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The innate resistome of “recalcitrant” Acinetobacter baumannii and the role of nanoparticles in combating these MDR pathogens

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Abstract

Acinetobacter baumannii, a nosocomial pathogen, and member of ESKAPE bacteria are currently a global threat. A. baumannii is equipped naturally laden with strong intrinsic resistance factors and is also capable of acquiring many resistance determinants against different antibiotic classes. Intrinsic resistome is defined as a mechanism of antibiotic resistance that is innately expressed/chromosomally encoded, irrespective of prior antibiotic exposure. Although these innate resistance factors are themselves poorly effective in conferring a high-level resistance, together with other resistance factors their force can be large enough to confer an organism multidrug resistant (MDR). In A. baumannii, which are predominantly of environmental origin (an opportunistic pathogen), weight on the impact of extreme resistance and evolution is often laid on their intrinsic antibiotic resistance phenotype. This review is focused on emphasizing the role of intrinsic resistome involved in the antibiotic resistance of A. baumannii, the understanding of which will be very helpful in combating this opportunistic pathogen. With a dead-end in the treatment of infections due to MDR A. baumannii, different avenues have to be explored for a better treatment option. This review will also discuss the application of nanoparticles as antimicrobials and as a conjugate for restoring the bioactivity of the available drugs against MDR pathogens.

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Abbreviations

ESKAPE:

Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species

MDR:

Multidrug-resistant

XDR:

Extensive drug-resistant

PDR:

Pan-drug resistant

BAP:

Biofilm-associated protein

LPS:

Lipopolysaccharides

OMVs:

Outer membrane vesicles

PBP:

Penicillin-binding proteins

ADC:

Acinetobacter-derived cephalosporinases

RND:

Resistance nodulation division

CRAB:

Carbapenem-resistant

MBL:

Metallo β-lactamase

CHDLs:

Chromosomally mediated carbapenem hydrolyzing oxacillinase

OMPs:

Outer membrane proteins

CarO:

Carbapenem resistance-associated Omp

MFS:

Major facilitator superfamily

MATE:

Multidrug and toxic compound extrusion

QRDRs:

Quinolone resistance-determining regions

NP:

Nanoparticles

ROS:

Reactive-oxygen species

Ag:

Silver, Au- Gold, CeO2-cerium oxide nanoparticles

FeO:

Ferrous oxide

Cu:

Copper

NiO:

Nickle oxide

ZnO:

Zinc oxide

TiO2 :

Titanium dioxide

Al2O3 :

Aluminium oxide

References

  • Adams MD, Nickel GC, Bajaksouzian S et al (2009) Resistance to colistin in Acinetobacter baumannii associated with mutations in the Pmrab two-component system. Antimicrob Agents Chemother 53:3628–3634

    Article  CAS  Google Scholar 

  • Alvarez-Ortega C, Wiegand I, Olivares J et al (2011) The intrinsic resistome of pseudomonas aeruginosa to β-lactams. Virulence 2:144–146

    Article  Google Scholar 

  • Ansari MA, Khan HM, Alzohairy MA et al (2015) Green synthesis of Al2O3 nanoparticles and their bactericidal potential against clinical isolates of multi-drug resistant pseudomonas aeruginosa. World J Microbiol Biotechnol 31:153–164

    Article  CAS  Google Scholar 

  • Ashajyothi C, Harish KH, Dubey N et al (2016) Antibiofilm activity of biogenic copper and zinc oxide nanoparticles-antimicrobials collegiate against multiple drug resistant bacteria: a nanoscale approach. J Nanostructure Chem 6:329–341

    Article  CAS  Google Scholar 

  • Aydemir H, Akduman D, Piskin N et al (2013) Colistin Vs. the combination of colistin and rifampicin for the treatment of carbapenem-resistant Acinetobacter baumannii ventilator-associated pneumonia. Epidemiol Infect 141:1214–1222

    Article  CAS  Google Scholar 

  • Banoee M, Seif S, Nazari ZE et al (2010) Zno Nanoparticles enhanced antibacterial activity of ciprofloxacin against Staphylococcus aureus and Escherichia coli. J Biomed Mat Res 93:557–561

    Article  Google Scholar 

  • Baptista PV, McCusker MP, Carvalho A et al (2018) Nano-strategies to fight multidrug resistant bacteria—“a battle of the titans.” Front Microbiol 9:1441

    Article  Google Scholar 

  • Baranwal A, Srivastava A, Kumar P et al (2018) Prospects of nanostructure materials and their composites as antimicrobial agents. Front Microbiol 9:422

