Research Article

 

In-vivo and In-vitro Anti-Acinetobacter baumannii Activity of Citrate-Capped Silver Nanoparticles

 

Ibtesam Ghadban Auda 1 *, Istabreq Mohamed Ali Salman 1 *, Dalal Abed Al-Sattar 1 *, Jameelah Ghadban Oduha 2

 

1 Department of Biology, College of Science, Mustansiriyah University, Iraq.

2 Dept. of Microbiology, Al-Kindy College of Medical – Baghdad University, Iraq.

 

* Corresponding author. E-mail: stbg@uomustansiriyah.edu.iq.

 

Received: Nov. 20, 2020; Accepted: May 24, 2021; Published: Aug. 16, 2021

 

Citation: Ibtesam Ghadban Auda, Istabreq Mohamed Ali Salman, Dalal Abed Al-Sattar, and Jameelah Ghadban Oduha, In-vivo and In-vitro Anti-Acinetobacter Baumannii Activity of Citrate-Capped Silver Nanoparticles. Nano Biomed. Eng., 2021, 13(3): 229-239.

DOI: 10.5101/nbe.v13i3.p229-239.

 

Abstract

Silver nanoparticles (Ag NPs) are of potential interest because of their effective antibacterial and antiviral activities. Capping agents are used for exhibiting a better antibacterial activity than uncapped Ag NPs. There are very few reports that have shown the usage of Ag NPs for in-vivo antibacterial therapy. Citrate-capped silver nanoparticles were synthesized chemically by citrate reduction method; the size of Cit-Ag NPs was determined by an atomic force microscope (AFM) and was between 15 - 90 nm. Acinetobacter baumannii (A. baumannii) isolates were the only sensitive species to Cit-Ag NPs. MICs and MBC of Cit-Ag NPs were determined by using A. baumannii. The results showed an additive effect of Cit-Ag NPs. Four mice groups were infected with a sub-lethal dose of A. baumannii intraperitoneally, IP. The single daily dose of Cit-Ag NPs and imipenem plus Cit-Ag NPs combination were administered IP. Imipenem and phosphate buffer saline (PBS) was used as positive control and negative control, respectively. Interestingly, only the PBS-treated group showed growth of A. baumannii in the liver and spleen of sacrificed mice. Histopathologically, Cit-Ag NPs showed antibacterial activity and had an additive effect when combined with imipenem in vivo and in vitro. Moreover, the Cit-Ag NPs showed dose-dependent activity and the organs differed in the illumination of the toxicity effect of Cit-Ag NPs even after high dose administration. In conclusion, Cit-capped Ag NPs had antibacterial activity against multiple drug resistant (MDR) A. baumannii but not against K. pneumoniae and E. coli. Cit-capped Ag NPs increased the inhibition zone of imipenem in additive effect; the minimum inhibitory concentration and the minimum bactericidal concentration of Cit-capped Ag NPs were relatively low. Cit-capped Ag NPs eliminated A. baumannii infection in vivo when it was given alone or in combination with imipenem. The cytotoxicity of Cit-Ag NPs was dose-dependent and the organs differed in the illumination of the inflammatory effect of Cit-Ag NPs after high dose administration. It is not recommended to use Cit-capped Ag NPs systemically despite their valuable additive antibacterial effect especially with a high dose and the combination with imipenem, Topical administration needs to be evaluated. 

 

Keywords: Citrate capped silver nanoparticles, Acinetobacter baumannii, RecA gene, In vivo, In vitro

 

