Role of Aminoglycoside-Modifying Enzymes (AMEs) in Resistance to Aminoglycosides among Clinical Isolates of <i>Pseudomonas aeruginosa</i> in the North of Iran

Ahmadian, Leila; Norouzi Bazgir, Zahra; Ahanjan, Mohammad; Valadan, Reza; Goli, Hamid Reza

doi:https://doi.org/10.1155/2021/7077344

BioMed Research International

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Abstract Introduction Materials and Methods Results Discussion Conclusions Data Availability Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2021 | Article ID 7077344 | https://doi.org/10.1155/2021/7077344

Role of Aminoglycoside-Modifying Enzymes (AMEs) in Resistance to Aminoglycosides among Clinical Isolates of Pseudomonas aeruginosa in the North of Iran

Leila Ahmadian,^1,2Zahra Norouzi Bazgir,^2,3Mohammad Ahanjan,^1,2Reza Valadan,^1,4and Hamid Reza Goli^1,2

Academic Editor: Stefania Cantore

Received04 Jul 2021

Accepted07 Aug 2021

Published23 Aug 2021

Abstract

In recent years, the prevalence of resistance to aminoglycosides among clinical isolates of Pseudomonas aeruginosa is increasing. The aim of this study was to investigate the role of aminoglycoside-modifying enzymes (AMEs) in resistance to aminoglycosides in clinical isolates of P. aeruginosa. The clinical isolates were collected from different hospitals. Disk agar diffusion test was used to determine the antimicrobial resistance pattern of the clinical isolates, and the minimum inhibitory concentration of aminoglycosides was detected by microbroth dilution method. The PCR was performed for discovery of aminoglycoside-modifying enzyme-encoding genes. Among 100 screened isolates, 43 (43%) isolates were resistant to at least one tested aminoglycosides. However, 13 (13%) isolates were resistant to all tested aminoglycosides and 37 isolates were detected as multidrug resistant (MDR). The resistance rates of P. aeruginosa isolates against tested antibiotics were as follows: ciprofloxacin (41%), piperacillin-tazobactam (12%), cefepime (32%), piperacillin (26%), and imipenem (31%). However, according to the MIC method, 13%, 32%, 33%, and 37% of the isolates were resistant to amikacin, gentamicin, tobramycin, and netilmicin, respectively. The PCR results showed that AAC(6)-Ib was the most commonly (26/43, 60.4%) identified AME-encoding gene followed by AAC(6)-IIa (41.86%), APH(3)-IIb (34.8%), ANT(3)-Ia (18.6), ANT(2)-Ia (13.95%), and APH(3)-Ib (2.32%). However, APH(3)-Ib was not found in any of the studied isolates. The high prevalence of AME-encoding genes among aminoglycoside-resistant P. aeruginosa isolates in this area indicated the important role of AMEs in resistance to these antibiotics similar to most studies worldwide. Due to the transmission possibility of these genes between the Gram-negative bacteria, we need to control the prescription of aminoglycosides in hospitals.

