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. 1998 May;72(5):3863–3871. doi: 10.1128/jvi.72.5.3863-3871.1998

TABLE 2.

Laboratory findingsa

Animal no. VIb IFA/IPc PCR specific ford:
EHDV-specific AGID EHDV-2-specific RIPA EHDV-2-specific RT in situ PCR
EHDV-1 EHDV-2 BTV
1 + + + + +
2 + + + + +
3 + + + +
4 + + + + +
5 + + + + +
6 + + + + +
7 + + + + +
8
9
10
a

Animals 8 to 10 represent clinically healthy, lesion-free deer and antelope from the affected area. Antiserum to BTV was cross-reactive with BTV serotypes 2, 10, 11, 13, 17, and 20. 

b

VI, virus isolation. Erythrocyte lysates and/or tissue homogenates were inoculated into embryonated chicken eggs and/or CPAE cells. 

c

IFA/IP, indirect immunofluorescence (IFA) and/or immunoperoxidase (IP) stain. Fluorescein- or biotin-conjugated MAbs specific for EHDV (hybridoma 11C6.288) or BTV (hybridoma 1004.90) inner capsid protein (VP7) were reacted with CPAE cells which had been cocultivated with clinical samples. MAbs were provided as a gift by Michael Jochim, Veterinary Diagnostic Technology, Inc., Wheat Ridge, Colo. 

d

Erythrocyte-associated orbiviral nucleic acid was detected by RT nested PCR using nucleotide primers specific for EHDV-1 and EHDV-2 (1, 2, 58) or BTV (all North American serotypes) (57).