ArticleParasite (Paris, France)2026
Proteomic identification of Acanthamoeba castellanii excretory-secretory proteins associated with Klebsiella pneumoniae capsule enlargement: a candidate role for C-type lysozyme.
Article in Parasite (Paris, France), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundAcanthamoeba castellanii and Klebsiella pneumoniae are environmental commensals that co-exist in aquatic habitats. Our previous studies demonstrated that A. castellanii genotype T4 (AcT4) induces capsule enlargement and hypermucoviscosity in K. pneumoniae through small excretory-secretory proteins (ESPs; <10 kDa) that activate the Rcs two-component system, upregulating capsule biosynthesis genes independently of virulence plasmids. However, the molecular identity of these active ESPs remained undefined.
resultsTo identify candidate proteins, we performed label-free quantitative proteomics (LC-MS/MS) on conditioned medium from AcT4 co-cultured with K. pneumoniae (Ac/Kp) versus AcT4 alone (Ac only; n = 3 per group). A total of 391 A. castellanii proteins were identified; seven showed significantly increased extracellular abundance in Ac/Kp medium (log
conclusionsThis comparative secretome analysis provides the first proteomic catalogue of AcT4 extracellular proteins during co-culture with K. pneumoniae and identifies C-type lysozyme as a biologically plausible candidate mediating Rcs-dependent capsule induction. These findings lay the groundwork for future validation of AcT4-derived ESPs in protozoa-bacteria interactions and their potential role in the environmental emergence of hypervirulent K. pneumoniae.
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