EBOV tarvitsee ehdottomasti korkeampien organismien fosfoinositidilipidilaatuja virionin valmistukseen. ja ilmeisesti muihinkin vaiheisiin.
The Phosphatidylinositol-3-phosphate... (PDF Download Available). Available from: https://www.researchgate.net/publication/316078827_The_Phosphatidylinositol-3-phosphate_5-kinase_inhibitor_Apilimod_blocks_filoviral_entry_and_infection?_sg=jHD1ro2wp8OvvZ9-i_RrU8KdUSjG5m95aksJdi4LV3XOz-A4q8nBzgYUjn6qoD1H02-d45KZOdtfy1ITq6T3aZSqqTtfOCKNlg [accessed May 21 2018].
Abstract
Abstract
Phosphatidylinositol-3-phosphate 5-kinase (PIKfyve) is a lipid kinase involved in endosome maturation that emerged from a haploid genetic screen as being required for Ebola virus (EBOV) infection. Here we analyzed the effects of apilimod, a PIKfyve inhibitor that was reported to be well tolerated in humans in phase 2 clinical trials, for its effects on entry and infection of EBOV and Marburg virus (MARV). We first found that apilimod blocks infections by EBOV and MARV in Huh 7, Vero E6 and primary human macrophage cells, with notable potency in the macrophages (IC50, 10 nM). We next observed that similar doses of apilimod block EBOV-glycoprotein-virus like particle (VLP) entry and transcription-replication competent VLP infection, suggesting that the primary mode of action of apilimod is as an entry inhibitor, preventing release of the viral genome into the cytoplasm to initiate replication. After providing evidence that the anti-EBOV action of apilimod is via PIKfyve, we showed that it blocks trafficking of EBOV VLPs to endolysosomes containing Niemann-Pick C1 (NPC1), the intracellular receptor for EBOV. Concurrently apilimod caused VLPs to accumulate in early endosome antigen 1-positive endosomes. We did not detect any effects of apilimod on bulk endosome acidification, on the activity of cathepsins B and L, or on cholesterol export from endolysosomes. Hence by antagonizing PIKfyve, apilimod appears to block EBOV trafficking to its site of fusion and entry into the cytoplasm. Given the drug’s observed anti-filoviral activity, relatively unexplored mechanism of entry inhibition, and reported tolerability in humans, we propose that apilimod be further explored as part of a therapeutic regimen to treat filoviral infections.
The Phosphatidylinositol-3-phosphate... (PDF Download Available). Available from: https://www.researchgate.net/publication/316078827_The_Phosphatidylinositol-3-phosphate_5-kinase_inhibitor_Apilimod_blocks_filoviral_entry_and_infection?_sg=jHD1ro2wp8OvvZ9-i_RrU8KdUSjG5m95aksJdi4LV3XOz-A4q8nBzgYUjn6qoD1H02-d45KZOdtfy1ITq6T3aZSqqTtfOCKNlg [accessed May 21 2018].
Abstract
Phosphatidylinositol-3-phosphate 5-kinase (PIKfyve) is a lipid kinase involved in endosome maturation that emerged from a haploid genetic screen as being required for Ebola virus (EBOV) infection. Here we analyzed the effects of apilimod, a PIKfyve inhibitor that was reported to be well tolerated in humans in phase 2 clinical trials, for its effects on entry and infection of EBOV and Marburg virus (MARV).
We first found that apilimod blocks infections by EBOV and MARV in Huh 7, Vero E6 and primary human macrophage cells, with notable potency in the macrophages (IC50, 10 nM).
We next observed that similar doses of apilimod block EBOV-glycoprotein-virus like particle (VLP) entry and transcription-replication competent VLP infection, suggesting that the primary mode of action of apilimod is as an entry inhibitor, preventing release of the viral genome into the cytoplasm to initiate replication.
After providing evidence that the anti-EBOV action of apilimod is via PIKfyve, we showed that it blocks trafficking of EBOV VLPs to endolysosomes containing Niemann-Pick C1 (NPC1), the intracellular receptor for EBOV.
Concurrently apilimod caused VLPs to accumulate in early endosome antigen 1-positive endosomes.
We did not detect any effects of apilimod on bulk endosome acidification, on the activity of cathepsins B and L, or on cholesterol export from endolysosomes. Hence by antagonizing PIKfyve, apilimod appears to block EBOV trafficking to its site of fusion and entry into the cytoplasm.
Given the drug’s observed anti-filoviral activity, relatively unexplored mechanism of entry inhibition, and reported tolerability in humans, we propose that apilimod be further explored as part of a therapeutic regimen to treat filoviral infections.
We first found that apilimod blocks infections by EBOV and MARV in Huh 7, Vero E6 and primary human macrophage cells, with notable potency in the macrophages (IC50, 10 nM).
We next observed that similar doses of apilimod block EBOV-glycoprotein-virus like particle (VLP) entry and transcription-replication competent VLP infection, suggesting that the primary mode of action of apilimod is as an entry inhibitor, preventing release of the viral genome into the cytoplasm to initiate replication.
After providing evidence that the anti-EBOV action of apilimod is via PIKfyve, we showed that it blocks trafficking of EBOV VLPs to endolysosomes containing Niemann-Pick C1 (NPC1), the intracellular receptor for EBOV.
Concurrently apilimod caused VLPs to accumulate in early endosome antigen 1-positive endosomes.
We did not detect any effects of apilimod on bulk endosome acidification, on the activity of cathepsins B and L, or on cholesterol export from endolysosomes. Hence by antagonizing PIKfyve, apilimod appears to block EBOV trafficking to its site of fusion and entry into the cytoplasm.
Given the drug’s observed anti-filoviral activity, relatively unexplored mechanism of entry inhibition, and reported tolerability in humans, we propose that apilimod be further explored as part of a therapeutic regimen to treat filoviral infections.
The Phosphatidylinositol-3-phosphate... (PDF Download Available). Available from: https://www.researchgate.net/publication/316078827_The_Phosphatidylinositol-3-phosphate_5-kinase_inhibitor_Apilimod_blocks_filoviral_entry_and_infection?_sg=jHD1ro2wp8OvvZ9-i_RrU8KdUSjG5m95aksJdi4LV3XOz-A4q8nBzgYUjn6qoD1H02-d45KZOdtfy1ITq6T3aZSqqTtfOCKNlg [accessed May 21 2018].
Kts. ESCRT complex: endosomaalisessa kalvosaa PIP3 ja ESCRT-0 kompleksin jäsen Hrs, jolla on FYVE- domeeni, joka kiinnittyy PI3P molekyyliin.
https://openi.nlm.nih.gov/detailedresult.php?img=PMC2172707_200302136f7&req=4
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