Silva Marilene Neves, Vieira-Damiani Gislaine, Ericson Marna Elise, Gupta Kalpna, Gilioli Rovilson, de Almeida Amanda Roberta, Drummond Marina Rovani, Lania Bruno Grosselli, de Almeida Lins Karina, Soares Tânia Cristina Benetti, Velho Paulo Eduardo Neves Ferreira
Division of Dermatology, Department of Medicine, University of Campinas (UNICAMP) Medical School, Campinas, SP, Brazil.
Federal Institute of Education, Science and Technology, Jaguariaiva, PR, Brazil.
Transfusion. 2016 Jun;56(6 Pt 2):1556-9. doi: 10.1111/trf.13545. Epub 2016 Mar 10.
Bartonella spp. are neglected fastidious Gram-negative bacilli. We isolated Bartonella henselae from 1.2% of 500 studied blood donors and demonstrated that the bacteria remain viable in red blood cell units after 35 days of experimental infection. Now, we aim to evaluate the possibility of B. henselae transmission by blood transfusion in a mouse model.
Eight BALB/c mice were intraperitoneal inoculated with a 30 µL of suspension with 10(4) CFU/mL of B. henselae and a second group of eight mice were inoculated with saline solution and used as control. After 96 hours of inoculation, the animals were euthanized. We collected blood and tissue samples from skin, liver, and spleen. Thirty microliters of blood from four Bartonella-inoculated animals were transfused into a new group (n = 4). Another group received blood from the control animals. B. henselae infection was investigated by conventional and nested polymerase chain reaction (PCR).
Blood samples from all 24 mice were negative by molecular tests though half of the tissue samples were positive by nested PCR in the intraperitoneal Bartonella-investigated animals. Tissues from two of the four mice that received blood transfusions from Bartonella-inoculated animals were also nested PCR positives.
Transmission of B. henselae by transfusion is possible in mice even when donor animals have undetectable bloodstream infection. The impact of human Bartonella sp. transmission through blood transfusion recipients must be evaluated.
巴尔通体属是被忽视的苛养革兰氏阴性杆菌。我们从500名接受研究的献血者中分离出1.2%的亨氏巴尔通体,并证明在实验感染35天后,这些细菌在红细胞单位中仍具有活力。现在,我们旨在评估在小鼠模型中通过输血传播亨氏巴尔通体的可能性。
8只BALB/c小鼠腹腔接种30 μL含10⁴CFU/mL亨氏巴尔通体的悬液,另一组8只小鼠接种生理盐水作为对照。接种96小时后,对动物实施安乐死。我们采集了皮肤、肝脏和脾脏的血液及组织样本。将4只接种巴尔通体动物的30 μL血液输给一组新的小鼠(n = 4)。另一组接受来自对照动物的血液。通过常规和巢式聚合酶链反应(PCR)检测亨氏巴尔通体感染情况。
所有24只小鼠的血液样本经分子检测均为阴性,尽管在腹腔接种巴尔通体的动物中,一半的组织样本经巢式PCR检测呈阳性。接受接种巴尔通体动物输血的4只小鼠中有2只的组织经巢式PCR检测也呈阳性。
即使供体动物的血流感染无法检测到,输血传播亨氏巴尔通体在小鼠中也是可能的。必须评估人类巴尔通体通过输血传播给受血者的影响。