Acyl-Coa Thioesterases: A Rheostat That Controls Activated Fatty Acids Modulates Dengue Virus Serotype 2 Replication

During infection with dengue viruses (DENVs), the lipid landscape within host cells is significantly altered to assemble membrane platforms that support viral replication and particle assembly. Fatty acyl-CoAs are key intermediates in the biosynthesis of complex lipids that form these membranes. They also function as key signaling lipids in the cell. Here, we carried out loss of function studies on acyl-CoA thioesterases (ACOTs), a family of enzymes that hydrolyze fatty acyl-CoAs to free fatty acids and coenzyme A, to understand their influence on the lifecycle of DENVs. The loss of function of the type I ACOTs 1 (cytoplasmic) and 2 (mitochondrial) together significantly increased DENV serotype 2 (DENV2) viral replication and infectious particle release. However, isolated knockdown of mitochondrial ACOT2 significantly decreased DENV2 protein translation, genome replication, and infectious virus release. Furthermore, loss of ACOT7 function, a mitochondrial type II ACOT, similarly suppressed DENV2. As ACOT1 and ACOT2 are splice variants, these data suggest that functional differences and substrate specificities due to the location (cytosol and mitochondria, respectively) of these proteins may account for the differences in DENV2 infection phenotype. Additionally, loss of mitochondrial ACOT2 and ACOT7 expression also altered the expression of several ACOTs located in multiple organelle compartments within the cell, highlighting a complex relationship between ACOTs in the DENV2 virus lifecycle.


Introduction
Dengue viruses (DENVs) are arthropod-borne viruses that are transmitted by the Aedes aegypti mosquito [1,2]. These viruses infect over 400 million people each year. They are obligate intercellular parasites that rely on host cell metabolic pathways to fulfill their energy requirements and access substrates necessary for generating progeny virions [3]. It is widely established that the lifecycle of DENVs is reliant upon host lipid metabolic pathways [3][4][5][6]. Specifically, these viruses alter endoplasmic reticulum membranes to form scaffolds for viral protein translation and assembly of viral replication complexes [6,7]. Moreover, during viral particle assembly, host cell membranes are co-opted and incorporated into the viral envelope as a structural component of the virus particle [3,6,7]. Bank identifier 2QQ2 depicted. Type II ACOTs contain the "hot dog" domain composed of two alpha helixes surrounding a hydrophobic core. Although the composition of the active site is unknown within the "hot dog" domain, these enzymes are functionally analogous to type I ACOTs [10]. (C,D): Huh7 cells were transfected with an siRNA pool targeting both the ACOT1 and ACOT2 genes as well as indicated controls (IRR and DENV2) and then infected with DENV2 for 24 h (MOI = 3). (C) Infectious particle release was titrated via plaque assay. (D) Huh7 cells were collected, and Bank identifier 2QQ2 depicted. Type II ACOTs contain the "hot dog" domain composed of two alpha helixes surrounding a hydrophobic core. Although the composition of the active site is unknown within the "hot dog" domain, these enzymes are functionally analogous to type I ACOTs [10]. (C,D): Huh7 cells were transfected with an siRNA pool targeting both the ACOT1 and ACOT2 genes as well as indicated controls (IRR and DENV2) and then infected with DENV2 for 24 h (MOI = 3). (C) Infectious particle release was titrated via plaque assay. (D) Huh7 cells were collected, and relative copy number of viral RNA within cells was measured via qRT-PCR. qRT-PCR results were normalized to RPLP0. ACOT1/2: siRNA targeting acyl-CoA thioesterase 1 and 2, IRR: irrelevant siRNA control (no biological target for siRNA sequence), DENV2: siRNA targeting dengue virus, Given that fatty acyl-CoAs are integral to lipid metabolism and energy homeostasis, we investigated if perturbing fatty acyl-CoA homeostasis by altering ACOT enzyme expression modulated DENV2 infection. We also investigated if the ACOT enzyme location (cytoplasmic vs. mitochondrial) and/or specificity type (type I vs. type II) differentially influenced DENV2 replication. We examined three representative ACOT enzymes-ACOT1, ACOT2, and ACOT7-to understand their impact on the lifecycle of DENV2 in human hepatoma (liver) cells (Huh7s). siRNA-mediated loss of function studies of the type I ACOTs 1 and 2 together significantly increased DENV2 infectious particle release. However, isolated knockdown of ACOT2 significantly decreased DENV2 protein translation, genome replication, and infectious virus release. The loss of function of ACOT7, a mitochondrial type II ACOT, also similarly suppressed DENV2. Furthermore, our studies reveal a complex relationship between type I and type II ACOTs during DENV2 infection that suggests a functional interdependency of these enzymes.
For this study, dengue virus serotype 2 was used (DENV2, strain 16681) [17,18]. The virus was passaged in C6/36 cells. Viral titer was determined via plaque assay on BHK-21 cells as previously described [19]. Virus infections were carried out at room temperature for 1 h, allowing for viral adherence. Subsequently, the virus was removed, and cells were washed with 1×PBS before the addition of media supplemented with 2 mM nonessential amino acids, 2 mM L-glutamine, and 2% FBS. Cells were incubated at 37 • C with 5% CO 2 for 24 h.

