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. 2023 Oct 19;12(2):2265661. doi: 10.1080/22221751.2023.2265661

Table 1.

Summary of in vivo results using the three different recombinant ASFV.

    Pre-challenge Post-challenge
    Dosea Clinical signs Viremia   Clinical signs Viremia
Recombinant ASFV Group >40.5°C Signsb # pigs TCID50/mL Protectionc >40.5°C Signs # pigs HAD50/mLd
GΔKE_CmutQ96R K 104 2/6 0/6 6/6 100.75-6.25e 100.0% 0/6 0/6 2/6 100.75f
GΔKE_CmutQ96R/K108D O 104 2/6 0/6 5/6 100.75-3.75 83.3% 1/6 6/6 2/6 101.75-4.00
GΔDKE_CmutQ96R/K108D N, S 104 0/12 1/12 6/12 100.75-3.25 83.3% 5/12 3/12 7/12 100.75-6.25
GΔDKE_CmutQ96R/K108D T 105 1/6 1/6 5/6 100.75-4.25 100% 1/6 5/6 2/6 101.00-6.75
Georgia07/1g M, P, U 0% 9/9 9/9 9/9 107.25-8.25
a

Prime and boost dose is given as TCID50 and was administered intramuscularly in 1 ml PBS.

b

Signs refer to every other clinical signs observed daily besides temperatures >40.5°C.

c

Percentage of pigs that survived Georgia07/1 challenge.

d

Only challenge virus was detected post-challenge and the titres are expressed as HAD50/mL in all cases except for Group K.

e

Virus isolated from blood of Group K pigs was haemadsorbing.

f

Virus was isolated from 2 Group K pigs at low levels – one vaccine virus and the other challenge virus.

g

Non-immunized control pigs challenged at the same time as the immunized pigs.