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Viable Bacteria Associated with Red Blood Cells and Plasma in Freshly Drawn Blood Donations
被引:79
|作者:
Damgaard, Christian
[1
,2
]
Magnussen, Karin
[3
,4
]
Enevold, Christian
[1
,2
]
Nilsson, Martin
[5
]
Tolker-Nielsen, Tim
[5
]
Holmstrup, Palle
[1
]
Nielsen, Claus Henrik
[1
,2
]
机构:
[1] Univ Copenhagen, Fac Hlth & Med Sci, Dept Odontol, Sect Periodontol Microbiol & Community Dent, Copenhagen, Denmark
[2] Copenhagen Univ Hosp, Rigshosp, Inst Inflammat Res, Dept Infect Dis & Rheumatol, Copenhagen, Denmark
[3] Copenhagen Univ Hosp, Rigshosp, Dept Clin Immunol, Hvidovre, Denmark
[4] Copenhagen Univ Hosp, Rigshosp, Ctr Blood, Hvidovre, Denmark
[5] Univ Copenhagen, Costerton Biofilm Ctr, Dept Int Hlth Immunol & Microbiol, Fac Hlth & Med Sci, Copenhagen, Denmark
来源:
关键词:
DONOR-ARM DISINFECTION;
STAPHYLOCOCCUS-EPIDERMIDIS;
PROPIONIBACTERIUM-ACNES;
TRANSFUSION;
INFECTION;
RISK;
CONTAMINATION;
ENDOCARDITIS;
DIVERSION;
PRODUCTS;
D O I:
10.1371/journal.pone.0120826
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Objectives Infection remains a leading cause of post-transfusion mortality and morbidity. Bacterial contamination is, however, detected in less than 0.1% of blood units tested. The aim of the study was to identify viable bacteria in standard blood-pack units, with particular focus on bacteria from the oral cavity, and to determine the distribution of bacteria revealed in plasma and in the red blood cell (RBC)-fraction. Design Cross-sectional study. Blood were separated into plasma and RBC-suspensions, which were incubated anaerobically or aerobically for 7 days on trypticase soy blood agar (TSA) or blue lactose plates. For identification colony PCR was performed using primers targeting 16S rDNA. Setting Blood donors attending Capital Region Blood Bank, Copenhagen University Hospital, Rig-shospitalet, Hvidovre, Denmark, October 29th to December 10th 2013. Participants 60 donors (>= 50 years old), self-reported medically healthy. Results Bacterial growth was observed on plates inoculated with plasma or RBCs from 62% of the blood donations. Growth was evident in 21 (35%) of 60 RBC-fractions and in 32 (53%) of 60 plasma-fractions versus 8 of 60 negative controls (p = 0.005 and p = 2.6x10(-6), respectively). Propionibacterium acnes was found in 23% of the donations, and Staphylococcus epidermidis in 38%. The majority of bacteria identified in the present study were either facultative anaerobic (59.5%) or anaerobic (27.8%) species, which are not likely to be detected during current routine screening. Conclusions Viable bacteria are present in blood from donors self-reported as medically healthy, indicating that conventional test systems employed by blood banks insufficiently detect bacteria in plasma. Further investigation is needed to determine whether routine testing for anaerobic bacteria and testing of RBC-fractions for adherent bacteria should be recommended.
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