Introduction

The appearance of multidrug-resistant (MDR) bacteria is an international problem for human health. Biological, chemical, and physical properties of nanoparticles making them probable alternatives to some antimicrobial agents [1, 2]. Silver nanoparticles (AgNPs) have potent antiviral and antibacterial activities [3]. Starting from the 18th century, silver in the form of silver sulfadiazine, silver nitrate, etc., has been used for the management of wounds, burns, and maybe other infections. Thereby this feature led to the incorporation of silver into a variety of germicidal preparations [4-6]. Silver nanoparticles have been synthesized by a variety of methods, such as silver ions reduction on functionalized silica surface [7, 8], reduction and capping of silver ions by citrate [3], and reduction of silver ions by nitrate reductase enzyme [9]. The antibacterial activities of the AgNPs varied according to the different synthesis methods. On the other hand, capping agents are nanoparticles stabilizing agent, and exhibiting antimicrobial activity better than uncapped AgNPs [10, 11]. Regarding the action mechanism, a variety of hypotheses have been suggested by many authors. One study mechanism suggests that silver nanoparticles affect the permeability of the bacterial cell wall due to the deposition of silver [12] and electron-dense granules creation [13]. Other studies have shown DNA failure to replicate prior silver ions treatment and enzymatic inactivation by reaction with thiol groups [14]. Extensively proton leakage of membranes occurred in E. coli and Vibrio cholerae leading to the collapse of the proton motive force [15, 16]. The synthesis of metal colloid required a reductant, the commonly used one is citrate ion. Silver nanocrystallites interact strongly with the surface of citrate ions. Comparing with radiological and chemical synthesis methods. The slow growth of crystals resulting from citrate ions and silver surface interaction is distinctive.  Citrate ions addition to silver nitrate results in the complex formation of citrate with silver ions to produce citrate-capped silver nanoparticles, Cit-AgNPs [17]. Although the silver ions' antimicrobial activity is well-known, few works report the utilization of the AgNPs as an antibacterial agent for in vivo therapy [3]. The study aims to evaluate the antibacterial activities of Cit-AgNPs in vivo and in vitro as well as to evaluate the effect of Cit-AgNPs histopathologically on some vital organs.

 

Experimental

Bacterial isolates

Four A. baumannii isolates identified by the Vitek system were isolated from wounds of patients admitted to Baghdad hospitals\ Iraq. Four of uropathogenic K. pneumoniae and four of uropathogenic E. coli isolates were obtained from the same mentioned hospital and identified by the Vitek system.

 

Molecular detection of A. baumannii isolates

The recA gene (a housekeeping gene) was used for molecular detection of Acinetobacter baumannii using specific primers [18] forward primer, 5-CCTGAATCTTCGGTAAAAC-3, and reverse primer, 5-GTTTCTGGGCTGCCAAACATTAC-3. Template DNA was prepared by the boiling method by Auda et al. [19]. Briefly, loopful bacterial culture was suspended in 200 μl of lysis buffer containing 1% Triton X-100, 0.5% Tween 20, 10 mM Tris-HCl (pH = 8), and 1 mM EDTA and incubated for 3 minutes in a boiling water bath. After centrifugation for 2 minutes at 10,000 × g to sediment the debris. After centrifugation, the supernatant was used as template DNA. A negative control is the PCR mixture without the template DNA while the positive control is the PCR mixture with A. baumannii ATCC DNA as atemplate (Baghdad University- College of Science).

 

Antimicrobial susceptibility testing of A. baumannii

It was performed by the disk diffusion method according to the CLSI guidelines [20]. Five families of the antimicrobial were used. The following discs (μg/disc), were used CP: ciprofloxacin (5 μg), CT: cefotaxime (30 μg), IP: imipenem (10 μg), PI: pipracillin+ tazobactam (100/10 μg), TZ: ceftazidime (30 μg), gentamicin (10 μg), amoxicillin+ clavulanic acid (20/10 μg). These discs were obtained from Ninawa drug industries (NDI-Iraq).

 

Citrate-capped silver nanoparticles synthesis

Citrate-capped AgNPs (Cit-AgNPs) were prepared according to a method of Atta et al. [21] with little modifications. Briefly, 0.018% of the AgNO3 solution in deionized water was boiled, and 1% of sodium citrate solution was added dropwise under vigorous stirring. The solution was kept at boiling temperature for 10 minutes then kept in a boiling water bath for about 30 minutes. The change of color to a grayish-yellow indicated the formation of AgNPs and then the solution was cooled to room temperature before been used for further experiments. The prepared Cit-AgNPs were tested for stability at room temperature and refrigerator for no more than one week to ensure its stability at these two conditions. The prepared Cit-AgNPs was stable until 5 days after preparation.

