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新型隐球菌荚膜直径的定量分析。

Quantification of C. neoformans Capsule Diameter.

机构信息

Middle Tennessee State University, Murfreesboro, TN, USA.

Molecular Pathology Laboratory Network, Inc., Maryville, TN, USA.

出版信息

Methods Mol Biol. 2024;2775:225-237. doi: 10.1007/978-1-0716-3722-7_15.

Abstract

The polysaccharide capsule of Cryptococcus neoformans is the primary virulence factor and one of the most commonly studied aspects of this pathogenic yeast. Capsule size varies widely between strains, has the ability to grow rapidly when introduced to stressful or low-nutrient conditions, and has been positively correlated with strain virulence. For these reasons, the size of the capsule is of great interest to C. neoformans researchers. Inducing the growth of the C. neoformans capsule is used during phenotypic testing to help understand the effects of different treatments on the yeast or size differences between strains. Here, we describe one of the standard methods of capsule induction and detail two accepted methods of staining: (i) India ink, a negative stain, used in conjunction with conventional light microscopy and (ii) co-staining with fluorescent dyes of both the cell wall and capsule followed by confocal microscopy. Finally, we outline how to measure capsule diameter manually and offer a protocol for automated diameter measurement of India ink-stained samples using computational image analysis.

摘要

新型隐球菌的多糖荚膜是主要的毒力因子,也是该致病性酵母最常研究的方面之一。荚膜大小在菌株间差异很大,在引入应激或低营养条件下能够快速生长,并与菌株毒力呈正相关。由于这些原因,荚膜的大小是新型隐球菌研究人员非常关注的问题。诱导新型隐球菌荚膜生长用于表型测试,以帮助了解不同处理方法对酵母的影响或菌株间大小的差异。在这里,我们描述了一种荚膜诱导的标准方法,并详细介绍了两种公认的染色方法:(i)印度墨水,一种负染色,与传统的光学显微镜结合使用,(ii)细胞壁和荚膜的荧光染料共染色,然后进行共聚焦显微镜检查。最后,我们概述了如何手动测量荚膜直径,并提供了使用计算图像分析对印度墨水染色样本进行自动直径测量的方案。

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