Literature DB >> 17435510

Pseudomonas aeruginosa infection and inflammation during contact lens wear: a review.

Mark D P Willcox1.   

Abstract

Infection and inflammation during contact lens wear is often associated with microbial contamination of lenses. Several different types of microbes that colonize lenses can lead to infection and inflammation, but the most common cause of infection (microbial keratitis; MK) remains the Gram-negative bacterium Pseudomonas aeruginosa. P. aeruginosa has a battery of cell-associated and extracellular virulence factors it can use to initiate and maintain infection. Its ability to produce proteases, to either invade or kill corneal cells, and to coordinate expression of virulence factors via quorum-sensing have been shown to be important during MK. Another important factor that contributes to the destruction of the cornea during MK is excessive activation of the host defense system. P. aeruginosa can activate several pathways of the immune system during MK, and activation often involves receptors on the corneal epithelial cells called toll-like receptors (TLRs). These TLRs recognize e.g., lipopolysaccharide or flagella from P. aeruginosa and activate the epithelial cells to produce inflammatory mediators such as cytokines and chemokines. These cytokines or chemokines recruit white blood cells, predominantly polymorphonuclear leukocytes, to the infection in order that they can phagocytose and kill the P. aeruginosa. However, continued recruitment and presence of these polymorphonuclear neutrophils and other white blood cells in the corneal tissue leads to destruction of corneal cells and tissue components. This can ultimately lead to scarring and vision loss.

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Year:  2007        PMID: 17435510     DOI: 10.1097/OPX.0b013e3180439c3e

Source DB:  PubMed          Journal:  Optom Vis Sci        ISSN: 1040-5488            Impact factor:   1.973


  75 in total

Review 1.  Contact lens-related microbial keratitis: how have epidemiology and genetics helped us with pathogenesis and prophylaxis.

Authors:  F Stapleton; N Carnt
Journal:  Eye (Lond)       Date:  2011-12-02       Impact factor: 3.775

2.  EepR Mediates Secreted-Protein Production, Desiccation Survival, and Proliferation in a Corneal Infection Model.

Authors:  Kimberly M Brothers; Nicholas A Stella; Eric G Romanowski; Regis P Kowalski; Robert M Q Shanks
Journal:  Infect Immun       Date:  2015-08-31       Impact factor: 3.441

3.  The comparison of antimicrobial effectiveness of contact lens solutions.

Authors:  Ali Kal; Mustafa Ilker Toker; Serpil Kaya
Journal:  Int Ophthalmol       Date:  2016-10-13       Impact factor: 2.031

4.  A novel murine model for contact lens wear reveals clandestine IL-1R dependent corneal parainflammation and susceptibility to microbial keratitis upon inoculation with Pseudomonas aeruginosa.

Authors:  Matteo M E Metruccio; Stephanie J Wan; Hart Horneman; Abby R Kroken; Aaron B Sullivan; Tan N Truong; James J Mun; Connie K P Tam; Robin Frith; Laurence Welsh; Melanie D George; Carol A Morris; David J Evans; Suzanne M J Fleiszig
Journal:  Ocul Surf       Date:  2018-11-12       Impact factor: 5.033

5.  Evidence that WapB is a 1,2-glucosyltransferase of Pseudomonas aeruginosa involved in Lipopolysaccharide outer core biosynthesis.

Authors:  Dana Kocíncová; Youai Hao; Evgeny Vinogradov; Joseph S Lam
Journal:  J Bacteriol       Date:  2011-03-25       Impact factor: 3.490

6.  The ADP-ribosylation domain of Pseudomonas aeruginosa ExoS is required for membrane bleb niche formation and bacterial survival within epithelial cells.

Authors:  Annette A Angus; David J Evans; Joseph T Barbieri; Suzanne M J Fleiszig
Journal:  Infect Immun       Date:  2010-08-23       Impact factor: 3.441

7.  The complex interplay of iron, biofilm formation, and mucoidy affecting antimicrobial resistance of Pseudomonas aeruginosa.

Authors:  Amanda G Oglesby-Sherrouse; Louise Djapgne; Angela T Nguyen; Adriana I Vasil; Michael L Vasil
Journal:  Pathog Dis       Date:  2014-02-10       Impact factor: 3.166

8.  A spider web strategy of type IV pili-mediated migration to build a fibre-like Psl polysaccharide matrix in Pseudomonas aeruginosa biofilms.

Authors:  Shiwei Wang; Matthew R Parsek; Daniel J Wozniak; Luyan Z Ma
Journal:  Environ Microbiol       Date:  2013-02-20       Impact factor: 5.491

9.  TREM-2 promotes host resistance against Pseudomonas aeruginosa infection by suppressing corneal inflammation via a PI3K/Akt signaling pathway.

Authors:  Mingxia Sun; Min Zhu; Kang Chen; Xinxin Nie; Qiuchan Deng; Linda D Hazlett; Yongjian Wu; Meiyu Li; Minhao Wu; Xi Huang
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-05-17       Impact factor: 4.799

10.  Why does the healthy cornea resist Pseudomonas aeruginosa infection?

Authors:  David J Evans; Suzanne M J Fleiszig
Journal:  Am J Ophthalmol       Date:  2013-04-17       Impact factor: 5.258

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