key: cord-0022449-8qvn52oc
authors: Kumar, Sunil; Anwer, Razique; Azzi, Arezki
title: Virulence Potential and Treatment Options of Multidrug-Resistant (MDR) Acinetobacter baumannii
date: 2021-10-06
journal: Microorganisms
DOI: 10.3390/microorganisms9102104
sha: 2a09d812ef67272100c222d36deeb4fbe754c922
doc_id: 22449
cord_uid: 8qvn52oc

Acinetobacter baumannii is an opportunistic pathogen which is undoubtedly known for a high rate of morbidity and mortality in hospital-acquired infections. A. baumannii causes life-threatening infections, including; ventilator-associated pneumonia (VAP), meningitis, bacteremia, and wound and urinary tract infections (UTI). In 2017, the World Health Organization listed A. baumannii as a priority-1 pathogen. The prevalence of A. baumannii infections and outbreaks emphasizes the direct need for the use of effective therapeutic agents for treating such infections. Available antimicrobials, such as; carbapenems, tigecycline, and colistins have insufficient effectiveness due to the appearance of multidrug-resistant strains, accentuating the need for alternative and novel therapeutic remedies. To understand and overcome this menace, the knowledge of recent discoveries on the virulence factors of A. baumannii is needed. Herein, we summarized the role of various virulence factors, including; outer membrane proteins, efflux pumps, biofilm, penicillin-binding proteins, and siderophores/iron acquisition systems. We reviewed the recent scientific literature on different A. baumannii virulence factors and the effective antimicrobial agents for the treatment and management of bacterial infections.

Acinetobacter baumannii are non-motile, aerobic Gram-negative, glucose non-fermentative, catalase-positive, non-fastidious, oxidative-negative coccobacilli [1] . The phylogenetic classification and interpretation of the taxonomy of the genus Acinetobacterhas established over 60 known species within the genus ( Figure 1 ) [2] . Amongst all other species, A. baumannii is particularly associated with hospital-acquired infections (HAI) world wide [3] . Hospital-acquired pneumonia, meningitis, and skin and soft tissue infections are amongst the diverse infections caused by A. baumannii [4] . A. baumannii has also been known as "Iraqibacter" due to the infections among soldiers admitted to the US military hospitals during the Iraq and Afghanistan conflicts [5] . A. baumannii virulence factors have posed multiple challenges and outbreaks in treatment, particularly in critical patients admitted to the intensive care units (ICUs) of healthcare units [3] . Infections due to A. baumannii are recently emerging particularly in the hospital setting and constitute a challenge for clinicians to tackle their spread and treatment, especially in the ICUs [6] . Furthermore, multidrug resistance has significantly increased in the past two decades, including; resistance to last-resort antibiotics, such as colistin [7, 8] . A. baumannii infections are usually very difficult to treat; however, the organism has depicted a relatively low virulence potential in immunocompetent hosts [9] . However, recently, animal infection models have reported A. baumannii strains with increased pathogenicity [10, 11] . This might be due to phenotypic and genetic adaptations that could increase the resistance and virulence potential of A. baumannii [12, 13] .

Physico-chemical functions, including; cell communication, secretion of macromolecules, and surface-regulated attachments, are key factors for bacterial biofilm formation [14] . Several virulence genes enable A. baumannii to be a potent bacterial pathogen in animals and humans [15, 16] . K1 surface antigen protein 1, acinetobactin transporters, capsular polysaccharides, outer membrane porins, and iron acquisition systems are some of the factors which, along with acquired antibiotics resistance, have promoted A. baumannii as a significant nosocomial pathogen [17, 18] . A. baumannii has been reported to have a range of virulence genes that code for biofilmformation and its adherence on biotic and abiotic surfaces [19] . These virulence genes also facilitate A. baumannii in the viable state under different adverse environmental conditions and protect against antimicrobial agents [20] [21] [22] . Due to the fast development of severe infections and rising antimicrobial resistance of A. baumannii, inappropriate empirical therapy is given to the patient, most often with negative consequences [23] . Several studies have examined the effect of antibiotic exposures on the modulation of the virulence properties of resistant pathogens [24] [25] [26] [27] . Augmentation of virulence in A. baumannii has been seen by converting a normally low-virulence organism into a highly virulent one in response to variable antibiotic concentrations [28, 29] . Several novel treatment options have recently been approved for treating this deadly bug [30, 31] . Herein, we review the virulence factors of A. baumannii to assess the relationships between antimicrobial resistance, virulence, and the therapeutic options.

A. baumannii is capable of harboring acquired resistance to a variety of antibiotics used in therapy. Several antimicrobial agents, such aspenicillins, cephalosporins, tetracyclines, aminoglycosides, and quinolones have been tested as ineffective against A. baumannii treatment due to the augmentation of resistance determinants. The mechanism behind this might be the genetic alteration causing modification of the membrane fusion proteins (OMPs); overexpression of antimicrobial modifying enzymes; overexpression of efflux transporters; modification of target sites; and the insertion of new resistance determinants. Consequently, carbapenems are the only choice of treatment alternatives due to their enhanced activity and reduced toxicity for A. baumannii infections [32] . In the past few decades, A. baumannii causedan array of nosocomial infections, which were successfully treated with gentamicin, minocycline, nalidixic acid, ampicillin, or carbenicillin, either as monotherapy or in combinations, but global surveys have shown an increased resistance in the hospital isolates [33] [34] [35] . Several mechanisms of resistance have been implicated in the augmentation of resistance in A. baumannii:

Enzymatic mechanisms including; deferent β-lactamases.

Non-enzymatic mechanisms involving efflux pumps and membrane permeability.

Change in the sequence of penicillin-binding proteins (PBPs).

Among these, the first two are very crucial in imparting resistance to clinical isolates of A. baumannii [36] .The action of bacterial β-lactamase resulted in the rise of antibiotic resistance to the penicillins, cephalosporins, and carbapenems [37, 38] . A. baumannii gives rise to β-lactamases, which are coded by various chromosomal genes or plasmids genes.

Different classes of β-lactam antibiotics become hydrolyzed by the enzymes produced by bacterial cells, such as cephalosporins, carbapenems, penicillins, and monobactam, which are neutralized by β-lactamases. Beta-lactamases are classified into four major classes (A, B, C, and D) as per their gene sequence homology. On the basis ofthe inclusion of divalent cations in enzyme activation, these enzymes are classified into metallo-β-lactamases (class-B) and non-metallo-β-lactamases (classes A, C, and D) [39] . Overproduction of betalactamases has been associated with the escalated resistance to carbapenems in A. baumannii in many investigations.AmpC beta-lactamases come under the Ambler classification of preferred ESBL (extended-spectrum beta-lactamases) [40] . As per recent information on A. baumannii, the most significant mechanism is the carbapenemase behind carbapenem resistance, which is the most powerful class of β-lactamases. Divalent cations (zinc) are utilized by metallo-enzymes in addition to water moleculesin order to cleave the β-lactam ring. Carbapenem hydrolyzing class-D beta-lactamases (CHDL) are considered as another promising cause of carbapenem resistance in A. baumannii. These enzymes are also known as oxacillinases (OXAs) because of their capacity to hydrolyzeisoxazolyl-penicillin-oxacillin quicker than benzylpenicillin [41, 42] . To date, many types of OXAs have been discovered in the A. baumannii, such as OXA-23, OXA-51, OXA-40/24, OXA-48, OXA-58, and OXA-143 [32, 43] .

