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开发一种用于检测和区分布鲁氏菌属的诊断多重聚合酶链反应微阵列分析方法。

Development of a diagnostic multiplex polymerase chain reaction microarray assay to detect and differentiate Brucella spp.

机构信息

Friedrich Loeffler Institute, Institute of Bacterial Infections and Zoonoses, Jena, Germany.

出版信息

Diagn Microbiol Infect Dis. 2011 Dec;71(4):341-53. doi: 10.1016/j.diagmicrobio.2011.08.013. Epub 2011 Oct 5.

Abstract

Brucellosis is a worldwide zoonosis leading to tremendous economic losses and severe human illness. Fast and reliable laboratory tests are needed to detect disease in both humans and animals and to monitor the production of safe food products and feed. For rapid identification of the genus Brucella and differentiation of its species, a multiplex polymerase chain reaction microarray assay based on 11 signature sequences and redundant oligonucleotide probes was developed. The gene targets included genus-specific sequences in bcsp31, perA, cgs, and omp2b, as well as chromosomal regions displaying species-specific hybridization patterns. Brucella reference strains and a representative panel of 102 field isolates were unambiguously identified by their hybridization patterns. The differentiation of species, however, was limited in members of the groups B. suis bv 3/4/B. canis and B. neotomae/B. microti. In summary, the newly developed Brucella ArrayTube® assay is an easy-to-handle molecular test for high-throughput and parallel analysis.

摘要

布鲁氏菌病是一种全球性的动物传染病,给人类和动物带来了巨大的经济损失和严重的疾病。因此,需要快速、可靠的实验室检测方法来诊断人类和动物的疾病,并监测安全食品和饲料的生产。为了快速鉴定布鲁氏菌属并区分其种,我们开发了一种基于 11 个特征序列和冗余寡核苷酸探针的多重聚合酶链反应微阵列检测方法。基因靶标包括 bcsp31、perA、cgs 和 omp2b 中的属特异性序列,以及显示种特异性杂交模式的染色体区域。布鲁氏菌参考菌株和 102 个代表性野外分离株通过其杂交模式被明确鉴定。然而,在 B. suis bv 3/4/B. canis 和 B. neotomae/B. microti 等组的成员中,种的区分受到限制。总之,新开发的布鲁氏菌 ArrayTube®检测方法是一种易于操作的分子检测方法,适用于高通量和并行分析。

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