 

Determination of Cit-AgNPs size by atomic force microscope (AFM)

Synthesized Cit-AgNPs were precipitated on the slide, dried then sent to the Department of Chemistry/ University of Baghdad to determine the Cit-AgNPs size by atomic force microscope [22].

 

Antimicrobial activity of Cit-AgNPs

The antimicrobial activity of synthesized Cit-AgNPs was tested using 3 groups of pathogenic bacteria, A. baumannii, K. pneumoniae, and E. coli (four isolates of each group). The method by which the isolates were tested was the agar well diffusion method [3]. The effect of imipenem (5 µg/ ml) and Cit-AgNPs (11.25 μg/ml) combination on A. baumannii was also tested. The obtained inhibition zones resulted from such combination were compared with that resulted from each separately.

 

Determinations of MICs and MBCs

MICs of Cit-AgNPs were determined by using the broth microdilution method [23] with A. baumannii and two-fold dilutions of Cit-AgNPs (90, 45, 22.5, 11.25, 5.625, 2.81, 1.4, and 0.70 μg/ml). The lowest concentration showing no visible growth was considered as the MIC. From the clear wells, 100 μl of each sample was sub-cultured onto nutrient agar to determine the minimum bactericidal concentration (MBC).

 

In-vivo experiment

BALB/c mice were obtained from Pharmaceutical Censorship Center-Baghdad and housed at the animal house at Biology department/college of Science/ Mustansiriyah University. The used 25, 6-8 weeks’ mice were divided randomly into 5 groups (5 mice each). All procedures with animals were performed in agreement with the animal handling institution's ethics. Four mice groups were infected with a sub-lethal dose of A. baumannii intraperitoneal, IP, (1 × 107 CFU/mouse). Single daily dose of Cit-AgNPs (3.5 mg/kg) and imipenem plus Cit-AgNPs combination (5 mg + 1.75 mg/kg) were administered IP. Imipenem (10 mg/kg) and phosphate buffer saline (PBS) was used as the positive control and negative control respectively. The 4 groups received this treatment daily for 3 days as well as a 5th group receive only Cit-AgNPs (3.5 mg/kg) once daily for 3 days. An additional group (6th group) serves as normal healthy control. The first 4 mice groups were sacrificed on day 4, and the liver and spleen were aseptically separated and homogenized in sterile PBS. The homogenate was plated in on nutrients to determine the bacterial load in the liver and spleen. The 5th group was left for 15 days then were sacrificed. Vital organs including the liver, spleen, and kidney were separately collected and the histopathological section was made and stained with hematoxylin and eosin and examined by a microscope [3]. Fig. 1 shows the in-vivo experimental procedure.

 

Fig. 1 Experimental procedure.

 

Result and Discussion

Molecular identification of A. baumannii isolates

A. baumannii isolates were identified by recA gene amplification with specific primers, the obtained amplicon was 425 bp (Fig. 2).

 

Fig. 2 Agarose gel electrophoretogram of recA gene PCR products: Lane 1 is a 100bp molecular ladder; Lane 2, 3 and 4 are PCR products. All three lanes show bands of recA (425 bp). Agarose gel electrophoresis was performed using 1.5% agarose gel and the run last for 90min at 7 V/ cm.

 

Antimicrobial susceptibility testing

The antimicrobial susceptibility test of  A. baumannii isolates revealed that four tested isolates were resistant to all antimicrobial tested except imipenem. On the bases of these results, A. baumannii was used as a model for in vivo experiments, and imipenem was used as a positive control.  Genetically resourceful A. baumannii has grown to be endemic in hospitals, hence the genetic machinery of A. baumannii allows it to the rapid development of resistance. Therefore, Multidrug-resistant A. baumannii outbreaks in hospitals as a nosocomial infection are prevalent and were reported globally [24]. However, due to the recent unproductive therapeutic outcomes, the need to develop new antibacterial agents and understanding the role of other potential alternatives is necessary.

 

Synthesis of citrate-capped silver nanoparticles

Citrate-capped AgNPs (Cit-AgNPs) were prepared according to the chemical-boiling method as described above. The change of color to a grayish-yellow indicated the formation of Cit-AgNPs as shown in Fig. 3. 