    Article  Google Scholar 

  • Behdad R, Pargol M, Mirzaie A et al (2020) Efflux pump inhibitory activity of biologically synthesized silver nanoparticles against multidrug-resistant Acinetobacter baumannii clinical isolates. J Basic Microbiol 60:494–507

    Article  CAS  Google Scholar 

  • Bellio P, Luzi C, Mancini A et al (2018) Cerium oxide nanoparticles as potential antibiotic adjuvant. Effects of Ceo2 nanoparticles on bacterial outer membrane permeability. Biochim Biophys Acta Biomembr 1860:2428–2435

    Article  CAS  Google Scholar 

  • Bhattacharya M, Toth M, Antunes NT et al (2014) Structure of the extended-spectrum class C β-lactamase Adc-1 from Acinetobacter baumannii. Acta Crystallogr D Biol Crystallogr 70:760–771

    Article  CAS  Google Scholar 

  • Bogaerts P, Naas T, El Garch F et al (2010) Ges extended-spectrum β-lactamases in acinetobacter baumannii isolates in Belgium. Antimicrob Agents Chemother 54:4872–4878

    Article  CAS  Google Scholar 

  • Bou G, Cerveró G, Dominguez MA et al (2000) Characterization of a nosocomial outbreak caused by a multiresistant Acinetobacter baumannii strain with a carbapenem-hydrolyzing enzyme: high-level carbapenem resistance Ina. baumannii is not due solely to the presence of β-lactamases. J Clin Microbiol 38:3299–3305

    Article  CAS  Google Scholar 

  • Brown S, Amyes S (2005) Oxa β-lactamases in acinetobacter: the story so far. J Antimicro Chemother 57:1–3

    Article  Google Scholar 

  • Burygin G, Khlebtsov B, Shantrokha A et al (2009) On the enhanced antibacterial activity of antibiotics mixed with gold nanoparticles. Nanoscale Res Lett 4:794–801

    Article  CAS  Google Scholar 

  • Cai Y, Chai D, Wang R et al (2012) Colistin resistance of Acinetobacter baumannii: clinical reports, mechanisms and antimicrobial strategies. J Antimicrob Chemother 67:1607–1615

    Article  CAS  Google Scholar 

  • Carré G, Hamon E, Ennahar S et al (2014) Tio2 photocatalysis damages lipids and proteins in Escherichia coli. Appl Environ Microbiol 80:2573–2581

    Article  Google Scholar 

  • Catel-Ferreira M, Marti S, Guillon L et al (2016) The outer membrane porin Ompw of Acinetobacter baumannii is involved in iron uptake and colistin binding. FEBS Lett 590:224–231

    Article  CAS  Google Scholar 

  • Chamundeeswari M, Sobhana SL, Jacob JP et al (2010) Preparation, characterization and evaluation of a biopolymeric gold nanocomposite with antimicrobial activity. Biotechnol Appl Biochem 55:29–35

    Article  CAS  Google Scholar 

  • Chapartegui-Gonzalez I, Lazaro-Diez M, Bravo Z et al (2018) Acinetobacter baumannii maintains its virulence after long-time starvation. PLoS ONE 13:e0201961

    Article  Google Scholar 

  • Choi O, Deng KK, Kim N-J et al (2008) The inhibitory effects of silver nanoparticles, silver ions, and silver chloride colloids on microbial growth. Water Res 42:3066–3074

    Article  CAS  Google Scholar 

  • Chopra S, Galande A (2011) A fluoroquinolone-resistant Acinetobacter baumannii without the quinolone resistance-determining region mutations. J Antimicrob Chemother 66:2668–2670

    Article  CAS  Google Scholar 

  • Christena LR, Mangalagowri V, Pradheeba P et al (2015) Copper nanoparticles as an efflux pump inhibitor to tackle drug resistant bacteria. RSC Adv 5:12899–12909

    Article  CAS  Google Scholar 

  • Corbella X, Ariza J, Ardanuy C et al (1998) Efficacy of sulbactam alone and in combination with ampicillin in nosocomial infections caused by multiresistant Acinetobacter baumannii. J Antimicrob Chemother 42:793–802

    Article  CAS  Google Scholar 

  • Coyne S, Courvalin P, Perichon B (2011) Efflux-mediated antibiotic resistance in Acinetobacter spp. Antimicrob Agents Chemother 55:947–953

    Article  CAS  Google Scholar 

  • Coyne S, Guigon G, Courvalin P et al (2010) Screening and quantification of the expression of antibiotic resistance genes in Acinetobacter baumannii with a microarray. Antimicrob Agents Chemother 54:333–340

