Pseudomonas aeruginosa
Pseudomonas aeruginosa is a highly virulent and multidrug resistant bacterium, primarily targeting individuals with reduced immunity. It was firstly described, isolated and recognised as a pathogen in the end of 19th century. P. aeruginosa causes between 10% and 20% of all infections.[1] It is on the ‘critical’ category list of the World Health Organisation (WHO) for research and developing the new drugs.[2]
| Pseudomonas aeruginosa | |
|---|---|
| 240px | |
| Scanning electron micrograph of Pseudomonas aeruginosa | |
| Scientific classification | |
| Kingdom: | |
| Phylum: | |
| Class: | |
| Order: | |
| Family: | |
| Genus: | |
| Species: | P. aeruginosa
|
| Binomial name | |
| Pseudomonas aeruginosa (Schröter 1872)
Migula 1900 | |
Biology
P. aeruginosa is a Gram-negative, rod-shaped bacterium, known by its environmental abundance. It can be found in water, soil, animal, human and plant environments, which can be explained by its versatile energy metabolism; it can survive without oxygen (anaerobic).[3] It has multiple hair-like attachments (pili) which are found on the surface of many bacteria and archaea to attach to other cells, and one flagellum, which is another but longer hair-like structure which provide motility.
Pathogenesis
P. aeruginosa primarily causes clinical infections in individuals with compromised immune systems. For example, in patients with cystic fibrosis. These people build up mucus layers, which create an environment for the bacteria that somewhat protects them from antibiotics and the host immune system. People with cancer, large wounds, and individuals on immunosuppressant drugs after transplant surgery are also considered to be susceptible.
P. aeruginosa may cause different infections, depending on the organ affected. Infections may include: pneumonia, diarrhoea, meningitis, urinary tract infections, bloodstream, ear and wound infections.[4][5] It is spread through improper hygiene, water contamination and medical equipment which is not properly sterilised. Along with high predisposition of patients with weak immunity, infections can be easily acquired in hospital, through, for example, medical devices, such as breathing machine and catheters.[4]
Antibiotic resistance and research
P. aeruginosa is a Gram-negative bacteria, containing two lipid bilayers (acting as barriers) with thin peptidoglycan layer (composed of proteins) in the middle. Because its peptidoglycan is covered by a lipid bilayer, some of the antibiotics, such as penicillin are less effective, as they target proteins within peptidoglycan.
P. aeruginosa also contains small circular genetic material (plasmids) which carry antibiotic resistance genes. These genes make proteins which will protect bacteria from antibiotics. Some of these proteins in P. aeruginosa are efflux pumps - transport proteins which pump the antibiotic outside of cells. Efflux pumps were firstly described in P. aeruginosa as well.
Resistant genes can be acquired through gene transfers. In vertical gene transfer, the new gene appears, for example, through spontaneous mutation. In horizontal gene transfer, the gene is transferred from one bacterium to another. This type of gene transfer makes most of the evolution and determines the bacterium virulence and antibiotic resistance.[6][7]
Recent research shows that phage therapy (involving bacteriophages – bacterial viruses) might be considered as a possible treatment. Bacteriophages attack and destroy extracellular matrix (cell skeleton), increasing cell permeability to antibiotics.[8]
Diagnosis and treatment
P. aeruginosa diagnosis includes physical examination, along with fluid samples. Mild infections can be treated with certain antibiotics. It becomes difficult for the severe cases due to antibiotic resistance. Often the samples are taken into laboratory to see which antibiotics are effective for the strain.
Pseudomonas Aeruginosa Media
- Pseudomonas Aeruginosa.jpg
Pseudomonas aeruginosa in Petri dish
- Pseudomonas aeruginosa pigment production.jpg
Pigment production, growth on cetrimide agar, the oxidase test, plaque formation and Gram stain
A culture dish with Pseudomonas
Gram-stained P. aeruginosa bacteria (pink-red rods)
Susceptibility of P. aeruginosa to antibiotics
Phagocytosis of P. aeruginosa by neutrophil in patient with bloodstream infection (Gram stain)
Production of pyocyanin, water-soluble green pigment of P. aeruginosa (left tube)
Pseudomonas aeruginosa fluorescence under UV illumination
- Pseudomonas aeruginosa antibiogram.jpg
The antibiogram of P. aeruginosa on Mueller–Hinton agar
- Pseudomonas aeruginosa antibiotic susceptibility testing.jpg
Examples of antibiotic susceptibility testing of P. aeruginosa. The disk diffusion test (A) and the MIC test (B). P. aeruginosa is intrinsically resistant to ampicillin/sulbactam, tigecycline and trimethoprim/sulfamethoxazole (no breakpoints in Img. B).
References
- ↑ Lua error in Module:Citation/CS1/Identifiers at line 630: attempt to index field 'known_free_doi_registrants_t' (a nil value).
- ↑ Lua error in Module:Citation/CS1/Identifiers at line 630: attempt to index field 'known_free_doi_registrants_t' (a nil value).
- ↑ Encyclopedia of food microbiology. Carl A. Batt, Mary Lou Tortorello (2nd ed.). Amsterdam. 2014. ISBN 978-0-12-384733-1. OCLC 881482027.
{{cite book}}: CS1 maint: others (link) - ↑ 4.0 4.1 Lua error in Module:Citation/CS1/Identifiers at line 630: attempt to index field 'known_free_doi_registrants_t' (a nil value).
- ↑ Lua error in Module:Citation/CS1/Identifiers at line 630: attempt to index field 'known_free_doi_registrants_t' (a nil value).
- ↑ Lua error in Module:Citation/CS1/Identifiers at line 630: attempt to index field 'known_free_doi_registrants_t' (a nil value).
- ↑ Lua error in Module:Citation/CS1/Identifiers at line 630: attempt to index field 'known_free_doi_registrants_t' (a nil value).
- ↑ Chegini, Zahra; Khoshbayan, Amin; Taati Moghadam, Majid; Farahani, Iman; Jazireian, Parham; Shariati, Aref (2020-09-30). "Bacteriophage therapy against Pseudomonas aeruginosa biofilms: a review". Annals of Clinical Microbiology and Antimicrobials. 19 (1): 45. doi:10.1186/s12941-020-00389-5. ISSN 1476-0711. PMC 7528332. PMID 32998720.