 

Determination of Cit-AgNPs size by atomic force microscope

An atomic force microscope is a type of microscope that provides pictures of atoms in or on surfaces. Like the scanning electron microscope (SEM), the purpose of the AFM is to stare at substances on the atomic level. It is commonly used in nanotechnology [22]. The obtained results of AFM revealed that the average diameter of Cit-AgNPs was 59.39 nm and the range of Cit-AgNPs size was between 15-90 nm while 50% of Cit-AgNPs size was 60 nm. In a previous study, Cit-AgNPs size was between 10-55 nm [25], lower than that of this study, but the obtained Cit-AgNPs size was still at the nano-scale level. Table 1 and Fig. 3 and 4 summarized the Cit-AgNPs size as measured by AFM.

 

Table 1 Distribution of prepared citrate-capped silver nanoparticles according to particle size

Diameter (nm) <	Volume (%)	Cumulation (%)	Diameter (nm) <	Volume (%)	Cumulation (%)	Diameter (nm) <	Volume (%)	Cumulation (%)
15.00 20.00 25.00 30.00 35.00 40.00	0.72 0.72 3.14 2.42 4.11 5.80	0.72 1.45 4.59 7.00 11.11 16.91	45.00 50.00 55.00 60.00 65.00 70.00	7.97 5.31 7.00 10.14 11.59 7.73	24.88 30.19 37.20 47.34 58.94 66.67	75.00 80.00 85.00 90.00	8.94 9.18 9.66 5.56	75.60 84.78 94.44 100.00

Avg. diameter: 59.39 nm; <= 10% diameter: 30.00 nm; <= 50% diameter: 60.00 nm; <= 90% diameter: 80.00 nm.

 

Fig. 3 Citrate- capped silver nanoparticles. (a) and (b) Citrate- capped silver nanoparticles size on the slide as captured by an atomic force microscope; (c) Prepared citrate- capped silver nanoparticles.

 

Fig. 4 Granularity cumulation distribution chart: Percentage of Cit-AgNPs according to the size.

 

Anti-A. baumannii activity of Cit-AgNPs

Acinetobacter baumannii was the only sensitive group while K. pneumoniae and E. coli groups were resistant to Cit-AgNPs and showed no inhibition zone at all (Fig. 5 and Table 2). The effect of imipenem and Cit-AgNPs combination on A. baumannii in vitro was tested. Interestingly, the Cit-AgNPs increased the inhibition zone of imipenem about 4 mm in 4 tested A. baumannii isolates (Fig. 6 and Table 2). It was reported that AgNPs have antibacterial activities at very low concentrations and exhibit a synergistic effect with many other antibacterial drugs, such as penicillin, amoxicillin, erythromycin, and clindamycin [26]. Such an effect was observed when Cit-AgNPs combined with imipenem in this study and it was not reported previously.

 

Fig. 5 Antibacterial effect of Cit-AgNPs on pathogenic bacteria: (a) A. baumannii (4 isolates), (b) E. coli (4 isolates), and (c) K. pneumoniae (4 isolates). Cit-AgNPs: Citrate-capped silver nanoparticles. There are inhibition zones around Cit-AgNPs wells only in the culture plate of A. baumannii.

 

Fig. 6 Effect of imipenem - Cit-AgNPs combination against A. baumannii.

Imp: Imipenem; AgNPs: Silver nanoparticles; AgNPs + imp: Silver nanoparticles + imipenem.

 

Table 2 Mean and SD of inhibition zone diameter of imipenem, Cit-AgNPs, and imipenem-Cit-AgNPs combination against A. baumannii 

Isolate No.	Imipenem mean + SD (mm)	Cit-AgNPs mean + SD (mm)	Imipenem + Cit- mean + SD (mm)
1	24 + 0.32	13 + 0.39	28 + 0.73
2	24 + 0.53	16 + 0.50	28 + 0.75
3	30 + 0.41	15 + 0.50	34 + 0.72
4	27 + 0.36	15 + 0.38	31 + 0.70

 

 

 

 

 

 

 

 

 

 

Cit-AgNPs: Citrate-capped silver nanoparticles

 

Determinations of MICs and MBCs of Cit-AgNPs against A. baumannii

Four isolates of A. baumannii showed the same MIC value, 11.25 μg/ml. while all except one isolate showed the same MBC value, 22.5 μg/ml (Table 3). Some researchers found that the MIC of AgNPs was very low [26] and differ from that obtained by others who found it higher [3]. This diversity in results may be attributed to experiment design and the dilutions of AgNPs preparations that differ from each other according to experiment design.