    Article  CAS  Google Scholar 

  • Damier-Piolle L, Magnet S, Brémont S et al (2008) AdeIJK, a resistance-nodulation-cell division pump effluxing multiple antibiotics in Acinetobacter baumannii. Antimicrob Agents Chemother 52:557–562

    Article  CAS  Google Scholar 

  • Durante-Mangoni E, Signoriello G, Andini R et al (2013) Colistin and rifampicin compared with colistin alone for the treatment of serious infections due to extensively drug-resistant Acinetobacter baumannii: a multicenter, randomized clinical trial. Clin Infect Dis 57:349–358

    Article  CAS  Google Scholar 

  • Egger S, Lehmann RP, Height MJ et al (2009) Antimicrobial properties of a novel silver-silica nanocomposite material. Appl Environ Microbiol 75:2973–2976

    Article  CAS  Google Scholar 

  • Evans AB, Hamouda A, Amyes GBS (2013) The rise of carbapenem-resistant Acinetobacter baumannii. Curr Pharm Des 19:223–238

    Article  CAS  Google Scholar 

  • Fajardo A, Martínez-Martín N, Mercadillo M et al (2008) The neglected intrinsic resistome of bacterial pathogens. PLoS ONE 3:e1619

    Article  Google Scholar 

  • Fakhri A, Tahami S, Naji MJJ et al (2017) Synthesis and characterization of core-shell bimetallic nanoparticles for synergistic antimicrobial effect studies in combination with doxycycline on burn specific pathogens. J Photochem Photobiol B Biol 169:21–26

    Article  CAS  Google Scholar 

  • Falagas ME, Vardakas KZ, Roussos NS (2015) Trimethoprim/sulfamethoxazole for acinetobacter spp.: a review of current microbiological and clinical evidence. Int J Antimicrob Agents 46:231–241

    Article  CAS  Google Scholar 

  • Fernández-Reyes M, Rodríguez-Falcón M, Chiva C et al (2009) The cost of resistance to colistin in Acinetobacter baumannii: a proteomic perspective. Proteomics 9:1632–1645

    Article  Google Scholar 

  • Forsberg KJ, Reyes A, Wang B et al (2012) The shared antibiotic resistome of soil bacteria and human pathogens. Science 337:1107–1111

    Article  CAS  Google Scholar 

  • Furlan JPR, de Almeida OGG, De Martinis ECP et al (2019) Characterization of an environmental multidrug-resistant Acinetobacter seifertii and comparative genomic analysis reveals co-occurrence of antimicrobial resistance and metal tolerance determinants. Front Microbiol 10:2151

    Article  Google Scholar 

  • Fyfe C, Grossman TH, Kerstein K et al (2016) Resistance to macrolide antibiotics in public health pathogens. Cold Spring Harb Perspect Med 6:a025395

    Article  Google Scholar 

  • Gan H M, Wengert P, Penix T et al (2019) Insight into the resistome and quorum sensing system of a divergent Acinetobacter Pittii isolate from an untouched site of the lechuguilla cave. bioRxiv 745182

  • Gao W, Zhang LJNRM (2020) Nanomaterials arising amid antibiotic resistance. Nat Rev Microbiol 19(1):5–6

    Article  Google Scholar 

  • Gehrlein M, Leying H, Cullmann W et al (1991) Imipenem resistance in Acinetobacter baumanii is due to altered penicillin-binding proteins. Chemotherapy 37:405–412

    Article  CAS  Google Scholar 

  • Gleckman R, Blagg N, Joubert DW (1981) Trimethoprim: mechanisms of action, antimicrobial activity, bacterial resistance, pharmacokinetics, adverse reactions, and therapeutic indications. Pharmacotherapy 1:14–20

    Article  CAS  Google Scholar 

  • Govindaraju K, Vasantharaja R, Suganya KU et al (2020) Unveiling the Anticancer and Antimycobacterial Potentials of Bioengineered Gold Nanoparticles. Process Biochem 96:213–219

    Article  CAS  Google Scholar 

  • Grossman TH (2016) Tetracycline antibiotics and resistance. Cold Spring Harb Perspect Med 6:a025387

    Article  Google Scholar 

  • Gu H, Ho P, Tong E et al (2003) Presenting vancomycin on nanoparticles to enhance antimicrobial activities. Expert Rev Anti Infect Ther 3:1261–1263

