AI Article Synopsis

  • The study explored how different bacterial species, including Legionella pneumophila and various Pseudomonas strains, affect the growth of Acanthamoeba polyphaga in different environments.
  • At 30°C, L. pneumophila significantly decreased the amoeba's population over 11 days, while Burkholderia cepacia had a lesser impact.
  • Pseudomonas strains exhibited varying behaviors, with P. fluorescens causing cell lysis in the amoeba and P. aeruginosa showing less detrimental effects, highlighting the complex interactions between these bacteria and the protozoa.

Article Abstract

We investigated in solid medium, in water microcosm co-cultures and by light and transmission electron microscopy the influence of Legionella pneumophila Lp-1, Pseudomonas aeruginosa ATCC 27853, Burkholderia cepacia ATCC 25416 and Pseudomonas fluorescens SSD35 on the growth and survival of Acanthamoeba polyphaga. The infection with L. pneumophila was microscopically characterized by the presence of few bacteria inside protozoa at 4th h, and by the beginning of disruptive effects in late phase of trial. In water microcosm studies, performed at different temperature, the more significant interactions were observed at 30°C. In these conditions, L. pneumophila caused a marked reduction in trophozoite and cyst counts from the 4th day until the end of incubation (11 days). B. cepacia showed, by microscopic observation, few and generally single rods within protozoan phagosomes and caused a light reduction of trophozoite viability and cyst formation in co-cultures. A more invasive type of endocytosis, characterized by an early invasion with the presence of a high bacteria number inside amoebae, was observed for Pseudomonas strains. P. fluorescens produced a violent lysis of the host, whereas P. aeruginosa did not cause lysis or suffering. These results underline that water bacteria other than legionella are capable of intracellular survival in Acanthamoeba, influencing the protozoa viable cycle.

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Source
http://dx.doi.org/10.1007/s00203-010-0618-0DOI Listing

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