Jensen Henrik Elvang, Jensen Louise Kruse, Barington Kristiane, Pors Susanne Elisabeth, Bjarnsholt Thomas, Boye Mette
Department of Veterinary Disease Biology, Faculty of Health and Medical Sciences, University of Copenhagen, Ridebanevej 3, 1870, Frederiksberg C, Denmark,
Methods Mol Biol. 2015;1247:219-34. doi: 10.1007/978-1-4939-2004-4_17.
Fluorescence in situ hybridization (FISH) is an efficient technique for the identification of specific bacteria in tissue of both experimental and spontaneous infections. The method detects specific sequences of nucleic acids by hybridization of fluorescently labeled probes to complementary target sequences within intact cells. FISH allows direct histological localization of the bacteria in the tissue and thereby a correlation between the infection and the histopathological changes present. This chapter presents protocols for FISH identification of bacterial pathogens in fixed deparaffinized tissue samples mounted on glass slides. Two different methods are presented: one is illustrated with the use of peptide nucleic acid (PNA) that is carried out directly on glass slides (Method I), whereas the other is exemplified by using a DNA probe in a Shandon rack (Method II). In the two methods, both PNA and DNA probes can be used.
荧光原位杂交(FISH)是一种用于鉴定实验性感染和自发性感染组织中特定细菌的有效技术。该方法通过将荧光标记的探针与完整细胞内的互补靶序列杂交来检测核酸的特定序列。FISH可使细菌在组织中直接进行组织学定位,从而将感染与所呈现的组织病理学变化联系起来。本章介绍了用于在载玻片上固定的脱石蜡组织样本中进行细菌病原体FISH鉴定的方案。介绍了两种不同的方法:一种是使用直接在载玻片上进行的肽核酸(PNA)说明(方法I),而另一种是以在Shandon架中使用DNA探针为例(方法II)。在这两种方法中,PNA和DNA探针均可使用。