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一种用于预防母羊衣原体流产的商业疫苗的临床评估。

Clinical evaluation of a commercial vaccine against chlamydial abortion of ewes.

作者信息

Rodolakis A, Souriau A

出版信息

Ann Rech Vet. 1979;10(1):41-8.

PMID:539776
Abstract

The immunity of ewes vaccinated prior to breeding with an adjuvant vaccine prepared from yolk sac propagated chlamydiae, was challenged at 70 days of pregnancy by intravenous (IV) or intradermal (ID) inoculation of a suspension of virulent yolk sac propagated chlamydiae. The response to challenge inoculation was followed by recording rectal temperature, CF antibody titer, lambing performance and by chlamydial isolation from vaginal swabs. That vaccine did not protect against IV challenge: 7 of 10 vaccinated ewes, and 7 of 8 controls aborted. When the challenge was given by the ID route, the incidence of abortion was reduced: 4 of 9 vaccinated, and 9 of 9 control ewes aborted, but chlamydiae were isolated from vaginal swabs of 7 of the 9 vaccinated ewes.

摘要

在配种前用由卵黄囊繁殖的衣原体制备的佐剂疫苗接种的母羊,在怀孕70天时通过静脉注射(IV)或皮内注射(ID)接种毒力强的卵黄囊繁殖衣原体悬浮液来进行免疫挑战。通过记录直肠温度、CF抗体效价、产羔性能以及从阴道拭子中分离衣原体来跟踪对挑战接种的反应。该疫苗不能预防静脉注射挑战:10只接种疫苗的母羊中有7只,8只对照母羊中有7只流产。当通过皮内途径进行挑战时,流产发生率降低:9只接种疫苗的母羊中有4只,9只对照母羊中有9只流产,但9只接种疫苗的母羊中有7只的阴道拭子中分离出了衣原体。

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