Application of Laser Scanning Confocal Microscopy for the Visualization of M. tuberculosis in Lung Tissue Samples with Weak Ziehl-Neelsen Staining

被引:11
作者
Erokhina, Maria, V [1 ,2 ]
Lepekha, Larisa N. [1 ]
Voronezhskaya, Elena E. [1 ,3 ]
Nezlin, Leonid P. [1 ,3 ]
Avdienko, Vadim G. [4 ]
Ergeshov, Atadzhan E. [5 ]
机构
[1] Cent TB Res Inst, Dept Pathol Cell Biol & Biochem, 2 Yauzskaya Alleya, Moscow 107564, Russia
[2] Lomonosov Moscow State Univ, Fac Biol, 1-12 Leninskie Gory, Moscow 119991, Russia
[3] Russian Acad Sci, Koltsov Inst Dev Biol, Dept Comparat & Dev Physiol, Moscow 119334, Russia
[4] Cent TB Res Inst, Dept Immunol, 2 Yauzskaya Alleya, Moscow 107564, Russia
[5] Cent TB Res Inst, 2 Yauzskaya Alleya, Moscow 107564, Russia
关键词
pulmonary tuberculosis; sensitivity of M; tuberculosis detection in tissue; Ziehl-Neelsen staining; confocal laser scanning microscopy; polyclonal antibody; immunohistochemistry; COMPLEX SPECIFIC ANTIGEN; MYCOBACTERIUM-TUBERCULOSIS; IMMUNOCYTOCHEMICAL DETECTION; DIAGNOSIS; BACILLI; SARCOIDOSIS; IMPROVES; SPUTUM;
D O I
10.3390/jcm8081185
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
One of the key requirements for the diagnosis of pulmonary tuberculosis is the identification of M. tuberculosis in tissue. In this paper, we present the advantages of specific fluorescent antibody labelling, combined with laser scanning confocal microscopy (LSCM), for the detection of M. tuberculosis in histological specimens of lung tissues. We demonstrate that the application of LSCM allows: (i) The automatic acquisition of images of the whole slice and, hence, the determination of regions for subsequent analysis; (ii) the acquisition of images of thick (20-40 mu m) slices at high resolution; (iii) single bacteria identification; and (iv) 3D reconstruction, in order to obtain additional information about the distribution, size, and morphology of solitary M. tuberculosis; as well as their aggregates and colonies, in various regions of tuberculosis inflammation. LSCM allows for the discrimination of the non-specific fluorescence of bacteria-like particles and their aggregates presented in histological lung samples, from the specific fluorescence of labelled M. tuberculosis, using spectrum emission analysis. The applied method was effective in the identification of M. tuberculosis in lung histological samples with weak Ziehl-Neelsen staining. Altogether, combining immunofluorescent labelling with the application of LSCM visualization significantly increases the effectiveness of M. tuberculosis detection.
引用
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页数:14
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