Genetic identification of the main opportunistic mucorales by PCR-restriction fragment length polymorphism

被引:67
|
作者
Machouart, M [1 ]
Larché, J
Burton, K
Collomb, J
Maurer, P
Cintrat, A
Biava, MF
Greciano, S
Kuijpers, AFA
Contet-Audonneau, N
de Hoog, GS
Gérard, A
Fortier, B
机构
[1] CHU Brabois, Serv Parasitol Mycol, F-54511 Vandoeuvre Les Nancy, France
[2] CHU Brabois, Serv Reanimat Med, F-54511 Vandoeuvre Les Nancy, France
[3] Cent Bur Schimmelcultures, NL-3508 AD Utrecht, Netherlands
关键词
D O I
10.1128/JCM.44.3.805-810.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mucormycosis is a rare and opportunistic infection caused by fungi belonging to the order Mucorales. Recent reports have demonstrated an increasing incidence of mucormycosis, which is frequently lethal, especially in patients suffering from severe underlying conditions such as immunodeficiency. In addition, even though conventional mycology and histopathology assays allow for the identification of Mucorales, they often fail in offering a species-specific diagnosis. Due to the lack of other laboratory tests, a precise identification of these molds is thus notoriously difficult. In this study we aimed to develop a molecular biology tool to identify the main Mucorales involved in human pathology. A PCR strategy selectively amplifies genomic DNA from molds belonging to the genera Absidia, Mucor, Rhizopus, and Rhizomucor, excluding human DNA and DNA from other filamentous fungi and yeasts. A subsequent digestion step identified the Mucorales at genus and species level. This technique was validated using both fungal cultures and retrospective analyses of clinical samples. By enabling a rapid and precise identification of Mucorales strains in infected patients, this PCR-restriction fragment length polymorphism-based method should help clinicians to decide on the appropriate treatment, consequently decreasing the mortality of mucormycosis.
引用
收藏
页码:805 / 810
页数:6
相关论文
共 50 条
  • [31] Cryptosporidium parvum mixed genotypes detected by PCR-restriction fragment length polymorphism analysis
    Reed, C
    Sturbaum, GD
    Hoover, PJ
    Sterling, CR
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (01) : 427 - 429
  • [32] MOLECULAR CHARACTERIZATION BY PCR-RESTRICTION FRAGMENT LENGTH POLYMORPHISM OF TEM BETA-LACTAMASES
    ARLET, G
    BRAMI, G
    DECRE, D
    FLIPPO, A
    GAILLOT, O
    LAGRANGE, PH
    PHILIPPON, A
    FEMS MICROBIOLOGY LETTERS, 1995, 134 (2-3) : 203 - 208
  • [33] Evaluation of PCR-restriction profile analysis and IS2404 restriction fragment length polymorphism and amplified fragment length polymorphism fingerprinting for identification and typing of Mycobacterium ulcerans and M-marinum
    Chemlal, K
    Huys, G
    Fonteyne, PA
    Vincent, V
    Lopez, AG
    Rigouts, L
    Swings, J
    Meyers, WM
    Portaels, F
    JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (09) : 3272 - 3278
  • [34] Genetic variation of chloroplast DNA in Zingiberaceae taxa from Myanmar assessed by PCR-restriction fragment length polymorphism analysis
    Ahmad, D.
    Kikuchi, A.
    Jatoi, S. A.
    Mimura, M.
    Watanabe, K. N.
    ANNALS OF APPLIED BIOLOGY, 2009, 155 (01) : 91 - 101
  • [35] Detection and identification of human papillomavirus using a PCR-restriction fragment mass polymorphism assay
    Lee, Jin Kyung
    Hong, Young Jun
    Um, Tae Hyun
    Lee, Eun Hee
    Chi, Hyun-Sook
    Koh, Jae Soo
    Yim, Hyeon Woo
    Cha, Young Joo
    MOLECULAR MEDICINE REPORTS, 2011, 4 (04) : 645 - 650
  • [36] Use of PCR-restriction fragment length polymorphism for the identification of zoonotic mycobacteriosis in zebrafish caused by Mycobacterium abscessus and Mycobacterium chelonae
    Seok, Seung-Hyeok
    Koo, Hye Cheong
    Kasuga, Asako
    Kim, Yeun
    Lee, Eun Gae
    Lee, Hyeyoung
    Park, Jong-Hwan
    Baek, Min-Won
    Lee, Hui-Young
    Kim, Dong-Jae
    Lee, Byeung-Hee
    Lee, Yong-Soon
    Cho, Sang-Nae
    Park, Jae-Hak
    VETERINARY MICROBIOLOGY, 2006, 114 (3-4) : 292 - 297
  • [37] Identification of oral Peptostreptococcus isolates by PCR-restriction fragment length polymorphism analysis of 16S rRNA genes
    Riggio, MP
    Lennon, A
    JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (09) : 4475 - 4479
  • [38] Aspergillus Section Fumigati Typing by PCR-Restriction Fragment Polymorphism
    Staab, Janet F.
    Balajee, S. Arunmozhi
    Marr, Kieren A.
    JOURNAL OF CLINICAL MICROBIOLOGY, 2009, 47 (07) : 2079 - 2083
  • [39] Use of PCR-restriction fragment length polymorphism analysis for identification of yeast species isolated from bovine intramammary infection
    Fadda, M. E.
    Pisano, M. B.
    Scaccabarozzi, L.
    Mossa, V.
    Deplano, M.
    Moroni, P.
    Liciardi, M.
    Cosentino, S.
    JOURNAL OF DAIRY SCIENCE, 2013, 96 (12) : 7692 - 7697
  • [40] Use of PCR-restriction fragment length polymorphism analysis of the hsp65 gene for rapid identification of mycobacteria in Brazil
    Rocha, AD
    Leite, CD
    Torres, HM
    de Miranda, AB
    Lopes, MQP
    Degrave, WM
    Suffys, PN
    JOURNAL OF MICROBIOLOGICAL METHODS, 1999, 37 (03) : 223 - 229