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Acinetobacter

Acinetobacter is a genus of Gram-negative, aerobic, non-fermentative, oxidase-negative coccobacilli bacteria that are ubiquitous in the environment, commonly found in soil, water, sewage, and on human and animal skin.^[1]^[2]^[3] These nonmotile organisms exhibit versatile metabolic capabilities, including the degradation of aromatic compounds, hydrocarbons, and toxins, as well as phosphate solubilization, making some species valuable for bioremediation and plant growth promotion.^[3] While the genus encompasses over 80 species with diverse ecological roles as of 2024, certain members, particularly those in the A. baumannii complex such as Acinetobacter baumannii, are opportunistic pathogens that primarily cause nosocomial infections in healthcare settings.^[2]^[4]^[5] Clinically, Acinetobacter species are associated with infections including pneumonia, bacteremia, urinary tract infections, wound infections, and meningitis, predominantly affecting vulnerable populations such as immunocompromised patients, those in intensive care units (ICUs), individuals with prolonged hospital stays, ventilators, catheters, or chronic conditions like diabetes and lung disease.^[1]^[2] These infections are healthcare-associated, spreading through contaminated surfaces, equipment, or person-to-person contact via healthcare workers' hands, with A. baumannii being the most frequent culprit and linked to high mortality rates of 30-75% in cases of pneumonia and up to 70% in resistant strains.^[1]^[4] The genus's low inherent virulence is offset by its remarkable environmental persistence, surviving dry conditions for over four months on surfaces and forming biofilms that enhance colonization.^[2]^[4] A major public health concern with Acinetobacter is its propensity for antibiotic resistance, with many strains classified as multidrug-resistant (MDR), extensively drug-resistant (XDR), or even pan-drug-resistant (PDR), driven by mechanisms such as β-lactamases, efflux pumps, and porin alterations.^[2]^[4] The U.S. Centers for Disease Control and Prevention (CDC) designates carbapenem-resistant Acinetobacter as a "serious" antimicrobial resistance threat, complicating treatment and necessitating strategies like device removal, isolation of colonized patients, rigorous hand hygiene, and targeted antibiotics such as colistin or tigecycline when susceptible.^[1]^[2] Beyond pathogenesis, the genus's heterogeneity highlights its ecological significance, with non-pathogenic species contributing to food spoilage, wastewater treatment, and industrial applications, underscoring Acinetobacter's multifaceted role in both human health challenges and environmental processes.^[3]^[4]

Introduction

Description

_Acinetobacter is a genus of Gram-negative bacteria characterized by their coccobacilli morphology, appearing as short, paired rods or diplococci under microscopy. These organisms are strictly aerobic, non-motile, and incapable of spore formation, distinguishing them from many other Gram-negative bacteria. They typically stain Gram-negative but may occasionally appear Gram-variable due to challenges in decolorization during staining.^[6] Physiologically, Acinetobacter species are catalase-positive and oxidase-negative, enabling their identification in clinical and environmental settings. As strict aerobes, they rely on oxidative respiration for energy production and thrive in oxygen-rich environments without fermentative capabilities. These bacteria demonstrate remarkable adaptability, growing across a broad temperature range of 20–45°C, with an optimum around 37°C for most isolates, and they can proliferate on minimal media supplemented with basic nutrients.^[6]^[7]^[8] Biochemically, Acinetobacter exhibits oxidative metabolism of glucose, where the sugar is oxidized in the periplasm to gluconate before entering central metabolism, rather than through glycolysis. This genus can utilize a diverse array of carbon sources, including acetate and lactate, supporting their survival in nutrient-variable habitats. The cell envelope includes lipopolysaccharide (LPS) in the outer membrane, which provides structural integrity and contributes to barrier functions, alongside porins such as OmpA that facilitate nutrient uptake and environmental interactions.^[9]^[10]^[11]^[12]

