Open Access

Nutrition induced pleomorphism and budding mode of reproduction in Deinococcus radiodurans

BMC Research Notes20092:123

DOI: 10.1186/1756-0500-2-123

Received: 09 January 2009

Accepted: 07 July 2009

Published: 07 July 2009

Abstract

Background

Morphological adaptation is an important biological function of a microorganism to cope with its environment. Pleomorphism (to exist in a number of morphological forms) took centre stage in many discussions wherein a bacterium exhibits morphological transition and altered mode of reproduction in response to an environmental condition.

Findings

To strengthen the concept on pleomorphism in bacteria, we report here different cell morphologies of Deinococcus radiodurans in response to variation in nutrient concentration. From our studies we attempt primary evidence towards the presence of significant population of monomer cells of D. radiodurans in specific culture condition. In this report we also illustrate with scanning electron micrographs an unusual budding mode of reproduction in D. radiodurans which was not reported till date for this group of bacteria.

Conclusion

In a holistic view the study reflects on bacterial shape (morphotypes) and the physiological adaptation to a particular nutrient environment. The discovery of budding mode of reproduction in Deinococcus will be of interest to microbiologists. It can serve as a model system to understand the mechanism of budding process at molecular level.

Background

The Deinococcaceae are a family of non-spore-forming bacteria which exhibit extreme resistance to ionizing radiation and desiccation [13]. D. radiodurans strain R1 (the strain used in the present study) is the well characterized member of Deinococcaceae and exist as individual tetrads in its natural milieu [4]. During different growth phases, D. radiodurans predominantly exists as tetrads, with a fraction of population as aggregates of sextet or octets [5]. Daly et al., [6] observed that D. radiodurans grows in tryptone, glucose and yeast extract (TGY) medium as clusters of two cells (diplococci) in early stages of growth and as four cells (tetracocci) in late growth phase. Venkateswaran et al., [2] demonstrated that D. radiodurans grows as diplococci in a defined minimal medium (DMM) which contains mixture of amino acids and other constituents. Chou & Tan [7] reported that the concentration of mono/divalent cations (Na, K, Li, Mg and Ca) plays a major role in multicell formation in Deinococcus and low salt medium such as TGY or nutrient broth also produce similar multicell forms in salt added media. In response to salt addition the diploid/tetrad (2/4) cells grew and divided without separation and formed 8, 16 and 32 cell units in succession [7]. This phenomenon of morphological transition is termed pleomorphism i.e., to exist in a number of morphological forms or morphotypes in response to environmental conditions [8].

Methods

In this investigation we have grown D. radiodurans exclusively in TGY medium and observed different morphotypes of the bacterium by varying the culture medium concentration. During the study Deinococcus cells were harvested in the late log phase (48 hrs growth) and subjected to microscopic observation. To avoid any fundamental bias in determining bacterial shape and size measurements, we used confocal scanning laser microscopy, scanning electron microscopy and dynamic light scattering techniques for determination of the shape and size of the bacterium.

Culture conditions

The strain of Deinococcus radiodurans R1 (B 2906, NRRLB) was maintained on TGY (tryptone-glucose-yeast extract) medium consisting of 5 g tryptone, 3 g yeast extract, 1 g glucose and 1.5% agar was added to prepare solid medium for sub-culturing and culture purity study. Phosphate buffered saline [PBS] at pH 7.2 was prepared using dehydrated phosphate buffer powder (BBL, USA) and 0.85% NaCl as per the manufacturer protocol.

Growth conditions

The inoculated TGY broth cultures were incubated at 30°C in an orbital shaker at 100 rpm. The late log phase culture (48 hr of incubation) was centrifuged at 8,000 rpm for 5 minutes at 20°C. After two repeated washing with PBS, the bacterial cells were harvested, and used for further experimentation.

Dynamic Light Scattering (DLS)

DLS measurements on dilute suspensions of D. radiodurans were performed using a Malvern 4700 (Malvern Instruments, UK) light scattering unit equipped with a Malvern made goniometer, a multi-tau correlator, and a 2.5 W (Ar+ + Kr+) ion laser (Spectra-Physics (Mountain View, CA, model No. 2018-RM) operating at 514.5 nm. In DLS measurements, the incident laser beam was vertically polarized and the scattered intensity was collected using a Glan-Thompson prism (Melles Griot, Rochester, NY), placed in front of the PMT in the vertical and horizontal polarization respectively. For DLS measurements, the cell pellet was further washed twice with 0.2 μm filtered PBS buffer. The washed pellet was resuspended directly into the light scattering cell (quartz) of 8 mm inner diameter with 1 ml of ultra-filtered PBS buffer. Further dilutions were made with the same ultra-pure buffer to the required concentrations.

