Development of a loop-mediated isothermal amplification method for diagnosing Pneumocystis pneumonia
Uemura, Natsu and Makimura, Koichi and Onozaki, Masanobu and Otsuka, Yoshihito and Shibuya, Yasuhiro and Yazaki, Hirohisa and Kikuchi, Yoshimi and Abe, Shigeru and Kudoh, Shoji,, 57, 50-57 (2008),
doi = https://doi.org/10.1099/jmm.0.47216-0,
publicationName = Microbiology Society,
issn = 0022-2615,
abstract= Loop-mediated isothermal amplification (LAMP) is a novel, rapid nucleic acid amplification method with high specificity and sensitivity under isothermal conditions. In this study a LAMP assay for diagnosing Pneumocystis pneumonia (PCP) was developed. Oligonucleotide primers specific for Pneumocystis species were designed corresponding to 18S rRNA gene sequences. The assay, performed for 30 min at 61 °C, was capable of detecting 50 copies per tube (2×103 copies ml−1) in 30 min and did not show cross-reactivity to other species of fungi, including the genera Candida, Aspergillus and Cryptococcus. A total of 21 of 24 clinical specimens (sputum and bronchoalveolar lavage fluid) from patients with suspected PCP tested positive using the LAMP assay by real-time fluorescence detection. The results of the LAMP reaction were also observed by real-time turbidity detection and end-point visual turbidity or fluorescence detection. With real-time fluorescence detection, melting curves of the products were effective at distinguishing specific amplification from non-specific amplification or self-amplification. Visual detection was also possible as a rapid and easy assay using only a heat block and a black light.,
language=,
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