Department of Microbiology, Chiang Mai University, Chiang Mai, Thailand.
Med Mycol. 2009;47(5):549-53. doi: 10.1080/13693780802484875.
We previously reported a nested PCR assay for specific identification of 18S ribosomal DNA of Penicillium marneffei. In this study, the assay was used to detect the DNA of P. marneffei in serum samples. Sensitivity of the test was 4 pg/microl and 0.4 fg/microl when the cycle numbers used for nested reactions were 15 and 30, respectively. Twenty four out of 35 sera (68.6%) collected from patients with culture confirmed penicilliosis marneffei were positive, while normal healthy and non-P. marneffei infected HIV-positive sera were negative. The results suggested that the assay could be applied for the diagnosis of infections due to P. marneffei.
我们之前报道了一种巢式 PCR 检测方法,用于特异性鉴定马尔尼菲青霉的 18S 核糖体 DNA。在这项研究中,该方法用于检测血清样本中的马尔尼菲青霉 DNA。当嵌套反应的循环数分别为 15 和 30 时,该检测的灵敏度分别为 4 皮克/微升和 0.4 飞克/微升。从经培养证实患有马尔尼菲青霉病的患者中采集的 35 份血清中,有 24 份(68.6%)为阳性,而正常健康和非马尔尼菲青霉感染的 HIV 阳性血清均为阴性。结果表明,该检测方法可用于诊断马尔尼菲青霉引起的感染。