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In vitro study reveals that Filifactor alocis relieves arginine toxicity in Porphyromonas gingivalis via ArcA degradation, suggesting a cooperative metabolic survival mechanism in periodontitis.
Metabolic cross-feeding is a main driver of microbial mutualism under various stresses. Elevated arginine levels in the periodontal microenvironment reshape pathogen physiology. Here, we discovered that increased arginine levels disrupted the intracellular amino acid metabolism of the periodontal pathogen Porphyromonas gingivalis by repressing glutamate dehydrogenase activity and α-ketoglutarate production via the accumulation of NH3. This perturbation inhibited P. gingivalis growth and was accompanied by increased expression of the PorX/PorY-associated T9SS and enhanced small-peptide acquisition. Given the frequent co-occurrence of P. gingivalis and Filifactor alocis in periodontitis, our findings suggested that F. alocis partially relieved arginine-associated growth inhibition of P. gingivalis through ArcA-dependent arginine degradation, thereby promoting its persistence under high-arginine conditions. This cooperative arginine metabolism is critical for the resilience of microbial communities and may serve as a therapeutic target. Complex microbial communities are often shaped by cooperation. Here, the authors show that high arginine levels suppress the periodontal pathogen Porphyromonas gingivalis, while Filifactor alocis helps it persist by breaking down arginine, revealing a metabolic partnership.
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Zhou et al. (2026) studied this question.
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