A global lipid map reveals host dependency factors conserved across SARS-CoV-2 variants
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Abstract
A comprehensive understanding of host dependency factors for SARS-CoV-2 remains elusive. Here, we map alterations in host lipids following SARS-CoV-2 infection using nontargeted lipidomics. We find that SARS-CoV-2 rewires host lipid metabolism, significantly altering hundreds of lipid species to effectively establish infection. We correlate these changes with viral protein activity by transfecting human cells with each viral protein and performing lipidomics. We find that lipid droplet plasticity is a key feature of infection and that viral propagation can be blocked by small-molecule glycerolipid biosynthesis inhibitors. We find that this inhibition was effective against the main variants of concern (alpha, beta, gamma, and delta), indicating that glycerolipid biosynthesis is a conserved host dependency factor that supports this evolving virus.
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Dao Wen Wang
Review 3: "A global lipid map reveals host dependency factors conserved across SARS-CoV-2 variants"
This preprint examines lipid droplet plasticity as a feature of infection that can be stopped by glycolipid biosynthesis inhibitors and finds that they are a host dependency factor supporting COVID-19. Reviewers found this study reliable and informative for virus evolution.
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Aman Rajpal
Review 2: "A global lipid map reveals host dependency factors conserved across SARS-CoV-2 variants"
This preprint examines lipid droplet plasticity as a feature of infection that can be stopped by glycolipid biosynthesis inhibitors and finds that they are a host dependency factor supporting COVID-19. Reviewers found this study reliable and informative for virus evolution.
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Susmita Kaushik
Review 1: "A global lipid map reveals host dependency factors conserved across SARS-CoV-2 variants"
This preprint examines lipid droplet plasticity as a feature of infection that can be stopped by glycolipid biosynthesis inhibitors and finds that they are a host dependency factor supporting COVID-19. Reviewers found this study reliable and informative for virus evolution.
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Strength of evidence
Reviewers: Susmita Kaushik (Albert Einstein College of Medicine) |📘📘📘📘📘
Aman Rajpal (Case Western Reserve University) | 📗📗📗📗◻️
Dao Wen Wang (Tongji Medical College) -
SciScore for 10.1101/2022.02.14.480430: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics not detected. Sex as a biological variable not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Cell Line Authentication not detected. Table 2: Resources
Antibodies Sentences Resources Anti-dsRNA antibody was obtained from Millipore (identifier MABE1134); anti-mouse IgG AlexaFluor 647 was obtained from Invitrogen (Identifier A32628); anti-llama secondary HRP, goat IgG was obtained from Novus (identifier NB7242). anti-mouse IgGsuggested: Noneanti-llama secondary HRP, goat IgGsuggested: (Thermo Fisher Scientific Cat# A16060, RRID:AB_2534733)Cells were stained overnight with an anti-dsRNA antibody diluted 1:50 in blocking buffer. anti-dsRNAsuggested: NoneCells were … SciScore for 10.1101/2022.02.14.480430: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics not detected. Sex as a biological variable not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Cell Line Authentication not detected. Table 2: Resources
Antibodies Sentences Resources Anti-dsRNA antibody was obtained from Millipore (identifier MABE1134); anti-mouse IgG AlexaFluor 647 was obtained from Invitrogen (Identifier A32628); anti-llama secondary HRP, goat IgG was obtained from Novus (identifier NB7242). anti-mouse IgGsuggested: Noneanti-llama secondary HRP, goat IgGsuggested: (Thermo Fisher Scientific Cat# A16060, RRID:AB_2534733)Cells were stained overnight with an anti-dsRNA antibody diluted 1:50 in blocking buffer. anti-dsRNAsuggested: NoneCells were washed three times with PBS and then stained with an A647 secondary antibody for 1 hr. A647suggested: NonePlates were permeabilized in perm buffer (0.1% saponin, 0.1% BSA in PBS) for 30 minutes, then incubated with 50 μL primary antibody (alpaca anti-SARS-CoV-2 serum, diluted 1:5,000 in perm buffer) for either 2hr room temperature or overnight at 4 °C. anti-SARS-CoV-2suggested: NonePlates were incubated with 50 μL secondary antibody (anti-llama HRP, goat IgG) for either 2hr room temperature or overnight at 4 °C. anti-llama HRP, goat IgGsuggested: NoneExperimental Models: Cell Lines Sentences Resources Materials: Cell lines: Cell lines (HEK293T, HEK293T-ACE2, Vero-E6, and Caco2) were obtained from ATCC. HEK293Tsuggested: NoneViral strains: SARS-CoV-2 viral strains (isolate USA-WA1/2020: Identifier #NR-52281; isolate USA/CA_CDC_5574/2020: Identifier #NR-54011; isolate hCoV-19/South Africa/KRISP-K005325/2020: Identifier #NR-54009; hCoV-19/Japan/TY7-503/2021: Identifier #NR54982; isolate hCoV-19/USA/PHC658/2021: Identifier # NR-55611) were obtained from BEI resources and propagated in Vero E6 cells. Vero E6suggested: RRID:CVCL_XD71)Media for Vero-E6 cells, 293T (wt) and 293T-ACE2 cells was supplemented with 10% FBS while media for Caco2 cells was supplemented with 20% FBS. Vero-E6suggested: None293T-ACE2suggested: NoneWild-type 293T cells were seeded in 6cm dishes and transfected with varying amounts viral plasmids (based on optimal expression for each plasmid, see Table S1), as well as a PLVX empty vector control, using Lipofectamine 3000 (ThermoFisher Scientific) as per manufacturer’s instructions. 293Tsuggested: NoneLipid droplet immunofluorescence — Infection: 293T-ACE2 or Caco2 cells were seeded at 70% cell density in 24-well plates and allowed to grow overnight. Caco2suggested: NoneResults from OddPub: Thank you for sharing your data.
Results from LimitationRecognizer: An explicit section about the limitations of the techniques employed in this study was not found. We encourage authors to address study limitations.Results from TrialIdentifier: No clinical trial numbers were referenced.
Results from Barzooka: We found bar graphs of continuous data. We recommend replacing bar graphs with more informative graphics, as many different datasets can lead to the same bar graph. The actual data may suggest different conclusions from the summary statistics. For more information, please see Weissgerber et al (2015).
Results from JetFighter: We did not find any issues relating to colormaps.
Results from rtransparent:- Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
- Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
- No protocol registration statement was detected.
Results from scite Reference Check: We found no unreliable references.
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