Introduction
Acinetobacter lwoffii is a Gram-negative, aerobic, non-motile, and non-fermenting bacterium that belongs to the Acinetobacter genus. It is commonly found in the environment, particularly in soil and water, but can also be found on human skin and in hospital settings. A. lwoffii is a relatively uncommon cause of infections in humans, but when it does cause disease, it can be severe and difficult to treat due to its resistance to multiple antibiotics. A. lwoffii has been associated with a range of infections, including bloodstream infections, pneumonia, urinary tract infections, and wound infections. It is important to accurately identify A. lwoffii in the clinical setting to guide appropriate treatment and infection control measures.
Morphology
The morphology of Acinetobacter lwoffii is characterized by being a small, non-motile, Gram-negative coccobacillus (short rod-shaped bacterium). A. lwoffii cells are typically about 0.5 to 1.5 micrometers in width and 0.8 to 2.5 micrometers in length, and can occur singly, in pairs, or in short chains. They have a capsule that may be visualized with special staining techniques. In terms of colony morphology on agar plates, A. lwoffii typically forms smooth, cream-colored colonies that are non-hemolytic and have a slightly convex shape.
Pthogenicity
Acinetobacter lowffii can cause various infections in humans, particularly in immunocompromised patients. It can cause hospital-acquired infections such as pneumonia, urinary tract infections, bloodstream infections, and wound infections. It is also known to cause meningitis and endocarditis. The pathogenicity of A. lowffii is attributed to its ability to adhere to and colonize the host tissue, form biofilms, and produce virulence factors such as lipopolysaccharides and outer membrane proteins. Additionally, A. lowffii is often resistant to multiple antibiotics, making it difficult to treat.
Laboratory Diagnosis
Acinetobacter lwoffii can be identified in the laboratory using various methods. Some of them are:
- Gram staining: Acinetobacter lwoffii is a gram-negative bacillus that appears as short rods on gram stain.
- Culture: The bacterium can be cultured on various media like blood agar, MacConkey agar, and nutrient agar. It grows well at 37°C and produces smooth, circular, and opaque colonies.
- Biochemical tests: Biochemical tests like oxidase test, catalase test, and glucose fermentation test can help in the identification of Acinetobacter lwoffii.
- MALDI-TOF MS: Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) can also be used for the identification of Acinetobacter lwoffii.
- Molecular methods: Polymerase chain reaction (PCR) and DNA sequencing can also be used to identify Acinetobacter lwoffii.
- It is important to note that identification of Acinetobacter lwoffii in the laboratory should be performed by trained personnel using proper safety precautions due to its potential pathogenicity and antibiotic resistance.
Treatment
The treatment of Acinetobacter lwoffii infections depends on the severity of the infection, the site of infection, and the patient’s immune status. A. lwoffii is usually resistant to many commonly used antibiotics, including penicillin, cephalosporins, and aminoglycosides. However, it may be susceptible to carbapenems, fluoroquinolones, and tetracyclines. Therefore, the choice of antibiotics should be based on the results of antimicrobial susceptibility testing. In severe cases, combination therapy with two or more antibiotics may be necessary. In addition, supportive therapy should be provided, such as intravenous fluids, oxygen therapy, and other supportive measures.
Prevention
Prevention of Acinetobacter lwoffii infection involves a range of measures that can be taken to minimize the risk of transmission, especially in healthcare settings. Some preventive measures include:
- Good hand hygiene: Regular hand washing with soap and water or alcohol-based hand sanitizers can help prevent the spread of A. lwoffii infections.
- Personal protective equipment: Use of personal protective equipment, such as gloves, masks, and gowns, can help prevent the spread of A. lwoffii infections.
- Environmental cleaning and disinfection: Regular cleaning and disinfection of surfaces and equipment can help prevent the spread of A. lwoffii in healthcare settings.
- Antimicrobial stewardship: Rational use of antibiotics and avoiding unnecessary use of broad-spectrum antibiotics can help prevent the development and spread of A. lwoffii antibiotic resistance.
- Surveillance and monitoring: Regular surveillance and monitoring of A. lwoffii infections can help identify outbreaks and implement appropriate control measures.
Keynotes
Acinetobacter lwoffii is a gram-negative, non-motile, non-spore-forming, aerobic bacterium. It is an uncommon cause of human infections, but has been associated with various clinical conditions, such as bacteremia, pneumonia, and urinary tract infections.
In the laboratory, A. lwoffii can be identified by its characteristic morphology on agar plates, and confirmed by various biochemical tests, including the oxidase test, catalase test, and API systems. It is typically resistant to multiple antibiotics, making treatment challenging.
Prevention of A. lwoffii infections involves measures such as proper hand hygiene, disinfection of medical equipment, and appropriate use of antibiotics to prevent the emergence of resistant strains.
Overall, A. lwoffii is an opportunistic pathogen that can cause serious infections, particularly in immunocompromised individuals, and its accurate diagnosis and appropriate management is crucial for patient outcomes.
Further Reading
- Lefort A, Panhard X, Clermont O, Woerther PL, Branger C, Mentré F, Fantin B, Wolff M, Denamur E, Tenaillon O. Host factors and portal of entry outweigh bacterial determinants to predict the severity of Escherichia coli bacteremia. Journal of clinical microbiology. 2011 Nov 1;49(11):777-83.
- MDR Acinetobacter baumannii and Acinetobacter species: An emerging threat to public health. (2017). Journal of Medical Microbiology and Diagnosis, 6(267), 2.
- Perez F, Hujer AM, Hujer KM, Decker BK, Rather PN, Bonomo RA. Global challenge of multidrug-resistant Acinetobacter baumannii. Antimicrobial agents and chemotherapy. 2007 Oct 1;51(10):3471-84.
- Howard, A., O’Donoghue, M., Feeney, A., & Sleator, R. D. (2012). Acinetobacter baumannii: an emerging opportunistic pathogen. Virulence, 3(3), 243-250.
- Hujer, K. M., & Bonomo, R. A. (2011). Multidrug-resistant Acinetobacter baumannii: a menace to critically ill patients. Annu. Rev. Med., 62, 81-92.
- Giammanco, A., Calà, C., Fasciana, T., Dowzicky, M. J., & Mammina, C. (2016). Country-specific correlation between antibiotics consumed and resistance rates of Escherichia coli and Klebsiella pneumoniae at a tertiary care hospital in Malta. International journal of antimicrobial agents, 48(6), 698-704.
- Turton, J. F., Woodford, N., Glover, J., Yarde, S., & Kaufmann, M. E. (2006). Identification of Acinetobacter baumannii by detection of the blaOXA-51-like carbapenemase gene intrinsic to this species. Journal of clinical microbiology, 44(8), 2974-2976.
- Vaneechoutte, M., Dijkshoorn, L., & Nemec, A. (2019). Acinetobacter taxonomy: current status, challenges and outlook. FEMS microbiology reviews, 43(6), 877-902.
