Antigen-capture ELISA and immunochromatographic test strip to detect the H9N2 subtype avian influenza virus rapidly based on monoclonal antibodies

All the viruses used in this study are described in Table 1. All the viruses were obtained from the virus repository in our laboratory [20, 38‐41]. AIVs were stored at − 80 °C and propagated at 37 °C using 10-day old chicken embryos, as described previously [20]. Influenza B virus, avian paramyxovirus 4 (APMV-4), infectious bursal disease virus (IBDV), Newcastle disease virus (NDV), and infectious bronchitis virus (IBV) were also acquired from our laboratory virus repository. All viruses were determined using hemagglutinin (HA) and tissue culture infectious dose 50 (TCID50) assays according to standard methods [42]. The experiments involving H5 and H7 subtype AIVs were conducted in an accredited Biosafety Level 3 (BSL-3) containment laboratory at the First Affiliated Hospital of Zhejiang University.

Madin-Darby canine kidney (MDCK) cells and SP2/0 mouse myeloma cells were maintained in our laboratory. Purified HA protein from the H9N2 (A/chicken/Zhejiang/329/2011) subtype AIV was purchased from Sino Biological (Beijing, China) [43].

BALB/c mice (9 weeks old) were immunized with the purified H9N2 subtype AIV HA protein mixed Freund’s adjuvant (Sigma, St. Louis, MO, USA) intramuscularly, twice at 3 weeks apart. After 6 weeks, the mice were immunized once more with HA protein by tail vein injection. After 3 days, the spleen lymphocytes of the selected mice were fused with SP2/0 cells [43, 44]. The hybridoma cells were screened using a purified H9N2 HA protein-coated ELISA method. The positive monoclonal hybridoma cell line that was obtained after three consecutive limiting dilutions was continuously subcultured and then injected into mice intraperitoneally. To obtain MAbs, a Protein G column (GE Healthcare, Chicago, IL, USA) was used to purify ascites collected from the mice injected with the hybridoma cells [45].

Isotyping of the MAbs was performed using a Monoclonal Antibody Isotyping Kit (Bio-Rad, Hercules, CA, USA). The affinities of each MAb were measured using ELISA, as described previously [45]. In brief, the ELISA plate was coated with purified H9N2 HA protein (20 ng/well) overnight at 4 °C. MAbs were twofold serially diluted, starting at 1 mg/ml, and added to the plate. Incubation was carried out for 1 h at 37 °C. Then, goat anti-mouse IgG (Novus, St Charles, MO USA) was diluted 10,000 times and added as the secondary antibody. Incubation was carried out for 30 min at 37 °C. The color reaction was performed using the 3, 3′, 5, 5′-tetramethylbenzidine (TMB) reagent (KPL, Gaithersburg, MD, USA). After 10 min, the color reaction was stopped using the terminating reagent (KPL). Between each step, phosphate-buffered saline (PBS) with Tween 20 (PBST) was used to wash the plate five times. An ELISA plate reader (Bio-Rad) was read used to read the optical density (OD) at 450 nm, and the antibody’s affinity was estimated as the minimum concentration of the MAb required to provide a positive reaction. The variable genes of the heavy or light chains of the MAbs were sequenced by Sino Biological.

An immunofluorescence assay (IFA) was used to visualize the binding of the MAbs to the virus-infected MDCK cells [46, 47]. After incubation with the virus for 24 h, virus-infected MDCK cells were fixed with paraformaldehyde. Thereafter, the MDCK cells were permeabilized using Triton X-100. Then, MAbs 3G4 or 2G7 were added and incubated for 1 h at 37 °C. The goat anti-mouse IgG heavy plus light chain (H + L)-Alexa Fluor (Abcam, Cambridge, UK) was then added. The wells were washed with PBS three times between each step. The results were scored using an EVOS M7000 instrument (Thermo Fisher Scientific, Waltham, MA, USA).

The procedure for AC-ELISA (Fig. 1) was described previously [35, 48]. In brief, based on the results of MAb affinity measurements, MAb 3G4 was selected for capture and used to coat a 96-well ELISA plate at 80 ng/well in 100 μl of coating buffer at 4 °C. After 12 h, MAb 2G7, which was selected as the detection antibody, was labelled with horseradish peroxidase (HRP; Innoreagents, Huzhou, China). Then, the ELISA plate was washed and blocked with bovine serum albumin (BSA). After washing, samples were added into the ELISA plate and incubated for 1 h at 37 °C. Then, after washing the plate, 2G7-MAb-HRP (4 μg/ml) was added and incubated for 30 min at 37 °C. The plate was then washed and TMB solution was added at 100 μl/well. After 10 min, the TMB stop solution was added. The OD value (450 nm) was then detected using an ELISA reader. An OD value greater than 2.1 times that of the negative control was considered to indicate a positive reaction.

The procedure for using the ICT strip is shown in Fig. 1. The preparation of the colloidal gold solution was described previously [37, 49]. In brief, 0.01% HAuCl4 solution was heated to 100 °C, and then a trisodium citrate solution was added quickly with continuous vigorous stirring. Then, the colloidal gold solution was continuously boiled until the color changed to wine-red. After cooling, the pH of the solution was adjusted to 7.2 using potassium carbonate. Then, 10 ml of the colloidal gold solution placed into a glass bottle into which 100 μl MAb 3G4 (1 mg/ml) was added. Incubation was carried out for 30 min with gentle stirring. After blocking with BSA, the solution was centrifuged for 30 min at 4 °C. The colorless supernatant was discarded and the pellet was re-dissolved with 1 ml PBST (containing 1% BSA).

