Detection of bacterial DNA in blood samples from febrile patients: underestimated infection or emerging contamination?

被引:28
作者
Peters, RPH
Mohammadi, T
Vandenbroucke-Grauls, CMJE
Danner, SA
van Agtmael, MA
Savelkoul, PHM
机构
[1] Vrije Univ Amsterdam, Ctr Med, Dept Med Microbiol & Infect Control, NL-1007 MB Amsterdam, Netherlands
[2] Dept Res & Educ, Sanquin Blood Bank NW Reg, NL-1066 CX Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Ctr Med, Dept Internal Med, NL-1007 MB Amsterdam, Netherlands
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2004年 / 42卷 / 02期
关键词
bacteraemia; Burkholderia species; automated DNA isolation; MagNA pure; real-time PCR; contamination;
D O I
10.1016/j.femsim.2004.05.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We applied real-time broad-range polymerase chain reaction (PCR) to detect bacteraemia in blood from febrile patients. Interpretation of amplification results in relation to clinical data and blood culture outcome was complex, although the reproducibility of the PCR results was good. Sequencing analysis of the PCR products revealed the presence of Burkholderia species DNA while no Burkholderia species grew in culture. The source of this contamination was shown to be the commercial DNA isolation kit used in the automated MagNA Pure Isolation Robot. A high degree of suspicion is required when uncommon or unexpected pathogens are diagnosed by molecular methods as clinical consequences can be serious. (C) 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:249 / 253
页数:5
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