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. 2007 Sep 5;14(11):1529–1531. doi: 10.1128/CVI.00197-07

TABLE 1.

Concordance between the test antigens and the pooled in-house antigens using culture-positive seraa

Isolate from which the antigen was derived (country of origin) No. (%) of serum samples for which the titer was:
No. (%) of results that wered:
r (CI)e Pe
Sameb ±1 dilutionc ±2 dilutionsc ±3 or more dilutionsc Concordant Discordant
B. pseudomallei NCTC 13178 (Australia) 9 (36) 10 (40) 3 (12) 1 (4) 23 (92) 2 (8) 0.8135 (0.6088-0.9167) <0.0001
B. pseudomallei 145 (Papua New Guinea) 9 (36) 8 (32) 5 (20) 1 (4) 23 (92) 2 (8) 0.8506 (0.6795-0.9340) <0.0001
B. pseudomallei 148 (Sri Lanka) 8 (32) 11 (44) 1 (4) 4 (16) 24 (96) 1 (4) 0.7690 (0.5281-0.8953) <0.0001
B. thailandensis 5 (20) 4 (16) 5 (20) 8 (32) 22 (88) 3 (12) 0.1802 (−0.2432-0.5469) <0.3887
a

The number of serum samples was 25. The range of titers was from 1:10 to more than 1:5,120. CI, confidence interval.

b

Concordance with the in-house IHA implies that an identical IHA titer was obtained using the antigen named.

c

Concordance within ±1, ±2, or ±3 (or more) dilutions implies that the IHA titer obtained using the antigen named was either above or below the titer obtained in the in-house IHA by that factor.

d

A discordant result implies that the IHA result obtained using the antigen named was negative, while the in-house test result was positive. Sera tested using the B. cepacia antigen were uniformly negative.

e

For concordant results, Spearman rank correlation was carried out to obtain r and P values.