The relative contributions of physical structure and cell density to the antibiotic susceptibility of bacteria in biofilms

For many bacterial infections, noninherited mechanisms of resistance are responsible for extending the term of treatment and in some cases precluding its success. Among the most important of these noninherited mechanisms of resistance is the ability of bacteria to form biofilms. There is compelling evidence that bacteria within biofilms are more refractory to antibiotics than are planktonic cells. Not so clear, however, is the extent to which this resistance can be attributed to the structure of biofilms rather than the physiology and density of bacteria within them. To explore the contribution of the structure of biofilms to resistance in a quantitative way, we developed an assay that compares the antibiotic sensitivity of bacteria in biofilms to cells mechanically released from these structures. Our method, which we apply to Escherichia coli and Staphylococcus aureus each with antibiotics of five classes, controls for the density and physiological state of the treated bacteria. For most of the antibiotics tested, the bacteria in biofilms were no more resistant than the corresponding populations of planktonic cells of similar density. Our results, however, suggest that killing by gentamicin, streptomycin, and colistin is profoundly inhibited by the structure of biofilms; these drugs are substantially more effective in killing bacteria released from biofilms than cells within these structures.

Medienart:

E-Artikel

Erscheinungsjahr:

2012

Erschienen:

2012

Enthalten in:

Zur Gesamtaufnahme - volume:56

Enthalten in:

Antimicrobial agents and chemotherapy - 56(2012), 6 vom: 26. Juni, Seite 2967-75

Sprache:

Englisch

Beteiligte Personen:

Kirby, Amy E [VerfasserIn]
Garner, Kimberly [VerfasserIn]
Levin, Bruce R [VerfasserIn]

Links:

Volltext

Themen:

Anti-Bacterial Agents
Colistin
Gentamicins
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Streptomycin
Y45QSO73OB
Z67X93HJG1

Anmerkungen:

Date Completed 13.09.2012

Date Revised 21.10.2021

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1128/AAC.06480-11

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM216519292