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首页> 外文期刊>Tropical Animal Health and Production >A 3-year long study of Staphylococcus aureus isolates from subclinical mastitis in three Azawak zebu herds at the Sahelian experimental farm of Toukounous, Niger
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A 3-year long study of Staphylococcus aureus isolates from subclinical mastitis in three Azawak zebu herds at the Sahelian experimental farm of Toukounous, Niger

机译:在尼日尔Toukounous萨赫勒实验农场的3个Azawak zebu牛群中,从亚临床乳腺炎分离的金黄色葡萄球菌进行了为期3年的研究

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Staphylococcus (S.) aureus is one of the most important pathogens causing bovine mastitis. The aim of the present work was to follow in three herds and during the 3 years the clonality of S. aureus isolated from California Mastitis Test (CMT)-positive cows at the experimental station of Toukounous (Niger) by (i) comparing their pulsed field gel electrophoresis (PFGE) fingerprints, (ii) identifying their virulotypes by PCR amplification and (iii) assessing the production of capsule and the formation of biofilm. The 88 S. aureus isolates belonged to 14 different pulsotypes, 3 of them being predominant: A (30 %), D (27 %), B (15 %). A and B pulsotypes had the highest profile similarity coefficient (94 %), while others had similarity coefficients under 60 %. Seventy-five S. aureus isolates were further studied for their virulotypes, capsular antigens and biofilm production. Most surface factor-, leukocidin- and haemolysin-, but not the enterotoxin-encoding genes were detected in the majority (> 75 %) of the isolates and were evenly distributed between the A, B and D pulsotype isolates. The majority of the 72 S. aureus positive with the cap5H or cap8H PCR produced the CP5 (82 %) or the CP8 (88 %) capsular antigen, respectively. Biofilm production by the 57 icaA-positive isolates was strong for 8 isolates, moderate for 31 isolates but weak for 18 isolates, implying that the icaA gene may not be expressed in vitro by one third of the positive isolates. Similar to other studies, those results confirm that a restricted number of S. aureus clones circulate within the three herds at Toukounous and that their specific virulence-associated properties must still be further studied.
机译:金黄色葡萄球菌是引起牛乳腺炎的最重要的病原体之一。本研究的目的是追踪三只牛群,并在三年中通过以下方法从图克努斯(尼日尔)实验站的加利福尼亚乳腺炎测试(CMT)阳性母牛分离出的金黄色葡萄球菌的克隆性(i)比较它们的脉冲场凝胶电泳(PFGE)指纹,(ii)通过PCR扩增鉴定其病毒型,(iii)评估胶囊的产生和生物膜的形成。 88个金黄色葡萄球菌分离物属于14种不同的脉冲型,其中3种占主导地位:A(30%),D(27%),B(15%)。 A和B脉冲型的轮廓相似性系数最高(94%),而其他人的相似性系数小于60%。进一步研究了75株金黄色葡萄球菌的病毒型,荚膜抗原和生物膜产生。在大多数(> 75%)分离株中检测到大多数表面因子,白细胞介素和溶血素,但未检测到肠毒素编码基因,并在A,B和D脉冲型分离株之间均匀分布。在cap5H或cap8H PCR呈阳性的72株金黄色葡萄球菌中,大多数分别产生CP5(82%)或CP8(88%)荚膜抗原。 57株icaA阳性菌株的生物膜产量对8株菌株呈强势,对31株菌株呈中等,但对18株菌株则弱,这表明icaA基因可能无法在体外被三分之一的阳性菌株表达。与其他研究相似,这些结果证实,在Toukounous的三个牛群中有少量的金黄色葡萄球菌克隆在循环,并且它们与毒力相关的特性还必须进一步研究。

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