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. 2021 Jun 24;33(5):894–905. doi: 10.1177/10406387211027131

Table 2.

Viral infections detected on 3 farms by molecular (conventional or real-time RT-PCR) or serologic methods (ELISA, VNT).

Targeted virus Farm 1 (+ 30 cattle)
Farm 2
Farm 3 (+ 65 cattle)
Water buffalo (n = 17) Water buffalo (n = 26) Sheep (n = 19) Water buffalo (n = 5) Goats (n = 7)
Genome
 BuGyKV ND 22 11 ND ND
 Herpesviruses ND 1 BoHV6 15 OvHV2; 3 unass. sheep LHV ND 1 unass. goat LHV
Antibodies
 BoHV2 1 1 ND ND ND
 Ruminant pestiviruses 1 BVDV 2 BVDV; 1 BVDV/BDV 1 BDV 1 BVDV 1 BVDV
 BTV ND ND 1 3 ND
 SBV ND ND 8 ND 2

Viruses shared between water buffaloes and small ruminants (BuGyKV, BVDV/BDV), and possibly cattle (BoHV2), are marked in bold.

BDV = border disease virus; BoHV2 = bovine alphaherpesvirus 2; BoHV6 = bovine gammaherpesvirus 6; BTV = bluetongue virus; BuGyKV = bubaline-associated gemykrogvirus; BVDV = bovine viral diarrhea virus; LHV = lymphotropic herpesvirus; ND = not detected; OvHV2 = ovine gammaherpesvirus 2; RT-PCR = reverse-transcription PCR; SBV = Schmallenberg virus; unass. = unassigned; VNT = virus neutralization test.