Abstract

We investigated how Legionella pneumophila (Lp) JR32 interacts with Anteglaucoma CS11A and Colpoda E6, two ciliates that we isolated from sewage and sink trap sludge, respectively, using a handmade maze device containing a 96-well crafting plate. Our 18S rDNA-based phylogenetic analysis showed that Anteglaucoma CS11A and Colpoda E6 formed distinct clades. Scanning electron microscopy showed that Anteglaucoma CS11A had a bigger-sized body than Colpoda E6 and, unlike Tetrahymena IB (the reference strain), neither ciliate produced pellets, which are extracellular vacuoles. Fluorescence microscopic observations revealed that although the intake amounts differed, all three ciliates rapidly ingested LpJR32 regardless of the presence or absence of the icm/dot virulence genes, indicating that they all interacted with LpJR32. In co-cultures with Anteglaucoma CS11A, the LpJR32 levels were maintained but fell dramatically when the co-culture contained the LpJR32 icm/dot deletion mutant instead. Anteglaucoma CS11A died within 2 days of co-culture with LpJR32, but survived co-culture with the deletion mutant. In co-cultures with Colpoda E6, LpJR32 levels were maintained but temporarily decreased independently of the virulence gene. Concurrently, the Colpoda E6 ciliates survived by forming cysts, which may enable them to resist harsh environments, and by diminishing the sensitivity of trophozoites to Lp. In the Tetrahymena IB co-cultures with LpJR32 or Δicm/dot, the Lp levels were maintained, albeit with temporal decreases, and the Tetrahymena IB levels were also maintained. We conclude that unlike Tetrahymena IB with pellet production, Anteglaucoma CS11A can be killed by LpJR32 infection, and Colpoda E6 can resist LpJR32 infection through cyst formation and the low sensitivity of trophozoites to Lp. Thus, the two ciliates that we isolated had different susceptibilities to LpJR32 infection.

Highlights

  • Legionella pneumophila (Lp) is ubiquitous in a wide range of natural environments such as soil or pond water, where it interacts with amoebae [1,2,3]

  • We assessed the interaction of Lp with two wild ciliates, Anteglaucoma CS11A and Colpoda E6, which we isolated from sewage and sink trap sludge, respectively, using a handmade maze device fitted with a 96-well crafting plate

  • The 18S rDNA sequences from Anteglaucoma CS11A and Colpoda E6 described in this study under accession numbers LC573510 and have been deposited in the Characterization of the ciliates newly isolated from sewage and sink trap sludge by phylogenetic analysis and Scanning electron microscopy (SEM) observations

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Summary

Introduction

Legionella pneumophila (Lp) is ubiquitous in a wide range of natural environments such as soil or pond water, where it interacts with amoebae [1,2,3]. In the process of adapting to its cellular environment, Lp acquired a set of virulence genes encoding the Icm/Dot system that deliver effector proteins to support its successful phagocytosis and invasion, thereby favoring its growth inside human cells along with its own growth [4,5,6,7]. Lp prefers to colonize plumbing walls or gravel floors in hot springs, and Legionella outbreaks frequently occur when people take public baths in circulating water systems or in free-flowing hot springs where aerosols containing Lp are frequently formed [11,12,13]. From a public health perspective, the ability to control Lp requires better understanding of its interactions with amoebae

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