IDENTIFICATION OF HOST DNA BY AMPLIFIED FRAGMENT LENGTH POLYMORPHISM ANALYSIS - PRELIMINARY-ANALYSIS OF HUMAN CRAB LOUSE (ANOPLURA, PEDICULIDAE) EXCRETA

被引:35
作者
REPLOGLE, J
LORD, WD
BUDOWLE, B
MEINKING, TL
TAPLIN, D
机构
[1] UNIV MIAMI,SCH MED,DEPT DERMATOL & CUTANEOUS SURG,MIAMI,FL 33136
[2] UNIV MIAMI,DEPT EPIDEMIOL & PUBL HLTH,MIAMI,FL 33136
关键词
POLYMERASE CHAIN REACTION; DNA; LICE;
D O I
10.1093/jmedent/31.5.686
中图分类号
Q96 [昆虫学];
学科分类号
摘要
The ability to identify individual hosts of hematophagous arthropods via bloodmeal analyses is a continuing pursuit in both medical and forensic entomology. Characterization of human DNA from blood-feeding arthropods has been advanced substantially by preparation techniques, such as the polymerase chain reaction (PCR). Successful application of amplified fragment length polymorphism (AMP-FLP) analysis to excreta obtained from adult crab lice, Pthirus pubis (L.), fed on human volunteers is reported herein. Human DNA derived from crab louse excreta was typed successfully for two human DNA genetic markers, D1S80 and HUMTH01. Although preliminary, these results illustrate the ability of AMP-FLP analyses to provide individual human locus characterizations from desiccated arthropod excrement.
引用
收藏
页码:686 / 690
页数:5
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