    CAS  Google Scholar 

  • Hackel MA, Tsuji M, Yamano Y et al (2017) in vitro activity of the siderophore cephalosporin, cefiderocol, against a recent collection of clinically relevant gram-negative bacilli from North America and Europe, including carbapenem-nonsusceptible isolates (Sidero-Wt-2014 Study). Antimicrob Agents Chemother 61:e00093-e117

    Article  CAS  Google Scholar 

  • Harding CM, Hennon SW, Feldman MF (2018) Uncovering the mechanisms of Acinetobacter Baumannii virulence. Nat Rev Microbiol 16:91

    Article  CAS  Google Scholar 

  • Hemeg HA (2017) Nanomaterials for alternative antibacterial therapy. Int J Nanomedicine 12:8211

    Article  CAS  Google Scholar 

  • Héritier C, Poirel L, Fournier P-E et al (2005) Characterization of the naturally occurring oxacillinase of Acinetobacter baumannii. Antimicrob Agents Chemother 49:4174–4179

    Article  Google Scholar 

  • Higgins PG, Poirel L, Lehmann M et al (2009) Oxa-143, a novel carbapenem-hydrolyzing class D β-lactamase in Acinetobacter baumannii. Antimicrob Agents Chemother 53:5035–5038

    Article  CAS  Google Scholar 

  • Higgins PG, Stubbings W, Wisplinghoff H et al (2010) Activity of the investigational fluoroquinolone finafloxacin against ciprofloxacin-sensitive and-resistant Acinetobacter baumannii isolates. Antimicrob Agents Chemother 54:1613–1615

    Article  CAS  Google Scholar 

  • Hsu L-Y, Apisarnthanarak A, Khan E et al (2017) Carbapenem-resistant Acinetobacter baumannii and enterobacteriaceae in South and Southeast Asia. Clin Microbiol Rev 30:1–22

    Article  Google Scholar 

  • Hsueh S-C, Lee Y-J, Huang Y-T et al (2018) In vitro activities of cefiderocol, ceftolozane/tazobactam, ceftazidime/avibactam and other comparative drugs against imipenem-resistant pseudomonas aeruginosa and Acinetobacter baumannii, and Stenotrophomonas maltophilia, all associated with bloodstream infections in Taiwan. J Antimicrob Chemother 74:380–386

    Article  Google Scholar 

  • Huh AJ, Kwon YJJ (2011) “Nanoantibiotics”: a new paradigm for treating infectious diseases using nanomaterials in the antibiotics resistant era. J Control Release 156:128–145

    Article  CAS  Google Scholar 

  • Hujer KM, Hamza NS, Hujer AM et al (2005) Identification of a new allelic variant of the Acinetobacter baumannii cephalosporinase, Adc-7 β-lactamase: defining a unique family of class C enzymes. Antimicrob Agents Chemother 49:2941–2948

    Article  CAS  Google Scholar 

  • Hujer KM, Hujer AM, Endimiani A et al (2009) Rapid determination of quinolone resistance in Acinetobacter spp. J Clin Microbiol 47:1436–1442

    Article  CAS  Google Scholar 

  • Hwang I-S, Hwang JH, Choi H et al (2012) Synergistic effects between silver nanoparticles and antibiotics and the mechanisms involved. J Med Microbiol 61:1719–1726

    Article  CAS  Google Scholar 

  • Insua I, Majok S, Peacock AF et al (2017) Preparation and antimicrobial evaluation of polyion complex (Pic) nanoparticles loaded with polymyxin B. Eur Polym J 87:478–486

    Article  CAS  Google Scholar 

  • Jacob JM, John MS, Jacob A et al (2019) Bactericidal coating of paper towels via sustainable biosynthesis of silver nanoparticles using ocimum sanctum leaf extract. Mat Res Express 6:045401

    Article  Google Scholar 

  • Jelinkova P, Mazumdar A, Sur VP et al (2019) Nanoparticle-drug conjugates treating bacterial infections. J Control Release 307:166–185

    Article  CAS  Google Scholar 

  • Johnning A, Karami N, Hallbäck ET et al (2018) The resistomes of six carbapenem-resistant pathogens–a critical genotype-phenotype analysis. Microb Genom 4(11):e000233

    Google Scholar 

  • Josephson J (2006) The microbial resistome. Environ Sci Technol 40(21):6531–6534

    Article  CAS  Google Scholar 

  • Kadiyala U, Kotov NA, Scott VanEpps J (2018) Antibacterial metal oxide nanoparticles: challenges in interpreting the literature. Curr Pharm Des 24:896–903

