TABLE 2.
Characteristics of the Aino virus isolates used in this study
| Strain | Yr collected | Location | Patterna | Passage levelb | Origin |
|---|---|---|---|---|---|
| JaNAr28 | 1964 | Nagasaki | 1 | Sm12HL4 | Culex tritaeniorhynchus |
| B7974 | 1968 | Queensland, Australia | 4 | Sm6BHK2 | Culicoides brevitarsis |
| KSB-2/C/86 | 1986 | Kagoshima | 2 | BHK5 | Culicoides oxystoma |
| KSB-3/C/86 | 1986 | Kagoshima | 2 | BHK4 | Culicoides oxystoma |
| KSB-4/C/86 | 1986 | Kagoshima | 2 | BHK4 | Culicoides oxystoma |
| KSB-5/C/86 | 1986 | Kagoshima | 2 | BHK4 | Culicoides oxystoma |
| KSB-6/C/86 | 1986 | Kagoshima | 2 | BHK4 | Culicoides oxystoma |
| KSB-7/P/86 | 1986 | Kagoshima | 2 | BHK4 | Bovine plasma |
| KSB-8/P/86 | 1986 | Kagoshima | 2 | BHK4 | Bovine plasma |
| KSB-9/P/86 | 1986 | Kagoshima | 2 | BHK4 | Bovine plasma |
| KSB-10/P/86 | 1986 | Kagoshima | 2 | BHK4 | Bovine plasma |
| MZ-1/P/88 | 1988 | Miyazaki | 3 | BHK4 | Bovine plasma |
| KSB-2/C/88 | 1988 | Kagoshima | 3 | BHK5 | Culicoides oxystoma |
| KSB-3/P/88 | 1988 | Kagoshima | 3 | BHK4 | Bovine plasma |
| KSB-4/P/88 | 1988 | Kagoshima | 1 | BHK5 | Bovine plasma |
| KSB-1/C/89 | 1989 | Kagoshima | 1 | BHK5 | Culicoides oxystoma |
| KSB-2/C/89 | 1989 | Kagoshima | 1 | BHK4 | Culicoides punctatus |
| KSB-3/P/89 | 1989 | Kagoshima | 3 | BHK4 | Bovine plasma |
| KSB-4/P/89 | 1989 | Kagoshima | 1 | BHK4 | Bovine plasma |
| HG-1/B/95 | 1995 | Hyogo | 2 | BHK4 | Bovine blood |
| HG-2/B/95 | 1995 | Hyogo | 2 | BHK4 | Bovine blood |
| KSB-3/P/95 | 1995 | Kagoshima | 2 | BHK4 | Bovine plasma |
Pattern of the Aino virus isolates as determined by DIA.
Letters indicate cell lines and numbers indicate number of passages. Sm, brain of suckling mice; HL, HmLu-1 cells; BHK, BHK-21 cells.