Discrimination of all Members of the Anopheles punctulatus Complex by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism Analysis
A method has been developed to identify the members of the Anopheles punctulatus complex using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Members of the An. punctulatus complex are the most important vectors of malaria in the southwest Pacific and consist of 10 cr...
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Veröffentlicht in: | The American journal of tropical medicine and hygiene 1995-11, Vol.53 (5), p.478-481 |
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description | A method has been developed to identify the members of the Anopheles punctulatus complex using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Members of the An. punctulatus complex are the most important vectors of malaria in the southwest Pacific and consist of 10 cryptic species, An. farauti no. 1-7, An. punctulatus, An. sp. near punctulatus, and An. koliensis. For each species, PCR amplification of the ribosomal DNA internal transcribed spacer produced a 750-basepair product. Digestion with Msp I and electrophoresis on a 3.0% agarose gel results in banding patterns unique to each species. Isolates of the same species from different locations gave an identical pattern. The technique is sensitive enough so that a PCR-RFLP can be generated from as little as a single mosquito leg, allowing the rest of the mosquito to be used for other important epidemiologic analyses such as determining host feeding source, and for parasite detection. |
doi_str_mv | 10.4269/ajtmh.1995.53.478 |
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Members of the An. punctulatus complex are the most important vectors of malaria in the southwest Pacific and consist of 10 cryptic species, An. farauti no. 1-7, An. punctulatus, An. sp. near punctulatus, and An. koliensis. For each species, PCR amplification of the ribosomal DNA internal transcribed spacer produced a 750-basepair product. Digestion with Msp I and electrophoresis on a 3.0% agarose gel results in banding patterns unique to each species. Isolates of the same species from different locations gave an identical pattern. 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Members of the An. punctulatus complex are the most important vectors of malaria in the southwest Pacific and consist of 10 cryptic species, An. farauti no. 1-7, An. punctulatus, An. sp. near punctulatus, and An. koliensis. For each species, PCR amplification of the ribosomal DNA internal transcribed spacer produced a 750-basepair product. Digestion with Msp I and electrophoresis on a 3.0% agarose gel results in banding patterns unique to each species. Isolates of the same species from different locations gave an identical pattern. The technique is sensitive enough so that a PCR-RFLP can be generated from as little as a single mosquito leg, allowing the rest of the mosquito to be used for other important epidemiologic analyses such as determining host feeding source, and for parasite detection.</description><subject>Animals</subject><subject>Anopheles - classification</subject><subject>Anopheles - genetics</subject><subject>Anopheles punctulatus</subject><subject>Australia</subject><subject>Biological and medical sciences</subject><subject>Culicidae</subject><subject>Diptera</subject><subject>DNA Primers - chemistry</subject><subject>DNA, Ribosomal - analysis</subject><subject>DNA, Ribosomal - chemistry</subject><subject>Human protozoal diseases</subject><subject>Infectious diseases</subject><subject>Insect Vectors - classification</subject><subject>Insect Vectors - genetics</subject><subject>Malaria</subject><subject>Medical sciences</subject><subject>Melanesia</subject><subject>Papua New Guinea</subject><subject>Parasitic diseases</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Protozoal diseases</subject><subject>Species Specificity</subject><subject>Tropical medicine</subject><subject>Vanuatu</subject><issn>0002-9637</issn><issn>1476-1645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcuO1DAQRS0EGpqBD2CB5AWwS2M7fsTLUcMAUiPQCNaW46l0PLKTYCdq-jP4Y9wPzZaNX3XuLasuQq8pWXMm9Qf7MMd-TbUWa1GvuWqeoBXlSlZUcvEUrQghrNKyVs_Ri5wfCKENo_QKXSneCEXECv396LNLPvrBzn4c8NhhGwL-BrGFlI_XuQd8M4xTDwEynpbBzUuw85LxZoxTgD-4PeAfYzhESDYD3vTWD_gOrDsaVneQ5-RPZ3yb7C7CMOMtDLu5P6vGNPU-x9LDhkP2-SV61tmQ4dVlv0a_bj_93Hyptt8_f93cbCtXSzVXom20k1YRybjWZQQda8sbo6pzpKlrwZtO6I4rKIskjnCm2ntFOt20VDSsvkbvz75TGn8v5ZcmllFACHaAcclGKcVqSul_QaoIZZzVBaRn0KUx5wSdmcpkbToYSswxL3PKyxzzMqI2Ja-ieXMxX9oI94-KS0Cl_vZSt9nZ0CU7OJ8fMaapLFTB3p2x3u_6vU9gciw5FlNq9vt9aSZO7f4BEiCt4w</recordid><startdate>199511</startdate><enddate>199511</enddate><creator>Beebe, Nigel