Confocal Scanning Laser Microscopy (CSLM)

After harvesting the bacterial cells were washed twice with PBS buffer and finally suspended in 1 ml of PBS. 50 μl of D. radiodurans suspension was spread on to a glass slide and air-dried. The smear was stained with 20 μl of 0.02% of acridine orange (absorption maximum; 490 nm, emission maximum; 520 nm) for a few minutes (Acridine orange is an intercalating dye that binds to the double stranded DNA inside the bacteria cells, and these dye-tagged molecules of double-stranded DNA emit fluorescence signal in green when excited with an Argon ion laser operating at 488 nm). Excess stain was washed with ultra-pure water, and the stained sample was air-dried. A thin cover slip was placed on the smear and the slide was mounted on to the microscope stage for observation. A confocal laser scanning microscope (Leica TCS SP2 AOBS) equipped with a Leica DMIRE2 inverted microscope (Leica Microsystems, Germany) was used to acquire images of Deinococcus bacteria. Water immersion objective (63 × 1.2 NA) was used for observing the bacterial smears. A 488 nm line of Argon laser was used for excitation of the acridine orange stained sample. Emission was collected in the bandwidth 515 to 540 nm to detect cells exhibiting fluorescence. All the images were taken by scanning a frame of 512 × 512 pixels with the laser beam in the x, y plane, and each image was averaged over 40 frames for a better signal/noise ratio.

Scanning Electron Microscopy (SEM) Studies

A pure culture of D. radiodurans grown in 1:100 dilution TGY medium was processed to SEM analysis. The glutaraldehyde fixed cells were smeared on to glass slides and freeze dried. The specimens were later sputter coated with gold-palladium and observed in a Philips ESEM model XL30.

Results

In this study we have grown D. radiodurans exclusively in TGY medium and observed different forms of the bacterium morphology by varying the culture medium nutrient concentration. Distinct D. radiodurans monomer cells (size 1.62 μm), diploid cells (size 1.96 μm) were observed at 1:100 dilution. Tetrads (size 2.05 μm) were detected at 1:10 dilution and multimer forms (size 3.45 μm) at full strength. Table 1 describes the size measurement values recorded from DLS and CSLM technique of different morphologies of D. radiodurans. DLS values obtained in an earlier study were also compared. Figure 1(A–D) describes the Confocal Laser Scanning Microscope (CSLM) images of monomer, diploid, tetrad and multimer forms of the D. radiodurans. In the highly diluted medium, we have noticed for the first time significant population of D. radiodurans monococcus cells (Figure 1A, 2A, G & Fig 3b). Notably, we also report for the first time on the budding mode of reproduction in D. radiodurans R1 species. SEM and CSLM images demonstrate morphological evidence of the unusual budding process in D. radiodurans which was illustrated in Figure 2(A–G), Figure 3a and 3b.
https://static-content.springer.com/image/art%3A10.1186%2F1756-0500-2-123/MediaObjects/13104_2009_Article_261_Fig1_HTML.jpg
Figure 1

Epi-fluorescence and confocal laser microscopic images of nutrition induced morphotypes of D. radiodurans , A – Monomer cells (CSLM image); B – Dimer cells (CSLM image); C – Tetramer cells (CSLM image); D – Multimer forms (Epi-fluorecscence image). Scale bar = 10 μm. Culture condition for A = 1: 100 dilution of TGY; B = 1:100; C = 1:10; D = without dilution.

https://static-content.springer.com/image/art%3A10.1186%2F1756-0500-2-123/MediaObjects/13104_2009_Article_261_Fig2_HTML.jpg
Figure 2

SEM images of budding mode of reproduction in D. radiodurans along with schematic illustration. A – Monomer cells of D. radiodurans; B – Bud initiation in monomer cell; C – Bud elongation stage; D – Mature bud stage; E – Constriction formation between mother and daughter cell; F – Bud initiation before separation of cell; G – Separated daughter cells. Panel H shows a schematic model for budding mode of reproduction. Culture condition 1: 100 dilution in TGY; Grown at 30°C for 48 hrs.

https://static-content.springer.com/image/art%3A10.1186%2F1756-0500-2-123/MediaObjects/13104_2009_Article_261_Fig3_HTML.jpg
Figure 3

a: CSLM transmission image showing budding in Deinococcus radiodurans : A – Bud formation, B – elongation of cell, C – Detachment of daughter cell, D – Monomer cells. Culture condition 1: 100 dilution in TGY; Grown at 30°C for 48 hrs. 3b: Magnified view of CSLM image: Different stages of cell division, 1 – bud initiation, 2 – elongation, 3 – two daughter cells, 4 – monomer cells. Culture condition 1: 100 dilution in TGY; Grown at 30°C for 48 hrs.

Table 1

Size distribution of different forms of D. radiodurans using Confocal Laser Scanning Microscopy and Dynamic Light Scattering.

