Mycobacteria infect different cell types in the human lung and cause species dependent cellular changes in infected cells. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Ganbat, Dariimaa; Seehase, Sophie; Richter, Elvira; Vollmer, Ekkehard; Reiling, Norbert; Fellenberg, Kurt; Gaede, Karoline; Kugler, Christian; Goldmann, Torsten
• Is Part Of: BMC pulmonary medicine. Volume 16:Issue 1(2016)
• Page Start: 1
• Page End: 16
• Publication Date: 2016-12
• Subjects: Tuberculosis -- Ex vivo -- STST model -- Mycobacteria -- M. tuberculosis -- M. avium -- M. abscessus -- Cellular change -- HOPE-fixation -- Innate immunity -- Intracellular infection -- Tissue viability; Lungs -- Diseases -- Periodicals; 616.24005
• DOI: 10.1186/s12890-016-0185-5
• Languages: English
• ISSNs: 1471-2466

Abstract

Abstract Background Mycobacterial infections remain a significant cause of morbidity and mortality worldwide. Due to limitations of the currently available model systems, there are still comparably large gaps in the knowledge about the pathogenesis of these chronic inflammatory diseases in particular with regard to the human host. Therefore, we aimed to characterize the initial phase of mycobacterial infections utilizing a human ex vivo lung tissue culture model designated STST (Short-Term Stimulation of Tissues). Methods Human lung tissues from 65 donors with a size of 0.5–1 cm3 were infected each with two strains of three different mycobacterial species (M. tuberculosis, M. avium, andM. abscessus ), respectively. In order to preserve both morphology and nucleic acids, the HOPE® fixation technique was used. The infected tissues were analyzed using histo- and molecular-pathological methods. Immunohistochemistry was applied to identify the infected cell types. Results Morphologic comparisons between ex vivo incubated and non-incubated lung specimens revealed no noticeable differences. Viability of ex vivo stimulated tissues demonstrated by TUNEL-assay was acceptable. Serial sections verified sufficient diffusion of the infectious agents deep into the tissues. Infection was confirmed by Ziel Neelsen-staining and PCR to detect mycobacterial DNA. We observed the infection of different cell types, including macrophages, neutrophils, monocytes, and pneumocytes-II, which were critically dependent on the mycobacterial species used. Furthermore, different forms of nuclear alterations (karyopyknosis, karyorrhexis, karyolysis) resulting in cell death were detected in the infected cells, again with characteristic species-dependent differences. Conclusion We show the application of a human ex vivo tissue culture model for mycobacterial infections. The immediate primary infection of a set of different cell types and the characteristic morphologic changes observed in these infected human tissues significantly adds to the current understanding of the initial phase of human pulmonary tuberculosis. Further studies are ongoing to elucidate the molecular mechanisms involved in the early onset of mycobacterial infections in the human lung.