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Evaluation of DNA Extraction Methods for Detection of <i>Leishmania</i>by Polymerase Chain Reaction

Evaluation of DNA Extraction Methods for Detection of <i>Leishmania</i>by Polymerase Chain Reaction
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摘要 There are several methods used to obtain DNA from cells;however, the quantity, integrity, and purity of DNA vary among the methods, which may interfere with the polymerase chain reaction (PCR) results. The objective was to determine the most efficient and cost-effective method that provides the best DNA yield and PCR results. Three methods of DNA isolation were compared: 20% sodium dodecyl sulfate (SDS), guanidine isothiocyanate-phenol-chloroform (GTPC), and DNA extraction using a commercial kit (GE Healthcare GenomicPrep Blood DNA Isolation Kit<sup>TM</sup>). Human peripheral blood samples were inoculated with 10<sup>4</sup> promastigotes of <em>Leishmania infantum</em>. DNA was quantified and PCR was performed with 13A/13B primers. The results showed that a higher DNA yield was obtained using the GTPC technique (214.51 ng/μL), followed by SDS (26.16 ng/μL) and the commercial kit (10.99 ng/μL). We concluded that while all of the techniques were effective for obtaining DNA, the GTPC method provided the best yield and the brightest bands. There are several methods used to obtain DNA from cells;however, the quantity, integrity, and purity of DNA vary among the methods, which may interfere with the polymerase chain reaction (PCR) results. The objective was to determine the most efficient and cost-effective method that provides the best DNA yield and PCR results. Three methods of DNA isolation were compared: 20% sodium dodecyl sulfate (SDS), guanidine isothiocyanate-phenol-chloroform (GTPC), and DNA extraction using a commercial kit (GE Healthcare GenomicPrep Blood DNA Isolation Kit<sup>TM</sup>). Human peripheral blood samples were inoculated with 10<sup>4</sup> promastigotes of <em>Leishmania infantum</em>. DNA was quantified and PCR was performed with 13A/13B primers. The results showed that a higher DNA yield was obtained using the GTPC technique (214.51 ng/μL), followed by SDS (26.16 ng/μL) and the commercial kit (10.99 ng/μL). We concluded that while all of the techniques were effective for obtaining DNA, the GTPC method provided the best yield and the brightest bands.
作者 Letícia Surian Batalini Silvana de Oliveira Castro Carla Geórgia Rodrigues Guimarães Souto Herintha Coeto Neitzke-Abreu Manoel Sebastião da Costa Lima-Junior Letícia Surian Batalini;Silvana de Oliveira Castro;Carla Geórgia Rodrigues Guimarães Souto;Herintha Coeto Neitzke-Abreu;Manoel Sebastião da Costa Lima-Junior(Faculty of Health Sciences, Universidade Federal da Grande Dourados (UFGD), Dourados, Brazil;Postgraduate Program of Health Sciences, Universidade Federal da Grande Dourados (UFGD), Dourados, Brazil;Aggeu Magalh&#227;es Institute, Oswaldo Cruz Fundation (Fiocruz), Recife, Brazil)
出处 《American Journal of Molecular Biology》 2020年第4期265-272,共8页 美国分子生物学期刊(英文)
关键词 <i>Leishmania</i> DNA PURIFICATION PCR DIAGNOSIS <i>Leishmania</i> DNA Purification PCR Diagnosis
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