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. 1998 Jun;72(6):4650–4656. doi: 10.1128/jvi.72.6.4650-4656.1998

TABLE 4.

Inactivation of heterologous viruses by NHSa

Expt Virus Log10 PFU after treatment
NHS Heat-inactivated NHS MEM
1 HSV-SK <1 <1 3.5
HSV-SK-GT <1 <1 >3.7
SV-SK 3.2 3.5 3.6
SV-SK-GT 3.4 3.3 3.3
VSV-SK 2.2 3.6 4.1
VSV-SK-GT 2.0 4.0 3.9
2 NDV-SK 1.8 3.8 3.7
NDV-SK-GT <1 3.9 4.2
SV-SK 3.4 3.6 3.5
SV-SK-GT 3.5 3.4 3.7
VSV-SK 2.2 3.6 4.3
VSV-SK-GT 1.8 3.9 4.0
3 NDV-SK-STOCK 1 <1 3.0 3.1
NDV-SK-STOCK 2 1.7 4.0 4.1
NDV-SK-GT-STOCK 1 <1 3.4 3.4
NDV-SK-GT-STOCK 2 1.5 4.1 4.2
4 SV-GT-WT 2.9 4.1 4.2
SV-GT-KO 4.2 4.4 4.4
VSV-GT-WT <1 4.0 4.1
VSV-GT-KO 1.0 4.0 4.1
5 SV-GT-WT 3.5 4.0 4.3
SV-GT-WT + nanase 3.4 4.3 4.4
SV-GT-KO 4.2 4.3 4.4
SV-GT-KO + nanase 3.8 4.1 4.2
SV-SK 3.9 3.8 3.8
SV-SK + nanase 4.2 3.9 4.0
SV-SK-GT 3.6 3.7 3.7
SV-SK-GT + nanase 3.8 3.8 3.7
a

Viruses passaged through human SK and SK-GT or mouse GT-KO and GT-WT cells were treated with sera as described in Materials and Methods and assayed for PFU on Vero cell monolayers. In experiment 5, viruses, where designated, were incubated 1:1 with 0.3 U of Clostridium perfringens neuraminidase (nanase) (Sigma) per ml for 1 h at 37°C before treatment with sera.