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. 2013 Feb 6;2013:289295. doi: 10.1155/2013/289295

Table 2.

Detection of HeV in experimentally infected horses.

Day Microsphere array assay
Henipa N Henipa P qPCR (a) LAMP (a)
(MFI) (MFI) (Ct) (U/Pos)
Horse 1
 0 148 213 U U
 1 185 256 U U
 2 20 858 23 745 37.5 U
 3 22 088 24 593 34.7 Pos
 4 22 828 24 049 35.9 Pos
 5 23 734 24 985 29.5 Pos
 6 23 856 25 197 32.8 Pos

Horse 2
 0 219 104 U U
 1 197 296 U Pos
 2 22 304 23 547 36.3 Pos
 3 22 983 23 625 32.4 Pos
 4 11 638 8 142 38.9 Pos
 5 23 063 24 068 34.3 Pos
 6 22 914 23 333 31.1 Pos
 7 23 024 24 284 28.1 Pos
 8 22 900 24 145 29.2 Pos
 9 22 900 24 951 35.2 Pos

Horse 3
 0 186 301 U U
 1 221 288 U U
 2 10 734 375 42* Pos
 4 1 271 2 251 41.4* Pos
 5 5 406 7 018 43* Pos
 6 1 804 8 019 U U
 7 16 731 20 575 37.7 Pos

Pos control 23228 23451
NTC 226 298

Comparison of microsphere array assays performed on archival RNA extracted from daily nasal swabs of experimentally infected horses [21].

(a) Comparison with qPCR and loop-mediated amplification (LAMP) assay results [22] in retrospective analysis. Day indicates sampling day after challenge. MFI: median fluorescence intensity; U: undetected; Pos: positive reaction; *indicates qPCR indeterminate results; NTC: no template control. All positive results are in bold.