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用于肺炎链球菌分子分型的盒式PCR指纹图谱分析

BOX PCR Fingerprinting for Molecular Typing of Streptococcus pneumoniae.

作者信息

van Belkum A, Hermans P W

机构信息

Department of Medical Microbiology and Infectious Diseases, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.

出版信息

Methods Mol Med. 2001;48:159-68. doi: 10.1385/1-59259-077-2:159.

Abstract

A highly conserved repeated DNA element has been identified in the chromosome of Streptococcus pneumoniae (pneumococcus) and given the name of the BOX repetitive element (1). This was the first demonstration of the presence of such a repetitive DNA moiety in a Gram positive bacterial species. Approximately 25 of these elements are found in noncoding regions dispersed throughout the entire pneumococcal genome. The BOX repeat is found to consist of three discriminate regions: boxA, boxB, and boxC, which are 59, 45, and 50 basepairs in length, respectively. Various different combinations of these three elements are found to be present in different BOX loci and limited sequence heterogeneity is encountered among different elements from the same strain or elements sequenced from different strains. The first publication on the BOX repetitive elements also described its intricate secondary structure, supported by compensating basepairing in different loci where the repeat is encountered (see Fig. 1). Moreover, their location in the vicinity of genes involved in the regulation of various aspects of bacterial competence, genetic transformation and virulence suggest that the elements might well be involved in coordination of the control of gene expression. More recently, Saluja and Weiser (2) demonstrated that the presence of a BOX element is associated with variation in colony opacity of the pneumococcus. The frequency with which the colonies switched from transparent to opaque clearly depended on the Fig. 1. Predicted secondary structure of the consensus BOX sequence containing one copy of boxB. The figure is adapted from reference (1). Boxed basepairs indicate interactions that have been supported by phylogenetic comparisons, the basepairs themselves are highlighted by dots. The border between boxA and boxB is at nucleotide position 60, whereas boxB borders boxC at nucleotide 104. The PCR primer locations and the corresponding primer codes can be found in Table 1 . Table 1 Survey of the DNA Sequence for the Different Primers Used in Various Studies on BOX PCR for Typing of Streptococcus pneumoniae Primer Code Sequence 5' →3' Position in Fig. 1 Literature reference boxA1 CGTCAGCGTCGCCTTGCCGTAG 30-51 (5) boxA1R CTACGGCAAGGCGACGCTGACG 51-30 (5,8,9) boxA2R ACGTGGTTTGAAGAGATTTTCG 32-11 (5) boxA ATACTCTTCGAAAATCTCTTCAAAC 3-27 (6,10) boxB1 TTCGTCAGTTCTATCTACAACC 65-86 (5) boxB2 AACCTCAAAACAGTGTTTTGAG 83-104 (5) boxC1 TGCGGCTAGCTTCCTAGTTTGC 110-131 (5) boxC1R AGCAAACTAGGAAGCTAGCCGC 132-111 (5) boxC2 TTGCTCTTTGATTTTCATTGAG 128-149 (5) Note: The primers boxA1R and boxA have been employed most successfully for molecular typing of pneumococci. Although both primers derive from the boxA region there is no overlap in primary structure. Primers boxA1 and boxA1R are each others precise complement, as are primers boxC and boxC1R. See Fig. 1for a precise localisation of some of the primers in the entire BOX element.

摘要

在肺炎链球菌(肺炎球菌)的染色体中已鉴定出一种高度保守的重复DNA元件,并将其命名为BOX重复元件(1)。这是首次证明革兰氏阳性细菌物种中存在这种重复DNA部分。在整个肺炎球菌基因组中分散的非编码区域中发现了大约25个这样的元件。BOX重复序列由三个不同区域组成:boxA、boxB和boxC,其长度分别为59、45和50个碱基对。发现这三个元件的各种不同组合存在于不同的BOX位点,并且在来自同一菌株的不同元件或从不同菌株测序的元件之间遇到有限的序列异质性。关于BOX重复元件的第一篇出版物还描述了其复杂的二级结构,在遇到重复序列的不同位点通过互补碱基配对得到支持(见图1)。此外,它们位于参与细菌感受态、遗传转化和毒力等各个方面调控的基因附近,这表明这些元件很可能参与基因表达调控的协调。最近,萨卢贾和韦泽(2)证明BOX元件的存在与肺炎球菌菌落不透明度的变化有关。菌落从透明转变为不透明的频率显然取决于图1。包含一个boxB拷贝的共有BOX序列的预测二级结构。该图改编自参考文献(1)。带框的碱基对表示通过系统发育比较得到支持的相互作用,碱基对本身用点突出显示。boxA和boxB之间的边界在核苷酸位置60,而boxB在核苷酸104处与boxC接壤。PCR引物位置和相应的引物代码可在表1中找到。表1 用于肺炎链球菌BOX PCR分型的各种研究中使用的不同引物的DNA序列调查引物代码序列5'→3'在图1中的位置文献参考boxA1CGTCAGCGTCGCCTTGCCGTAG30 - 51(5)boxA1RCTACGGCAAGGCGACGCTGACG51 - 30(5,8,9)boxA2RACGTGGTTTGAAGAGATTTTCG32 - 11(5)boxAATACTCTTCGAAAATCTCTTCAAAC3 - 27(6,10)boxB1TTCGTCAGTTCTATCTACAACC65 - 86(5)boxB2AACCTCAAAACAGTGTTTTGAG83 - 104(5)boxC1TGCGGCTAGCTTCCTAGTTTGC110 - 131(5)boxC1RAGCAAACTAGGAAGCTAGCCGC132 - 111(5)boxC2TTGCTCTTTGATTTTCATTGAG128 - 149(5)注意:引物boxA1R和boxA在肺炎球菌的分子分型中最成功。虽然这两种引物都来自boxA区域,但一级结构没有重叠。引物boxA1和boxA1R彼此精确互补,引物boxC和boxC1R也是如此。有关一些引物在整个BOX元件中的精确位置,请见图1。

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