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. 2010 Mar 1;54(5):1834–1841. doi: 10.1128/AAC.01608-09

TABLE 2.

Chemiluminescent neuraminidase inhibition assay of A/Texas/12/2007 (H3N2) and plaque-purified clones

Strain designation Passage levelb NA mutation Mean IC50 ±SD (nM)a
Oseltamivir Zanamivir Peramivir A-315675
A/Texas/12/2007 X/C2 E119V 9.18 ± 1.10 1.09 ± 0.01 ND ND
A/Texas/12/2007 X/C3 E119(V/I) 8.06 ± 0.41 1.54 ± 0.47 0.51 ± 0.00 1.35 ± 0.15
A/Texas/12/2007 clone 1 X/C4 E119V 5.49 ± 0.03 1.38 ± 0.45 0.43 ± 0.02 1.25 ± 0.03
A/Texas/12/2007 clone 2 X/C4 E119I 33.25 ± 7.01 12.67 ± 5.33 0.90 ± 0.11 4.96 ± 0.47
A/Washington/01/2007 (sensitive control) None 0.16 ± 0.03 0.76 ± 0.08 0.28 ± 0.02 0.74 ± 0.01
a

Average IC50 of two independent chemiluminescent NI assays; IC50s of test viruses are compared with those of oseltamivir-sensitive control A/Washington/01/2007 (H3N2) to determine the fold difference in IC50. ND, not done due to insufficient specimen volume.

b

X denotes that the virus isolate was grown in the originating laboratory with an unknown passage number and cell culture, and C2, C3, and C4 denote that the same virus isolate was passaged an additional two, three, or four times, respectively, in MDCK cells at the CDC reference laboratory.