Batumin—A Selective Inhibitor of Staphylococci—Reduces Biofilm Formation in Methicillin Resistant Staphylococcus aureus ()
Received 15 October 2015; accepted 1 December 2015; published 4 December 2015
1. Introduction
Batumin, a polyketide antibiotic, produced by Pseudomonas batumici, has high and selective activity against staphylococci [1] [2] . This predetermined its use not only for treatment of infections and nasal carriage of staphylococci but also for diagnosis of staphylocococcal infection, using the “Diastaph” preparation, which consists of batumin-impregnated disks [3] . The high susceptibility of staphylococci to batumin distinguishes them from representatives of other taxons, as was demonstrated using “Diastaph” in several thousands of clinical isolates of bacteria [4] .
Bacteria growing as biofilm are highly resistant to antibiotics [5] . However, our previous studies have shown that addition of half the concentration of the batumin MIC (0.125 μg/ml) to the media considerably reduced biofilm formation in 80% of nasal staphylococcal strains, which had initially high levels of biofilm formation [6] .
The objective of this work was to broaden our knowledge about batumin activity against Staphylococcus species, against atypical forms of this pathogen, i.e. small staphylococcal colony variants (SSCVs), and to obtain more detailed insights into the influence of batumin on biofilm formation by using atomic-force microscopy.
2. Materials and Methods
Batumin, obtained by fermentation of Pseudomonas batumici and purified by silica gel preparative chromatography to 85% of purity, was used.
Batumin is commercially available from Santa Cruz Biotechnology (Santa Cruz, CA) or Enzo Life Sciences (Antwerp, Belgium).
Type and collection strains of 30 different species belonging to the genus Staphylococcus (Table 1) and 50 methicillin resistant S. aureus (MRSA) strains isolated in the
Institute
of
Traumatology
and Orthopedics, Medical Science Academy of Ukraine, from patients with osteomyelitis, were included. 20 Staphylococcus aureus strains, 19 Staphylococcus epidermidis and 4 Staphylococcus intermedius strains, isolated from skin microbial biocenosis and nasal mucous membrane (microbial collection of the Institute of cellular and intracellular symbiosis Ural Branch of Russian Academy of Sciences, Orenburg, Russia) were also studied for their susceptibility to batumin and for its antibiotic effect upon biofilm formation. Thus, in total 123 strains of staphylococci were included.
Identification of MRSA was carried out according to methods described in [7] . Susceptibility of staphylococcal clinical strains to a wide spectrum of antibiotics was tested by the Kirby-Bauer method. NCCLS criteria [8] were used to interpret the susceptibility to antibiotics.
Thirty strains of SSCVs were isolated as subpopulations on Columbia agar with 5% sheep blood, as pinpoint colonies (0.1 - 0.3 mm) after 48 hours of aerobic incubation at 37˚C, among the more numerous colonies (2 - 3 mm) with normal Staphylococcus morphology, considered as the parental isolates of the SSCVs. Identification of the staphylococci was carried out according to standard methods [9] .
The atypical forms of staphylococci were previously identified by standard methods and using tDNA-PCR analysis and were assigned to three species: S. aureus, S. epidermidis and S. haemolyticus. Their detailed description was presented previously [10] .
The minimal inhibitory concentration (MIC) of batumin was studied according to CLSI Standards (2005) in Mueller-Hinton agar or broth [11] . The microbial load of SSCVs was 0.5 × 108 cfu/ml and the Petri dishes were incubated at 37°С for 48 hours.
Half the MIC of batumin was used to study its effect upon biofilm formation in staphylococci. Biofilm formation was studied by a photometric method determining the bacterial capacity to adhere onto the 96-hole polystyrole plane-table surface with subsequent crystal violet colouring [12] . Optical density measurement was done using a photometer ELx808 (
BioTek
,
USA
) at a wavelength of 630 nm. Degree of biofilm formation was expressed in conditional units (un.) which was the optical density of studied strain (experiment) in relation to the nutrient broth density (the control).
For the study of batumin effect on biofilm formation we used S. aureus B-904 (UCM) as test-culture. For biofilm production, glass coverslips were immersed into Luria-Bertani broth with 0.125 μg/ml of batumin and incubated for 48 h at 37˚C.
