Effects of PslG on the Surface Movement of Pseudomonas aeruginosa

• Published in: Applied and environmental microbiology 2018-07, Vol.84 (13), p.e00219-18
• Main Authors: Zhang, Jingchao, He, Jing, Zhai, Chunhui, Ma, Luyan Z, Gu, Lichuan, Zhao, Kun
• Format: Article
• Language: English
• Subjects: Bacteria; Biofilms; Biomedical materials; Cellular biology; Environmental Microbiology; Motility; Pseudomonas aeruginosa
• ISSN: 0099-2240; 1098-5336
• DOI: 10.1128/AEM.00219-18

PslG attracted a lot of attention recently due to its great potential abilities in inhibiting biofilms of However, how PslG affects biofilm development still remains largely unexplored. Here, we focused on the surface motility of bacterial cells, which is critical for biofilm development. We studied the effects of PslG on bacterial surface movement in early biofilm development at a single-cell resolution by using a high-throughput bacterial tracking technique. The results showed that compared with no exogenous PslG addition, when PslG was added to the medium, bacterial surface movement was significantly (4 to 5 times) faster and proceeded in a more random way with no clear preferred direction. A further study revealed that the fraction of walking mode increased when PslG was added, which then resulted in an elevated average speed. The differences of motility due to PslG addition led to a clear distinction in patterns of bacterial surface movement and retarded microcolony formation greatly. Our results provide insight into developing new PslG-based biofilm control techniques. Biofilms of are a major cause for hospital-acquired infections. They are notoriously difficult to eradicate and pose serious health hazards to human society. So, finding new ways to control biofilms is urgently needed. Recent work on PslG showed that PslG might be a good candidate for inhibiting/disassembling biofilms of through Psl-based regulation. However, to fully explore PslG functions in biofilm control, a better understanding of PslG-Psl interactions is needed. Toward this end, we examined the effects of PslG on the surface movement of in this work. The significance of our work is in greatly enhancing our understanding of the inhibiting mechanism of PslG on biofilms by providing a detailed picture of bacterial surface movement at a single-cell level, which will allow a full understanding of PslG abilities in biofilm control and thus present potential applications in biomedical fields.