2008
DOI: 10.1186/1471-2415-8-7
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Specific detection of fungal pathogens by 18S rRNA gene PCR in microbial keratitis

Abstract: Background: The sensitivity and specificity of 18S rRNA polymerase chain reaction (PCR) in the detection of fungal aetiology of microbial keratitis was determined in thirty patients with clinical diagnosis of microbial keratitis.

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Cited by 64 publications
(49 citation statements)
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“…In nonendemic areas, systemic mycosis is seen in individuals who visit endemic areas, with the risk of acquisition increasing with immune suppression. 6,7 The asexual form A. dermatitidis exists as a mold in nature. Airborne conidia, when inhaled, gets lodged in the alveoli, where it undergoes transition to yeast form, which is seen in mammalian tissue and culture at 37 C. Wet earth enriched with animal droppings, rotting wood, and decaying vegetables is considered to be the ecological niche for B. dermatitidis.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…In nonendemic areas, systemic mycosis is seen in individuals who visit endemic areas, with the risk of acquisition increasing with immune suppression. 6,7 The asexual form A. dermatitidis exists as a mold in nature. Airborne conidia, when inhaled, gets lodged in the alveoli, where it undergoes transition to yeast form, which is seen in mammalian tissue and culture at 37 C. Wet earth enriched with animal droppings, rotting wood, and decaying vegetables is considered to be the ecological niche for B. dermatitidis.…”
Section: Discussionmentioning
confidence: 99%
“…6 DNA extraction was done using the yeast Genomic DNA Kit (Himedia Laboratories Pvt. Ltd., Mumbai, India).…”
Section: Case Reportmentioning
confidence: 99%
“…PCR primers used to detect the 18S rRNA gene of Aspergillus sp. : PFPRIM-F3 5 0 GACTCAACACGGGGAA ACT3 0 and PFPRIM-R4 5 0 ATTCCTCGTTGAAGAGCA3 0 (Embong et al 2008). The amplification reaction was conducted in 50 ll that contained 19 Taq DNA polymerase buffer (10 mM Tris-HCl, pH 9.0, 50 mM NaCl, 0.01 M Triton X-100, and 2 mM MgCl 2 ), 2 mM of each dNTP, 10 mM of each primer, 50 ng of genomic DNA, and 5 units of Taq DNA polymerase.…”
Section: Isolation and Screening Of Decolorizing Fungal Isolatesmentioning
confidence: 99%
“…Otros autores han encontrado que Fusarium spp. es el principal patógeno encontrado en las muestras oculares (24,25,26).…”
Section: Carlos Pérez Díaz Patricia Barrios Castañeda José David MIunclassified