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. Author manuscript; available in PMC: 2017 Jun 20.
Published in final edited form as: Euro Surveill. 2015 May 7;20(18):21122. doi: 10.2807/1560-7917.es2015.20.18.21122

Table 1. Antigenic properties of study samples measured by HI assays using ferret or sheep antisera raised against contemporary influenza A(H3N2) strains.

HA GenBank or EpiFlua accession number HA clade Antigens used to generate ferret sera Antigens used to generate sheep sera
rA/Perth/16/2009 rA/Victoria/361/2011-likeb (cell-grown) rA/Victoria/361/2011 (egg-grown) rA/Indiana/8/2011 (H3N2v) A/Victoria/361/2011 A/Texas/50/2012
Reference antigensc
rA/Perth/16/2009 (cell-grown) GQ293081.1 1 320 320 113 <20 453 1,280
rA/Victoria/361/2011 (cell-grown) EPI349103 3C.1 640 453 538 20 905 >2,560
rA/Victoria/361/2011 (egg-grown) EPI353906 3C.1 226 320 905 40 1,280 >2,560
rA/Indiana/8/2011 (H3N2v) JN638733.1 N/A <20 <20 <20 320 <80 <80
Test antigens
A/Texas/JMM_3/2012 CY134748.1 5 226 453 113 <20 320 1,810
A/Texas/JMM_48/2012 CY135076.1 3A 226 57 160 <20 <80 905
A/Texas/JMM_20/2012 CY134868.1 3C.2 320 226 320 <20 320 1,810
A/Texas/JMM_37/2012 CY134996.1 3C.3 80 <20 28 <20 <80 <80
A/Texas/JMM_4/2012 CY134756.1 3C-2012/13 80 <20 40 <20 <80 <80

HA: haemagglutinin; NA: neuraminidase; N/A: not applicable.

a

The authors gratefully acknowledge the originating (WHO Collaborating Centre for Reference and Research on Influenza in North Melbourne, Victoria, Australia) and submitting (Centers for Disease Control and Prevention, Atlanta, Georgia, US) laboratories that contributed the cell-and egg-grown A/Victoria/361/2011 sequences to GISAID's EpiFlu database.

b

rA/South_Australia/3/2011, which has the same amino acid sequence as A/Victoria/361/2011 (cell-grown) except for one change in the signal peptide.

c

These reassortant viruses are named for the strain from which the HA and NA were obtained; the six internal genes match A/Puerto Rico/8/1934(H1N1), A/New York/238/2005(H3N2) or A/New York/1682/2009(H1N1pdm09) sequences.

Highlighted cells indicate two-way HI results, where the specified serum is tested using the same (or a very similar) antigen to that used to generate the serum. An ‘r’ before the strain name indicates the virus was generated using gene synthesis and reverse genetics. Results from one experimental replicate are presented and are representative of the results obtained from at least two additional experimental replicates performed on a different day. All HA controls were between 3 and 8 HA units.