Harland N M, Leigh J A, Collins M D
AFRC Institute of Food Research, Reading Laboratory, UK.
J Appl Bacteriol. 1993 May;74(5):526-31.
23S ribosomal RNa (rRNA) gene sequences of Streptococcus uberis and Strep. parauberis were determined by direct polymerase chain reaction (PCR) sequencing. Oligonucleotide probes specific for Strep. uberis and Strep. parauberis were designed from variable regions of the 23S rRNA gene sequence data. Molecular hybridizations with PCR-amplified rRNA gene targets provided a precise and reliable means of differentiating Strep. uberis and Strep. parauberis from each other and from other streptococcal species.
通过直接聚合酶链反应(PCR)测序确定了乳房链球菌和副乳房链球菌的23S核糖体RNA(rRNA)基因序列。根据23S rRNA基因序列数据的可变区设计了针对乳房链球菌和副乳房链球菌的寡核苷酸探针。用PCR扩增的rRNA基因靶标进行分子杂交,为区分乳房链球菌和副乳房链球菌以及它们与其他链球菌物种提供了一种精确而可靠的方法。