Olszewska Magdalena A, Kocot Aleksandra M, Nynca Anna, Łaniewska-Trokenheim Łucja
Chair of Industrial and Food Microbiology, Faculty of Food Science, University of Warmia and Mazury in Olsztyn, Plac Cieszyński 1, 10-726 Olsztyn, Poland.
Chair of Industrial and Food Microbiology, Faculty of Food Science, University of Warmia and Mazury in Olsztyn, Plac Cieszyński 1, 10-726 Olsztyn, Poland.
Microbiol Res. 2016 Nov;192:239-246. doi: 10.1016/j.micres.2016.07.011. Epub 2016 Aug 1.
pH stress is recognized as an important feature for Lactobacillus in relation to lifestyle and commercial utility. Hence, this study aims to investigate the cell function of Lactobacilli cells subjected to pHs between 7.0 and 2.0. For this purpose, the Lactobacilli isolates of vegetable origin were first hybridized with fluorescent oligonucleotide rRNA probes for detecting Lactobacillus species. Then, cells were exposed to pH stress and labelled with fluorescent probes, carboxyfluorescein diacetate (CFDA) and propidium iodine (PI), which provided the insight into esterase activity and membrane integrity of cells. Among isolates, fluorescence in situ hybridization (FISH) enabled us to specifically detect L. plantarum and L. brevis. Interestingly, FCM analysis revealed that at pHs between 7.0 and 4.0 the cell membrane was intact, while after the exposure at pH 3.0, and 2.0 became perturbed or impaired. Finally, L. brevis and L. plantarum differed from each other in fluorescence labeling behaviour and culturability. However, the results showed that the same standard protocol for labeling enables discrimination of subpopulations of tested species. Depending on the species, the substantial culturability loss was observed at pH 3.0 and 2.0. These results suggest that the taxonomic and physiological fluorescent probes could be suitable for in situ detection of specific bacteria and rapid assessment of the physiological status of cells.
pH胁迫被认为是乳酸杆菌与生活方式和商业用途相关的一个重要特征。因此,本研究旨在调查乳酸杆菌细胞在pH值介于7.0和2.0之间时的细胞功能。为此,首先将植物源乳酸杆菌分离株与用于检测乳酸杆菌种类的荧光寡核苷酸rRNA探针杂交。然后,使细胞遭受pH胁迫,并用荧光探针羧基荧光素二乙酸酯(CFDA)和碘化丙啶(PI)进行标记,这为了解细胞的酯酶活性和膜完整性提供了线索。在分离株中,荧光原位杂交(FISH)使我们能够特异性地检测植物乳杆菌和短乳杆菌。有趣的是,流式细胞术分析表明,在pH值介于7.0和4.0之间时细胞膜是完整的,而在暴露于pH 3.0和2.0之后,细胞膜变得紊乱或受损。最后,短乳杆菌和植物乳杆菌在荧光标记行为和可培养性方面彼此不同。然而,结果表明,相同的标记标准方案能够区分受试物种的亚群。根据物种的不同,在pH 3.0和2.0时观察到了显著的可培养性损失。这些结果表明,分类学和生理学荧光探针可能适用于特定细菌的原位检测以及细胞生理状态的快速评估。