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Open AccessJournal ArticleDOI

Overview of mechanisms of antibiotic resistance in Pseudomonas aeruginosa: an ocular perspective.

TLDR
The types of mobile genetic elements (MGEs) such as plasmids, integrons and transposons that are frequently associated with drug resistance in P. aeruginosa are reviewed to provide valuable information on the emergence of new antibiotic resistance and potential to treat resistant strains.
Abstract
Treatment of Pseudomonas aeruginosa eye infections often becomes a challenge due to the ability of this bacterium to be resistant to antibiotics via intrinsic and acquired mechanisms. Transfer of resistance due to interchangeable genetic elements is an important mechanism for the rapid transfer of antibiotic resistance in this pathogen. As a result, drug-resistant strains are becoming increasingly prevalent worldwide. This review systematically analyses data from recent publications to describe the global prevalence and antibiotic sensitivity of ocular P. aeruginosa. Thirty-seven studies were selected for review from PubMed-based searches using the criteria 'microbial keratitis OR eye infection AND Pseudomonas aeruginosa AND antibiotic resistance' and limiting to papers from 2011 onward, to demonstrate the antibiotic resistance from isolates from around the world. Subsequently, we reviewed the ways in which P. aeruginosa can become resistant to antibiotics. Both the rate of isolation of bacteria in general (79 per cent of cases), and prevalence of P. aeruginosa (68 per cent of all isolates) were highest in contact lens-related microbial keratitis. The average resistance rate to common ocular antibiotics such as ciprofloxacin (9 per cent), gentamicin (22 per cent) and ceftazidime (13 per cent) remained relatively low. However, there were large variations in resistance rates reported in studies from different countries, for example resistance to ciprofloxacin reached up to 33 per cent. We next reviewed the types of mobile genetic elements (MGEs) such as plasmids, integrons and transposons that are frequently associated with drug resistance in P. aeruginosa. MGEs are important for the transmission of resistance to beta-lactams and aminoglycosides and recently have been shown to be potential factors for the transmission of fluoroquinolone resistance. Studies on the molecular mechanisms of resistance transfer in ocular P. aeruginosa have begun to be reported and will provide valuable information on the emergence of new antibiotic resistance and potential to treat resistant strains.

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Citations
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Journal ArticleDOI

Antibiotic resistance in Pseudomonas aeruginosa: mechanisms and alternative therapeutic strategies

TL;DR: The mechanism of antibiotic resistance in P. aeruginosa is a recently characterized mechanism, which includes biofilm-mediated resistance and formation of multidrug-tolerant persister cells, and is responsible for recalcitrance and relapse of infections.
Journal ArticleDOI

Prevalence and hazardous impact of pharmaceutical and personal care products and antibiotics in environment: A review on emerging contaminants

TL;DR: In this article, the major sources responsible for emergence of antibiotic resistance are elucidated and a variety of introductory sources and fate of PPCPs in aquatic environment including human and veterinary wastes, aquaculture and agriculture related wastes, and other anthropogenic activities have been discussed.
Journal ArticleDOI

Pseudomonas aeruginosa and microbial keratitis

TL;DR: Ongoing evidence to suggest that keratitis infections are associated with a phylogenetic subgroup of P. aeruginosa isolates carrying the gene encoding the potent cytotoxin exotoxin U, one of two mutually exclusive exotoxins secreted via the type III secretion system could contribute to the development of resistance to both antibiotics and disinfectants.
Journal ArticleDOI

Pseudomonas aeruginosa: pathogenesis, virulence factors, antibiotic resistance, interaction with host, technology advances and emerging therapeutics

TL;DR: In this article , the authors comprehensively review the progress and discuss the current status of Pseudomonas aeruginosa biophysical traits, behaviors, virulence factors, invasive regulators, and host defense patterns against its infection, which point out new directions for future investigation and add to the design of novel and/or alternative therapeutics.
Journal ArticleDOI

Queensland Microbial Keratitis Database: 2005-2015.

TL;DR: The estimated incidence of microbial keratitis in Queensland was 0.66 cases per 10 000 people, the rate of antibiotic susceptibility is high and stable, the incidence of ker atitis secondary to protozoa is likely to be decreasing whileThe incidence of Keratitis culturing yeast is increasing.
References
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Journal Article

The Antibiotic Resistance Crisis: Part 1: Causes and Threats

TL;DR: Decades after the first patients were treated with antibiotics, bacterial infections have again become a threat because of the rapid emergence of resistant bacteria-a crisis attributed to abuse of these medications and a lack of new drug development.
Journal ArticleDOI

Carbapenemases: the versatile beta-lactamases.

TL;DR: The characteristics, epidemiology, and detection of the carbapenemases found in pathogenic bacteria are updates and metallo-β-lactamases are detected primarily in Pseudomonas aeruginosa.
Journal ArticleDOI

Updated Functional Classification of β-Lactamases

TL;DR: The functional classification scheme updated herein is based on the 1995 proposal and includes group 1 (class C) cephalosporinases; group 2 (classes A and D) broad-spectrum, inhibitor-resistant, and extended-spectrums β-lactamases and serine carbapenemases; and group 3 metallo-β-lacticamases.
Journal ArticleDOI

AmpC β-Lactamases

TL;DR: Overexpression confers resistance to broad-spectrum cephalosporins including cefotaxime, ceftazidime, and ceftriaxone and is a problem especially in infections due to Enterobacter aerogenes and Enterobacteria cloacae, where an isolate initially susceptible to these agents may become resistant upon therapy.
Journal ArticleDOI

The structure of beta-lactamases.

TL;DR: In this article, it was shown that the β-lactamases have a polyphyletic origin and all the enzymes of currently known amino acid sequence belong to one homology group, called class A enzymes.
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