siRNA Transfection and Knockdown Confirmation
ACOT1/2, ACOT2, and ACOT7 loss of function was conducted by transfecting Huh7 cells with pooled siRNAs (Horizon Discovery/Dharmacon, Lafayette, CO, USA; Sigma-Aldrich, St. Louis, MO, USA-see Supplementary Table S1) as described previously [20] using RNAiMAX (Invitrogen, Carlsbad, CA, USA) and incubating for 48 h at 37 • C with Viruses 2022, 14, 240 4 of 12 5% CO 2 . At 48 h post transfection, cells were either collected for a cytotoxicity assay (described below), knockdown confirmation, or infected with DENV2 (as described above). At 24 hpi, cells and viral supernatant were collected for further analysis. Viral titration was completed via plaque assay. RNA was extracted from cells, and qRT-PCR analysis was used to confirm knockdown of ACOT2 and ACOT7 mRNA transcripts. Cellular transcripts were normalized to RPLP0, and the ACOT2 and ACOT7 siRNA-treated samples were then compared to an irrelevant control (IRR) using the delta-delta cq method described in [21]. The IRR control siRNA is a scrambled RNA with no homology to any human mRNA sequences (described in [20]). Cytotoxicity of siRNA treatment was determined using a 1:10 dilution of resazurin (ThermoFisher, Ward Hill, MA, USA) in cell culture media, and incubating cells for 1-2 h. Fluorescence was read on a Victor 1420 Multilabel plate reader (Perkin Elmer, Waltham, MA, USA) at 560 nm/590 nm (excitation/emission).

RNA Extraction and qRT-PCR
RNA was extracted from cells and viral supernatant using TRIzol or TRIzol LS (Ther-moFisher), respectively, following standard TRIzol extraction methods. For qRT-PCR, the Brilliant III Ultra-Fast SYBR ® Green one-step qRT-PCR kit (Agilent, Carlsbad, CA, USA) was used, and all reactions were set up according to manufacturer's protocols on a LightCycler 96-well real-time PCR machine (Roche, Indianapolis, IN, USA). The following cycling parameters were employed: 20 min at 50 • C for reverse transcription, 5 min at 95 • C, followed by 45 two-step cycles of 95 • C for 5 secs, and 60 • C for 60 secs. A melt curve followed each step, starting at 65 • C and ending at 97 • C. (Primer sequences are reported in Supplementary Table S1). A standard curve was generated using in vitro transcribed viral RNA from a DENV2 cDNA subclone (derived from strain 16681 full-length clone) in order to quantify DENV2 genome copies. All cellular RNA transcript copy numbers were normalized to Ribosomal Protein Lateral Stalk Subunit P0 (RPLP0) RNA using the delta-delta cq method as described previously [21,22].

