Denaturing HPLC for identifying bacteria

被引:61
作者
Hurtle, W
Shoemaker, D
Henchal, E
Norwood, D
机构
[1] USA, Med Res Inst Infect Dis, Diagnost Syst Div, Ft Detrick, MD 21702 USA
[2] Clin Res Management, N Royalton, OH USA
关键词
D O I
10.2144/02332rr05
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Denaturing HPLC (DHPLC) is used in a wide variety of genetic applications. Here we introduce a new application for this technique, the identification of bacteria. We combined the capability of DHPLC to detect sequence variation with the principles of rRNA genotyping analysis to develop a high-throughput method of identifying microorganisms. Thirty-nine bacterial species from a broad spectrum of genera were tested to determine if DHPLC could be used for identification. Most (36 of 39) species of bacteria had a unique peak profile that could be used as a molecular fingerprint. Furthermore, a blind panel of 65 different bacterial isolates was analyzed to demonstrate the diagnostic capability of this method to specifically identify Yersinia pestis and Bacillus anthracis. All the Y. pestis samples (70 of 10) and the majority of B. anthracis samples (12 of 74) were correctly identified. The procedure had an overall specificity of 100%, overall sensitivity of 97.7%, and a predictive value of 96.9%. The data suggest that DHPLC of products spanning regions of genetic variability will be a useful application for bacterial identification.
引用
收藏
页码:386 / +
页数:5
相关论文
共 18 条
[1]  
Arnold N, 1999, HUM MUTAT, V14, P333, DOI 10.1002/(SICI)1098-1004(199910)14:4<333::AID-HUMU9>3.3.CO
[2]  
2-3
[3]  
Bennasar Antonio, 2000, International Microbiology, V3, P31
[4]   Characterization of single-nucleotide polymorphisms in coding regions of human genes [J].
Cargill, M ;
Altshuler, D ;
Ireland, J ;
Sklar, P ;
Ardlie, K ;
Patil, N ;
Lane, CR ;
Lim, EP ;
Kalyanaraman, N ;
Nemesh, J ;
Ziaugra, L ;
Friedland, L ;
Rolfe, A ;
Warrington, J ;
Lipshutz, R ;
Daley, GQ ;
Lander, ES .
NATURE GENETICS, 1999, 22 (03) :231-238
[5]  
Gross E, 2000, HUM MUTAT, V16, P345, DOI 10.1002/1098-1004(200010)16:4<345::AID-HUMU7>3.0.CO
[6]  
2-#
[7]  
HaywardLester A, 1996, BIOTECHNIQUES, V20, P250
[8]   Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography [J].
Hoogendoorn, B ;
Owen, RJ ;
Oefner, PJ ;
Williams, N ;
Austin, J ;
O'Donovan, MC .
HUMAN GENETICS, 1999, 104 (01) :89-93
[9]   Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in Marfan syndrome and related connective tissue disorders [J].
Liu, WO ;
Oefner, PJ ;
Qian, CP ;
Odom, RS ;
Francke, U .
GENETIC TESTING, 1997, 1 (04) :237-242
[10]   Targeted screening for induced mutations [J].
McCallum, CM ;
Comai, L ;
Greene, EA ;
Henikoff, S .
NATURE BIOTECHNOLOGY, 2000, 18 (04) :455-457