Real Time Polymerase Chain Reaction (rt-PCR): A New Patent to Diagnostic Purposes for Paracoccidioidomycosis

被引:9
|
作者
Rocha-Silva, Fabiana [1 ]
Gomes, Luciana I. [2 ]
Gracielle-Melo, Cidiane [1 ]
Goes, Alfredo M. [3 ]
Caligiorne, Rachel B. [1 ]
机构
[1] Nucleo Posgrad & Pesquisa Santa Casa Belo Horizon, Belo Horizonte, MG, Brazil
[2] Fiocruz MS, Ctr Pesquisas Rene Rachou, Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Dept Bioquim & Imunol, Belo Horizonte, MG, Brazil
关键词
Diagnosis; paracoccidioidomycosis; Paracocciodioides brasiliensis; Paracocciodioides lutzii; Pb; 27; protein; real time-PCR;
D O I
10.2174/1872214810666160905150958
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Paracoccidioidomycosis (PCM) is a systemic mycosis caused by dimorphic fungi Paracoccidioides brasiliensis and Paracoccidioides lutzii. It is prevalent in Latin American, mainly in Brazil. Therefore, PCM has fundamental impact on the Brazilian global economy, especially in public health system, since it is affecting economical active population in different country regions. Objective: The present study aimed to standardize the Real Time-Polymerase Chain Reaction (rt-PCR) for an efficient and safe PCM diagnosis amplifying the recombinant protein PB27 gene, only expressed by specimens of Paracoccidioides genus. Methods: To standardize a methodology of rt-PCR using species-specific primers and probe designed for annealing in this specific region of the fungi's genome, amplifying the recombinant protein PB27 gene, only expressed by specimens of Paracoccidioides genus. Followed by design in silico, experiments were performed in vitro to determine rt-PCR specificity, efficiency and genome detection limit. Results: The primers and probe sequences were deposited in Brazilian Coordination of Technological Innovation and Transfer (CTIT), under patent reference number BR1020160078830. The present study demonstrated the rt-PCR applicability for support on diagnosis of paracoccidioidomycosis, presenting low cost, which makes it affordable for public health services in developing countries as Brazil. It is noteworthy that it is necessary to validate this methodology using clinical samples before to use as a safe method of diagnosis. A review of all patents related to this topic was performed and it was shown that, to date, there are no records of patent on kits for paracoccidioidomycosis's diagnostic. Indeed, there is still a lot to go to reach this goal. Conclusion: The reaction developed was standardized and patented, opening perspectives to molecular diagnosis development for paracoccidioidomycosis, since rt-PCR can be applied to a broad spectrum of infectious diseases. It would need to be tested in biological samples in order to validate this method and then generate a diagnostic kit for Paracoccidioidomycosis.
引用
收藏
页码:143 / 149
页数:7
相关论文
共 50 条
  • [21] Detection of micrometastases in peritoneal washings of gastric cancer patients by quantitative real time reverse transcriptase-polymerase chain reaction (RT-PCR)
    Dalal, Kimberly M.
    Woo, Yanghee
    Galanis, Charles
    Gonen, Mithat
    Fong, Yuman
    Coit, Daniel G.
    GASTROENTEROLOGY, 2007, 132 (04) : A892 - A892
  • [22] Detection of micrometastases in peritoneal washings of pancreatic cancer patients by quantitative real time reverse transcriptase-polymerase chain reaction (RT-PCR)
    Dalal, Kimberly M.
    Woo, Yanghee
    Galanis, Charles
    Gonen, Mithat
    Allen, Peter J.
    Dematteo, Ronald P.
    Fong, Yuman
    Coit, Daniel G.
    GASTROENTEROLOGY, 2007, 132 (04) : A835 - A836
  • [23] BRCA1 expression evaluated by real-time reverse transriptase polymerase chain reaction (RT-PCR) in operable breast cancer
    Potemski, P.
    Pluciennik, E.
    Bednarek, A. K.
    Kusinska, R.
    Debska, S.
    Kubiak, R.
    Kordek, R. M.
    JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15)
  • [24] Development of real-time reverse transcriptase-polymerase chain reaction (rt RT-PCR) targeting four genes of peste des petits ruminants virus
    Dincer, Ender
    Ozkul, Aykut
    ANKARA UNIVERSITESI VETERINER FAKULTESI DERGISI, 2015, 62 (04): : 283 - 287
  • [25] Detection of neuroblastoma cells in blood by reverse transcriptase-polymerase chain reaction(RT-PCR)
    高亚
    李恭才
    张宪生
    徐泉
    郑百俊
    中华医学杂志(英文版), 1997, (05) : 21 - 25
  • [26] Detection of Citrus tatter leaf virus with reverse transcription—polymerase chain reaction (RT-PCR)
    D. L. Hailstones
    K. L. Bryant
    P. Broadbent
    C. Zhou
    Australasian Plant Pathology, 2000, 29 : 240 - 248
  • [27] Detection of malignancy markers in thyroid nodules by reverse transcriptase polymerase chain reaction (RT-PCR)
    Pineda, P
    Rojas, P
    Liberman, C
    Moyano, L
    Goecke, L
    REVISTA MEDICA DE CHILE, 2003, 131 (09) : 965 - 972
  • [28] Detection of circulating breast cancer cells by reverse transcriptase polymerase chain reaction (RT-PCR)
    Hu, XC
    Chow, LWC
    EUROPEAN JOURNAL OF SURGICAL ONCOLOGY, 2000, 26 (06): : 530 - 535
  • [29] DIAGNOSIS OF FLAME CHLOROSIS BY REVERSE TRANSCRIPTION-POLYMERASE CHAIN-REACTION (RT-PCR)
    HABER, S
    RYMERSON, RT
    PROCUNIER, JD
    MURRAY, G
    CVITKOVITCH, SE
    PLANT DISEASE, 1995, 79 (06) : 626 - 630
  • [30] Detection of viable Vibrio cholerae by reverse-transcriptase polymerase chain reaction (RT-PCR)
    Bej, AK
    Ng, WY
    Morgan, S
    Jones, DD
    Mahbubani, MH
    MOLECULAR BIOTECHNOLOGY, 1996, 5 (01) : 1 - 10