Use of a semi-nested PCR diagnosis test to evaluate antifolate resistance of Plasmodium falciparum isolates
The antifols, inhibitors of the dihydrofolate reductase (DHFR), such as pyrimethamine and proguanil, have been used against Plasmodium falciparum in the areas where chloroquine resistance is widespread. This use has selected resistant strains in Southeast Asia and South America. The resistance is co...
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Veröffentlicht in: | Molecular and cellular probes 1995-12, Vol.9 (6), p.391-397 |
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creator | Eldin de Pecoulas, P Abdallah, B Dje, M K Basco, L K le Bras, J Mazabraud, A |
description | The antifols, inhibitors of the dihydrofolate reductase (DHFR), such as pyrimethamine and proguanil, have been used against Plasmodium falciparum in the areas where chloroquine resistance is widespread. This use has selected resistant strains in Southeast Asia and South America. The resistance is correlated with point mutations in precise positions of the DHFR gene. A reliable semi-nested PCR diagnosis test was established and used to determine the genotypic features of 29 isolates of P. falciparum originating from Africa. The results obtained by the PCR technique were compared with those of the in vitro drug sensitivity test. Some isolates were found to be polyclonal. Among the mutations tested, only mutations on codon 108 which generate an asparagine induce a decrease in sensitivity to pyrimethamine and cycloguanil, whereas mutation on codon 59 strengthens resistance to both antifols. No mutation on codon 16 or codon 164 was found. |
doi_str_mv | 10.1006/mcpr.1995.0061 |
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This use has selected resistant strains in Southeast Asia and South America. The resistance is correlated with point mutations in precise positions of the DHFR gene. A reliable semi-nested PCR diagnosis test was established and used to determine the genotypic features of 29 isolates of P. falciparum originating from Africa. The results obtained by the PCR technique were compared with those of the in vitro drug sensitivity test. Some isolates were found to be polyclonal. Among the mutations tested, only mutations on codon 108 which generate an asparagine induce a decrease in sensitivity to pyrimethamine and cycloguanil, whereas mutation on codon 59 strengthens resistance to both antifols. No mutation on codon 16 or codon 164 was found.</description><identifier>ISSN: 0890-8508</identifier><identifier>DOI: 10.1006/mcpr.1995.0061</identifier><identifier>PMID: 8808309</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; Antimalarials - pharmacology ; Base Sequence ; Codon - genetics ; DNA Mutational Analysis ; DNA, Protozoan - genetics ; Drug Resistance - genetics ; Folic Acid Antagonists - pharmacology ; Molecular Sequence Data ; Plasmodium falciparum - drug effects ; Plasmodium falciparum - enzymology ; Plasmodium falciparum - genetics ; Point Mutation ; Polymerase Chain Reaction - methods ; Proguanil - pharmacology ; Protozoan Proteins - antagonists & inhibitors ; Protozoan Proteins - genetics ; Pyrimethamine - pharmacology ; Sensitivity and Specificity ; Tetrahydrofolate Dehydrogenase - genetics</subject><ispartof>Molecular and cellular probes, 1995-12, Vol.9 (6), p.391-397</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8808309$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eldin de Pecoulas, P</creatorcontrib><creatorcontrib>Abdallah, B</creatorcontrib><creatorcontrib>Dje, M K</creatorcontrib><creatorcontrib>Basco, L K</creatorcontrib><creatorcontrib>le Bras, J</creatorcontrib><creatorcontrib>Mazabraud, A</creatorcontrib><title>Use of a semi-nested PCR diagnosis test to evaluate antifolate resistance of Plasmodium falciparum isolates</title><title>Molecular and cellular probes</title><addtitle>Mol Cell Probes</addtitle><description>The antifols, inhibitors of the dihydrofolate reductase (DHFR), such as pyrimethamine and proguanil, have been used against Plasmodium falciparum in the areas where chloroquine resistance is widespread. This use has selected resistant strains in Southeast Asia and South America. The resistance is correlated with point mutations in precise positions of the DHFR gene. A reliable semi-nested PCR diagnosis test was established and used to determine the genotypic features of 29 isolates of P. falciparum originating from Africa. The results obtained by the PCR technique were compared with those of the in vitro drug sensitivity test. Some isolates were found to be polyclonal. Among the mutations tested, only mutations on codon 108 which generate an asparagine induce a decrease in sensitivity to pyrimethamine and cycloguanil, whereas mutation on codon 59 strengthens resistance to both antifols. No mutation on codon 16 or codon 164 was found.