• 中国科学论文统计源期刊
  • 中国科技核心期刊
  • 美国化学文摘(CA)来源期刊
  • 日本科学技术振兴机构数据库(JST)

临床输血与检验 ›› 2026, Vol. 28 ›› Issue (4): 533-539.DOI: 10.3969/j.issn.1671-2587.2026.04.011

• 临床输血 • 上一篇    下一篇

体外模拟输血相关血液制品中细菌污染的生存特性与生物膜形成研究*

李丹丹1, 王佳琦2, 李婧3, 程红1, 陶雪2, 王志成1, 张振2, 夏荣1   

  1. 1复旦大学附属华山医院输血科,上海 200040;
    2上海德济医院检验科,上海 200331;
    3复旦大学附属华山医院检验科,上海 200040
  • 收稿日期:2026-07-07 出版日期:2026-08-20 发布日期:2026-08-26
  • 通讯作者: 夏荣,主要从事输血相关免疫调节研究,(E-mail)rongxia@fudan.edu.cn。
  • 作者简介:李丹丹,主要从事血液制品的细菌污染防控方面研究,(E-mail)danny0606@foxmail.com。
  • 基金资助:
    *本课题受国家自然科学基金面上项目(No.82470234)、中国输血协会圣湘基金(No.CSBT-SX-2024-05)、中国输血协会威高基金(No.CSBT-WG-2024-01)资助

Survival Characteristics and Biofilm Formation of Bacterial Contamination in Transfusion-related Blood Products

LI Dandan1, WANG Jiaqi2, LI Jing3, CHENG Hong1, TAO Xue2, WANG Zhicheng1, ZHANG Zhen2, XIA Rong1   

  1. 1Department of Blood Transfusion, Huashan Hospital Affiliated to Fudan University, Shanghai 200040;
    2Department of Clinical Laboratory, Shanghai Deji Hospital, Shanghai 200331;
    3Department of Clinical Laboratory, Huashan Hospital Affiliated to Fudan University, Shanghai 200040
  • Received:2026-07-07 Online:2026-08-20 Published:2026-08-26

摘要: 目的 比较分离自健康志愿者肘正中皮肤并经鉴定的表皮葡萄球菌(Staphylococcus epidermidis)在全血、红细胞悬液及浓缩血小板中的生存差异,并初步探索血液制品保存袋内壁的生物膜形成情况。方法 采集5份健康志愿者全血,手工分离红细胞悬液和浓缩血小板。使用无菌棉拭子采集健康志愿者肘正中皮肤菌群,分离鉴定优势菌为表皮葡萄球菌。将各组血制品分别加入终浓度约10 CFU/mL的表皮葡萄球菌菌液,同时设置无菌对照。全血和红细胞悬液于4 ℃保存,浓缩血小板于(22±2)℃振荡保存。于加菌第1天(2 h内)、第3天、第5天、第7天、第9天取样进行血平板培养,48 h后计数菌落数。实验结束后,采用结晶紫染色法检测保存袋内壁生物膜形成。结果 加菌第1天,三组均能检出少量细菌(1~8 CFU/100 μL),组间无差异(H=1.792,P=0.436)。此后三组趋势截然不同:全血组从第3天起逐步清除细菌,至第9天4份标本无菌生长,仅1份持续检出1 CFU/100 μL;红细胞悬液组第3天菌落数上升至19(8,32)CFU/100 μL,至第9天3份标本无菌生长;浓缩血小板组第3天即大量增殖,菌落数上升至81(33,300)CFU/100 μL,第7天起全部不可计数。结晶紫染色显示,全血组及红悬组袋内壁有紫色着色,其中无菌生长的袋壁亦见着色。结论 全血和红细胞悬液对表皮葡萄球菌具有一定自净能力,而浓缩血小板极易促进细菌增殖。细菌可能在血袋内壁形成生物膜,导致常规培养和检测假阴性。

关键词: 表皮葡萄球菌, 全血, 红细胞悬液, 浓缩血小板, 细菌污染, 生物膜, 输血安全

Abstract: Objective To compare the survival of Staphylococcus epidermidis in whole blood, red blood cell suspensions, and platelet concentrates, and to preliminarily investigate biofilm formation on the inner wall of blood storage bags. Methods Whole blood was collected from five healthy volunteers, and red blood cell suspensions and platelet concentrates were manually prepared. Skin flora from the antecubital region was sampled using sterile swabs, and the predominant isolate was identified as S. epidermidis. Each blood component was spiked with the bacterial suspension to a final concentration of approximately 10 CFU/mL, with sterile controls set up in parallel. Whole blood and red blood cell suspensions were stored at 4 ℃, while platelet concentrates were agitated at (22±2) ℃. Samples were taken on days 1 (within 2 h), 3, 5, 7, and 9 post-inoculation, plated on blood agar, and colonies were counted after 48 h of incubation. At the end of the experiment, crystal violet staining was used to assess biofilm formation on the inner bag surface. Results On day 1, all three groups yielded small numbers of bacteria (1~8 CFU/100 μL), with no significant difference among groups (H=1.792, P=0.436). Thereafter, the three groups showed distinctly different trends: in the whole-blood group, bacteria were progressively cleared from day 3 onward, with 4 of 5 specimens becoming sterile by day 9 and the remaining one showing only 1 CFU/100 μL. In the red blood cell suspension group, counts rose to 19 (8, 32) CFU/100 μL on day 3, but by day 9, 3 specimens were sterile. In the platelet concentrate group, massive proliferation occurred as early as day 3, with counts reaching 81 (33 300) CFU/100 μL, and all specimens became uncountable from day 7 onward. Crystal violet staining revealed purple coloration on the inner bag walls in both the whole-blood and red blood cell suspension groups, including bags that had become sterile. Conclusion Whole blood and red blood cell suspensions exhibit a certain capacity for self-clearance against S. epidermidis, whereas platelet concentrates strongly support bacterial proliferation. Bacteria may form biofilms on the inner bag surface, potentially leading to false-negative results in routine culture and detection.

Key words: Staphylococcus epidermidis, Whole blood, Red blood cell suspension, Platelet concentrate, Bacterial contamination, Biofilm, Transfusion safety

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