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. 2015 Jul 17;2(9):1179–1185. doi: 10.1016/j.ebiom.2015.07.018

Table 1.

Results of the qPCRgyrALp assay with melting temperature (Tm), and presence or absence of the gyrA83/T83I QRDR change determined by PCR amplification and sequencing (PCR-Seq), and Next-Generation Sequencing (NGS, with the percentage of gyrA83 mutant alleles among sequencing reads) for the 139 respiratory samples collected from the 82 patients.

Patients (n = 82)
Respiratory samples (n = 139)
Day of samplinga
qPCRgyrALp
T83I GyrA change
FQ No FQ NAb Total (Tm) PCR-Seq NGS
n = 20 8 2 10 20 Negative ND
n = 58 3 0 1 4 Negative ND
54 10c 40 104 Positive (~ 60 °C) ND Yes (< 0.5%)
#1 1 1 D1 Positive (~ 60 °C) NPA No
1 1 D3 Positive (~ 56 °C) NPA Yes (< 0.5%)
1 1 D7 Negative ND ND
#2 1 1 D0 Positive (~ 60 °C) No Yes (2.9%)
1 1 D4 Positive (~ 56 °C) Yes Yes (94%)
1 1 D4 Positive (~ 56 °C) ND ND
#3 1 1 D0 Positive (~ 56 °C) No No
#4 1 1 D0 Positive (~ 60 °C) No Yes (1.05%)
1 1 D2 Positive (~ 60 °C) ND ND
1 1 D3 Positive (~ 56 °C) Yes Yes (75%)
1 1 D5 Positive (~ 56 °C) Yes Yes (85%)
Total 75 13 51 139

Data are given according to the patient's fluoroquinolone (FQ) treatment status at the time of respiratory sample collection. ND: not determined. NPA: no PCR amplification.

a

Days of sampling are given according to the day of legionellosis diagnosis (D0).

b

FQ treatment information not available.

c

Including three D0 samples tested by NGS for the three control patients.