Puig de Centorbi O N, de Cuadrado A M, Alcaraz L E, Laciar A L, de Milán M C
Cátedra de Bacteriología II, Facultad de Química Bioquímica y Farmacia, Universidad Nacional de San Luis, Argentina.
Rev Argent Microbiol. 1992 Apr-Jun;24(2):73-80.
In order to detect subclinical mastitis by means of California Mastitis Test and recounting of somatic cells, 163 cows from the dairies of San Luis city, Argentina, were examined. Seventy six individuals (46.6%) exhibited an inflammatory response ranging > or = 2+ grade and a cellular recounting value of > or = 5 x 10(5), data compatible with those of subclinical mastitis. Staphylococcus aureus was isolated from 39 (51.3%) cultures as estimated by the sum of the two last values listed in Table 1. Organisms were isolated by plating on brain heart infusion agar with 5% of sheep blood and on Baird-Parker media. One hundred and three S. aureus isolates recovered from 51 of 63 cows were characterized by coagulase activity by the tube method using human and bovine plasma; clumping factor; glucose and mannitol fermentation; thermonuclease (TNase), pigment, gelatinase, fibrinolysin, acetoin, hemolysin production; egg yolk, tellurite and catalase reaction and crystal violet types. All isolates were susceptible to cephalothin, clindamycin, methicillin, gentamycin and vancomycin; 94.1% were susceptible to chloramphenicol and 53.8% to G penicillin. Sixty three isolates (61.1%) were classified according to Hájek and Marsálek scheme as biotype C (bovine and ovine ecovar), 33 isolates (32.0%) were classified as biotype B (swine and poultry ecovar); 1 isolated (0.9%) as intermediate between B and D; 5 isolates (4.8%) as biotype A (human ecovar) and 1 isolated (0.9%) as biotype D (ecovar silvestres spp) (Table 2). Production of enterotoxins A to E and toxic shock syndrome toxin-1 (TSST-1) was determined by the optimal susceptibility plate method on 27 isolates (26.2%) which were coagulase 3+ to 4+ and TNase highly positive. None of them produced enterotoxins including TSST-1. The subclinical mastitis data and the prevalence of S. aureus coincide with those of other authors, both from Argentina and from other countries.
为了通过加利福尼亚乳房炎检测法和体细胞计数来检测亚临床型乳腺炎,对来自阿根廷圣路易斯市奶牛场的163头奶牛进行了检查。76头奶牛(46.6%)表现出炎症反应,等级≥2+,体细胞计数值≥5×10⁵,这些数据与亚临床型乳腺炎的数据相符。根据表1中列出的最后两个值的总和估计,从39份(51.3%)培养物中分离出了金黄色葡萄球菌。通过接种在含5%绵羊血的脑心浸液琼脂和贝尔德-帕克培养基上分离出这些微生物。从63头奶牛中的51头奶牛身上分离出的103株金黄色葡萄球菌,通过使用人血浆和牛血浆的试管法检测凝固酶活性、聚集因子、葡萄糖和甘露醇发酵、耐热核酸酶(TNase)、色素、明胶酶、纤维蛋白溶酶、3-羟基丁酮、溶血素产生情况、蛋黄、亚碲酸盐和过氧化氢酶反应以及结晶紫类型进行鉴定。所有分离株对头孢噻吩、克林霉素、甲氧西林、庆大霉素和万古霉素敏感;94.1%对氯霉素敏感,53.8%对G青霉素敏感。根据哈杰克和马尔萨克方案,63株分离株(61.1%)被分类为生物型C(牛和羊生态变种),33株分离株(32.0%)被分类为生物型B(猪和家禽生态变种);1株分离株(0.9%)被分类为B和D之间的中间型;5株分离株(4.8%)被分类为生物型A(人生态变种),1株分离株(0.9%)被分类为生物型D(野生生态变种)(表2)。通过最佳敏感性平板法对27株凝固酶为3+至4+且TNase高度阳性的分离株(26.2%)检测了A至E型肠毒素和中毒性休克综合征毒素-1(TSST-1)的产生情况。它们均未产生包括TSST-1在内的肠毒素。亚临床型乳腺炎数据和金黄色葡萄球菌的流行情况与来自阿根廷和其他国家的其他作者的数据一致。