Institute of Medical Microbiology and Hospital Hygiene, University of Rostock, Schillingallee 70, 18057, Rostock, Germany.
BMC Genomics. 2012 Oct 13;13:550. doi: 10.1186/1471-2164-13-550.
Small non-coding RNAs (sRNAs) have attracted attention as a new class of gene regulators in both eukaryotes and bacteria. Genome-wide screening methods have been successfully applied in Gram-negative bacteria to identify sRNA regulators. Many sRNAs are well characterized, including their target mRNAs and mode of action. In comparison, little is known about sRNAs in Gram-positive pathogens. In this study, we identified novel sRNAs in the exclusively human pathogen Streptococcus pyogenes M49 (Group A Streptococcus, GAS M49), employing a whole genome intergenic tiling array approach. GAS is an important pathogen that causes diseases ranging from mild superficial infections of the skin and mucous membranes of the naso-pharynx, to severe toxic and invasive diseases.
We identified 55 putative sRNAs in GAS M49 that were expressed during growth. Of these, 42 were novel. Some of the newly-identified sRNAs belonged to one of the common non-coding RNA families described in the Rfam database. Comparison of the results of our screen with the outcome of two recently published bioinformatics tools showed a low level of overlap between putative sRNA genes. Previously, 40 potential sRNAs have been reported to be expressed in a GAS M1T1 serotype, as detected by a whole genome intergenic tiling array approach. Our screen detected 12 putative sRNA genes that were expressed in both strains. Twenty sRNA candidates appeared to be regulated in a medium-dependent fashion, while eight sRNA genes were regulated throughout growth in chemically defined medium. Expression of candidate genes was verified by reverse transcriptase-qPCR. For a subset of sRNAs, the transcriptional start was determined by 5' rapid amplification of cDNA ends-PCR (RACE-PCR) analysis.
In accord with the results of previous studies, we found little overlap between different screening methods, which underlines the fact that a comprehensive analysis of sRNAs expressed by a given organism requires the complementary use of different methods and the investigation of several environmental conditions. Despite a high conservation of sRNA genes within streptococci, the expression of sRNAs appears to be strain specific.
小非编码 RNA(sRNAs)作为真核生物和细菌中新的一类基因调控因子引起了关注。全基因组筛选方法已成功应用于革兰氏阴性菌,以鉴定 sRNA 调控因子。许多 sRNAs 已经得到了很好的描述,包括它们的靶 mRNA 和作用模式。相比之下,革兰氏阳性病原体中的 sRNAs 知之甚少。在这项研究中,我们采用全基因组基因间平铺阵列方法,鉴定了专性人类病原体酿脓链球菌 M49(A 组链球菌,GAS M49)中的新型 sRNAs。GAS 是一种重要的病原体,可引起从轻度皮肤和鼻咽喉黏膜浅表感染到严重毒性和侵袭性疾病的各种疾病。
我们在 GAS M49 的生长过程中鉴定了 55 个推定的 sRNAs,其中 42 个是新的。新鉴定的 sRNAs 中的一些属于 Rfam 数据库中描述的常见非编码 RNA 家族之一。我们的筛选结果与最近发表的两种生物信息学工具的结果进行比较,结果显示推定的 sRNA 基因之间的重叠程度较低。此前,通过全基因组基因间平铺阵列方法,已在 GAS M1T1 血清型中检测到 40 个潜在的 sRNA 表达。我们的筛选检测到在两种菌株中表达的 12 个推定 sRNA 基因。20 个 sRNA 候选基因似乎呈培养基依赖性调节,而 8 个 sRNA 基因在化学定义培养基中的生长过程中受到调节。通过逆转录 qPCR 验证候选基因的表达。通过 5' 快速扩增 cDNA 末端-PCR(RACE-PCR)分析,确定了一部分 sRNA 的转录起始点。
与先前研究的结果一致,我们发现不同筛选方法之间的重叠很少,这强调了一个事实,即全面分析给定生物体表达的 sRNAs 需要互补使用不同的方法,并研究几种环境条件。尽管链球菌中的 sRNA 基因高度保守,但 sRNA 的表达似乎是菌株特异性的。