ABSTRACT

Nanobacteria individual cases under the name of suggesting the bacteria mycoplasma and L-transformed forms of bacteria that imitate their size are nanobacteria that a separate systematic units remains controversial; the introduction of new high-resolution analytical microscopy techniques of prokaryote and eukaryote has revealed new structures in the structures of bacteria, which are the target of physical, chemical and biologically active stressors. The purpose of this work is, through a comparative retrospective analysis, to find out the motivation of “nanobacteria” ultrastructure public and visualize the structure of Gram-negative bacteria and viruses like symbiont of entamoeba.

Subject Areas:

Cell Biology

Keywords:

Nanolike, Bacteria, Symbiont, Electron Microscopy

1. Introduction

At the present time, despite the large number of publications about nanobacteria [1] [2] [3] , the issues on their presence as a separate systematic units remain controversial. For the characterization of bacteria as “nanobacteria”, they can be attributed to the filtering of L-transformed forms, to mycoplasmas and to dormant forms of the bacteria [4] [5] . Introduction to new high-resolution analytical microscopy techniques of prokaryotes and eukaryotes has revealed new structures in constructing of uncultivated bacteria and symbiont of entamoeba [6] , which are the target of physical, chemical and biological active stressors factors. To nanobacteria, as to pathogenic factors, they are attributed such diseases as kidney stone disease, calcification of the placenta, malignant tumors and other diseases [7] - [9] . Study of nanobiotes and mixing them with nanobacteria, calcium and other mineral salts will probably make reveal etiological factors for various pathologies, as well as the mechanisms of formation of biofilm from bacteria [10] - [12] .

The purpose of this work: through a comparative retrospective analysis to find out the ultrastructure motivations of publicly available visualized nanolike structures of bacteria and endosymbiont of entamoeba.

2. Material and Methods

2.1. Experimental Materials

In this study has been used a wide range of cultures of micro-organisms, belonging to different taxonomic groups causative agents of intestinal infections: enteropathogen Escherichia coli (strain 1257), Shigella flexnerii (strain 130), Salmonella typhimurium (strain 546), Entamoeba moshkovskii (strain “Er”). E. coli 1257 and S. flexnerii 130 and S. typhimurium 546, in order to follow the changes in bacterial cells in death phase of growth and after the treatment of antibiotics.

Bacteria were grown anaerobically in LB medium (48 hours, 37˚C), solidified with 1.8% agar, when necessary. The following antibiotics were used: ampicillin (35 μg/ml), and the quaternary ammonium compound (QAC) ?“A −660” (0.5 mg/ml). The latter was done by serial dilutions as well as according to the instructions of bactericidal properties of new disinfectants. Ultrastructure analysis of antibiotics action was carried out according to the methods of determining the minimum inhibitory concentration (MIC) of antibiotics of the penicillin series-ampicillin (4000 units/ml) was used. The E. moshkovskii “Yer” cultures (wastewater treatment plant is off) were irradiated with lethal doses 1000 Grey of γ-ionizing radiation.

2.2.Preparation of Specimens for Electron Microscopy

Cell cultures of bacteria and entamoeba were separated after centrifugation at low speeds for/during 20 min, and were fixed with 2.5% glutaraldehyde in 0.1 M cacodylate buffer at pH 7.4 during 2 h. After washing three times in cacodylate buffer, the post-fixation was performed with the help of 1% osmium tetroxide in 0.1 M cacodylate buffer at pH 7.4 during at least 1h. After washing in the same buffer, dehydratation of biological samples was performed with ethanol or acetone of increasing concentrations (30%, 50%, 70%, 96% and 100%), followed by impregnation and by pouring the mixture of araldite according to Luft [13] . After polymerization in the thermostat at temperatures of 37˚C and 59˚C, we obtained ultrathin sections on the ultramicrotome “Reichert-Jung” (Austria). Ultrathin sections were then stained with aqueous uranyl acetate and 3%, and by Reynolds lead citrate [14] . They were registered in the transmission electron microscope (TEM) JEM-100C and Tesla-500, operating at accelerating voltage of 80 kV. Electron microscopy imaging analysis was performed using the digital program system “Video-Test Structure-5 of Nanotechnology”.

3. Results

The formation of spherical granules in 40 - 100 nm surrounding by membrane structures of S. flexnerii in growth and death phase (Figure 1(a) Figure 1(b)), leaving the cell vacuoles unicultived forms of bacteria differing with compact citoplasme (Figure 1(c)), as well as the formation of outgrowths on S. typhimu- rium cell walls with different length during the ampicillin-treatment (Figure 1(d)) were detected in these studies. These formations could be discussed as a basis for the development of nanobacteria under the specific conditions of environment [15] .

After the action of the quaternary ammonium compound A-660 on E.coli, was detected the formation of “nanobacteria”, which had the structure of Gram- negative bacteria, closely adjacent to the surface of the cell wall of E. coli (Figure 2(a) Figure 2(b)). Some of them are connected by the little bridge to the cell wall of bacteria, thus creating the appearance of budding. In the same biosamples, were installed the outgrowths of the cell wall of the outer membrane of various lengths (Figure 2(c)).

At nano-like symbiotic bacteria of Ent. moshkovskii, after exposure to γ- radiation, have been identified previously unknown structures in the form of electron dense granules with different diameter from 8 to 35 nm (Figure 3). The particles “O₁” on ultrathin sections were examined it should be said that the diameter of the large granule “O₁” was 35 nm, the area-885 nm²; and the diameter of the small “O₂”-8 nm, the area-45 nm². After irradiation, the morphometric parameters of virus-like symbionts, on ultrathin sections, were equated in length within 160 nm in diameter-94 nm, the total area-11036 nm². “O₁” granules with their electron density and sizes resemble volutin-acidocalcisom (AC) (Figure 3) of bacteria and unicellular eukaryotes after the action of stress factor [16] .

One can consider the formation of nano-like bacteria as one of the forms of survival of bacteria and symbionts under the influence of stress factors. The results of our searches have shown various forms of nanosphere transformation under the action of antibiotics, quaternary ammonium compounds and ionizing radiation, which is comparable with the literature data of nanomicrobiology [2] [12] .

4. Conclusions

The data we obtained witness the fact that the formation of nano-like structures

in/at E. coli, Shigella flexnerii, Salmonella typhimurium was type connected with the cultures aging, as well as by the action of bio-organic, chemical and physical stress factors of the environment, as well as they testify the possibility of the presence of acidocalcisome in nanobacteria of symbionts in entamoeba cells with γ-ionizing radiation.

Our attempts to analyze nanobacteria-like formations and the obtained results allowed to establish different types of nanostructures in studied Gram-negative bacteria and symbiont of entamoeba performed using the digital program.

Acknowledgements

The study was done within the framework supported by Ministry of Education and Scene of the Republic of Armenia (Basic support).

Conflict of Interests

The authors declare no conflict of interests with respect to the present paper.

Cite this paper

Hovnanyan, K., Hovnanyan, M. and Trchounian, A. (2017) Electronmicroscopic Study of Nanolike Bacteria. Open Access Library Journal, 4: e3485. https://doi.org/10.4236/oalib.1103485

References