Parasit Host Dis.  2023 Nov;61(4):397-404. 10.3347/PHD.23088.

Phagocytosis-associated genes in Acanthamoeba castellanii feeding on Escherichia coli

Affiliations
  • 1Department of Biomedical Science, Graduate School, Kyung Hee University, Seoul 02447, Korea
  • 2Department of Medical Zoology, Kyung Hee University School of Medicine, Seoul 02447, Korea
  • 3Medical Research Center for Bioreaction to Reactive Oxygen Species and Biomedical Science Institute, Core Research Institute, School of Medicine, Kyung Hee University, Seoul 02447, Korea
  • 4Department of Parasitology, Dong-A University College of Medicine, Busan 49201, Korea

Abstract

Acanthamoeba species are free-living amoebae those are widely distributed in the environment. They feed on various microorganisms, including bacteria, fungi, and algae. Although majority of the microbes phagocytosed by Acanthamoeba spp. are digested, some pathogenic bacteria thrive within them. Here, we identified the roles of 3 phagocytosis-associated genes (ACA1_077100, ACA1_175060, and AFD36229.1) in A. castellanii. These 3 genes were upregulated after the ingestion of Escherichia coli. However, after the ingestion of Legionella pneumophila, the expression of these 3 genes was not altered after the consumption of L. pneumophila. Furthermore, A. castellanii transfected with small interfering RNS (siRNA) targeting the 3 phagocytosis-associated genes failed to digest phagocytized E. coli. Silencing of ACA1_077100 disabled phagosome formation in the E. coli-ingesting A. castellanii. Alternatively, silencing of ACA1_175060 enabled phagosome formation; however, phagolysosome formation was inhibited. Moreover, suppression of AFD36229.1 expression prevented E. coli digestion and consequently led to the rupturing of A. castellanii. Our results demonstrated that the ACA1_077100, ACA1_175060, and AFD36229.1 genes of Acanthamoeba played crucial roles not only in the formation of phagosome and phagolysosome but also in the digestion of E. coli.

Keyword

gene expression; gene silencing; phagocytosis; phagolysosome; phagosome; siRNA
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