ABSTRACT

Acinetobacter baumannii is one of the most frequent nosocomial pathogen capable of acquiring resistance to different antimicrobials. The aim of this study was to investigate the activity of tetracycline, doxycycline and minocycline, the prevalence of tet(A) and tet(B) determinants, and the role of efflux pump in tetracycline resistance among the A. baumannii clinical isolates. Susceptibility of 98 A. baumannii isolates to tetracyclines was evaluated by disk diffusion method. The presence of active efflux pump was investigated by determination of the minimum inhibitory concentration (MIC) of tetracycline using the carbonyl cyanide 3-chlorophenylhydrazone (CCCP). Polymerase chain reaction (PCR) was performed to investigate the presence of tet(A) and tet(B) determinants in tetracycline-resistant isolates. The rate of resistance to tetracycline, doxycycline and minocycline was 47.95%, 0%, and 30.61%, respectively. Among the 47 tetracycline-resistant isolates, 29.79% were originated from burned patients and showed MIC ranging from 128-256 μg/mL with both MIC ₅₀ and MIC₉₀ values of 256 μg/mL, while 70.21% were from ventilator-associated pneumonia (VAP) patients and had MIC values ranging from 32-1024 μg/mL, with MIC₅₀ and MIC₉₀ of 512 μg/mL and 1024 μg/mL, respectively. The tet(B) gene was found in 61.7% of tetracycline-resistant isolates, while none of the isolates carried the tet(A) gene. CCCP led to 2-128-fold reduction in tetracycline MIC of the tested isolates. The results showed that doxycycline and minocycline are promising agents for the treatment of A. baumannii infections. This study has also revealed the role of efflux activity in the resistance to tetracycline of A. baumannii isolates. The emergence of resistance to these agents is likely due to the spread of clones presenting with a higher prevalence of resistance determinants.

KEYWORDS:
Acinetobacter baumannii; Efflux pump; Tet(A), Tet(B); Tetracycline resistance

INTRODUCTION

Acinetobacter baumannii is an opportunistic microorganism that has emerged as one of the most troublesome pathogens worldwide ¹1. Carvalho KR, Carvalho-Assef AP, Peirano G, Santos LC, Pereira MJ, Asensi MD. Dissemination of multidrug-resistant Acinetobacter baumannii genotypes carrying bla(OXA-23) collected from hospitals in Rio de Janeiro, Brazil. Int J Antimicrob Agents. 2009;34:25-8.^,22. Pournajaf A, Rajabnia R, Razavi S, Solgi S, Ardebili A, Yaghoubi S, et al. Molecular characterization of carbapenem-resistant Acinetobacter baumannii isolated from pediatric burns patients in an Iranian hospital. Trop J Pharm Res. 2018;17:135-41. . This pathogen is responsible for severe infections, such as ventilator-associated pneumonia (VAP), bloodstream, urinary tract, and wound infections ³3. Razavi Nikoo H, Ardebili A, Mardaneh J. Systematic review of antimicrobial resistance of clinical Acinetobacter baumannii isolates in Iran: an update. Microb Drug Resist. 2017;23:744-56.^,44. Lari AR, Ardebili A, Hashemi A. AdeR-AdeS mutations & overexpression of the AdeABC efflux system in ciprofloxacin-resistant Acinetobacter baumannii clinical isolates. Indian J Med Res. 2018;147:413-21. . VAP is the most frequent ICU-acquired infection, occurring in 9 to 24% of patients intubated for longer than 48 h ⁵5. Coyne S, Guigon G, Courvalin P, Périchon B. Screening and quantification of the expression of antibiotic resistance genes in Acinetobacter baumannii with a microarray. Antimicrob Agents Chemother. 2010;54:333-40. . Even more worrisome, the ability of this microorganism to acquire resistance to multiple antimicrobial agents makes it difficult to treat under certain clinical conditions, especially in critically ill patients. Thus, there are currently only a few antibiotics expected to be effective against the severe forms of A. baumannii infections leading to the increment of mortality rates, as well as health care costs ³3. Razavi Nikoo H, Ardebili A, Mardaneh J. Systematic review of antimicrobial resistance of clinical Acinetobacter baumannii isolates in Iran: an update. Microb Drug Resist. 2017;23:744-56. .

