Nutrient supplementation of culture media improves the detection of Cutibacterium acnes in platelet components by an automated culture system

Abstract

AbstractBackground and ObjectivesPlatelet concentrates (PCs) contaminated with Cutibacterium acnes are often transfused prior to detection by the BACT/ALERT system. Though C. acnes is implicated in mild transfusion reactions, delayed clinical effects are unknown. This study assessed the ability to enhance C. acnes detection by supplementing culture media with Tween 80 (T80, an oleic acid source) and a commercial nutrient supplement.Materials and MethodsAnaerobic culture bottles (BPN) were supplemented with T80 or oleic acid. T80‐supplemented BPN bottles were inoculated with four C. acnes isolates (10 or 100 colony‐forming units [CFU]/bottle) or other transfusion‐relevant bacteria (10 CFU/bottle). Samples of plasma containing SSP+ (platelet additive solution [PAS]) (PAS‐plasma) at different concentrations, plasma‐PCs and PAS‐PCs, spiked with two C. acnes isolates (10 CFU/bottle), were inoculated into T80‐supplemented BPN bottles. Furthermore, plasma‐PCs were spiked with C. acnes and tested in BPN bottles supplemented with the BD Difco Supplement VX (BDVx). Bottles were incubated in the BACT/ALERT system and times to detection (TtoD) were compared (N = 3).ResultsA reduction in TtoD of ≤3.5 days was observed for C. acnes in T80‐supplemented BPN, while other species did not show the same effect. However, false positives were observed when T80‐supplemented BPN was inoculated with PAS‐plasma (except for 70% PAS:30% plasma), plasma‐PCs or PAS‐PCs. Oleic acid supplementation also resulted in false positives. Interestingly, BDVx‐supplemented BPN reduced the TtoD of C. acnes in PCs by ≤1.2 days (p < 0.05), with no false‐positive results.ConclusionBDVx supplementation for detection of C. acnes from PCs could result in timely unit retrieval, preventing the transfusion of contaminated products. In clinical settings, T80 supplementation could significantly enhance C. acnes detection from non‐blood‐derived samples.