Kamiya Regianne Umeko, Höfling José Francisco, Gonçalves Reginaldo Bruno
Department of Oral Diagnosis, Microbiology and Immunology Division, Piracicaba Dental School, Campinas University, Piracicaba, SP, Brazil.
J Med Microbiol. 2008 May;57(Pt 5):626-635. doi: 10.1099/jmm.0.47749-0.
The aim of this study was to analyse the frequency and expression of biosynthesis genes in 47 Streptococcus mutans isolates with different mutacin-producing phenotypes. Detection of the frequency and expression of genes encoding mutacin types I, II, III and IV were carried out by PCR and semi-quantitative RT-PCR, respectively, using primers specific for each type of biosynthesis gene. In addition, a further eight genes encoding putative bacteriocins, designated bsm 283, bsm 299, bsm 423, bsm 1889c, bsm 1892c, bsm 1896, bsm 1906c and bsm 1914, were also screened. There was a high phenotypic diversity; some Streptococcus mutans isolates presented broad antimicrobial spectra against other Streptococcus mutans clinical isolates, including bacteria resistant to common antibiotics, as well as Staphylococcus aureus, Staphylococcus epidermidis, Enterococcus faecalis and Streptococcus pyogenes. The expression frequency of the bsm gene was higher than that of the previously characterized mutacins (I-IV). There was no positive correlation between the number of indicator strains inhibited (antimicrobial spectra) and the number of biosynthesis genes expressed (Spearman correlation test, r=-0.03, P>0.05). In conclusion, the high diversity of mutacin-producing phenotypes, associated with high frequency of expression of the biosynthesis genes screened, reveals a broad repertoire of genetic determinants encoding antimicrobial peptides that can act in different combinations.
本研究的目的是分析47株具有不同变链菌素产生表型的变形链球菌分离株中生物合成基因的频率和表达情况。分别使用针对每种生物合成基因类型的特异性引物,通过PCR和半定量RT-PCR检测编码I型、II型、III型和IV型变链菌素的基因的频率和表达。此外,还筛选了另外8个编码假定细菌素的基因,命名为bsm 283、bsm 299、bsm 423、bsm 1889c、bsm 1892c、bsm 1896、bsm 1906c和bsm 1914。存在高度的表型多样性;一些变形链球菌分离株对其他变形链球菌临床分离株具有广泛的抗菌谱,包括对常用抗生素耐药的细菌,以及金黄色葡萄球菌、表皮葡萄球菌、粪肠球菌和化脓性链球菌。bsm基因的表达频率高于先前鉴定的变链菌素(I-IV)。被抑制的指示菌株数量(抗菌谱)与表达的生物合成基因数量之间没有正相关(Spearman相关性检验,r=-0.03,P>0.05)。总之,产生变链菌素表型的高度多样性,与所筛选的生物合成基因的高表达频率相关,揭示了编码抗菌肽的广泛遗传决定因素库,这些抗菌肽可以以不同组合发挥作用。