Due to the continued emergence and spread of A. baumannii- resistant strains and a few number of therapeutic options, other antibiotics have been analyzed for use in clinical practice. Tetracyclines, including minocycline and doxycycline, have shown promising clinical and microbiological effectiveness for treating A. baumannii infections. The successful use oftetracyclines in combination with other antibiotics has been reported in 71.9% of respiratory infections and 87.5% of blood stream infections ⁶6. Falagas ME, Vardakas KZ, Kapaskelis A, Triarides NA, Roussos NS. Tetracyclines for multidrug-resistant Acinetobacter baumannii infections. Int J Antimicrob Agents. 2015;45:455-60. .

The efflux system, found in many bacterial genera, is responsible for reducing the antibiotic accumulation and is known as an potent mechanism of drug resistance ⁷7. Vila J, Martí S, Sanchez-Céspedes J. Porins, efflux pumps and multidrug resistance in Acinetobacter baumannii. J Antimicrob Chemother. 2007;59:1210-5.^,88. Huys G, Cnockaert M, Vaneechoutte M, Woodford N, Nemec A, Dijkshoorn L, et al. Distribution of tetracycline resistance genes in genotypically related and unrelated multiresistant Acinetobacter baumannii strains from different European hospitals. Res Microbiol. 2005;156:348-55. . Efflux pump-encoding genes are carried either by genetic elements, e.g., TetA and CmlA systems in resistance to tetracycline and chloramphenicol, respectively, or by a chromosome, being therefore responsible for acquired or intrinsic resistances when they are overexpressed ⁹9. Coyne S, Courvalin P, Périchon B. Efflux-mediated antibiotic resistance in Acinetobacter spp. Antimicrob Agents Chemother. 2011;55:947-53. . Similar to other Gram-negative bacteria, the efflux pump is a main mechanism involved in resistance to tetracycline in A. baumannii⁸8. Huys G, Cnockaert M, Vaneechoutte M, Woodford N, Nemec A, Dijkshoorn L, et al. Distribution of tetracycline resistance genes in genotypically related and unrelated multiresistant Acinetobacter baumannii strains from different European hospitals. Res Microbiol. 2005;156:348-55. . The most common tetracycline-specific efflux pumps are members of the major transporters facilitator superfamily (MFS) ¹⁰10. Chopra I, Roberts M. Tetracycline antibiotics: mode of action, applications, molecular biology, and epidemiology of bacterial resistance. Microbiol Mol Biol Rev. 2001;65:232-60. . These systems expel tetracycline molecules from the inside of cells at the expense of a proton. Several Tet efflux pumps from the MFS superfamily leading to resistance to tetracycline have been acquired by clinical isolates of A. baumannii¹¹11. Mak JK, Kim MJ, Pham J, Tapsall J, White PA. Antibiotic resistance determinants in nosocomial strains of multidrug-resistant Acinetobacter baumannii. J Antimicrob Chemother. 2009;63:47-54. . Tet(A) and Tet(B) are the most prevalent, with Tet(A) efflux conferring resistance to tetracycline but not to minocycline or doxycycline and Tet(B) conferring resistance to tetracycline and minocycline but not to tigecycline ¹²12. Grossman TH. Tetracycline antibiotics and resistance. Cold Spring Harb Perspect Med. 2016;6:a025387.^,1313. Martí S, Fernández-Cuenca F, Pascual A, Ribera A, Rodríguez-Baño J, Bou G, et al. Prevalencia de los genes tetA y tetB como mecanismo de resistencia a tetraciclina y minociclina en aislamientos clínicos de Acinetobacter baumannii. Enferm Infecc Microbiol Clin. 2006;24:77-80. . It has also been found that Tet(A) acts sinergically with the resistance—nodulation—division (RND) superfamily of efflux pumps, such as AdeABC and AdeIJK, serving as an important resistance mechanism of resistance to tigecycline in A. baumannii¹⁴14. Foong WE, Wilhelm J, Tam HK, Pos KM. Tigecycline efflux in Acinetobacter baumannii is mediated by TetA in synergy with RND-type efflux transporters. J Antimicrob Chemother. 2020;75:1135-9. . The tet(B) gene was found in at least 50% of tetracycline-resistant A. baumannii isolates and tet(A) in 14-46% ¹⁵15. Ribera A, Roca I, Ruiz J, Gibert I, Vila J. Partial characterization of a transposon containing the tet(A) determinant in a clinical isolate of Acinetobacter baumannii. J Antimicrob Chemother. 2003;52:477-80.^,1616. Srinivasan VB, Rajamohan G, Pancholi P, Stevenson K, Tadesse D, Patchanee P, et al. Genetic relatedness and molecular characterization of multidrug resistant Acinetobacter baumannii isolated in central Ohio, USA. Ann Clin Microbiol Antimicrob. 2009;8:21. . The genetic basis of these determinants remains largely unknown. A partially characterized Tn1721-like transposon containing the tet(R) and tet(A) genes, encoding, a regulatory protein and a resistance protein ¹⁵15. Ribera A, Roca I, Ruiz J, Gibert I, Vila J. Partial characterization of a transposon containing the tet(A) determinant in a clinical isolate of Acinetobacter baumannii. J Antimicrob Chemother. 2003;52:477-80. , respectively, and tet(B) is carried by 5 to 9-kb plasmids in the multidrug resistant of A. baumannii¹⁷17. Agersø Y, Petersen A. The tetracycline resistance determinant Tet 39 and the sulphonamide resistance gene sulII are common among resistant Acinetobacter spp. isolated from integrated fish farms in Thailand. J Antimicrob Chemother. 2007;59:23-7. .