1. Introduction

Pseudomonas aeruginosa, as an opportunist pathogen, is responsible for several nosocomial infections such as bacteremia; urinary tract, blood, respiratory, burn, and soft tissue infections; external otitis; and endocarditis in clinical settings, which are often difficult to treat [1, 2]. Aminoglycosides, fluoroquinolones, and β-lactams are clinically effective antibiotics in the treatment of infections caused by P. aeruginosa, while carbapenems are the last-line option before colistin [3–5]. Increasing resistance to fluoroquinolones and β-lactams has led to attentiveness in clinical applications of aminoglycosides against Gram-negative bacteria [6]. However, P. aeruginosa can survive in hospital environments for a long time due to the high-level resistance against biocides and can acquire and/or spread the antibiotic resistance genes [7]. Transfer of these genes, especially in hospital environments, can further complicate the treatment of the infected patients [8]. Some of the most important resistance genes transferable between the Gram-negative bacteria, especially in P. aeruginosa, are the aminoglycoside-modifying enzyme- (AME-) encoding genes [6]. Enzymatic modification is one of the important mechanisms leading to resistance against aminoglycosides, while these antibiotics are counting as the most potent drugs of choice for the treatment of life-threatening infections caused by P. aeruginosa [8]. The AMEs are classified as acetyltransferases (AACs), nucleotidyltransferases (ANTs), and phosphotransferases (APH) [9]. These enzymes started N-acetylation, O-nucleotidylation, and/or O-phosphorylation of the aminoglycosides resulting in inactivation of the drugs and therapeutic failure [9, 10]. AAC(6)-I, AAC (6)-II, ANT(2)-I, and APH(3) are the most common AME-encoding genes in P. aeruginosa [11]. The mobile genetic elements such as integrons, plasmids, and transposons can help in the rapid spreading of these clinically important genes [12]. Recently, Thirumalmuthu et al. found that the presence of AME genes was the main cause for resistance to aminoglycosides in multidrug-resistant (MDR) ocular isolates of P. aeruginosa [13]. Therefore, understanding the prevalence of these genes is important for the practical control of antibiotic resistance. This study was aimed at evaluating the role of aminoglycoside-modifying enzyme-encoding genes in resistance to these antibiotics in the clinical isolates of P. aeruginosa collected from hospitalized patients in the north of Iran.

2. Materials and Methods

2.1. Sample Collection and Identification of the Bacteria

One hundred consecutive nonduplicated clinical isolates of P. aeruginosa were collected during 2018-2019 from 5 different teaching and therapeutic hospitals in the north of Iran. The isolates were obtained from different sources including sputum, urine, wound, catheter, blood, stool, and eye. After identification of the isolates by different conventional microbiological and biochemical methods [14], the pure overnight isolates were cultured in trypticase soy broth (Merck, Germany) containing 10% glycerol and were stocked at -20°C for the next investigations. The isolates which were detected as P. aeruginosa were included in the study and others were rejected.

2.2. Antibiotic Susceptibility Testing

The antimicrobial susceptibility pattern of the clinical P. aeruginosa isolates was determined by the Kirby-Bauer disk agar diffusion method on Mueller–Hinton agar (Merck, Germany), according to the Clinical and Laboratory Standards Institute (CLSI) recommendations against 4 different antibiotics [15]. The following antibiotics were exploited in this study: ciprofloxacin (5 μg), cefepime (30 μg), piperacillin (100 μg), piperacillin/tazobactam (100/10 μg), and imipenem (10 μg) (Rosco, Denmark). However, the minimum inhibitory concentrations (MICs) of amikacin, gentamicin, tobramycin, and netilmicin (Sigma, Germany) were detected using the microbroth dilution method conferring to the CLSI guidelines [15], and the lowest concentration of the antibiotics that inhibited the bacterial growth was reported as the MIC. P. aeruginosa ATCC 27853 was used as the control strain in antimicrobial susceptibility testing.

2.3. DNA Extraction and Amplification of AME-Encoding Genes

The alkaline lysis method based on sodium dodecyl sulfate (SDS) (Sigma) and NaOH (Sigma) was used for DNA extraction [16]. Briefly, we solved 0.5 g SDS and 0.4 g NaOH in 200 ml distilled water and suspended the bacterial colony in 20 μl of this extraction buffer. Then, the suspension was warmed at 95°C for 10 min and centrifuged infor 3 min. Next, 180 μl distilled water was added to it and saved at -20°C as extracted DNA until use. All isolates which were resistant to at least one aminoglycoside were examined by the polymerase chain reaction (PCR) method, and the presence of aminoglycoside-modifying enzyme-encoding genes was detected using specific primers (Table 1). The detection of ANT(3)-Ia, ANT (2)-Ia, APH(3)-IIb, AAC(6)-Ib, APH (3)-Ib, APH (3)-Ib, and AAC (6)-IIa genes was performed by the PCR method. The PCRs were done in a final volume of 15 μl reaction mixtures containing 7.5 μl of Master Mix (Ampliqon, Denmark), 300 ng of the extracted DNA, and 10 pmol of each primer and added distilled water to the final volume. The thermal cycler (Bio-Rad, USA) running condition was as follows: an initial denaturation for 5 min at 94°C and 35 cycles including denaturation at 94°C for 60 seconds, annealing for 1 min at specific primer set temperatures (Table 1), and extension at 72°C for 2 min, and after the cycles, a final extension of the amplicons happened at 72°C for 10 min. Finally, the amplified DNAs were visualized by electrophoresis on 1% agarose gel (Sigma, Germany) containing a 3% safe stain (SinaClon, Iran). Distilled water was used as the negative control in PCR.