Etymology

The genus name Acinetobacter derives from the Ancient Greek prefix a- (ἀ-, meaning "without" or "non-") and kinētos (κινῆτος, meaning "able to move" or "motile"), combined with the suffix -bakter (from bakterion, βακτήριον, meaning "rod" or "staff"), thus translating to "non-motile rod."^[13] This nomenclature directly reflects the defining morphological trait of non-motility observed in these Gram-negative coccobacilli.^[14] The name was first proposed in 1954 by French microbiologists Jean Brisou and Augustin R. Prévot in their taxonomic revision of the heterogeneous Achromobacter group, aiming to delineate non-motile, oxidase-negative strains from the motile pseudomonads and related aerobes previously lumped together.^[15] Their seminal paper, published in the Annales de l'Institut Pasteur, established Acinetobacter as a distinct genus to accommodate these saprophytic, strictly aerobic bacteria, separating them based on phenotypic characteristics such as lack of motility and oxidase activity.^[6] Although initially proposed in 1954, the genus faced taxonomic uncertainty and was not universally accepted until the late 1960s and 1970s, when it was reclassified as a separate entity from Moraxella. In 1968, Peter Baumann and colleagues proposed transferring oxidase-negative, rod-shaped members of Moraxella (previously classified under group II Moraxella) into Acinetobacter based on physiological and biochemical distinctions.^[16] This separation was officially acknowledged in 1971 by the Subcommittee on the Taxonomy of Moraxella and Allied Bacteria of the International Committee on Bacteriological Nomenclature, supported by early nucleic acid homology studies.^[6] Specifically, pulse-labeled RNA-DNA hybridization experiments in 1970 demonstrated low genetic relatedness between Acinetobacter strains and typical Moraxella or Neisseria species, providing molecular evidence for the genus-level distinction and reinforcing its independence within the emerging family Moraxellaceae.^[17]

Taxonomy and Phylogeny

Classification

Acinetobacter is a genus of Gram-negative bacteria classified within the family Moraxellaceae, order Moraxellales, class Gammaproteobacteria, and phylum Pseudomonadota.^[18] This placement reflects its phylogenetic position among aerobic, non-motile coccobacilli that share metabolic and genetic traits with other members of the Moraxellaceae family, such as Moraxella and Psychrobacter.^[19] Species delineation in the genus relies primarily on DNA-DNA hybridization (DDH) thresholds, where values greater than 70% indicate conspecific strains, complemented by 16S rRNA gene sequence similarities typically exceeding 97% for genus-level assignment.^[20] Increasingly, average nucleotide identity (ANI) values of 95-96% are used as a genomic proxy for the 70% DDH threshold, facilitating species delineation with whole-genome sequences.^[21] Due to limited intraspecies variation in 16S rRNA genes, DDH remains the gold standard for resolving closely related taxa, as demonstrated in foundational studies identifying multiple genomic species.^[22] This polyphasic approach has led to the recognition of over 90 validly named species, with ongoing genomic sequencing refining boundaries and identifying additional taxa.^[23]^[24] Phylogenetic analyses, based on core-genome orthologs and multi-locus sequence data, reveal a monophyletic genus divided into a core group (encompassing genomic species 1–15) and peripheral species.^[24] The core group includes clinically significant taxa like A. baumannii (genomic species 2) and forms a tight clade with shared orthologous proteins (approximately 950 families), while peripheral species exhibit greater divergence and adaptation to environmental niches.^[25] This structure highlights the genus's ancient diversification, with the core-peripheral split reflecting ecological specialization.^[24] One genomic study suggested an ancient origin for the genus, with protein sequence similarities indicating the last common ancestor may date back over 500 million years, comparable to major bacterial radiations.^[24]