    Article  CAS  Google Scholar 

  • Kesavan D, Vasudevan A, Wu L et al (2020) Integrative analysis of outer membrane vesicles proteomics and whole-cell transcriptome analysis of eravacycline induced Acinetobacter baumannii strains. BMC Microbiol 20:31

    Article  CAS  Google Scholar 

  • Khashan KS, Sulaiman GM, Abdul Ameer FAK et al (2016) Synthesis, characterization and antibacterial activity of colloidal Nio nanoparticles. Pak J Pharm Sci 29(2):541–546

    CAS  Google Scholar 

  • Krause KM, Serio AW, Kane TR et al (2016) Aminoglycosides: an overview. Cold Spring Harb Perspect Med 6(6):a027029

    Article  Google Scholar 

  • Kuo S-C, Lee Y-T, Yang Lauderdale T-L et al (2015) Contribution of acinetobacter-derived cephalosporinase-30 to sulbactam resistance in Acinetobacter baumannii. Front Microbiol 6:231

    Article  Google Scholar 

  • Kwon HI, Kim S, Oh MH et al (2019) Distinct role of outer membrane protein a in the intrinsic resistance of Acinetobacter baumannii and Acinetobacter nosocomialis. Infect Genet Evol 67:33–37

    Article  CAS  Google Scholar 

  • Lambert T, Gerbaud G, Galimand M et al (1993) Characterization of acinetobacter haemolyticus Aac (6’)-Ig Gene encoding an aminoglycoside 6’-N-acetyltransferase which modifies amikacin. Antimicrob Agents Chemother 37:2093–2100

    Article  CAS  Google Scholar 

  • Lari AR, Ardebili A, Hashemi A (2018) Ader-ades mutations and overexpression of the adeabc efflux system in ciprofloxacin-resistant Acinetobacter baumannii clinical isolates. Indian J Med Res 147:413

    Article  CAS  Google Scholar 

  • Lean SS, Suhaili Z, Ismail S et al (2014) prevalence and genetic characterization of carbapenem- and polymyxin-resistant Acinetobacter baumannii isolated from a Tertiary Hospital in Terengganu Malaysia. ISRN Microbiol 2014:953417

    Article  Google Scholar 

  • Lee C-R, Lee JH, Park M et al (2017) Biology of Acinetobacter baumannii: pathogenesis, antibiotic resistance mechanisms, and prospective treatment options. Front Cell Infect Microbiol 7:55

    Article  Google Scholar 

  • Lenhard JR, Bulman ZP, Tsuji BT et al (2019) Shifting Gears: the future of polymyxin antibiotics. Antibiotics 8:42

    Article  CAS  Google Scholar 

  • Levin AS (2002) Multiresistant acinetobacter infections: a role for sulbactam combinations in overcoming an emerging worldwide problem. Clin Microbiol Infect 8:144–153

    Article  CAS  Google Scholar 

  • Li P, Li J, Wu C et al (2005) Synergistic antibacterial effects of β-lactam antibiotic combined with silver nanoparticles. Nanotechnology 16:1912

    Article  CAS  Google Scholar 

  • Lin M-F, Lan C-Y (2014) Antimicrobial resistance in Acinetobacter baumannii: from bench to bedside. WJCC 2:787

    Article  Google Scholar 

  • Magnet S, Courvalin P, Lambert T (2001) Resistance-Nodulation-cell division-type efflux pump involved in aminoglycoside resistance in Acinetobacter baumannii strain Bm4454. Antimicrob Agents Chemother 45:3375–3380

    Article  CAS  Google Scholar 

  • Manchanda V, Sanchaita S, Singh N (2010) Multidrug resistant acinetobacter. J Glob Infect Dis 2:291–304

    Article  Google Scholar 

  • Mapara N, Sharma M, Shriram V et al (2015) Antimicrobial potentials of helicteres isora silver nanoparticles against extensively drug-resistant (Xdr) clinical isolates of pseudomonas aeruginosa. Appl Microbiol Biotechnol 99:10655–10667

    Article  CAS  Google Scholar 

  • Mitscher LA (1978) The chemistry of the tetracycline antibiotics. Marcel Dekker Inc, New York, N.Y.

