THE ANOPHELES-PUNCTULATUS COMPLEX - DNA PROBES FOR IDENTIFYING THE AUSTRALIAN SPECIES USING ISOTOPIC, CHROMOGENIC, AND CHEMILUMINESCENCE DETECTION SYSTEMS

被引:51
作者
COOPER, L
COOPER, RD
BURKOT, TR
机构
[1] QUEENSLAND INST MED RES,TROP HLTH PROGRAM,BRAMSTON TERRACE,HERSTON,QLD 4006,AUSTRALIA
[2] ARMY MALARIA RES UNIT,INGELBURN,NSW 2174,AUSTRALIA
关键词
ANOPHELES-PUNCTULATUS COMPLEX; ANOPHELES-FARAUTI; MOSQUITOS; DNA PROBES; CHEMILUMINESCENCE; DEOXYRIBONUCLEIC ACID (DNA); SODIUM DODECYL SULFATE (SDS); SODIUM CHLORIDE TRISODIUM CITRATE BUFFER (SSC); DEOXYCYTIDINE TRIPHOSPHATE (DCTP); HYDROCHLORIC ACID (HCL); SODIUM CHLORIDE (NACL); ENHANCED CHEMILUMINESCENCE (ECL); ETHYLENEDIAMINETETRAACETIC ACID (EDTA); CESIUM CHLORIDE (CSCL); TRIS [HYDROXYMETHYL]AMINOMETHANE (TRIS);
D O I
10.1016/0014-4894(91)90004-G
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Isotopic and enzyme-labeled species-specific DNA probes were made for the three known members of the Anopheles punctulatus complex of mosquitoes in Australia (Anopheles farauti Nos. 1, 2, and 3). Species-specific probes were selected by screening total genomic libraries made from the DNA of individual species with 32P-labeled DNA of homologous and heterologous mosquito species. The 32P-labeled probes for A. farauti Nos. 1 and 2 can detect less than 0.2 ng of DNA while the 32P-labeled probe forA. farauti No. 3 has a sensitivity of 1.25 ng of DNA. Probes were then enzyme labeled for chromogenic and Chemiluminescence detection and compared to isotopic detection using 32P-labeled probes. Sequences of the probe repeat regions are presented. Species identifications can be made from dot blots or squashes of freshly killed mosquitoes or mosquitoes stored frozen, dried, and held at room temperature or fixed in isopropanol or ethanol with isotopic, chromogenic, or Chemiluminescence detection systems. The use of nonisotopic detection systems will enable laboratories with minimal facilities to identify important regional vectors. © 1991.
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页码:27 / 35
页数:9
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