Key Species

Acinetobacter baumannii is recognized as the primary human pathogen within the genus, classified as genomic species 2 in the Acinetobacter calcoaceticus-A. baumannii complex.^[26] Its genome typically measures approximately 4 Mb, enabling a compact structure that supports rapid adaptation in clinical environments.^[27] This species exhibits high genomic plasticity, largely driven by the acquisition and mobilization of plasmids that carry resistance genes and virulence factors, facilitating its persistence in hospital settings.^[28] Acinetobacter calcoaceticus, an environmental species, is commonly isolated from soil and water sources rather than clinical samples.^[29] It is frequently misidentified due to phenotypic similarities with other complex members, complicating accurate surveillance.^[21] A distinguishing feature is its ability to utilize acetate as a primary carbon source, reflecting adaptations to nutrient-limited natural habitats.^[30] Acinetobacter lwoffii serves as a commensal organism on human skin and mucous membranes, contributing to the normal microbiome without typically causing disease.^[31] It is considered less virulent than pathogenic congeners, with infections rare and often linked to immunocompromised states.^[32] Differentiation from other species relies on biochemical profiles, including variable utilization of carbon sources and enzymatic activities.^[33] Emerging species such as Acinetobacter nosocomialis and Acinetobacter pittii are increasingly associated with hospital-acquired infections, forming part of the A. calcoaceticus-A. baumannii complex alongside A. baumannii.^[34] These are distinguished genomically through multilocus sequence typing (MLST), which reveals sequence variations in housekeeping genes to resolve species boundaries.^[35] Phenotypically, they show subtle differences in growth characteristics and antibiotic susceptibilities compared to A. baumannii.^[36]

Biology and Ecology

Habitat

Acinetobacter species are ubiquitous environmental bacteria, commonly found in soil, freshwater, sewage, and various food sources such as milk and vegetables. This wide distribution is attributed to their remarkable tolerance to desiccation, nutrient limitation, and fluctuating environmental conditions, allowing them to thrive as free-living saprophytes in diverse ecosystems.^[3]^[37]^[38] In human-associated habitats, Acinetobacter serves as a transient component of the normal skin and respiratory tract flora in healthy individuals, with carriage rates typically ranging from 15% to 43%. This colonization is often asymptomatic and reflects the bacterium's adaptability to human skin's relatively dry and nutrient-poor microenvironments.^[39]^[40]^[41] Within hospital environments, Acinetobacter demonstrates exceptional persistence on dry inanimate surfaces, such as bed rails, ventilators, and countertops, surviving for weeks to months—up to four months in some cases—due to its capacity for biofilm formation. These biofilms protect cells from desiccation and disinfectants, enabling prolonged environmental reservoirs that facilitate transmission.^[42]^[43]^[44]^[45] Ecologically, Acinetobacter plays a key role in nutrient cycling processes, particularly in soil and aquatic systems, where it contributes to organic matter decomposition and nutrient mobilization for plant growth. Certain species are also prominent in bioremediation, degrading hydrocarbons in polluted sites like oil-contaminated soils and sediments, thereby aiding in the restoration of contaminated environments.^[46]^[37]^[47]^[48]