In the present study, we investigated (i) the activity of tetracycline, doxycycline and minocycline, (ii) the prevalence of tet(A) and tet(B) efflux determinants, and (iii) the presence of efflux activity among clinical isolates of A. baumannii .

MATERIALS AND METHODS

Ethics statement

The present study was approved by the Ethics Committee of the Iran University of Medical Sciences, protocol N° IR.IUMS.REC 1395.9221133207. The included patients did not directly participate in this study. All experiments were performed on bacteria isolated from clinical specimens of hospitalized patients.

Bacterial identification

This cross-sectional study was performed on A. baumannii isolates from patients admitted at the burn unit and intensive care unit (ICU) of two hospitals, Shahid Motahari and Rasoul Akram, in Tehran, Iran, from 2016 to 2017. Each isolate was recovered from a particular patient, and only one sample was taken from each patient. The standard microbiological and biochemical tests, such as Gram staining, oxidase and catalase tests, triple sugar iron (TSI) agar culture, SIM (sulfide, indole, motility) agar culture, and oxidation-fermentation (OF) media culture (Merck, Darmstadt, Germany) were grown at 44 °C, used in the initial identification of isolates ¹⁸18. Ardebili A, Azimi L, Mohammadi-Barzelighi H, Owlia P, Beheshti M, Talebi M, et al. Determination of resistance pattern of isolated Acinetobacter baumannii from hospitalized burned patients in Motahari Hospital, Tehran. J Adv Med Biomed Res. 2012;20:112-9. , and then, submitted to PCR-sequencing of bla OXA-51-like gene to confirm the isolates as A. baumannii⁴4. Lari AR, Ardebili A, Hashemi A. AdeR-AdeS mutations & overexpression of the AdeABC efflux system in ciprofloxacin-resistant Acinetobacter baumannii clinical isolates. Indian J Med Res. 2018;147:413-21. . This sequencing was deposited in GenBank data library with the accession number MG920243. All isolates were stored in Luria-Bertani broth (Merck Co., Darmstadt, Germany) containing 20% glycerol at −70 °C for further use. A. baumannii ATCC^® 19606 (American Type Culture Collection, VA, USA) was used as the quality control.

