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原发性人呼吸道上皮细胞上分枝杆菌生物膜的发育、可视化及定量分析方案

Protocol for development, visualization, and quantification of mycobacterial biofilms on primary human airway epithelial cells.

作者信息

Barclay Amy M, Limpens Ronald W A L, Bárcena Montserrat, Ottenhoff Tom H M, Hiemstra Pieter S, van der Does Anne M, Joosten Simone A

机构信息

Leiden University Center for Infectious Diseases (LUCID), Leiden University Medical Center (LUMC), 2333ZA Leiden, the Netherlands.

Cell and Chemical Biology (CCB), LUMC, 2333ZA Leiden, the Netherlands.

出版信息

STAR Protoc. 2025 Jun 20;6(2):103872. doi: 10.1016/j.xpro.2025.103872. Epub 2025 Jun 4.

Abstract

Tuberculosis (TB) displays several characteristics commonly linked to biofilm-associated infections, including recurrence of infection and resistance to antibiotics. Studying biofilm formation by mycobacteria on relevant mucosal surfaces advances our understanding of its role in TB pathogenesis and drug tolerance. Here, we present a protocol to promote biofilm formation by mycobacteria on differentiated primary pseudostratified human bronchial epithelial cell cultures. We then detail procedures to visualize and quantify biofilm matrix and biomass using electron and confocal microscopy and crystal violet staining. For complete details on the use and execution of this protocol, please refer to Barclay et al..

摘要

结核病(TB)具有一些通常与生物膜相关感染有关的特征,包括感染复发和对抗生素的耐药性。研究分枝杆菌在相关粘膜表面形成生物膜有助于我们了解其在结核病发病机制和药物耐受性中的作用。在这里,我们提出了一种促进分枝杆菌在分化的原代假复层人支气管上皮细胞培养物上形成生物膜的方案。然后,我们详细介绍了使用电子显微镜、共聚焦显微镜和结晶紫染色来观察和量化生物膜基质及生物量的程序。有关本方案使用和实施的完整详细信息,请参考巴克利等人的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aa6/12169759/a7842d435d91/fx1.jpg

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