Abstract

Bacteria in genus Mycoplasma spp. are the smallest and simplest form of freely replicating bacteria, with 16 species known to infect humans. In the mouth, M. salivarium is the most frequently identified species. Mycoplasma spp. are parasites with small genomes. Although most of the Mycoplasma spp. that infect humans remain attached to the host cell surface throughout their life cycle, we have previously reported the presence of Mycoplasma salivarium in the epithelial cells of oral leukoplakia and oral lichen planus. However, the mechanism underlying the pathogenicity of M. salivarium has remained unclear. Further studies are needed to identify the process of infection of human cells and the stages in the life cycle of M. salivarium. Electron microscopy (EM) is the method of choice for morphological investigation of Mycoplasma spp. in cells or tissues. This study was performed to clarify and detail the ultrastructure of M. salivarium in tissue biopsies of oral mucosal leukoplakia, using three EM methods: (1) a standard EM processing method; (2) an ultracryotomy and immunolabeling method; and (3) the LR White resin post-embedding and immunolabeling method. This study included five oral leukoplakia tissue samples showing hyperplasia and hyperkeratosis. Although there was some variation in ultrastructural appearances between the three EM methods used, there were four ultrastructural appearances that are believed to reflect the stages of the M. salivarium life cycle in the epithelial cells of the oral mucosa: (1) small, electron-dense cellular-like structures or elementary bodies of M. salivarium; (2) large structures of M. salivarium; (3) M. salivarium organisms in cell division; (4) the sequence of events in the life cycle of M. salivarium that includes: (a) elementary bodies of M. salivarium deep in the oral mucosal epithelium; (b) replication by binary fission and daughter cell division from the elementary bodies; (c) maturation or degeneration of M. salivarium in the epithelial cells mainly in the upper part of the epithelium; and (d) death of the organisms in the granular and/or keratinized layer. These ultrastructural images may provide a useful reference for the identification of M. salivarium in diagnostic cytology or biopsy material.

Highlights

  • Bacteria in the genus Mycoplasma spp. are the smallest and simplest form of freely replicating bacteria and are characterized by the lack of a rigid cell wall, being bound by a single plasma membrane (McElhaney, 1992)

  • The results of IHC of the oral leukoplakia tissues using a monoclonal antibody against Mycoplasma salivarium showed fine, granular, brown immunostaining in the epithelium

  • The Electron microscopy (EM) images of M. salivarium in the epithelial cells of oral leukoplakia tissue depended on the method, four ultrastructural appearances of M. salivarium were obtained: (1) small, electron-dense cellularlike structures, or elementary bodies of M. salivarium; (2)

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Summary

Introduction

Bacteria in the genus Mycoplasma spp. are the smallest and simplest form of freely replicating bacteria and are characterized by the lack of a rigid cell wall, being bound by a single plasma membrane (McElhaney, 1992). There are 16 species of Mycoplasma known to infect humans, including M. pneumoniae, M. salivarium, M. buccale, M. orale, M. faucium, M. lipophilum, and M. fermentans, which are commensal organisms of the oropharynx (Blancherd and Bebear, 2002). M. salivarium and M. orale have been identified more frequently than the other species of Mycoplasma (Watanabe et al, 1986). Mycoplasma spp. have extremely small genomes that range in size from 580 to 2,200 kb, with their metabolic options for replication and survival being limited by their small genome (Rottem, 2003). Mycoplasma spp. exhibit strict host and tissue specificities. Most of the organisms that infect humans remain attached to the host cell surface throughout their life cycle, except for M. pneumoniae, M. penetrans, M. genitalium, M. hominis, and M. fermentans, which may reside within non-phagocytic cells under certain circumstances (Razin et al, 1998)

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