Table 1. Glycosylation site conservation and recombinant LCMV genetic stability.
Mutation | Conservationa | Stabilityb | |||
OW | NW | Epithelial | Neurons | Macrophages | |
WT Arm 5 | n/a | n/a | 10 | 10 | 10 |
F260L | n/a | n/a | 10 | 10 | 10 |
Deletion of N-glycosylation site | |||||
T87A (1) | 8/8 | 15/20 | 0 | 0 | 0 |
S97A (2) | 8/8 | 20/20 | 0 | 0 | 0 |
S116A (4) | 7/8 | 7/20 | 1 | 0 | 0 |
T126A (5) | 8/8 | 18/20 | 10 | 10 | 10 |
T173A (6) | 7/8 | 20/20 | 10 | 10 | 10 |
T234A (7) | 8/8 | 17/20 | 10 | 10 | 6 |
S373A (8) | 8/8 | 20/20 | 7 | 3 | 3 |
S398A (10) | 8/8 | 19/20 | 10 | 10 | 10 |
T403A (11) | 8/8 | 20/20 | 10 | 10 | 10 |
Addition of N-glycosylation site | |||||
G104N (3) | 5/8 | 9/20 | 10 | 10 | 10 |
E379N/A381T(9) | 5/8 | 20/20 | 10 | 10 | 10 |
Specific mutations of N-glycosylation sites were engineered to delete or add N-glycan on the LCM virus glycoprotein.
Conservation of the glycosylation site from alignment of arenavirus GP sequences performed using CLC Sequence Viewer software. The 8 Old Word arenaviruses are: Lassa virus (LASV), X52400; Ippy virus (IPPYV), DQ328877; Mobala virus (MOBV), AY342390; Mopeia virus (MOPV), DQ328874; Morogoro virus (MORV), EU914103; Dandenong virus (DANV), EU136038; Lymphocytic choriomeningitis virus (LCMV), AY847350; Lujo virus (LUJV), FJ952384; while the 20 New World arenaviruses are: Pirital virus (PIRV), AF277659; Allpahuayo virus (ALLV), AY012687; Pichinde virus (PICV), NC_006447, Parana virus (PARV), AF512829; Flexal virus (FLEV), AF512831; Oliveros virus (OLVV), U34248; Latino virus (LATV), AF512830; Machupo virus (MACV), NC_005078; Junin virus (JUNV), D10072; Tacaribe virus (TCRV), NC_004293; Chapare virus (CHAV), EU260463; Sabia virus (SABV), NC_006317; Guanarito virus (GTOV), NC_005077; Amapari virus (AMAV), AF512834; Cupixi virus (CPXV), AF512832; Skinner Tank virus (SKTV), EU123328; Whitewater Arroyo virus (WWAV), AF228063; Catarina virus (CATV), DQ865245; Tamiami virus (TAMV), AF512828; Bear Canyon virus (BCNV), AF512833.
Stability controlled by sequencing of GP for each rescued virus mutant 72 h post infection in (i) epithelial cell lines: Vero E6 and HEK293T, (ii) neurons: cell line OBL21A and primary mouse cortical neuron, (iii) macrophages: cell line RAW264.7 and bone marrow derived macrophages. Stability was measured on a scale from 0–10 and represents the stability of the mutants during 10 passages, on epithelial cells, or during a 72 h infection, on primary cells. ‘0′ means no rLCMV rescued and ‘10′ mutation stable for more than 10 passages on epithelial cells and more than 72 h on primary cells.