Yang Z Q, Wei Y F, Rao S Q, Gao L, Yin Y Q, Xue F, Fang W M, Gu R X, Jiao X A
College of Food Science and Engineering, Yangzhou University, Yangzhou, Jiangsu, China.
Jiangsu Key Laboratory of Dairy Biotechnology and Safety Control, Yangzhou University, Yangzhou, Jiangsu, China.
J Appl Microbiol. 2016 Nov;121(5):1406-1415. doi: 10.1111/jam.13275.
Piliated Lactobacillus rhamnosus (pLR) strains have attracted much attention owing to their excellent mucus adhering capacity and immunomodulatory effects. Here, we aimed to develop a rapid, sensitive method for isolating pLR strains in complex ecosystems using immunomagnetic separation (IMS) with colony immunoblotting (CIB).
Magnetic nanobeads (diameter: 180 nm) conjugated with anti-pLR SpaA pilin antibodies (anti-SpaA) were prepared and used to preconcentrate pLR strains in samples, followed by confirmation with anti-SpaA-based CIB analysis. Under optimized experimental conditions, IMS-CIB selectively recovered pLR strains from 10 CFU ml of faecal microbiota samples spiked with 2·9 × 10 to 2·4 × 10 CFU ml of pLR strains. No positive colonies were detected in samples without addition of pLR strains. The detection limit of IMS-CIB was 29 CFU pLR ml of faecal microbiota, which is much lower than that of CIB without IMS preconcentration (2·0 × 10 CFU ml ).
IMS-CIB allowed selective preconcentration of pLR strains in highly heterogeneous bacterial suspensions and direct detection of pLR colonies, which remained readily available for subsequent isolation.
Our findings established an effective method for selective enrichment and detection of pLR strains.
由于其出色的黏液黏附能力和免疫调节作用,有菌毛的鼠李糖乳杆菌(pLR)菌株备受关注。在此,我们旨在开发一种快速、灵敏的方法,通过免疫磁珠分离(IMS)结合菌落免疫印迹(CIB),从复杂生态系统中分离pLR菌株。
制备了与抗pLR SpaA菌毛蛋白抗体(抗SpaA)偶联的磁性纳米珠(直径:180 nm),用于预富集样品中的pLR菌株,随后通过基于抗SpaA的CIB分析进行确认。在优化的实验条件下,IMS-CIB能从每毫升粪便微生物群样本中选择性回收pLR菌株,这些样本中添加了每毫升2.9×10至2.4×10 CFU的pLR菌株。未添加pLR菌株的样本中未检测到阳性菌落。IMS-CIB对粪便微生物群中pLR菌株的检测限为每毫升29 CFU,远低于未经过IMS预富集的CIB的检测限(每毫升2.0×10 CFU)。
IMS-CIB能够在高度异质的细菌悬液中选择性预富集pLR菌株,并直接检测pLR菌落,这些菌落仍易于用于后续分离。
我们的研究结果建立了一种有效选择性富集和检测pLR菌株的方法。