Class-A (GES and KPC) and class-B carbapenemases (NDM, IMP, SIM, and VIM) have also been screened in A. baumannii. Many class-A carbapenemases are crystallized (e.g., SME-1, KPC-2, andNmcA). Most of the class-C β-lactamases show weaker activity in the hydrolysis of carbapenems. OXA-23 is the most prominently found CHDL beta-lactamase, primarily found on a plasmid of the A. baumannii strain in Scotland and represented as the first oxacillinase harboring carbapenemase activity [44] . Later on, the blaOXA-23 gene was identified both on plasmids and on chromosomes all over globe. It is exclusively found in the genus Acinetobacter with the exception of a Proteus mirabilis isolate from France [45] . OXA-24/40, initially isolated from Spain, were predicted the first time as separate enzymes but re-sequencing confirmed them as identical later on [46] .

OXA-58 has also been identified in A. baumannii, which shares a 59% protein sequence similarity with OXA-51/69 [47] . OXA-58 is particularly coded by a plasmid gene, which has been circulated extensively all over the world. Initially, OXA-58 was more prevalent in Greece and Italy [48] [49] [50] [51] [52] because of frequent outbreaks in intensive care units and pediatric wards [53] [54] [55] . Nowadays, OXA-58 is found in A. baumannii in every corner of the world [56] . OXA-143 is the more recently identified group of CHDLs, which were formerly traced in the clinical isolate of A. baumannii in Brazil [57] . CHDLs hydrolyze the carbapenems typically very effectively; therefore, as a substrate, imipenem is given preference over meropenem and hence raises a debate on the contributing role of CHDLs in carbapenem resistance [58, 59] . Some of the studies have tried to prove this by implementing either knock-out mutants or by using transformation experiments to see the changes in susceptibility to carbapenems.

Efflux pumps are the components of the bacterial cell membrane which excrete toxic substances, metabolic end-products, and even antimicrobials [60] . Overexpression of chromosomally encoded efflux pumps is one of the several mechanisms responsible for multidrug resistance in A. baumannii [61] . Efflux pumps have been presented as the first step in the augmentation of an MDR phenotype [62] . Most of the efflux pumps are prevalently described in the Gram-negative bacteria, which are comprised of three protein components [63] . The resistance-nodulation-division (RND) efflux family, which most commonly fetches antimicrobial resistance in A. baumannii, is composed of a periplasmic MFP (membrane fusion protein) interacting with an inner cytoplasmic membrane transporter protein at one end and an OMP (outer membrane protein) on other end to facilitate the extrusion of antimicrobials [64, 65] . Such efflux systems are the MexAB-OprM system (previously studied as MexAB-OprK) of P. aeruginosa [66] and the AcrAB system in E. coli.

In the Burkholderiacepacia complex, RND efflux pumps have also been explored for the association of antimicrobial drug resistance to different antimicrobials [67] . Apart from the MexAB-OprM system, three more RND efflux systems have been characterized: MexEF-OprN, MexXY-OprM, and MexCD-OprJ [60, 68] . To date, many RND efflux pump systems have been described in A. baumannii, including; AdeABC, AdeFGH, and AdeIJK [36, [69] [70] [71] . Each of these efflux pumps is regulated by a two-component regulatory system, e.g.,AdeRS regulates the AdeABC in A. baumannii [72] ;AdeL (LysR-type transcriptional regulator) regulates the AdeFGH [70] ; and AdeN regulates the AdeIJK for TetR transcriptional regulation [73] . Overexpression of the efflux pumps by up-regulation has led to increased antimicrobial resistance in A. baumannii [36, 74] . The MF (Major Facilitator) and MATE (Multidrug And Toxic compound Extrusion) super family efflux pumps have also been observed contributing to antimicrobial resistance in A. baumannii [69, 72, 75] .

Multiple virulence factors facilitate A. baumannii in passing on a disease to the host efficiently ( Figure 2 ) [15] . Only a meager understanding is available about the A. baumannii virulence potential and the host responses to infection caused by this bacterium [76, 77] . Virulence factor identification and the underlying mechanisms of pathogenesis can help in the synthesis of new treatment substitutes to control the disease by this bug [24] . 

Outer membrane proteins of Gram-negative bacteria are investigated for their association with antimicrobial resistance, pathogenesis, and variation in the adherence of the host cell [78] . A. baumannii isolates have shown a few OMPs, which are symbolized as the most prevalent ones among other species as well [79] . A. baumannii OmpA (AbOmpA) is reported as an impending virulence factor bringing numerous significant properties to signal processing and pathogenesis [80] . AbOmpA of A. baumannii is a major surface-bound protein, which facilitates the attachment process and host cell invasion and helps in the commencement of apoptosis at the onset of infection. OmpA adds to the initiation of cell apoptosis, the invasion of epithelial cells, and serum resistance [81, 82] . Gram-negative bacteria generally produce outer membrane vesicles (OMVs) that assist in confronting virulence factors by host cells [83] . Lipo-polysaccharides (LPS), lipids, proteins, and DNA or RNA are the main constituents of OMVs, which have a diameter range of approximately 20-200 nm [84, 85] . OMVs deliver the virulence factor to host cells and transfer resistance genes from one bacteria to another [86] .

Biofilm is a complex structure of diversified bacterial cells usually found adhered to the biotic or abiotic surfaces, embedded in an extracellular matrix of polymers (involving nucleic acids, carbohydrates, proteins, and other constituents) and representing a shielding mechanism to thrive in unfavorable environmental conditions and at the time of host infection [87, 88] . One of the essential virulence factors required for adherence to biotic and abiotic surfaces and biofilm formation is 38 kDa (OmpA) outer membrane protein A [80, 89] . Initial attachment to the abiotic surface is mediated by pili production controlled by the usher-chaperone assembly structure (CsuA/BABCDE) and regulated by BfmS/BfmR (a 2-component system) [90] . Formation and regulation of biofilms depend upon several host factors, such as growth condition, cell density, quorum sensing, light, and free iron [91, 92] . A significant component of exopolysaccharide is PNAG (Poly-β-1,6-N-acetyl -glucosamine), which constitutes biofilms [93] . The effortless adherence to epithelial cells, diverse medical devices, and equipment is crucial for A. baumannii invasion in the susceptible hosts and persistence in hospitals [94] . Such bacteria show a higher resistance against variable antibiotics, stressors, or disinfectants than the motile ones and hence the capacity to produce biofilms symbolizes a critical factor of virulence. Biofilm formation can be manipulated by general features, such as bacterial appendages, bacterial surface constituents, availability of nutrition medium, macromolecular secretions, and quorum sensing systems [91] . The capability of clinical strains of A. baumannii to synthesize biofilm is attributed to a resistance phenotype, particularly on abiotic surfaces, catheter-associated infections, sepsis or urinary tract catheters and even in the patients with shunt-related meningitis [95] [96] [97] .

