24Pseudomonas aeruginosa can cause severe infections in humans. This bacteria often 25 adopt a biofilm lifestyle that is hard to treat. In several previous studies, the 26 PprA-PprB two-component system (TCS), which controls the expression of type IVb 27 pili, BapA adhesin, and CupE fimbriae, was shown to be involved in biofilm 28 formation. However, signals or environmental conditions that can trigger the 29 PprA-PprB TCS are still unknown, and the molecular mechanisms of PprB-mediated 30 biofilm formation are poorly characterized. Here we report that carbon starvation 31 stress (CCS) can induce the expression of pprB and genes in the PprB regulon. The 32 stress response sigma factor RpoS, rather than the two-component sensor PprA, was 33 determined to mediate the induction of pprB transcription. We also observed a strong 34 negative regulation of PprB to the transcription of itself. Further experiments showed 35 that PprB overexpression greatly enhanced cell-cell adhesion (CCA) and cell-surface 36 adhesion (CSA) in P. aeruginosa. Specially, under the background of PprB 37 overexpression, both of the BapA adhesin and CupE fimbriae displayed positive effect 38 on CCA and CSA, while the type IVb pili showed an unexpected negative effect on 39 CCA and no effect on CSA. In addition, expression of the PprB regulon genes 40 displayed significant increases in 3-day colony biofilms, indicating a possible carbon 41 limitation state in these biofilms. The CSS-RpoS-PprB-Bap/Flp/CupE/Tad pathway 42 identified in this study provides a new perspective on the process of biofilm formation 43 under carbon-limited environments.44 3 / 44 IMPORTANCE 45 46Typically, determining the external signals that can trigger a regulatory system is 47 crucial to understand the regulatory logic and inward function of that system. The
48PprA-PprB two-component system was reported to be involved in biofilm formation 49 in Pseudomonas aeruginosa, but the signals that can trigger this system are unknown.
50In this study, we found that carbon starvation stress (CSS) can induce the transcription 51 of pprB and genes in PprB regulon, through an RpoS dependent pathway. Increase of 52 PprB expression leads to enhanced cell-cell and cell-surface adhesions in P. 53 aeruginosa, both of which are dependent mainly on the Bap adhesin secretion system 54 and partially on the CupE fimbriae. Our findings suggest that PprB reinforces the 55 structure of biofilms under carbon-limited conditions, and the Bap secretion system 56 and CupE fimbriae are two potential targets for biofilm treatment.57 58 KEYWORDS 59 Pseudomonas aeruginosa, carbon starvation stress, biofilm formation, PprB 60 61 62 63 64 65 66 4 / 44 Pseudomonas aeruginosa is a ubiquitous opportunistic pathogen responsible for many 67 human infections, especially the cystic fibrosis found in some immunocompromised 68 individuals (1-3). In most cases of chronic infections, bacteria live in biofilm 69 communities, and increasingly, they are becoming resistant to human immunity and 70 antibiotic treatment...