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Center for Biofilm Engineering

Movie Description:  

Staphylococcus aureus biofilm rolling along the lumen of a glass tube


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Staphylococcus aureus, an opportunistic human pathogen, is commonly associated with nosocomial infections and often colonizes medical devices such as catheters. Using glass flow cells, biofilms can be monitored in situ microscopically.

This is a 11.5 hour time-lapse video sequence showing a side view of a S. aureus biofilm microcolony rolling along the side wall of a square glass tube. Water containing brain-heart infusion broth was flowing through the tube at a flow rate of 1 ml/min, giving an average flow velocity of 1.7 cm/s. The biofilm microcolony appeared to be attached to the glass by sticky appendages or "tethers". The rolling motion appeared to be caused by the continual attachment and detachment of the biofilm from the glass surface. First the microcolony detaches from the upstream side, where presumably the shear force overcomes the attachment force of the tether. It then jerks forward in a rolling motion and tethers reattach at the downstream side.


The migration of bacterial microcolonies along the lumen of catheters (tubes used to deliver fluids into the body or drain fluids from the body), endotracheal tubes (tubes used to maintain an airway), or dental unit water lines may be an important consideration in the dissemination of pathogens such as S. aureus into patients. In industrial systems, the movement of biofilms along the walls of process pipes may result in the spread of contamination to other parts of the system. By moving along the pipe wall, the biofilm can spread without detaching and entering a planktonic (free swimming or floating) phase in which the bacteria are often more susceptible to antimicrobial agents such as antibiotics or biocides.

Acknowledgments: This work was supported by the National Institutes of Health grant RO1 GM60052 and the W. M. Keck Foundation. The movie sequence is also available at the ASM MicrobeLibrary (www.microbelibrary.org).

 

Movie Author:  Rupp, C.J., Wilson, S, and Stoodley, P.

 

Reference:

 

Rupp, C.J., C. Fux, and P. Stoodley. 2005. Viscoelasticity of Staphylococcus aureus biofilms in response to fluid shear resists detachment and facilitates rolling migration. Appl. Envron. Microbiol. 71(4): 2175-2178.

 

Further Reading:

 

Klapper, I., C. J. Rupp, R. Cargo, B. Purevdorj, and P. Stoodley. 2002. A viscoelastic fluid description of bacterial biofilm material properties. Biotechnol. Bioeng. 80: 289-96.

Stoodley, P., Z. Lewandowski, J. D. Boyle, and H. M. Lappin-Scott. 1999.
Structural deformation of bacterial biofilms caused by short term fluctuations in flow velocity: an in situ demonstration of biofilm viscoelasticity. Biotechnol. Bioeng. 65:83-92.

 

 

 

Viscoelasticity of Staphylococcus aureus biofilm

 
 
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This time-lapse video sequence shows Staphylococcus aureus biofilm cell clusters in a glass flow cell stretching and contracting as the flow rate of the nutrient feed is turned up and down between 0 and 9 ml/min. The amount of stretching (strain) can be related to the shear stress caused by the fluid flowing in the flow cell. The strain is then used to investigate the material properties of the attached biofilm. This data demonstrates that the S. aureus biofilm is a viscoelastic material. S. aureus is commonly found on the skin and as part of the naturally occurring oral, nasal, and vaginal microbial flora, where in most people it lives harmlessly. However, S. aureus is also an opportunistic human pathogen and is commonly associated with nosocomial infections. S. aureus often colonizes on medical devices such as venous and renal catheters and is associated with infections such as osteomyelitis (infection of the bone), endocarditis (infection of the heart valves), and bacteremia (infection of the blood). An understanding of the material properties of biofilms is important in predicting how biofilms may respond when exposed to fluid shear forces. Detachment of clumps of pathogenic bacteria from biofilms, or the flow of biofilms across surfaces, may be an important consideration in the dissemination of the infection in the host or from catheters and other medical delivery systems. Additionally, this information may be useful in designing novel strategies for biofilm removal or stabilization.

Acknowledgments: This work was supported by the National Institutes of Health grant RO1 GM60052 and the W. M. Keck Foundation. The movie sequence is also available at the ASM MicrobeLibrary (www.microbelibrary.org).

 

Movie Authors:  Rupp, C.J., Wilson, S, and Stoodley, P.
Reference:

 

Rupp, C.J., C. Fux, and P. Stoodley. 2005. Viscoelasticity of Staphylococcus aureus biofilms in response to fluid shear resists detachment and facilitates rolling migration. Appl. Envron. Microbiol. 71(4): 2175-2178.

 

 

Further Reading:

 

Klapper, I., C. J. Rupp, R. Cargo, B. Purevdorj, and P. Stoodley. 2002. A viscoelastic fluid description of bacterial biofilm material properties. Biotechnol. Bioeng. 80: 289-296.

Stoodley, P., Z. Lewandowski, J. D. Boyle, and H. M. Lappin-Scott. 1999.
Structural deformation of bacterial biofilms caused by short term fluctuations in flow velocity: an in situ demonstration of biofilm viscoelasticity. Biotechnol. Bioeng. 65:83-92.

 

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