PBPs are enzymes usually found as membrane-bound in the cytoplasm of bacteria and share a familiar evolutionary origin [98] . These enzymes are essential for synthesizing peptidoglycan, the bacterial cell wall's principal constituent, and coupled with cell division and morphogenesis [99] . Disorientation in the cell wall is caused by the inhibition of PBPs, which further inhibit growth or cell lysis. PBPs have been categorized into low and highmolecular weight PBPs. Low molecular weight PBPs help cell segregation and the remodeling of peptidoglycan, whereas highmolecular weight PBPs are responsible for cell wall and peptidoglycan synthesis [100] . Using rat soft-tissue infection models, Russo et al. also showed that a mutant derivative of the wild A. baumannii (PBP-7/8 deficient) is added tothe A. baumannii pathogenesis and is involved in its survival and growth in the ascites of humans [101] . A few studies also portrayed the role of penicillin-binding proteins in pathogenesis due to A. baumannii [102] .

Pathogenic bacteria face one major challenge in their hosts, which is the shortage of freely accessible iron. Iron is almost unavailable in mammals for invading bacteria and is mostly integrated into storage proteins and iron transport. The ability of the host to withhold iron significantly diminishes the accessibility of iron to infecting bacteria and is accounted for as an essential module of innate immunity [17] . Siderophores are secreted and bind to ferric ions and enable A. baumannii to capture iron under an iron-shortage condition [103] . Bacterial cells acquire siderophores loaded with Fe 3+ and heme through specific protein receptors. These receptors are usually present on the outer membrane of Gram-negative bacteria where siderophore-Fe 2+ complexes are internalized, coupled with the indulgence of the proton gradient on the bacterial inner membrane [104] . TonB protein complexmediates the energy transduction in the periplasmic space from the inner to the outer membrane [105] . Recently, a novel siderophore, cefiderocol (siderophorecephalosporin conjugate), investigated in a subject suffering from kidney impairment, was found to be well tolerated as a treatment for multidrug-resistant strains [106] . Synthesis of fimsbactin A and B has also been studied recently, based on the synthesis routes as stereoisomeric analogues [107] . A gamma-lactam antimicrobial has been effectively tested upon MDR A. baumannii in the USA recently [108] . Some studies also explained the roles of phospholipase D and capsular polysaccharide as virulence factors which add to the pathogenicity of A. baumannii [109, 110] .

A. baumannii infections are commonly severe and complicated to cure because of escalating multidrug resistance, specifically among clinical isolates [111, 112] . Consecutive surveys have revealed the mounting resistance in clinical isolates. The majority of A. baumannii strains have become resistant against clinically attainable doses of nearly all prevalent utilized antimicrobials, such as ureidopenicillins, aminoglycosides, aminopenicillins, fluoroquinolones, chloramphenicol, and cephalosporins [113, 114] . The rate of resistance of sulbactam is also rising periodically despite being bactericidal to many other species of the genus Acinetobacter [115] . Carbapenems, in particular meropenem and imipenem, were previously very successful in in vitro treatment. Carbapenems are considered as the last resort of the treatment for managing infections caused by MDR A. baumannii. Still, the rate of resistance against carbapenems has increased in clinical strains of A. baumannii, particularly in Europe, Latin America, Asia, and Australia ( Figure 3 ) [56, [116] [117] [118] . Such carbapenem-resistant A. baumannii (CRAB) isolates are generally resistant to other conservatively used common antibiotics [56, 113, 119] . Imipenem has a higher affinity for certain oxacillinase enzymes than meropenem. The susceptibility to tigecycline or polymyxins at present remains satisfactory [120, 121] . A global surveillance from 2007-2011 suggested the escalating susceptibility of minocycline ranging from 72.5% to 91.7% [122, 123] . In a study from Italy, an increase in resistance to the latest generation of antimicrobials has been observed in sepsis cases [124] . Most of the A. baumannii isolates have been reported resistant to most of the antibiotics (95-99%) in another investigation [125] . Minocycline showed bactericidal effects against A. baumannii isolates as well as synergistic effects with other antimicrobials. 

Although the microbiological clearance rates in the A. baumannii severe infections are considerably higher with the use of combined therapy, recent analysis stated that there is an inadequacy of clinical effectiveness (mortality or cure rate) using combination therapy comparative to monotherapy. Absence of regulated clinical trials renders it complicated to judge the effect of combination therapy or synergy for treating MDR A. baumannii infections [126] . Combined therapy is recommended when all conventional drugs become ineffective against the A. baumannii [127] . Synergy and combinations of drugs through in vitro andin vivoexperiments have shown extremely bactericidal activity against the hospital strains of MDR A. baumannii [128, 129] . Two or three classes of the following antibiotics are included in such synergic combinations: rifampin, polymixins, sulbactam, tigecycline, aminoglycosides, or β-lactams, such as broad-spectrum cephalosporins or carbapenems [130] [131] [132] . However, all antibiotics should be tested individually against each strain and combined with suitable in vitro methods as multiple diverse resistance mechanisms are prevalent in the clinical isolates.

Conflicting results have been found in a few studies when different investigators used the same antimicrobial combinations. Montero et al., performed a study on a murine pneumonia host model of MDR A. baumannii. They concluded that rifampin combinedtherapy with tobramycin, imipenem, or colistin were the most efficient treatment options [133] . However, a follow-up clinical study suggested not using a combination of rifampin and imipenem for CRAB treatment because of a high failure rate. It acknowledged the increased resistance to rifampin in 70% of treated patients with this regimen [134] . To treat the imipenem-resistant pneumonia using a guinea pig model, amikacin and imipenem combined therapy gave a worse outcome than imipenem alone; however, the in vitro results represented the synergism among the antimicrobials [135] . The in vitro synergy benefits are still not clear. A broad category of additional antimicrobials usage put a limit on the capability to describe the overall outcome of combined therapy. In contrast to colistin parenteral monotherapy, most combination therapy outcomes were equivalent with respect to cure rates. Additional clinical studies with controlled parameters are required to conclude whether any suitable combination of antimicrobials could be translated to useful therapeutic strategies.

The dosage and drug of choice relied upon in vitro susceptibility surveys but not on rigorous clinical trials. The persistence and spread of specific epidemic lineages of A. baumannii in the different geographical locations indicatethat information on the prevail-ing local susceptibility pattern is critical for treating Acinetobacter infection. A. baumannii susceptible isolates could be quickly treated with conservative antimicrobial agents, spanning over the third and fourth generations of cephalosporin, fluoroquinolones, or carbapenems [136] . Aminoglycosides in combination with other antibiotics are usually prescribed for treating meningitis or bacteremia and have shown promising activity against A. baumannii in in vivo and in vitro studies [119, 137] . Tetracycline is also preferred to treat A. baumannii infections in several experimental and clinical studies [138] .

It is essential to understand the fact that A. baumannii clinical isolates are increasingly reported as multidrug resistant and a few of them are resistant to almost all the routinely used antibiotics [139] . Therefore, it is necessary to have complete antimicrobial susceptibility testing [140] . Carbapenems have been the drug of choice for the last 20 years for treating A. baumannii infections when susceptibility data were generally not available [141] . However, the outbreak of epidemic clonal lineages worldwide with increased resistance to carbapenems has been documented during the last decade [56, 142, 143] . Before the availability of antimicrobial susceptibility tests, a combination of carbapenem withother antibiotics (sulbactam, tigecycline, or polymyxins) is perhaps an accepted choice for empirical therapy to treat A. baumannii infections [126] . The following antibiotics, either as monotherapy or in combined therapy, have been utilized for treating MDR isolates of A. baumannii with a lower success rate.

