Extraction of human DNA for PCR from chewed residues of betel quid using anovel "PVP/CTAB" method

Citation
Fs. Chiou et al., Extraction of human DNA for PCR from chewed residues of betel quid using anovel "PVP/CTAB" method, J FOREN SCI, 46(5), 2001, pp. 1174-1179
Citations number
15
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology
Journal title
JOURNAL OF FORENSIC SCIENCES
ISSN journal
00221198 → ACNP
Volume
46
Issue
5
Year of publication
2001
Pages
1174 - 1179
Database
ISI
SICI code
0022-1198(200109)46:5<1174:EOHDFP>2.0.ZU;2-0
Abstract
Residues of chewed betel quid (BQ) are often found on crime scenes in Taiwa n and possibly some of the Southeast Asian countries. Although these residu es are important biological evidences relating to the suspects, the forensi c analysis of BQ evidence has been hindered by failures in extraction of hu man DNA for PCR analysis. Therefore, it is a prerequisite for relevant fore nsic casework to establish a reliable method for extracting DNA from chewed BQ residues. Three conventional methods (salt/chloroform, 5% Chelex-100 resin, and QIAam p) were first tested for extraction of human DNA from 33 mock BQ samples, w hich had been stored for less than two months, and 50 four-year-old forensi c BQ samples. PCR amplifications from the HLA-DQA1&PM and the STR loci were then used to test the quality of the extracted DNA. For the mock samples, three observations were made. First, PCR amplification of DNA extracted by using these conventional methods had low success rate. Second, the addition of extra Taq DNA polymerase could compensate the lost enzyme activities du e to putative inhibitors and, thus, increase the yield. Third, using the Ce ntricon (TM) -100 column to remove putative inhibitors substantially improv ed the efficiency of PCR. However, for the four-year-old forensic BQ sample s, none of the attempts for PCR were successful. In order to solve the problem in PCR analysis of DNA from old BQ samples, w e developed a DNA extraction method based on the use of polyvinyl pyrrolido ne (PVP) and cetyltrimethylammonium bromide (CTAB), which bind to two commo n classes of PCR inhibitors in plants, polyphenols, and polysaccharides, re spectively. The result showed that this "PVP/CTAB" method is completely suc cessful for the mock BQ samples, and 92% (46 out of 50) successful for the four-year-old forensic BQ samples. To our best knowledge, this is the first report of a reliable method for the extraction of human DNA for PCR from c hewed BQ residues. This method should provide a useful means for forensic i dentification in countries where betel chewing is common.