Research Article

Microsphere Suspension Array Assays for Detection and Differentiation of Hendra and Nipah Viruses

Table 2

Detection of HeV in experimentally infected horses.

DayMicrosphere array assay
Henipa NHenipa PqPCR (a)LAMP (a)
(MFI)(MFI)(Ct)(U/Pos)

Horse 1
 0148213UU
 1185256UU
 220 85823 74537.5U
 322 08824 59334.7Pos
 422 82824 04935.9Pos
 523 73424 98529.5Pos
 623 85625 19732.8Pos

Horse 2
 0219104UU
 1197296UPos
 222 30423 54736.3Pos
 322 98323 62532.4Pos
 411 6388 14238.9Pos
 523 06324 06834.3Pos
 622 91423 33331.1Pos
 723 02424 28428.1Pos
 822 90024 14529.2Pos
 922 90024 95135.2Pos

Horse 3
 0186301UU
 1221288UU
 210 73437542*Pos
 41 2712 25141.4*Pos
 55 4067 01843*Pos
 61 8048 019UU
 716 73120 57537.7Pos

Pos control2322823451
NTC226298

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.