2017
DOI: 10.1186/s12866-017-1093-4
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Evaluation of trypan blue stain in a haemocytometer for rapid detection of cerebrospinal fluid sterility in HIV patients with cryptococcal meningitis

Abstract: BackgroundQuantitative culture is the most common method to determine the fungal burden and sterility of cerebrospinal fluid (CSF) among persons with cryptococcal meningitis. A major drawback of cultures is a long turnaround-time. Recent evidence demonstrates that live and dead Cryptococcus yeasts can be distinguished using trypan blue staining. We hypothesized that trypan blue staining combined with haemocytometer counting may provide a rapid estimation of quantitative culture count and detection of CSF steri… Show more

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Cited by 9 publications
(4 citation statements)
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References 12 publications
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“…Indeed, automation is pivotal in cell manufacturing applications, as it increases reproducibility and reduce time consumption, paving the way to industrial translation [20] . More specifically, the counting time using an hematocytometer has been found to increase almost linearly with sample concentration [21] , ranging from around 30 seconds with 4 × 10 4 cells/mL to around 3 min with 8 × 10 5 cells/mL [22] . On the other hand, the analysis time using an automated cell counter is independent on cell concentration.…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, automation is pivotal in cell manufacturing applications, as it increases reproducibility and reduce time consumption, paving the way to industrial translation [20] . More specifically, the counting time using an hematocytometer has been found to increase almost linearly with sample concentration [21] , ranging from around 30 seconds with 4 × 10 4 cells/mL to around 3 min with 8 × 10 5 cells/mL [22] . On the other hand, the analysis time using an automated cell counter is independent on cell concentration.…”
Section: Discussionmentioning
confidence: 99%
“…Live cells (unstained) that did not take the stain were considered. Dead cells were stained [ 22 ]. Cell survivability or viability was counted using formula [ 23 ] (Supplementary Figure S1).…”
Section: Methodsmentioning
confidence: 99%
“…Cell viability, which is essential to assess the kinetics of growth, is performed by the selective staining of the sample using various staining approaches. Vital exclusion stains are commonly used to mark cells that have lost membrane integrity such as Trypan Blue or inclusion stains which mark cells retaining membrane integrity such as Fluorescein Diacetate (Kwizera et al, 2017). Hemocytometer is not limited to certain staining methods and allows all staining techniques according to the purpose of the analyses.…”
Section: Hemocytometermentioning
confidence: 99%