While inadequate therapeutic options are in hand, clinicians have revisited the use of polymyxin E (colistin) or polymyxin B for MDR Acinetobacter infections [144] . The mode of action of colistin is the disrupting of the cell membrane by interacting with the lipopolysaccharide, increasing the membrane permeability, and resulting in bacterial cell fatality [145] . Colistin acts as a bactericidal drug and its effect is dependent upon the concentration utilized against A. baumannii [146] . There are two routes of colistin medicationwhere colistin sulphate is given through an oral route andfor topical useand, colistin sulphomethate sodium is administered intravenously [147] . Polymyxins, either in mono-or combined therapy, have proved effective intravenously in the clinical outcomes of patients suffering with meningitis or pneumonia (VAP) [148, 149] . Toxicity rates, predominantly nephrotoxicity due to colistin, are usually lower than those reported earlier, but some investigators have shown the rates of AKI (Acute Kidney Injury) reaching up to 50% [150] . Lack of alternate antibiotics, failure to examine the renal functions, and various factors for renal injury make it difficult to access the outcomes of such studies. Polymyxins share similar PK-PD (pharmacokinetics/pharmacodynamics) with aminoglycosides; a trim level prospective study demonstrated the safety and efficiency of an elevated dose of colistin in critical patients [151] . Polymyxins in conjugation with other antimicrobial agents in aerosol form can also be given intravenously, which showed effectiveness in patients with A. baumannii nosocomial pneumonia [152] . When the intravenous colistin, or other antimicrobials, combined with aerosolized colistin, the outcome was improved in the subjective reports [153] . However, the combination of intravenous colistin had no discriminating benefit in a randomized study [152] . However, in critical patients, the extensive use of polymyxins for treating A. baumannii infections may lead to an escalating and increasing resistance [154] . Hetero-resistance to colistin has also been reported in A. baumannii isolates [155] . Consequently, combination therapy has been recommended with polymyxins and other antimicrobials [144] .

Sulbactam, which is a predominant β-lactamase inhibitor, has an inherent mechanism against A. baumannii isolates [30] . In vivo and in vitro assays of sulbactam have shown promising results against A. baumannii infections [129] . Ampicillin, a β-lactam agent, combined with the beta-lactamase inhibitor, did not materialize to enhance the synergy or activity [156] . Use of sulbactam alone is not recommended for severe Acinetobacter infections. However, Qin et al. reported extensive sulbactam use in the treatment of 114 patients with MDR Acinetobacter pulmonary infections, resulting in similar clinical outcomes among patients treated with sulbactam and cefoperazone alone [157] . Recently, sulbactam combined with meropenem therapy resulted in decreased biomass and mean thickness, raised the roughness of the Acinetobacter biofilm, and showed synergism against biofilmembedded CRAB [158] . In another investigation, antimicrobial susceptibility results of MIC tests (broth microdilution method) in 176 isolates of A. baumannii of β-lactam/β-lactamase combinations showed a 99.4% susceptibility, which suggested future prophylactic and therapeutic options [159] .

According to the particular geographical area, the in vitro susceptibility of A. baumannii differs extensively for sulbactam [160] . No substantial randomized clinical trial has been available with sulbactam. Studies have shown that compared to other successful antibiotics for treating resistant A. baumannii, sulbactam, either in combination or alone, has shown similar efficacy [161] . A higher sulbactam dose of >6 g/day is recommended in serious patients, and a regimen of 9 g/day of sulbactam has been used effectively, exclusive of significant side effects [162] . However, due to rampant clinical use, the antimicrobial efficacy of sulbactam has declined extensively against A. baumannii isolates and resistance to sulbactam is frequently increasing in certain geographical regions [163] .

Tigecycline is a relatively new glycylcycline agent, a synthetic derivative of minocycline, and possesses a specific mechanism of action. Tigecycline has been found to have bacteriostatic activity against CRAB isolates [164] . Some MDR Acinetobacter isolates have reported increased resistance to tigecycline by rapidly evading tigecycline by up-regulating efflux pumps encoded by chromosomal genes [165, 166] . Clinical reports described the combination regimens of tigecycline to treat A. baumannii infections, such as bacteremia, VAP, soft tissue, and skin infections [126, 167] . A poor correlation has been reported through studies between microbiological and clinical outcomes, mainly among patients under treatment for respiratory tract infections [120, 168, 169] . A low rate (48%) of microbiological eradication with tigecycline treatment has been noticed in A. baumannii hospital-acquired pneumonia (HAP) in some patients, probably due to the lack of adequate tigecycline concentration [170] . Another study recommended the high dose of tigecycline over a smalldose by PK-PD interpretation and partial clinical investigations sustain its safety and efficiency [171, 172] . In a study of UTI (urinary tract infections) from Italy, 85% of uro-pathogens were Gram-negative bacteria [173] . For treating UTI, tigecycline is not recommended as the right choice drug as it is not excreted via urine [174] . The development of tigecycline resistance in P. aeruginosa, A. baumannii, and K. pneumoniae infections was also reported during therapy [119] . Therefore, it is crucial to avoid tigecycline use as a monotherapy for A. baumannii infection treatment. After discussing these findings, tigecycline is considered a good option for salvage therapy of infectious diseases [167, 175] .

Tobramycin and amikacin are aminoglycoside agents utilized as therapeutic options for infections with MDR A. baumannii that keep hold of their susceptibility [176, 177] . Such agents are frequently utilized in combination with a different potent antibiotic [178] . Numerous MDR Acinetobacter isolates maintain intermediate susceptibility to tobramycin or amikacin and increasing resistance to these agents is coupled with efflux pump mechanisms of aminoglycoside modifying enzymes [179] . Recently, the role of the outermembrane protein 'A' has been associated with increased resistance to gentamicin [180] . However, in vitro studies have reported a rise in resistance to aminoglycosides [181] .

In a recent study from North India, a combination therapy of tetracycline with nalidixic acid showed a synergistic effect on MDR isolates of A. baumannii [182] . Minocycline has shown considerable results through an in vitro pharmacodynamics model against carbapenem-resistant and susceptible isolates of A. baumannii in monotherapy and combination with other antimicrobials [123] . Data from a few investigations have shown that more than 90% of isolates of A. baumannii were susceptibile to minocycline [183] . Subjective data has recommended minocycline in combinations with other antibiotics through intravenous route in critically ill patients with MDR Acinetobacter infections after the noticeable in vitro activity and constructive pharmacodynamics profiles [184] . However, large scale relative studies with an adequate number of patients are essential to validatethe minocycline efficacy. A study of over 2000 samples was recently conducted with a novel derivative of tetracycline (omadacycline) where 90% of the A. baumannii isolates were inhibited with a concentration of ≤4 µg/mL [185] . However, resistance to tetracycline has been reported in a number of investigations due to the overexpression of tet efflux pumps [186] .

Due to the high level of antimicrobial resistance, it is very difficult to control the A. baumannii infections. It is really difficult to get A. baumannii eliminated from a healthcare unit once it gets endemic. However, when a stubborn approach is implemented to infection prevention and control (IPC), it is not impossible to eliminate this organism from a unit. WHO guidelines were enforced in 2017 and should be strictly followed to effectively manage A. baumannii infections [187] . Although regular surveillance programs to control the infection are deficient in controlling the transmission of resistant Acinetobacter infections, inclusion of a variety of improvised action plans covering the assurance of all sorts of frontline hospital staff have revealed an indication of improvement ( Figure 3 ) [188] . Detection of the source of transmission, cleaning of the environment, judicious feedback of information and medical equipment disinfection, strengthening of standard precautions, and hand hygiene are all necessary steps to prevent the hospital outbreaks [189] . The patients should be kept in isolated sites; for patients receiving mechanical ventilation, a closed tracheal suction system should be used to prevent contamination [190] . However, there are many other examples where it has been compulsory to put into practice a closure of wards for a period of up to one month, so that outbreaks of A. baumannii could be controlled [191] At genome level, further investigations are required to screen novel genomic islands responsible for a high virulence potential [192] .

