Literature DB >> 9467744

Increased sensitivity of malaria detection by nested polymerase chain reaction using simple sampling and DNA extraction.

J Cox-Singh1, S Mahayet, M S Abdullah, B Singh.   

Abstract

Malaria remains a disease of underdeveloped and remote regions of the world. The application of polymerase chain reaction (PCR) technology to malaria epidemiology has the potential for increasing our knowledge and understanding of this disease. In order to study malaria in all geographical locations it is important that specimen collection and DNA extraction for PCR be kept simple. Here we report a method for extracting DNA from dried blood spots on filter paper which is capable of detecting one Plasmodium falciparum and two Plasmodium vivax parasites/microliter of whole blood by nested PCR without compromising the simplicity of specimen collection or DNA extraction.

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Year:  1997        PMID： 9467744     DOI： 10.1016/s0020-7519(97)00147-1

Source DB:  PubMed          Journal:  Int J Parasitol        ISSN： 0020-7519            Impact factor:   3.981


  27 in total

Review 1.  Microfluidic approaches to malaria detection.

Authors:  Peter Gascoyne; Jutamaad Satayavivad; Mathuros Ruchirawat
Journal:  Acta Trop       Date:  2004-02       Impact factor: 3.112

2.  Plasmodium knowlesi malaria in humans is widely distributed and potentially life threatening.

Authors:  Janet Cox-Singh; Timothy M E Davis; Kim-Sung Lee; Sunita S G Shamsul; Asmad Matusop; Shanmuga Ratnam; Hasan A Rahman; David J Conway; Balbir Singh
Journal:  Clin Infect Dis       Date:  2008-01-15       Impact factor: 9.079

3.  High specificity of semi-nested multiplex PCR using dried blood spots on DNA Banking Card in comparison with frozen liquid blood for detection of Plasmodium falciparum and Plasmodium vivax.

Authors:  S Ataei; M Nateghpour; H Hajjaran; G H Edrissian; A Rahimi Foroushani
Journal:  J Clin Lab Anal       Date:  2011       Impact factor: 2.352

4.  Comparative analysis of three methods from dried blood spots for expeditious DNA extraction from mosquitoes; suitable for PCR based techniques.

Authors:  Barsa Baisalini Panda; Nitika Pradhan; Rupenangshu K Hazra
Journal:  Mol Biol Rep       Date:  2018-11-16       Impact factor: 2.316

5.  Reverse Transcription-Polymerase Chain Reaction Testing on Filter Paper-Dried Serum for Laboratory-Based Dengue Surveillance-American Samoa, 2018.

Authors:  Emily J Curren; Aifili John Tufa; William Thane Hancock; Brad J Biggerstaff; June S Vaifanua-Leo; Catherine A Montalbo; Tyler M Sharp; Marc Fischer; Susan L Hills; Carolyn V Gould
Journal:  Am J Trop Med Hyg       Date:  2020-03       Impact factor: 2.345

Review 6.  Application of nucleic acid amplification in clinical microbiology.

Authors:  G Lisby
Journal:  Mol Biotechnol       Date:  1999-08       Impact factor: 2.695

7.  Two techniques for simultaneous identification of Plasmodium ovale curtisi and Plasmodium ovale wallikeri by use of the small-subunit rRNA gene.

Authors:  Hans-Peter Fuehrer; Marie-Therese Stadler; Katharina Buczolich; Ingrid Bloeschl; Harald Noedl
Journal:  J Clin Microbiol       Date:  2012-09-26       Impact factor: 5.948

8.  Clinical and laboratory features of human Plasmodium knowlesi infection.

Authors:  Cyrus Daneshvar; Timothy M E Davis; Janet Cox-Singh; Mohammad Zakri Rafa'ee; Siti Khatijah Zakaria; Paul C S Divis; Balbir Singh
Journal:  Clin Infect Dis       Date:  2009-09-15       Impact factor: 9.079

Review 9.  Human infections and detection of Plasmodium knowlesi.

Authors:  Balbir Singh; Cyrus Daneshvar
Journal:  Clin Microbiol Rev       Date:  2013-04       Impact factor: 26.132

10.  Clinical and parasitological response to oral chloroquine and primaquine in uncomplicated human Plasmodium knowlesi infections.

Authors:  Cyrus Daneshvar; Timothy M E Davis; Janet Cox-Singh; Mohammad Z Rafa'ee; Siti K Zakaria; Paul C S Divis; Balbir Singh
Journal:  Malar J       Date:  2010-08-19       Impact factor: 2.979
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