Hale J D F, Balakrishnan Balakrishnan, Tagg J R
Department of Microbiology,University of Otago, Dunedin, New Zealand.
Indian J Med Res. 2004 May;119 Suppl:247-51.
BACKGROUND & OBJECTIVES: The mutans streptococci (MS) are a group of 7 species of dental cariesassociated bacteria of which Streptococcus mutans and Streptococcus sobrinus are the most important in humans. Many MS produce bacteriocin-like inhibitory substances (BLIS), some of which have been characterised as small peptides capable of inhibiting the growth of closely-related species. These peptides have most commonly been referred to as mutacins. S. mutans strains N and UA140 appear to have closely similar BLIS activities. Both produce mutacins that seem to target the same species of bacteria. On closer analysis however, these two strains have been shown to produce distinctly different mutacins, known as mutacin N and mutacin I respectively. In the present study the mutacin N structural gene (mutN) was cloned and compared with the mutacin I structural gene (mutA).
Cloning and sequencing of S. mutans N was done. The distribution of mutN using DNA from 216 streptococcal strains was determined by dot blotting.
Mut N was cloned and sequenced from an 1800 bp Bam HI/Eco RI fragment. PCR with the mutN primers mutNF and mutNR on the four mutN-positive strains identified identical bands to S. mutans N. The location of mutN differs significantly from that of mutA in that it is directly upstream of comC, a gene encoding a putative competence stimulating factor.
INTERPRETATION & CONCLUSION: The close upstream proximity of mutN to comC suggests a link between mutacin N production and competence development. Further studies need to be done to detect competence-related genes in S. mutans strain N.
变形链球菌(MS)是一组7种与龋齿相关的细菌,其中变形链球菌和远缘链球菌在人类中最为重要。许多MS会产生类细菌素抑制物质(BLIS),其中一些已被鉴定为能够抑制密切相关菌种生长的小肽。这些肽最常被称为变链菌素。变形链球菌菌株N和UA140似乎具有非常相似的BLIS活性。两者都产生似乎靶向相同细菌种类的变链菌素。然而,经过更仔细的分析,已证明这两种菌株产生明显不同的变链菌素,分别称为变链菌素N和变链菌素I。在本研究中,克隆了变链菌素N结构基因(mutN)并与变链菌素I结构基因(mutA)进行比较。
对变形链球菌N进行克隆和测序。通过斑点杂交测定使用来自216株链球菌菌株的DNA的mutN分布。
从一个1800 bp的Bam HI/Eco RI片段中克隆并测序了Mut N。用mutN引物mutNF和mutNR对四个mutN阳性菌株进行PCR,鉴定出与变形链球菌N相同的条带。mutN的位置与mutA的位置有显著差异,因为它直接位于comC的上游,comC是一个编码假定的感受态刺激因子的基因。
mutN在comC上游的紧密相邻表明变链菌素N的产生与感受态发展之间存在联系。需要进一步研究以检测变形链球菌菌株N中的感受态相关基因。