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. 2011 Apr;49(4):1389–1394. doi: 10.1128/JCM.00710-10

Table 3.

Results on viruses used in this study using RT-PCR method with the oligonucleotide primers for the dual priming oligonucleotide system

Family Genus Species Straina Resultb
Expected Observed
Bunyaviridae Bunyavirus Aino virus KSA9910 X X
Orthobunyavirus Akabane virus 93FMX X X
Phlebovirus RVFV Smithburn O O
Flaviviridae Flavivirus JEV Anyang300 X X
WNV NY385-99 X X
WNV B956 X X
Pestivirus BVDV KD26-1 X X
BVDV 95002 X X
Paramyxoviridae Morbillivirus CDV Onderstepoort X X
RPV L O O
RPV LA O O
RPV LATC O O
PPRV Nigeria 75/1 O O
Picornaviridae Aphthovirus FMDV O/SKR/2002 X X
Enterovirus SVDV UK27/72 X X
Reoviridae Orbivirus BTV RSArrr/01 (serotype 1) O O
BTV RSArrr/02 (serotype 2) O O
BTV RSArrr/03 (serotype 3) O O
BTV RSArrr/04 (serotype 4) O O
BTV RSArrr/05 (serotype 5) O O
BTV RSArrr/06 (serotype 6) O O
BTV RSArrr/07 (serotype 7) O O
BTV RSArrr/08 (serotype 8) O O
BTV RSArrr/09 (serotype 9) O O
BTV RSArrr/10 (serotype 10) O O
BTV RSArrr/11 (serotype 11) O O
BTV RSArrr/12 (serotype 12) O O
BTV RSArrr/13 (serotype 13) O O
BTV RSArrr/14 (serotype 14) O O
BTV RSArrr/15 (serotype 15) O O
BTV RSArrr/16 (serotype 16) O O
BTV RSArrr/17 (serotype 17) O O
BTV RSArrr/18 (serotype 18) O O
BTV RSArrr/19 (serotype 19) O O
BTV RSArrr/20 (serotype 20) O O
BTV RSArrr/21 (serotype 21) O O
BTV RSArrr/22 (serotype 22) O O
BTV RSArrr/23 (serotype 23) O O
BTV RSArrr/24 (serotype 24) O O
BTV MAY1987/01(serotype 1) O O
BTV IND2003/01(serotype 2) O O
BTV ISA1991/01(serotype 16) O O
BTV IND1998/01(serotype 23) O O
BTV IND2001/01(serotype 1) O O
BTV Station (serotype 10) O O
BTV 6245S (serotype 11) O O
BTV 67-41B (serotype 13) O O
BTV CSIRO 19 O O
Chuzan virus YoungAm X X
EHDV-1 NewJersey X X
EHDV-2 Alberta X X
EHDV-2 Ibaraki X X
Rhabdoviridae Vesiculovirus VSV Indiana X X
Togaviridae Alphavirus WEEV Unidentified X X
EEEV Unidentified* X X
WEEV Unidentified* X X
VEEV Unidentified* X X
a

*, RNAs extracted from the Cephalovac VEWT vaccine (Boehringer Ingelheim Vetmedica, St. Joseph, MO).

b

O, the multiplex RT-PCR used in this study produced amplicons of exactly the expected sizes, and they were clearly distinguishable by agarose gel electrophoresis; X, no band was observed.