Identification

Acinetobacter species are typically identified in the laboratory through a combination of phenotypic and molecular methods, as their morphological similarities to other Gram-negative bacteria necessitate targeted approaches for accurate differentiation from clinical or environmental samples. Initial phenotypic characterization involves culturing isolates on selective media such as MacConkey agar, where Acinetobacter grows as non-lactose-fermenting, colorless colonies, aiding in preliminary screening from lactose-fermenting Enterobacteriaceae.^[49] Further biochemical testing using systems like the API 20NE panel (bioMérieux) assesses key traits, including oxidase negativity, catalase positivity, urease negativity, and variable citrate utilization, achieving approximately 92% accuracy for genus-level identification when compared to conventional biochemical tests.^[50] These methods rely on the bacteria's non-motile, coccobacillary Gram-negative morphology observed via hanging drop preparation and Gram staining.^[51] Molecular tools provide higher specificity, particularly for species-level identification within the Acinetobacter calcoaceticus-baumannii (Acb) complex. Polymerase chain reaction (PCR) targeting the blaOXA-51-like carbapenemase gene is a rapid and reliable marker for Acinetobacter baumannii, highly specific for A. baumannii, though rare false positives in other Acinetobacter species have been reported, distinguishing most strains from other species lacking this intrinsic gene.^[52] Recent advances as of 2025 include pan-genome-derived specific targets for nucleic acid amplification tests (NATs), enhancing detection accuracy for A. baumannii.^[53] Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) enables quick proteomic profiling, with updated databases improving accuracy to over 95% for clinically relevant species like A. baumannii, A. pittii, and A. nosocomialis, though performance may vary for rare or novel taxa.^[54] For unresolved cases, sequencing the rpoB gene (RNA polymerase beta subunit) offers robust phylogenetic resolution, achieving 98.2% accuracy in delineating Acb complex species based on nucleotide variability.^[55] Serological and phage typing methods, while historically employed, have limited contemporary use primarily for epidemiological strain tracking in outbreak investigations. Serotyping based on lipopolysaccharide antigens can classify A. baumannii into over 20 serovars, facilitating source attribution in nosocomial settings, but cross-reactivity and lack of standardization reduce reliability.^[56] Phage typing, using bacteriophages specific to Acinetobacter, identifies lysis patterns for subtyping, with studies demonstrating utility in correlating strains during hospital epidemics, though it is supplanted by genomic methods due to reproducibility issues.^[57] A major challenge in Acinetobacter identification is misclassification as Enterobacteriaceae, stemming from overlapping phenotypic traits like Gram-negative coccobacillary morphology and growth on common media, which automated systems such as VITEK 2 exacerbate through incomplete databases.^[55] This error can lead to inappropriate therapeutic decisions, as Acinetobacter exhibits distinct resistance profiles. Resolution often requires confirmatory molecular approaches like rpoB gene sequencing to achieve precise species assignment, underscoring the need for integrated phenotypic-molecular workflows in diagnostic laboratories.^[52]

Natural Transformation

Natural transformation in Acinetobacter species enables the uptake and integration of exogenous DNA, contributing to genetic diversity and adaptability. This process is particularly well-characterized in A. baumannii, a clinically significant pathogen, where competence is inducible by specific environmental cues such as human serum albumin and calcium ions (Ca²⁺), which enhance DNA uptake frequencies by up to several orders of magnitude compared to basal levels.^[58] In contrast, the model organism A. baylyi exhibits constitutive natural competence across growth phases, with peak efficiency during late exponential phase, though nutrient limitation can further promote DNA uptake as a nutrient acquisition strategy.^[59] These induction mechanisms allow Acinetobacter cells to respond to host-associated or stressful conditions, facilitating rapid genetic exchange. The DNA uptake machinery in Acinetobacter relies on type IV pili (T4P) for initial binding and translocation of extracellular DNA. T4P, composed of pilin subunits like PilA and accessory proteins such as PilT (retraction ATPase), bind double-stranded DNA at the cell surface, followed by retraction that pulls the DNA toward the periplasm.^[60] Once in the periplasm, DNA is processed into single strands by nucleases and translocated across the inner membrane via the ComEC channel, with ComEA acting as a DNA-binding protein to stabilize the process.^[61] Integration of the incoming DNA into the genome occurs through RecA-mediated homologous recombination, enabling stable incorporation of genetic elements without the need for plasmids in many cases.^[62] This T4P-dependent pathway is conserved across Acinetobacter species and shares components with twitching motility systems, highlighting multifunctional roles in bacterial physiology.^[63] Under laboratory conditions optimized for competence (e.g., addition of serum albumin and Ca²⁺ in A. baumannii), transformation frequencies can reach up to 10⁻⁴ transformants per recipient cell, representing a significant proportion of the population capable of DNA uptake.^[64] In A. baylyi, frequencies are comparably high, often exceeding 10⁻³ in rich media, underscoring the efficiency of this genus in horizontal gene transfer (HGT).^[59] Evolutionarily, natural transformation promotes HGT of antibiotic resistance cassettes in Acinetobacter, allowing rapid adaptation to selective pressures such as antimicrobial exposure. For instance, in clinical isolates of A. baumannii, transformation facilitates the acquisition of resistance genes like those encoding carbapenemases, enhancing intraspecies and interspecies gene flow in polymicrobial environments.^[65] This mechanism contributes to the emergence of multidrug-resistant strains, underscoring its role in pathogenicity and ecological persistence.^[66]