2.4. Ethical Approval Statements

We received the clinical samples without names from the laboratories of the hospitals affiliated to the Mazandaran University of Medical Sciences. This study was conducted in accordance with the Declaration of Helsinki; however, written informed consent form was provided by the patients or a close relative before hospitalization, and classifying information of each sample was kept secret. Also, this study was approved by the Iran National Committee for Ethics in Biomedical Research with the national ethical code (consent ref number) IR.MAZUMS.REC.1398.980.

3. Results

3.1. Patients and Samples

A total of 100 P. aeruginosa clinical isolates, collected from 60 males and 40 females with an average age of 46 years, were analyzed in the present study. The isolates were collected from five educational-therapeutic hospitals including Zare (burn center, 11 isolates), Razi (infectious center, 22 isolates), Bu-Ali Sina (pediatric center, 17 isolates), Fatemeh Zahra (heart center, 10 isolates), and Imam Khomeini (general center, 40 isolates). However, the isolates were collected from different hospital wards counting intensive care unit (ICU) (48 isolates), burn (9 isolates), internal medicine (4 isolates), operation room (3 isolates), men (3 isolates), women (2 isolates), emergency (13 isolates), surgery (3 isolates), oncology (1 isolate), cardiac care unit (CCU) (6 isolates), neurology (2 isolates), and pediatric (6 isolates). In terms of sample type, the isolates were obtained from sputum (), urine (), wound (), catheter (), blood (), stool (), and eye ().

3.2. Antimicrobial Susceptibility Pattern of the Isolates

The resistance rates against all tested antibiotics are shown in Figure 1. According to the antimicrobial susceptibility testing, 43 (43%) isolates were resistant to at least one tested aminoglycoside. However, 13 (13%) isolates were resistant to all tested aminoglycosides in the present study. The highest aminoglycoside resistance rate was observed against gentamicin (), while 39 and 28 isolates were resistant towards tobramycin and amikacin, respectively. Piperacillin-tazobactam was the most effective antibiotic in this study, while the highest resistance rate was shown against gentamicin and ciprofloxacin. Also, 37 isolates were detected as MDR in the present study.

The microbroth dilution results indicated that 6, 23, 12, and 2 isolates were high-level resistant ( μg/ml) to amikacin, gentamicin, tobramycin, and netilmicin, respectively (Table 2).

3.3. Genotypic Detection of AME-Encoding Genes

The PCR amplification exhibited that 34/43 (79%) of aminoglycoside-resistant isolates were positive for AME-encoding genes (Table 3). AAC(6)-Ib was the most commonly (26/43, 60.4%) identified gene followed by AAC(6)-IIa (41.86%), APH(3)-IIb (34.8%), ANT(3)-Ia (18.6%), ANT(2)-Ia (13.95%), and APH(3)-Ib (2.32%). APH(3)-Ib was not found in any of the studied isolates. Among the 34 isolates that contained at least one of the studied genes, 12 (35.29%) isolates were carrying only one AME-encoding gene; however, 12 (35.29%) isolates were positive for two genes, 4 (11.76%) isolates had 3 genes, 4 (11.76%) others contained 4 AME-encoding genes, and 2 (5.88%) isolates had 5 AME genes. We did not detect any isolates containing all studied genes in the present study (Table 3). The simultaneous presence of the genes encoding aminoglycoside-modifying enzymes had a significant effect on the increase of the MICs of gentamicin and tobramycin (), whereas the combination of the two genes had less effect on the increasing of amikacin and netilmicin MICs. Interestingly, among 26 ICU isolates in this study, 22 (84.61%) of them have contained at least one AME-encoding gene, while this rate among burn isolates was 6/8 (75%). Also, Table 4 exhibits the relation between the aminoglycoside resistance phenotype and the simultaneous presence of AME-encoding genes in the studied isolates. According to this table, most aminoglycoside resistance phenotype (29/43, 67.44%) was the simultaneous resistance against gentamicin and tobramycin. However, different resistance phenotypes in the present study showed similar resistance gene profile.

