Development and evaluation of loop-mediated isothermal amplification (LAMP) for the rapid diagnosis of Penicillium marneffei in archived tissue samples

被引:2
作者
Sun, Jiufeng [1 ]
Li, Xiqing [1 ]
Zeng, Hanxiang [1 ]
Xie, Zhi [1 ]
Lu, Changming [1 ]
Xi, Liyan [1 ]
de Hoog, Gert S. [2 ,3 ,4 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 2, Dept Dermatol, Guangzhou 510120, Peoples R China
[2] CBS KNAW Fungal Biodivers Ctr, Utrecht, Netherlands
[3] Univ Amsterdam, Inst Biodivers & Ecosyst Dynam, NL-1012 WX Amsterdam, Netherlands
[4] Peking Univ, Hlth Sci Ctr, Res Ctr Med Mycol, Beijing 100871, Peoples R China
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2010年 / 58卷 / 03期
基金
中国国家自然科学基金;
关键词
Penicillium marneffei; penicilliosis; rapid diagnosis; LAMP; ACUTE RESPIRATORY SYNDROME; MYCOBACTERIUM-TUBERCULOSIS; IDENTIFICATION; ASSAY; PCR; HYBRIDIZATION; DNA; INFECTION; YEAST; CORONAVIRUS;
D O I
10.1111/j.1574-695X.2009.00647.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Penicillium marneffei is the etiologic agent of a severe systemic disease in immunocompromised hosts in Southeast Asia. In the present study, a novel method, known as loop-mediated isothermal amplification (LAMP), is described for the rapid and specific detection of the species, using a primer set derived from the internal transcribed spacer (ITS) region of the rRNA gene. Amplification products can be detected macroscopically by visual inspection in vials using SYBR Green I as well as by electrophoresis on agarose gel. The LAMP assay resulted in specific amplification of P. marneffei ITS using pure cultures after a 1-h reaction at 65 degrees C in a water bath; no cross-reactivity with other fungi including other biverticillate penicillia was observed. The detectable DNA limit was two copies. In addition, specific amplification was achieved using paraffin wax-embedded tissue samples from patients with penicilliosis marneffei and tissue samples from bamboo rats. The method provides a powerful tool for rapid diagnostics in the clinical lab, and has potential for use in ecological studies.
引用
收藏
页码:381 / 388
页数:8
相关论文
共 39 条
[21]   Loop-mediated isothermal amplification of DNA [J].
Notomi, Tsugunori ;
Okayama, Hiroto ;
Masubuchi, Harumi ;
Yonekawa, Toshihiro ;
Watanabe, Keiko ;
Amino, Nobuyuki ;
Hase, Tetsu .
NUCLEIC ACIDS RESEARCH, 2000, 28 (12)
[22]   Rapid identification of Ochroconis gallopava by a loop-mediated isothennal amplification (LAMP) method [J].
Ohori, Akira ;
Endo, Shigeo ;
Sano, Ayako ;
Yokoyama, Koji ;
Yarita, Kyoko ;
Yamaguchi, Masashi ;
Kamei, Katsuhiko ;
Miyaji, Makoto ;
Nishimura, Kazuko .
VETERINARY MICROBIOLOGY, 2006, 114 (3-4) :359-365
[23]   Development of a monoclonal antibody-based enzyme-linked immunosorbent assay for the diagnosis of Penicillium marneffei infection [J].
Panichakul, T ;
Chawengkirttikul, R ;
Chaiyaroj, SC ;
Sirisinha, S .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2002, 67 (04) :443-447
[24]   Evaluation of real-time reverse transcriptase PCR and real-time loop-mediated amplification assays for severe acute respiratory syndrome - Coronavirus detection [J].
Poon, LLM ;
Wong, BWY ;
Chan, KH ;
Ng, SSF ;
Yuen, KY ;
Guan, Y ;
Peiris, JSM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (07) :3457-3459
[25]   Rapid detection of the severe acute respiratory syndrome (SARS) coronavirus by a loop-mediated isothermal amplification assay [J].
Poon, LLM ;
Leung, CSW ;
Tashiro, M ;
Chan, KH ;
Wong, BWY ;
Yuen, KY ;
Guan, Y ;
Peiris, JSM .
CLINICAL CHEMISTRY, 2004, 50 (06) :1050-1052
[26]   Development and evaluation of a one-tube seminested PCR assay for the detection and identification of Penicillium marneffei [J].
Prariyachatigul, C ;
Chaiprasert, A ;
Geenkajorn, K ;
Kappe, R ;
Chuchottaworn, C ;
Termsetjaroen, S ;
Srimuang, S .
MYCOSES, 2003, 46 (11-12) :447-454
[27]  
SUN J, 2009, J MICROBIOL METH, DOI DOI 10.1016/J.MIMET.2009.1010.1002
[28]   DISSEMINATED PENICILLIUM-MARNEFFEI INFECTION IN SOUTHEAST-ASIA [J].
SUPPARATPINYO, K ;
KHAMWAN, C ;
BAOSOUNG, V ;
NELSON, KE ;
SIRISANTHANA, T .
LANCET, 1994, 344 (8915) :110-113
[29]  
Ukarapol Nuthapong, 1998, Journal of the Medical Association of Thailand, V81, P637
[30]   Rapid identification of Penicillium marneffei by PCR-based detection of specific sequences on the rRNA gene [J].
Vanittanakom, N ;
Vanittanakom, P ;
Hay, RJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (05) :1739-1742