Laboratory of Pharmaceutical Microbiology, Ghent University , Ghent , Belgium.
PeerJ. 2015 Feb 24;3:e787. doi: 10.7717/peerj.787. eCollection 2015.
Multispecies biofilms are an important healthcare problem and may lead to persistent infections. These infections are difficult to treat, as cells in a biofilm are highly resistant to antimicrobial agents. While increasingly being recognized as important, the properties of multispecies biofilms remain poorly studied. In order to do so, the quantification of the individual species is needed. The current cultivation-based approaches can lead to an underestimation of the actual cell number and are time-consuming. In the present study we set up a culture-independent approach based on propidium monoazide qPCR (PMA-qPCR) to quantify Pseudomonas aeruginosa in a multispecies biofilm. As a proof of concept, we explored the influence of the combined presence of Staphylococcus aureus, Streptococcus anginosus and Burkholderia cenocepacia on the antimicrobial susceptibility of P. aeruginosa using this PMA-qPCR approach.
多物种生物膜是一个重要的医疗保健问题,可能导致持续感染。这些感染很难治疗,因为生物膜中的细胞对抗菌药物具有高度抗性。尽管多物种生物膜越来越被认为是重要的,但它们的特性仍未得到充分研究。为了做到这一点,需要对各个物种进行定量。目前基于培养的方法可能会导致对实际细胞数量的低估,并且耗时。在本研究中,我们建立了一种基于吖啶橙单加合物 qPCR(PMA-qPCR)的非培养方法,用于定量多物种生物膜中的铜绿假单胞菌。作为概念验证,我们使用这种 PMA-qPCR 方法探索了金黄色葡萄球菌、咽峡炎链球菌和洋葱伯克霍尔德菌的共同存在对铜绿假单胞菌抗菌敏感性的影响。