Matsumura K, Kazuta Y, Endo R, Tanaka K, Inoue T, Matsuda H
Yamaguchi Prefectural Research Institute of Health, Japan.
Vet Parasitol. 1988 Mar;27(3-4):337-44. doi: 10.1016/0304-4017(88)90047-7.
This study describes an enzyme (horseradish peroxidase)-linked immunosorbent assay using nitrocellulose (NC) paper (Dot-ELISA) for the detection of antibodies against Dirofilaria immitis in dogs. Dirofilarial antigens prepared were directly bound on NC paper set into a microfiltration apparatus to ensure their uniformity. Of the 23 infected dogs tested, 21 were determined positive by visual observation of brown-colored spots on NC paper. The positive and negative readings were further confirmed by using a densitometer. Sera from 15 non-infected and 17 other parasite-infected dogs were all negative, i.e. no false positive readings and low cross-reactivities were found using this technique. Also, a large number of samples could be assayed simultaneously within 1.5 h. The Dot-ELISA technique reported here may be useful to veterinarians and also may be a means of field surveying human filariasis.
本研究描述了一种使用硝酸纤维素(NC)纸的酶(辣根过氧化物酶)联免疫吸附测定法(斑点酶联免疫吸附测定法),用于检测犬体内抗犬恶丝虫的抗体。制备的恶丝虫抗原直接结合在置于微滤装置中的NC纸上,以确保其均匀性。在检测的23只感染犬中,通过目视观察NC纸上的褐色斑点,确定21只为阳性。阳性和阴性读数通过密度计进一步确认。来自15只未感染和17只其他寄生虫感染犬的血清均为阴性,即使用该技术未发现假阳性读数且交叉反应性较低。此外,大量样本可在1.5小时内同时进行检测。此处报道的斑点酶联免疫吸附测定法可能对兽医有用,也可能是一种现场调查人类丝虫病的方法。