Abstract
We investigated the antimicrobial effects of colistin (CST) and tigecycline (TGC), either alone or in combination, on biofilm-dispersed and biofilm-embedded multidrug-resistant Acinetobacter baumannii (MDRAB) strains R1 and R2. The bacterial growth of biofilm-dispersed MDRAB was inhibited by CST or TGC. However, the inhibitory effects were attenuated by a combination of CST and low concentrations of TGC. The bactericidal effects of CST, but not TGC, were observed on biofilm-dispersed MDRAB. Notably, the bactericidal effects increased with a combination of CST and high concentrations of TGC, whereas they were attenuated with the combination of CST and low concentrations of TGC. Although biofilm formation by MDRAB decreased with increasing concentrations of CST or TGC, there was no complete disruption of the biofilms. Additionally, the biofilms increased with a combination of 1–2 μg/mL CST and TGC at 2 μg/mL and 2–4 μg/mL for strains R1 and R2, respectively. Biofilm-embedded MDRAB was eradicated with CST, but not TGC. Notably, the eradication effects increased with a combination of CST and high concentrations of TGC, whereas attenuation happened with the combination of CST and low concentrations of TGC. These results provide information on the combined effects of CST and TGC in the treatment of biofilm-associated MDRAB infection.
Similar content being viewed by others
Introduction
Acinetobacter baumannii is an important opportunistic pathogen associated with nosocomial infections, such as bacteremia, pneumonia, meningitis, urinary tract infections, and wound infections1,2. Additionally, A. baumannii is included among the six nosocomial pathogens: Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp. (ESKAPE) that acquire multidrug resistance and virulence3,4. Therefore, A. baumannii, especially multidrug-resistant A. baumannii (MDRAB), has gained importance as a human pathogen in hospital environments.
Although A. baumannii is regarded as a low-virulence pathogen5, recent studies have shown that A. baumannii exhibits several forms of pathogenicity, such as biofilm formation, adherence, invasion of lung epithelial cells, host cell death, and iron acquisition6. Recently, Colquhoun et al. hypothesized that biofilms are, at least in part, responsible for the high prevalence of A. baumannii nosocomial and recurrent infections because they frequently contaminate hospital surfaces and patient indwelling devices7. A. baumannii is capable of forming biofilms2,5,6; biofilm persister cells are protected from antimicrobial agents and immune responses and are therefore difficult to eliminate8, suggesting bacterial colonization in hosts and promoting persistent infections. Therefore, understanding A. baumannii biofilm formation, maturation, and dispersal is important for developing effective strategies to inhibit its growth and proliferation.
Colistin (CST) and tigecycline (TGC) are the last resort antibiotics used against a number of multidrug resistant bacteria9, although there have been reports of antibiotic resistance against these antibiotics worldwide10,11. Previous studies have suggested that a combination of TGC with CST, levofloxacin (LVX), amikacin (AMK), and imipenem (IPM) may be an effective therapy to synergistically prevent the emergence of resistance during treatment of MDRAB infections12,13. Moreover, Wang et al. reported the synergistic effects of the combinations of meropenem (MEPM), IPM, sulbactam (SBT), CST, and TGC on biofilm-embedded carbapenem-resistant A. baumannii and carbapenem-susceptible A. baumannii strains14. Meanwhile, other studies reported that no synergistic effects of CST and TGC were observed in A. baumannii clinical isolates15,16. Therefore, the combined effects of antibiotics on A. baumannii may depend on bacterial strains. Additionally, we have reported that clinical isolates of MDRAB showed different degrees of biofilm formation in the presence of sub-minimum inhibitory concentrations (sub-MICs) of CST and TGC17, suggesting that A. baumannii is emerging as a highly pathogenic bacterium and that the characteristics of A. baumannii vary under different environmental stress conditions, such as in the presence of multiple antimicrobial agents. Therefore, in this study, we focused on the combined effects of CST and TGC on MDRAB biofilms, that is, the inhibitory and bactericidal effects of these antibiotics on biofilm-dispersed and biofilm-embedded MDRAB. Furthermore, we analyzed the combined effects of CST and TGC on biofilms formed by MDRAB.