Western Blotting
Huh7 cells were lysed in RIPA Buffer. Total protein in each sample was measured using the Qubit BR Protein Assay (ThermoFisher, Carlsbad, CA, USA) on a Qubit Flex Fluorometer. Equal total protein was loaded from each of the indicated cell lysates and run on a Criterion TM XT 4-12% Bis-Tris protein gel (Bio-Rad, Hercules, CA, USA). Protein was transferred at 4 • C to nitrocellulose membrane for 2 h at 50 V. Following transfer, blocking was performed overnight at 4 • C with a 5% milk solution in 1 × PBS supplemented with 0.1% Tween 20. The primary antibodies used were a 1:300 dilution of antibody against the DENV2 NS3 protein (mouse polyclonal antibody raised against the DENV2 NS3 protein as described in 20), and 1:100 dilution of β-actin (rabbit polyclonal antibody, Invitrogen). The secondary antibodies used were a 1:3000 dilution of goat-anti-mouse IRDye 800CW, and goat-anti-rabbit IRDye 680RD (Li-Cor Biosciences, Lincoln, NE, USA). Blots were imaged on a ChemiDoc MP Imaging System (Bio-Rad, Hercules, CA, USA), and quantified in ImageJ utilizing area under the curve analysis.

Statistical Analysis
In each figure and/or figure legend, statistical analysis details are noted. All results are expressed as mean values with standard deviation. Statistical significance was determined using a one-way Analysis of Variance (ANOVA) with Dunnett's multiple comparisons test, or an unpaired t test using Prism software version 9.0 (GraphPad Software, La Jolla, CA, USA).

Combined Loss of ACOT1 and ACOT2 Function Increases DENV2 Genome Replication and Infectious Particle Release
As ACOTs act as a rheostat for intracellular levels of FFAs and fatty acyl-CoAs, we hypothesized that ACOT functionality, which purportedly limits the availability of fatty acyl-CoAs, may have an inhibitory effect on the DENV2 lifecycle. To determine if ACOT enzymes affect DENV2 replication, we used siRNA-mediated knockdown to decrease the expression of type I ACOTs 1 and 2 in Huh7 cells. ACOT1 is located in the cytoplasm and ACOT2 in the mitochondria. There is~94% homology between the mRNAs of ACOT1 and ACOT2, with only an insertion of 90-110 nucleotides differentiating ACOT2 mRNA from ACOT1 mRNA [23][24][25]. We included a non-target, irrelevant siRNA (IRR) to control for off-target effects of siRNA treatment and a DENV2-specific siRNA as a positive control for viral inhibition. We found that loss of ACOT1 and ACOT2 together resulted in an increase (~178%) in infectious viral release ( Figure 1C) and in viral genome replication (~470%, Figure 1D) compared to the IRR control. Due to the sequence similarity between ACOT1 and 2, we were unable to target siRNAs specific to ACOT1, but we were able to target specific siRNAs to ACOT2. Therefore, as shown below, we were able to parse out the influence of ACOT2 on this phenotype.

