TABLE 1.
γHV68Δ9743 phenotype | Tissue | Time: (days) p.i. | Route of infection | Candidate genea |
---|---|---|---|---|
Reactivation, 5× increase | Peritoneal cells | 42 | i.p. | M1 (M1Δ511) (ref. 11) |
Acute-phase titer, 10× decrease | Spleen | 9 | i.p. | M2 (M2.Stop) (ref. 19) |
Latent load and reactivation, 24× and >13× decreases | Spleen | 17 | i.n. | M2 (M2.Stop) (ref. 19) |
Acute-phase titer, 10× decrease | Lung | 6 | i.n. | ? |
Latent load, 15× decrease | Spleen | 42 | i.n. | ? |
Reactivation, >12× increase | Peritoneal cells | 42 | i.n. | M1?b |
Candidate genes are based on specific gene mutations that have given similar phenotypes. ref., reference.
While M1 mutants exhibit increased reactivation from latency in peritoneal cells following i.p. infection (11), it is unknown whether these viruses show increased reactivation following i.n. infection.