Comparison of the diagnostic performance of microscopic examination with nested polymerase chain reaction for optimum malaria diagnosis in Upper Myanmar
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 submicr...
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creator | Kang, Jung-Mi Cho, Pyo-Yun Moe, Mya Lee, Jinyoung Jun, Hojong Lee, Hyeong-Woo Ahn, Seong Kyu Kim, Tae Im Pak, Jhang Ho Myint, Moe Kyaw Lin, Khin Kim, Tong-Soo Na, Byoung-Kuk |
description | 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.
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.
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.
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. |
doi_str_mv | 10.1186/s12936-017-1765-4 |
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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.
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.
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.</description><identifier>ISSN: 1475-2875</identifier><identifier>EISSN: 1475-2875</identifier><identifier>DOI: 10.1186/s12936-017-1765-4</identifier><identifier>PMID: 28302168</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Accuracy ; Antigens ; Blood ; Deoxyribonucleic acid ; Diagnosis ; DNA ; Endemic species ; Erythrocytes ; Health care ; Human diseases ; Humans ; Infections ; Malaria ; Malaria, Falciparum - diagnosis ; Malaria, Vivax - diagnosis ; Methods ; Microscopy ; Microscopy - standards ; Myanmar ; Nucleotide sequence ; Parasites ; PCR ; Plasmodium ; Plasmodium falciparum - isolation & purification ; Plasmodium vivax - isolation & purification ; Polymerase chain reaction ; Polymerase Chain Reaction - standards ; Reproducibility of Results ; Species ; Specificity ; Vector-borne diseases</subject><ispartof>Malaria journal, 2017-03, Vol.16 (1), p.119-119, Article 119</ispartof><rights>2017. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-af1780db09032b3814a3ad36958563e93c4f59019db07071908a7f7cc83aa963</citedby><cites>FETCH-LOGICAL-c427t-af1780db09032b3814a3ad36958563e93c4f59019db07071908a7f7cc83aa963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356273/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356273/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28302168$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kang, Jung-Mi</creatorcontrib><creatorcontrib>Cho, Pyo-Yun</creatorcontrib><creatorcontrib>Moe, Mya</creatorcontrib><creatorcontrib>Lee, Jinyoung</creatorcontrib><creatorcontrib>Jun, Hojong</creatorcontrib><creatorcontrib>Lee, Hyeong-Woo</creatorcontrib><creatorcontrib>Ahn, Seong Kyu</creatorcontrib><creatorcontrib>Kim, Tae Im</creatorcontrib><creatorcontrib>Pak, Jhang Ho</creatorcontrib><creatorcontrib>Myint, Moe Kyaw</creatorcontrib><creatorcontrib>Lin, Khin</creatorcontrib><creatorcontrib>Kim, Tong-Soo</creatorcontrib><creatorcontrib>Na, Byoung-Kuk</creatorcontrib><title>Comparison of the diagnostic performance of microscopic examination with nested polymerase chain reaction for optimum malaria diagnosis in Upper Myanmar</title><title>Malaria journal</title><addtitle>Malar J</addtitle><description>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.
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.
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.
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.</description><subject>Accuracy</subject><subject>Antigens</subject><subject>Blood</subject><subject>Deoxyribonucleic acid</subject><subject>Diagnosis</subject><subject>DNA</subject><subject>Endemic species</subject><subject>Erythrocytes</subject><subject>Health care</subject><subject>Human diseases</subject><subject>Humans</subject><subject>Infections</subject><subject>Malaria</subject><subject>Malaria, Falciparum - diagnosis</subject><subject>Malaria, Vivax - diagnosis</subject><subject>Methods</subject><subject>Microscopy</subject><subject>Microscopy - standards</subject><subject>Myanmar</subject><subject>Nucleotide sequence</subject><subject>Parasites</subject><subject>PCR</subject><subject>Plasmodium</subject><subject>Plasmodium falciparum - isolation & purification</subject><subject>Plasmodium vivax - isolation & purification</subject><subject>Polymerase chain reaction</subject><subject>Polymerase Chain Reaction - standards</subject><subject>Reproducibility of Results</subject><subject>Species</subject><subject>Specificity</subject><subject>Vector-borne diseases</subject><issn>1475-2875</issn><issn>1475-2875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdkc1O3TAQhS1UxP8DdFNZ6oZNin8S29lUqq4KrQTqhq6tuY7DNYrt1E7a3jfhcXG4gGhXtjTfnJkzB6H3lHyiVImLTFnLRUWorKgUTVXvoSNay6ZiSjbv3vwP0XHO96SASrIDdMgUJ4wKdYQeVtGPkFyOAcceTxuLOwd3IebJGTza1MfkIRi7VL0zKWYTx1Kyf8G7AJMrjX_ctMHB5sl2eIzD1tsE2WKzARdwsmCeqKKE4zg5P3vsYShD4WWWy7iQP8cyD99sIXhIp2i_hyHbs-f3BN1efr1dfauuf1x9X325rkzN5FRBXzyRbk1awtmaK1oDh46LtlGN4Lblpu6bltC2IJJI2hIFspfGKA7QCn6CPu9kx3ntbWdsmBIMekyu7LDVEZz-txLcRt_F37rhjWCSF4HzZ4EUf83lBtq7bOwwQLBxzpoqqRRjlNYF_fgfeh_nFIo7zXitmOBSsULRHbXcOifbvy5DiV5i17vYdUlTL7HrRfnDWxevHS8580cJDKxh</recordid><startdate>20170316</startdate><enddate>20170316</enddate><creator>Kang, Jung-Mi</creator><creator>Cho, Pyo-Yun</creator><creator>Moe, Mya</creator><creator>Lee, Jinyoung</creator><creator>Jun, Hojong</creator><creator>Lee, Hyeong-Woo</creator><creator>Ahn, Seong