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用于分离流产布鲁氏菌RB51菌株的选择性培养基。

Selective media for isolation of Brucella abortus strain RB51.

作者信息

Hornsby R L, Jensen A E, Olsen S C, Thoen C O

机构信息

Zoonotic Diseases Research Unit, National Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, 2300 Dayton Ave., Ames, IA 50010, USA.

出版信息

Vet Microbiol. 2000 Apr 4;73(1):51-60. doi: 10.1016/s0378-1135(00)00149-8.

Abstract

Brucella abortus strain RB51 (SRB51) is the standard vaccine used to protect cattle against brucellosis and is currently being used to vaccinate bison in the United States (US). Currently available media for culture of Brucella have not been evaluated for their ability to support growth of SRB51. In this study, five selective media for isolating brucellae, four commercially available media for gram-negative bacteria, and tryptose agar with 5% bovine serum (TSA) were compared to two SRB51 selective media developed in this study (rifampin brucellae medium (RBM), and malachite green brucellae medium (MGB)), for their ability to support growth and enhance recovery of SRB51. Four of the five media currently used for isolation of brucellae and two of the four media used for other Gram-negative bacteria did not support growth of SRB51. Modified Kuzdas and Morse (MKM), Brilliant Green, Skirrow's, RBM, and MGB supported growth of SRB51 in a manner similar to TSA. Recovery of SRB51 from tissues of SRB51-vaccinated bison was attempted on TSA, MKM, RBM, and MGB. From a total of 436 samples, SRB51 was isolated from 9.6, 4.3, 5.5, and 9.0% on TSA, MKM, RBM, or MGB media, respectively. Strain RB51 was recovered on only one medium (nine on TSA; three on RBM; and 9 on MGB) from 21 samples. Overgrowth of contaminating bacteria prevented potential detection of SRB51 from 9. 4, 5.5, 0.07, and 5.9% of samples on TSA, MKM, RBM, or MGB, respectively. These data suggest that the use of RBM and MGB, in combination with TSA, enhances the ability to recover SRB51 from tissue samples.

摘要

布鲁氏菌流产菌株RB51(SRB51)是用于保护牛免受布鲁氏菌病侵害的标准疫苗,目前正在美国用于给野牛接种疫苗。目前可用于培养布鲁氏菌的培养基尚未评估其支持SRB51生长的能力。在本研究中,将五种用于分离布鲁氏菌的选择性培养基、四种市售的革兰氏阴性菌培养基以及含5%牛血清的胰蛋白胨琼脂(TSA)与本研究开发的两种SRB51选择性培养基(利福平布鲁氏菌培养基(RBM)和孔雀石绿布鲁氏菌培养基(MGB))进行比较,以评估它们支持SRB51生长和提高其回收率的能力。目前用于分离布鲁氏菌的五种培养基中的四种以及用于其他革兰氏阴性菌的四种培养基中的两种不支持SRB51生长。改良的库兹达斯和莫尔斯培养基(MKM)、亮绿培养基、斯基罗培养基、RBM和MGB支持SRB51生长的方式与TSA相似。尝试在TSA、MKM、RBM和MGB上从接种SRB51的野牛组织中回收SRB51。在总共436个样本中,分别在TSA、MKM、RBM或MGB培养基上从9.6%、4.3%、5.5%和9.0%的样本中分离出SRB51。从21个样本中仅在一种培养基上回收了RB51菌株(TSA上9个;RBM上3个;MGB上9个)。污染菌的过度生长分别阻止了在TSA、MKM、RBM或MGB上从9.4%、5.5%、0.07%和5.9%的样本中检测到潜在的SRB51。这些数据表明,将RBM和MGB与TSA联合使用可提高从组织样本中回收SRB51的能力。

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