Results
Inhibitory and bactericidal effects of CST and TGC on biofilm-dispersed and biofilm-embedded MDRAB
We have previously reported the MICs of CST and TGC for MDRAB strains R1 and R2 in a previous study17. The MICs of CST on MDRAB strains R1 and R2 were at 2 μg/mL, and those of TGC were at 0.5 μg/mL, respectively (Table 1). We analyzed the bactericidal concentrations of CST and TGC on planktonic cells of MDRAB strains R1 and R2. The minimum bactericidal concentration (MBC) of CST on these cells was 8 μg/mL (i.e., a 4-fold increase in MIC) (Table 1). Meanwhile, the MBCs of TGC on these cells were > 256 and 256 μg/mL for R1 and R2, respectively (i.e., > 512 and 512-fold MIC increase, respectively) (Table 1). We further analyzed the inhibitory and bactericidal concentrations of CST and TGC on biofilm-dispersed MDRAB. Bacterial growth of biofilm-dispersed MDRAB strains R1 and R2 was inhibited with CST at 16 and 32 μg/mL (i.e., 8- and 16-fold MIC increase), and inhibited with TGC at 4 μg/mL, respectively (i.e., 8-fold MIC increase, respectively) (Table 1). The MBCs of CST on these cells were 32 μg/mL for R1 and R2, respectively (i.e., 16-fold MIC increase, respectively) (Table 1). Meanwhile, the MBCs of TGC on these cells were > 256 μg/mL for R1 and R2, respectively (i.e., > 512-fold MIC increase, respectively) (Table 1). Additionally, we analyzed the bactericidal concentrations of CST and TGC on biofilm-embedded MDRAB (i.e., minimum biofilm eradication concentrations: MBECs). The MBECs of CST on MDRAB strains R1 and R2 were 16 and 32 μg/mL, respectively (i.e., 8- and 16-fold MIC increase, respectively). Meanwhile, TGC had no bactericidal effects on MDRAB cells in strains R1 and R2, even at a concentration of 256 μg/mL (i.e., > 512-fold MIC increase) (Table 1). These results suggest that CST at 32 μg/mL has antibiotic effects not only for biofilm-dispersed but also for biofilm-embedded MDRAB, whereas TGC is an effective antibiotic for the inhibition of bacterial growth of biofilm-dispersed but not biofilm-embedded MDRAB.
Inhibitory effects of the combinations of CST and TGC on the bacterial growth of biofilm-dispersed MDRAB
We analyzed the inhibitory effects of combinations of CST and TGC on the growth of biofilm-dispersed MDRAB. The growth of biofilm-dispersed MDRAB strain R1 was inhibited with 16 μg/mL of CST and 4 μg/mL of TGC (Tables 1 and 2). However, the inhibitory effects were slightly attenuated with the combination of CST at 16 μg/mL and TGC at 0.25–1 μg/mL (Table 2). Additionally, the inhibitory effect of CST at 8 μg/mL was significantly attenuated with the combination of TGC at 0.5 μg/mL (Table 2). Bacterial growth of biofilm-dispersed MDRAB strain R2 was inhibited with 32 μg/mL of CST and 4 μg/mL of TGC, respectively (Tables 1 and 3). However, the inhibitory effects were slightly attenuated by the combination of CST at 8 and 16 μg/mL and TGC at 0.25–1 μg/mL (Table 3). These results suggest that the inhibitory effects of CST on the bacterial growth of biofilm-dispersed MDRAB were attenuated when used in combination with low concentrations of TGC.