To study A. baumannii pathogenesis and virulence, model systems have now been established, including; in vitro and in vivo systems in invertebrates and mammals [193] [194] [195] . C. elegans has been used as a host model to detect the variations in virulence factors amongst a variety of A. baumannii isolates with already identified virulence factors and resistance mechanisms [28] . Several studies have investigated high levels of antibiotic resistance over the last two decades [145] . To a large extent, the in vivo work in association with the quick adjustment of A. baumannii in the presence of antibioticshas been conducted by defining its genetic architecture spanning hospitalsettings [195, 196] . Several other investigations have also underlined the significance of supplementary virulence factors [197, 198] . The knowledge of the association of the fitness cost and the virulence factors with the resistance mechanisms of A. baumannii stillis lacking; however, both the virulence and fitness costs are thought to be connected with antimicrobial resistance [196, 199] . A. baumannii virulence factors and pathogenetic potential allow it to grow and survive in the various habitats and environmental conditions where several other bacteria could not continue to exist [200, 201] . Multiple investigations have used mammalian infection models for inventing fitness and virulence assays of A. baumannii and other related bacterial pathogens, especially in the rodent models [202] . Vertebrate host models require multifarious infrastructure, amenities and trained manpower to handle, maintain and monitor large number of animals. Therefore, the invertebrate host models have become popular nowadays as alternative host models with less expenditure, a short life span, and low cost maintenance [203, 204] .

Over the last decade, developed invertebrate models decreased the cost and complications of mammalian model experiments and the need for animal care [205] . Moreover, no ethical issues are involved with the use of invertebrate models [206] . Such merits enable the large-scale infection model trials, which are predominantly utilized for high throughput selection of mutated bacterial strains [207] . Established invertebrate models to study the virulence include Drosophila melanogaster [208] , C. elegans [196] , Galleria mellonella [203] , Bombyx mori [209] , and Dictyostelium discoideum [210] .

G. mellonella and C. elegans have been demonstrated as the leading significant and standard host models in the laboratories to study bacterial virulence and pathogenic islands [211] . As a host model of A. baumannii, C. elegans possesses numerous merits over G. mellonella in targeting the host-bacterial relations, such as a small size; a petite generation time; a transparent body; a short genome; a simple lifecycle; ease of maintenance; no requirement for external suppliers; accessibility of a plentiful choice of genetically modified mutants; the full knowledge of its lineage; and the simplicity of the animal [212, 213] .

A. baumannii is a notorious, nosocomial pathogen responsible for hospital-acquired infections. It has an ability to survive in a variety of hospital environments and to accumulate antimicrobial resistance. Multidrug resistance is the most troublesome feature of A. baumannii, due to which new treatment agents are ineffective against it. Antibiotic resistance mechanisms of A. baumannii include β-lactamases; modification of aminoglycosides; overexpression of multidrug efflux pumps; under-expression of outer membrane porins; and modifications of target sites. As per recent studies, polymyxin B, another polymyxin antibiotic, has been proposed as a prospective therapeutic option to colistin. Various animal models are crucial to investigating the pathogenicity and virulenceassociated with A. baumannii. G. mellonella larvae have identified hundreds of genes necessary for in vivo A. baumannii survival. Additionally, other model animals using transposon screening will underscore the probability of a novel insight into the pathogenesis of A. baumannii. However, the pathogenicity and toxicity of A. baumannii still remain unclear despite recent advancements. Patients with severe infections should be included as hotspots from areas with high resistance rates for targeting future treatment options and trials. Rapid detection and implementation of thorough infection control measures, development of novel antibiotics and maintenance of effectiveness of already available antibiotics are the key factors for controlling the A. baumannii infections successfully. 

The authors declare no conflict of interest.

Role of the BaeSR two-component system in the regulation of Acinetobacter baumannii adeAB genes and its correlation with tigecycline susceptibility

Defining bacterial species in the genomic era: Insights from the genus Acinetobacter

Increase in Hospital-Acquired Carbapenem-Resistant Acinetobacter baumannii Infection and Colonization in an Acute Care Hospital During a Surge in COVID-19 Admissions-New Jersey

Prediction of the Risk of Hospital Deaths in Patients with Hospital-Acquired Pneumonia Caused by Multidrug-Resistant Acinetobacter baumannii Infection: A Multi-Center Study

Acinetobacter baumannii: Emergence of a successful pathogen

Integrated Co-functional Network Analysis on the Resistance and Virulence Features in Acinetobacter baumannii

Prevalence of multi-drug resistant (MDR) and extensively drug-resistant (XDR) phenotypes of Pseudomonas aeruginosa and Acinetobacter baumannii isolated in clinical samples from Northeast of Iran

Colistin Resistance in Environmental Isolates of Acinetobacter baumannii

A lethal pneumonia model of Acinetobacter baumannii: An investigation in immunocompetent mice

A Porcine Wound Model of Acinetobacter baumannii Infection

Assessing Acinetobacter baumannii Virulence and Persistence in a Murine Model of Lung Infection

Interplay Between Antibiotic Resistance and Virulence During Disease Promoted by Multidrug-Resistant Bacteria

Multiple roles for a novel RND-type efflux system in Acinetobacter baumannii AB5075

Anti-biofilm and anti-virulence effects of zerumbone against Acinetobacter baumannii

Uncovering the mechanisms of Acinetobacter baumannii virulence

Acinetobacter baumannii can use multiple siderophores for iron acquisition, but only acinetobactin is required for virulence

Characterization of surface antigen protein 1 (SurA1) from Acinetobacter baumannii and its role in virulence and fitness

Antibiofilm and antivirulence efficacy of myrtenol enhances the antibiotic susceptibility of Acinetobacter baumannii

The role of biofilms as environmental reservoirs of antibiotic resistance

Antimicrobial resistance patterns and their encoding genes among clinical isolates of Acinetobacter baumannii in Ahvaz

Pathobiology of Multidrug Resistant Acinetobacterbaumannii: An update

Excess mortality due to pandrug-resistant Acinetobacter baumannii infections in hospitalized patients

Attenuation of Acinetobacter baumannii virulence by inhibition of polyphosphate kinase 1 with repurposed drugs

Antimicrobial and biofilm inhibiting potential of an amide derivative [N-(2 , 4 -dinitrophenyl)-3beta-hydroxyurs-12-en-28-carbonamide] of ursolic acid by modulating membrane potential and quorum sensing against colistin resistant Acinetobacter baumannii

Septicemia by Pseudomonas stutzeri Vb-3: First report from India

Relationship Between Different Resistance Mechanisms and Virulence in Acinetobacter baumannii

Disruption of tetR type regulator adeN by mobile genetic element confers elevated virulence in Acinetobacter baumannii

Therapeutic options for difficult-to-treat Acinetobacter baumannii infections: A 2020 perspective