    Google Scholar 

  • Moffatt JH, Harper M, Adler B et al (2011) Insertion sequence isaba11 is involved in colistin resistance and loss of lipopolysaccharide in Acinetobacter baumannii. Antimicrob Agents Chemother 55:3022–3024

    Article  CAS  Google Scholar 

  • Moffatt JH, Harper M, Harrison P et al (2010) Colistin Resistance in Acinetobacter baumannii is mediated by complete loss of lipopolysaccharide production. Antimicrob Agents Chemother 54:4971–4977

    Article  CAS  Google Scholar 

  • Munawer U, Raghavendra VB, Ningaraju S et al (2020) Biofabrication of gold nanoparticles mediated by the endophytic cladosporium species: photodegradation, in vitro anticancer activity and in vivo antitumor studies. Int J Pharm 588:119729

    Article  CAS  Google Scholar 

  • Nallathamby PD, Lee KJ, Desai T et al (2010) Study of the multidrug membrane transporter of single living pseudomonas aeruginosa cells using size-dependent plasmonic nanoparticle optical probes. Biochemistry 49:5942–5953

    Article  CAS  Google Scholar 

  • Nejabatdoust A, Zamani H, Salehzadeh AJMDR (2019) Functionalization of Zno nanoparticles by glutamic acid and conjugation with thiosemicarbazide alters expression of efflux pump genes in multiple drug-resistant Staphylococcus aureus strains. Microb Drug Resist 25:966–974

    Article  CAS  Google Scholar 

  • Nie D, Hu Y, Chen Z et al (2020) Outer membrane protein a (Ompa) as a potential therapeutic target for Acinetobacter baumannii infection. J Biomed Sci 27:1–8

    Article  Google Scholar 

  • Papp-Wallace KM, Endimiani A, Taracila MA et al (2011) Carbapenems: past, present, and future. Antimicrob Agents Chemother 55:4943–4960

    Article  CAS  Google Scholar 

  • Patra P, Mitra S, Debnath N et al (2014) Ciprofloxacin conjugated zinc oxide nanoparticle: a camouflage towards multidrug resistant bacteria. Bull Mater Sci 37:199–206

    Article  CAS  Google Scholar 

  • Peleg AY, Potoski BA, Rea R et al (2006) Acinetobacter baumannii bloodstream infection while receiving tigecycline: a cautionary report. J Antimicrob Chemother 59:128–131

    Article  Google Scholar 

  • Peleg AY, Seifert H, Paterson DL (2008) Acinetobacter baumannii: emergence of a successful pathogen. Clin Microbiol Rev 21:538–582

    Article  CAS  Google Scholar 

  • Pelgrift RY, Friedman AJ (2013) Nanotechnology as a therapeutic tool to combat microbial resistance. Adv Drug Deliv Rev 65:1803–1815

    Article  CAS  Google Scholar 

  • Penwell WF, Shapiro AB, Giacobbe RA et al (2015) Molecular mechanisms of sulbactam antibacterial activity and resistance determinants in Acinetobacter baumannii. Antimicrob Agents Chemother 59:1680–1689

    Article  Google Scholar 

  • Perez F, Hujer AM, Hujer KM et al (2007) Global challenge of multidrug-resistant Acinetobacter baumannii. Antimicrob Agents Chemother 51:3471–3484

    Article  CAS  Google Scholar 

  • Périchon B, Goussard S, Walewski V et al (2014) Identification of 50 class D β-lactamases and 65 acinetobacter-derived cephalosporinases in acinetobacter spp. Antimicrob Agents Chemother 58:936–949

    Article  Google Scholar 

  • Perry JA, Westman EL, Wright GD (2014) The antibiotic resistome: what’s new? Curr Opin Microbiol 21:45–50

    Article  CAS  Google Scholar 

  • Perry JA, Wright GD (2014) Forces shaping the antibiotic resistome. BioEssays 36:1179–1184

    Article  Google Scholar 

  • Poirel L, Naas T, Nordmann P (2010) Diversity, epidemiology, and genetics of class D β-lactamases. Antimicrob Agents Chemother 54:24–38

    Article  CAS  Google Scholar 

  • Poirel L, Nordmann P (2006) Carbapenem resistance in Acinetobacter baumannii: mechanisms and epidemiology. Clin Microbiol Infect 12:826–836

    Article  CAS  Google Scholar 

  • Pollitt S, Zalkin HJJ (1983) Role of primary structure and disulfide bond formation in beta-lactamase secretion. J Bacteriol 153:27–32

    Article  CAS  Google Scholar 

  • Richmond GE, Evans LP, Anderson MJ et al (2016) The Acinetobacter baumannii two-component system AdeRS regulates genes required for multidrug efflux, biofilm formation, and virulence in a strain-specific manner. Mbio 7:e00430-e516

