The Role of Steroids in the Management of Acanthamoeba Keratitis, Fungal Keratitis, and Epidemic Keratoconjunctivitis

1994 ◽  
Vol 34 (3) ◽  
pp. 19-31 ◽  
Author(s):  
Roberto Pineda ◽  
Claes H. Dohlman
2021 ◽  
Vol 202 ◽  
pp. 108372
Author(s):  
Bethany Mills ◽  
Naveen Radhakrishnan ◽  
Siva Ganesa Karthikeyan Rajapandian ◽  
Gunasekaran Rameshkumar ◽  
Prajna Lalitha ◽  
...  
Keyword(s):  

Pathogens ◽  
2020 ◽  
Vol 9 (5) ◽  
pp. 321 ◽  
Author(s):  
Steven Rolland ◽  
Luce Mengue ◽  
Cyril Noël ◽  
Stéphanie Crapart ◽  
Anne Mercier ◽  
...  

Acanthamoeba castellanii is a ubiquitous free-living amoeba. Pathogenic strains are causative agents of Acanthamoeba keratitis and granulomatous amoebic encephalitis. In response to adverse conditions, A. castellanii differentiate into cysts, which are metabolically inactive and resistant cells. This process, also named encystment, involves biochemical and genetic modifications that remain largely unknown. This study characterizes the role of the ACA1_384820 Acanthamoeba gene during encystment. This gene encodes a putative N-acetyltransferase, belonging to the Gcn5-related N-acetyltransferase (GNAT) family. We showed that expression of the ACA1_384820 gene was down-regulated as early as two hours after induction of encystment in A. castellanii. Interestingly, overexpression of the ACA1_384820 gene affects formation of cysts. Unexpectedly, the search of homologs of ACA1_384820 in the Eukaryota gene datasets failed, except for some species in the Acanthamoeba genus. Bioinformatics analysis suggested a possible lateral acquisition of this gene from prokaryotic cells. This study enabled us to describe a new Acanthamoeba gene that is down-regulated during encystment.


2015 ◽  
Vol 114 (9) ◽  
pp. 3283-3289 ◽  
Author(s):  
Ismail Soner Koltas ◽  
Fadime Eroglu ◽  
Elif Erdem ◽  
Meltem Yagmur ◽  
Ferdi Tanır

2021 ◽  
Vol 33 (4) ◽  
pp. 408
Author(s):  
Dhouha Gouider ◽  
Asma Khallouli ◽  
Afef Maalej ◽  
Sana Khochtali ◽  
Moncef Khairallah

2021 ◽  
Vol 14 (5) ◽  
pp. e241709
Author(s):  
Mohit Chhabra ◽  
Ruchi Goel ◽  
Samreen Khanam ◽  
Sonam Singh

Side port infection and corneal abscess after cataract surgery can produce devastating outcomes. Topical antibacterial drugs are the mainstay in management of these cases. Although intrastromal antifungal agents are an established modality for fungal keratitis, such use of antibacterial agents is rarely reported due to better pharmacokinetic profile of antibacterial agents.We report a case of methicillin-resistant Staphylococcus aureus corneal abscess following phacoemulsification that responded to intrastromal vancomycin injection in addition to conventional therapy.This case of postphacoemulsification corneal abscess highlights the importance of postoperative hygiene practices, use of anterior segment optical coherence tomography for monitoring these patients and use of intrastromal vancomycin as an adjunct to topical and systemic therapy.


Author(s):  
J. Y. Niederkorn ◽  
H. Alizadeh ◽  
H. Leher ◽  
S. Apte ◽  
S. El Agha ◽  
...  

2016 ◽  
Vol 27 (1) ◽  
pp. 10-15 ◽  
Author(s):  
Ágnes Füst ◽  
Jeannette Tóth ◽  
Gyula Simon ◽  
László Imre ◽  
Zoltán Z. Nagy

Purpose To report on the presence of 4 different structures visualized by confocal microscopy in patients whose clinical presentation suggested infection by Acanthamoeba. Methods Data and charts of 28 consecutive patients were analyzed in a retrospective study. Four types of structures were recognized by confocal microscopy performed with HRT II Rostock Cornea Module: trophozoites, double-walled cysts, signet rings, and bright spots. The 28 patients (mean age 30.8 years, range 17-61 years, 10 male, 18 female) were divided into 4 groups according to the diagnosis established later by microscopic examination of smear, culture, response to therapy, and the course of keratitis. The 4 groups were Acanthamoeba keratitis (AK), Acanthamoeba suspect (AK-suspect), bacterial keratitis (BK), and fungal keratitis (FK). Results The rate of patients in AK, AK-suspect, FK, and BK groups where bright spots were found were 100%, 100%, 40%, and 55%, respectively. The sensitivity of presence of bright spots in the in vivo confocal microscopy in Acanthamoeba keratitis was 100% (95% confidence interval [CI] 73.5% to 100.00%) and specificity was 50% (CI 24.7% to 75.4%). When cases where the only signs of Acanthamoeba were bright spots were excluded, and only those cases were counted where any of cysts, trophozoites, or signet rings were also found, the sensitivity was 67% (95% CI 34. 9% to 90.1%) and the specificity was 94% (95% CI 69.8% to 99.8%). Conclusions The relatively high rate of bright spots in non- Acanthamoeba keratitis challenges the assumption that bright spots seen by confocal microscopy are a specific indication of Acanthamoeba keratitis.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
M. Barbariga ◽  
F. Vallone ◽  
E. Mosca ◽  
F. Bignami ◽  
C. Magagnotti ◽  
...  

Abstract Corneal neo-vascularization (CNV) is a highly prevalent medical condition which impairs visual acuity. The role of specific proteins in modulating CNV has been extensively reported, although no studies have described the entire human proteome in CNV corneas. In this paper, we performed a proteomic analysis of vascularized vs healthy corneal stroma, in a CNV mouse model and in CNV-affected patients, with a specific focus on extracellular matrix (ECM) proteins. We identified and quantified 2315 murine proteins, 691 human proteins and validated 5 proteins which are differentially expressed in vascularized samples and conserved in mice and humans: tenascin-C and fibronectin-1 were upregulated, while decorin, lumican and collagen-VI were downregulated in CNV samples. Interestingly, among CNV patients, those affected with Acanthamoeba keratitis showed the highest levels of fibronectin-1 and tenascin-C, suggesting a specific role of these two proteins in Acanthamoeba driven corneal CNV. On a broader picture, our findings support the hypothesis that the corneal stroma in CNV samples is disorganized and less compact. We are confident that the dissection of the human corneal proteome may shed new light on the complex pathophysiology of human CNV, and finally lead to improved treatments.


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