Callister S M, Case K L, Agger W A, Schell R F, Johnson R C, Ellingson J L
Microbiology Research Laboratory, Gundersen Medical Foundation, La Crosse, Wisconsin.
J Clin Microbiol. 1990 Feb;28(2):363-5. doi: 10.1128/jcm.28.2.363-365.1990.
The ability of decreasing inocula of Borrelia burgdorferi to grow in otherwise identical Barbour-Stoenner-Kelly (BSK) media containing different lots of bovine serum albumin (fraction V) was determined. These media differed significantly in ability to detect B. burgdorferi. Some BSK media required inocula of 2 x 10(5) organisms per ml for detection, while other media could stimulate growth after inoculation with less than 2 organisms per ml. In addition, organisms from the less sensitive BSK media were thinner, longer, and less tightly coiled. The endpoint dilutions of indirect fluorescent-antibody titers, especially immunoglobulin M, exhibited up to 16-fold decreases, and both immunoglobulin G and M titers were more difficult to interpret with diagnostic slides prepared from some longer, thinner B. burgdorferi. These results demonstrate that, when performing laboratory investigations which rely on B. burgdorferi, it is essential that the quality of the BSK medium be determined.
测定了伯氏疏螺旋体接种量降低时在其他方面相同但含有不同批次牛血清白蛋白(第V组分)的巴伯-斯托纳-凯利(BSK)培养基中的生长能力。这些培养基在检测伯氏疏螺旋体的能力上有显著差异。一些BSK培养基检测时每毫升需要接种2×10⁵个菌体,而其他培养基接种每毫升少于2个菌体后就能刺激生长。此外,来自敏感性较低的BSK培养基的菌体更细、更长且螺旋更松散。间接荧光抗体效价的终点稀释倍数,尤其是免疫球蛋白M,最多降低了16倍,并且用一些更长、更细的伯氏疏螺旋体制备诊断玻片时,免疫球蛋白G和M的效价都更难解读。这些结果表明,在进行依赖伯氏疏螺旋体的实验室研究时,确定BSK培养基的质量至关重要。