Visualization of the biofilms was done by atomic force microscopy using the SMM-2000 microscope (Proton- MIET Closed JOINT Stock Company, Russia), in contact mode in air environment [13] [18] .
3. Results and Discussion
The susceptibility to batumin of Staphylococcus species reference strains of some collection strains and of methicillin-resistant S. aureus strains are presented in (Table 1). It is of interest to note the high uniformity of the susceptibility to batumin for the different Staphylococcus species. Batumin inhibited most of the studied strains and species, including MRSA, at concentrations between 0.25 and 0.5 μg/ml, and rarely 1.0 μg/ml was needed.
Table 1. Susceptibility to batumin of species belonging to different 16S RNA complexes of the genus Staphylococcus.
The strain numbers of the Ukrainian Collection of Microorganisms (UCM) are presented. Numbers from АТСС or from other collections between brackets.
Our data show that the most susceptible species to batumin were species of the S. epidermidis complex (МIC 0.0625 - 0.125 μg/ml). Strains of this complex demonstrated the highest batumin susceptibility also during previous clinical trials (unpublished data).
Figure 1 shows the antibiotic-resistance profile of the studied MRSA strains, indicating that these strains are resistant to all commonly used antibiotics. At the same time, all 50 strains―regardless their origin and their susceptibility to different antibiotics―were inhibited by 0.5 μg/ml of batumin.
Batumin is also effective against macrococci which were set separately from the genus Staphylococcus and included in the new genus Macrococcus. On the other hand, Gemella morbillorum and G. haemolysans, isolated from osteomyelitis patients, did not show growth inhibition zones around batumin disks [14] , despite their relationship to staphylococci. Batumin was also not effective against bacilli, Listeria, planococci and other bacteria which belong to the order of the Bacillales, comprising the family of the Staphylococcaceaе [2] [4] .
Data presented here, as well as studies of the past years, demonstrate high activity of batumin against metabolically normal members of the genus Staphylococcus [2] [3] , as well as against atypical forms of staphylococci, the so-called small colony-variants (SSCVs). SSCVs are formed as a result of mutations and characterized by a complex pleiotropic phenotype which can be largely explained by defective electron transport [15] [16] .
All 30 SSCVs included in this study were isolated on solid growth media as a subpopulation among the larger number of colonies with normal for staphylococci morphology. They were characterized by altered colony morphology, delayed growth and lack of pigmentation. Moreover, many of them lacked lecithinase, phosphatase, coagulase and haemolytic activity and the metabolism of carbohydrates such as sucrose, lactose and fructose was altered, which is consistent with the literature and with our previous results [10] [17] .
Coming from our previous data on batumin antimicrobial action against SSCVs we first estimated this effect studying the growth inhibiting concentrations.
Most of the SSCVs were inhibited by a concentration of 0.25 μg batumin/ml. Strain S. aureus 71 was most resistant, with an MIC of 0.5 μg/ml.
So the data presented in this work and first obtained using strains of practically all known staphylococci species, multiresistant clinical isolates and atypical forms of this pathogen give evidence that batumin is highly active selective inhibitor of representatives of the genus Staphylococcus.
Susceptibility of nasal and skin clinical isolates of staphylococci to batumin was the same as of type and collection strains of different species of the genus Staphylococcus studied before [6] . At the same time, the antibiotic effect against biofilm formation was different in different strains and species. Their biofilm formation values varied from 2.6 - 3.1 CU for S. aureus to 1.8 - 2.3 for S. epidermidis and 1.7 - 1.9 for S. intermedius strains (Table 2). Presence of half of batumin MIC in the broth reduced the biofilm formation in 85% of studied
Figure 1. The antibiotic resistance profiles of 50 methicillin-resistant Staphylococcus aureus strains. Legend: x-axis: studied antibiotics; y-axis: % of MRSA strains, resistant to these antibiotics.
Table 2. Batumin effect against biofilm formation by staphylococci.
*The ratio of the optical density of the samples in the experiment and control. Expressed as conventional unit (CU) = OD630 in experimental samples/OD630 in control samples. Optic density of control samples is 0.05, which is the nutrient broth density.
