Magnarelli L A, Oliver J H, Hutcheson H J, Anderson J F
Department of Entomology, Connecticut Agricultural Experiment Station, New Haven 06504.
J Wildl Dis. 1991 Oct;27(4):562-8. doi: 10.7589/0090-3558-27.4.562.
An enzyme-linked immunosorbent assay (ELISA) was developed to detect serum antibodies to Borrelia burgdorferi, the causative agent of Lyme borreliosis, in deer (Odocoileus virginianus) and raccoons (Procyon lotor). Blood samples were collected from these mammals in Connecticut, Maryland, North Carolina, Georgia and Florida. Seropositivity for deer was highest in Connecticut (56% of 353 sera) and Maryland (51% of 35 sera). Raccoons in Connecticut, Maryland, North Carolina, and Florida also had antibodies to B. burgdorferi, but prevalence of positive sera was highest in Maryland (79% of 14 samples). Based on adsorption tests, the immunoglobulins detected in these mammals were probably specific to B. burgdorferi. The ELISA was more sensitive than an indirect fluorescent antibody staining method and was more suitable for analyzing large numbers of serum samples.
开发了一种酶联免疫吸附测定(ELISA)法,用于检测鹿(弗吉尼亚白尾鹿)和浣熊(北美浣熊)血清中针对莱姆病病原体伯氏疏螺旋体的抗体。在康涅狄格州、马里兰州、北卡罗来纳州、佐治亚州和佛罗里达州采集了这些哺乳动物的血样。鹿的血清阳性率在康涅狄格州最高(353份血清中的56%),在马里兰州次之(35份血清中的51%)。康涅狄格州、马里兰州、北卡罗来纳州和佛罗里达州的浣熊也有针对伯氏疏螺旋体的抗体,但阳性血清的患病率在马里兰州最高(14份样本中的79%)。基于吸附试验,在这些哺乳动物中检测到的免疫球蛋白可能对伯氏疏螺旋体具有特异性。ELISA法比间接荧光抗体染色法更灵敏,更适合分析大量血清样本。