Brief report: Mutations in SIV Nef that disrupt and restore tetherin downregulation
Abstract The H196residue in SIVmac239 Nef is conserved across nearly all HIV and SIV isolates, lies immediately adjacent to the AP-2 (adaptor protein 2) interacting domain (ExxxLM195), and is critical for several described AP-2 dependent Nef functions, including the downregulation of tetherin (BST-2/CD317). Surprisingly, many stocks of the closely related SIVmac251 swarm virus harbor anefallele encoding a Q196, which is associated with loss of multiple AP-2 dependent functions in SIVmac239. Publicly available sequences for SIVmac251 stocks were mined for variants linked to Q196that might compensate for functional defects associated with this mutation. Variants were engineered into the SIVmac239 parental plasmid and mutant viruses were used to test tetherin downregulatory capacity in primary CD4 T cells using flow cytometry. SIVmac251 stocks that encode a Q196residue in Nef uniformly also encode an upstream R191residue. We show that R191restores the ability of Nef to downregulate tetherin in the presence of Q196. However, a published report showed Q196commonly evolves to H196in vivo, suggesting a fitness cost. R191may represent compensatory evolution to restore the ability to downregulate tetherin lost in viruses harboring Q196..
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Preprint| Erscheinungsjahr: |
2021 |
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| Erschienen: |
2021 |
| Enthalten in: |
bioRxiv.org - (2021) vom: 15. Dez. Zur Gesamtaufnahme - year:2021 |
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| Sprache: |
Englisch |
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| Beteiligte Personen: |
Maness, Nicholas J [VerfasserIn] |
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| Links: |
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| doi: |
10.1101/833137 |
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| PPN (Katalog-ID): |
XBI000664952 |
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| 520 | |a Abstract The H196residue in SIVmac239 Nef is conserved across nearly all HIV and SIV isolates, lies immediately adjacent to the AP-2 (adaptor protein 2) interacting domain (ExxxLM195), and is critical for several described AP-2 dependent Nef functions, including the downregulation of tetherin (BST-2/CD317). Surprisingly, many stocks of the closely related SIVmac251 swarm virus harbor anefallele encoding a Q196, which is associated with loss of multiple AP-2 dependent functions in SIVmac239. Publicly available sequences for SIVmac251 stocks were mined for variants linked to Q196that might compensate for functional defects associated with this mutation. Variants were engineered into the SIVmac239 parental plasmid and mutant viruses were used to test tetherin downregulatory capacity in primary CD4 T cells using flow cytometry. SIVmac251 stocks that encode a Q196residue in Nef uniformly also encode an upstream R191residue. We show that R191restores the ability of Nef to downregulate tetherin in the presence of Q196. However, a published report showed Q196commonly evolves to H196in vivo, suggesting a fitness cost. R191may represent compensatory evolution to restore the ability to downregulate tetherin lost in viruses harboring Q196. | ||
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