The ICT strip contained an absorbent pad, nitrocellulose (NC) membranes, a MAb-gold conjugated, pad and a sample pad. The NC membranes were coated with MAb 2G7 as the test line and with goat anti-mouse IgG (Solarbio, Beijing, China) as the control line.

The specificity of the assays was tested using different subtypes of AIV (19 H9N2 AIVs and 25 other AIV subtypes), and other viruses (IBDV, IBV, APMV-4, NDV, and influenza B virus). To determine the sensitivity, twofold serial dilutions of H9N2 AIV allantoic fluid and purified H9N2 proteins were used. A twofold serial dilution of H10N7 AIV allantoic fluid was used as the negative control. To evaluate repeatability, all samples were tested in triplicate, and all assays were repeated three times.

To assess the clinical application of the two methods, 200 cloacal swabs (100 from chickens and 100 from ducks) collected from 10 poultry farms in Zhejiang Province were detected using multiplex qRT-PCR, AC-ELISA, and ICT strip methods. There were 20 samples for every farm. An Influenza A virus universal PCR kit (Liferiver Bio-Tech, Shanghai, China) was used to perform the qRT-PCR assay [37].

Five murine MAbs (3G4, 2G7, 1B12, 1C12, and 2F1) were screened using ELISA. MAbs 3G4, 2G7, 1B12, and 1C12 belonged to the IgG1 subclass, and Mab 2F1 belonged to the IgG2a subclass. Among these MAbs, MAbs 3G4 and 2G7 were chosen to develop the detection method because of their high affinity (Table 2). Although none of the five MAbs displayed hemagglutination inhibition (HI) or virus neutralization (VN) activity against H9N2 subtype AIV, these MAbs reacted with all H9N2 subtype AIVs available in our laboratory (Table 1). Therefore, MAbs 3G4 and 2G7 were complementary to each other and hence likely to be suitable for rapid detection of H9N2 subtype AIVs.

IFA was used to analyze whether the MAbs could recognize H9N2 subtype AIV in MDCK cells. Neither MAb exhibited non-specific binding to MDCK cells infected with H5N1, H6N1, and H7N3 subtype AIVs; However, MAbs 3G4 and 2G7 showed strong reactivity toward MDCK cells infected with H9N2 subtype AIV (Fig. 2).

To determine its specificity, AC-ELISA was tested using different strains of viruses, including H9N2 subtype AIVs and other virus strains (Table 1 and Fig. 3a). No cross-reactivity was observed for any of the other subtypes of influenza A virus (H1, H2, H3, H4, H5, H6, H7, H10, and H11) or for the other viruses tested (NDV, APMV-4, IBV, IBDV, and influenza B virus).

To determine the sensitivity of AC-ELISA, three different H9N2 subtype AIVs were assessed alongside the H10N8 subtype AIV as a negative control. The four selected viruses were twofold serially diluted to determine the detection limit (Table 1 and Fig. 3b). The detection limits were 4 HA titer in 100 μl of virus sample (A/chicken/Zhejiang/329/2011, A/quail/Zhejiang/D485/2011 and A/chicken/Zhejiang/221/2011). The detection limit of AC-ELISA for the H9N2 HA protein was 31.5 ng/ml (Fig. 3c).

To evaluate repeatability, twofold serially diluted H9N2 subtype AIV was detected (A/chicken/Zhejiang/329/2011). In the intra- and inter-batch repeatability tests, the coefficient of variation (CV%) was < 5% (Table 3 and Table 4), which showed that the AC-ELISA method possessed good reproducibility.

The specificity of the ICT strip was tested using H9N2 viruses and other non-H9N2 viruses, as described above. Only the H9N2 subtype AIV samples showed positive results (Fig. 4a). The result suggested that the ICT strip could specifically detect H9N2 subtype AIVs (Table 1).

Two-fold serially diluted allantoic fluid from H9N2 subtype AIV (A/chicken/Zhejiang/329/2011)-infected chicken eggs was used to test the sensitivity of the strip. The detection limit of the ICT strip was 100 μl of allantoic fluid containing a 4 HA titer of the virus or a median tissue culture infectious dose (TCID50) of 10^3.15 (Fig. 4b).

To verify their stability, the ICT strips were tested after being assembled for 30 and 60 days, and the results revealed comparable specificity and sensitivity to newly assembled ICT strips.

To assess the actual clinical application of the methods, cloacal swabs were collected from poultry in farms and subjected to analysis by qRT-PCR, AC-ELISA, and ICT strips (Table 5). We used the results of qRT-PCR as the standard, using which, 44 samples were determined to be positive. By comparison, the results of AC-ELISA showed that 41 of the 200 poultry samples were positive, and the ICT strip assay result identified 40 of 200 poultry samples as positive. Furthermore, the positive samples identified by qRT-PCR and AC-ELISA were confirmed to be the same samples. The sensitivity and specificity of the AC-ELISA method were calculated as 93.2% (41/44) and 98.1% (153/156), respectively. The sensitivity and specificity of the ICT strips were 90.9% (40/44) and 97.4% (152/156), respectively. These results indicated that both AC-ELISA and ICT strip methods exhibited high sensitivity and specificity for environmental sample detection.