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YFV-17D induces mitochondrial hyper-functionality and energetic overcommitment.

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posted on 2025-04-21, 17:50 authored by Samantha G. Muccilli, Benjamin Schwarz, Byron Shue, Forrest Jessop, Jeffrey G. Shannon, Charles L. Larson, Adam Hage, Seon-Hui Hong, Eric Bohrnsen, Thomas Hsu, Alison W. Ashbrook, Gail L. Sturdevant, Shelly J. Robertson, Joseph W. Guarnieri, Justin Lack, Douglas C. Wallace, Catharine M. Bosio, Margaret R. MacDonald, Charles M. Rice, Jonathan W. Yewdell, Sonja M. Best

(A) Seahorse XF cell mito stress test profile of HepG2 cells infected with mock, YFV-17D (MOI 0.1), or DENV2 (MOI 1) at 12hpi, 24hpi, and 48hpi. (B) Quantification of Seahorse XF mito stress test parameters (basal respiration, maximal respiration, ATP-linked respiration, and spare respiratory capacity) in mock, YFV-17D, or DENV2 infected HepG2 cells over 48 h. (C) Quantification of intracellular ATP levels in mock, YFV-17D, and DENV2 infected HepG2 cells at 24 hpi and 48 hpi. (D) Quantification of mitochondrial membrane potential (TMRE) in mock, YFV-17D, and DENV2 infected HepG2 cells between 24 hpi and 72 hpi. (E) Mitochondrial membrane potential at 48 hpi with molecular clone-derived YFV variants. Values represent the mean ± SD (B: n = 12, C: n = 4, D: n = 3, E: n = 4). Statistical significance was assessed using two-way ANOVA followed by Dunnett’s multiple comparisons test. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001.

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