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. 2007 May 30;45(8):2726–2730. doi: 10.1128/JCM.00321-07

TABLE 1.

Results of testing of different specimens with real-time PCR assays based on the amplification of parts of the P1 gene and the repetitive element repMp1 of M. pneumoniae

Sample Descriptiona M. pneumoniae strain Real-time PCR CP ± SDb (n = 8)
Purified plasmid pET-30 (containing P1 sequence) 102 GE/5 μl M129 (subtype 1) P1 36.45 ± 0.37 (1.0)
104 GE/5 μl 29.20 ± 0.08 (0.3)
106 GE/5 μl 22.21 ± 0.07 (0.3)
Purified plasmid pET-30 (containing repMp1 sequence) 102 GE/5 μl M129 (subtype 1) RepMp1 35.19 ± 0.30 (0.8)
104 GE/5 μl 28.43 ± 0.14 (0.5)
106 GE/5 μl 21.55 ± 0.04 (0.2)
Extracted DNA from bouillon cultures 0.2 CFU/5 μl M129 (subtype 1) P1 NEc (CP > 42)
(0.4 fg of DNA/5 μl) RepMp1 34.16 ± 0.22 (0.6)
1.9 CFU/5 μl P1 40.56 ± 1.25 (3.1)
(4.2 fg of DNA/5 μl) RepMp1 33.64 ± 0.31 (0.9)
19.0 CFU/5 μl P1 36.44 ± 0.41 (1.1)
(42.2 fg of DNA/5 μl) RepMp1 31.15 ± 0.48 (0.6)
Extracted DNA from bouillon cultures FH (subtype 2) P1 29.98 ± 0.08 (0.3)
RepMp1 26.02 ± 0.06 (0.2)
4817 (variant 1) P1 30.95 ± 0.10 (0.3)
RepMp1 26.05 ± 0.09 (0.3)
ST (variant 2) P1 29.58 ± 0.10 (0.3)
RepMp1 24.70 ± 0.04 (0.2)
a

GE, genome equivalent.

b

The arithmetic mean of crossing points ± the standard deviation is indicated; the coefficient of variation (%) is given in parentheses. CP, crossing point.

c

NE, not evaluable.