Bactericidal effects of combinations of CST and TGC on biofilm-dispersed MDRAB
We further analyzed the bactericidal effects of combinations of CST and TGC on biofilm-dispersed MDRAB. The MBC of CST on biofilm-dispersed MDRAB strain R1 was 32 μg/mL, whereas TGC had no bactericidal effect even with treatment at 256 μg/mL (Tables 1 and 4). Meanwhile, the synergistic bactericidal effect of CST at 16 μg/mL in combination with TGC at > 1 μg/mL were observed in these cells (Table 4). However, the bactericidal effects of CST at 16 and 32 μg/mL were attenuated when used in combination with TGC at < 1 μg/mL (Table 4). The MBC of CST on biofilm-dispersed MDRAB strain R2 was 32 μg/mL, whereas that of TGC on these cells was > 256 μg/mL (Tables 1 and 5). Meanwhile, the synergistic bactericidal effects of CST at 16 μg/mL in combination with TGC at > 1 μg/mL were observed in these cells (Table 5). However, the bactericidal effects of CST at 16 and 32 μg/mL were attenuated when used in combination with 0.5 μg/mL of TGC (Table 5). These results suggest that the CST-TGC combination exhibits synergistic bactericidal effects on biofilm-dispersed MDRAB; however, the bactericidal effects of CST on these cells are attenuated when used in combination with low concentrations of TGC.
Bactericidal effects of combinations of CST and TGC on biofilm-embedded MDRAB
We analyzed the bactericidal effects of the combinations of CST and TGC on biofilm-embedded MDRAB, that is, the biofilm eradication effects of these antibiotics. The MBEC of CST on biofilm-embedded MDRAB strain R1 was 16 μg/mL, whereas no bactericidal effect was observed even when 256 μg/mL of TGC was used on these cells (Tables 1 and 6). Meanwhile, synergistic bactericidal effects of CST at 8 μg/mL on these cells were observed when used in combination with 128 μg/mL of TGC (Table 6). However, the bactericidal effects of CST at 8–32 μg/mL were attenuated when used in combination with < 32 μg/mL of TGC (Table 6). Similarly, the MBEC of CST on biofilm-embedded MDRAB strain R2 was 32 μg/mL, whereas no bactericidal effect was observed even with treatment of 256 μg/mL of TGC on these cells (Tables 1 and 7). Meanwhile, a synergistic bactericidal effect of CST at 16 μg/mL on these cells was observed when used in combination with 32 μg/mL of TGC (Table 7). However, the bactericidal effects of CST at 16 μg/mL were attenuated when used in combination with 0.5–2 μg/mL of TGC (Table 7). Additionally, the inhibitory effects of TGC at 128 μg/mL were attenuated when used in combination with 2 μg/mL of CST on biofilm-embedded MDRAB strains R1and R2 (Tables 6 and 7). These results suggest that the combination of CST and a high concentration of TGC, except for when used in combination with 2 μg/mL of CST and 128 μg/mL of TGC, exhibits synergistic bactericidal effects on biofilm-embedded MDRAB; however, the bactericidal effects of CST on these cells were attenuated when used in combination with low concentrations of TGC.
Effects of CST and TGC used alone or in combination on biofilm formation of MDRAB
We further analyzed whether CST and TGC affected the biofilms formed by MDRAB. Biofilms formed by MDRAB of strains R1 and R2 decreased depending on the concentration of CST, whereas they decreased slightly depending on the concentration of TGC (Tables 8 and 9). However, the biofilms formed by MDRAB strain R1 significantly increased with the combination of 1 μg/mL of CST and 2 μg/mL of TGC (Table 8). Meanwhile, biofilms formed by MDRAB in strain R2 increased with the combination of 1–2 μg/mL of CST and 2–4 μg/mL of TGC (Table 9). Additionally, there was no synergistic disruptive effect of the combination of CST and TGC on these biofilms (Tables 8 and 9).
Discussion
Acinetobacter baumannii has recently emerged as a major nosocomial pathogen1,2, and an increase in outbreaks of MDRAB worldwide is becoming a cause of concern3,4. Additionally, it is possible that A. baumannii causes biofilm-associated infections, such as bacteremia, via patient indwelling devices5,7,18,19 because A. baumannii is capable of forming biofilms2,5,6. Khazaal et al. suggested that biofilms formed in endotracheal tubes lead to the development of ventilator-associated pneumonia (VAP)20. Moreover, catheter-related urinary or bloodstream infections are caused by biofilm-forming strains21. Therefore, biofilm formation is thought to be an important pathogenic feature, especially in relation to intravascular line infections and VAP, so treatment strategies for inhibition of biofilm formation may lead to a reduced risk of severe A. baumannii infection.