Loss of ACOT2 Function Reduces DENV2 Replication, Infectious Particle Release and Infectivity
Given the above observations from combined loss of ACOT1 and ACOT2 function, and that ACOT1 and ACOT2 share the same substrate specificity (18), we hypothesized that loss of ACOT2 function alone would also result in increased viral replication and release. Therefore, we repeated knockdown studies with siRNAs specifically targeting ACOT2 in Huh7 cells. Surprisingly, we found that loss of ACOT2 function resulted in a significant reduction (~76%) in infectious virus release ( Figure 2A) compared to the IRR control. Additionally, DENV2 genome replication was reduced by~50% following ACOT2 knockdown ( Figure 2B). In our previous studies, we found that inhibition of specific enzymes involved in fatty acid metabolism resulted in the release of partially immature virions, thereby reducing particle infectivity [25]. To determine if loss of ACOT2 function also reduced particle infectivity, we compared the ratios of viral RNA copies to infectious virions (particle/pfu ratio) in the supernatant of each of our treatment groups ( Figure 2C). The data showed that there was a significant increase in the DENV particle/pfu ratio following ACOT2 knockdown compared to the IRR control, thus suggesting a decrease in particle infectivity. We also found that viral protein translation was reduced by~50% ( Figure 2D and Supplementary Figure S1). We further confirmed that siRNA treatment was not cytotoxic to Huh7 cells ( Figure 2E) and was also effective at reducing ACOT2 mRNA levels ( Figure 2F). Overall, these data suggest that ACOT2 functionality is critical to the DENV2 lifecycle. This contrasts with the phenotype from the combined loss of function of ACOT1 and 2, suggesting that ACOT1 has a unique influence on viral replication. following ACOT2 knockdown compared to the IRR control, thus suggesting a decrease in particle infectivity. We also found that viral protein translation was reduced by ~50% (Figures 2D and Supplementary Figure S1). We further confirmed that siRNA treatment was not cytotoxic to Huh7 cells ( Figure 2E) and was also effective at reducing ACOT2 mRNA levels ( Figure 2F). Overall, these data suggest that ACOT2 functionality is critical to the DENV2 lifecycle. This contrasts with the phenotype from the combined loss of function of ACOT1 and 2, suggesting that ACOT1 has a unique influence on viral replication.

Mitochondrial ACOTs Are Vital for Productive DENV2 Infection
ACOT2 is suggested to be an important mediator of β-oxidation [26,27]. This is the process of gaining ATP from the breakdown of fatty acyl-CoA to 2-carbon acetyl-CoA molecules. As this process occurs in the mitochondria, mitochondrial ACOTs may be important in regulating the balance of FFAs and fatty acyl-CoAs through shuttling fatty acyl-CoAs into β-oxidation [26,27]. Previous studies indicate that β-oxidation is elevated during infection

Mitochondrial ACOTs Are Vital for Productive DENV2 Infection
ACOT2 is suggested to be an important mediator of β-oxidation [26,27]. This is the process of gaining ATP from the breakdown of fatty acyl-CoA to 2-carbon acetyl-CoA molecules. As this process occurs in the mitochondria, mitochondrial ACOTs may be important in regulating the balance of FFAs and fatty acyl-CoAs through shuttling fatty acyl-CoAs into β-oxidation [26,27]. Previous studies indicate that β-oxidation is elevated during infection of host cells by DENVs (reviewed in [3]). Both type I and type II ACOTs exist in the mitochondria. ACOT7 is a type II ACOT, and is functionally homologous to ACOT2 (both hydrolyze long-chain FAs) [25]. Therefore, we investigated if loss of ACOT7 function also resulted in suppression of DENV2 infection. Similar to ACOT2 knockdown, we found that loss of ACOT7 function significantly reduced DENV2 infectious particle release (~77%) in Huh7 cells ( Figure 3A). Interestingly, ACOT7 inhibition resulted in a greater reduction of viral protein translation (~75% reduction, Figure 3D and Supplementary Figure S1) and viral genome replication (~70% reduction, Figure 3B) compared to the effect of the loss of function of ACOT2 ( Figure 2B). Similar to the ACOT2 study, loss of ACOT7 function significantly decreased particle infectivity ( Figure 3C). We confirmed that these results were also not due to cytotoxicity of the siRNA treatment ( Figure 3E), and that the ACOT7 siRNA effectively reduced ACOT7 mRNA levels ( Figure 3F). Taken together, these studies suggest that two of the mitochondrial ACOTs have a vital role in the DENV2 lifecycle. viral protein translation (~75% reduction, Figure 3D and Supplementary Figure S1) and viral genome replication (~70% reduction, Figure 3B) compared to the effect of the loss of function of ACOT2 ( Figure 2B). Similar to the ACOT2 study, loss of ACOT7 function significantly decreased particle infectivity ( Figure 3C). We confirmed that these results were also not due to cytotoxicity of the siRNA treatment ( Figure 3E), and that the ACOT7 siRNA effectively reduced ACOT7 mRNA levels ( Figure 3F). Taken together, these studies suggest that two of the mitochondrial ACOTs have a vital role in the DENV2 lifecycle.