Medical and Clinical Aspects

Clinical Significance

_Acinetobacter species, particularly A. baumannii, are opportunistic pathogens primarily responsible for nosocomial infections in healthcare settings. They commonly cause ventilator-associated pneumonia (VAP), accounting for approximately 10–20% of VAP isolates in some intensive care unit (ICU) populations, as well as bacteremia and urinary tract infections (UTIs). These infections often arise from prior colonization rather than primary invasion, with outbreaks frequently reported in ICUs due to the organism's environmental persistence.^[67]^[2] Patients at highest risk include immunocompromised individuals, such as those with neutropenia, trauma victims (e.g., from combat injuries), and individuals requiring mechanical ventilation. Epidemiologically, A. baumannii infections surged in the 2000s, particularly in Europe and Asia, with multihospital outbreaks documented across these regions and beyond. The World Health Organization designated carbapenem-resistant A. baumannii as a critical priority pathogen in 2017, highlighting its global threat due to high morbidity and mortality rates, which can reach up to 70% in cases of multidrug-resistant strains.^[2]^[68]^[69] Key virulence factors contribute to A. baumannii's pathogenicity and persistence. The polysaccharide capsule shields the bacterium from complement-mediated killing by the host immune system, while adhesins such as pili facilitate attachment to host cells, biofilm formation, and twitching motility. Efflux pumps enable the extrusion of antimicrobial agents and potentially other toxic compounds, aiding immune evasion and survival in hostile environments.^[2]^[70]

Treatment

Acinetobacter species, particularly A. baumannii, were historically susceptible to carbapenems such as imipenem, with minimum inhibitory concentrations (MICs) typically ≤2 µg/mL qualifying as susceptible according to Clinical and Laboratory Standards Institute (CLSI) breakpoints. However, as of the early 2020s, the global prevalence of multidrug-resistant (MDR) A. baumannii isolates is estimated at approximately 80% (range 74-85%), defined as non-susceptibility to at least one agent in three or more antimicrobial categories, complicating effective therapy.^[5] Key resistance mechanisms in Acinetobacter include the production of beta-lactamases, such as carbapenem-hydrolyzing class D oxacillinases (e.g., OXA-23) and metallo-beta-lactamases (e.g., NDM-1), which hydrolyze beta-lactam antibiotics including carbapenems.^[71] Aminoglycoside resistance often arises from modifying enzymes like aminoglycoside 3'-phosphotransferase (APH(3')) and acetyltransferases (AAC), reducing efficacy of agents like amikacin; susceptibility is assessed via CLSI/EUCAST MIC breakpoints, with amikacin susceptible at ≤16 µg/mL (CLSI).^[71] Efflux pumps and porin alterations further contribute to MDR phenotypes, elevating MICs for multiple classes.^[72] Current treatment guidelines for carbapenem-resistant A. baumannii (CRAB) infections, as per the Infectious Diseases Society of America (IDSA) guidance as of July 2024, recommend sulbactam-durlobactam (2 g every 6 hours via 3-hour infusion) combined with a carbapenem (e.g., imipenem-cilastatin or meropenem) as the preferred regimen for severe infections; supporting trial data showed reduced mortality (19% vs. 32%) compared to colistin-based therapy.^[73] For alternatives when sulbactam-durlobactam is unavailable, high-dose ampicillin-sulbactam (9 g sulbactam daily) plus a second agent (e.g., polymyxin B or tigecycline) is advised, with combination therapy emphasized to improve outcomes in MDR cases.^[73] Colistin (or polymyxin B) and tigecycline serve as last-resort options, typically in high doses and combinations (e.g., sulbactam plus carbapenem for CRAB), though colistin MIC breakpoints are ≤2 mg/L for susceptible (EUCAST) and carry risks of nephrotoxicity. Emerging strategies include phage therapy trials in the 2020s, which have shown promise in treating refractory MDR A. baumannii infections, such as pneumonia and bacteremia, through targeted bacteriophage cocktails that lyse resistant strains in preclinical and compassionate-use cases; as of 2025, phase III trials are ongoing.^[74] Additionally, sulbactam-durlobactam received FDA approval in May 2023 as a novel beta-lactamase inhibitor combination specifically addressing OXA-type enzymes in Acinetobacter.^[73]

