Lima-Junior, M.S.C., Zorzenon, D.C.R., Dorval, M.E.C., Pontes, E.R.J.C., Oshiro, E.T., Cunha, R., Andreotti, R. and Matos, M.F.C. (2013) Sensitivity of PCR and Real-Time PCR for the Diagnosis of Human Visceral Leishmaniasis Using Peripheral Blood. Asian Pacific Journal of Tropical Disease, 3, 10-15.
https://doi.org/10.1016/S2222-1808(13)60003-1

has been cited by the following article:

• TITLE: Evaluation of DNA Extraction Methods for Detection of Leishmania by Polymerase Chain Reaction

  AUTHORS: Letícia Surian Batalini, Silvana de Oliveira Castro, Carla Geórgia Rodrigues Guimarães Souto, Herintha Coeto Neitzke-Abreu, Manoel Sebastião da Costa Lima-Junior

  KEYWORDS: Leishmania, DNA, Purification, PCR, Diagnosis

  JOURNAL NAME: American Journal of Molecular Biology, Vol.10 No.4, September 15, 2020

  ABSTRACT: 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 KitTM). Human peripheral blood samples were inoculated with 104 promastigotes of Leishmania infantum. 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.