4. Discussion

The aminoglycosides as the broad-spectrum antibiotics have remained useful as antipseudomonal choice agents for the treatment of life-threatening infections [17]. Therefore, the continuous increase of aminoglycoside resistance levels among the clinical isolates of Gram-negative bacteria will become a growing clinical concern in the future [17, 18]. The lowest resistance to aminoglycosides in the present study was seen against amikacin (13%) with the MICs ranging from 0.25 to 2048 μg/ml, whereas 37% of the P. aeruginosa isolates were resistant to netilmicin with the MICs ranging from 4 μg/ml to 2048 μg/ml. Moreover, Kashfi et al. reported that amikacin was more effective than gentamicin against P. aeruginosa isolated from burned patients [19], while their MICs ranged from 2 μg/ml to 256 μg/ml. These lowest resistances against amikacin may be due to the lower prescription of this aminoglycoside in hospitals of Iran. On the other hand, the rate of resistance to aminoglycosides is different in various regions and countries, even in different hospitals of the same region in a similar country. These variabilities may be due to the different causes such as overuse of these drugs in hospitals, arbitrary use of the drugs by people without a prescription, geographical and cultural differences, countries’ health levels, and hygienic condition [20].

Aminoglycoside resistance in P. aeruginosa is often related to the production of various aminoglycoside-modifying enzymes [19], so the more prevalence of these enzymes is an important problem. In this study, the aminoglycoside resistance rate was 43%, while 79% of the resistant isolates carried AME-encoding genes. In total, 34 AME patterns (28 combinations and 6 single-gene forms) were identified, which showed different levels of aminoglycoside resistance. As an important result of the present study, we found that the simultaneous presence of AME genes was the cause of increasing the MIC ranges of gentamicin and tobramycin. This shows that these genes were the most effective factor in resistance to tested aminoglycosides, while this effect was lower about amikacin and netilmicin. According to the study conducted by Panahi et al. in 2020, AMEs were highly prevalent (96.2%) among the aminoglycoside nonsusceptible P. aeruginosa isolates [21]. However, Odumosu et al. in Nigeria reported that the AME-encoding genes AAC(6)–I and ANT(2)–I were found only in 22.22% of their isolates [8].

In the present study, AAC(6)-Ib, AAC(6)-IIa, and APH(3)-IIb were more prevalent than the ANT(3)-Ia, ANT(2)-Ia, and APH(3)-Ib genes among P. aeruginosa clinical isolates. Also, APH(3)-Ib was not found in any of the isolates. The more prevalence of AAC(6)-Ib in our study was similar to the previous reports from Iran [22, 23], while it was significantly higher compared with another research conducted by Vaziri et al. in Iran which reported a 7% prevalence of this gene [17]. Our results confirmed that the presence of AAC(6)-Ib gene may be more effective in resistance of P. aeruginosa towards tested aminoglycosides, although probably other mechanisms contribute to this type of resistance, too [24]. However, the high prevalence of this gene in P. aeruginosa clinical isolates collected from Iranian patients demonstrates its key role in resistance to aminoglycosides and its high distribution in Iran [21–23]. While the high prevalence of the AAC(6)-I gene can result in a higher resistance level to amikacin [10], our MIC results showed that 42.3% of AAC(6)-Ib-positive isolates were resistant to this antibiotic.