Kyu</creator><creator>Kim, Tae Im</creator><creator>Pak, Jhang Ho</creator><creator>Myint, Moe Kyaw</creator><creator>Lin, Khin</creator><creator>Kim, Tong-Soo</creator><creator>Na, Byoung-Kuk</creator><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7SS</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>K9.</scope><scope>L.G</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170316</creationdate><title>Comparison of the diagnostic performance of microscopic examination with nested polymerase chain reaction for optimum malaria diagnosis in Upper Myanmar</title><author>Kang, Jung-Mi ; Cho, Pyo-Yun ; Moe, Mya ; Lee, Jinyoung ; Jun, Hojong ; Lee, Hyeong-Woo ; Ahn, Seong Kyu ; Kim, Tae Im ; Pak, Jhang Ho ; Myint, Moe Kyaw ; Lin, Khin ; Kim, Tong-Soo ; Na, Byoung-Kuk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-af1780db09032b3814a3ad36958563e93c4f59019db07071908a7f7cc83aa963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Accuracy</topic><topic>Antigens</topic><topic>Blood</topic><topic>Deoxyribonucleic acid</topic><topic>Diagnosis</topic><topic>DNA</topic><topic>Endemic species</topic><topic>Erythrocytes</topic><topic>Health care</topic><topic>Human diseases</topic><topic>Humans</topic><topic>Infections</topic><topic>Malaria</topic><topic>Malaria, Falciparum - diagnosis</topic><topic>Malaria, Vivax - diagnosis</topic><topic>Methods</topic><topic>Microscopy</topic><topic>Microscopy - standards</topic><topic>Myanmar</topic><topic>Nucleotide sequence</topic><topic>Parasites</topic><topic>PCR</topic><topic>Plasmodium</topic><topic>Plasmodium falciparum - isolation & purification</topic><topic>Plasmodium vivax - isolation & purification</topic><topic>Polymerase chain reaction</topic><topic>Polymerase Chain Reaction - standards</topic><topic>Reproducibility of Results</topic><topic>Species</topic><topic>Specificity</topic><topic>Vector-borne diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kang, Jung-Mi</creatorcontrib><creatorcontrib>Cho, Pyo-Yun</creatorcontrib><creatorcontrib>Moe, Mya</creatorcontrib><creatorcontrib>Lee, Jinyoung</creatorcontrib><creatorcontrib>Jun, Hojong</creatorcontrib><creatorcontrib>Lee, Hyeong-Woo</creatorcontrib><creatorcontrib>Ahn, Seong Kyu</creatorcontrib><creatorcontrib>Kim, Tae Im</creatorcontrib><creatorcontrib>Pak, Jhang Ho</creatorcontrib><creatorcontrib>Myint, Moe Kyaw</creatorcontrib><creatorcontrib>Lin, Khin</creatorcontrib><creatorcontrib>Kim, Tong-Soo</creatorcontrib><creatorcontrib>Na, Byoung-Kuk</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Malaria journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kang, Jung-Mi</au><au>Cho, Pyo-Yun</au><au>Moe, Mya</au><au>Lee, Jinyoung</au><au>Jun, Hojong</au><au>Lee, Hyeong-Woo</au><au>Ahn, Seong Kyu</au><au>Kim, Tae Im</au><au>Pak, Jhang Ho</au><au>Myint, Moe Kyaw</au><au>Lin, Khin</au><au>Kim, Tong-Soo</au><au>Na, Byoung-Kuk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of the diagnostic performance of microscopic examination with nested polymerase chain reaction for optimum malaria diagnosis in Upper Myanmar</atitle><jtitle>Malaria journal</jtitle><addtitle>Malar J</addtitle><date>2017-03-16</date><risdate>2017</risdate><volume>16</volume><issue>1</issue><spage>119</spage><epage>119</epage><pages>119-119</pages><artnum>119</artnum><issn>1475-2875</issn><eissn>1475-2875</eissn><abstract>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.
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.
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.
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.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>28302168</pmid><doi>10.1186/s12936-017-1765-4</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Accuracy Antigens Blood Deoxyribonucleic acid Diagnosis DNA Endemic species Erythrocytes Health care Human diseases Humans Infections Malaria Malaria, Falciparum - diagnosis Malaria, Vivax - diagnosis Methods Microscopy Microscopy - standards Myanmar Nucleotide sequence Parasites PCR Plasmodium Plasmodium falciparum - isolation & purification Plasmodium vivax - isolation & purification Polymerase chain reaction Polymerase Chain Reaction - standards Reproducibility of Results Species Specificity Vector-borne diseases |
title | Comparison of the diagnostic performance of microscopic examination with nested polymerase chain reaction for optimum malaria diagnosis in Upper Myanmar |
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