CST and TGC remain the only effective antibiotics for the treatment of MDRAB9. CST is an old antibiotic member of the polymyxin family, which are membrane-active peptides with bactericidal capabilities that can disrupt the outer bacterial cell membrane22. It is currently used as a last-resort antibiotic for the treatment of multidrug-resistant gram-negative bacterial infections23. Meanwhile, TGC is a member of the glycylcycline class of semisynthetic antimicrobial agents developed for the treatment of polymicrobial infections caused by multidrug-resistant gram-positive and gram-negative bacteria and acts as a bacteriostatic agent against these bacteria24. In fact, the bactericidal effects of CST were observed on biofilm-dispersed and biofilm-embedded MDRAB, whereas TGC had no bactericidal effect on these cells. These results reflect the reasonable action of these antibiotics. Furthermore, we demonstrated that the combination of CST and TGC exhibited synergistic bactericidal effects on biofilm-dispersed and biofilm-embedded MDRAB. However, although the synergistic effects of CST on these cells increased when used in combination with high concentrations of TGC, they were attenuated when used in combination with low concentrations of TGC. It remains unclear why the antibiotic activity of CST on MDRAB is attenuated when used in combination with low concentrations of TGC. Efflux pumps play an important role in antimicrobial resistance and virulence for A. baumannii25. Lin et al. reported that EmrB-deleted mutant of A. baumannii was more susceptible to CST, suggesting that EmrAB pump systems in A. baumannii contribute to the resistance to CST26. Additionally, Cheng et al. reported that the expression of efflux pumps including EmrAB in A. baumannii upregulated under the pressure of TGC at a low concentration27. With considering these results, we speculate that bactericidal effects of CST were attenuated when used in combination with low concentrations of TGC because of EmrAB efflux pumps upregulated by TGC at low concentrations. Additionally, these results suggest that the antibiotic resistance characteristics of A. baumannii vary under different environmental stress conditions (e.g., changes in antibiotic concentrations, combination of various antibiotics, etc.). We previously reported that clinical isolates of MDRAB showed different degrees of biofilm formation in the presence of sub-MICs of CST and TGC17. Moreover, we demonstrated that biofilm formation by MDRAB increased even more upon treatment with CST in combination with TGC at concentrations less than the MBC, suggesting that the characteristics of A. baumannii vary in the presence of antibiotics at low concentrations. We have reported that the number of biofilm cells was positively and significantly correlated with the mRNA levels of genes encoding efflux pumps (adeB and adeG) and autoinducer synthase (abaI), which are biofilm-related genes in MDRAB strain R2 in the presence of CST17. Additionally, several reports demonstrated that mRNA levels of genes encoding efflux pumps, porins, virulence factors, and biofilm-related genes in A. baumannii were altered in the presence of various antibiotics at sub-MICs28,29. Therefore, we speculate that the expression of biofilm-related genes in biofilm-embedded MDRAB is altered in the presence of CST and TGC because these cells are exposed to low concentrations of antibiotics that slightly infiltrate into biofilms. Therefore, exposure to a lethal dose of bactericidal concentrations of CST and TGC in patients is necessary for the treatment of A. baumannii infection.
In summary, we demonstrated the combined effects of CST and TGC on biofilm-dispersed MDRAB, biofilm-embedded MDRAB, and biofilms formed by MDRAB. Since MDRAB clinical isolates showed different characteristics upon treatment with antibiotics, further studies are required to understand the mechanism of the biofilm-related characteristics of A. baumannii in the presence of antibiotics.
Materials and methods
All methods were carried out in accordance with relevant guidelines and regulations.