Both Type I and Type II ACOTs Are Differentially Expressed upon ACOT2 or ACOT7 Knockdown
Currently, there are ten human ACOTs known to exist in different subcellular compartments, and they have substrate specificity for a wide range of fatty acyl-CoAs [24,25]. However, the functional overlap and/or ability of each ACOT to compensate for the loss of function of the others is unknown. As mitochondrial ACOTs seem to play vital roles in fatty acid metabolism and energy production, we determined whether other ACOTs could compensate for loss of ACOT2 or ACOT7 function, both within and without the context of DENV2 infection. To investigate this, we carried out similar siRNA-mediated knockdown of ACOT2 and ACOT7 in both mock-infected and DENV2-infected Huh7 cells. An IRR siRNA control was also included. 24 h post infection (hpi), mock-and DENV2-infected In both mock-infected and DENV2-infected samples, we observed similar trends in the mRNA expression of other ACOTs upon knockdown of ACOT2 ( Figure 4A,B) or ACOT7 ( Figure 4C,D). Specifically, we observed that in both mock-and DENV2-infected Huh7 cells, knockdown of ACOT2 significantly reduced the mRNA expression of ACOTs 1, 6, 8, and 11 ( Figure 4A,B). A decrease in ACOT9 and ACOT12 mRNA expression was only observed in DENV2-infected ACOT2 knockdown samples. We found loss of ACOT7 significantly reduced mRNA expression of ACOTs 2,4,8,9,and 11 in both mock-and DENV2-infected cells, (Figure 4C,D). Additionally, in DENV2 infected cells, ACOT6 and ACOT13 mRNA expression was decreased in ACOT7 siRNA-treated cells. It should be noted that the siRNAs for ACOT2 and ACOT7 do not have any sequence similarity to the other ACOT mRNAs. Therefore, these data suggest that other ACOTs may be functionally dependent on the activity of ACOT2 and 7. Intriguingly, inhibiting ACOT7 also reduced expression of ACOT2 ( Figure 4C,D); however, inhibition of ACOT2 did not impact the expression of ACOT7 ( Figure 4A,B). Thus, while both mitochondrial ACOTs are functionally similar, neither compensates for the loss of the other at a transcriptional level, and ACOT2 functionality may rely upon ACOT7.

Mitochondrial ACOTs Are Upregulated at Early Timepoints of Infection
In previous studies, it has been demonstrated that DENV2 infection results in both viral-and host-mediated modulation of enzymes involved in fatty acid metabolism [3][4][5][6][7][8][9]24]. As our loss of function studies of ACOT2 and ACOT7 indicated that these enzymes are vital for the DENV2 lifecycle, we analyzed whether ACOT2 and ACOT7 mRNA expression was altered over a time course of DENV2 infection. For this study, we collected both mock-infected and DENV2-infected cells at 0, 6, 24, and 48 hpi. These time points represent early, peak, and late viral replication. ACOT mRNA expression was analyzed using qRT-PCR ( Figure 5). We observed that ACOT2 and ACOT7 mRNA expression was significantly upregulated at 6 hpi in DENV2-infected cells, but downregulated at 24 and 48 hpi ( Figure 5A). A similar trend was noted when we compared mRNA expression be-

