Department of Basic Sciences, Division of Microbiology and Molecular Genetics, School of Medicine, Loma Linda University, Loma Linda, CA 92354, USA.
FEMS Microbiol Lett. 2010 Nov;312(1):24-32. doi: 10.1111/j.1574-6968.2010.02093.x. Epub 2010 Aug 27.
Extracytoplasmic function (ECF) sigma factors are known to play an important role in the bacterial response to various environmental stresses and can significantly modulate their pathogenic potential. In the genome of Porphyromonas gingivalis W83, six putative ECF sigma factors were identified. To further evaluate their role in this organism, a PCR-based linear transformation method was used to inactivate five ECF sigma factor genes (PG0162, PG0214, PG0985, PG1660, and PG1827) by allelic exchange mutagenesis. All five isogenic mutants formed black-pigmented colonies on blood agar. Mutants defective in PG0985, PG1660, and PG1827 genes were more sensitive to 0.25 mM of hydrogen peroxide compared with the wild-type strain. Isogenic mutants of PG0162 and PG1660 showed a 50% decrease in gingipain activity. Reverse transcription-PCR analysis showed that there was no alteration in the expression of rgpA, rgpB, and kgp gingipain genes in these mutants. Hemolytic and hemagglutination activities were decreased by more than 50% in the PG0162 mutant compared with the wild type. Taken together, these findings suggest that ECF sigma factors can modulate important virulence factors in P. gingivalis. ECF sigma factors encoded by the PG0162 and PG1660 genes might also be involved in the post-transcriptional regulation of the gingipains.
细胞外功能(ECF)σ因子在细菌对各种环境应激的反应中起着重要作用,并能显著调节其致病潜能。在牙龈卟啉单胞菌 W83 的基因组中,鉴定出了六个推定的 ECFσ因子。为了进一步评估它们在该生物体中的作用,使用基于 PCR 的线性转化方法通过等位基因交换诱变使五个 ECFσ因子基因(PG0162、PG0214、PG0985、PG1660 和 PG1827)失活。所有五个同基因突变体在血琼脂上形成黑色色素菌落。与野生型菌株相比,PG0985、PG1660 和 PG1827 基因缺陷型突变体对 0.25mM 过氧化氢更敏感。PG0162 和 PG1660 的同基因突变体的牙龈蛋白酶活性降低了 50%。逆转录-PCR 分析表明,这些突变体中 rgpA、rgpB 和 kgp 牙龈蛋白酶基因的表达没有改变。与野生型相比,PG0162 突变体的溶血和红细胞凝集活性降低了 50%以上。总之,这些发现表明 ECFσ因子可以调节牙龈卟啉单胞菌中的重要毒力因子。PG0162 和 PG1660 基因编码的 ECFσ因子也可能参与了牙龈蛋白酶的转录后调节。