S. aureus strains. It should be noted that batumin is more effective against Staphylococcus strains with strong biofilm formation (CU values between 2.6 and 3.1).
Analysis of experimental data on batumin effect on the stages of biofilm formation in S. aureus demonstrated that the effectiveness of batumin depended on the stage of biofilm formation (Table 3). Simultaneous batumin addition with S. aureus into culture medium promoted reduction of biofilm formation values in all studied staphylococci strains, at that already formed film was more resistant to studied preparation.
More detailed study of batumin action upon S. aureus biofilm formation was carried out using atomic force microscopy. The object of this study was the reference strain S. aureus UCM B-904. This strain formed biofilm on the surface of the glass, as can be seen from Figure 2(a). Surface biofilm was formed by exopolymeric matrix with cells of round shape immersed in it (Figure 2(b)).
For strain S. aureus B-904, the effect of batumin with regard to biofilm formation disturbance corresponded to a more than fourfold decrease of the number of adherent cells. Moreover, in the presence of batumin, the cells of staphylococci were observed in the form of monolayer of separate islets (Figure 2(c)). Particles of exopolymeric matrix were determined with average values of thickness of 63 - 62 nm, located between the cells and on their surface (Figure 2(d)). In this case the transverse dimension of cells was 0.64 ± 0.08 mm, not significantly different from control values. A detailed study of the surface of bacterial cells treated with batumin allows to establish significant reduction of their roughness values (Table 4). Observed values were typical for planktonic S. aureus cells [19] .
Atomic force microscopy revealed qualitative and quantitative changes in the exopolymeric matrix due to batumin treatment, as well as a significant reduction in the number of cells adhered to the coverslip, preventing formation of S. aureus biofilm.
It is known that some biofilms are covered by a surface film composed of lipid components similar to those in bacterial membranes which are a barrier for the penetration of antibiotics [20] . We have previously shown that batumin has significant effects on lipid metabolism of S. aureus [21] . Based on the similarity of a biofilm matrix lipid on the one hand and membrane of bacterial cell on the other hand, it can be assumed that batumin penetrates well into staphylococcal biofilm, explaining the significant changes of exopolymeric matrix that can be observed.
4. Conclusions
The data presented in this work show that batumin is a highly active antimicrobial agent, inhibiting all species of staphylococci and macrococci, regardless their origin or antibiotic susceptibility. The MIC-values for batumin
Table 3. Influence of batumin (0.125 mg/ml) on the steps of biofilm formation by Staphylococcus aureus.
Figure 2. Аtomic force microscopy-topography images of Staphylococcus aureus B-904. ((а) (b)) S. aureus B-904 without batumin; ((c) (d)) S. aureus B-904 grown in the presence of 0.125 μg/ml of batumin. Arrows: 1: particles of exopolymeric matrix; 2 bacterial cells; Scale―2 μm ((a) (b)); 1 μm ((c) (d)).
Table 4. Morphological characteristics of cells and adherence to glass of S. aureus B-904 in the presence of 0.125 µg/ml batumin.
*p < 0.05 (Mann-Whitney U-test). **To determine bacterial cell length and width, cells that were at least immersed into exopolymeric matrix were selected. However, height determination of the cells in this case would have been incorrect and therefore was not implemented.
range between 0.25 and 0.5 µg/ml, rarely reaching 1.0 μg/ml. It should be noted that these results were obtained with 85% pure batumin, whereas, according to [22] , the MIC of 95% pure batumin against S. aureus was much higher, i.e. 0.05 μg/ml.
Probably batumin differs in its mechanism of antimicrobial action from all antibiotic substances used at present in clinical practice, and the nature of its selectivity is connected with some peculiarity of staphylococcal metabolism which sets them apart from other genetically related bacteria. Taking into account, the polyketide nature of batumin and our earlier data about batumin activity upon Staphylococcus lipids [21] , we may suppose that these distinctions are determined by specific characteristics of the staphylococcal fatty acids metabolism.
The obtained data on atomic force microscopy explain one of the mechanisms of the antimicrobial action of batumin, based оn preventing formation of S. aureus biofilm that allows considering it as a promising agent in treatment of staphylococcal biofilm-associated infections.
NOTES
*Corresponding author.