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. Author manuscript; available in PMC: 2013 Dec 1.
Published in final edited form as: J Virol Methods. 2012 Jul 27;186(1-2):73–77. doi: 10.1016/j.jviromet.2012.07.024

Table 4.

Specificity validation of multiple real-time qPCR assays detecting known EEHV species.

EEHV Speciesa NAP No.b Samplec EEHV1 (Cq) EEHV2 (Cq) EEHV3/4 (Cq) EEHV5 (Cq) EEHV6 (Cq)
1A 31 Blood 23.7d >40 >40 >40 >40
1A 33 Blood 28.7d >40 >40 >40 >40
1A/B 19 Blood 27.9d >40 >40 >40 >40
1B 45 TWe 16.4 >40 >40 >40 >40
2 12 Blood >40 29.5 >40 >40 >40
3 27 Colon >40d >40 26.4 >40 >40
4 22 Blood >40d >40 26.6 >40 >40
5 50 Blood >40 >40 >40 33.3 >40
6 35 Blood >40 >40 >40 >40 36.5
None Nonef Blood >40 >40 >40 >40 >40
a

EEHV species previously detected in archival elephant DNA sample.

b

North American Proboscivirus (NAP) number assigned to the test sample. If no NAP number was previously assigned to the case, the elephant’s name is given.

c

Tissue or fluid from which the test DNA sample was obtained.

d

Previously published in Stanton et al. 2010.

e

Trunk wash

f

Negative control Asian elephant with no detectable EEHV in genomic DNA sample