 

Table 3 The effect of citrate-capped silver nanoparticle concentrations on A. baumannii

Isolate No.	MIC (μg/ml)	MBC (μg/ml)
1	11.25	11.25
2	11.25	22.5
3	11.25	22.5
4	11.25	22.5

 

 

 

 

 

 

 

 

 

 

MIC: Minimum inhibitory concentration, MBC: minimum bactericidal concentration

 

In-vivo experiment

On the fourth day, the animals in 5 groups and the liver and spleen were plated on nutrient agar. The results revealed that only PBS-treated group showed growth of A. baumannii. In vivo, serum albumin interacts with uncapped AgNPs affecting the antibacterial activity of AgNPs. However, capped AgNPs [with citrate or poly(vinylpyrrolidone)] exhibited antibacterial activity in vivo due to minimized interactions with proteins of serum (3). Based on these facts, Cit-AgNPs was prepared to be used in vivo. Histopathological study: the main targets of AgNPs are kidneys, spleen, and liver [27, 28]. The tissue of three vital organs of 5 groups was stained and examined microscopically. Kidneys of the imipenem treated group showed necrosis, degeneration of glomeruli, distal, proximal tubules cells and mucin secretion. Imipenem plus Cit-AgNPs group showed the same picture as the imipenem group. The pathological changes in these two groups may be due to A. baumannii infection and Cit-AgNPs at 1.75 mg/kg of this study have no detectable effect of AgNPs at low concentration with minimal side effect on kidneys that’s belongs to large size of AgNPs [29]. The kidneys of mice groups treated with Cit-AgNPs and PBS reveal severe degeneration and necrosis, excessive mucin secretion in distill and proximal tubules, and loss of glomeruli structure and atrophy.   At a high dose of  3.5 mg/kg Cit-AgNPs, as considered by some researchers [30], there are marked histopathological lesions that were observed in kidneys of the Cit-AgNPs group of this study and as reported previously [31]. At a relatively high dose, AgNps induce several histopathological changes represented by hemorrhage, severe atrophy of glomeruli, loss of morphology, degeneration, congestion of proximal, distal convoluted tubules, and Henley loop epithelial cell distraction. The severity of these changes depends on the administrated dose of AgNPs [29]. The severe signs and lesions of PBS treated groups are due to A. baumannii infection hence no other possible causes were found. After 14 days of high dose (3.5 mg/kg) Cit-AgNPs administration, the lesions appeared to be less than lesions of mice groups treated with Cit-AgNPs and PBS but the evidence of degeneration, necrosis, and mucin secretion is still visible (Fig. 7). The excretion of AgNPs from the body is slow and delayed and it was observed that the level of AgNPs in urine is high until day 14 then AgNPs concentration was a decline [30]. The slow AgNPs excretion may explain the delay and slow regeneration of kidney tissue. On the other hand, the excretion routes of AgNPs depend on the size of the nanoparticles. Small size AgNPs are excreted mainly through the urinary tract while larger size through the liver then out with feces [32]. Spleen and liver are the main targets for the accumulation of AgNPs. Phagocytes, like spleen B cells and macrophages and liver Kupffer cells,  play a major role in such a process [33]. Regarding the spleens of the groups, the spleen of the imipenem treated group showed well define tissue and normal red and white pulps and trabeculae but there is bleeding throughout the tissue. Imipenem plus Cit-AgNPs group showed bleeding and loss of red and white pulps structures. The same was observed in the spleen of the group treated with Cit-AgNPs. Cit-AgNPs have a toxic effect on the spleen at both low and high doses hence the severity of the increased lesion as compared with imipenem treated. The 20 nm AgNPs were mainly deposited into the liver, the kidneys, and spleen, whereas the larger AgNPs were mainly distributed to the spleen followed by the liver and lung after injection of Cit-AgNPs [31]. Most Cit-AgNPs of this study are relatively large particles (50% of Cit-AgNPs size was 60 nm) which may explain spleen toxicity. Phosphate buffer-treated mice showed massive tissue distraction, severe bleeding, and necrosis. In the group treated with Cit-AgNPs for 14 days, no bleeding was observed and evidence of regeneration is begun (Fig. 8). The livers of the group treated with imipenem were severely congested. Degeneration, necrosis, and bleeding are also observed this may be contributed to A. baumannii infection. While livers of groups treated imipenem plus Cit-AgNPs, AgNPs only, and PBS showed severe congestion, loss of tissue structure, necrosis as well as inclusion body degeneration and swelling degeneration and bleeding. The effect of both A. baumannii infection and  Cit-AgNPs maybe double the toxic effect. The severity of these lesions is obvious in AgNPs and PBS that showed severe bleeding and necrosis. After 14 days of AgNPs treatment, the liver was normal as the control mice group, and no evidence of tissue inflammation was observed (Fig. 8). This finding may be due to the amazing ability of the liver to generate and heal [34]. Moreover, AgNPs induce the expression of some genes related to apoptosis and oxidative stress [35, 36]. In conclusion, Cit-capped AgNPs have antibacterial activity against MDR A. baumannii but not against K. pneumoniae and E. coli. Cit-capped AgNPs increase the inhibition zone of imipenem in additive effect and MIC and MBC of Cit-capped AgNPs are relatively low. Cit-capped AgNPs eliminate A. baumannii infection in vivo when it was given alone or in combination with imipenem. The cytotoxicity of Cit-AgNPs is dose-dependent and the organs differ in the illumination of the inflammatory effect of Cit-AgNPs after high dose administration.

