Skip to main content
. 2013 May 4;9:95. doi: 10.1186/1746-6148-9-95

Table 1.

Outline of examined BLV-infected but clinically normal cattle

Cattle Age (years) WBC (/μl) Lymphocyte (/μl) (%) Clinical stagea ELISAb Proviral loadc
(Copies/1 × 105cells)
Syncytium assayd
(Number/5 × 106cells)
BLV-free normal cattle
N790
2.5
9,540
6,382 (66.9)
-
-
0
0
N791
2.5
8,260
4,956 (60.0)
-
-
0
0
BLV-infected cattle
1) Cattle with < 100 proviral load
N818
2.0
9,410
5,147 (54.7)
AL
+
8
0
N789
2.5
5,472
5,472 (60.2)
AL
+
26
1
2) Cattle with > 100 proviral load
N787 N733
2.5
8,730
4,487 (51.4)
AL
+
294
250
2.5
8,230
6,313 (68.4)
AL
+
1,614
400
N823
2.0
9,340
6,239 (66.8)
AL
+
11,112
11,000
N788
2.5
9,620
5,435 (56.5)
AL
+
18,094
17,500
O10 15.0 12,200 7,900 (64.8) PL + 10,689 9,086

aThe clinical stage of BLV infection was evaluated according to the lymphocyte count (per 1 μl), the detection of atypical mononuclear cells, and the age of the animal [19]. AL, BLV-infected but clinically and hematologically normal cattle; PL, BLV-infected but clinically normal cattle showing an increase in the number of apparently normal B lymphocytes. In the latter case, three separate lymphocyte counts were performed at different times and all yielded the same results.

bELISA was performed using an anti-BLV ELISA kit according to the manufacturer’s instructions (JNC Inc., Tokyo, Japan). +, positive for anti-BLV antibodies; -, negative for anti-BLV antibodies.

cThe proviral load (expressed as the copy number per 105 peripheral blood mononuclear cells [PBMCs]) was evaluated by BLV-CoCoMo-qPCR as previously described [19].

dPBMCs were mixed with CC81 cells and 4 μg/ml polybrene (Sigma, St. Louis, MO) and used in the syncytium formation assay [19]. Syncytia were counted under a light microscope.