TRANSFUSION-TRANSMITTED YERSINIA-ENTEROCOLITICA INFECTION - PROTECTION THROUGH BUFFY COAT REMOVAL AND FAILURE OF THE BACTERIA TO GROW IN PLATELET-RICH OR PLATELET-POOR PLASMA
J. Gong et al., TRANSFUSION-TRANSMITTED YERSINIA-ENTEROCOLITICA INFECTION - PROTECTION THROUGH BUFFY COAT REMOVAL AND FAILURE OF THE BACTERIA TO GROW IN PLATELET-RICH OR PLATELET-POOR PLASMA, Vox sanguinis, 65(1), 1993, pp. 42-46
In a previous study, removal of white blood cells (WBC), by filtration
5 h after deliberate contamination of whole blood with a type 0:3 str
ain of Yersinia enterocolitica, was shown to be an effective way of av
oiding bacterial growth in red blood cells (RBC) during storage. In th
e present study the Opti-System technique was used to remove the buffy
coat from whole blood, leaving 10-20% of the original number of WBC i
n the RBC preparation. In one series of experiments, all of 4 units of
RBC suspension, from which buffy coats were removed 2 h after inocula
tion of 112 colony-forming units (cfu) per ml of Y. enterocolitica, be
came Yersinia-free, while abundant bacterial growth occurred in all of
4 units where RBC suspension and buffy coat had been recombined. In a
second series of 10 experiments, with an inoculum of 80 cfu/ml, no gr
owth was found in platelet-poor plasma stored for 42 days at 4-degrees
-C. Five out of 10 RBC suspensions in SAGM additive solution remained
Yersinia-free throughout a 6-week storage period; 4 of these 10 units
showing growth of Yersinia after 4 weeks and 5 after 6 weeks. In the b
uffy coats bacterial growth was found in 1 out of 10 units after 1 wee
k, 4 after 2 weeks, and in all of 10 units after 4 weeks. In 2 control
experiments with WBC-reduced RBC inoculated with the same bacterial d
ose, growth started within 24 h and was abundant after 1 week. In plat
elet-rich plasma (PRP), prepared from 4 units of whole blood that had
been inoculated with Y enterocolitica (106 cfu/ml), no bacterial growt
h was found during 10 days of storage at 22-degrees-C. Also, after Y e
nterocolitica inoculation (114 cfu/ml) directly into PRP, bacteria fai
led to grow. We conclude that removal of the buffy coat from whole blo
od that had been previously contaminated with a moderate inoculation o
f Y. enterocolitica partly protects the red cells from bacterial growt
h during storage. The risk of transmitting Y enterocolitica with plate
let-poor plasma, liquid stored at 4-degrees-C, seems minimal. This bac
terial species shows very poor capacity to grow in PRP at 22-degrees-C
.