The frequency of AAC(6)-IIa in similar studies was 1.9% in France [25], 18.5% in Nigeria [8], and 10% in another study carried out in Iran [19]. However, 18% of our all clinical isolates were AAC(6)-IIa positive, indicating the increasing frequency of this gene in our region. Furthermore, AAC(6)-IIa was known as the most prevalent aminoglycoside resistance gene in Europe [26]. On the other hand, this gene can spread by integrons, causing the high prevalence of this resistance gene which plays an effective role in resistance to aminoglycosides [27]. AAC(6)-II has a key role in resistance towards gentamicin, tobramycin, netilmicin, and kanamycin [27]. However, among the AAC(6)-IIa-positive isolates of this study, 83%, 88%, and 77% of the isolates were resistant to gentamicin, tobramycin, and netilmicin, respectively.

It seems that ANT(2)-Ia has a relatively important role in resistance against gentamicin and tobramycin in P. aeruginosa isolates [28]. Interestingly, all ANT(2)-Ia-positive isolates in the present study were resistant to these aminoglycosides. However, 13.9% of our isolates were positive for this gene that was comparable with another study conducted in Iran [22]. On the other hand, other studies conducted in Iran and South Korea reported the ANT(2)-Ia gene as the most common aminoglycoside resistance gene [19, 29]. Moreover, Michalska et al. in Poland and Odumosu et al. in Nigeria detected 36% and 16.6% of this gene in their P. aeruginosa clinical isolates, respectively [8, 30].

The results of our study revealed that 18.6% of the P. aeruginosa clinical isolates were carrying ANT(3)-Ia gene similar to the study of Aghazadeh et al. in Iran [22], while 87.5% of other research in Tehran contained this gene [19]. This significant difference may be due to the different sources of the isolates, as 38% of the bacteria in the first study were isolated from the sputum of the cystic fibrosis patients and 62% of their isolates were collected from burned patients [22], while all isolates in another mentioned study [19] were collected from burned patients. Generally, burn patients are at high risk for bacterial infections, so isolates collected from burn injuries may show a higher resistance level [31].

Although APH(3)-Ib is responsible for streptomycin resistance in Enterobacteriaceae [10], 2.32% of our isolates were positive for this gene. This was comparable to Michalska et al.’s study in Poland from which 8% of their isolates were carrying this gene [30]. On the other hand, besides the fact that we found that 34.8% of our isolates were APH(3)-IIb positive, this was lower than the similar studies carried out in Iran and Thailand with the rate of 61.8% and 57%, respectively [22, 32]. Besides, we detected any isolates with the presence of the APH(3)-Ib gene, while in other studies conducted in Iran, the frequency of this gene was 60% and 46%, respectively [19, 22].

5. Conclusions

The aminoglycoside-modifying enzyme-encoding genes are highly prevalent among Pseudomonas aeruginosa clinical isolates worldwide, especially in Iran. The inappropriate and indiscriminate prescription of aminoglycosides was probably one of the main reasons for the high prevalence of some aminoglycoside resistance genes in this study. Due to the high ability of P. aeruginosa in the distribution of these genes, an appropriate antibiotic stewardship policy is required for the prevention of AME gene spreading and to decrease the aminoglycoside resistance rates.

Data Availability

All data generated or analyzed during this study are included in this published article.

Conflicts of Interest

The authors declare no conflict of interest.

Authors’ Contributions

Study concept and design were performed by Hamid Reza Goli. Acquisition of data was performed by Leila Ahmadian, Zahra Norouzi Bazgir, and Hamid Reza Goli. Analysis and interpretation of data were performed by Mohammad Ahanjan and Reza Valadan. Drafting of the manuscript was performed by Leila Ahmadian. Review of the article was performed by Hamid Reza Goli.

Acknowledgments

We thank the laboratory staff of Zare, Razi, Bu-Ali Sina, Fatemeh Zahra, and Imam Khomeini hospitals for providing patients’ information and the collection of the clinical isolates. This study is a report of a database from MSc student thesis registered and carried out in Molecular and Cell Biology Research Center in Mazandaran University of Medical Sciences, Sari, Iran, with grant no. 1293 and the national ethical code IR.MAZUMS.REC.1398.980.

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Copyright © 2021 Leila Ahmadian et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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