Literature DB >> 24951167

Acanthamoeba DNA can be directly amplified from corneal scrapings.

Nagwa Mostafa El-Sayed1, Mohamed Saad Younis, Azza Mohamed Elhamshary, Amina Ibrahim Abd-Elmaboud, Shereen Magdy Kishik.   

Abstract

This study evaluated the performance of direct amplification of Acanthamoeba-DNA bypassing DNA extraction in the diagnosis of Acanthamoeba keratitis in clinically suspected cases in comparison to direct microscopic examination and in vitro culture. Corneal scrapings were collected from 110 patients who were clinically suspected to have Acanthamoeba keratitis, 63 contact lens wearers (CLW), and 47 non-contact lens wearers (NCLW). Taken samples were subjected to direct microscopic examination, cultivation onto the non-nutrient agar plate surface seeded with Escherichia coli, and PCR amplification. The diagnostic performance of these methods was statistically compared. The results showed that Acanthamoeba infection was detected in 21 (19.1%) of clinically suspected cases (110); 17 (81%) of them were CLW and the remaining 4 (19%) positive cases were NCLW. Regarding the used diagnostic methods, it was found that direct amplification of Acanthamoeba DNA bypassing nucleic acid extraction was superior to microscopy and culture in which 21 cases (19.1%) were positive for Acanthamoeba by PCR compared to 19 positive cases by culture (17.3%) and one case (0.9%) by direct smear. The difference in detection rates between culture and direct smear was highly statistically significant (P = 0.001). On the other hand, there was no significant difference in detection rates between culture and PCR (P = 0.86). On using culture as the gold standard, PCR showed three false-positive samples that were negative by culture and one false-negative sample that was positive by culture. At the same time, direct smear showed 18 false-negative samples. The sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy of PCR were 94.7, 96.7, 85.7, 98.9, and 96.4, respectively, while those of direct smear were 5.3, 100, 100, 83.5, and 83.6, respectively. In conclusion, direct amplification of Acanthamoeba-DNA bypassing DNA extraction is a reliable, specific, sensitive method in the diagnosis of Acanthamoeba keratitis in clinically suspected cases. It should set up in ophthalmological centers as an easy diagnostic tool.

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Year:  2014        PMID: 24951167     DOI: 10.1007/s00436-014-3989-3

Source DB:  PubMed          Journal:  Parasitol Res        ISSN: 0932-0113            Impact factor:   2.289


  33 in total

1.  In vitro amoebicidal activity of ethanol extracts of Arachis hypogaea L., Curcuma longa L. and Pancratium maritimum L. on Acanthamoeba castellanii cysts.

Authors:  Nagwa Mostafa El-Sayed; Khadiga Ahmed Ismail; Sabah Abd-El-Ghany Ahmed; Mona Hafez Hetta
Journal:  Parasitol Res       Date:  2011-12-07       Impact factor: 2.289

2.  Identification of 18S ribosomal DNA genotype of Acanthamoeba from patients with keratitis in North China.

Authors:  Yan Zhang; Xuguang Sun; Zhiqun Wang; Ran Li; Shiyun Luo; Xiuying Jin; Shijing Deng; Wei Chen
Journal:  Invest Ophthalmol Vis Sci       Date:  2004-06       Impact factor: 4.799

3.  Development of a real-time PCR assay for quantification of Acanthamoeba trophozoites and cysts.

Authors:  Delphine Rivière; Florence Ménard Szczebara; Jean-Marc Berjeaud; Jacques Frère; Yann Héchard
Journal:  J Microbiol Methods       Date:  2005-05-31       Impact factor: 2.363

Review 4.  Acanthamoeba: biology and increasing importance in human health.

Authors:  Naveed Ahmed Khan
Journal:  FEMS Microbiol Rev       Date:  2006-07       Impact factor: 16.408

5.  New tool for the simultaneous detection of 10 different genotypes of Acanthamoeba available from the American Type Culture Collection.

Authors:  P Goldschmidt; S Degorge; D Benallaoua; C Saint-Jean; L Batellier; C Alouch; L Laroche; C Chaumeil
Journal:  Br J Ophthalmol       Date:  2009-04-28       Impact factor: 4.638

6.  Rose bengal and lissamine green inhibit detection of herpes simplex virus by PCR.

Authors:  Gerami D Seitzman; Vicky Cevallos; Todd P Margolis
Journal:  Am J Ophthalmol       Date:  2006-04       Impact factor: 5.258

7.  Acanthamoeba keratitis in non-contact lens wearers in India: DNA typing-based validation and a simple detection assay.

Authors:  Savitri Sharma; Gunisha Pasricha; Debashish Das; Ramesh K Aggarwal
Journal:  Arch Ophthalmol       Date:  2004-10

8.  Resistance of Acanthamoeba cysts to disinfection in multiple contact lens solutions.

Authors:  Stephanie P Johnston; Rama Sriram; Yvonne Qvarnstrom; Sharon Roy; Jennifer Verani; Jonathan Yoder; Suchita Lorick; Jacquelin Roberts; Michael J Beach; Govinda Visvesvara
Journal:  J Clin Microbiol       Date:  2009-04-29       Impact factor: 5.948

9.  Resistance of Acanthamoeba to classic DNA extraction methods used for the diagnosis of corneal infections.

Authors:  P Goldschmidt; S Degorge; C Saint-Jean; H Yera; H Year; F Zekhnini; L Batellier; L Laroche; C Chaumeil
Journal:  Br J Ophthalmol       Date:  2007-10-26       Impact factor: 4.638

Review 10.  Pathogenic and opportunistic free-living amoebae: Acanthamoeba spp., Balamuthia mandrillaris, Naegleria fowleri, and Sappinia diploidea.

Authors:  Govinda S Visvesvara; Hercules Moura; Frederick L Schuster
Journal:  FEMS Immunol Med Microbiol       Date:  2007-04-11
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  3 in total

1.  In vitro amoebicidal effect of Aloe vera ethanol extract and honey against Acanthamoeba spp. cysts.

Authors:  Ghada Mohamed Kadry; Mousa A M Ismail; Nagwa Mostafa El-Sayed; Hanan S El-Kholy; Dina M Hamdy El-Akkad
Journal:  J Parasit Dis       Date:  2020-10-15

2.  Diagnosis of Acanthamoeba keratitis in Mashhad, Northeastern Iran: A Gene-Based PCR Assay.

Authors:  Nazgol Khosravinia; Abdolmajid Fata; Elham Moghaddas; Bibi Razieh Hosseini Farash; Mohammad Reza Sedaghat; Ali Raza Eslampour; Lida Jarahi
Journal:  Iran J Parasitol       Date:  2021 Jan-Mar       Impact factor: 1.012

3.  Colony-PCR Is a Rapid Method for DNA Amplification of Hyphomycetes.

Authors:  Georg Walch; Maria Knapp; Georg Rainer; Ursula Peintner
Journal:  J Fungi (Basel)       Date:  2016-04-19
  3 in total

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