Bacterial strains and growth conditions
R1 and R2 strains of A. baumannii were isolated from the Teikyo University Hospital during an outbreak that occurred around 2010. The bacteria were isolated on CHROMagar™ Acinetobacter and incubated for 24 h at 37 °C. The R1 strain was isolated from the sputum of a patient with interstitial pneumonia. The R2 strain was isolated from a urine sample of a patient with malignant lymphoma and pneumonia. The isolates were streaked onto blood agar plates and cultivated for 24 h to obtain monoclonal colonies and were identified as A. baumannii through DNA sequencing of the partial RNA polymerase β-subunit (rpoB) gene30. Additionally, the isolates were confirmed to be non-clonal via pulsed-field gel electrophoresis (data not shown). After identification, the isolates were stored in glycerol stocks at − 80 °C at the Department of Microbiology & Immunology, Teikyo University School of Medicine. Antimicrobial susceptibility testing was performed using two strains of A. baumannii based on the MICs of IPM, AMK, and ciprofloxacin (CPFX). Against these two strains, the MICs of IPM, AMK, and CPFX were > 8, > 32, and > 2 mg/L, respectively. Thus, these strains were identified as MDRAB strains. The MIC of CST against MDRAB in strains R1 and R2 was determined to be 2 mg/L17. The MIC of TGC against these strains was found to be 0.5 mg/L17. These bacteria were cultured on Luria–Bertani (LB) agar plates (Becton, Dickinson and Company, MD, USA) for 16 h at 37 °C. Thereafter, the bacteria were suspended in LB broth at a concentration of OD595 = 0.1, then the concentration was adjusted via optical density (OD) measurements at 595 nm. The bacterial suspensions obtained were used for biofilm formation.
Determination of inhibitory and bactericidal effects of antibiotics on biofilm-dispersed MDRAB, biofilm-embedded MDRAB, and biofilms formed by MDRAB
To analyze the combined effects of CST and TGC on biofilm-dispersed MDRAB, biofilm-embedded MDRAB, and biofilms formed by MDRAB, bacterial strains were added to 96-well microtiter plates containing the Biofilm Formation Assay Kit or Biofilm Viability Assay Kit (DOJINDO, Kumamoto, Japan)31. Then, the plate was covered with a 96-pin microtiter plate lid and incubated for 24 h at 37 °C. After incubation, the 96-pin lid with established biofilms was washed three times with sterile PBS and then placed onto a fresh 96-well microtiter plate with each well containing LB with various concentrations of antibiotics. After incubation for 24 h at 37 °C, to analyze the inhibitory effects of antibiotics on biofilm-dispersed MDRAB, the 96-pin lid was removed and the culture broth was measured at A595. To analyze the bactericidal effects of antibiotics on biofilm-dispersed MDRAB, 5 μL of culture broth was plated onto LB agar, and the presence of viable cells was confirmed through the growth from the bacterial suspension after 24 h of incubation at 37 °C. To analyze the number of biofilm cells, the 96-pin lid was washed three times with sterile PBS and then placed onto a fresh 96-well microtiter plate with each well containing 0.1% crystal violet solution. After staining for 30 min, the 96-pin lid with stained biofilms was washed three times with sterile PBS to remove unreacted crystal violet. Then, the 96-pin lid was placed onto a fresh 96-well microtiter plate with each well containing 99.5% ethanol and extracted for 15 min. The amount of crystal violet extracted was measured using A595. The viability of biofilm-embedded MDRAB was determined using the Biofilm Viability Assay Kit (DOJINDO) according to the manufacturer’s protocol. After the incubation of biofilms in the presence of antibiotics, the 96-pin lid was washed three times with sterile PBS to remove planktonic and nonattached cells and then placed onto a fresh 96-well microtiter plate with each well containing LB broth with WST solution. After incubation for 24 h, the 96-pin lid was removed, and the LB broth was measured at A450.
References
Dijkshoorn, L., Nemec, A. & Seifert, H. An increasing threat in hospitals: Multidrug-resistant Acinetobacter baumannii. Nat. Rev. Microbiol. 5, 939–951 (2007).
Antunes, L. C., Visca, P. & Towner, K. J. Acinetobacter baumannii: Evolution of a global pathogen. Pathog. Dis. 71, 292–301 (2014).
Rice, L. B. Federal funding for the study of antimicrobial resistance in nosocomial pathogens: No ESKAPE. J. Infect. Dis. 197, 1079–1081 (2008).
