Point-of-care molecular diagnosis of Mycoplasma pneumoniae including macrolide sensitivity using quenching probe polymerase chain reaction

Macrolides are generally considered to be the drugs of choice for treatment of patients with Mycoplasma pneumoniae infection. However, macrolide-resistant M. pneumoniae has been emerging since about 2000. The Smart Gene.sup.® system (MIZUHO MEDY Co., Ltd., Tosu, Japan) is a novel fully automated sys...

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Veröffentlicht in:PloS one 2021-10, Vol.16 (10), p.e0258694-e0258694
Hauptverfasser: Ishiguro, Nobuhisa, Sato, Rikako, Mori, Toshihiko, Tanaka, Hiroshi, Narita, Mitsuo, Nagano, Takashi, Owaku, Masato, Miyajima, Kensuke, Manabe, Atsushi
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Sprache:eng
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Zusammenfassung:Macrolides are generally considered to be the drugs of choice for treatment of patients with Mycoplasma pneumoniae infection. However, macrolide-resistant M. pneumoniae has been emerging since about 2000. The Smart Gene.sup.® system (MIZUHO MEDY Co., Ltd., Tosu, Japan) is a novel fully automated system for detection of pathogens using the method of quantitative polymerase chain reaction (qPCR) with QProbe (QProbe PCR). The entire procedure is completed within 50 min and the size of the instrument is small (15 x 34 x 30 cm). The purpose of this study was to evaluate the usefulness of the Smart Gene.sup.® system for detection of M. pneumoniae and detection of a point mutation at domain V of the 23S rRNA gene of M. pneumoniae. Pharyngeal swab samples were collected from 154 patients who were suspected of having respiratory tract infections associated with M. pneumoniae. Compared with the results of qPCR, the sensitivity and specificity of the Smart Gene.sup.® system were 98.7% (78/79) and 100.0% (75/75), respectively. A point mutation at domain V of the 23S rRNA gene was detected from 7 (9.0%) of 78 M. pneumoniae-positive samples by the Smart Gene.sup.® system and these results were confirmed by direct sequencing. The minimum inhibitory concentrations of clarithromycin among the 5 isolates of M. pneumoniae with a point mutation at domain V of the 23S rRNA gene were >64 [mu]g/ml and those among the 33 isolates without a mutation in the 23S rRNA gene were
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0258694