Infection Prevention

Preventing infections caused by Acinetobacter species, particularly multidrug-resistant strains like carbapenem-resistant Acinetobacter baumannii (CRAB), relies on multifaceted strategies in healthcare settings to interrupt transmission. These measures emphasize standard infection control practices tailored to the organism's environmental persistence and resistance profile.^[75] Hand hygiene is a cornerstone of prevention, including the use of alcohol-based sanitizers, which are effective against Acinetobacter. Chlorhexidine-based washes can be used for decolonization and skin preparation in high-risk settings. Studies have shown that daily chlorhexidine gluconate (CHG) bathing significantly reduces A. baumannii colonization in intensive care unit (ICU) patients, lowering the risk of subsequent infections by up to 50% in high-prevalence settings. Contact precautions, including gown and glove use upon entry to patient rooms, are recommended for colonized or infected individuals to minimize direct and indirect transmission, as per CDC guidelines for multidrug-resistant organisms (MDROs).^[76]^[77]^[78] Environmental cleaning plays a critical role given Acinetobacter's ability to survive on dry surfaces for extended periods. In ICUs, disinfection with bleach (sodium hypochlorite at 1:10 to 1:100 dilutions) or hydrogen peroxide-based agents effectively eliminates surface contamination, reducing bioburden by over 90% in outbreak scenarios. Enhanced protocols, such as daily cleaning of high-touch areas and terminal disinfection with hydrogen peroxide vapor, have been associated with decreased acquisition rates in affected units.^[79]^[80] Aseptic techniques are essential to prevent device-related entry points for Acinetobacter, which frequently causes catheter-associated urinary tract infections and ventilator-associated pneumonia (VAP). Strict sterile procedures during insertion and maintenance of central venous catheters, urinary catheters, and endotracheal tubes—such as using full-barrier precautions and daily chlorhexidine site care—limit bacterial ingress. Implementation of VAP prevention bundles, which include head-of-bed elevation, oral care with chlorhexidine, and daily sedation interruption, has been shown to reduce VAP incidence by 40–60% in mechanically ventilated patients, thereby curbing Acinetobacter as a common pathogen in these cases.^[76]^[81] Active surveillance enhances early detection and containment, particularly in high-risk units like ICUs. CDC guidelines recommend screening high-risk patients using rectal swabs (combined with axillary-groin swabs if needed) to identify asymptomatic colonization, which occurs in up to 20–40% of cases and precedes infection; this approach, updated in MDRO management strategies as of 2024, facilitates targeted isolation and has reduced transmission in endemic settings by prompting timely interventions.^[82]^[83]

