Sayama Yusuke, Zamoto-Niikura Aya, Matsumoto Chieko, Saijo Masayuki, Ishihara Chiaki, Matsubayashi Keiji, Nagai Tadashi, Satake Masahiro
Central Blood Institute, Blood Service Headquarters, Japanese Red Cross Society, National Institute of Infectious Diseases, Tokyo, Japan.
Department of Virology I, National Institute of Infectious Diseases, Tokyo, Japan.
Transfusion. 2018 May;58(5):1234-1244. doi: 10.1111/trf.14558. Epub 2018 Mar 9.
Human babesiosis is caused mainly by Babesia microti and has recently become a public health concern due to an increase in transfusion-transmitted infection. Thus, the development of an antibody detection method with high specificity and sensitivity is a priority. Seroreactivity against B. microti has been reported to be highly specific not only to B. microti lineages but also to sublineages. This study aimed to elucidate the human antibody reactivity against various lineages, including US, Kobe, and Hobetsu, and sublineages (North America and East Asia) in the US lineage.
Twenty samples obtained from individuals infected with B. microti in the United States were tested for the presence of anti-B. microti antibodies using indirect immunofluorescence assay (IFA) and Western blotting (WB) to indicate antigens of each (sub-)lineage.
By IFA, 20 samples showed reactivity to the North America sublineage (titer range, 64-4096), 16 to the East Asia sublineage (64-512), 10 to the Kobe (64-128), and five to the Hobetsu (64). Antibody titers to the East Asia sublineage, Kobe, and Hobetsu were significantly lower than those to the North America sublineage (p < 0.01). By WB, in parallel with the IFA results, 18 samples showed strong reactions to the North America sublineage, weak reactions to the East Asia sublineage, and near-zero reactions to the Kobe and Hobetsu.
Human antibodies induced by B. microti infection are highly specific against B. microti lineages and sublineages with low cross-reactivity. Developing a precise antibody detection method may require specific antigens based on B. microti lineages and sublineages.
人类巴贝斯虫病主要由微小巴贝斯虫引起,由于输血传播感染的增加,最近已成为一个公共卫生问题。因此,开发一种具有高特异性和敏感性的抗体检测方法是当务之急。据报道,针对微小巴贝斯虫的血清反应性不仅对微小巴贝斯虫谱系具有高度特异性,而且对亚谱系也具有高度特异性。本研究旨在阐明人类针对包括美国、神户和北别在内的各种谱系以及美国谱系中的亚谱系(北美和东亚)的抗体反应性。
从美国感染微小巴贝斯虫的个体中获取20份样本,使用间接免疫荧光法(IFA)和蛋白质印迹法(WB)检测抗微小巴贝斯虫抗体的存在,以指示每个(亚)谱系的抗原。
通过IFA,20份样本对北美亚谱系有反应(滴度范围为64 - 4096),16份对东亚亚谱系有反应(64 - 512),10份对神户谱系有反应(64 - 128),5份对北别谱系有反应(64)。对东亚亚谱系、神户谱系和北别谱系的抗体滴度显著低于对北美亚谱系的抗体滴度(p < 0.01)。通过WB,与IFA结果一致,18份样本对北美亚谱系有强烈反应,对东亚亚谱系有微弱反应,对神户谱系和北别谱系几乎无反应。
微小巴贝斯虫感染诱导的人类抗体对微小巴贝斯虫谱系和亚谱系具有高度特异性,交叉反应性低。开发精确的抗体检测方法可能需要基于微小巴贝斯虫谱系和亚谱系的特异性抗原。