Sunday 10 March 2013

It's snot impossible to break down biofilms


Chronic Rhinosinusitis is one of the most common respiratory tract disorders in Europe, affecting 10% of the population. This disease is characterised by inflammation of the paranasal sinuses and nasal airway and is classified as chronic if it lasts for 12 consecutive weeks or more. Current therapy involves topical steroids and nasal douching for chronic disorders and antibiotics for acute, however these methods have been criticised as ineffective and in some exacerbated cases surgery may be warranted to remove mucin build up and nasal blockage. This recalcitrance to medical therapy is due to the biofilm forming capabilities of the bacteria responsible (mostly Staphylococci spp.) which enables a 1000fold increase in resistance to antibiotics. Several novel methods have been proposed for treating biofilms, most predominant of which involves degrading the extracellular DNA (eDNA) which provides stabilisation of the biofilm structure, enhanced adhesion capabilities and enhanced exchange of genetic material. Extracellular deoxyribonucleases (eDNAses) exist which catabolise the eDNA, thus disrupting the existing biofilm.

The authors of this study collected mucin from patients suffering from Chronic Rhinosinusitis and applied the afore mentioned eDNAse, called NucB, isolated from a marine strain of the gram positive bacterium Bacillus licheniformis. Confirmation of biofilm formation and structure was obtained using transmission electron microscopy. The authors applied the NucB to the infected mucus and observed the subsequent degradation of the biofilm. The results of this study show no extracellular biofilm observed in the treated samples.

The authors conclude that this test shows a novel therapeutic methodology which shows promising prospects for the future and whilst I agree with this, I can’t help but point out that this study is only in vitro and clinical trials are a very lengthy and very costly process, often ending prematurely and in disappointment. Nevertheless, ultimately all medical therapies must start somewhere and this study shows that NucB undoubtedly has potential for the control of biofilms. It will be interesting to see the results of the in vivo study on the same enzyme, which is currently being undertaken by the same research group in Newcastle (this is stated in the paper and as far as I know is still underway). 

REF: Shields, R.C., Mokhtar, N., Ford, M. et al (2013) Efficacy of a Marine Bacterial Nuclease against Biofilm Forming Microorganisms Isolated from Chronic Rhinosinusitis. PLoS One, 8 (2)e55339. (Published online)

Available fromhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575374/

4 comments:

  1. Hello there Harrison, what an interesting read! I was just wondering if the NucB enzyme can be used to degrade biofilms ex vivo on oil pipe lines? Also, do you know if it works on Staphylococci species?
    One more thing, could you please put the reference up for the paper you have used?
    Thanks!

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  2. Sorry I meant does it work without Staphylococci species!

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  3. Hey Hannah,

    Sorry I always forget to reference! I've edited the post so it should be on there.

    In answer to your questions; The authors did mention the possibility of an ex vivo usage, but from what I could gather they were far more interested in the medical potential than the engineering potential of the enzyme. From purely speculation I would guess that maybe the amount of enzyme needed to significantly degrade biofilm ex vivo would be impractical due to washing away, eating etc. whereas in vivo the enzyme is contained.
    Due to the specificity of enzymes I would assume that NucB only works on staph spp., however the authors do make mention of Neisseria gonorrhoeae and Vibrio cholerae, but state that they produce "thicker biofilms" and offer no further explanation of if the enzyme would work or not!


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  4. Brilliant, do you know of any similar papers which look in to the bioengineering side of these applications?

    Thanks for the quick response!

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