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All five study isolates shared very similar phenotypic characteristics. Cells grew well on Trypticase soy agar (TSA) and MacConkey agar media. On TSA, bacterial ...
[48]
Advances in automated techniques to identify Acinetobacter ... - NIH
The objective of this review is to recapitulate the current evolution in phenotypic and automated techniques used to identify the ACB complex.
[49]
Identification of genus Acinetobacter: Standardization of in-house ...
The identification is mostly based on preliminary tests such as Gram's stain, catalase test, oxidase test, and hanging drop preparation for motility.
[50]
Accurate identification of clinically important Acinetobacter spp. - NIH
Jun 27, 2019 · The genus Acinetobacter includes a heterogeneous group of bacteria that have been considered 'the most troublesome' by clinicians and scientists ...
[51]
Identification of Acinetobacter Species Using Matrix-Assisted Laser ...
Apr 25, 2016 · MALDI-TOF MS enables the prompt and accurate identification of clinically significant Acinetobacter species when used with the improved database.
[52]
Accurate Identification of Clinically Important Acinetobacter Spp.
The 16S rRNA gene of bacteria contains nine hypervariable regions that show sequence diversity among the different bacterial species and are therefore used for ...
[53]
Acinetobacter baumannii serotyping for delineation of outbreaks of ...
A total of 152 clinical isolates of Acinetobacter baumannii from 152 patients were identified by carbon source utilization tests and examined serologically.
[54]
Species, biotype, and bacteriophage type determinations compared ...
Acinetobacter baumannii was the most commonly found species in isolates from clinical sources, followed by Acinetobacter species 3. Nine biotypes were observed ...
[55]
Serum Albumin and Ca2+ Are Natural Competence Inducers in the ...
Serum Albumin and Ca2+ Are Natural Competence Inducers in the Human Pathogen Acinetobacter baumannii. Authors: German Matias Traglia, Brettni Quinn, Sareda ...
[56]
Costs and benefits of natural transformation in Acinetobacter baylyi
Feb 15, 2017 · Increased transformation rates were observed when homologous DNA, but not heterologous DNA, was added after exposure of cells to UV-light [33].Methods · Strains, Media And Dna · Genomic Integration Of...<|control11|><|separator|>
[57]
DNA Uptake by the Nosocomial Pathogen Acinetobacter baumannii ...
Physiological characterization of natural transformation in Acinetobacter calcoaceticus. ... Attenuation of quorum sensing in the pathogen Acinetobacter ...
[58]
Natural Transformation in Acinetobacter baumannii W068: A Genetic ...
... induction of competence. A global regulator protein, cAMP receptor protein (CRP), is a major shared activator that controls the development of competence in ...
[59]
DNA modifications impact natural transformation of Acinetobacter ...
We describe a methylome-dependent phenomenon that impacts intra- and inter-species DNA exchange by the competent A. baumannii strain A118.
[60]
Acinetobacter baylyi regulates type IV pilus synthesis by employing ...
Jun 18, 2021 · Bacteria use extracellular appendages called type IV pili (T4P) for diverse behaviors including DNA uptake, surface sensing, virulence, ...
[61]
Fluorescence-Based Detection of Natural Transformation in Drug ...
baumannii population, the frequency of transformants does not usually exceed 10 ... transformation frequencies seem to reach saturation and remained around 10−4.
[62]
The Impact of Natural Transformation on the Acquisition of Antibiotic ...
May 12, 2022 · ... natural transformation as a mechanism of intraspecies and interspecies exchange of genetic material occurs in Acinetobacter spp. This study ...
[63]
Manipulation of natural transformation by AbaR-type islands ... - PNAS
Manipulation of natural transformation by AbaR-type islands promotes fixation of antibiotic resistance in Acinetobacter baumannii.
[64]
Hospital-acquired and Ventilator-associated Pneumonia (HAP/VAP)
