GIMAP EA 3064 (Groupe Immunité des Muqueuses et Agents Pathogènes), University of Lyon, Faculty of Medicine of Saint-Etienne, Saint-Etienne, France.
Laboratory of Infectious Agents and Hygiene, University Hospital of Saint-Etienne, Saint-Etienne, France.
Biomed Res Int. 2018 Nov 21;2018:7013470. doi: 10.1155/2018/7013470. eCollection 2018.
Rapid bacterial identification of positive blood culture is important for adapting the antimicrobial therapy in patients with blood stream infection. The aim of this study was to evaluate the performance of the multiplex FilmArray Blood Culture Identification (BCID) assay by comparison to an in-house protocol based on MALDI-TOF MS identification of microcolonies after a 4-hour culture, for identifying on the same day the microorganisms present in positive blood culture bottles. One hundred and fifty-three positive bottles from 123 patients were tested prospectively by the 3 techniques of bacterial identification: 11 bottles yielding negative results by the 3 tests were considered false positive (7.2%). The reference MALDI-TOF MS technique identified 134 monomicrobial (87.6%) and 8 double infections (5.2%), which resulted in a total of 150 microorganisms. Globally, 137 (91.3%) of these 150 pathogens were correctly identified by the fully automated multiplex FilmArray BCID system at the species or genus level on day of growth detection, versus 117 (78.8%) by MALDI-TOF MS identification on nascent microcolonies after a 4-hour culture ( < 0.01). By combining the two approaches, 140 (93.5%) of the positive bottles were identified successfully at day 0. These results confirm the excellent sensitivity of the FilmArray BCID assay, notably in case of multimicrobial infection. Due to the limited number of targets included into the test, it must be coupled to another identification strategy, as that presented in this study relying on MALDI-TOF MS identification of microcolonies obtained after a very short culture period.
快速鉴定阳性血培养中的细菌对于调整血流感染患者的抗菌治疗非常重要。本研究旨在评估多重 FilmArray 血培养鉴定(BCID)分析与基于 MALDI-TOF MS 鉴定微菌落的内部方案的性能,该方案在 4 小时培养后,用于鉴定阳性血培养瓶中当天存在的微生物。通过 3 种细菌鉴定技术对 123 例患者的 153 个阳性瓶进行了前瞻性检测:3 种检测方法中,11 个阴性结果的瓶被认为是假阳性(7.2%)。参考 MALDI-TOF MS 技术鉴定了 134 种单微生物(87.6%)和 8 种双感染(5.2%),共鉴定出 150 种微生物。总体而言,在生长检测日,全自动多重 FilmArray BCID 系统在种或属水平上正确鉴定了 137 种(91.3%)这些 150 种病原体,而通过 MALDI-TOF MS 鉴定 4 小时培养后初生微菌落的方法仅鉴定了 117 种(78.8%)(<0.01)。通过结合这两种方法,在第 0 天成功鉴定了 140 个(93.5%)阳性瓶。这些结果证实了 FilmArray BCID 分析的出色灵敏度,尤其是在多重感染的情况下。由于测试中包含的目标数量有限,它必须与另一种鉴定策略结合使用,如本研究中使用的基于 MALDI-TOF MS 鉴定非常短培养期后获得的微菌落的方法。