van Belkum A, Scherer S, van Leeuwen W, Willemse D, van Alphen L, Verbrugh H
Department of Bacteriology, University Hospital Rotterdam, The Netherlands.
Infect Immun. 1997 Dec;65(12):5017-27. doi: 10.1128/iai.65.12.5017-5027.1997.
An algorithm capable of identifying short repeat motifs was developed and used to screen the whole genome sequence available for Haemophilus influenzae, since some of these repeats have been shown to affect bacterial virulence. Various di- to hexanucleotide repeats were identified, confirming and extending previous findings on the existence of variable-number-of-tandem-repeat loci (VNTRs). Repeats with units of 7 or 8 nucleotides were not encountered. For all of the 3- to 6-nucleotide repeats in the H. influenzae chromosome, PCR tests capable of detecting allelic polymorphisms were designed. Fourteen of 18 of the potential VNTRs were indeed highly polymorphic when different strains were screened. Two of the potential VNTRs appeared to be short and homogeneous in length; another one may be specific for the H. influenzae Rd strain only. One of the primer sets generated fingerprint-type DNA banding patterns. The various repeat types differed with respect to intrinsic stability as well. It was noted for separate colonies derived from a single clinical specimen or strains passaged for several weeks on chocolate agar plates that the lengths of the VNTRs did not change. When several strains from different patients infected during an outbreak of lung disease were analyzed, increased but limited variation was encountered in all VNTR sites analyzed. One of the 5-nucleotide VNTRs proved to be hypervariable. This variability may reflect the molecular basis of a mechanism used by H. influenzae bacteria to successfully colonize and infect different human individuals.
开发了一种能够识别短重复基序的算法,并用于筛选流感嗜血杆菌的全基因组序列,因为其中一些重复序列已被证明会影响细菌毒力。鉴定出了各种二核苷酸至六核苷酸重复序列,证实并扩展了先前关于串联重复序列可变数目的位点(VNTR)存在的研究结果。未发现具有7或8个核苷酸单位的重复序列。对于流感嗜血杆菌染色体中的所有3至6核苷酸重复序列,设计了能够检测等位基因多态性的PCR检测方法。在筛选不同菌株时,18个潜在的VNTR中有14个确实具有高度多态性。其中两个潜在的VNTR似乎较短且长度均匀;另一个可能仅对流感嗜血杆菌Rd菌株具有特异性。一组引物产生了指纹型DNA条带模式。各种重复类型在内在稳定性方面也有所不同。对于来自单个临床标本的分离菌落或在巧克力琼脂平板上传代数周的菌株,发现VNTR的长度没有变化。当分析在肺部疾病暴发期间感染的不同患者的几种菌株时,在所有分析的VNTR位点都遇到了增加但有限的变异。其中一个5核苷酸VNTR被证明是高度可变的。这种变异性可能反映了流感嗜血杆菌成功定殖和感染不同人类个体所使用机制的分子基础。