Literature DB >> 25392356

Development of an immunochromatographic assay kit using fluorescent silica nanoparticles for rapid diagnosis of Acanthamoeba keratitis.

Koji Toriyama1, Takashi Suzuki2, Tomoyuki Inoue1, Hiroshi Eguchi3, Saichi Hoshi4, Yoshitsugu Inoue5, Hideki Aizawa6, Kazutomi Miyoshi6, Michio Ohkubo6, Eiji Hiwatashi7, Hiroshi Tachibana8, Yuichi Ohashi1.   

Abstract

We developed an immunochromatographic assay kit that uses fluorescent silica nanoparticles bound to anti-Acanthamoeba antibodies (fluorescent immunochromatographic assay [FICGA]) and evaluated its efficacy for the detection of Acanthamoeba and diagnosis of Acanthamoeba keratitis (AK). The sensitivity of the FICGA kit was evaluated using samples of Acanthamoeba trophozoites and cysts diluted to various concentrations. A conventional immunochromatographic assay kit with latex labels (LICGA) was also evaluated to determine its sensitivity in detecting Acanthamoeba trophozoites. To check for cross-reactivity, the FICGA was performed by using samples of other common causative pathogens of infectious keratitis, such as Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, and Candida albicans. Corneal scrapings from patients with suspected AK were tested with the FICGA kit to detect the presence of Acanthamoeba, and the results were compared with those of real-time PCR. The FICGA kit detected organisms at concentrations as low as 5 trophozoites or 40 cysts per sample. There were no cross-reactivities with other pathogens. The FICGA was approximately 20 times more sensitive than the LICGA for the detection of Acanthamoeba trophozoites. The FICGA kit yielded positive results for all 10 patients, which corresponded well with the real-time PCR results. The FICGA kit demonstrated high sensitivity for the detection of Acanthamoeba and may be useful for the diagnosis of AK.
Copyright © 2015, American Society for Microbiology. All Rights Reserved.

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Year:  2014        PMID: 25392356      PMCID: PMC4290933          DOI: 10.1128/JCM.02595-14

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  33 in total

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Authors:  A H Chagla; A J Griffiths
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3.  The Purkinje shift.

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6.  Two cases of acanthamoeba keratitis diagnosed only by real-time polymerase chain reaction.

Authors:  Michiko Kandori; Tomoyuki Inoue; Fumihiko Takamatsu; Yoshinao Kojima; Yuichi Hori; Naoyuki Maeda; Yasuo Tano
Journal:  Cornea       Date:  2010-02       Impact factor: 2.651

7.  Use of 18S rRNA gene-based PCR assay for diagnosis of acanthamoeba keratitis in non-contact lens wearers in India.

Authors:  Gunisha Pasricha; Savitri Sharma; Prashant Garg; Ramesh K Aggarwal
Journal:  J Clin Microbiol       Date:  2003-07       Impact factor: 5.948

8.  Rapid growth of Acanthamoeba in defined media; induction of encystment by glucose-acetate starvation.

Authors:  T J Byers; R A Akins; B J Maynard; R A Lefken; S M Martin
Journal:  J Protozool       Date:  1980-05

Review 9.  Acanthamoeba spp. as agents of disease in humans.

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Journal:  Clin Microbiol Rev       Date:  2003-04       Impact factor: 26.132

10.  Delay in diagnosis and outcome of Acanthamoeba keratitis.

Authors:  I Claerhout; A Goegebuer; C Van Den Broecke; Ph Kestelyn
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2004-08       Impact factor: 3.117

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4.  A DNA dot hybridization model for molecular diagnosis of parasitic keratitis.

Authors:  Fu-Chin Huang; Hsin-Yi Hsieh; Tsung C Chang; Shu-Li Su; Shin-Ling Tseng; Yu-Hsuan Lai; Ming-Tse Kuo
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