Skip to main content
. 2004 Sep;11(5):825–834. doi: 10.1128/CDLI.11.5.825-834.2004

TABLE 2.

NanH ELISA screening of rabbits housed in research facilities

Sourcea No. of rabbits negative/total no. tested (%) No. of rabbits positive for the following/total no. tested (%):
IgMb IgGb IgM and IgGc Total
Facility 1d 3/3 (100) 0/3 (0) 0/3 (0) 0/3 (0) 0/3 (0)
Facility 2 15/15 (100) 0/15 (0) 0/15 (0) 0/15 (0) 0/15 (0)
Facility 3 6/11 (55) 1/11 (9) 4/11 (36) 0/11 (0) 5/11 (45)
Facility 4 3/21 (14) 0/21 (0) 6/21 (29) 12/21 (57) 18/21 (86)
Facility 5d 9/15 (60) 2/15 (13) 3/15 (20) 1/15 (7) 6/15 (40)
Facility 6 0/4 (0) 1/4 (25) 2/4 (50) 1/4 (25) 4/4 (100)
Facility 7 3/7 (43) 1/7 (14) 3/7 (43) 0/7 (0) 4/7 (57)
Facility 8d 3/10 (30) 2/10 (20) 4/10 (40) 1/10 (10) 7/10 (70)
    Total 42/86 (49) 7/86 (8) 22/86 (26) 15/86 (17) 44/86 (51)
a

All research facilities except facilities 1 and 2 reported a recent history of pasteurellosis among rabbits in the same area.

b

Sample positive only for IgG or IgM but not both. To be considered positive for NanH antibody, samples exhibited an OD at 490 nm of 0.2 or above at a 1:16 dilution by the NanH IgG assay or an OD of 0.13 or above at a dilution of 1:8 by the NanH IgM assay. The NanH IgG ELISA detected nonisotype-specific IgG.

c

Samples positive for both IgM and IgG NanH antibodies.

d

Some samples from facilities 1, 5, and 8 were also tested by the whole-cell-lysate ELISA as described by Kawamoto et al. (29). Samples from facility 1 did not produce antibodies; however, both facilities 5 and 8 possessed rabbits positive for antibodies to whole-cell lysates.