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. 2025 Aug 21;30(33):2500183. doi: 10.2807/1560-7917.ES.2025.30.33.2500183

Table 2. Qualitative inter-laboratory analysis of an anonymised panel of influenza samples using the JRC-HA and JRC-MP digital PCR assays (n = 40).

Subtype Pathotype Lineage/clade HA IZSVe + HA JRC + % HA agreement MP IZSVe + MP JRC + % MP agreement
H1N1 LPAI Avian 0/1 0/1 100 1/1 1/1 100
H1N1 LPAI Swine 1A.3.3.2 [37] 0/1 0/1 100 1/1 1/1 100
H3N2 LPAI Swine 0/1 0/1 100 1/1 1/1 100
H3N8 LPAI Eurasian 0/2 0/2 100 2/2 2/2 100
H5N1 HPAI Eurasian, 2.3.4.4b 26/26 26/26 100 26/26 26/26 100
H5N1 LPAI Eurasian 0/1 0/1 100 1/1 1/1 100
H5N2 LPAI Eurasian 0/1 0/1 100 1/1 1/1 100
H5N3 LPAI Eurasian 0/1 0/1 100 1/1 1/1 100
H7N7 HPAI Eurasian 0/1 0/1 100 1/1 1/1 100
H7N7 LPAI Eurasian 0/1 0/1 100 1/1 1/1 100
H9N2 LPAI Eurasian, clade Y8 [38] 0/1 0/1 100 1/1 1/1 100
Allantoic fluid 0/3 0/3 100 0/3 0/3 100
Total 40 40 100 40 40 100

+: only the positive results are reported; HA: JRC-HA assay ; HPAI: high pathogenic avian influenza virus; IZSVe: Istituto Zooprofilattico Sperimentale delle Venezie; JRC: Joint Research Centre; LPAI: low pathogenic avian influenza virus; MP: JRC-MP assay.

The number of positive samples over the total number of isolates for a given subtype is shown. Unless otherwise specified, all samples were originally isolated from bird species.