Antimicrobial susceptibility testing

Susceptibility of A. baumannii isolates to three tetracyclines (Mast, Merseyside, UK), including tetracycline (30 μg), doxycycline (30 μg) and minocycline (30 μg) was evaluated by the Kirby-Bauer disk diffusion method according to the Clinical and Laboratory Standard Institute recommendations ¹⁰10. Chopra I, Roberts M. Tetracycline antibiotics: mode of action, applications, molecular biology, and epidemiology of bacterial resistance. Microbiol Mol Biol Rev. 2001;65:232-60.^,1919. Clinical and Laboratory Standards Institute. Performance standards for antimicrobial susceptibility testing: M100S. 26thed. Wayne: CLSI; 2016. . Pseudomonas aeruginosa ATCC^® 27853 (American Type Culture Collection, VA, USA) was used as the control.

Detection of active efflux phenotypes

The presence of active efflux systems was investigated in tetracycline-resistant isolates. The minimal inhibitory concentration (MIC) of tetracycline was determined by the agar dilution method before and after treatment of the efflux pump inhibitor with carbonylcyanide 3-chlorophenylhydrazone (CCCP) (Sigma-Aldrich, Dorset, United Kingdom) ²⁰20. Clinical and Laboratory Standards Institute. Method for dilution antimicrobial susceptibility tests for bacteria that grow aerobically, approved standard. 9thed. Wayne: CLSI; 2012.^,2121. Pumbwe L, Glass D, Wexler HM. Efflux pump overexpression in multiple-antibiotic-resistant mutants of Bacteroides fragilis. Antimicrob Agents Chemother. 2006;50:3150-3. . The addition of CCCP to Mueller-Hinton (M-H) agar plates led to increased intracellular concentration of the antibiotic, reducing the MIC in isolates having any active efflux pumps. Briefly, 50 μg/mL of CCCP were added to each M-H agar plates containing 0.5 to 1024 μg/mL of tetracycline. Then, the MIC of tetracycline was determined for all tetracycline-resistant isolates against the A. baumannii ATCC 19606^® (American Type Culture Collection, VA, USA). M-H agar plates with CCCP without antibiotic were used as controls. The effect of the efflux pump inhibitor was determined by the detection of a 4-fold or higher increment in the susceptibility after treatment with CCCP ²¹21. Pumbwe L, Glass D, Wexler HM. Efflux pump overexpression in multiple-antibiotic-resistant mutants of Bacteroides fragilis. Antimicrob Agents Chemother. 2006;50:3150-3. .

Polymerase chain reaction (PCR)

Genomic DNA was extracted by the boiling method. One to three colonies were dissolved in 500 μL of sterile distilled water in microtubes, and then placed in a boiling water bath at 100 °C for 10 min, and immediately centrifuged at 12000×g for 5 min. The supernatant containing total DNA was stored at −80 °C until further used. The presence of Tet efflux genes, tet(A) and tet(B) , was examined in tetracycline-resistant A. baumannii isolates using the following specific primers16. F, 5'-GCGCGATCTGGTTCACTCG-3' and R, 5'-AGTCGACAGYRGCGCCGGC-3' for tet(A) , and F, 5'-TACGTGAATTTATTGCTTCGG-3' and R, 5'-ATACAGCATCCAAAGCGCAC-3' for tet(B) . PCR amplification was performed in a total volume of 25 μL containing 12.5 μL of 2×Taq Master Mix RED (Ampliqon, Odense, Denmark) (150 mM Tris-HCl [pH 8.5], 40 mM (NH₄)₂SO₄, 4 mM MgCl₂, 0.2% Tween^® 20, 0.4 mM of each dNTP), 0.05 units/μL Ampliqon Taq DNA polymerase, 1 μL of 10 pmol of each primer, 1 μL (20 ng) of DNA template, and 9.5 μL of sterile distilled water. The thermal cycling protocol for PCR of both tet(A) and tet(B) genes was as initial denaturation at 94 °C for 5 min, followed by 30 cycles of denaturation at 94 °C for 1 min, annealing at 57 °C for 1 min, and extension at 72 °C for 1 min, with a final extension at 72 °C for 5 min. The PCR products were electrophoresed using 1.5% agarose gel with ethidium bromide and photographed under UV light.

