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      Development of loop-mediated isothermal amplification method for detecting Wuchereria bancrofti DNA in human blood and vector mosquitoes.

      Parasitology International
      Animals, Base Sequence, Brugia, genetics, Culex, DNA, Helminth, analysis, Dirofilaria, Filariasis, blood, diagnosis, parasitology, Humans, Molecular Sequence Data, Nucleic Acid Amplification Techniques, Repetitive Sequences, Nucleic Acid, Sensitivity and Specificity, Wuchereria bancrofti, isolation & purification

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          Abstract

          We have developed loop-mediated isothermal amplification (LAMP) method to detect Wuchereria bancrofti DNA. The sensitivity and specificity of LAMP method were equivalent to those of PCR method which detects SspI repeat sequence in W. bancrofti genomic DNA: both methods detected one thousandth of W. bancrofti DNA from one microfilaria (Mf), and did not cross-react with DNAs of Brugia malayi, B. pahangi, Dirofilaria immitis, human and Culex quinquefasciatus. We also examined the sensitivity of LAMP using the mimic samples of patient's blood or blood-fed mosquitoes containing one W. bancrofti Mf per sample. The LAMP method was able to detect W. bancrofti DNA in 1000 μl of blood or in a pool of 60 mosquitoes, indicating its usefulness in detecting/monitoring W. bancrofti infection in humans and vector mosquitoes in endemic areas. Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

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