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通过肽核酸荧光原位杂交快速鉴定嗜麦芽窄食单胞菌

Rapid identification of Stenotrophomonas maltophilia by peptide nucleic acid fluorescence in situ hybridization.

作者信息

Hansen N, Rasmussen A K I, Fiandaca M J, Kragh K N, Bjarnsholt T, Høiby N, Stender H, Guardabassi L

机构信息

Department of Veterinary Disease Biology, Faculty of Health and Medical Sciences, University of Copenhagen Stigbøjlen, Frederiksberg, Denmark.

Dako Denmark A/S Produktionsvej, Glostrup, Denmark.

出版信息

New Microbes New Infect. 2014 May;2(3):79-81. doi: 10.1002/nmi2.38. Epub 2014 Mar 25.

Abstract

The objective of this study was to develop a novel peptide nucleic acid (PNA) probe for Stenotrophomonas maltophilia identification by fluorescence in situ hybridization (FISH). The probe was evaluated using 33 human and veterinary clinical S. maltophilia isolates and 45 reference strains representing common bacterial species in the respiratory tract. The probe displayed 100% sensitivity and 100% specificity on pure cultures and allowed detection in sputum from cystic fibrosis patients. The detection limit was 10(4) CFU/mL in spiked tracheal aspirate and bronchoalveolar lavage from healthy horses. Altogether the study shows that this species-specific PNA FISH probe facilitates rapid detection of S. maltophilia in biological specimens.

摘要

本研究的目的是开发一种新型肽核酸(PNA)探针,用于通过荧光原位杂交(FISH)鉴定嗜麦芽窄食单胞菌。使用33株人和兽医临床嗜麦芽窄食单胞菌分离株以及45株代表呼吸道常见细菌种类的参考菌株对该探针进行了评估。该探针对纯培养物显示出100%的敏感性和100%的特异性,并能够在囊性纤维化患者的痰液中进行检测。在健康马匹的气管吸出物和支气管肺泡灌洗物加标样本中,检测限为10(4) CFU/mL。总之,该研究表明这种种特异性PNA FISH探针有助于在生物标本中快速检测嗜麦芽窄食单胞菌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3da/4184662/528699f59fea/nmi20002-0079-f1.jpg

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