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首页> 外文期刊>BMC Microbiology >Identification and characterization of intervening sequences within 23S rRNA genes from more than 200 Campylobacter isolates from seven species including atypical campylobacters
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Identification and characterization of intervening sequences within 23S rRNA genes from more than 200 Campylobacter isolates from seven species including atypical campylobacters

机译:鉴定和鉴定来自7种物种的200多种弯曲杆菌中23S rRNA基因中的插入序列,包括非典型弯曲杆菌

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Background Identification and characterization of intervening sequences (IVSs) within 23S rRNA genes from Campylobacter organisms including atypical campylobacters were carried out using two PCR primer pairs, designed to generate helix 25 and 45 regions. Results Only C. sputorum biovar sputorum LMG7975 and fecalis LMG8531, LMG8534 and LMG6728 of a total of 204 Campylobacter isolates (n = 56 C. jejuni; n = 11 C. coli; n = 33 C. fetus; n = 43 C. upsaliensis; n = 30 C. hyointestinalis; n = 4 C. sputorum biovar sputorum; n = 5 C. sputorum biovar fecalis; n = 5 C. sputorum biovar paraureolyticus; n = 10 C. concisus; n = 7 C. curvus) were shown to carry IVSs in helix 25 region. C. sputorum biovar fecalis LMG8531 and LMG8534, interestingly, carried two different kinds of the 23S rRNA genes with and without the IVS, respectively. Consequently, in a total of 265 isolates of 269, including 65 C. lari isolates examined previously, the absence of IVSs was identified in the helix 25 region. In the helix 45 region, all the C. hyointestinalis, C. sputorum and C. concisus isolates were shown not to carry any IVSs. However, the 30 of 56 C. jejuni isolates (54%), 5 of 11 C. coli (45%), 25 of 33 C. fetus (76%), 30 of 43 C. upsaliensis (70%) and 6 of 7 C. curvus (90%) were shown to carry IVSs. In C. jejuni and C. upsaliensis isolates, two different kinds of the 23S rRNA genes were also identified to occur with and without IVSs in the helix 45 region, respectively. Conclusions Secondary structure models were also constructed with all the IVSs identified in the present study. In the purified RNA fractions from the isolates which carried the 16S or 23S rRNA genes with the IVSs, no 16S or 23S rRNA was evident, respectively.
机译:背景使用两个PCR引物对对来自弯曲杆菌属(包括非典型弯曲杆菌)的23S rRNA基因中的插入序列(IVS)进行鉴定和表征,该引物对设计用于产生25和45螺旋区。结果总共204株弯曲杆菌中仅存在C. sputorum biovar sputorum LMG7975和fecalis LMG8531,LMG8534和LMG6728(n = 56空肠弯曲杆菌; n = 11大肠杆菌; n = 33胎儿; n = 43 C.upsaliensis ; n = 30 C. hyointestinalis; n = 4 C. sputorum biovar sputorum; n = 5 C. sputorum biovar fecalis; n = 5 C. sputorum biovar paraureolyticus; n = 10 C. conconsus; n = 7 C. curvus)显示在螺旋25区携带IVS。有趣的是,C。sputorum biovar fecalis LMG8531和LMG8534分别携带有和没有IVS的两种23S rRNA基因。因此,在总共269个265个分离株中,包括先前检查的65个C. lari分离株,在螺旋25区中鉴定出没有IVS。在螺旋45区,显示所有的豚肠弯曲杆菌,孢子囊弯曲杆菌和结膜弯曲杆菌分离株均不携带任何IVS。但是,空肠弯曲杆菌56株中有30株(54%),11株大肠杆菌5株(45%),33株胎儿25株(76%),43株upsaliensis有30株(70%)和6株显示7个弯曲弯曲杆菌(90%)携带IVS。在空肠弯曲菌和upsaliensis分离株中,还鉴定出两种不同类型的23S rRNA基因分别在螺旋45区有或没有IVS时发生。结论还建立了二级结构模型,并在本研究中确定了所有IVS。在带有带有IVS的带有16S或23S rRNA基因的分离株的纯化RNA级分中,分别没有明显的16S或23S rRNA。

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