Abstract

Bacterial type 4 pili (T4P) are extracellular polymers that serve both as adhesins and molecular motors. Functionally, they are involved in adhesion, colony formation, twitching motility, and horizontal gene transfer. T4P of the human pathogen Neisseria gonorrhoeae have been shown to enhance survivability under treatment with antibiotics or hydrogen peroxide. However, little is known about the effect of external stresses on T4P production and motor properties. Here, we address this question by directly visualizing gonococcal T4P dynamics. We show that in the absence of stress gonococci produce T4P at a remarkably high rate of ∼200 T4P min–1. T4P retraction succeeds elongation without detectable time delay. Treatment with azithromycin or ceftriaxone reduces the T4P production rate. RNA sequencing results suggest that reduced piliation is caused by combined downregulation of the complexes required for T4P extrusion from the cell envelope and cellular energy depletion. Various other stresses including inhibitors of cell wall synthesis and DNA replication, as well as hydrogen peroxide and lactic acid, inhibit T4P production. Moreover, hydrogen peroxide and acidic pH strongly affect pilus length and motor function. In summary, we show that gonococcal T4P are highly dynamic and diverse external stresses reduce piliation despite the protective effect of T4P against some of these stresses.

Highlights

  • Type 4 pili (T4P) are polymeric cell appendages that are responsible for a remarkable variety of functions in the bacterial world

  • Deletion of the retraction ATPase PilT inhibited T4P dynamics (Supplementary Figure 6), confirming that the observed dynamics depends on PilT

  • Since we found the azithromycin and ceftriaxone reduce the rate of T4P production, we addressed the question whether genes involved in T4P biogenesis were downregulated during antibiotic treatment

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Summary

Introduction

Type 4 pili (T4P) are polymeric cell appendages that are responsible for a remarkable variety of functions in the bacterial world. These functions include adhesion to host cells and other surfaces, microcolony formation, twitching motility, horizontal gene transfer, and surface sensing (Berry and Pelicic, 2015; Craig et al, 2019). The potential mechanisms include hindered diffusion of the drug within the colony (Tseng et al, 2013; Singh et al, 2016), stress responses (Nguyen et al, 2011; Secor et al, 2018), and community-related differentiation (Yan and Bassler, 2019). Aggregation is controlled by T4P and piliation and T4P dynamics likely affect stress tolerance

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