    CAS  Google Scholar 

  • Roberts MC (1996) Tetracycline resistance determinants: mechanisms of action, regulation of expression, genetic mobility, and distribution. FEMS Microbiol Rev 19:1–24

    Article  CAS  Google Scholar 

  • Rogalski W (1985) Chemical modification of the tetracyclines. Springer, Heidelberg, Berlin, pp 179–316

    Book  Google Scholar 

  • Roy AS, Parveen A, Koppalkar AR et al (2010) Effect of nano-titanium dioxide with different antibiotics against methicillin-resistant Staphylococcus aureus. J Biomater Nanobiotechnol 1:37

    Article  CAS  Google Scholar 

  • Ruddaraju LK, Pammi SVN, Guntuku GS et al (2020) A review on anti-bacterials to combat resistance: from ancient era of plants and metals to present and future perspectives of green nano technological combinations. Asian j Pharm Sci 15:42–59

    Article  Google Scholar 

  • Saravanan M, Niguse S, Abdulkader M et al (2018) Review on emergence of drug-resistant tuberculosis (Mdr & Xdr-Tb) and its molecular diagnosis in Ethiopia. Microb Pathog 117:237–242

    Article  Google Scholar 

  • Sathiyavimal S, Vasantharaj S, Veeramani V et al (2021) Green chemistry route of biosynthesized copper oxide nanoparticles using psidium guajava leaf extract and their antibacterial activity and effective removal of industrial dyes. J Environ Chem Eng 9:105033

    Article  CAS  Google Scholar 

  • Shaikh S, Nazam N, Rizvi SMD et al (2019) Mechanistic insights into the antimicrobial actions of metallic nanoparticles and their implications for multidrug resistance. Int J Mol Sci 20:2468

    Article  Google Scholar 

  • Shaker MA, Shaaban MIJ (2017) Formulation of carbapenems loaded gold nanoparticles to combat multi-antibiotic bacterial resistance: in vitro antibacterial study. Int j Pharm 525:71–84

    Article  CAS  Google Scholar 

  • Shaw K, Rather P, Hare R et al (1993) Molecular genetics of aminoglycoside resistance genes and familial relationships of the aminoglycoside-modifying enzymes. Microbiol Mol Biol Rev 57:138–163

    CAS  Google Scholar 

  • Simakov N, Leonard DA, Smith JC et al (2017) A distal disulfide bridge in Oxa-1 β-lactamase stabilizes the catalytic center and alters the dynamics of the specificity determining Ω loop. J Phys Chem B 121:3285–3296

    Article  CAS  Google Scholar 

  • Singla P, Sikka R, Deeep A et al (2014) Co-production of Esbl and Ampc Β-lactamases in clinical isolates of A. baumannii and A. lwoffii in a tertiary care hospital from Northern India. J Clin Diagn Res 8:16

    Google Scholar 

  • Siroy A, Cosette P, Seyer D et al (2006) Global comparison of the membrane subproteomes between a multidrug-resistant Acinetobacter baumannii strain and a reference strain. J Proteome Res 5:3385–3398

    Article  CAS  Google Scholar 

  • Sood D, Kumar N, Singh A et al (2018) Antibacterial and pharmacological evaluation of fluoroquinolones: a chemoinformatics approach. Genomics Inform 16:44–51

    Article  Google Scholar 

  • Soon RL, Nation RL, Cockram S et al (2010) Different surface charge of colistin-susceptible and-resistant Acinetobacter baumannii cells measured with zeta potential as a function of growth phase and colistin treatment. J Antimicrob Chemother 66:126–133

    Article  Google Scholar 

  • Storm DR, Rosenthal KS, Swanson PE (1977) Polymyxin and related peptide antibiotics. Annu Rev Biochem 46:723–763

    Article  CAS  Google Scholar 

  • Strydom SJ, Rose WE, Otto DP et al (2013) Poly (Amidoamine) dendrimer-mediated synthesis and stabilization of silver sulfonamide nanoparticles with increased antibacterial activity. Nanomedicine: NBM 9:85–93

    Article  CAS  Google Scholar 

  • Sultan I, Rahman S, Jan AT et al (2018) Antibiotics, resistome and resistance mechanisms: a bacterial perspective. Front Microbiol 21:9–2066

    Google Scholar 

  • Thaker M, Spanogiannopoulos P, Wright GD (2010) The tetracycline resistome. Cell Mol Life Sci 67:419–431

    Article  CAS  Google Scholar 

  • Tian G-B, Adams-Haduch JM, Taracila M et al (2011) Extended-spectrum Ampc cephalosporinase in Acinetobacter baumannii: Adc-56 confers resistance to cefepime. Antimicrob Agents Chemother 55:4922–4925