Mitochondrial ACOTs Are Upregulated at Early Timepoints of Infection
In previous studies, it has been demonstrated that DENV2 infection results in both viral-and host-mediated modulation of enzymes involved in fatty acid metabolism [3-9,24].
Viruses 2022, 14, 240 9 of 12 As our loss of function studies of ACOT2 and ACOT7 indicated that these enzymes are vital for the DENV2 lifecycle, we analyzed whether ACOT2 and ACOT7 mRNA expression was altered over a time course of DENV2 infection. For this study, we collected both mock-infected and DENV2-infected cells at 0, 6, 24, and 48 hpi. These time points represent early, peak, and late viral replication. ACOT mRNA expression was analyzed using qRT-PCR ( Figure 5). We observed that ACOT2 and ACOT7 mRNA expression was significantly upregulated at 6 hpi in DENV2-infected cells, but downregulated at 24 and 48 hpi ( Figure 5A). A similar trend was noted when we compared mRNA expression between DENV2 and mock-infected samples at each timepoint, although the increased expression at 6 hpi was not statistically significant ( Figure 5B). These results, combined with our results in Figures 2 and 3, suggest that ACOT2 and ACOT7 functionality is required for early stages of the DENV2 life cycle.

Discussion
The ACOT family of enzymes are suggested to be key regulators of the intercellular balance of activated fatty acids (fatty acyl-CoAs) and FFAs [10,25]. As previous studies have shown that DENVs are reliant upon activated fatty acids for completion of their lifecycle ( [8,9,20,21,28,29], reviewed in [3]), our present study investigated whether ACOT enzymes were important modulators of DENV2 infection. The ACOT enzymes chosen represented both type I (ACOT1 and ACOT2) and type II ACOTs (ACOT7), as well as ACOTs found within the same organelle (ACOT2 and ACOT7 in the mitochondria). Interestingly, we found that the loss of function of these enzymes had a divergent effect on the DENV2 lifecycle that was independent of their substrate specificity, and, instead, highlighted a more nuanced relationship between DENV2 and the subcellular regulation of fatty acid metabolism. Specifically, we found that the loss of function of the cytoplasmic ACOT1 enzyme resulted in increased DENV2 genome replication and infectious virus release, indicating that its normal function may be antiviral. However, the loss of function of the mitochondrial ACOT2 and ACOT7 enzymes resulted in the suppression of multiple stages of the DENV2 lifecycle, indicating that the function of these enzymes is vital for effective DENV2 infection. Furthermore, our analyses revealed a functional dependency between enzymes within the ACOT family.
Because ACOTs act directly on activated fatty acids, it is predicted that they play a significant role in the modulation of fatty acid metabolism [10,11,21,25,30]. However, mechanistic insight as to the specific functions of ACOT enzymes is limited. One challenge is that the ester bond that links coenzyme A with fatty acids is labile, which limits the ability to obtain a true ratio of activated fatty acids and FFAs in cells with traditional

