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Amoebae as training grounds for microbial pathogens.
Price, Christopher T D; Hanford, Hannah E; Al-Quadan, Tasneem; Santic, Marina; Shin, Cheon J; Da'as, Manal S J; Abu Kwaik, Yousef.
Affiliation
  • Price CTD; Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky, USA.
  • Hanford HE; Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky, USA.
  • Al-Quadan T; Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky, USA.
  • Santic M; University of Rijeka, Rijeka, Croatia.
  • Shin CJ; Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky, USA.
  • Da'as MSJ; Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky, USA.
  • Abu Kwaik Y; Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky, USA.
mBio ; : e0082724, 2024 Jul 08.
Article in En | MEDLINE | ID: mdl-38975782
ABSTRACT
Grazing of amoebae on microorganisms represents one of the oldest predator-prey dynamic relationships in nature. It represents a genetic "melting pot" for an ancient and continuous multi-directional inter- and intra-kingdom horizontal gene transfer between amoebae and its preys, intracellular microbial residents, endosymbionts, and giant viruses, which has shaped the evolution, selection, and adaptation of microbes that evade degradation by predatory amoeba. Unicellular phagocytic amoebae are thought to be the ancient ancestors of macrophages with highly conserved eukaryotic processes. Selection and evolution of microbes within amoeba through their evolution to target highly conserved eukaryotic processes have facilitated the expansion of their host range to mammals, causing various infectious diseases. Legionella and environmental Chlamydia harbor an immense number of eukaryotic-like proteins that are involved in ubiquitin-related processes or are tandem repeats-containing proteins involved in protein-protein and protein-chromatin interactions. Some of these eukaryotic-like proteins exhibit novel domain architecture and novel enzymatic functions absent in mammalian cells, such as ubiquitin ligases, likely acquired from amoebae. Mammalian cells and amoebae may respond similarly to microbial factors that target highly conserved eukaryotic processes, but mammalian cells may undergo an accidental response to amoeba-adapted microbial factors. We discuss specific examples of microbes that have evolved to evade amoeba predation, including the bacterial pathogens- Legionella, Chlamydia, Coxiella, Rickettssia, Francisella, Mycobacteria, Salmonella, Bartonella, Rhodococcus, Pseudomonas, Vibrio, Helicobacter, Campylobacter, and Aliarcobacter. We also discuss the fungi Cryptococcus, and Asperigillus, as well as amoebae mimiviruses/giant viruses. We propose that amoeba-microbe interactions will continue to be a major "training ground" for the evolution, selection, adaptation, and emergence of microbial pathogens equipped with unique pathogenic tools to infect mammalian hosts. However, our progress will continue to be highly dependent on additional genomic, biochemical, and cellular data of unicellular eukaryotes.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: MBio Year: 2024 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: MBio Year: 2024 Document type: Article Affiliation country: Estados Unidos
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