Statistical data analysis

All obtained data were recorded, edited and entered using the SPSS statistic software package, version 18.0 (SPSS Inc., Chicago, IL, USA). The differences between categorical variables, including clinical specimen types, antibiotic resistance pattern, and distribution of tet genes were compared by the χ² (chi-square) test. A P -value <0.05 was considered as statistically significant.

RESULTS

Bacterial isolates and susceptibility testing

A total of 98 isolates of A. baumannii were obtained from patients, of which 66.36% (65/98) were from wounds and 33.67% (33/98) from respiratory tract infections of burned VAP patients, respectively. Doxycycline was the most active antibiotic tested, followed by minocycline and tetracycline, with susceptibility rates of 96.93% (95/98), 71.57% (68/98), and 43.87% (43/98), respectively ( Table 1 ). Among the 47 tetracycline-resistant isolates, 29.79% (14/47) were from burned patients and showed MIC values ranging from 128-256 μg/mL with both, MIC₅₀ and MIC₉₀ of 256 μg/mL, while 70.21% (33/47) were from VAP patients and had MIC ranges ranging from 32-1024 μg/mL, with MIC₅₀ and MIC₉₀ of 512 μg/mL and 1024 μg/mL, respectively. Except for doxycycline, resistance rates for both, tetracycline and minocycline, were significantly higher in VAP isolates than in isolates from burns (100% and 87.87% versus 21.53% and 1.53% of resistance against tetracycline and minocycline, respectively) (p<0.0001) ( Table 1 ).

Active efflux phenotypes

The MIC of tetracycline in A. baumannii tetracycline-resistant isolates was tested in the presence of CCCP. In the absence of CCCP, MICs ranged from 128-256 μg/mL and 32-1024 μg/mL, respectively, in isolates from burns and VAP ( Table 2 ). In the presence of CCCP, all tested isolates sshowed tetracycline MIC ranging from 2-128 μg/mL, with a 2-128-fold reduction compared to when CCCP was not added. Furthermore, all bacteria grew well in M-H agar plates with CCCP but without tetracycline (as control), indicating that 50 μg/mL CCCP had no intrinsic antibacterial activity.

Detection of tet efflux genes

PCR results were positive for the tet(B) gene in 61.7% (29/47) of tetracycline-resistant isolates, while none of the isolates carried the tet(A) gene. In addition, 38.3% of A. baumannii tested isolates (18/47) had no genes studied. The prevalence of tet(B) gene in burned and VAP isolates was 7.14% (1/14) and 84.84% (28/33), respectively (p<0.0001).