D. radiodurans morphotype

CSLMa

DLSa

DLSb

Monomer

1.62 ± 0.15

1.55 ± 0.02

ND

Dimer

1.96 ± 0.12

2.12 ± 0.04

2.06 ± 0.03

Tetramer

2.05 ± 0.08

2.32 ± 0.03

2.22 ± 0.02

Multimer

3.45 ± 0.12

3.55 ± 0.05

3.61 ± 0.04

a = present study; b = Jena et al., [9]; ND = not detected

Discussion

Among the technologies currently being developed for treatment of toxic wastes bioremediation using extremely radiation-resistant organism, Deinococcus radiodurans shows promising application [1]. Deinococcus radiodurans is a non-pathogenic, desiccation-resistant, solvent-tolerant soil bacterium that can survive acute (short) exposure to an ionizing irradiation (~1.5 Mrads). This bacterium can also grow in the presence of chronic (continuous) gamma irradiation [4]. The Deinococcus radiodurans cells are usually spherical in nature, dividing in pairs and are non- motile [9]. Deinococcus radiodurans generally exist as tetrads, with fraction of population as sextet or octet in TGY (tryptone-glucose-yeast extract) medium [9]. There were reports that D. radiodurans can grow in multimeric forms under the influence of salt concentration or as diploid cells in defined minimal media (DMM) [4, 7]. This report illustrates significant presence of D. radiodurans monococcus cells at low nutrient concentrations (Figure 1A, 2A, G & Figure 3b). This unusual observation of monomeric units of D. radiodurans contradicts the findings of Daly et al., [6] who reported that D. radiodurans does not grow as monomers and survival of single cell population cannot be determined experimentally. However, Oyazu et al., [10] reported that Deinococcus grandis grows as single cells in either TGY or DMM. The observations from the present data demonstrate that using different concentrations/dilutions of the basic medium TGY one can decipher various morphologies of D. radiodurans. We attribute this phenomenon (i.e., variation in morphology) to nutrition induced pleomorphism. The observed pleomorphism in D. radiodurans implies that, limitations on the sizes of a bacterium are not due to the ability to take up nutrients per se but arise from the competition for available nutrients as described by Young [11]. Nutrient concentration, chiefly results in formation of smaller, faster growing cells like monomer and dimer forms compared to larger size (tetrads or multimers). The presence of monomer or dimer units is the result of size oriented higher surface to volume ratio, which aid in nutrient scavenging in a deficient environment. In effect a bacterium can enhance its survival by simply adapting its morphological forms to propagate in a particular environment [12]. Although, there are many established reports indicating pleomorphism in different species of bacteria [1214] still the phenomena is debated. Young, [11] suggested that, by accruing evidence for cell shape, it is possible to manipulate bacterial morphology with enough confidence. Concurrently, one can also arrive at how morphological changes affect survival in different nutrient deficit conditions. This investigation divulges with experimental evidence that cell shape per se is influenced by nutrient acquisition property. The study also provides impetus for further experimentation in varied nutritional situations which facilitate favourable conditions for one bacterial shape over another. This report concludes that nutrient concentration in a culture media of D. radiodurans incites pleomorphism and we support this general concept in bacteria.

Generally, bacteria follow simple binary fission for propagation but unusual reproductive ways such as budding is also exhibited in some cases [15]. For example the filamentous Bacillus sp., strain NAF 001 exhibits budding growth [16], which is not culture-dependent. However, in the present study we consider the budding process in D. radiodurans is culture condition dependent. The dilute nutrient environment could have resulted in the monomer forms, consequently resulting in the bud formation (Figure 2A–G). Commonly, budding results in formation of smaller daughter cell which subsequently detaches and grow independently. We conclude that the dilute nutrient condition could also have induced budding mode of reproduction in D. radiodurans.

This study has significant ramifications primarily on growth and reproduction of Deinococcus and related bacteria. In a holistic view it reflects on bacterial shape (morphotypes) and the physiological adaptation to a particular environment. The conflicting aspect of the true morphology of the bacterium in natural environment and observed morphology in laboratory conditions always posed questions to microbiologists. It can be surmised that the dilute nutrient condition of the culture broth represents the natural nutrient environment of the D. radiodurans which is largely nutrient depleted [10]. A recent report [17] describes that Deinococcus sp could be isolated only in ten times diluted culture media instead of full strength medium, this observation also corroborates our findings. Similarly, we conjecture that nutrient starvation conditions can result in cell asymmetry and further budding type of cell division. This phenomenon of nutrient depletion seems to be analogous to the spore formation process of Bacillus subtilis, wherein nutrient limitation leads to formation of cellular asymmetry and spore formation. The discovery of budding mode of reproduction in Deinococcus will be of great interest to microbiologists. It can serve as a model system to understand the mechanism of budding at molecular level particularly in case of some extremophiles.

Declarations

Acknowledgements

Both the authors thank Dr. S.V.Narasimhan, Associate Director, Chemistry Group, BARC, & Head, WSCD; Dr. V.P. Venugopalan, Head, BBPS, WSCD, for support and encouragement during the course of this investigation.

Authors’ Affiliations

(1)
Biofouling & Biofilm Processes Section, Water & Steam Chemistry Division, Bhabha Atomic Research Centre Facilities

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Copyright

© Toleti et al; licensee BioMed Central Ltd. 2009

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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