Discussion
The ACOT family of enzymes are suggested to be key regulators of the intercellular balance of activated fatty acids (fatty acyl-CoAs) and FFAs [10,25]. As previous studies have shown that DENVs are reliant upon activated fatty acids for completion of their lifecycle ( [8,9,20,21,28,29], reviewed in [3]), our present study investigated whether ACOT enzymes were important modulators of DENV2 infection. The ACOT enzymes chosen represented both type I (ACOT1 and ACOT2) and type II ACOTs (ACOT7), as well as ACOTs found within the same organelle (ACOT2 and ACOT7 in the mitochondria). Interestingly, we found that the loss of function of these enzymes had a divergent effect on the DENV2 lifecycle that was independent of their substrate specificity, and, instead, highlighted a more nuanced relationship between DENV2 and the subcellular regulation of fatty acid metabolism. Specifically, we found that the loss of function of the cytoplasmic ACOT1 enzyme resulted in increased DENV2 genome replication and infectious virus release, indicating that its normal function may be antiviral. However, the loss of function of the mitochondrial ACOT2 and ACOT7 enzymes resulted in the suppression of multiple stages of the DENV2 lifecycle, indicating that the function of these enzymes is vital for effective DENV2 infection. Furthermore, our analyses revealed a functional dependency between enzymes within the ACOT family.
Because ACOTs act directly on activated fatty acids, it is predicted that they play a significant role in the modulation of fatty acid metabolism [10,11,21,25,30]. However, mechanistic insight as to the specific functions of ACOT enzymes is limited. One challenge is that the ester bond that links coenzyme A with fatty acids is labile, which limits the ability to obtain a true ratio of activated fatty acids and FFAs in cells with traditional methods [10,31]. Thus, much of what the field understands about the function of these enzymes is concluded from studies characterizing their biophysical and biochemical properties, or from mouse models studying the impact of ACOT gene deletion on cardiac, neurological, and metabolic disorders [10][11][12][13][14][15][23][24][25][26][27]31]. During the curation of this paper, we successfully developed an LC-MS assay that allowed us to distinguish between arachidonic acid, SH-CoA, and arachidonoyl-CoA (the primary substrate of ACOT7, discussed in 25 and 27). However, due to limitations in the scalability of siRNA treatment, the levels of these metabolites were below our limits of detection. As a future direction, use of knockdown cell lines may further characterize ACOT enzyme functionality. Moreover, an additional challenge was that ACOT1 and ACOT2 enzymes share 98% similarity at the protein level, and 94% nucleotide sequence homology [11,24]. This inhibited differentiation of these enzymes at the protein level. However, we were able to design specific siRNA and primer sequences that targeted the mitochondrial localization sequence of ACOT2, allowing us to characterize these enzymes based on their mRNA expression.
In an ACOT1 knockout mouse model, ACOT1 was shown to modulate liver fatty acid metabolism during fasting, and the loss of function of this enzyme led to increased triglyceride turnover and beta oxidation [23]. Importantly, infection with DENV2 mimics a fasting state in the cell, and previous studies have established that triglyceride hydrolysis and beta-oxidation are increased in DENV2-infected cells [20,28,29]. Thus, inhibition of ACOT1 may further enhance these processes, leading to a more favorable environment for DENV2 replication. Mitochondrial functional assays have suggested that ACOT2 and ACOT7 functions to decrease beta-oxidation overload, possibly by mediating efflux of fatty acids from the mitochondrial matrix [28,30,31]. Thus, loss of ACOT2 and ACOT7 function may have resulted in a buildup of fatty acyl-CoAs levels in the mitochondria, decreased turnover of CoA and fatty acid precursor molecules, and increased oxidative stress-all of which would antagonize the DENV2 lifecycle. Interestingly, we found that, following ACOT2 or ACOT7 knockdown, there was no compensation by any of the other mitochondrial ACOTs (ACOT2, 7 or 9). However, ACOT2 and ACOT7 knockdown decreased peroxisomal ACOT4, ACOT6, and ACOT8 expression. Peroxisomal ACOTs are important in the degradation of very long-chain fatty acids that cannot be directly shuttled to the mitochondria [10,11]. Peroxisomes are becoming recognized as important mediators for controlling or facilitating virus infection, including antiviral immune responses, interactions with viral capsid proteins, and influencing membrane fluidity [32,33]. Therefore, another possibility is that ACOT2 or ACOT7 knockdown is indirectly suppressing DENV2 replication through an altering of the expression of peroxisomal ACOTs, which may impact peroxisomal lipid degradation activity. The role of peroxisomes in these biochemical interactions between virus and host is as yet an uncharted territory.
In summary, we found there is a differential impact of ACOTs on DENV2 genome replication and infectious particle release that could be influenced by the subcellular location of these enzymes. We also observed that the loss of function of a single ACOT impacted the expression of multiple ACOTs in different cellular locations, highlighting the complexity of understanding how ACOTs influence viral replication. Overall, our current study underscores that DENV2 is reliant upon careful coordination of fatty acid metabolism to complete its lifecycle. Future studies aimed at characterizing the exact substrate specificities would increase our understanding of how the loss of function of specific enzymes regulates infection. Additionally, our data suggest that determining the functional relationship between ACOTs is warranted.

Supplementary Materials:
The following are available online at https://www.mdpi.com/article /10.3390/v14020240/s1, Table S1: siRNA and oligonucleotide resources used in this study. Figure S1: Loss of function of mitochondrial ACOTs inhibits viral protein translation.