DISCUSSION

Due to the increased rate of A. baumannii resistance to most antimicrobial agents, evaluating the antimicrobial susceptibility of “old” antibiotics that are not used as first line drugs in clinical practice is of interest. This study showed adequate in vitro activity of doxycycline and minocycline in burned patients and only of doxycycline in VAP, showing promising clinical and microbiological effectiveness of tetracyclines either as monotherapy or in combination with other agents for the treatment of A. baumannii infections. Similarly, previous epidemiological studies reported high susceptibility rates of A. baumannii to doxycycline (100%) ²²22. Vila J, Marcos A, Marco F, Abdalla S, Vergara Y, Reig R, et al. In vitro antimicrobial production of beta-lactamases, aminoglycoside-modifying enzymes, and chloramphenicol acetyltransferase by and susceptibility of clinical isolates of Acinetobacter baumannii. Antimicrob Agents Chemother. 1993;37:138-41. and minocycline (56%-94.3%) ²³23. Adibhesami H, Douraghi M, Rahbar M, Abdollahi A. Minocycline activity against clinical isolates of multidrug-resistant Acinetobacter baumannii. Clin Microbiol Infect. 2015;21:e79-80.^,2424. Dimitriadis P, Protonotariou E, Varlamis S, Poulou A, Vasilaki O, Metallidis S, et al. Comparative evaluation of minocycline susceptibility testing methods in carbapenem-resistant Acinetobacter baumannii. Int J Antimicrob Agents. 2016;48:321-3. . In contrast, tetracycline exhibited no optimal antibacterial activity for the use in clinical practice. In a study by Adibhesami et al . ²³23. Adibhesami H, Douraghi M, Rahbar M, Abdollahi A. Minocycline activity against clinical isolates of multidrug-resistant Acinetobacter baumannii. Clin Microbiol Infect. 2015;21:e79-80. the number of minocycline and doxycycline-susceptible A. baumannii isolates was significantly higher than the number of tetracycline-susceptibleones. Maleki et al . ²⁵25. Maleki MH, Sekawi Z, Soroush S, Azizi-Jalilian F, Asadollahi K, Mohammadi S, et al. Phenotypic and genotypic characteristics of tetracycline resistant Acinetobacter baumannii isolates from nosocomial infections at Tehran hospitals. Iran J Basic Med Sci. 2014;17:21-6. have also found a resistance rate of 18% to doxycycline and 19% to minocycline against A. baumannii isolates, while 80% of isolates showed resistant to tetracycline. Additionally, VAP isolates showed high levels of resistance to tetracycline and high resistance rates to both, tetracycline and minocycline, in comparison with isolates from burned patients. The majority of VAP isolates carried the tet(B) gene in comparison with isolates from burned patients. Although the clinical outcomes of patients participating in the present study were not assessed, VAP infections due to A. baumannii have been associated with a high mortality rate, prolonged stay in the intensive care unit, and the rapid development of antimicrobial resistance to commonly used antimicrobials ²⁶26. Chang HC, Chen YC, Lin MC, Liu SF, Chung YH, Su MC, et al. Mortality risk factors in patients with Acinetobacter baumannii ventilator-associated pneumonia. J Formos Med Assoc. 2011;110:564-71. , indicating the increased risk of more serious infections in critically ill patients.

In addition, our study described A. baumannii isolates presenting with the efflux pump phenotype in tetracycline-resistant isolates recovered from burned and VAP patients. The results of the present study showed that the MIC for 43 of 47 tetracycline-resistant isolates (91.48%) was significantly reduced, by 4-16-fold in the presence of the efflux pump inhibitor. Similarly, Ardehali et al . ²⁷27. Ardehali SH, Azimi T, Fallah F, Owrang M, Aghamohammadi N, Azimi L. Role of efflux pumps in reduced susceptibility to tigecycline in Acinetobacter baumannii. New Microbes New Infect. 2019;30:100547. found that CCCP reduced considerably the MIC of 51.25% of tigecycline-resistant A. baumannii isolates by 2-4-fold. The MICs of isolates resistant to minocycline, doxycycline, and tetracycline in the presence of different efflux pump inhibitors, such as CCCP, phenyl-arginine-b-naphthylamide, 1-(1-naphthylmethyl)-piperazine, reserpine, and verapamil were significantly reduced ²⁸28. Meshkat Z, Salimizand H, Amini Y, Khakshoor M, Mansouri D, Farsiani H, et al. Molecular characterization and genetic relatedness of clinically Acinetobacter baumanii isolates conferring increased resistance to the first and second generations of tetracyclines in Iran. Ann Clin Microbiol Antimicrob. 2017;16:51. . Consistent with these findings, our results revealed that active efflux pumps could be involved in the increased rate of resistance to tetracycline in A. baumannii .

