Skip to main content
. 2019 Jul 15;13(7):e0007473. doi: 10.1371/journal.pntd.0007473

Table 2. Summary of West Nile virus infectious cDNA clone derived glycosylation mutant viruses that were generated.

Parental Virusα Nucleotide Substitutions made to parental WNV.ICβ Rescued WNV Glycosylation Mutant Virus Amino Acid Motif Amino Acid Translationβ Predicted glycosylation status
WNV.IC (NYS) AAT-TAC-TCC WNV.IC NYS Asn- Tyr- Ser (+)
AAC-TAC-ACC WNV.NYT.IC NYT Asn- Tyr- Thr (+)
AAC-TAC-CCC WNV.NYP.IC NYP Asn- Tyr- Pro (-)
AAT-TAC-TTC WNV.NYF.IC NYF Asn- Tyr- Phe (-)
AGC-TAC-TCC WNV.SYS.IC SYS Ser- Tyr- Ser (-)
AGC-TAC-CCC WNV.SYP.IC SYP Ser- Tyr- Pro (-)
AAA-TAC-TCC WNV.KYS.IC KYS Lys- Tyr- Ser (-)
AAT-TAC-TCC WNV.A’DEL.IC A’DEL (-)

α The N-linked NYS (AAT-TAC-TCC) glycosylation motif of the parental WNV.IC envelope protein was mutagenized to generate seven new WNV glycosylation mutant viruses that are described in the third column.

β Nucleotides and/or amino acids that were substituted are highlighted in bold and underlined.