</description><subject>Animals</subject><subject>Antimalarials - pharmacology</subject><subject>Base Sequence</subject><subject>Codon - genetics</subject><subject>DNA Mutational Analysis</subject><subject>DNA, Protozoan - genetics</subject><subject>Drug Resistance - genetics</subject><subject>Folic Acid Antagonists - pharmacology</subject><subject>Molecular Sequence Data</subject><subject>Plasmodium falciparum - drug effects</subject><subject>Plasmodium falciparum - enzymology</subject><subject>Plasmodium falciparum - genetics</subject><subject>Point Mutation</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Proguanil - pharmacology</subject><subject>Protozoan Proteins - antagonists & inhibitors</subject><subject>Protozoan Proteins - genetics</subject><subject>Pyrimethamine - pharmacology</subject><subject>Sensitivity and Specificity</subject><subject>Tetrahydrofolate Dehydrogenase - genetics</subject><issn>0890-8508</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotkDFPwzAQhT2ASimsbEie2FKcOHHtEVVQkCpRITpHF_uMDHESYgeJf49bqhvu3tOnp7sj5CZny5wxce_1MC5zpaplUvkZmTOpWCYrJi_IZQifjDFVMjkjMymZ5EzNydc-IO0tBRrQu6zDENHQ3fqNGgcfXR9coDGZNPYUf6CdICKFLjrbt4dxxERE6PQxZddC8L1xk6cWWu0GGNPowpENV-Q8uQGvT31B9k-P7-vnbPu6eVk_bLOhYCJmshQojGRCgwAteGGLdEeJulGcc8OFsWhL0MibqoQmiUbbPC_QHgoMX5C7_9xh7L-ntHztXdDYttBhP4V6tVKFqJRI4O0JnBqPph5G52H8rU_f4X8XV2iq</recordid><startdate>19951201</startdate><enddate>19951201</enddate><creator>Eldin de Pecoulas, P</creator><creator>Abdallah, B</creator><creator>Dje, M K</creator><creator>Basco, L K</creator><creator>le Bras, J</creator><creator>Mazabraud, A</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19951201</creationdate><title>Use of a semi-nested PCR diagnosis test to evaluate antifolate resistance of Plasmodium falciparum isolates</title><author>Eldin de Pecoulas, P ; Abdallah, B ; Dje, M K ; Basco, L K ; le Bras, J ; Mazabraud, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p206t-846e6d806ca6ac632f20894ecb9333d36dfef4ace3b54abfefbcf112efefefad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Antimalarials - pharmacology</topic><topic>Base Sequence</topic><topic>Codon - genetics</topic><topic>DNA Mutational Analysis</topic><topic>DNA, Protozoan - genetics</topic><topic>Drug Resistance - genetics</topic><topic>Folic Acid Antagonists - pharmacology</topic><topic>Molecular Sequence Data</topic><topic>Plasmodium falciparum - drug effects</topic><topic>Plasmodium falciparum - enzymology</topic><topic>Plasmodium falciparum - genetics</topic><topic>Point Mutation</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Proguanil - pharmacology</topic><topic>Protozoan Proteins - antagonists & inhibitors</topic><topic>Protozoan Proteins - genetics</topic><topic>Pyrimethamine - pharmacology</topic><topic>Sensitivity and Specificity</topic><topic>Tetrahydrofolate Dehydrogenase - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eldin de Pecoulas, P</creatorcontrib><creatorcontrib>Abdallah, B</creatorcontrib><creatorcontrib>Dje, M K</creatorcontrib><creatorcontrib>Basco, L K</creatorcontrib><creatorcontrib>le Bras, J</creatorcontrib><creatorcontrib>Mazabraud, A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular and cellular probes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eldin de Pecoulas, P</au><au>Abdallah, B</au><au>Dje, M K</au><au>Basco, L K</au><au>le Bras, J</au><au>Mazabraud, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Use of a semi-nested PCR diagnosis test to evaluate antifolate resistance of Plasmodium falciparum isolates</atitle><jtitle>Molecular and cellular probes</jtitle><addtitle>Mol Cell Probes</addtitle><date>1995-12-01</date><risdate>1995</risdate><volume>9</volume><issue>6</issue><spage>391</spage><epage>397</epage><pages>391-397</pages><issn>0890-8508</issn><abstract>The antifols, inhibitors of the dihydrofolate reductase (DHFR), such as pyrimethamine and proguanil, have been used against Plasmodium falciparum in the areas where chloroquine resistance is widespread. This use has selected resistant strains in Southeast Asia and South America. The resistance is correlated with point mutations in precise positions of the DHFR gene. A reliable semi-nested PCR diagnosis test was established and used to determine the genotypic features of 29 isolates of P. falciparum originating from Africa. The results obtained by the PCR technique were compared with those of the in vitro drug sensitivity test. Some isolates were found to be polyclonal. Among the mutations tested, only mutations on codon 108 which generate an asparagine induce a decrease in sensitivity to pyrimethamine and cycloguanil, whereas mutation on codon 59 strengthens resistance to both antifols. No mutation on codon 16 or codon 164 was found.</abstract><cop>England</cop><pmid>8808309</pmid><doi>10.1006/mcpr.1995.0061</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Antimalarials - pharmacology Base Sequence Codon - genetics DNA Mutational Analysis DNA, Protozoan - genetics Drug Resistance - genetics Folic Acid Antagonists - pharmacology Molecular Sequence Data Plasmodium falciparum - drug effects Plasmodium falciparum - enzymology Plasmodium falciparum - genetics Point Mutation Polymerase Chain Reaction - methods Proguanil - pharmacology Protozoan Proteins - antagonists & inhibitors Protozoan Proteins - genetics Pyrimethamine - pharmacology Sensitivity and Specificity Tetrahydrofolate Dehydrogenase - genetics |
title | Use of a semi-nested PCR diagnosis test to evaluate antifolate resistance of Plasmodium falciparum isolates |
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