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. 2005 Jan 6;124(1):183–190. doi: 10.1016/j.jviromet.2004.11.022

Table 2.

Sample to residual ratio quantification using RRT-PCR results for known IBV strains

Strain Serotypea Anti-Massachusetts Anti-Arkansas Anti-Connecticut Anti-Delaware/Georgia 98 Assay serotype
Beaudette Massachusetts +b (4.74) c (−1.15) − (−0.80) − (0.03) Massachusetts
Florida 18288 Florida − (−0.80) − (−1.70) − (−1.47) − (−1.85) Not typeable
Arkansas 99 Arkansas − (−1.13) + (3.35) − (−1.70) − (−2.46) Arkansas
3668-4 Arkansas − (−0.82) + (2.48) − (−0.66) − (−0.37) Arkansas
GAV92/4595/92 GAV92 − (0.16) − (0.85) − (0.65) − (−1.01) Not typeable
0470 GA98 − (−0.29) − (−0.55) − (−1.27) + (2.06) Delaware/GA98
CAV 56b California Variant − (−0.22) − (0.27) − (−0.48) − (0.5) Not typeable
15172 C Nebraska 95 − (−0.51) − (0.55) − (−0.99) − (−1.17) Not typeable

Calculated SRRQ values are given in parentheses.

a

Serotype as determined by virus neutralization or RT-PCR/RFLP.

b

A plus sign denotes that the sample RNA incubated with the particular chimeric oligonucleotide amplified at least two cycles later as compared with the uncleaved control RNA.

c

A negative sign denotes that the sample RNA incubated with the particular chimeric oligonucleotide amplified no later than 1.99 cycles as compared with the uncleaved control RNA.