Laboratorio de Inmunomicrobiología, Escuela Nacional de Ciencias Biológicas del Instituto Politécnico Nacional, Mexico City, Mexico.
Functional Genomics of Prokaryotes, Center for Genomic Sciences, National Autonomous University of Mexico, Cuernavaca, Mexico.
Arch Microbiol. 2022 Apr 21;204(5):274. doi: 10.1007/s00203-022-02891-0.
The Staphylococcus aureus SdrG protein is glycosylated by SdgA and SdgB for protection against its degradation by the neutrophil cathepsin G. So far, there is no information about the role of Staphylococcus epidermidis SdgA or SdgB in biofilm-forming; therefore, the focus of this work was to determine the distribution and expression of the sdrG, sdgA and sdgB genes in S. epidermidis under in vitro and in vivo biofilm conditions. The frequencies of the sdrG, sdgA and sdgB genes were evaluated by PCR in a collection of 75 isolates. Isolates were grown in dynamic (non-biofilm-forming) or static (biofilm-forming) conditions. The expression of sdrG, sdgA and sdgB was determined by RT-qPCR in cells grown under dynamic conditions (CGDC), as well as in planktonic and sessile cells from a biofilm and cells adhered to a catheter implanted in Balb/c mice. The sdrG and sdgB genes were detected in 100% of isolates, while the sdgA gene was detected in 71% of the sample (p < 0.001). CGDC did not express sdrG, sdgA and sdgB mRNAs. Planktonic and sessile cells expressed sdrG and sdgB, and the same was observed in cells adhered to the catheter. In particular, one isolate, capable of inducing a biofilm under treatment with cathepsin G, expressed sdrG and sdgB in planktonic and sessile cells and cells adhering to the catheter. This suggests that bacteria require biofilm conditions as an important factor for the transcription of the sdgA, sdgB and sdrG genes.
金黄色葡萄球菌 SdrG 蛋白被 SdgA 和 SdgB 糖基化,以防止中性粒细胞组织蛋白酶 G 的降解。到目前为止,还没有关于表皮葡萄球菌 SdgA 或 SdgB 在生物膜形成中的作用的信息;因此,这项工作的重点是确定 sdrG、sdgA 和 sdgB 基因在表皮葡萄球菌在体外和体内生物膜条件下的分布和表达。通过 PCR 评估了 75 株分离株中 sdrG、sdgA 和 sdgB 基因的频率。在动态(非生物膜形成)或静态(生物膜形成)条件下培养分离株。通过 RT-qPCR 确定了在动态条件下生长的细胞(CGDC)中 sdrG、sdgA 和 sdgB 的表达,以及生物膜中的浮游细胞和定殖细胞以及植入 Balb/c 小鼠的导管上粘附的细胞。sdrG 和 sdgB 基因在 100%的分离株中被检测到,而 sdgA 基因在 71%的样本中被检测到(p<0.001)。CGDC 不表达 sdrG、sdgA 和 sdgB mRNAs。浮游细胞和定殖细胞表达 sdrG 和 sdgB,在粘附在导管上的细胞中也观察到了同样的情况。特别是,一株能够在组织蛋白酶 G 处理下诱导生物膜形成的分离株,在浮游细胞和定殖细胞以及粘附在导管上的细胞中表达 sdrG 和 sdgB。这表明细菌需要生物膜条件作为转录 sdgA、sdgB 和 sdrG 基因的重要因素。