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Central European Journal of Immunology
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1/2016
vol. 41
 
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Experimental immunology

The effect of clindamycin and amoxicillin on neutrophil extracellular trap (NET) release

Weronika Bystrzycka
,
Aneta Moskalik
,
Sandra Sieczkowska
,
Aneta Manda-Handzlik
,
Urszula Demkow
,
Olga Ciepiela

(Cent Eur J Immunol 2016; 41 (1): 1-5)
Online publish date: 2016/03/24
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Introduction

Neutrophil extracellular traps (NETs), described for the first time in 2004, are threads of extracellular DNA complexed with antimicrobial proteins released from neutrophils to fight and kill pathogens, such as bacteria and fungi [1]. Pathogens are trapped and immobilised within a viscous web-like structure, and influenced by high concentrations of antimicrobial compounds, such as neutrophil elastase, myeloperoxidase, and histones [1-3]. Many physiological and non-physiological agents induce NET release, including S. aureus, C. glabrata, HIV, interleukin-8, tumour necrosis factor  (TNF-), calcium ions, phorbol myristate acetate (PMA), or calcium ionophore [4]. In line with phagocytosis and oxidative burst, release of NETs is an efficient mechanism of innate immunity [2, 3, 5]. On the other hand, NETs were found to be a source of antigens for production of anti-nuclei auto-antibodies. Significant formation of NETs accompanied by insufficient clearance of DNA from extracellular matrix are two important mechanisms involved in many autoimmune diseases [4].
Antibiotics are widely used for treatment of bacterial infections. Depending on their biochemical structure and mechanisms of action, they can act not only as bactericidal compounds but may also influence neutrophil or lymphocyte functions [6, 7]. Moreover, they can influence release of cytokines or delayed-type hypersensitivity reactions [6, 8, 9]. However, the influence of antibiotics on NET release is largely unknown. Jerjomiceva et al. found that enrofloxacin increases NET release from bovine granulocytes [10]. Clindamycin was found to inhibit nuclease activity of Staphylococcus aureus, which resulted in increased human NET efficacy in bacteria elimination [11]. Recently, Konstantinidis et al. showed that clarithromycin may induce NET formation in human both in vivo and in vitro [12].
Clindamycin belongs to the group of antibiotics called lincosamides. It has a bacteriostatic effect, and after binding to bacterial ribosomes it acts as an inhibitor of protein synthesis. It was found that clindamycin influences chemotaxis of neutrophils in a dose-dependent manner; the concentration that is obtained physiologically during infection treatment with the antibiotic enhances chemotaxis. Moreover, clindamycin increases oxidative burst of neutrophils [13]. In several studies clindamycin showed a positive effect on phagocytosis [7, 14, 15]. Amoxicillin belongs to the -lactam antibiotics, and its action is based on inhibition of the synthesis of bacterial cell wall. No influence of amoxicillin on phagocytosis was previously reported in in vitro studies. Interestingly, amoxicillin showed a positive effect on neutrophil chemotaxis in vitro [7]. No direct influence of both antibiotics on neutrophil extracellular traps formation was studied so far.
The aim of this study was to investigate whether amoxicillin and clindamycin influence NET release and phagocytosis of human neutrophils.

Material and methods

Neutrophil isolation

Whole blood from six healthy volunteers was collected into tubes containing 3.2% sodium citrate. Then, neutrophils were isolated using the density gradient centrifugation method. After rich-platelet plasma was discarded after centrifugation for 10 minutes at 200 g, a double plasma volume of 0.9% solution of NaCl was added and diluted blood was layered onto a Histopaque 1077 (Sigma Aldrich) and centrifuged for 30 minutes at 400 g. The supernatant (mononuclear cells and isolation media layers) was carefully removed and the layer containing polymorphonuclear and red blood cells was mixed with 5 ml of 1% polyvinyl alcohol and left for 20 minutes for erythrocyte sedimentation. The top layer consisting of alcohol and neutrophils was collected and centrifuged. The remaining red blood cells were lysed with distilled water for 40 seconds and the lysis was stopped by adding two-times-concentrated phosphate buffered saline (2 × PBS). Granulocytes were then washed twice and the cell pellet was resuspended in a cell culture medium (RPMI 1640 without phenol red, supplemented with 10 mM HEPES; Gibco, Waltham, USA).

Phagocytosis

Neutrophils (5 × 105/ml) were incubated for 2 hours at 37˚C, 5% CO2 with clindamycin (1 mg/l, Sigma Aldrich) or amoxicillin (50 µg/ml, Sigma Aldrich), with or without addition of cytochalasin D (10 µg/ml, Sigma Aldrich), an inhibitor of phagocytosis, and negative control. Subsequently, cells were incubated with Escherichia coli (5 µl, BioParticles, fluorescein conjugate) for 30 minutes at 37˚C, 5% CO2. Then the cells were washed with PBS, treated with 0.4% Trypan Blue (Sigma Aldrich) to quench fluorescence of non-phagocyted, adherent bacteria and centrifuged for five minutes at 200 g. Fluorescence of neutrophils was analysed with a Cytomics FC500 flow cytometer (Beckman Coulter, USA) equipped with an argon laser at the first channel of fluorescence.

