Immunomics analysis of Babesia microti protein markers by high-throughput screening assay

被引:6
作者
Zhou, Xia [1 ,2 ]
Huang, Ji-Lei [2 ]
Shen, Hai-Mo [2 ]
Xu, Bin [2 ]
Chen, Jun-Hu [2 ]
Zhou, Xiao-Nong [2 ]
机构
[1] Soochow Univ, Med Sch, 199 Renai Rd, Suzhou 215123, Peoples R China
[2] Chinese Minist Hlth, Key Lab Parasite & Vector Biol, Natl Ctr Int Res Trop Dis,WHO Collaborating Ctr T, Natl Inst Parasit Dis,Chinese Ctr Dis Control & P, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金;
关键词
Babesia microti; Antigens; Immunoproteomics; Protein microarray; PLASMODIUM-VIVAX INFECTION; NATURAL ANTIBODY-RESPONSES; CHINA-MYANMAR BORDER; CELL INVASION; PCR CLONING; GENOME; MALARIA; IDENTIFICATION; PARASITOLOGY; MICROARRAY;
D O I
10.1016/j.ttbdis.2018.07.004
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Babesia microti is a protozoan considered to be a major etiological agent of emerging human babesiosis. It imposes an increasing public-health threat and can be overlooked because of low parasitemia or mixed infection with other pathogens. More sensitive and specific antigens are needed to improve the diagnosis of babesiosis. To screen the immune diagnostic antigens of B. microti, 204 sequences from homologue proteins between B. microti and B. bovis genome sequences in PiroplasmaDB were selected. The high throughput cloned and expressed B. microti proteins were screened with the sera from the BALB/c mice infected by B. microti using protein arrays. Ten (5.9%, 10/169) highly immunoreactive proteins were identified, and most (80%, 8/10) of these highly immunoreactive proteins had not been characterized before, making them potentially useful as candidate antigens for the development of diagnostic tools for babesiosis.
引用
收藏
页码:1468 / 1474
页数:7
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