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在自然感染或实验感染的澳大利亚犬科动物中检测细粒棘球绦虫粪抗原。

Detection of Echinococcus granulosus coproantigens in Australian canids with natural or experimental infection.

作者信息

Jenkins D J, Fraser A, Bradshaw H, Craig P S

机构信息

Australian Hydatid Control and Epidemiology Program, Fyshwick, Australian Capital Territory.

出版信息

J Parasitol. 2000 Feb;86(1):140-5. doi: 10.1645/0022-3395(2000)086[0140:DOEGCI]2.0.CO;2.

Abstract

Coproparasitological and purging methods for diagnosing canids infected with the intestinal helminth Echinococcus granulosus, an important zoonotic parasite, are unreliable. Detection of coproantigens in feces of infected dogs by enzyme-linked immunosorbent assay (ELISA) is suitable for detecting patent and prepatent infections with a high degree of sensitivity and specificity. In the present study, natural and experimental infections in domestic and wild Australian canids were investigated using a coproantigen capture ELISA. Experimental infection of dogs with E. granulosus was detected at between 14 and 22 days postinfection (PI), and optical density (OD) values remained high until termination of experiments 35 days PI. After chemotherapy, coproantigen levels in infected dogs dropped rapidly, becoming negative 2-4 days after treatment. In experimentally infected red foxes (Vulpes vulpes), the coproantigen excretion profile was different, with ELISA OD levels peaking 15-17 days PI, then falling to low or undetectable levels by 30 days PI. Coproantigens were detected in the feces of naturally infected Australian wild dogs (dingoes, dingo/domestic dog hybrids) with infection levels ranging between 2 worms and 42,600. Preliminary data on the stability of coproantigen in dog feces exposed to environmental conditions indicated that there was no change in antigenicity over 6 days. The results suggest the coproantigen ELISA could be successfully used to monitor E. granulosus prevalence rates in Australian domestic dogs, foxes, and wild dogs.

摘要

用于诊断感染肠道蠕虫细粒棘球绦虫(一种重要的人畜共患寄生虫)的犬科动物的粪便寄生虫学和驱虫方法并不可靠。通过酶联免疫吸附测定(ELISA)检测感染犬粪便中的粪抗原,适用于检测显性和隐性感染,具有高度的敏感性和特异性。在本研究中,使用粪抗原捕获ELISA对澳大利亚家养和野生犬科动物的自然感染和实验感染进行了调查。犬感染细粒棘球绦虫后,在感染后14至22天可检测到实验感染,并且光密度(OD)值在感染后35天实验结束前一直保持较高水平。化疗后,感染犬的粪抗原水平迅速下降,治疗后2 - 4天变为阴性。在实验感染的赤狐(赤狐)中,粪抗原排泄情况不同,ELISA OD水平在感染后15 - 17天达到峰值,然后在感染后30天降至低水平或无法检测到的水平。在自然感染的澳大利亚野狗(澳洲野犬、澳洲野犬/家犬杂交种)粪便中检测到粪抗原,感染水平在2条虫至42,600条虫之间。关于暴露于环境条件下的犬粪便中粪抗原稳定性的初步数据表明,6天内抗原性没有变化。结果表明,粪抗原ELISA可成功用于监测澳大利亚家犬、狐狸和野狗中细粒棘球绦虫的流行率。

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