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关于一种抗乳房炎无乳链球菌活疫苗效力的进一步研究。

Further studies on the efficacy of a live vaccine against mastitis caused by Streptococcus uberis.

作者信息

Finch J M, Winter A, Walton A W, Leigh J A

机构信息

Institute for Animal Health, Compton Laboratory, Berks., UK.

出版信息

Vaccine. 1997 Jul;15(10):1138-43. doi: 10.1016/s0264-410x(96)00307-6.

Abstract

Three groups of dairy cows were immunized by subcutaneous (s.c.) administration of a preparation of live Streptococcus uberis (strain 0140J) and an intramammary infusion of a soluble surface extract derived from same the bacteria. Animals in Groups 1 and 2 received two s.c. vaccinations plus an intramammary inoculation. Animals in Group 3 received two s.c. vaccinations but did not receive the intramammary infusion. In addition to the vaccinated animals, each group also contained two non-vaccinated (control) animals. All animals were challenged experimentally by intramammary infusion (in two quarters per animal) of ca 100 c.f.u. of S. uberis (strain 0140J or C221) and monitored for clinical signs of disease, bacterial numbers in milk, somatic cell count in milk, and daily milk yield for the following 10 days. Animals in Group I were challenged with strain 0140J. Only one out of six challenged quarters of three vaccinated cows developed clinical disease compared to all (four out of four) quarters of non-vaccinated cows. Animals in Group 2 were challenged with strain C221. All challenged quarters of three vaccinated (six out of six) and two non-vaccinated (four out of four) cows developed clinical mastitis. Animals in Group 3 were challenged with strain 0140J. Five out of eight quarters on four vaccinated cows developed clinical mastitis but the onset was delayed in comparison with that in both non-vaccinated cows in which four out of four challenged quarters developed clinical mastitis. These results indicated that vaccination with live S. uberis protects against challenge with the homologous strain but was less effective against a heterologous strain. Reduced protection was also seen when the intramammary booster was omitted.

摘要

三组奶牛通过皮下注射活的乳房链球菌(菌株0140J)制剂以及乳房内注入源自相同细菌的可溶性表面提取物进行免疫。第1组和第2组的动物接受两次皮下接种加一次乳房内接种。第3组的动物接受两次皮下接种,但未接受乳房内注入。除了接种疫苗的动物外,每组还包含两只未接种疫苗的(对照)动物。所有动物通过乳房内注入(每只动物两个乳腺)约100 c.f.u.的乳房链球菌(菌株0140J或C221)进行实验性攻毒,并在接下来的10天内监测疾病的临床症状、牛奶中的细菌数量、牛奶中的体细胞计数和每日产奶量。第I组的动物用菌株0140J进行攻毒。与未接种疫苗的奶牛的所有(四分之四)乳腺相比,三只接种疫苗的奶牛的六个攻毒乳腺中只有一个出现临床疾病。第2组的动物用菌株C221进行攻毒。三只接种疫苗的奶牛的所有攻毒乳腺(六分之六)和两只未接种疫苗的奶牛的所有攻毒乳腺(四分之四)都发生了临床乳腺炎。第3组的动物用菌株0140J进行攻毒。四只接种疫苗的奶牛的八个乳腺中有五个发生了临床乳腺炎,但与未接种疫苗的奶牛相比,发病时间延迟,未接种疫苗的奶牛的四个攻毒乳腺中有四个发生了临床乳腺炎。这些结果表明,用活的乳房链球菌接种疫苗可预防同源菌株的攻毒,但对异源菌株的效果较差。省略乳房内加强接种时也观察到保护作用降低。

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