Profile of immunoglobulins, clinical and bacteriological cure after different treatment routes of clinical bovine mastitis

被引:2
作者
Lima, M. G. B. [1 ]
Blagitz, M. G. [1 ]
Souza, F. N. [1 ]
Sanchez, E. M. R. [1 ]
Batista, C. F. [1 ]
Bertagnon, H. G. [1 ,3 ]
Diniz, S. A. [2 ]
Silva, M. X. [2 ]
Della Libera, A. M. M. P. [1 ]
机构
[1] Univ Sao Paulo, Sao Paulo, SP, Brazil
[2] Univ Fed Minas Gerais, Belo Horizonte, MG, Brazil
[3] Univ Ctr Oeste Parana UNICENTRO, Guarapuava, PR, Brazil
关键词
therapy; intramammary infection; humoral immunity; somatic cell count; dairy cow; STAPHYLOCOCCUS-AUREUS MASTITIS; ESCHERICHIA-COLI; MAMMARY-GLAND; DAIRY HERDS; MILK; COWS; EFFICACY; BLOOD; CEFQUINOME; IMMUNITY;
D O I
10.1590/1678-4162-9695
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The present study aimed to evaluate the profile of immunoglobins profile, clinical and bacteriological cure after different treatment routes of clinical bovine mastitis. Here, 30 Holstein cows with clinical mastitis in one quarter were uniformly divided into: 10 dairy cows that received 8.5mg of cefquinome sulphate administrated intramammarily during three consecutive milkings and 2.5mg/kg of enrofloxacin administrated parenterally during three consecutive days (Group 1); 10 dairy cows that received 8.5mg of cefquinome sulphate administrated intramammarily during three consecutive milkings (Group 2); and 10 dairy cows that received 2.5mg/kg of enrofloxacin administrated parenterally during three consecutive days (Group 3). Milk samples for somatic cell count, California Mastitis Test (CMT), bacteriological culture and quantification of IgG(1), IgG(2), IgM and IgA were collected before antimicrobial treatment, and after two, five and 12 days after the antimicrobial treatment. The combined treatment was more effective in the clinical cure rate, reduction of somatic cell count and CMT scores. Furthermore, the results demonstrated that milk concentration of different Igs classes were not related to prognosis of bovine clinical mastitis, and then cannot be considered as robust markers associated with clinical and bacteriological cures.
引用
收藏
页码:1141 / 1149
页数:9
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