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      Comparison of the diagnostic performance of microscopic examination with nested polymerase chain reaction for optimum malaria diagnosis in Upper Myanmar

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          Abstract

          Background

          Accurate diagnosis of Plasmodium infection is crucial for prompt malaria treatment and surveillance. Microscopic examination has been widely applied as the gold standard for malaria diagnosis in most part of malaria endemic areas, but its diagnostic value has been questioned, particularly in submicroscopic malaria. In this study, the diagnostic performance of microscopic examination and nested polymerase chain reaction (PCR) was evaluated to establish optimal malaria diagnosis method in Myanmar.

          Methods

          A total of 1125 blood samples collected from residents in the villages and towns located in Naung Cho, Pyin Oo Lwin, Tha Beik Kyin townships and Mandalay of Upper Myanmar were screened by microscopic examination and species-specific nested PCR method.

          Results

          Among the 1125 blood samples, 261 samples were confirmed to be infected with malaria by microscopic examination. Evaluation of the 1125 samples by species-specific nested PCR analysis revealed that the agreement between microscopic examination and nested PCR was 87.3% (261/299). Nested PCR successfully detected 38 Plasmodium falciparum or Plasmodium vivax infections, which were missed in microscopic examination. Microscopic examinations also either misdiagnosed the infected Plasmodium species, or did not detect mixed infections with different Plasmodium species in 31 cases.

          Conclusions

          The nested PCR method is more reliable than conventional microscopic examination for the diagnosis of malaria infections, and this is particularly true in cases of mixed infections and submicroscopic infections. Given the observed higher sensitivity and specificity of nested PCR, the molecular method holds enormous promise in malaria diagnosis and species differentiation, and can be applied as an effective monitoring tool for malaria surveillance, control and elimination in Myanmar.

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          Most cited references51

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          A review of malaria diagnostic tools: microscopy and rapid diagnostic test (RDT).

          The absolute necessity for rational therapy in the face of rampant drug resistance places increasing importance on the accuracy of malaria diagnosis. Giemsa microscopy and rapid diagnostic tests (RDTs) represent the two diagnostics most likely to have the largest impact on malaria control today. These two methods, each with characteristic strengths and limitations, together represent the best hope for accurate diagnosis as a key component of successful malaria control. This review addresses the quality issues with current malaria diagnostics and presents data from recent rapid diagnostic test trials. Reduction of malaria morbidity and drug resistance intensity plus the associated economic loss of these two factors require urgent scaling up of the quality of parasite-based diagnostic methods. An investment in anti-malarial drug development or malaria vaccine development should be accompanied by a parallel commitment to improve diagnostic tools and their availability to people living in malarious areas.
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            Development of a real-time PCR assay for detection of Plasmodium falciparum, Plasmodium vivax, and Plasmodium ovale for routine clinical diagnosis.

            A TaqMan-based real-time PCR qualitative assay for the detection of three species of malaria parasites-Plasmodium falciparum, P. ovale, and P. vivax-was devised and evaluated using 122 whole-blood samples from patients who had traveled to areas where malaria is endemic and who presented with malaria-like symptoms and fever. The assay was compared to conventional microscopy and to an established nested-PCR assay. The specificity of the new assay was confirmed by sequencing the PCR products from all the positive samples and by the lack of cross-reactivity with Toxoplasma gondii and Leishmania infantum DNA. Real-time PCR assay showed a detection limit (analytical sensitivity) of 0.7, 4, and 1.5 parasites/ micro l for P. falciparum, P. vivax, and P. ovale, respectively. Real-time PCR, like nested PCR, brought to light errors in the species identification by microscopic examination and revealed the presence of mixed infections (P. falciparum plus P. ovale). Real-time PCR can yield results within 2 h, does not require post-PCR processing, reduces sample handling, and minimizes the risks of contamination. The assay can therefore be easily implemented in routine diagnostic malaria tests. Future studies are warranted to investigate the clinical value of this technique.
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              • Abstract: not found
              • Article: not found

              Nested PCR analysis of Plasmodium parasites.

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                Author and article information

                Contributors
                gjm9951001@hanmail.net
                chopy74@hanmail.net
                myamoee.dmr@gmail.com
                jylee5492@gmail.com
                hojongi2@inha.ac.kr
                rainlee67@naver.com
                asksay@daum.net
                taeim1018@gmail.com
                jhpak@amc.seoul.kr
                dr.myintmoekyaw@gmail.com
                dr.khinlin.dir@gmail.com
                tongsookim@inha.ac.kr
                bkna@gnu.ac.kr
                Journal
                Malar J
                Malar. J
                Malaria Journal
                BioMed Central (London )
                1475-2875
                16 March 2017
                16 March 2017
                2017
                : 16
                : 119
                Affiliations
                [1 ]ISNI 0000 0001 0661 1492, GRID grid.256681.e, Department of Parasitology and Tropical Medicine, and Institute of Health Sciences, , Gyeongsang National University School of Medicine, ; Jinju, 52727 Republic of Korea
                [2 ]ISNI 0000 0001 0661 1492, GRID grid.256681.e, BK21Plus Team for Anti-Aging Biotechnology and Industry, Department of Convergence Medical Science, , Gyeongsang National University, ; Jinju, 52727 Republic of Korea
                [3 ]ISNI 0000 0001 2364 8385, GRID grid.202119.9, Department of Tropical Medicine and Inha Research Institute for Medical Sciences, , Inha University School of Medicine, ; Incheon, 22212 Republic of Korea
                [4 ]Department of Medical Research Pyin Oo Lwin Branch, Pyin Oo Lwin, Myanmar
                [5 ]ISNI 0000 0001 0842 2126, GRID grid.413967.e, Department of Convergence Medicine, , University of Ulsan College of Medicine and Asan Institute for Life Sciences, Asan Medical Center, ; Seoul, 05505 Republic of Korea
                Article
                1765
                10.1186/s12936-017-1765-4
                5356273
                28302168
                1688e60a-b2e1-4c03-835a-c914eba155bf
                © The Author(s) 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 1 December 2016
                : 28 February 2017
                Funding
                Funded by: NRF-2015K1A3A9A01034893
                Award ID: NRF-2015K1A3A9A01034893
                Award Recipient :
                Funded by: NRF-2015R1A2A2A01004310
                Award ID: NRF-2015R1A2A2A01004310
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2017

                Infectious disease & Microbiology
                malaria,microscopic examination,species-specific nested pcr,diagnosis,myanmar

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