Landin Håkan, Mörk Marie Jansson, Larsson Maria, Waller Karin Persson
Växa Sverige, SE-104 25, Stockholm, Sweden.
Evidensia Djurkliniken Näset, SE-236 32, Höllviken, Sweden.
Acta Vet Scand. 2015 Nov 25;57:81. doi: 10.1186/s13028-015-0171-6.
Staphylococcus aureus is a common udder pathogen in dairy cows, and may cause severe mastitis problems in some herds. In herds where normal control measures are not successful, vaccination might be an additional tool to use if sufficiently efficient. The aim of the present study was to evaluate the efficacy of a commercially available vaccine (Startvac(®), Hipra, Spain) in two commercial Swedish dairy herds where the control programs for S. aureus mastitis had been unsuccessful. Within each herd cows were randomly assigned to vaccine or control groups, and effects on udder health and milk production during 120 days after calving, and survival during the following lactation were evaluated.
A field study was performed in two high producing Swedish herds having approximately 600 (herd A) and 200 (herd B) cows. During 12 months, cows with odd numbers were vaccinated three times around calving according to label protocol, while cows with even numbers constituted the not vaccinated control group. Quarter milk samples for bacteriological culturing were collected from all cases of clinical and subclinical mastitis. The outcome was evaluated during 120 days after calving using data on SCC and daily milk yield at monthly milk recordings, and incidence of mastitis due to S. aureus, coagulase-negative staphylococci, streptococci and coliforms. Cow survival throughout lactation was also studied. In herd A, 239 and 240 cows were included in the vaccinated and control groups, respectively. Corresponding numbers for herd B was 126 and 151 cows. Significant differences between vaccinated and control groups were not found in any of the parameters investigated.
Vaccination with a commercial polyvalent vaccine did not have any beneficial effects on udder health, milk production or survival in two commercial dairy herds with mastitis problems due to S. aureus.
金黄色葡萄球菌是奶牛常见的乳房病原体,在某些牛群中可能导致严重的乳腺炎问题。在常规控制措施未成功的牛群中,如果疫苗足够有效,接种疫苗可能是一种额外的手段。本研究的目的是评估一种市售疫苗(Startvac(®),西班牙喜普生物)在瑞典两个商业奶牛群中的效果,这两个牛群的金黄色葡萄球菌乳腺炎控制计划均未成功。在每个牛群中,奶牛被随机分配到疫苗组或对照组,并评估产犊后120天内对乳房健康和产奶量的影响,以及随后泌乳期的存活率。
在瑞典两个高产牛群中进行了一项实地研究,牛群A约有600头奶牛,牛群B约有200头奶牛。在12个月期间,奇数编号的奶牛在产犊前后按照标签说明接种三次疫苗,而偶数编号的奶牛组成未接种疫苗的对照组。从所有临床和亚临床乳腺炎病例中采集四分位牛奶样本进行细菌培养。使用每月牛奶记录中的体细胞计数(SCC)和每日产奶量数据,以及由金黄色葡萄球菌、凝固酶阴性葡萄球菌、链球菌和大肠菌群引起的乳腺炎发病率,在产犊后120天内评估结果。还研究了整个泌乳期奶牛的存活率。在牛群A中,疫苗组和对照组分别纳入了239头和240头奶牛。牛群B的相应数字分别为126头和151头奶牛。在所研究的任何参数中,疫苗组和对照组之间均未发现显著差异。
在两个因金黄色葡萄球菌导致乳腺炎问题的商业奶牛群中,接种一种商业多价疫苗对乳房健康、产奶量或存活率没有任何有益影响。