Michel A L, Buchholz G S, Van der Lugt J J
Virology Division, Onderstepoort Veterinary Intitute, South Africa.
Onderstepoort J Vet Res. 1995 Jun;62(2):109-15.
The DNA probe SW15 derived from the laboratory-attenuated Alcelaphine Herpesvirus-1 (AHV-1) strain WC11 as well as from the polymerase chain-reaction test (Hsu, Shih, Castro & Zee 1990), was used to detect viral DNA of malignant catarrhal fever (MCF) in six experimentally infected cattle. Heparinized blood samples were collected and tested at least three times a week over a period of up to 142 d. Results of hybridization and PCR tests were compared with the results of clinical examinations, and on various occasions with those of viral isolation and serum-neutralization assays as well as with those of pathology. Three animals developed clinical signs and lesions typical of MCF, while the other three animals remained clinically healthy. All cattle seroconverted, and viral nucleic acid was detected by DNA hybridization and PCR at various intervals during the observation period. Virus isolation was successful in two of the clinical cases and all cattle seroconverted. Storage of blood samples at 4 degrees C for up to 10 d did not influence the hybridization and DNA-amplification results.
源自实验室减毒的非洲猪瘟病毒1型(AHV-1)毒株WC11以及聚合酶链反应检测(Hsu、Shih、Castro和Zee,1990年)的DNA探针SW15,用于检测6头实验感染牛的恶性卡他热(MCF)病毒DNA。采集肝素化血样,在长达142天的时间内每周至少检测3次。将杂交和PCR检测结果与临床检查结果进行比较,并在不同情况下与病毒分离、血清中和试验结果以及病理学结果进行比较。3头动物出现了典型的MCF临床症状和病变,而其他3头动物临床健康。所有牛均发生血清转化,在观察期内不同时间通过DNA杂交和PCR检测到病毒核酸。在2例临床病例中病毒分离成功,所有牛均发生血清转化。血样在4℃保存长达10天不影响杂交和DNA扩增结果。