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应用线性肽段检测嗜吞噬细胞无形体和微小巴贝斯虫抗体。

Detection of antibodies to Anaplasma phagocytophilum and Babesia microti using linear peptides.

作者信息

Tagliafierro Teresa, Joshi Shreyas, Sameroff Stephen, Marques Adriana, Dumler J Stephen, Mishra Nischay, Sanchez-Vicente Santiago, Wormser Gary P, Marcos Luis A, Lipkin W Ian, Tokarz Rafal

机构信息

Center for Infection and Immunity, Mailman School of Public Health, Columbia University, 722 West 168th Street, Room 1701, New York, NY 10032, United States.

Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.

出版信息

Ticks Tick Borne Dis. 2022 Sep;13(5):101999. doi: 10.1016/j.ttbdis.2022.101999. Epub 2022 Jul 1.

Abstract

Anaplasma phagocytophilum and Babesia microti are emerging tick-borne pathogens in the United States. Although active infection is typically diagnosed by direct diagnostic tests, such as blood smear or polymerase chain reaction assay, serologic assays can be helpful to identify past infections, and the use of acute plus convalescent testing can potentially identify recent infections. We employed a peptide array to select sets of linear peptides for serologic diagnosis of infections with A. phagocytophilum and B. microti. Three optimal peptides were selected for each agent based on their performance with clinical specimens. All three A. phagocytophilum peptides were located within the conserved fragments of the MSP2 antigen. Two B. microti peptides were located in the N terminus of the SA-1 antigen; the third was in the BMN 1-17 antigen. We found that these peptides can be a useful tool for detection of antibody reactivity to both of these pathogens.

摘要

嗜吞噬细胞无形体和微小巴贝斯虫是美国新出现的蜱传病原体。虽然直接诊断检测(如血涂片或聚合酶链反应检测)通常可用于诊断活动性感染,但血清学检测有助于确定既往感染,采用急性期加恢复期检测可潜在地确定近期感染。我们采用肽芯片选择了用于诊断嗜吞噬细胞无形体和微小巴贝斯虫感染的线性肽组合。根据与临床标本的检测结果,针对每种病原体选择了 3 个最佳的肽。嗜吞噬细胞无形体的 3 个最佳肽均位于 MSP2 抗原的保守片段内。微小巴贝斯虫的 2 个最佳肽位于 SA-1 抗原的 N 末端;第 3 个位于 BMN 1-17 抗原。我们发现,这些肽可作为检测这两种病原体抗体反应性的有用工具。

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