Amram Eytan, Borovok Ilya, Nachum-Biala Yaarit, Ayling Roger, Lerner Uri, Harrus Shimon, Lysnyansky Inna
Mycoplasma Unit, Division of Avian and Aquatic Diseases, Kimron Veterinary Institute, Beit Dagan, Israel Koret School of Veterinary Medicine, The Hebrew University of Jerusalem, Rehovot, Israel.
Department of Molecular Microbiology and Biotechnology, Tel Aviv University, Tel Aviv, Israel.
Appl Environ Microbiol. 2016 Oct 14;82(21):6386-6394. doi: 10.1128/AEM.01628-16. Print 2016 Nov 1.
Insertion sequences (ISs) are widespread in the genome of Mycoplasma bovis strain PG45, but no ISs were identified within its two tandemly positioned rRNA operons (rrn1 and rrn2). However, characterization of the rrn locus in 70 M. bovis isolates revealed the presence of ISs related to the ISMbov1 (IS30 family) and ISMbov4 (IS4 family) isomers in 35 isolates. ISs were inserted into intergenic region 1 (IGR-1) or IGR-3, which are the putative promoter regions of rrn1 and rrn2, respectively, and into IGR-5, located downstream of the rrl2 gene. Seven different configurations (A to G) of the rrn locus with respect to ISs were identified, including those in five annotated genomes. The transcriptional start site for the single rrn operon in M. bovis strain 88127 was mapped within IGR-1, 60 bp upstream of the rrs gene. Notably, only 1 nucleotide separated the direct repeat (DR) for ISMbov1 and the promoter -35 element in configuration D, while in configuration F, the -35 motif was a part of the ISMbov1 DR. Relative quantitative real-time (qRT) PCR analysis and growth rate comparisons detected a significant increase (P < 0.05) in the expression of the rrs genes and in the number of viable cells during log phase growth (8, 12, and 16 h) in the strains with configuration F in comparison to strains with one or two rrn operons that did not have ISs. A high prevalence of IS elements within or close to the M. bovis rrn operon-promoter region may reflect their important role in regulation of both ribosome synthesis and function.
Data presented in this study show a high prevalence of diverse ISs within the M. bovis rrn locus resulting in intraspecies variability and diversity. Such abundance of IS elements near or within the rrn locus may offer a selective advantage to M. bovis Moreover, the fact that expression of the rrs genes as well as the number of viable cells increased in the group of strains with IS element insertion within a putative promoter -35 sequence (configuration F) in comparison to that in strains with one or two rrn operons that do not have ISs may serve as a basis for understanding the possible role of M. bovis IS elements in fundamental biological processes such as regulation of ribosome synthesis and function.
插入序列(ISs)在牛支原体PG45菌株的基因组中广泛存在,但在其两个串联排列的rRNA操纵子(rrn1和rrn2)中未发现ISs。然而,对70株牛支原体分离株rrn位点的特征分析显示,35株分离株中存在与ISMbov1(IS30家族)和ISMbov4(IS4家族)异构体相关的ISs。ISs插入到基因间隔区1(IGR-1)或IGR-3中,它们分别是rrn1和rrn2的假定启动子区域,以及插入到位于rrl2基因下游的IGR-5中。鉴定出rrn位点相对于ISs的七种不同构型(A至G),包括五个注释基因组中的构型。牛支原体88127菌株中单个rrn操纵子的转录起始位点定位在IGR-1内,rrs基因上游60 bp处。值得注意的是,在构型D中,ISMbov1的直接重复序列(DR)与启动子-35元件仅相隔1个核苷酸,而在构型F中,-35基序是ISMbov1 DR的一部分。相对定量实时(qRT)PCR分析和生长速率比较检测到,与没有ISs的一个或两个rrn操纵子的菌株相比,构型F的菌株在对数生长期(8、12和16小时)rrs基因的表达和活细胞数量显著增加(P<0.05)。牛支原体rrn操纵子启动子区域内或附近IS元件的高流行率可能反映了它们在核糖体合成和功能调控中的重要作用。
本研究提供的数据表明,牛支原体rrn位点内多种ISs的高流行率导致种内变异性和多样性。rrn位点附近或内部如此丰富的IS元件可能为牛支原体提供了选择优势。此外,与没有ISs的一个或两个rrn操纵子的菌株相比,在假定启动子-35序列(构型F)内插入IS元件的菌株组中rrs基因的表达以及活细胞数量增加,这一事实可能为理解牛支原体IS元件在核糖体合成和功能调控等基本生物学过程中的可能作用提供依据。