Evaluation of a new generation of plastic culture bottles with an automated microbial detection system for nine common contaminating organisms found in PLT components

Transfusion ◽  
2004 ◽  
Vol 44 (3) ◽  
pp. 359-363 ◽  
Author(s):  
M.E. Brecher ◽  
S.N. Hay ◽  
S.J. Rothenberg
Separations ◽  
2020 ◽  
Vol 7 (4) ◽  
pp. 64
Author(s):  
Ryan Thompson ◽  
John D. Perry ◽  
Stephen P. Stanforth ◽  
John R. Dean

Development of a rapid approach for universal microbial detection is required in the healthcare, food and environmental sectors to aid with medical intervention, food safety and environmental protection. This research investigates the use of enzymatic hydrolysis of a substrate by a microorganism to generate a volatile organic compound (VOC). One such enzyme activity that can be used in this context is nitroreductase as such activity is prevalent across a range of microorganisms. A study was developed to evaluate a panel of 51 microorganisms of clinical interest for their nitroreductase activity. Two enzyme substrates, nitrobenzene and 1-fluoro-2-nitrobenzene, were evaluated for this purpose with evolution, after incubation, of the VOCs aniline and 2-fluoroaniline, respectively. Detection of the VOCs was done using headspace-solid phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) with obtained limits of quantitation (LOQ) of 0.17 and 0.03 µg/mL for aniline and 2-fluoroaniline, respectively. The results indicated that both enzyme substrates were reduced by the same 84.3% of microorganisms producing the corresponding volatile anilines which were detected using HS-SPME-GC-MS. It was found that nitroreductase activity could be detected after 6–8 h of incubation for the selected pathogenic bacteria investigated. This approach shows promise as a rapid universal microbial detection system.


2018 ◽  
Vol 79 (7-8) ◽  
pp. 5225-5242 ◽  
Author(s):  
Dinesh Jackson Samuel R ◽  
Rajesh Kanna B

Transfusion ◽  
2011 ◽  
Vol 51 (10) ◽  
pp. 2219-2227 ◽  
Author(s):  
Larry J. Dumont ◽  
Shauna N. Hay ◽  
Louise Herschel ◽  
Barbara Brantigan ◽  
Jaime Houghton ◽  
...  

2006 ◽  
Vol 157 (5) ◽  
pp. 433-436 ◽  
Author(s):  
Fusun Zeynep Akcam ◽  
Guler Yayli ◽  
Ersin Uskun ◽  
Onur Kaya ◽  
Canan Demir

2008 ◽  
Vol 167 (4) ◽  
pp. 191-195
Author(s):  
Erik Munson ◽  
Tina Endes ◽  
Katharine Vaughan ◽  
Timothy Block ◽  
Jeanne E. Hryciuk

Author(s):  
Mary Adamik ◽  
Anne Hutchins ◽  
Jasmin Mangilit ◽  
Betsy Katzin ◽  
Heather Totty ◽  
...  

Abstract Delayed entry of patient blood culture samples into a microbial detection system is unavoidable at times, due to off-shift staffing or transporting samples to centralized laboratories. Pre-incubation time and temperature of blood culture bottles are the most critical factors impacting recovery and detection of microorganisms. A total of 1377 BACT/ALERT® (BTA) Fastidious Antimicrobial Neutralization (FAN® PLUS) bottles (FA PLUS, FN PLUS, and PF PLUS) were tested after delayed entry times of 24 and 36 h at 20–25 °C (room temperature, RT) prior to loading into the BACT/ALERT® VIRTUO® microbial detection system (VIRTUO). Clinically relevant organisms were inoculated into bottles with 5–84 colony forming units (CFU) per bottle, and human blood (0 to 10 mL), and then loaded into the VIRTUO. When bottles were loaded without delay, a mean time to detection (TTD) of 9.6 h was observed. For delayed bottles, the TTD reported by the VIRTUO was added to the 24-h and 36-h delay times and resulted in average time to results of 32.5 h and 42.5 h, respectively. The FAN PLUS bottles in conjunction with the VIRTUO produced acceptable results when delays up to 24 h at 20–25 °C occur in loading.


Pathology ◽  
2017 ◽  
Vol 49 (6) ◽  
pp. 656-658 ◽  
Author(s):  
Christopher J. McIver ◽  
Noel Er ◽  
Robert Stevens ◽  
Peter C. Taylor

2001 ◽  
Vol 7 (S2) ◽  
pp. 1132-1133
Author(s):  
John A. Hunt ◽  
Frank E. Dickerson ◽  
A. Abbott ◽  
Gabriel Szantai ◽  
Paul E. Mooney

The Gatan Enfina EELS spectrometer, featuring a new generation of detection system, was recently developed to upgrade or replace Gatan PEELS / DigiPEELS systems. Major advantages of the system include significant improvements to the detector point spread function, readout speed, sensitivity, readout noise, and increased number of detection channels. This design was until now not available for VG STEM systems because compatible detectors must not significantly degrade the UHV column vacuum and must survive column baking. in this abstract we report on a new detector system with comparable specifications to the standard Enfina system but designed for new or for upgrading existing Gatan UHV PEELS / DigiPEELS systems on the VG STEM.The standard Enfina design has the scintillator, fibers, CCD, CCD socket board, flex-cables, thermo electric cooler and coupling grease in the shared vacuum of the EELS spectrometer and the electron microscope.


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