Jul 14, 2016 · aeruginosa (approximately 10%–20% of isolates), enteric gram-negative bacilli (approximately 20%–40% of isolates), and Acinetobacter baumannii ( ...
[65]
WHO publishes list of bacteria for which new antibiotics are urgently ...
Feb 27, 2017 · WHO priority pathogens list for R&D of new antibiotics. Priority 1: CRITICAL. Acinetobacter baumannii, carbapenem-resistant; Pseudomonas ...
[66]
Mapping Global Prevalence of Acinetobacter baumannii and Recent ...
Jun 1, 2021 · Acinetobacter baumannii is a leading cause of nosocomial infections that severely threaten public health. The formidable adaptability and ...
[67]
Carbapenem-Resistant Acinetobacter baumannii: Virulence Factors ...
Aug 26, 2025 · Adhesins are key virulence factors that help bacteria resist mechanical stress from bodily fluids. In A. baumannii, they include pili proteins, ...
[68]
Trends in Antimicrobial Resistance of Acinetobacter baumannii and ...
Jun 24, 2025 · baumannii isolates are carbapenem-resistant. Globally, over 71% are multidrug-resistant. In the United States, 27% of mechanically ventilated ...
[69]
Acinetobacter baumannii Antibiotic Resistance Mechanisms - PMC
Beta-lactamases are enzymes that catalyze the hydrolysis of beta-lactam antibiotics and can be divided into four classes based on sequence motifs and ...
[70]
Acinetobacter baumannii: an evolving and cunning opponent
Jan 21, 2024 · These β-lactamases feature has carboxylated lysine at its center, which leads to its distinct catalytic mechanism. The presence of MBLs and OXA ...
[71]
IDSA 2024 Guidance on the Treatment of Antimicrobial Resistant ...
This guidance document provides recommendations to clinicians for treatment of infections caused by extended-spectrum β-lactamase producing Enterobacterales ...
[72]
https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2024.1332108/full
[73]
Multidrug-resistant Organisms (MDRO) Management Guidelines
Apr 12, 2024 · This guideline provides recommendations for management of multidrug-resistant organisms in healthcare settings.MDRO Containment Strategy · MDRO Prevention and Control · Updates · Authors
[74]
Acinetobacter infection: Treatment and prevention - UpToDate
A. baumannii are included in the Acinetobacter calcoaceticus baumannii complex, which also includes A. calcoaceticus, A. pittii, and A. nosocomialis. For the ...Missing: MLST | Show results with:MLST
[75]
Effect of chlorhexidine bathing on colonization or infection with ...
This study suggests that CHG bathing significantly reduces colonization of A. baumannii in the ICU setting.
[76]
Carbapenem-resistant Acinetobacter baumannii (CRAB)
Use gown and gloves (e.g., Contact Precautions in Acute Care settings and Enhanced Barrier Precautions in long-term care settings for patients/residents who are ...
[77]
Environmental Cleaning Procedures | HAIs - CDC
Mar 19, 2024 · Typically, chlorine-based disinfectants at 500-5000ppm free chlorine (1:100 or 1:10 dilution of 5% chlorine-bleach; depending on the size of the ...Cleaning Programs · Cleaning Supplies and... · Appendix B1 · Risk-assessment for
[78]
The effect of temporary closure and enhanced terminal disinfection ...
Jul 14, 2020 · At Makassed Hospital's open-bay intensive care unit (ICU), enhanced terminal disinfection (ETD) using hydrogen peroxide (H2O2) was performed ...
[79]
Ventilator‐Associated Pneumonia Bundled Strategies: An Evidence ...
Dec 5, 2008 · Evidence shows that VAPB practices decrease VAP rates. Bundled practices result in decreased ventilator days, intensive care unit length of stay, and mortality ...
[80]
Summary of Recommendations | Infection Control - CDC
Mar 18, 2024 · Recommendations for all healthcare settings independent of the prevalence of multidrug resistant organism (MDRO) infections or the population served.Hicpac Recommendation... · V.A. General Recommendations · V.A. 5. Infection Control...
[81]
Detecting carbapenem-resistant Acinetobacter baumannii (CRAB ...
Screening for carbapenem-resistant Acinetobacter baumannii (CRAB) has been recommended to control outbreaks, but no specific recommendations have been made ...