tet(A) and tet(B) determinants conferring efflux phenotypes of resistance to tetracycline have been known in A. baumannii isolates ¹²12. Grossman TH. Tetracycline antibiotics and resistance. Cold Spring Harb Perspect Med. 2016;6:a025387. . The prevalence of tet(B) and tet(A) genes have been reported in at least 50% and 14%-46% of tetracycline-resistant A. baumannii isolates ⁹9. Coyne S, Courvalin P, Périchon B. Efflux-mediated antibiotic resistance in Acinetobacter spp. Antimicrob Agents Chemother. 2011;55:947-53. . Our study showed a high prevalence (61.7%) of tet(B) but not of tet(A) gene in tetracycline-resistant isolates. Similarly, in two independenpt studies from Iran, Meshkat et al . ²⁸28. Meshkat Z, Salimizand H, Amini Y, Khakshoor M, Mansouri D, Farsiani H, et al. Molecular characterization and genetic relatedness of clinically Acinetobacter baumanii isolates conferring increased resistance to the first and second generations of tetracyclines in Iran. Ann Clin Microbiol Antimicrob. 2017;16:51. and Mosavat et al . ²⁹29. Mosavat A, Soleimanpour S, Farsiani H, Salimizand H, Kebriaei A, Jamehdar SA, et al. Moderate genetic diversity with extensive antimicrobial resistance among multidrug-resistant Acinetobacter baumannii in a referral hospital in Northeast Iran. Jundishapur J Microbiol. 2018;11:e14412. detected the tet(B) determinant in a significant percentage of A. baumannii isolates (100% and 95%, respectively); interestingly, tet(A) was not found in any of the isolates. These results were surprisingly different from those reported by other studies ⁸8. Huys G, Cnockaert M, Vaneechoutte M, Woodford N, Nemec A, Dijkshoorn L, et al. Distribution of tetracycline resistance genes in genotypically related and unrelated multiresistant Acinetobacter baumannii strains from different European hospitals. Res Microbiol. 2005;156:348-55.^,2525. Maleki MH, Sekawi Z, Soroush S, Azizi-Jalilian F, Asadollahi K, Mohammadi S, et al. Phenotypic and genotypic characteristics of tetracycline resistant Acinetobacter baumannii isolates from nosocomial infections at Tehran hospitals. Iran J Basic Med Sci. 2014;17:21-6.^,3030. Asadollahi P, Akbari M, Soroush S, Taherikalani M, Asadollahi K, Sayehmiri K, et al. Antimicrobial resistance patterns and their encoding genes among Acinetobacter baumannii strains isolated from burned patients. Burns. 2012;38:1198-203. . Importantly, the fact that there was neither tet(B) nor tet(A) in some isolates in this study indicates that additional genetic determinants other than tet genes may play a role in the expression of resistance to tetracycline in some of these strains ²⁷27. Ardehali SH, Azimi T, Fallah F, Owrang M, Aghamohammadi N, Azimi L. Role of efflux pumps in reduced susceptibility to tigecycline in Acinetobacter baumannii. New Microbes New Infect. 2019;30:100547.^,3131. Chen Y, Pi B, Zhou H, Yu Y, Li L. Triclosan resistance in clinical isolates of Acinetobacter baumannii. J Med Microbiol. 2009;58:1086-91.^–3333. Damier-Piolle L, Magnet S, Brémont S, Lambert T, Courvalin P. AdeIJK, a resistance-nodulation-cell division pump effluxing multiple antibiotics in Acinetobacter baumannii. Antimicrob Agents Chemother. 2008;52:557-62. .

In conclusion, doxycycline presented with a good activity and minocycline with a moderate activity, being promising drugs for the effective treatment of A. baumannii infections. In addition, this study revealed that resistance to tetracyclines in the studied isolates is mediated by active efflux pumps. Since tetracyclines are not routinely used to treat Acinetobacter infections, the presence of tetracycline-resistant strains is likely due to the spread of clones presenting with a higher prevalence of resistance determinants. Hygienic surveillance programs and stringent infection control strategies are needed to prevent further dissemination.

ACKNOWLEDGMENTS

The authors thank all the participating patients as well as the staff of the two hospitals, Shahid Motahari and Rasoul Akram, Iran University of Medical Sciences, Tehran, Iran for their support in the study.

REFERENCES

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