    Article  CAS  Google Scholar 

  • Tiwari V, Mishra N, Gadani K et al (2018) Mechanism of anti-bacterial activity of zinc oxide nanoparticle against carbapenem-resistant Acinetobacter baumannii. Front Microbiol 9:1218

    Article  Google Scholar 

  • Tiwari V, Vashistt J, Kapil A et al (2012) Comparative proteomics of inner membrane fraction from carbapenem-resistant Acinetobacter baumannii with a reference strain. PLoS ONE 7:e39451

    Article  CAS  Google Scholar 

  • Trebosc V, Gartenmann S, Tötzl M et al (2019) Dissecting colistin resistance mechanisms in extensively drug-resistant Acinetobacter baumannii clinical isolates. Mbio 10:e01083-e1119

    Article  CAS  Google Scholar 

  • Turton JF, Ward ME, Woodford N et al (2006a) The role of Is Aba1 in expression of oxa carbapenemase genes in Acinetobacter baumannii. FEMS Microbiol Lett 258:72–77

    Article  CAS  Google Scholar 

  • Turton JF, Woodford N, Glover J et al (2006b) Identification of Acinetobacter baumannii by detection of the blaoxa-51-like carbapenemase gene intrinsic to this species. J Clin Microbiol 44:2974–2976

    Article  CAS  Google Scholar 

  • Venter H, Mowla R, Ohene-Agyei T et al (2015) Rnd-type drug efflux pumps from gram-negative bacteria: molecular mechanism and inhibition. Front Microbiol 6:377

    Article  Google Scholar 

  • Vila J, Martí S, Sanchez-Céspedes J (2007) Porins, efflux pumps and multidrug resistance in Acinetobacter baumannii. J Antimicrob Chemother 59:1210–1215

    Article  CAS  Google Scholar 

  • Wang L, Hu C, Shao LJ (2017a) The antimicrobial activity of nanoparticles: present situation and prospects for the future. Int J Nanomedicine 12:1227

    Article  CAS  Google Scholar 

  • Wang Y, Wu C, Zhang Q et al (2012) Identification of New Delhi Metallo-β-Lactamase 1 in Acinetobacter lwoffii of food animal origin. PLoS ONE 7:37152

    Article  Google Scholar 

  • Wang Z, Dong K, Liu Z et al (2017b) Activation of biologically relevant levels of reactive oxygen species by Au/G-C3n4 hybrid nanozyme for bacteria killing and wound disinfection. Biomaterials 113:145–157

    Article  CAS  Google Scholar 

  • Wencewicz TA (2019) Crossroads of antibiotic resistance and biosynthesis. J Mol Biol 23(18):3370–3399

    Article  Google Scholar 

  • Williamson R, Collatz E, Gutmann L (1986) Mechanisms of action of β-lactam antibiotics and mechanisms of Non-enzymatic resistance. Presse Med 15:2282–2289

    CAS  Google Scholar 

  • Yu Z, Qin W, Lin J (2015) Antibacterial mechanisms of polymyxin and bacterial resistance. Biomed Res Int 2015:679109

    Article  Google Scholar 

  • Yun S-H, Choi C-W, Kwon S-O et al (2011) quantitative proteomic analysis of cell wall and plasma membrane fractions from multidrug-resistant Acinetobacter baumannii. J Proteome Res 10:459–469

    Article  CAS  Google Scholar 

  • Yun S-H, Choi C-W, Park S-H et al (2008) Proteomic analysis of outer membrane proteins from Acinetobacter baumannii Du202 in tetracycline stress condition. J Microbiol 46:720–727

    Article  CAS  Google Scholar 

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Funding

National Natural Science Foundation of China (grant no.81771756). The Postdoctoral Foundation of Jiangsu Province (grant no.1601002C).

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Aparna Vasudevan and Dineshkumar Kesavan wrote the manuscript. Zhaoliang Su critically reviewed and edited the manuscript. Shengjun Wang revised for its integrity and accuracy. Huaxi Xu approved the final version of this manuscript and takes responsibility for its contents.

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Correspondence to Huaxi Xu.

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Aparna, V., Dineshkumar, K., Su, Z. et al. The innate resistome of “recalcitrant” Acinetobacter baumannii and the role of nanoparticles in combating these MDR pathogens. Appl Nanosci 13, 1–14 (2023). https://doi.org/10.1007/s13204-021-01877-6

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