 

Fig. 7 Histological sections of mice kidney (40 ×). Imp: Imipenem (10 mg /kg); Imp+Ag: Imipenem plus Cit-AgNPs combination (5 mg + 1.75 mg /kg); Ag: Cit-AgNPs (3.5 mg/kg); PBS: Phosphate buffer saline receiving mice for 3 days; 14 days-Ag: Cit-AgNPs (3.5 mg/kg) receiving mice for 3 days and sacrificed after 14 days. C: normal healthy control. Atrophy and loss of glomeruli structure (black arrows), necrosis and degeneration proximal and distal convoluted tubules (white arrows), and mucin secretion (curved arrows) are seen in all sections except healthy control.

 

Fig. 8 Histological sections of mice spleen (40 ×). Imp: Imipenem (10 mg /kg); Imp+Ag: Imipenem plus Cit-AgNPs combination (5 mg +1.75 mg/kg); Ag: Cit-AgNPs (3.5 mg/kg); PBS: Phosphate buffer saline receiving mice for 3 days; 14 days-Ag: Cit-AgNPs (3.5 mg/kg) receiving mice for 3 days and sacrificed after 14 days; C: Normal healthy control. Necrosis and degeneration (black arrows), interstitial bleeding (white arrows), and massive tissue distraction (curved arrow) are seen.

 

Fig. 9 Histological sections of mice liver (40 ×). Imp: Imipenem (10 mg /kg); Imp+Ag: Imipenem plus Cit-AgNPs combination (5 mg + 1.75 mg/kg); Ag: Cit-AgNPs (3.5 mg/kg); PBS: Phosphate buffer saline receiving mice for 3 days; 14 days-Ag: Cit-AgNPs (3.5 mg/kg) receiving mice for 3 days and sacrificed after 14 days; C: Normal healthy control. Severe congestion and bleeding especially in Ag treated mice liver (black arrows), necrosis (curved arrows), and inclusion body degeneration (white arrows) are seen.

 

Acknowledgments

The authors are thankful to Mustansiriyah University (www.uomustansiriyah.edu.iq) for supporting. Mustansiriyah university is the funding source for the current article.

 

Conflict of Interests

The authors declare that no competing interest exists.

 

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Copyright© Ibtesam Ghadban Auda, Istabreq Mohamed Ali Salman, Dalal Abed Al-Sattar, and Jameelah Ghadban Oduha. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.