Therapeutic Potential of Novel Mastoparan-Chitosan Nanoconstructs Against Clinical MDR Acinetobacter baumannii: In silico, in vitro and in vivo Studies

The Rise of Carbapenem-Resistant Acinetobacter baumannii

In vitro activities of new beta-lactam antibiotics against Acinetobacter spp

Evolution of Acinetobacter calcoaceticus in the hospital milieu, from 1971 to 1984

In-vitro and in-vivo activities of antimicrobial agents against Acinetobacter calcoaceticus

Over-expression of RND and MATE efflux pumps contribute to decreased susceptibility in clinical isolates of carbapenem resistant Acinetobacter baumannii

Mechanisms of multidrug resistance in Acinetobacter species and Pseudomonas aeruginosa

Emergence of PER and VEB extended-spectrum beta-lactamases in Acinetobacter baumannii in Belgium

Structural basis for carbapenem-hydrolyzing mechanisms of carbapenemases conferring antibiotic resistance

Stormy waters ahead": Global emergence of carbapenemases

Diversity, epidemiology, and genetics of class D beta-lactamases

Carbapenemase genes and genetic platforms in Gram-negative bacilli: Enterobacteriaceae, Pseudomonas and Acinetobacter species

OXA beta-lactamases

ARI 1: Beta-lactamase-mediated imipenem resistance in Acinetobacter baumannii

Chromosome-encoded class D beta-lactamase OXA-23 in Proteus mirabilis

Characterization of a nosocomial outbreak caused by a multiresistant Acinetobacter baumannii strain with a carbapenem-hydrolyzing enzyme: High-level carbapenem resistance in A. baumannii is not due solely to the presence of beta-lactamases

Genetic environment and expression of the extended-spectrum betalactamase blaPER-1 gene in gram-negative bacteria

Epidemic multidrug-resistant Acinetobacter baumannii related to European clonal types I and II in Rome (Italy)

Molecular epidemiology of carbapenem-resistant Acinetobacter baumannii in a newly established Greek hospital

Molecular characterization of acinetobacter isolates collected in intensive care units of six hospitals in Florence, Italy, during a 3-year surveillance program: A population structure analysis

Molecular epidemiological investigation of multidrug-resistant Acinetobacter baumannii strains in four Mediterranean countries with a multilocus sequence typing scheme

Evolution of multidrug-resistant Acinetobacter baumannii clonal lineages: A 10 year study in Greece

Genetic structures at the origin of acquisition and expression of the carbapenem-hydrolyzing oxacillinase gene blaOXA-58 in Acinetobacter baumannii

Outbreak of multiple clones of imipenem-resistant Acinetobacter baumannii isolates expressing OXA-58 carbapenemase in an intensive care unit

Clusters of imipenemresistant Acinetobacter baumannii clones producing different carbapenemases in an intensive care unit

Molecular epidemiology of carbapenem-resistant Acinetobacter baumannii isolates reveals the emergence of blaOXA-23 and blaNDM-1 encoding international clones in India

OXA-143, a novel carbapenem-hydrolyzing class D betalactamase in Acinetobacter baumannii

The versatile beta-lactamases

Contribution of acquired carbapenem-hydrolyzing oxacillinases to carbapenem resistance in Acinetobacter baumannii

Clinically relevant chromosomally encoded multidrug resistance efflux pumps in bacteria

Acinetobacter baumannii Efflux Pumps and Antibiotic Resistance

Pneumonia in multiple injured patients: A prospective controlled trial on early prediction using clinical and immunological parameters

Multidrug efflux pumps of gram-negative bacteria

The RND permease superfamily: An ancient, ubiquitous and diverse family that includes human disease and development proteins

Multidrug resistance mechanisms: Drug efflux across two membranes

Expression of Pseudomonas aeruginosa multidrug efflux pumps MexA-MexB-OprM and MexC-MexD-OprJ in a multidrug-sensitive Escherichia coli strain

Exploring the Interplay of Resistance Nodulation Division Efflux Pumps, AmpC and OprD in Antimicrobial Resistance of Burkholderiacepacia Complex in Clinical Isolates

Characterization of MexE-MexF-OprN, a positively regulated multidrug efflux system of Pseudomonas aeruginosa

Resistance-nodulation-cell division-type efflux pump involved in aminoglycoside resistance in Acinetobacter baumannii strain BM4454

Overexpression of resistance-nodulation-cell division pump AdeFGH confers multidrug resistance in Acinetobacter baumannii

AdeIJK, a resistance-nodulation-cell division pump effluxing multiple antibiotics in Acinetobacter baumannii

Expression of the RND-type efflux pump AdeABC in Acinetobacter baumannii is regulated by the AdeRS two-component system

Expression of the resistance-nodulation-cell division pump AdeIJK in Acinetobacter baumannii is regulated by AdeN, a TetR-type regulator

Nosocomial infections caused by Acinetobacter baumannii: A major threat worldwide

AbeM, an H+-coupled Acinetobacter baumannii multidrug efflux pump belonging to the MATE family of transporters

Insights into Acinetobacter baumannii pathogenicity

Inhibition of Virulence Factors and Biofilm Formation of Acinetobacter baumannii by Naturally-derived and Synthetic Drugs

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

Highly conserved exposed immunogenic peptides of Omp34 against Acinetobacter baumannii: An innovative approach

Outer membrane protein A (OmpA) as a potential therapeutic target for Acinetobacter baumannii infection

A bovine myeloid antimicrobial peptide (BMAP-28) and its analogs kill pan-drug-resistant Acinetobacter baumannii by interacting with outer membrane protein A (OmpA)

Identification of antigens from nosocomial Acinetobacter baumannii clinical isolates in sera from ICU staff and infected patients using the antigenome technique

Interspecies Outer Membrane Vesicles (OMVs) Modulate the Sensitivity of Pathogenic Bacteria and Pathogenic Yeasts to Cationic Peptides and Serum Complement

Extraction and Analysis of RNA Isolated from Pure Bacteria-Derived Outer Membrane Vesicles

Outer Membrane Vesicles (OMVs) of Gram-negative Bacteria: A Perspective Update

Vesicle-Mediated Gene Transfer in Acinetobacter baumannii

Biofilm Formation in Acinetobacter baumannii: Genotype-Phenotype Correlation

Structural basis for Acinetobacter baumannii biofilm formation

The Acinetobacter baumannii 19606 OmpA protein plays a role in biofilm formation on abiotic surfaces and in the interaction of this pathogen with eukaryotic cells

Quorum-sensing system in Acinetobacter baumannii: A potential target for new drug development

Pneumonia infection in mice reveals the involvement of the feoA gene in the pathogenesis of Acinetobacter baumannii

Glycomics Microarrays Reveal Differential In Situ Presentation of the Biofilm Polysaccharide Poly-N-acetylglucosamine on Acinetobacter baumannii and Staphylococcus aureus Cell Surfaces

Biofilm contamination of high-touched surfaces in intensive care units: Epidemiology and potential impacts

Virulence characteristics of multidrug resistant biofilm forming Acinetobacter baumannii isolated from intensive care unit patients

A method to assess influence of different medical tubing on biofilm formation by Acinetobacter baumannii

Bloodstream infections caused by ST2 Acinetobacter baumannii: Risk factors, antibiotic regimens, and virulence over 6 years period in China

