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. 2023 Jul;29(7):1492–1495. doi: 10.3201/eid2907.230296

Table. Detection of seroconversion and of influenza A viral loads in tissues and nasal swabs of experimentally infected pigs exposed by intranasal or alimentary inoculation with HPAI virus H5N1 clade 2.3.4.4b virus* .

 
Infection route
Day postinoculation
Animal ID
GEq, by qRT-PCR
NP-ELISA
Seroconversion
Nasal swabs†
Conchae nasalis
Trachea
Lung
Ileocaecal tonsil
Colon
Brain
Intranasal
4 1 30
4 2 150
14 3 30 10
14 4 10 60 10 170 200 350 +
14
Sentinel








Alimentary
4 1 5
4 2 30
14 3 20
14 4 140
14
Sentinel



10




Intranasal positive control‡ 4 1 300,000 10,000 860,000 5,400 NA NA NA
4 2 83,000 35,000 56,000 1,500 NA NA NA
4 3 750,000 4,300 1,600,000 1,500 NA NA NA
4 4 710,000 29,000 520,000 1,100 NA NA NA

*Shown are only tissues for which >1 animal has tested positive. GEq, genome copy equivalents per 0.1 mL calculated on the basis of qRT-PCR quantification of cycle values; HPAIV, highly pathogenic avian influenza; ID, identification; NA, not applicable; qRT-PCR, quantitative reverse transcription PCR; +, positive; –, negative. †Nasal swabs positive at day 2 postinfection for the intranasal group and day 4 postinfection for the alimentary group. ‡Four pigs, infected with the same device and dose of a swine-adapted influenza A virus strain (subtype H1avN1, clade 1C2.1) of a former study are included for comparison (9). Pigs were sacrificed at day 4 post infection when no seroconversion was to be expected; gastrointestinal tissues and brain were not examined.