TABLE 4.
Neutralization of pseudoviruses constructed from different env clones
Serumb | Reciprocal of NA titer againsta:
|
||||||
---|---|---|---|---|---|---|---|
MN virus | MN virus-derived pseudovirus:
|
MNE4 | MNE4-derived pseudovirus:
|
||||
PV-V5 | PV-V32 | PV-V36 | PV-E6 | PV-E14 | |||
Reference 1 | >5,120 | 4,096 | 2,048 | 2,048 | 8 | 64 | 128 |
Reference 2 | >5,120 | 4,096 | 4,096 | 2,048 | 128 | 64 | 256 |
NY-2 | 12,800 | 16,384 | NTd | NT | NT | 512 | NT |
NY-3c | 25,600 | 8,192 | NT | NT | <8 | 32 | NT |
NY-4 | 25,600 | 8,192 | NT | NT | <8 | 256 | NT |
NY-5 | 12,800 | 16,384 | NT | NT | 16 | 16 | NT |
NY-7 | 6,400 | 8,192 | NT | NT | <8 | 512 | NT |
NY-8 | 25,600 | 16,384 | NT | NT | NT | 256 | NT |
NY-9 | 51,200 | ≥32,768 | NT | NT | NT | 512 | NT |
NY-10 | 6,400 | 16,384 | NT | NT | NT | 512 | NT |
Neutralization of MN virus and MNE4 was assayed with Molt 3 cells, and the assays for the pseudoviruses were done with PM1 cells as described in Materials and Methods.
Human sera obtained from the NYBC (NY designations) and reference sera were used.
Serum that was used for selection of NR variants.
NT, not tested.