Septal Class A Penicillin-Binding Protein Activity and ld-Transpeptidases Mediate Selection of Colistin-Resistant Lipooligosaccharide-Deficient Acinetobacter baumannii

A penicillin-binding protein inhibits selection of colistin-resistant, lipooligosaccharide-deficient Acinetobacter baumannii

The Novel beta-Lactam Enhancer Zidebactam Augments the In Vivo Pharmacodynamic Activity of Cefepime in a Neutropenic Mouse Lung Acinetobacter baumannii Infection Model

Penicillin-binding protein 7/8 contributes to the survival of Acinetobacter baumannii in vitro and in vivo

Humanized Exposures of a beta-Lactam-beta-Lactamase Inhibitor, Tazobactam, versus Non-beta-Lactam-beta-Lactamase Inhibitor, Avibactam, with or without Colistin, against Acinetobacter baumannii in Murine Thigh and Lung Infection Models

Pharmacokinetic and Pharmacodynamic Profiles of Cefiderocol, a Novel Siderophore Cephalosporin

Activity of cefiderocol against high-risk clones of multidrug-resistant Enterobacterales, Acinetobacter baumannii, Pseudomonas aeruginosa and Stenotrophomonas maltophilia

Siderophore-based iron acquisition and pathogen control. Microbiol

Siderophore Cephalosporin for Gram-Negative Bacterial Infections: Pharmacokinetics and Safety in Subjects with Renal Impairment

Total Syntheses of Fimsbactin A and B and Their Stereoisomers to Probe the Stereoselectivity of the Fimsbactin Uptake Machinery in Acinetobacter baumannii

A gamma-lactam siderophore antibiotic effective against multidrug-resistant Pseudomonas aeruginosa, Klebsiella pneumoniae, and Acinetobacter spp

In vivo synthesis of monolysocardiolipin and cardiolipin by Acinetobacter baumannii phospholipase D and effect on cationic antimicrobial peptide resistance

Diversity and Function of Capsular Polysaccharide in Acinetobacter baumannii

Biology of Acinetobacter baumannii: Pathogenesis, Antibiotic Resistance Mechanisms, and Prospective Treatment Options

New Treatment Options against Carbapenem-Resistant Acinetobacter baumannii Infections

Transforming Acinetobacter baumannii into a Yet More Dangerous Menace

Ventilator-Associated Pneumonia due to Drug-Resistant Acinetobacter baumannii: Risk Factors and Mortality Relation with Resistance Profiles, and Independent Predictors of In-Hospital Mortality

Meropenem/colistin versus meropenem/ampicillin-sulbactam in the treatment of carbapenem-resistant pneumonia

Epidemiology and Diagnostics of Carbapenem Resistance in Gram-negative Bacteria

Emergence, molecular mechanisms and global spread of carbapenem-resistant Acinetobacter baumannii. Microb. Genom. 2019, 5, e000306

Emergence and spread of carbapenem-resistant Acinetobacter baumannii international clones II and III in Lima

Treatment options for K. pneumoniae, P. aeruginosa and A. baumannii co-resistant to carbapenems, aminoglycosides, polymyxins and tigecycline: An approach based on the mechanisms of resistance to carbapenems

Efficacy and safety of tigecycline in treatment of pneumonia caused by MDR Acinetobacter baumannii: A systematic review and meta-analysis

Clinical efficacy and safety of polymyxins based versus non-polymyxins based therapies in the infections caused by carbapenem-resistant Acinetobacter baumannii: A systematic review and meta-analysis

Resistance surveillance program report for selected European nations

Minocycline Alone and in Combination with Polymyxin B, Meropenem, and Sulbactam against Carbapenem-Susceptible and -Resistant Acinetobacter baumannii in an In Vitro Pharmacodynamic Model

Sepsis-A Retrospective Cohort Study of Bloodstream Infections

Lower Respiratory Tract Pathogens and Their Antimicrobial Susceptibility Pattern: A 5-Year Study

Triple combination therapy with high-dose ampicillin/sulbactam, high-dose tigecycline and colistin in the treatment of ventilator-associated pneumonia caused by pan-drug resistant Acinetobacter baumannii: A case series study

Polymyxin-resistant, carbapenem-resistant Acinetobacter baumannii is eradicated by a triple combination of agents that lack individual activity

In vitro and in vivo assessment of the antibacterial activity of colistin alone and in combination with other antibiotics against Acinetobacter baumannii and Escherichia coli

In vitro synergistic activity of the sulbactam/avibactam combination against extensively drug-resistant Acinetobacter baumannii

Combined Rifampin and Sulbactam Therapy for Multidrug-Resistant Acinetobacter baumannii Ventilator-Associated Pneumonia in Pediatric Patients

Polymyxin monotherapy or in combination against carbapenem-resistant bacteria: Systematic review and meta-analysis

Synergistic Effect of Tazobactam on Amikacin MIC in Acinetobacter baumannii Isolated from Burn Patients in Tehran

Antibiotic combinations for serious infections caused by carbapenem-resistant Acinetobacter baumannii in a mouse pneumonia model

Trends in Drug Resistance of Acinetobacter baumannii over a 10-year Period: Nationwide Data from the China Surveillance of Antimicrobial Resistance Program

Managing Acinetobacter baumannii infections

Plazomicin: A Novel Aminoglycoside for the Treatment of Resistant Gram-Negative Bacterial Infections

-7072, a Novel Third-Generation Tetracycline, against 531 Recent Geographically Diverse and Molecularly Characterized Acinetobacter baumannii Species Complex Isolates

Risk Factors and Drug Resistance of the MDR Acinetobacter baumannii in Pneumonia Patients in ICU

Antibiotic susceptibility signatures identify potential antimicrobial targets in the Acinetobacter baumannii cell envelope

Carbapenem use in critically ill patients

Genome Sequence of Acinetobacter baumannii Strain 5021_13, Isolated from Cerebrospinal Fluid

Genome Sequence of Acinetobacter baumannii Strain 10441_14 Belonging to ST451, Isolated from India

Enhanced bacterial killing with colistin/sulbactam combination against carbapenem-resistant Acinetobacter baumannii

Colistin and its role in the Era of antibiotic resistance: An extended review

Colistin Dependence in Extensively Drug-Resistant Acinetobacter baumannii Strain Is Associated with ISAjo2 and ISAba13 Insertions and Multiple Cellular Responses

Antimicrobial susceptibility among Acinetobacter calcoaceticus-baumannii complex and Enterobacteriaceae collected as part of the Tigecycline Evaluation and Surveillance Trial

Colistin versus Colistin Combined with Ampicillin-Sulbactam for Multiresistant Acinetobacter baumannii Ventilator-associated Pneumonia Treatment: An Open-label Prospective Study

Outcomes of adjunctive therapy with intrathecal or intraventricular administration of colistin for post-neurosurgical meningitis and ventriculitis due to carbapenem-resistant Acinetobacter baumannii

The effectiveness and nephrotoxicity of loading dose colistin combined with or without meropenem for the treatment of carbapenem-resistant A. baumannii

Dose Optimization of Colistin Combinations against Carbapenem-Resistant Acinetobacter baumannii from Patients with Hospital-Acquired Pneumonia in China by Using an In Vitro Pharmacokinetic/Pharmacodynamic Model

Intravenous vs intravenous plus aerosolized colistin for treatment of ventilator-associated pneumonia-A matched case-control study in neonates