Mulani, M. S. et al. Emerging strategies to combat ESKAPE pathogens in the era of antimicrobial resistance: A review. Front. Microbiol. 10, 539. https://doi.org/10.3389/fmicb.2019.00539 (2019).
Peleg, A. Y., Seifert, H. & Paterson, D. L. Acinetobacter baumannii: Emergence of a successful pathogen. Clin. Microbiol. Rev. 21, 538–582 (2008).
Uppalapati, S. R. et al. The outer membrane proteins OmpA, CarO, and OprD of Acinetobacter baumannii confer a two-pronged defense in facilitating its success as a potent human pathogen. Front. Microbiol. 11, 589234. https://doi.org/10.3389/fmicb.2020.589234 (2020).
Colquhoun, J. M. et al. Insights into mechanisms of biofilm formation in Acinetobacter baumannii and implications for uropathogenesis. Front. Cell. Infect. Microbiol. 10, 253. https://doi.org/10.3389/fcimb.2020.00253 (2020).
Lewis, K. Riddle of biofilm resistance. Antimicrob. Agents Chemother. 45, 999–1007 (2001).
Osei Sekyere, J. et al. Colistin and tigecycline resistance in carbapenemase-producing Gram-negative bacteria: Emerging resistance mechanisms and detection methods. J. Appl. Microbiol. 121, 601–617 (2016).
Cai, Y. et al. Colistin resistance of Acinetobacter baumannii: Clinical reports, mechanisms and antimicrobial strategies. J. Antimicrob. Chemother. 67, 1607–1615 (2012).
Al-Sweih, N. A., Al-Hubail, M. A. & Rotimi, V. O. Emergence of tigecycline and colistin resistance in Acinetobacter species isolated from patients in Kuwait hospitals. J. Chemother. 223, 13–16 (2011).
Principe, L. et al. In vitro activity of tigecycline in combination with various antimicrobials against multidrug resistant Acinetobacter baumannii. Ann. Clin. Microbiol. Antimicrob. 8, 18. https://doi.org/10.1186/1476-0711-8-18 (2009).
Cai, X. et al. Pharmacodynamics of tigecycline alone and in combination with colistin against clinical isolates of multidrug-resistant Acinetobacter baumannii in an in vitro pharmacodynamic model. Int. J. Antimicrob. Agents. 49, 609–616 (2017).
Wang, Y. C. et al. Individual or combined effects of meropenem, imipenem, sulbactam, colistin, and tigecycline on biofilm-embedded Acinetobacter baumannii and biofilm architecture. Antimicrob. Agents Chemother. 60, 4670–4676 (2016).
Petersen, P. J., Labthavikul, P., Jones, C. H. & Bradford, P. A. In vitro antibacterial activities of tigecycline in combination with other antimicrobial agents determined by chequerboard and time-kill kinetic analysis. J. Antimicrob. Chemother. 57, 573–576 (2006).
Arroyo, L. A., Mateos, I., González, V. & Aznar, J. In vitro activities of tigecycline, minocycline, and colistin-tigecycline combination against multi- and pandrug-resistant clinical isolates of Acinetobacter baumannii group. Antimicrob. Agents Chemother. 53, 1295–1296 (2009).
Sato, Y. et al. Sub-minimum inhibitory concentrations of colistin and polymyxin B promote Acinetobacter baumannii biofilm formation. PLoS ONE 13, e0194556. https://doi.org/10.1371/journal.pone.0194556 (2018).
Di Venanzio, G. et al. Urinary tract colonization is enhanced by a plasmid that regulates uropathogenic Acinetobacter baumannii chromosomal genes. Nat. Commun. 10, 2763. https://doi.org/10.1038/s41467-019-10706-y (2019).
Chen, H. P. et al. Predictors of mortality in Acinetobacter baumannii bacteremia. J. Microbiol. Immunol. Infect. 38, 127–136 (2005).
Khazaal, S. S. et al. Immunomodulation by Acinetobacter baumannii of endotracheal tube biofilm in ventilator-associated pneumonia. Meta Gene 24, 100672. https://doi.org/10.1016/j.mgene.2020.100672 (2020).