Neutrophil extracellular traps quantification

Isolated neutrophils were seeded into 96-well black plates at density 1 × 105 cells/well, treated with clindamycin, amoxicillin, or RPMI 1640 alone and incubated for two hours at 37˚C, 5% CO2. After incubation, NET formation was stimulated with 100 nM PMA (Sigma Aldrich) for three hours at 37°C, 5% CO2. Unstimulated neutrophils were used as a control. Following incubation, 500 mIU of micrococcal nuclease (ThermoFisher Scientific, Waltham, USA) was added to detach the DNA from the cell surface and the plate was incubated for 20 minutes at 37°C, 5% CO2. After 20 minutes of incubation, the reaction was stopped with 5 mM EDTA and the plates were centrifuged (10 minutes at 415 g). Subsequently, supernatant was collected and 100 nM Sytox green fluorescent dye (Life Technologies, Waltham, USA) was added. The amount of extracellular DNA release was measured in a FluroStar OMEGA plate reader (BMG Labtech, Ortenberg, Germany) and the results were expressed in relative fluorescence units (rfu).

Neutrophil extracellular traps visualization

Neutrophils were seeded in eight-well Lab-Tek chamber slides (2.5 × 104 cells/well; Nunc, Waltham, USA) and treated with clindamycin, amoxicillin, or RPMI 1640 for two hours at 37˚C, 5% CO2. After the incubation period the cells were stimulated with 100 nM PMA for three hours at 37˚C, 5% CO2. Then the samples were fixed with 4% paraformaldehyde, blocked with 0.1% Triton X (Sigma Aldrich), and incubated overnight with FITC-conjugated MPO antibody (0.1 mg/ml, Abcam ab11729). Post incubation, DNA was stained with 100 µM Sytox Orange fluorescent dye (Life Technologies, Waltham, USA). NETs were visualised using a Leica DMi8 fluorescent microscope.
The study was approved by the Local Ethical Committee at Medical University of Warsaw. Informed, written consent was obtained from all subjects enrolled in the study.

Statistical analysis

Statistical analysis was performed using GraphPad Prism v. 5.0 (GraphPad Software, La Jolla California USA). The results have been expressed as mean ± SD. Nonparametric analysis was performed using Mann-Whitney test for unpaired data and Wilcoxon matched paired test for paired data. Results were considered statistically significant at p < 0.05

Results

Effect of clindamycin and amoxicillin on phagocytosis

Cytochalasin D, as expected, inhibited the uptake of bacteria in each case, causing a decrease of cells fluorescence of 30 ±25%, 53 ±8%, and 55 ±24% in samples with culture media, clindamycin, and amoxicillin, respectively. Both of the antibiotics influenced the phagocytic function of neutrophils. Incubation with amoxicillin resulted in 74.65 ±122.9% higher phagocytic activity of neutrophils, and with clindamycin in 48.09 ±40.69% higher phagocytic activity of isolated cells (Fig. 1) than in samples pre-incubated only with culture medium. No significant difference between both antibiotics with respect to the control was observed.

Neutrophil extracellular traps and visualisation quantification assay

The quantity of released DNA was analysed using a fluorescence reader. The results show that clindamycin does not affect PMA-induced NET formation (78,628 ±17,290 rfu for PMA-stimulated sample vs. 78,628 ±10,249 rfu for amoxicillin-pretreated, PMA-stimulated sample p = 0.2), while amoxicillin increases NETS release (59,972 ±9755 rfu for PMA-stimulated sample and 74,306 ±9519 rfu for amoxicillin-pretreated, PMA-stimulated sample, p = 0.03) (Fig. 2). Neutrophil extracellular traps visualisation using immunofluorescent microscopy confirmed these observations (Fig. 3).

Discussion

In the present study we showed that antibiotics can affect NET release and phagocyte functions of human neutrophils. Previously, an effect of different antibiotics on physiological functions of neutrophils was described [7]. Only a few papers describe the influence of different antibiotics on neutrophil extracellular trap release, none regarding -lactams [10-12]. The results presented in our paper may shed new light on the immunomodulatory effect of antibiotics. We showed that clindamycin does not affect NET release, despite influencing phagocytosis. On the contrary, we found that amoxicillin may enhance NET formation, which could be an additional mechanism of bactericidal action of a studied -lactam.
In our study, neutrophils that were preincubated with clindamycin showed higher intake of fluorescein-conjugated Escherichia coli. This is in line with previous reports describing the influence of lincosamides on granulocyte functions [14, 15]. However, we did not find any influence on NET formation in vitro after stimulation with PMA. This is in agreement with the findings of Schilcher et al. They found that clindamycin does not directly change neutrophil ability to release NETs, but it inhibits bacterial nucleases activity, thus decreasing degradation of webs by trapped bacteria [11].
So far there have been no papers regarding the influence of amoxicillin on NET formation. Of all -lactams cefotaxime was shown to influence oxidative burst and decrease release of cytokines, especially interleukin-8 and TNF-, which are important proinflammatory cytokines triggering NET formations [13]. In the present paper we have shown that amoxicillin increases NET release after stimulation with PMA. The study was performed in vitro, so no effect on proinflammatory cytokines, the release of which might be affected by an antibiotic, could be associated with the observed NET release. We have also indicated that phagocyte activity after incubation with amoxicillin was enhanced. Taken together, our observations point to a strong immunomodulatory effect of -lactams. In our previous study (in press) we did not find any effect of cefotaxime on NET release. Thus, it is probable that amoxicillin acts differentially from cephalosporins, despite their similar antimicrobial effect.
Studies regarding the influence of antibiotics on neutrophil extracellular traps may profit from new findings, which may widen our knowledge regarding immumodulatory effects of antimicrobial drugs. Further analysis will be performed with wider analysis of mechanisms of action and other groups of antibiotics.

This project was financed by the Grant for Young Scientists No. 1WW/PM11/15 funded by the Dean of the First Faculty of Medicine, Medical University of Warsaw.
The authors declare no conflict of interest.

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Copyright: © 2016 Polish Society of Experimental and Clinical Immunology This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
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