080 1465-2080 |
DOI: | 10.1099/mic.0.000933 |