Composite particle formulations of colistin and meropenem with improved in-vitro bacterial killing and aerosolization for inhalation

Comparative efficacy and safety of combination therapy with high-dose sulbactam or colistin with additional antibacterial agents for multiple drug-resistant and extensively drug-resistant Acinetobacter baumannii infections: A systematic review and network meta-analysis

Deciphering colistin heteroresistance in Acinetobacter baumannii clinical isolates from Wenzhou

In vitro synergistic effect of colistin and ampicillin/sulbactam with several antibiotics against clinical strains of multi-drug resistant Acinetobacter baumannii

Effectiveness of Cefoperazone-sulbactam alone and Combined with Tigecycline in the Treatment of Multi-drug Resistant Acinetobacter baumannii Pulmonary Infection

Individual or Combined Effects of Meropenem, Imipenem, Sulbactam, Colistin, and Tigecycline on Biofilm-Embedded Acinetobacter baumannii and Biofilm Architecture

A prospective multicenter study on the evaluation of antimicrobial resistance and molecular epidemiology of multidrug-resistant Acinetobacter baumannii infections in intensive care units with clinical and environmental features

Sulbactam enhances the in vitro activity of sitafloxacin against extensivelydrug resistant Acinetobacter baumannii

Treatment efficacy of tigecycline in comparison to cefoperazone/ sulbactam alone or in combination therapy for carbapenenm-resistant Acinetobacter baumannii infections

Ampicillin/sulbactam: Its potential use in treating infections in critically ill patients

Molecular Epidemiology and Mechanism of Sulbactam Resistance in Acinetobacter baumannii Isolates with Diverse Genetic Backgrounds in China

Comparison of the treatment efficacy between tigecycline plus highdose cefoperazone-sulbactam and tigecycline monotherapy against ventilator-associated pneumonia caused by extensively drug-resistant Acinetobacter baumannii

Overexpression of AdeABC efflux pump associated with tigecycline resistance in clinical Acinetobacter nosocomialis isolates

Tigecycline efflux in Acinetobacter baumannii is mediated by TetA in synergy with RND-type efflux transporters

Comparison of the clinical efficacy between tigecycline plus extended-infusion imipenem and sulbactam plus imipenem against ventilator-associated pneumonia with pneumonic extensively drug-resistant Acinetobacter baumannii bacteremia, and correlation of clinical efficacy with in vitro synergy tests

Intraventricular Tigecycline as a Last Resort Therapy in a Patient with Difficult-to-Treat Healthcare-Associated Acinetobacter baumannii Ventriculitis: A Case Report. SN Compr

Pseudomonas oleovorans Sepsis in a Child: The First Reported Case in India

Clinical experience with tigecycline in the treatment of hospital-acquired pneumonia caused by multidrug resistant Acinetobacter baumannii

Bad bug, no test: Tigecycline susceptibility testing challenges and way forward

Optimization of tigecycline dosage regimen for different infections in the patients with hepatic or renal impairment

Trend of Bacterial Uropathogens and Their Susceptibility Pattern: Study of Single Academic High

Tigecycline in treatment of multidrug-resistant Gram-negative bacillus urinary tract infections: A systematic review

Tigecycline salvage therapy for ventriculoperitoneal shunt meningitis due to extensively drugresistant Acinetobacter baumannii

Meropenem and Amikacin for Management of Post-Neurosurgical Infections from Acinetobacter baumannii

Eradication of persister cells of Acinetobacter baumannii through combination of colistin and amikacin antibiotics

Aminoglycoside Heteroresistance in Acinetobacter baumannii AB5075. mSphere

Distinct role of outer membrane protein A in the intrinsic resistance of Acinetobacter baumannii and Acinetobacter nosocomialis

In vitro activity of apramycin against multidrug-, carbapenem-and aminoglycoside-resistant Enterobacteriaceae and Acinetobacter baumannii

Mechanistic insights into synergy between nalidixic acid and tetracycline against clinical isolates of Acinetobacter baumannii and Escherichia coli

The Role of Minocycline in the Treatment of Nosocomial Infections Caused by Multidrug, Extensively Drug and Pandrug Resistant Acinetobacter baumannii: A Systematic Review of Clinical Evidence

Pharmacodynamics of Minocycline against Acinetobacter baumannii in a Rat Pneumonia Model

Activity of Omadacycline and Other Tetracyclines Against Contemporary Gram-Negative Pathogens from New York City Hospitals

Tetracycline resistance mediated by tet efflux pumps in clinical isolates of Acinetobacter baumannii

Guidelines for the Prevention and Control of Carbapenem-Resistant Enterobacteriaceae, Acinetobacter baumannii and Pseudomonas aeruginosa in Health Care Facilities

Prevention and Control of Multidrug-Resistant Gram-Negative Bacteria in Adult Intensive Care Units: A Systematic Review and Network Meta-analysis

Control of a multidrug-resistant Acinetobacter baumannii outbreak

A multimodal intervention program to control a long-term Acinetobacter baumannii endemic in a tertiary care hospital

Control of Acinetobacter baumannii outbreak in the neonatal intensive care unit in Latvia: Whole-genome sequencing powered investigation and closure of the ward

Genomics Reveals a Unique Clone of Burkholderiacenocepacia Harboring an Actively Excising Novel Genomic Island

Direct interaction between RecA and a CheW-like protein is required for surface-associated motility, chemotaxis and the full virulence of Acinetobacter baumannii strain ATCC 17978

Genome-Scale Metabolic Modeling Reveals Metabolic Alterations of Multidrug-Resistant Acinetobacter baumannii in a Murine Bloodstream Infection Model

In vitro and in vivo fitness of clinical isolates of carbapenem-resistant and -susceptible Acinetobacter baumannii

Virulence role of the outer membrane protein CarO in carbapenem-resistant Acinetobacter baumannii

Global Transcriptomic Analysis During Murine Pneumonia Infection Reveals New Virulence Factors in Acinetobacter baumannii

Pimenta Oil as A Potential Treatment for Acinetobacter baumannii Wound Infection: In Vitro and In Vivo Bioassays in Relation to Its Chemical Composition

Surface-Related Features and Virulence Among Acinetobacter baumannii Clinical Isolates Belonging to International Clones I and II

Mechanisms Protecting Acinetobacter baumannii against Multiple Stresses Triggered by the Host Immune Response, Antibiotics and Outside-Host Environment

Mouse Models of Acinetobacter baumannii Infection

Antibiotics Act with vB_AbaP_AGC01 Phage against Acinetobacter baumannii in Human Heat-Inactivated Plasma Blood and Galleria mellonella Models

An Invertebrate Burn Wound Model That Recapitulates the Hallmarks of Burn Trauma and Infection Seen in Mammalian Models

Ton-That, H. Corynebacterium diphtheriae Virulence Analyses Using a Caenorhabditis elegans Model

Animal infection models using non-mammals

Characterization of RelA in Acinetobacter baumannii

A Tractable Drosophila Cell System Enables Rapid Identification of Acinetobacter baumannii Host Factors

Bombyx mori, as an alternative model organism in toxicological research

Dictyosteliumdiscoideum as a non-mammalian biomedical model

Exophiala dermatitidis isolates from various sources: Using alternative invertebrate host organisms (Caenorhabditis elegans and Galleria mellonella) to determine virulence

Caenorhabditis elegans as a model for intracellular pathogen infection

Caenorhabditis elegans as a Model for Microbiome Research