Rodríguez-Baño, J. et al. Biofilm formation in Acinetobacter baumannii: Associated features and clinical implications. Clin. Microbiol. Infect. 14, 276–278 (2008).
Hancock, R. E. Peptide antibiotics. Lancet 349, 418–422 (1997).
Olaitan, A. O. et al. Mechanisms of polymyxin resistance: Acquired and intrinsic resistance in bacteria. Front. Microbiol. 5, 643. https://doi.org/10.3389/fmicb.2014.00643 (2014).
Yaghoubi, S. et al. Tigecycline antibacterial activity, clinical effectiveness, and mechanisms and epidemiology of resistance: Narrative review. Eur. J. Clin. Microbiol. Infect. Dis. 5, 1–20 (2021).
Ayoub Moubareck, C. et al. Insights into Acinetobacter baumannii: A review of microbiological, virulence, and resistance traits in a threatening nosocomial pathogen. Antibiotics 9, 119. https://doi.org/10.3390/antibiotics9030119 (2020).
Lin, M. F., Lin, Y. Y. & Lan, C. Y. Contribution of EmrAB efflux pumps to colistin resistance in Acinetobacter baumannii. J. Microbiol. 55, 130–136 (2017).
Cheng, J. et al. Genome and transcriptome analysis of A. baumannii’s “Transient” increase in drug resistance under tigecycline pressure. J. Glob. Antimicrob. Resist. 22, 219–225 (2020).
He, X. et al. Biofilm formation caused by clinical Acinetobacter baumannii isolates is associated with overexpression of the AdeFGH efflux pump. Antimicrob. Agents Chemother. 59, 4817–4825 (2015).
Navidifar, T., Amin, M. & Rashno, M. Effects of sub-inhibitory concentrations of meropenem and tigecycline on the expression of genes regulating pili, efflux pumps and virulence factors involved in biofilm formation by Acinetobacter baumannii. Infect. Drug Resist. 12, 1099–1111 (2019).
La Scola, B., Gundi, V. A., Khamis, A. & Raoult, D. Sequencing of the rpoB gene and flanking spacers for molecular identification of Acinetobacter species. J. Clin. Microbiol. 44, 827–832 (2006).
Tsukatani, T. et al. A rapid and simple measurement method for biofilm formation inhibitory activity using 96-pin microtiter plate lids. World J. Microbiol. Biotechnol. 36, 189. https://doi.org/10.1007/s11274-020-02964-6 (2020).
Acknowledgements
This research was supported by JSPS KAKENHI (Grant Number 20K08827 and 21K08516). We thank our colleagues from the Department of Microbiology and Immunology, Teikyo University School of Medicine, for their constructive discussions regarding this study. We thank Honyaku Center Inc. (www.honyakuctr.com/) for editing the draft of this manuscript.
Author information
Authors and Affiliations
Contributions
Y.S. and Y.O. conducted the experiments. Y.S. performed the experiments and analyzed the data. Y.S., T.U., S.T.-N, and Y.Y. validated the data. Y.S. prepared the manuscript. All authors contributed to the scientific discussion of the manuscript.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Sato, Y., Ubagai, T., Tansho-Nagakawa, S. et al. Effects of colistin and tigecycline on multidrug-resistant Acinetobacter baumannii biofilms: advantages and disadvantages of their combination. Sci Rep 11, 11700 (2021). https://doi.org/10.1038/s41598-021-90732-3
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-021-90732-3
This article is cited by
-
Murraya koenigii (L.) Sprengel seeds and pericarps in relation to their chemical profiles: new approach for multidrug resistant Acinetobacter baumannii ventilator-associated pneumonia
Applied Biological Chemistry (2024)
-
The use of combination therapy for the improvement of colistin activity against bacterial biofilm
Brazilian Journal of Microbiology (2024)
-
Multiple heteroresistance to tigecycline and colistin in Acinetobacter baumannii isolates and its implications for combined antibiotic treatment
Journal of Biomedical Science (2023)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.