W</creator><creator>Saul, Allan</creator><general>ASTMH</general><general>Allen Press</general><scope>IQODW</scope><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>7SS</scope><scope>7X8</scope></search><sort><creationdate>199511</creationdate><title>Discrimination of all Members of the Anopheles punctulatus Complex by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism Analysis</title><author>Beebe, Nigel W ; Saul, Allan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c367t-5b89c6a7062499199f2b5b8217fc0833548f59f47e9f460c0427bd70f98b15823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Anopheles - classification</topic><topic>Anopheles - genetics</topic><topic>Anopheles punctulatus</topic><topic>Australia</topic><topic>Biological and medical sciences</topic><topic>Culicidae</topic><topic>Diptera</topic><topic>DNA Primers - chemistry</topic><topic>DNA, Ribosomal - analysis</topic><topic>DNA, Ribosomal - chemistry</topic><topic>Human protozoal diseases</topic><topic>Infectious diseases</topic><topic>Insect Vectors - classification</topic><topic>Insect Vectors - genetics</topic><topic>Malaria</topic><topic>Medical sciences</topic><topic>Melanesia</topic><topic>Papua New Guinea</topic><topic>Parasitic diseases</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Protozoal diseases</topic><topic>Species Specificity</topic><topic>Tropical medicine</topic><topic>Vanuatu</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beebe, Nigel W</creatorcontrib><creatorcontrib>Saul, Allan</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of tropical medicine and hygiene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beebe, Nigel W</au><au>Saul, Allan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Discrimination of all Members of the Anopheles punctulatus Complex by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism Analysis</atitle><jtitle>The American journal of tropical medicine and hygiene</jtitle><addtitle>Am J Trop Med Hyg</addtitle><date>1995-11</date><risdate>1995</risdate><volume>53</volume><issue>5</issue><spage>478</spage><epage>481</epage><pages>478-481</pages><issn>0002-9637</issn><eissn>1476-1645</eissn><coden>AJTHAB</coden><abstract>A method has been developed to identify the members of the Anopheles punctulatus complex using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Members of the An. punctulatus complex are the most important vectors of malaria in the southwest Pacific and consist of 10 cryptic species, An. farauti no. 1-7, An. punctulatus, An. sp. near punctulatus, and An. koliensis. For each species, PCR amplification of the ribosomal DNA internal transcribed spacer produced a 750-basepair product. Digestion with Msp I and electrophoresis on a 3.0% agarose gel results in banding patterns unique to each species. Isolates of the same species from different locations gave an identical pattern. The technique is sensitive enough so that a PCR-RFLP can be generated from as little as a single mosquito leg, allowing the rest of the mosquito to be used for other important epidemiologic analyses such as determining host feeding source, and for parasite detection.</abstract><cop>Lawrence, KS</cop><pub>ASTMH</pub><pmid>7485705</pmid><doi>10.4269/ajtmh.1995.53.478</doi><tpages>4</tpages></addata></record> |
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subjects | Animals Anopheles - classification Anopheles - genetics Anopheles punctulatus Australia Biological and medical sciences Culicidae Diptera DNA Primers - chemistry DNA, Ribosomal - analysis DNA, Ribosomal - chemistry Human protozoal diseases Infectious diseases Insect Vectors - classification Insect Vectors - genetics Malaria Medical sciences Melanesia Papua New Guinea Parasitic diseases Polymerase Chain Reaction Polymorphism, Restriction Fragment Length Protozoal diseases Species Specificity Tropical medicine Vanuatu |
title | Discrimination of all Members of the Anopheles punctulatus Complex by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism Analysis |
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