Evaluation of trypan blue stain in the TC20 automated cell counter as a point-of-care for the enumeration of viable cryptococcal cells in cerebrospinal fluid. (9th October 2017)

• Record Type: Journal Article
• Authors: Kwizera, Richard; Akampurira, Andrew; Kandole, Tadeo K; Nabaggala, Maria S; Williams, Darlisha A; Kambugu, Andrew; Meya, David B; Rhein, Joshua; Boulware, David R
• Is Part Of: Medical mycology. Volume 56:Number 5(2018)
• Page Start: 559
• Page End: 564
• Publication Date: 2017-10-09
• Subjects: Cryptococcal infection -- HIV -- diagnostic techniques -- point-of-care systems -- quantitation -- TC20; Medical mycology -- Periodicals; Veterinary mycology -- Periodicals; Mycology -- Periodicals; Mycoses -- Periodicals; Pathogenic fungi -- Periodicals; 616.969005
• DOI: 10.1093/mmy/myx076
• Languages: English
• ISSNs: 1369-3786

Abstract

Abstract: Cerebrospinal fluid (CSF) culture can determine a quantitative viability of Cryptococcus yeasts; however, culture has a long turnaround-time. The TC20 automated cell counter (Bio-Rad) is a benchtop instrument used to count cells in 30 seconds. In vitro studies suggest trypan blue staining can distinguish between viable and dead cryptococcal yeasts. We hypothesized that trypan blue staining with automated cell counting may provide rapid quantification of viable CSF Cryptococcus yeasts. In sum, 96 HIV-infected participants with cryptococcal meningitis were enrolled and provided 194 CSF specimens in Kampala, Uganda. Cryptococcosis was diagnosed by CSF cryptococcal antigen (CRAG). CSF was stained with trypan blue and quantified yeasts with the TC20 cell counter. We compared the log10 transformed cell counter readings with gating of 4–10 μm versus log10 quantitative Cryptococcus cultures/ml. TC20 showed more positive results (95.4%) overall than culture (78.4%) with reference to CSF CRAG. TC20 had higher readings compared to culture in most cases with only a 25% level of agreement between the two methods. TC20 had a poor correlation to culture throughout the 14 days of antifungal therapy. The median of log10 transformed counts were 5.22 (IQR = 4.79–5.44) for the TC20 and 3.99 (IQR = 2.59–5.14) for culture. Overall, a linear regression showed no significant relationship between the TC20 and culture ( r = −0.0025; P = .92). TC20 automated cell counting with trypan blue staining was poorly predictive of the quantitative CSF culture and could not be used as a substitute for quantitative culture.